Other mutations in this stock |
Total: 221 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700001K19Rik |
TTC |
TTCATC |
12: 110,634,881 (GRCm39) |
|
probably benign |
Het |
1700001K19Rik |
TTC |
TTCGTC |
12: 110,634,884 (GRCm39) |
|
probably benign |
Het |
Abt1 |
TTCTTGCT |
TT |
13: 23,607,881 (GRCm39) |
|
probably benign |
Het |
AI837181 |
GGC |
GGCCGC |
19: 5,475,257 (GRCm39) |
|
probably benign |
Het |
Akap12 |
AAA |
AAACAA |
10: 4,303,837 (GRCm39) |
|
probably benign |
Het |
Alg1 |
GCTCACTCAC |
GCTCAC |
16: 5,062,425 (GRCm39) |
|
probably null |
Homo |
Alg9 |
G |
GCGA |
9: 50,686,731 (GRCm39) |
|
probably benign |
Het |
Amfr |
GCC |
GCCGGCGCGAGCTCC |
8: 94,738,920 (GRCm39) |
|
probably benign |
Het |
Anapc2 |
TGGCGGTGGCGGCGGCGGCGGCGGCGGCGG |
TGGCGGCGGCGGCGGCGG |
2: 25,162,544 (GRCm39) |
|
probably benign |
Het |
Anxa7 |
C |
T |
14: 20,519,479 (GRCm39) |
G113E |
probably damaging |
Homo |
Apc |
AATAAAGC |
AATAAAGCCTATAAAGC |
18: 34,415,053 (GRCm39) |
|
probably benign |
Het |
Apc |
CCAATAAAG |
CCAATAAAGTCAATAAAG |
18: 34,415,051 (GRCm39) |
|
probably benign |
Het |
Apc |
AAGC |
AAGCCAATATAGC |
18: 34,415,057 (GRCm39) |
|
probably null |
Het |
Atad3a |
C |
A |
4: 155,838,396 (GRCm39) |
R207L |
probably damaging |
Homo |
Blm |
ACCT |
ACCTCCCT |
7: 80,113,515 (GRCm39) |
|
probably benign |
Homo |
Blm |
TCCTCCTCCTCCTCCTCCTCCTCC |
TCCTCCTCCTCCACCTCCTCCTCCTCCTCCTCCTCC |
7: 80,162,655 (GRCm39) |
|
probably benign |
Het |
Bmp5 |
GAGGAGT |
G |
9: 75,683,657 (GRCm39) |
|
probably benign |
Homo |
Bpifa6 |
A |
T |
2: 153,828,296 (GRCm39) |
Q134L |
probably benign |
Homo |
Bpifa6 |
A |
T |
2: 153,828,318 (GRCm39) |
R141S |
probably benign |
Homo |
Btnl10 |
AGA |
AGAGGA |
11: 58,814,755 (GRCm39) |
|
probably benign |
Homo |
Cacna1a |
ACC |
ACCGCC |
8: 85,365,346 (GRCm39) |
|
probably benign |
Het |
Cacna1a |
ACC |
ACCTCC |
8: 85,365,355 (GRCm39) |
|
probably benign |
Het |
Calhm1 |
TGGCTGTGGCTG |
TGGCTGTGGCTGCGGCTGTGGCTG |
19: 47,129,701 (GRCm39) |
|
probably benign |
Het |
Catsper2 |
TGTC |
TGTCGTC |
2: 121,228,260 (GRCm39) |
|
probably benign |
Homo |
Catsper2 |
C |
CTTTTACTTTTTT |
2: 121,228,023 (GRCm39) |
|
probably benign |
Homo |
Catsper2 |
ATCGTCGTCGTC |
ATCGTCGTCGTCGTC |
2: 121,228,276 (GRCm39) |
|
probably benign |
Het |
Catsper2 |
CAT |
CATTAT |
2: 121,228,263 (GRCm39) |
|
probably benign |
Het |
Ccdc170 |
ACCGCC |
ACCGCCGCC |
10: 4,511,008 (GRCm39) |
|
probably benign |
Het |
Ccdc170 |
AC |
ACCTC |
10: 4,511,029 (GRCm39) |
|
probably benign |
Het |
Ccdc170 |
ACC |
ACCGCC |
10: 4,511,023 (GRCm39) |
|
probably benign |
Het |
Ccnk |
TTCCCAC |
T |
12: 108,168,766 (GRCm39) |
|
probably benign |
Het |
Cdx1 |
GGGCTGC |
GGGCTGCGGCTGC |
18: 61,152,939 (GRCm39) |
|
probably benign |
Het |
Cdx1 |
GCTGCT |
GCTGCTTCTGCT |
18: 61,152,941 (GRCm39) |
|
probably benign |
Het |
Cep112 |
G |
GCTCT |
11: 108,316,178 (GRCm39) |
|
probably benign |
Het |
Cep89 |
GACT |
G |
7: 35,109,066 (GRCm39) |
|
probably benign |
Het |
Cfap46 |
CCTTCT |
CCTTCTTCT |
7: 139,218,846 (GRCm39) |
|
probably benign |
Homo |
Chd4 |
GC |
GCTCCCTC |
6: 125,099,094 (GRCm39) |
|
probably benign |
Homo |
Cluh |
GCCTGA |
GCCTGAACCTGA |
11: 74,560,346 (GRCm39) |
|
probably benign |
Het |
Cnpy3 |
CCT |
CCTACT |
17: 47,047,673 (GRCm39) |
|
probably null |
Het |
Cntnap1 |
CCCAGC |
CCCAGCACCAGC |
11: 101,080,398 (GRCm39) |
|
probably benign |
Het |
Cntnap1 |
CCAGCC |
CCAGCCTCAGCC |
11: 101,080,411 (GRCm39) |
|
probably benign |
Het |
Cntnap1 |
GCCCCA |
GCCCCACCCCCA |
11: 101,080,414 (GRCm39) |
|
probably benign |
Het |
Cntnap1 |
A |
ACCCCCC |
11: 101,080,395 (GRCm39) |
|
probably benign |
Het |
Col4a3 |
CGTTTTTTTTTTTTTTTT |
C |
1: 82,696,627 (GRCm39) |
|
probably null |
Het |
Cpne1 |
AGA |
AGAGAGA |
2: 155,913,945 (GRCm39) |
|
probably null |
Homo |
Cracdl |
C |
A |
1: 37,664,117 (GRCm39) |
E594* |
probably null |
Homo |
Cracdl |
A |
G |
1: 37,664,183 (GRCm39) |
S47P |
probably damaging |
Homo |
Cracdl |
T |
A |
1: 37,664,116 (GRCm39) |
E594V |
probably benign |
Homo |
Ctsm |
AGTG |
AGTGGGTG |
13: 61,685,650 (GRCm39) |
|
probably null |
Homo |
Cttnbp2 |
GCTGCT |
GCTGCTTCTGCT |
6: 18,367,466 (GRCm39) |
|
probably benign |
Het |
Cttnbp2 |
GCTGCT |
GCTGCTCCTGCT |
6: 18,367,460 (GRCm39) |
|
probably benign |
Het |
Cul9 |
TCC |
TCCGCC |
17: 46,811,776 (GRCm39) |
|
probably benign |
Het |
Cul9 |
TCC |
TCCCCC |
17: 46,811,779 (GRCm39) |
|
probably benign |
Het |
Cul9 |
TCC |
TCCCCC |
17: 46,811,782 (GRCm39) |
|
probably benign |
Het |
Cul9 |
CTTC |
CTTCTTC |
17: 46,811,774 (GRCm39) |
|
probably benign |
Het |
Cybrd1 |
GAAT |
G |
2: 70,968,855 (GRCm39) |
|
probably benign |
Homo |
Dbr1 |
AGGAGG |
AGGAGGCGGAGG |
9: 99,465,742 (GRCm39) |
|
probably benign |
Het |
Dbr1 |
AGGAGG |
AGGAGGCGGAGG |
9: 99,465,745 (GRCm39) |
|
probably benign |
Het |
Dbr1 |
AGG |
AGGAGGCGG |
9: 99,465,754 (GRCm39) |
|
probably benign |
Het |
Dbr1 |
GG |
GGAGGAAG |
9: 99,465,755 (GRCm39) |
|
probably benign |
Het |
Dcaf8 |
C |
T |
1: 172,000,423 (GRCm39) |
H194Y |
probably damaging |
Homo |
Dennd10 |
ACTC |
ACTCCTC |
19: 60,803,056 (GRCm39) |
|
probably benign |
Homo |
Dennd10 |
T |
TTCA |
19: 60,803,060 (GRCm39) |
|
probably benign |
Homo |
Dnaaf9 |
C |
CTCG |
2: 130,612,673 (GRCm39) |
|
probably benign |
Het |
Dnaaf9 |
TCC |
TCCCCC |
2: 130,612,659 (GRCm39) |
|
probably benign |
Het |
Dnaaf9 |
TCC |
TCCACC |
2: 130,612,662 (GRCm39) |
|
probably benign |
Het |
Dnajc19 |
AC |
ACGC |
3: 34,112,143 (GRCm39) |
|
probably null |
Het |
Dthd1 |
GAC |
GACTAC |
5: 63,000,367 (GRCm39) |
|
probably benign |
Homo |
Dusp10 |
G |
T |
1: 183,769,253 (GRCm39) |
C73F |
probably damaging |
Homo |
Eif3a |
A |
ATTTTT |
19: 60,763,729 (GRCm39) |
|
probably benign |
Homo |
Ermn |
CTT |
CTTGTT |
2: 57,938,092 (GRCm39) |
|
probably benign |
Het |
Ermn |
TC |
TCTAC |
2: 57,938,100 (GRCm39) |
|
probably benign |
Het |
Fbxo38 |
TGCAGC |
TGC |
18: 62,648,418 (GRCm39) |
|
probably benign |
Het |
Frem3 |
CT |
CTTGT |
8: 81,341,870 (GRCm39) |
|
probably benign |
Homo |
Gabre |
T |
TGAGGCC |
X: 71,314,028 (GRCm39) |
|
probably benign |
Homo |
Gabre |
AGGCT |
AGGCTGCGGCT |
X: 71,314,024 (GRCm39) |
|
probably benign |
Homo |
Gm10800 |
A |
AC |
2: 98,497,378 (GRCm39) |
|
probably null |
Homo |
Gm14393 |
T |
G |
2: 174,903,613 (GRCm39) |
N98T |
probably benign |
Het |
Gm16503 |
G |
A |
4: 147,625,710 (GRCm39) |
G68E |
unknown |
Het |
Gm28040 |
TG |
TGGCACCTTTCGAG |
1: 133,255,061 (GRCm39) |
|
probably benign |
Homo |
Gm4340 |
AGC |
AGCCGC |
10: 104,031,940 (GRCm39) |
|
probably benign |
Het |
Gm6309 |
C |
T |
5: 146,104,993 (GRCm39) |
V307I |
probably benign |
Het |
Golga5 |
G |
A |
12: 102,441,919 (GRCm39) |
|
probably null |
Homo |
Gpatch11 |
AGGAA |
AGGAAGTGGAA |
17: 79,149,609 (GRCm39) |
|
probably benign |
Het |
Gpatch11 |
GAGGAA |
GAGGAATAGGAA |
17: 79,149,602 (GRCm39) |
|
probably null |
Het |
Gpatch11 |
AGAGGA |
AGAGGATGAGGA |
17: 79,149,601 (GRCm39) |
|
probably benign |
Het |
Gpatch11 |
AAGAGG |
AAGAGGCAGAGG |
17: 79,149,600 (GRCm39) |
|
probably benign |
Het |
Gpatch11 |
GAAGAG |
GAAGAGCAAGAG |
17: 79,149,599 (GRCm39) |
|
probably benign |
Het |
H2-K2 |
GTTT |
G |
17: 34,216,016 (GRCm39) |
|
probably benign |
Homo |
Hcn1 |
GCAGC |
GCAGCGACAGC |
13: 118,112,344 (GRCm39) |
|
probably benign |
Homo |
Hoxa10 |
T |
A |
6: 52,211,166 (GRCm39) |
Q250L |
possibly damaging |
Homo |
Igf1r |
C |
CTGGAGATGGAGA |
7: 67,875,934 (GRCm39) |
|
probably benign |
Het |
Igf1r |
TGGAGC |
TGGAGCTGGAGAGGGAGC |
7: 67,875,929 (GRCm39) |
|
probably benign |
Het |
Il17rd |
CGG |
CGGTGG |
14: 26,804,634 (GRCm39) |
|
probably benign |
Het |
Il2 |
GG |
GGGGCTTGAAGTAG |
3: 37,179,978 (GRCm39) |
|
probably benign |
Het |
Ipo9 |
TCC |
TCCCCC |
1: 135,314,019 (GRCm39) |
|
probably benign |
Het |
Iqcc |
T |
TGTCAGCCTCCTTGTACCC |
4: 129,510,469 (GRCm39) |
|
probably benign |
Het |
Irag2 |
CACATTG |
CACATTGAGGACATTG |
6: 145,119,511 (GRCm39) |
|
probably benign |
Homo |
Isg20l2 |
AAG |
AAGTAG |
3: 87,839,022 (GRCm39) |
|
probably null |
Het |
Kcng4 |
G |
T |
8: 120,360,258 (GRCm39) |
Y39* |
probably null |
Homo |
Kmt2b |
CCTCCT |
CCTCCTACTCCT |
7: 30,285,789 (GRCm39) |
|
probably null |
Het |
Kmt2b |
TCCTCC |
TCCTCCACCTCC |
7: 30,285,791 (GRCm39) |
|
probably benign |
Het |
Kmt2b |
CCTCCT |
CCTCCTGCTCCT |
7: 30,285,798 (GRCm39) |
|
probably benign |
Het |
Kmt2b |
TCCTCC |
TCCTCCCCCTCC |
7: 30,285,785 (GRCm39) |
|
probably benign |
Het |
Kmt2b |
CTCCTC |
CTCCTCGTCCTC |
7: 30,285,787 (GRCm39) |
|
probably benign |
Het |
Kmt2c |
TGCTGCTGCTGTTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCT |
TGCTGCTGCTGCTGCTGTTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCT |
5: 25,520,761 (GRCm39) |
|
probably benign |
Homo |
Krtap9-3 |
AC |
ACAGGTGCCTC |
11: 99,488,830 (GRCm39) |
|
probably benign |
Homo |
Las1l |
A |
AGGC |
X: 94,984,439 (GRCm39) |
|
probably benign |
Het |
Las1l |
AGG |
AGGGGG |
X: 94,984,433 (GRCm39) |
|
probably benign |
Het |
Las1l |
GA |
GAGAA |
X: 94,984,438 (GRCm39) |
|
probably benign |
Het |
Lce1m |
TGCCAC |
TGCCACTGCTGCAGCCAC |
3: 92,925,455 (GRCm39) |
|
probably benign |
Het |
Leo1 |
GGTACCATGCAG |
GG |
9: 75,357,854 (GRCm39) |
|
probably benign |
Het |
Lrit3 |
CATA |
CATAAATA |
3: 129,597,559 (GRCm39) |
|
probably benign |
Homo |
Mamld1 |
GCA |
GCAACA |
X: 70,162,424 (GRCm39) |
|
probably benign |
Het |
Mamld1 |
GCAACA |
GCAACAACA |
X: 70,162,418 (GRCm39) |
|
probably benign |
Het |
Mast4 |
TGG |
TGGGGGCGG |
13: 102,872,820 (GRCm39) |
|
probably benign |
Het |
Mast4 |
GGACAAGCTGTGAGTTGGGGAACCCGGGAG |
GG |
13: 102,875,755 (GRCm39) |
|
probably null |
Homo |
Med12l |
GCA |
GCACCA |
3: 59,183,398 (GRCm39) |
|
probably benign |
Het |
Mn1 |
CAG |
CAGAAG |
5: 111,567,568 (GRCm39) |
|
probably benign |
Het |
Morf4l2 |
T |
C |
X: 135,634,371 (GRCm39) |
K286E |
probably benign |
Het |
Msantd4 |
A |
T |
9: 4,384,937 (GRCm39) |
I221F |
possibly damaging |
Homo |
Mup21 |
TT |
TTTTTATATACT |
4: 62,067,587 (GRCm39) |
|
probably benign |
Het |
Nacad |
C |
CAGGGTA |
11: 6,549,763 (GRCm39) |
|
probably benign |
Het |
Nacad |
A |
ACCAGGG |
11: 6,549,749 (GRCm39) |
|
probably benign |
Het |
Nacad |
TCAGGG |
TCAGGGACAGGG |
11: 6,549,756 (GRCm39) |
|
probably benign |
Het |
Nars1 |
CCACTCAC |
CCAC |
18: 64,643,516 (GRCm39) |
|
probably benign |
Homo |
Ndufc2 |
C |
T |
7: 97,049,481 (GRCm39) |
P29L |
probably damaging |
Het |
Nkx2-6 |
C |
T |
14: 69,412,678 (GRCm39) |
T282M |
probably damaging |
Homo |
Noc2l |
CTG |
CTGGTG |
4: 156,324,555 (GRCm39) |
|
probably benign |
Het |
Noc2l |
AGGC |
AGGCGGC |
4: 156,324,549 (GRCm39) |
|
probably benign |
Homo |
Nolc1 |
AGC |
AGCAGCAGCGGC |
19: 46,069,814 (GRCm39) |
|
probably benign |
Het |
Nolc1 |
CAG |
CAGAAGCAGAAG |
19: 46,069,795 (GRCm39) |
|
probably benign |
Het |
Or10j2 |
GGGCTGCTTGTGGCAAT |
G |
1: 173,098,197 (GRCm39) |
|
probably null |
Het |
Or51f1e |
T |
TTAC |
7: 102,747,516 (GRCm39) |
|
probably benign |
Homo |
Or51v8 |
AG |
AGAGG |
7: 103,320,173 (GRCm39) |
|
probably benign |
Homo |
Or52b4 |
A |
AAACCG |
7: 102,184,888 (GRCm39) |
|
probably null |
Homo |
Or5af2 |
T |
A |
11: 58,708,266 (GRCm39) |
V144D |
possibly damaging |
Homo |
Patl2 |
GCT |
GCTTCT |
2: 121,956,622 (GRCm39) |
|
probably benign |
Het |
Patl2 |
CTG |
CTGGTG |
2: 121,956,620 (GRCm39) |
|
probably benign |
Het |
Patl2 |
C |
CTGA |
2: 121,956,626 (GRCm39) |
|
probably benign |
Het |
Patl2 |
GC |
GCTTC |
2: 121,956,625 (GRCm39) |
|
probably benign |
Het |
Pdik1l |
ACCACC |
ACCACCCCCACC |
4: 134,006,817 (GRCm39) |
|
probably benign |
Homo |
Phc1 |
TG |
TGCTGCGG |
6: 122,300,559 (GRCm39) |
|
probably benign |
Het |
Phf3 |
ACTGCCGCTCCCGCTCC |
AC |
1: 30,844,104 (GRCm39) |
|
probably benign |
Het |
Pick1 |
TTC |
TTCTC |
15: 79,140,146 (GRCm39) |
|
probably null |
Homo |
Piezo1 |
G |
A |
8: 123,222,308 (GRCm39) |
R503W |
probably damaging |
Homo |
Pik3ap1 |
AG |
AGGGG |
19: 41,270,384 (GRCm39) |
|
probably benign |
Homo |
Pik3c2g |
AGAGG |
AGAGGGAGG |
6: 139,612,652 (GRCm39) |
|
probably null |
Homo |
Pitrm1 |
TTTTA |
T |
13: 6,610,632 (GRCm39) |
|
probably benign |
Homo |
Pogz |
GTAAT |
G |
3: 94,782,006 (GRCm39) |
|
probably benign |
Het |
Ppp1r3f |
C |
A |
X: 7,426,575 (GRCm39) |
G562V |
probably damaging |
Homo |
Ppp2r5c |
G |
T |
12: 110,507,172 (GRCm39) |
|
probably null |
Homo |
Prag1 |
CCGC |
CCGCCGC |
8: 36,571,037 (GRCm39) |
|
probably benign |
Homo |
Prr13 |
CTC |
CTCTTC |
15: 102,370,611 (GRCm39) |
|
probably benign |
Homo |
Prr13 |
CACT |
CACTACT |
15: 102,370,606 (GRCm39) |
|
probably benign |
Homo |
Ptms |
TCT |
TCTCCT |
6: 124,891,417 (GRCm39) |
|
probably benign |
Homo |
Ptpn23 |
G |
T |
9: 110,216,701 (GRCm39) |
P1052T |
probably benign |
Homo |
Raph1 |
GG |
GGGGG |
1: 60,528,426 (GRCm39) |
|
probably benign |
Homo |
Rpa1 |
TGCTGCC |
T |
11: 75,209,345 (GRCm39) |
|
probably benign |
Het |
Rpgrip1 |
GGA |
GGATGA |
14: 52,386,851 (GRCm39) |
|
probably benign |
Het |
Rpgrip1 |
GGAAGAAGA |
GGA |
14: 52,387,001 (GRCm39) |
|
probably benign |
Het |
Rps19 |
AGCGG |
AG |
7: 24,588,421 (GRCm39) |
|
probably benign |
Homo |
Rsf1 |
G |
GACC |
7: 97,229,116 (GRCm39) |
|
probably benign |
Homo |
Serpina3m |
A |
G |
12: 104,324,882 (GRCm39) |
|
probably null |
Homo |
Setd1a |
TGGTGGTGGT |
TGGTGGTGGTGGTGGTGGT |
7: 127,384,479 (GRCm39) |
|
probably benign |
Homo |
Setd1a |
TAGTGGTGG |
TAGTGGTGGGAGTGGTGG |
7: 127,384,488 (GRCm39) |
|
probably benign |
Het |
Sfswap |
ACTCAGCCC |
ACTCAGCCCCCTCAGCCC |
5: 129,646,815 (GRCm39) |
|
probably benign |
Het |
Sh3pxd2b |
GCCTGT |
GCCTGTGCCTGT |
11: 32,373,060 (GRCm39) |
|
probably benign |
Homo |
Sh3pxd2b |
CCTGTG |
CCTGTGTCTGTG |
11: 32,373,055 (GRCm39) |
|
probably benign |
Het |
Shroom4 |
GCAGCAACA |
GCA |
X: 6,536,128 (GRCm39) |
|
probably benign |
Het |
Six3 |
GCG |
GCGTCG |
17: 85,928,786 (GRCm39) |
|
probably benign |
Het |
Six3 |
CG |
CGGGG |
17: 85,928,799 (GRCm39) |
|
probably benign |
Het |
Skint8 |
C |
T |
4: 111,796,099 (GRCm39) |
L258F |
probably benign |
Homo |
Smoc2 |
AGTT |
A |
17: 14,621,824 (GRCm39) |
|
probably benign |
Homo |
Smpx |
CCCCCA |
C |
X: 156,503,920 (GRCm39) |
|
probably benign |
Homo |
Snx1 |
C |
CTTT |
9: 66,012,212 (GRCm39) |
|
probably benign |
Homo |
Snx1 |
TC |
TCTGC |
9: 66,012,211 (GRCm39) |
|
probably benign |
Homo |
Sp110 |
CT |
CTAAT |
1: 85,515,210 (GRCm39) |
|
probably benign |
Het |
Spaca1 |
CGCTCT |
CGCTCTTGCTCT |
4: 34,049,849 (GRCm39) |
|
probably benign |
Het |
Spaca1 |
GCTCTC |
GCTCTCCCTCTC |
4: 34,049,844 (GRCm39) |
|
probably benign |
Het |
Spag17 |
GGA |
GGACGA |
3: 99,963,571 (GRCm39) |
|
probably benign |
Het |
Spag17 |
AGG |
AGGTGG |
3: 99,963,570 (GRCm39) |
|
probably benign |
Het |
Srebf2 |
G |
T |
15: 82,069,536 (GRCm39) |
A693S |
probably damaging |
Homo |
Sry |
T |
TGGG |
Y: 2,662,841 (GRCm39) |
|
probably benign |
Homo |
Stard8 |
AGG |
AGGTGG |
X: 98,110,119 (GRCm39) |
|
probably benign |
Het |
Stard8 |
AGG |
AGGTGG |
X: 98,110,131 (GRCm39) |
|
probably benign |
Het |
Stk10 |
CCCA |
C |
11: 32,564,520 (GRCm39) |
|
probably benign |
Homo |
Tap2 |
ACTG |
ACTGCTG |
17: 34,424,673 (GRCm39) |
|
probably benign |
Homo |
Tbc1d5 |
G |
C |
17: 51,106,959 (GRCm39) |
H532Q |
probably benign |
Homo |
Tbc1d5 |
C |
G |
17: 51,106,971 (GRCm39) |
Q528H |
probably benign |
Homo |
Tfeb |
GCA |
GCAACA |
17: 48,097,019 (GRCm39) |
|
probably benign |
Het |
Tmcc1 |
G |
A |
6: 116,170,341 (GRCm39) |
|
probably benign |
Homo |
Tob1 |
AGC |
AGCCGC |
11: 94,105,298 (GRCm39) |
|
probably benign |
Het |
Tpsab1 |
TTGCACCTCCT |
TT |
17: 25,562,756 (GRCm39) |
|
probably benign |
Het |
Trav15-2-dv6-2 |
GAA |
GAATAA |
14: 53,887,211 (GRCm39) |
|
probably null |
Het |
Trav15-2-dv6-2 |
G |
GAAC |
14: 53,887,214 (GRCm39) |
|
probably benign |
Homo |
Trim16 |
GTGA |
GTGATGA |
11: 62,711,515 (GRCm39) |
|
probably benign |
Homo |
Tsbp1 |
AGC |
AGCGGC |
17: 34,679,032 (GRCm39) |
|
probably benign |
Het |
Tsbp1 |
AGC |
AGCGGC |
17: 34,679,035 (GRCm39) |
|
probably benign |
Het |
Tsen2 |
AGG |
AGGCGG |
6: 115,537,027 (GRCm39) |
|
probably benign |
Homo |
Ubtf |
TC |
TCCGC |
11: 102,197,785 (GRCm39) |
|
probably benign |
Het |
Vmn1r124 |
G |
T |
7: 20,993,861 (GRCm39) |
Q228K |
possibly damaging |
Het |
Vmn1r71 |
A |
C |
7: 10,482,048 (GRCm39) |
S147R |
probably benign |
Homo |
Vmn2r99 |
G |
A |
17: 19,614,547 (GRCm39) |
G756R |
probably damaging |
Homo |
Vps13b |
G |
T |
15: 35,847,103 (GRCm39) |
A2629S |
probably damaging |
Homo |
Wdr75 |
AAATAA |
AAA |
1: 45,862,564 (GRCm39) |
|
probably benign |
Homo |
Zfp111 |
T |
G |
7: 23,898,462 (GRCm39) |
K383T |
probably damaging |
Homo |
Zfp111 |
A |
ATCG |
7: 23,899,232 (GRCm39) |
|
probably benign |
Homo |
Zfp26 |
C |
A |
9: 20,349,842 (GRCm39) |
A241S |
probably benign |
Homo |
Zfp282 |
CGG |
CGGTGG |
6: 47,881,724 (GRCm39) |
|
probably benign |
Het |
Zfp335 |
TCC |
TCCACC |
2: 164,749,398 (GRCm39) |
|
probably benign |
Het |
Zfp335 |
CTC |
CTCTTC |
2: 164,749,394 (GRCm39) |
|
probably benign |
Het |
Zfp459 |
A |
AGTGG |
13: 67,556,395 (GRCm39) |
|
probably null |
Homo |
Zfp459 |
TGA |
TGAGAGA |
13: 67,556,393 (GRCm39) |
|
probably null |
Homo |
Zfp459 |
GA |
GAGTTA |
13: 67,556,394 (GRCm39) |
|
probably null |
Homo |
Zfp462 |
ACC |
ACCTCAGCCACAGCCGCC |
4: 55,009,760 (GRCm39) |
|
probably benign |
Het |
Zfp462 |
CC |
CCTCAGCCACAGCCATC |
4: 55,009,761 (GRCm39) |
|
probably benign |
Het |
Zfp598 |
CCACAGGC |
CC |
17: 24,898,346 (GRCm39) |
|
probably benign |
Het |
Zfp598 |
ACCACC |
ACCACCCCCACC |
17: 24,899,756 (GRCm39) |
|
probably benign |
Het |
Zfp683 |
AG |
AGGGG |
4: 133,786,190 (GRCm39) |
|
probably benign |
Homo |
Zpld2 |
TG |
TGCCG |
4: 133,929,941 (GRCm39) |
|
probably benign |
Homo |
|
Other mutations in Fsip2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00094:Fsip2
|
APN |
2 |
82,820,730 (GRCm39) |
missense |
probably benign |
0.18 |
IGL00557:Fsip2
|
APN |
2 |
82,821,657 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL01343:Fsip2
|
APN |
2 |
82,830,163 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL01387:Fsip2
|
APN |
2 |
82,823,326 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL01523:Fsip2
|
APN |
2 |
82,807,863 (GRCm39) |
missense |
probably benign |
|
IGL01554:Fsip2
|
APN |
2 |
82,807,622 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL01650:Fsip2
|
APN |
2 |
82,821,430 (GRCm39) |
missense |
probably benign |
0.33 |
IGL01809:Fsip2
|
APN |
2 |
82,808,691 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL01826:Fsip2
|
APN |
2 |
82,812,983 (GRCm39) |
missense |
probably benign |
0.18 |
IGL01830:Fsip2
|
APN |
2 |
82,815,273 (GRCm39) |
missense |
probably benign |
|
IGL01918:Fsip2
|
APN |
2 |
82,822,482 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL01932:Fsip2
|
APN |
2 |
82,824,349 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL01989:Fsip2
|
APN |
2 |
82,824,211 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02096:Fsip2
|
APN |
2 |
82,822,204 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL02153:Fsip2
|
APN |
2 |
82,809,065 (GRCm39) |
missense |
probably benign |
|
IGL02155:Fsip2
|
APN |
2 |
82,828,696 (GRCm39) |
missense |
probably benign |
|
IGL02219:Fsip2
|
APN |
2 |
82,808,174 (GRCm39) |
missense |
probably benign |
0.07 |
IGL02248:Fsip2
|
APN |
2 |
82,813,116 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL02316:Fsip2
|
APN |
2 |
82,809,137 (GRCm39) |
missense |
probably benign |
|
IGL02478:Fsip2
|
APN |
2 |
82,814,736 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02504:Fsip2
|
APN |
2 |
82,809,199 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL02572:Fsip2
|
APN |
2 |
82,822,347 (GRCm39) |
missense |
probably benign |
0.32 |
IGL02625:Fsip2
|
APN |
2 |
82,779,836 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02665:Fsip2
|
APN |
2 |
82,823,407 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02668:Fsip2
|
APN |
2 |
82,828,662 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02676:Fsip2
|
APN |
2 |
82,812,501 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL02717:Fsip2
|
APN |
2 |
82,781,370 (GRCm39) |
splice site |
probably benign |
|
IGL02805:Fsip2
|
APN |
2 |
82,823,839 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02943:Fsip2
|
APN |
2 |
82,822,701 (GRCm39) |
missense |
probably benign |
0.32 |
IGL02965:Fsip2
|
APN |
2 |
82,813,398 (GRCm39) |
missense |
probably benign |
0.33 |
IGL03001:Fsip2
|
APN |
2 |
82,820,968 (GRCm39) |
intron |
probably benign |
|
IGL03076:Fsip2
|
APN |
2 |
82,812,482 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL03229:Fsip2
|
APN |
2 |
82,808,420 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL03353:Fsip2
|
APN |
2 |
82,807,737 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL03401:Fsip2
|
APN |
2 |
82,820,814 (GRCm39) |
missense |
probably benign |
|
bubblegum
|
UTSW |
2 |
82,823,184 (GRCm39) |
missense |
probably benign |
0.16 |
Dao
|
UTSW |
2 |
82,823,494 (GRCm39) |
missense |
probably damaging |
0.97 |
engulf
|
UTSW |
2 |
82,815,120 (GRCm39) |
missense |
probably damaging |
0.98 |
envelope
|
UTSW |
2 |
82,811,085 (GRCm39) |
missense |
probably benign |
0.07 |
gladius
|
UTSW |
2 |
82,812,293 (GRCm39) |
missense |
possibly damaging |
0.68 |
glove
|
UTSW |
2 |
82,808,738 (GRCm39) |
missense |
possibly damaging |
0.85 |
Katana
|
UTSW |
2 |
82,819,860 (GRCm39) |
missense |
probably benign |
0.07 |
scarf
|
UTSW |
2 |
82,817,235 (GRCm39) |
missense |
probably benign |
|
Sock
|
UTSW |
2 |
82,828,524 (GRCm39) |
missense |
probably benign |
0.00 |
swaddle
|
UTSW |
2 |
82,813,772 (GRCm39) |
missense |
possibly damaging |
0.93 |
wrap
|
UTSW |
2 |
82,817,164 (GRCm39) |
missense |
probably benign |
0.04 |
Wrapper
|
UTSW |
2 |
82,820,430 (GRCm39) |
missense |
possibly damaging |
0.71 |
D4186:Fsip2
|
UTSW |
2 |
82,818,756 (GRCm39) |
missense |
probably benign |
0.32 |
FR4976:Fsip2
|
UTSW |
2 |
82,814,709 (GRCm39) |
critical splice acceptor site |
probably benign |
|
PIT4382001:Fsip2
|
UTSW |
2 |
82,821,196 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0017:Fsip2
|
UTSW |
2 |
82,822,416 (GRCm39) |
missense |
probably damaging |
0.98 |
R0017:Fsip2
|
UTSW |
2 |
82,822,416 (GRCm39) |
missense |
probably damaging |
0.98 |
R0021:Fsip2
|
UTSW |
2 |
82,830,201 (GRCm39) |
splice site |
probably benign |
|
R0054:Fsip2
|
UTSW |
2 |
82,817,299 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0054:Fsip2
|
UTSW |
2 |
82,817,299 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0054:Fsip2
|
UTSW |
2 |
82,806,952 (GRCm39) |
missense |
probably damaging |
0.96 |
R0104:Fsip2
|
UTSW |
2 |
82,809,317 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0104:Fsip2
|
UTSW |
2 |
82,809,317 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0127:Fsip2
|
UTSW |
2 |
82,815,269 (GRCm39) |
missense |
probably benign |
0.28 |
R0131:Fsip2
|
UTSW |
2 |
82,821,465 (GRCm39) |
missense |
probably benign |
|
R0149:Fsip2
|
UTSW |
2 |
82,805,849 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0167:Fsip2
|
UTSW |
2 |
82,811,151 (GRCm39) |
missense |
possibly damaging |
0.53 |
R0190:Fsip2
|
UTSW |
2 |
82,815,521 (GRCm39) |
missense |
possibly damaging |
0.73 |
R0323:Fsip2
|
UTSW |
2 |
82,816,240 (GRCm39) |
missense |
probably benign |
0.33 |
R0358:Fsip2
|
UTSW |
2 |
82,813,677 (GRCm39) |
missense |
possibly damaging |
0.56 |
R0361:Fsip2
|
UTSW |
2 |
82,805,849 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0369:Fsip2
|
UTSW |
2 |
82,814,908 (GRCm39) |
missense |
probably benign |
0.33 |
R0394:Fsip2
|
UTSW |
2 |
82,821,419 (GRCm39) |
missense |
possibly damaging |
0.70 |
R0532:Fsip2
|
UTSW |
2 |
82,808,129 (GRCm39) |
missense |
probably benign |
0.33 |
R0595:Fsip2
|
UTSW |
2 |
82,777,296 (GRCm39) |
missense |
probably damaging |
0.99 |
R0613:Fsip2
|
UTSW |
2 |
82,824,139 (GRCm39) |
missense |
probably damaging |
0.99 |
R0614:Fsip2
|
UTSW |
2 |
82,807,877 (GRCm39) |
missense |
probably benign |
0.15 |
R0619:Fsip2
|
UTSW |
2 |
82,774,484 (GRCm39) |
missense |
probably damaging |
1.00 |
R0626:Fsip2
|
UTSW |
2 |
82,819,302 (GRCm39) |
missense |
probably benign |
0.06 |
R0644:Fsip2
|
UTSW |
2 |
82,807,241 (GRCm39) |
missense |
probably benign |
0.02 |
R0661:Fsip2
|
UTSW |
2 |
82,816,513 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0680:Fsip2
|
UTSW |
2 |
82,821,703 (GRCm39) |
missense |
possibly damaging |
0.73 |
R0688:Fsip2
|
UTSW |
2 |
82,812,683 (GRCm39) |
missense |
probably benign |
0.18 |
R0881:Fsip2
|
UTSW |
2 |
82,816,617 (GRCm39) |
missense |
possibly damaging |
0.52 |
R0919:Fsip2
|
UTSW |
2 |
82,815,828 (GRCm39) |
missense |
possibly damaging |
0.53 |
R0973:Fsip2
|
UTSW |
2 |
82,807,436 (GRCm39) |
missense |
probably benign |
0.05 |
R0973:Fsip2
|
UTSW |
2 |
82,807,436 (GRCm39) |
missense |
probably benign |
0.05 |
R0974:Fsip2
|
UTSW |
2 |
82,807,436 (GRCm39) |
missense |
probably benign |
0.05 |
R0976:Fsip2
|
UTSW |
2 |
82,828,375 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1025:Fsip2
|
UTSW |
2 |
82,819,780 (GRCm39) |
nonsense |
probably null |
|
R1026:Fsip2
|
UTSW |
2 |
82,818,805 (GRCm39) |
missense |
possibly damaging |
0.52 |
R1140:Fsip2
|
UTSW |
2 |
82,805,378 (GRCm39) |
missense |
probably damaging |
0.99 |
R1170:Fsip2
|
UTSW |
2 |
82,821,844 (GRCm39) |
missense |
possibly damaging |
0.72 |
R1180:Fsip2
|
UTSW |
2 |
82,805,570 (GRCm39) |
missense |
probably damaging |
0.99 |
R1188:Fsip2
|
UTSW |
2 |
82,805,361 (GRCm39) |
missense |
possibly damaging |
0.96 |
R1226:Fsip2
|
UTSW |
2 |
82,811,355 (GRCm39) |
missense |
probably damaging |
0.96 |
R1248:Fsip2
|
UTSW |
2 |
82,820,107 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1273:Fsip2
|
UTSW |
2 |
82,819,752 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1323:Fsip2
|
UTSW |
2 |
82,816,096 (GRCm39) |
missense |
probably damaging |
1.00 |
R1323:Fsip2
|
UTSW |
2 |
82,816,096 (GRCm39) |
missense |
probably damaging |
1.00 |
R1356:Fsip2
|
UTSW |
2 |
82,820,089 (GRCm39) |
missense |
probably benign |
0.38 |
R1413:Fsip2
|
UTSW |
2 |
82,818,762 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1430:Fsip2
|
UTSW |
2 |
82,828,407 (GRCm39) |
missense |
possibly damaging |
0.71 |
R1475:Fsip2
|
UTSW |
2 |
82,817,539 (GRCm39) |
missense |
probably damaging |
0.99 |
R1489:Fsip2
|
UTSW |
2 |
82,810,155 (GRCm39) |
missense |
probably benign |
|
R1520:Fsip2
|
UTSW |
2 |
82,811,058 (GRCm39) |
missense |
possibly damaging |
0.96 |
R1543:Fsip2
|
UTSW |
2 |
82,811,931 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1581:Fsip2
|
UTSW |
2 |
82,816,626 (GRCm39) |
missense |
probably damaging |
0.98 |
R1590:Fsip2
|
UTSW |
2 |
82,813,131 (GRCm39) |
missense |
probably benign |
0.26 |
R1646:Fsip2
|
UTSW |
2 |
82,808,861 (GRCm39) |
missense |
probably benign |
0.07 |
R1678:Fsip2
|
UTSW |
2 |
82,816,689 (GRCm39) |
missense |
probably benign |
|
R1700:Fsip2
|
UTSW |
2 |
82,822,081 (GRCm39) |
missense |
probably benign |
0.33 |
R1717:Fsip2
|
UTSW |
2 |
82,805,289 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1741:Fsip2
|
UTSW |
2 |
82,820,256 (GRCm39) |
missense |
probably benign |
0.32 |
R1760:Fsip2
|
UTSW |
2 |
82,818,055 (GRCm39) |
missense |
possibly damaging |
0.71 |
R1760:Fsip2
|
UTSW |
2 |
82,815,240 (GRCm39) |
missense |
probably benign |
0.07 |
R1760:Fsip2
|
UTSW |
2 |
82,830,185 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1789:Fsip2
|
UTSW |
2 |
82,807,906 (GRCm39) |
missense |
probably benign |
0.00 |
R1850:Fsip2
|
UTSW |
2 |
82,814,933 (GRCm39) |
missense |
possibly damaging |
0.72 |
R1854:Fsip2
|
UTSW |
2 |
82,823,601 (GRCm39) |
missense |
possibly damaging |
0.84 |
R1888:Fsip2
|
UTSW |
2 |
82,774,504 (GRCm39) |
missense |
probably benign |
0.04 |
R1888:Fsip2
|
UTSW |
2 |
82,774,504 (GRCm39) |
missense |
probably benign |
0.04 |
R1905:Fsip2
|
UTSW |
2 |
82,813,772 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1907:Fsip2
|
UTSW |
2 |
82,813,772 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1920:Fsip2
|
UTSW |
2 |
82,817,164 (GRCm39) |
missense |
probably benign |
0.04 |
R1921:Fsip2
|
UTSW |
2 |
82,817,164 (GRCm39) |
missense |
probably benign |
0.04 |
R1921:Fsip2
|
UTSW |
2 |
82,811,127 (GRCm39) |
nonsense |
probably null |
|
R1931:Fsip2
|
UTSW |
2 |
82,817,077 (GRCm39) |
missense |
probably damaging |
0.99 |
R1934:Fsip2
|
UTSW |
2 |
82,810,902 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1959:Fsip2
|
UTSW |
2 |
82,821,894 (GRCm39) |
missense |
probably benign |
|
R1965:Fsip2
|
UTSW |
2 |
82,823,124 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1966:Fsip2
|
UTSW |
2 |
82,823,124 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1983:Fsip2
|
UTSW |
2 |
82,810,175 (GRCm39) |
missense |
probably benign |
|
R1988:Fsip2
|
UTSW |
2 |
82,806,861 (GRCm39) |
missense |
possibly damaging |
0.56 |
R2016:Fsip2
|
UTSW |
2 |
82,813,076 (GRCm39) |
missense |
possibly damaging |
0.53 |
R2017:Fsip2
|
UTSW |
2 |
82,813,076 (GRCm39) |
missense |
possibly damaging |
0.53 |
R2026:Fsip2
|
UTSW |
2 |
82,819,788 (GRCm39) |
missense |
possibly damaging |
0.71 |
R2034:Fsip2
|
UTSW |
2 |
82,819,838 (GRCm39) |
missense |
probably benign |
0.43 |
R2037:Fsip2
|
UTSW |
2 |
82,808,856 (GRCm39) |
missense |
probably damaging |
0.99 |
R2070:Fsip2
|
UTSW |
2 |
82,806,699 (GRCm39) |
missense |
probably damaging |
0.98 |
R2072:Fsip2
|
UTSW |
2 |
82,839,159 (GRCm39) |
missense |
possibly damaging |
0.53 |
R2075:Fsip2
|
UTSW |
2 |
82,818,923 (GRCm39) |
missense |
possibly damaging |
0.85 |
R2143:Fsip2
|
UTSW |
2 |
82,820,615 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2207:Fsip2
|
UTSW |
2 |
82,807,823 (GRCm39) |
missense |
probably benign |
0.02 |
R2256:Fsip2
|
UTSW |
2 |
82,793,095 (GRCm39) |
missense |
probably benign |
0.07 |
R2315:Fsip2
|
UTSW |
2 |
82,805,437 (GRCm39) |
missense |
probably benign |
|
R2344:Fsip2
|
UTSW |
2 |
82,820,257 (GRCm39) |
missense |
possibly damaging |
0.71 |
R2377:Fsip2
|
UTSW |
2 |
82,806,593 (GRCm39) |
missense |
probably benign |
0.29 |
R2403:Fsip2
|
UTSW |
2 |
82,811,064 (GRCm39) |
missense |
possibly damaging |
0.53 |
R2441:Fsip2
|
UTSW |
2 |
82,815,685 (GRCm39) |
missense |
possibly damaging |
0.53 |
R2504:Fsip2
|
UTSW |
2 |
82,809,954 (GRCm39) |
missense |
possibly damaging |
0.86 |
R2510:Fsip2
|
UTSW |
2 |
82,816,782 (GRCm39) |
missense |
probably benign |
|
R2511:Fsip2
|
UTSW |
2 |
82,816,782 (GRCm39) |
missense |
probably benign |
|
R2511:Fsip2
|
UTSW |
2 |
82,782,001 (GRCm39) |
missense |
probably damaging |
1.00 |
R2512:Fsip2
|
UTSW |
2 |
82,808,511 (GRCm39) |
missense |
probably benign |
0.04 |
R2568:Fsip2
|
UTSW |
2 |
82,820,775 (GRCm39) |
missense |
probably benign |
0.14 |
R2656:Fsip2
|
UTSW |
2 |
82,809,389 (GRCm39) |
missense |
possibly damaging |
0.83 |
R2883:Fsip2
|
UTSW |
2 |
82,821,868 (GRCm39) |
missense |
possibly damaging |
0.86 |
R3417:Fsip2
|
UTSW |
2 |
82,816,854 (GRCm39) |
missense |
possibly damaging |
0.51 |
R3431:Fsip2
|
UTSW |
2 |
82,822,354 (GRCm39) |
missense |
possibly damaging |
0.85 |
R3441:Fsip2
|
UTSW |
2 |
82,817,071 (GRCm39) |
missense |
probably benign |
0.00 |
R3605:Fsip2
|
UTSW |
2 |
82,815,253 (GRCm39) |
missense |
probably benign |
0.28 |
R3620:Fsip2
|
UTSW |
2 |
82,810,602 (GRCm39) |
missense |
probably benign |
0.00 |
R3621:Fsip2
|
UTSW |
2 |
82,810,602 (GRCm39) |
missense |
probably benign |
0.00 |
R3726:Fsip2
|
UTSW |
2 |
82,819,311 (GRCm39) |
missense |
possibly damaging |
0.84 |
R3755:Fsip2
|
UTSW |
2 |
82,808,561 (GRCm39) |
missense |
probably benign |
0.26 |
R3789:Fsip2
|
UTSW |
2 |
82,813,058 (GRCm39) |
missense |
probably damaging |
0.96 |
R3836:Fsip2
|
UTSW |
2 |
82,781,290 (GRCm39) |
missense |
probably damaging |
1.00 |
R3844:Fsip2
|
UTSW |
2 |
82,819,950 (GRCm39) |
missense |
possibly damaging |
0.52 |
R3846:Fsip2
|
UTSW |
2 |
82,816,759 (GRCm39) |
missense |
possibly damaging |
0.52 |
R3861:Fsip2
|
UTSW |
2 |
82,815,120 (GRCm39) |
missense |
probably damaging |
0.98 |
R3981:Fsip2
|
UTSW |
2 |
82,789,006 (GRCm39) |
missense |
probably benign |
0.08 |
R4014:Fsip2
|
UTSW |
2 |
82,813,862 (GRCm39) |
missense |
probably benign |
|
R4042:Fsip2
|
UTSW |
2 |
82,813,896 (GRCm39) |
missense |
probably benign |
0.02 |
R4075:Fsip2
|
UTSW |
2 |
82,813,245 (GRCm39) |
missense |
probably benign |
0.26 |
R4154:Fsip2
|
UTSW |
2 |
82,817,413 (GRCm39) |
missense |
possibly damaging |
0.71 |
R4210:Fsip2
|
UTSW |
2 |
82,805,493 (GRCm39) |
missense |
probably damaging |
0.99 |
R4211:Fsip2
|
UTSW |
2 |
82,805,493 (GRCm39) |
missense |
probably damaging |
0.99 |
R4327:Fsip2
|
UTSW |
2 |
82,817,403 (GRCm39) |
missense |
probably benign |
0.25 |
R4332:Fsip2
|
UTSW |
2 |
82,808,201 (GRCm39) |
missense |
probably benign |
0.00 |
R4440:Fsip2
|
UTSW |
2 |
82,821,550 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4454:Fsip2
|
UTSW |
2 |
82,821,120 (GRCm39) |
missense |
possibly damaging |
0.70 |
R4455:Fsip2
|
UTSW |
2 |
82,821,120 (GRCm39) |
missense |
possibly damaging |
0.70 |
R4457:Fsip2
|
UTSW |
2 |
82,821,120 (GRCm39) |
missense |
possibly damaging |
0.70 |
R4458:Fsip2
|
UTSW |
2 |
82,821,120 (GRCm39) |
missense |
possibly damaging |
0.70 |
R4540:Fsip2
|
UTSW |
2 |
82,782,009 (GRCm39) |
missense |
probably benign |
|
R4549:Fsip2
|
UTSW |
2 |
82,819,972 (GRCm39) |
missense |
probably damaging |
0.99 |
R4558:Fsip2
|
UTSW |
2 |
82,815,297 (GRCm39) |
missense |
possibly damaging |
0.73 |
R4573:Fsip2
|
UTSW |
2 |
82,816,510 (GRCm39) |
missense |
possibly damaging |
0.71 |
R4583:Fsip2
|
UTSW |
2 |
82,809,017 (GRCm39) |
missense |
probably benign |
0.33 |
R4618:Fsip2
|
UTSW |
2 |
82,818,103 (GRCm39) |
missense |
probably benign |
|
R4700:Fsip2
|
UTSW |
2 |
82,817,373 (GRCm39) |
missense |
probably benign |
0.32 |
R4716:Fsip2
|
UTSW |
2 |
82,805,203 (GRCm39) |
missense |
probably damaging |
0.96 |
R4739:Fsip2
|
UTSW |
2 |
82,805,697 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4749:Fsip2
|
UTSW |
2 |
82,819,629 (GRCm39) |
missense |
probably benign |
0.06 |
R4791:Fsip2
|
UTSW |
2 |
82,812,452 (GRCm39) |
missense |
possibly damaging |
0.53 |
R4793:Fsip2
|
UTSW |
2 |
82,818,044 (GRCm39) |
nonsense |
probably null |
|
R4819:Fsip2
|
UTSW |
2 |
82,818,786 (GRCm39) |
missense |
probably benign |
0.06 |
R4832:Fsip2
|
UTSW |
2 |
82,820,515 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4840:Fsip2
|
UTSW |
2 |
82,779,739 (GRCm39) |
missense |
probably benign |
0.01 |
R4840:Fsip2
|
UTSW |
2 |
82,815,815 (GRCm39) |
missense |
probably benign |
0.26 |
R4865:Fsip2
|
UTSW |
2 |
82,821,295 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4876:Fsip2
|
UTSW |
2 |
82,805,202 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4885:Fsip2
|
UTSW |
2 |
82,818,438 (GRCm39) |
missense |
probably benign |
0.02 |
R4911:Fsip2
|
UTSW |
2 |
82,811,837 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4918:Fsip2
|
UTSW |
2 |
82,824,114 (GRCm39) |
missense |
possibly damaging |
0.51 |
R4936:Fsip2
|
UTSW |
2 |
82,815,384 (GRCm39) |
missense |
probably benign |
0.18 |
R4950:Fsip2
|
UTSW |
2 |
82,777,276 (GRCm39) |
missense |
probably damaging |
0.97 |
R4950:Fsip2
|
UTSW |
2 |
82,807,758 (GRCm39) |
missense |
probably benign |
0.03 |
R4959:Fsip2
|
UTSW |
2 |
82,815,169 (GRCm39) |
missense |
probably benign |
0.00 |
R4971:Fsip2
|
UTSW |
2 |
82,816,222 (GRCm39) |
missense |
probably benign |
0.38 |
R4973:Fsip2
|
UTSW |
2 |
82,815,169 (GRCm39) |
missense |
probably benign |
0.00 |
R4976:Fsip2
|
UTSW |
2 |
82,818,535 (GRCm39) |
missense |
probably damaging |
0.99 |
R5022:Fsip2
|
UTSW |
2 |
82,809,773 (GRCm39) |
missense |
probably benign |
0.33 |
R5027:Fsip2
|
UTSW |
2 |
82,819,477 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5030:Fsip2
|
UTSW |
2 |
82,818,836 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5048:Fsip2
|
UTSW |
2 |
82,823,494 (GRCm39) |
missense |
probably damaging |
0.97 |
R5096:Fsip2
|
UTSW |
2 |
82,821,460 (GRCm39) |
missense |
probably benign |
0.00 |
R5097:Fsip2
|
UTSW |
2 |
82,822,329 (GRCm39) |
missense |
probably benign |
|
R5119:Fsip2
|
UTSW |
2 |
82,818,535 (GRCm39) |
missense |
probably damaging |
0.99 |
R5138:Fsip2
|
UTSW |
2 |
82,811,768 (GRCm39) |
missense |
probably benign |
0.12 |
R5152:Fsip2
|
UTSW |
2 |
82,808,916 (GRCm39) |
missense |
probably benign |
0.43 |
R5174:Fsip2
|
UTSW |
2 |
82,811,085 (GRCm39) |
missense |
probably benign |
0.07 |
R5193:Fsip2
|
UTSW |
2 |
82,813,338 (GRCm39) |
missense |
possibly damaging |
0.53 |
R5245:Fsip2
|
UTSW |
2 |
82,823,505 (GRCm39) |
missense |
probably benign |
0.02 |
R5282:Fsip2
|
UTSW |
2 |
82,808,925 (GRCm39) |
missense |
possibly damaging |
0.61 |
R5323:Fsip2
|
UTSW |
2 |
82,818,489 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5326:Fsip2
|
UTSW |
2 |
82,812,207 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5378:Fsip2
|
UTSW |
2 |
82,820,185 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5380:Fsip2
|
UTSW |
2 |
82,805,742 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5396:Fsip2
|
UTSW |
2 |
82,821,262 (GRCm39) |
missense |
probably benign |
0.00 |
R5422:Fsip2
|
UTSW |
2 |
82,812,572 (GRCm39) |
missense |
probably benign |
0.00 |
R5481:Fsip2
|
UTSW |
2 |
82,810,230 (GRCm39) |
missense |
probably benign |
0.26 |
R5482:Fsip2
|
UTSW |
2 |
82,815,654 (GRCm39) |
missense |
possibly damaging |
0.80 |
R5513:Fsip2
|
UTSW |
2 |
82,815,542 (GRCm39) |
missense |
possibly damaging |
0.72 |
R5513:Fsip2
|
UTSW |
2 |
82,781,256 (GRCm39) |
missense |
probably benign |
0.07 |
R5513:Fsip2
|
UTSW |
2 |
82,781,252 (GRCm39) |
missense |
probably damaging |
1.00 |
R5536:Fsip2
|
UTSW |
2 |
82,817,403 (GRCm39) |
missense |
probably benign |
0.25 |
R5542:Fsip2
|
UTSW |
2 |
82,812,207 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5553:Fsip2
|
UTSW |
2 |
82,793,090 (GRCm39) |
missense |
probably benign |
|
R5568:Fsip2
|
UTSW |
2 |
82,816,908 (GRCm39) |
missense |
probably benign |
0.25 |
R5581:Fsip2
|
UTSW |
2 |
82,828,472 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5664:Fsip2
|
UTSW |
2 |
82,818,439 (GRCm39) |
missense |
probably benign |
0.05 |
R5672:Fsip2
|
UTSW |
2 |
82,817,838 (GRCm39) |
nonsense |
probably null |
|
R5712:Fsip2
|
UTSW |
2 |
82,839,192 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5762:Fsip2
|
UTSW |
2 |
82,808,260 (GRCm39) |
missense |
probably benign |
0.33 |
R5772:Fsip2
|
UTSW |
2 |
82,815,084 (GRCm39) |
missense |
probably benign |
|
R5881:Fsip2
|
UTSW |
2 |
82,814,785 (GRCm39) |
missense |
possibly damaging |
0.72 |
R5919:Fsip2
|
UTSW |
2 |
82,822,953 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5920:Fsip2
|
UTSW |
2 |
82,818,852 (GRCm39) |
nonsense |
probably null |
|
R5934:Fsip2
|
UTSW |
2 |
82,817,092 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5938:Fsip2
|
UTSW |
2 |
82,807,835 (GRCm39) |
missense |
probably benign |
0.00 |
R5974:Fsip2
|
UTSW |
2 |
82,793,657 (GRCm39) |
missense |
possibly damaging |
0.68 |
R5991:Fsip2
|
UTSW |
2 |
82,820,812 (GRCm39) |
missense |
probably benign |
0.28 |
R6019:Fsip2
|
UTSW |
2 |
82,818,283 (GRCm39) |
missense |
possibly damaging |
0.52 |
R6020:Fsip2
|
UTSW |
2 |
82,822,471 (GRCm39) |
missense |
probably damaging |
0.99 |
R6056:Fsip2
|
UTSW |
2 |
82,816,017 (GRCm39) |
missense |
probably benign |
0.01 |
R6057:Fsip2
|
UTSW |
2 |
82,809,777 (GRCm39) |
missense |
probably damaging |
0.99 |
R6139:Fsip2
|
UTSW |
2 |
82,821,388 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6145:Fsip2
|
UTSW |
2 |
82,824,112 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6160:Fsip2
|
UTSW |
2 |
82,818,289 (GRCm39) |
nonsense |
probably null |
|
R6161:Fsip2
|
UTSW |
2 |
82,817,601 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6166:Fsip2
|
UTSW |
2 |
82,811,071 (GRCm39) |
missense |
probably benign |
0.00 |
R6187:Fsip2
|
UTSW |
2 |
82,812,798 (GRCm39) |
missense |
probably benign |
0.33 |
R6196:Fsip2
|
UTSW |
2 |
82,820,227 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6217:Fsip2
|
UTSW |
2 |
82,818,762 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6276:Fsip2
|
UTSW |
2 |
82,810,785 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6278:Fsip2
|
UTSW |
2 |
82,819,242 (GRCm39) |
missense |
probably benign |
0.16 |
R6349:Fsip2
|
UTSW |
2 |
82,823,416 (GRCm39) |
missense |
probably benign |
0.05 |
R6351:Fsip2
|
UTSW |
2 |
82,823,028 (GRCm39) |
missense |
possibly damaging |
0.51 |
R6401:Fsip2
|
UTSW |
2 |
82,820,430 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6404:Fsip2
|
UTSW |
2 |
82,820,430 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6405:Fsip2
|
UTSW |
2 |
82,820,430 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6437:Fsip2
|
UTSW |
2 |
82,813,836 (GRCm39) |
missense |
possibly damaging |
0.73 |
R6478:Fsip2
|
UTSW |
2 |
82,820,430 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6479:Fsip2
|
UTSW |
2 |
82,820,430 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6480:Fsip2
|
UTSW |
2 |
82,820,430 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6481:Fsip2
|
UTSW |
2 |
82,820,430 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6521:Fsip2
|
UTSW |
2 |
82,820,430 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6529:Fsip2
|
UTSW |
2 |
82,812,657 (GRCm39) |
missense |
probably benign |
|
R6621:Fsip2
|
UTSW |
2 |
82,820,158 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6639:Fsip2
|
UTSW |
2 |
82,813,571 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6649:Fsip2
|
UTSW |
2 |
82,798,161 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6714:Fsip2
|
UTSW |
2 |
82,820,430 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6714:Fsip2
|
UTSW |
2 |
82,809,878 (GRCm39) |
missense |
probably benign |
0.01 |
R6749:Fsip2
|
UTSW |
2 |
82,808,738 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6765:Fsip2
|
UTSW |
2 |
82,816,776 (GRCm39) |
missense |
probably benign |
|
R6790:Fsip2
|
UTSW |
2 |
82,821,283 (GRCm39) |
missense |
possibly damaging |
0.53 |
R6793:Fsip2
|
UTSW |
2 |
82,819,838 (GRCm39) |
missense |
probably benign |
0.43 |
R6795:Fsip2
|
UTSW |
2 |
82,811,303 (GRCm39) |
missense |
probably benign |
0.08 |
R6818:Fsip2
|
UTSW |
2 |
82,815,544 (GRCm39) |
missense |
probably benign |
0.04 |
R6844:Fsip2
|
UTSW |
2 |
82,813,969 (GRCm39) |
missense |
possibly damaging |
0.72 |
R6848:Fsip2
|
UTSW |
2 |
82,813,131 (GRCm39) |
missense |
probably benign |
0.26 |
R6945:Fsip2
|
UTSW |
2 |
82,823,184 (GRCm39) |
missense |
probably benign |
0.16 |
R6950:Fsip2
|
UTSW |
2 |
82,816,332 (GRCm39) |
missense |
probably benign |
0.03 |
R6951:Fsip2
|
UTSW |
2 |
82,812,293 (GRCm39) |
missense |
possibly damaging |
0.68 |
R6974:Fsip2
|
UTSW |
2 |
82,809,061 (GRCm39) |
missense |
probably damaging |
0.96 |
R6987:Fsip2
|
UTSW |
2 |
82,778,630 (GRCm39) |
nonsense |
probably null |
|
R6989:Fsip2
|
UTSW |
2 |
82,807,298 (GRCm39) |
missense |
probably benign |
0.00 |
R7001:Fsip2
|
UTSW |
2 |
82,817,269 (GRCm39) |
missense |
probably damaging |
1.00 |
R7002:Fsip2
|
UTSW |
2 |
82,819,687 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7016:Fsip2
|
UTSW |
2 |
82,820,979 (GRCm39) |
missense |
probably benign |
0.25 |
R7066:Fsip2
|
UTSW |
2 |
82,821,235 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7067:Fsip2
|
UTSW |
2 |
82,811,078 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7077:Fsip2
|
UTSW |
2 |
82,813,496 (GRCm39) |
missense |
probably benign |
0.18 |
R7099:Fsip2
|
UTSW |
2 |
82,817,968 (GRCm39) |
missense |
probably benign |
|
R7126:Fsip2
|
UTSW |
2 |
82,813,485 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7156:Fsip2
|
UTSW |
2 |
82,813,085 (GRCm39) |
missense |
probably benign |
0.00 |
R7165:Fsip2
|
UTSW |
2 |
82,811,541 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7171:Fsip2
|
UTSW |
2 |
82,816,571 (GRCm39) |
nonsense |
probably null |
|
R7189:Fsip2
|
UTSW |
2 |
82,823,581 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7217:Fsip2
|
UTSW |
2 |
82,819,412 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7222:Fsip2
|
UTSW |
2 |
82,814,015 (GRCm39) |
missense |
probably benign |
|
R7228:Fsip2
|
UTSW |
2 |
82,822,651 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7238:Fsip2
|
UTSW |
2 |
82,812,484 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7244:Fsip2
|
UTSW |
2 |
82,823,607 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7251:Fsip2
|
UTSW |
2 |
82,809,425 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7259:Fsip2
|
UTSW |
2 |
82,812,474 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7291:Fsip2
|
UTSW |
2 |
82,810,863 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7316:Fsip2
|
UTSW |
2 |
82,820,035 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7323:Fsip2
|
UTSW |
2 |
82,819,860 (GRCm39) |
missense |
probably benign |
0.07 |
R7335:Fsip2
|
UTSW |
2 |
82,813,462 (GRCm39) |
missense |
probably benign |
|
R7343:Fsip2
|
UTSW |
2 |
82,809,711 (GRCm39) |
missense |
probably benign |
0.07 |
R7346:Fsip2
|
UTSW |
2 |
82,828,524 (GRCm39) |
missense |
probably benign |
0.00 |
R7389:Fsip2
|
UTSW |
2 |
82,819,140 (GRCm39) |
missense |
possibly damaging |
0.51 |
R7391:Fsip2
|
UTSW |
2 |
82,820,663 (GRCm39) |
missense |
possibly damaging |
0.70 |
R7397:Fsip2
|
UTSW |
2 |
82,815,601 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7426:Fsip2
|
UTSW |
2 |
82,810,441 (GRCm39) |
missense |
probably damaging |
0.98 |
R7450:Fsip2
|
UTSW |
2 |
82,782,024 (GRCm39) |
missense |
probably benign |
0.30 |
R7538:Fsip2
|
UTSW |
2 |
82,818,894 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7542:Fsip2
|
UTSW |
2 |
82,815,196 (GRCm39) |
missense |
possibly damaging |
0.96 |
R7549:Fsip2
|
UTSW |
2 |
82,824,337 (GRCm39) |
missense |
probably damaging |
0.99 |
R7564:Fsip2
|
UTSW |
2 |
82,819,361 (GRCm39) |
missense |
probably benign |
0.02 |
R7565:Fsip2
|
UTSW |
2 |
82,779,856 (GRCm39) |
missense |
probably damaging |
0.97 |
R7583:Fsip2
|
UTSW |
2 |
82,805,585 (GRCm39) |
missense |
probably benign |
0.12 |
R7641:Fsip2
|
UTSW |
2 |
82,817,256 (GRCm39) |
nonsense |
probably null |
|
R7655:Fsip2
|
UTSW |
2 |
82,807,886 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7656:Fsip2
|
UTSW |
2 |
82,807,886 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7665:Fsip2
|
UTSW |
2 |
82,812,149 (GRCm39) |
missense |
probably benign |
0.03 |
R7672:Fsip2
|
UTSW |
2 |
82,820,455 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7764:Fsip2
|
UTSW |
2 |
82,811,252 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7790:Fsip2
|
UTSW |
2 |
82,818,723 (GRCm39) |
missense |
probably benign |
|
R7811:Fsip2
|
UTSW |
2 |
82,828,797 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7838:Fsip2
|
UTSW |
2 |
82,807,044 (GRCm39) |
missense |
probably benign |
0.00 |
R7873:Fsip2
|
UTSW |
2 |
82,779,856 (GRCm39) |
missense |
probably damaging |
0.97 |
R7902:Fsip2
|
UTSW |
2 |
82,808,168 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7920:Fsip2
|
UTSW |
2 |
82,781,365 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7959:Fsip2
|
UTSW |
2 |
82,816,120 (GRCm39) |
missense |
possibly damaging |
0.51 |
R8009:Fsip2
|
UTSW |
2 |
82,818,793 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8031:Fsip2
|
UTSW |
2 |
82,817,235 (GRCm39) |
missense |
probably benign |
|
R8034:Fsip2
|
UTSW |
2 |
82,819,699 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8037:Fsip2
|
UTSW |
2 |
82,816,322 (GRCm39) |
missense |
possibly damaging |
0.72 |
R8110:Fsip2
|
UTSW |
2 |
82,789,017 (GRCm39) |
missense |
probably benign |
0.00 |
R8117:Fsip2
|
UTSW |
2 |
82,823,296 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8138:Fsip2
|
UTSW |
2 |
82,806,141 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8175:Fsip2
|
UTSW |
2 |
82,818,021 (GRCm39) |
missense |
probably benign |
0.16 |
R8175:Fsip2
|
UTSW |
2 |
82,815,088 (GRCm39) |
missense |
probably benign |
0.06 |
R8182:Fsip2
|
UTSW |
2 |
82,806,951 (GRCm39) |
missense |
probably damaging |
0.99 |
R8206:Fsip2
|
UTSW |
2 |
82,820,808 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8229:Fsip2
|
UTSW |
2 |
82,808,487 (GRCm39) |
missense |
possibly damaging |
0.63 |
R8239:Fsip2
|
UTSW |
2 |
82,819,687 (GRCm39) |
missense |
possibly damaging |
0.71 |
R8245:Fsip2
|
UTSW |
2 |
82,811,346 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8303:Fsip2
|
UTSW |
2 |
82,818,724 (GRCm39) |
missense |
probably benign |
0.00 |
R8336:Fsip2
|
UTSW |
2 |
82,821,099 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8347:Fsip2
|
UTSW |
2 |
82,818,198 (GRCm39) |
missense |
probably benign |
0.16 |
R8351:Fsip2
|
UTSW |
2 |
82,822,239 (GRCm39) |
missense |
possibly damaging |
0.73 |
R8352:Fsip2
|
UTSW |
2 |
82,814,937 (GRCm39) |
missense |
probably benign |
|
R8419:Fsip2
|
UTSW |
2 |
82,808,963 (GRCm39) |
missense |
probably damaging |
0.96 |
R8431:Fsip2
|
UTSW |
2 |
82,811,910 (GRCm39) |
missense |
probably damaging |
1.00 |
R8439:Fsip2
|
UTSW |
2 |
82,807,430 (GRCm39) |
missense |
probably benign |
0.24 |
R8452:Fsip2
|
UTSW |
2 |
82,814,937 (GRCm39) |
missense |
probably benign |
|
R8459:Fsip2
|
UTSW |
2 |
82,810,022 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8465:Fsip2
|
UTSW |
2 |
82,810,284 (GRCm39) |
missense |
probably benign |
0.26 |
R8473:Fsip2
|
UTSW |
2 |
82,777,336 (GRCm39) |
missense |
probably damaging |
0.99 |
R8703:Fsip2
|
UTSW |
2 |
82,821,871 (GRCm39) |
missense |
probably damaging |
0.98 |
R8711:Fsip2
|
UTSW |
2 |
82,815,246 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8713:Fsip2
|
UTSW |
2 |
82,811,453 (GRCm39) |
missense |
probably damaging |
1.00 |
R8789:Fsip2
|
UTSW |
2 |
82,815,822 (GRCm39) |
missense |
possibly damaging |
0.73 |
R8805:Fsip2
|
UTSW |
2 |
82,813,453 (GRCm39) |
missense |
possibly damaging |
0.46 |
R8840:Fsip2
|
UTSW |
2 |
82,821,606 (GRCm39) |
missense |
probably benign |
0.03 |
R8855:Fsip2
|
UTSW |
2 |
82,810,521 (GRCm39) |
missense |
probably benign |
0.04 |
R8866:Fsip2
|
UTSW |
2 |
82,810,521 (GRCm39) |
missense |
probably benign |
0.04 |
R8875:Fsip2
|
UTSW |
2 |
82,820,782 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8883:Fsip2
|
UTSW |
2 |
82,809,524 (GRCm39) |
missense |
possibly damaging |
0.68 |
R8903:Fsip2
|
UTSW |
2 |
82,807,681 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8907:Fsip2
|
UTSW |
2 |
82,816,984 (GRCm39) |
missense |
probably benign |
0.20 |
R8912:Fsip2
|
UTSW |
2 |
82,810,938 (GRCm39) |
missense |
probably benign |
|
R8926:Fsip2
|
UTSW |
2 |
82,823,927 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8991:Fsip2
|
UTSW |
2 |
82,815,370 (GRCm39) |
missense |
probably benign |
0.33 |
R9014:Fsip2
|
UTSW |
2 |
82,806,898 (GRCm39) |
missense |
probably benign |
0.32 |
R9014:Fsip2
|
UTSW |
2 |
82,817,075 (GRCm39) |
missense |
possibly damaging |
0.71 |
R9039:Fsip2
|
UTSW |
2 |
82,828,545 (GRCm39) |
missense |
probably benign |
0.32 |
R9054:Fsip2
|
UTSW |
2 |
82,806,180 (GRCm39) |
missense |
possibly damaging |
0.68 |
R9114:Fsip2
|
UTSW |
2 |
82,807,301 (GRCm39) |
missense |
probably benign |
0.00 |
R9124:Fsip2
|
UTSW |
2 |
82,816,103 (GRCm39) |
missense |
probably benign |
0.00 |
R9131:Fsip2
|
UTSW |
2 |
82,813,170 (GRCm39) |
missense |
probably benign |
|
R9149:Fsip2
|
UTSW |
2 |
82,812,374 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9180:Fsip2
|
UTSW |
2 |
82,815,574 (GRCm39) |
missense |
possibly damaging |
0.96 |
R9192:Fsip2
|
UTSW |
2 |
82,817,844 (GRCm39) |
missense |
probably benign |
0.06 |
R9216:Fsip2
|
UTSW |
2 |
82,820,425 (GRCm39) |
missense |
probably damaging |
0.99 |
R9218:Fsip2
|
UTSW |
2 |
82,823,062 (GRCm39) |
missense |
probably damaging |
0.97 |
R9222:Fsip2
|
UTSW |
2 |
82,815,958 (GRCm39) |
missense |
probably benign |
0.00 |
R9262:Fsip2
|
UTSW |
2 |
82,807,662 (GRCm39) |
missense |
probably benign |
0.00 |
R9340:Fsip2
|
UTSW |
2 |
82,818,604 (GRCm39) |
missense |
possibly damaging |
0.71 |
R9342:Fsip2
|
UTSW |
2 |
82,818,747 (GRCm39) |
missense |
possibly damaging |
0.71 |
R9368:Fsip2
|
UTSW |
2 |
82,811,039 (GRCm39) |
missense |
possibly damaging |
0.68 |
R9372:Fsip2
|
UTSW |
2 |
82,822,756 (GRCm39) |
missense |
possibly damaging |
0.71 |
R9385:Fsip2
|
UTSW |
2 |
82,819,793 (GRCm39) |
missense |
possibly damaging |
0.84 |
R9432:Fsip2
|
UTSW |
2 |
82,805,907 (GRCm39) |
missense |
probably damaging |
0.98 |
R9434:Fsip2
|
UTSW |
2 |
82,816,702 (GRCm39) |
missense |
possibly damaging |
0.71 |
R9445:Fsip2
|
UTSW |
2 |
82,806,132 (GRCm39) |
missense |
probably damaging |
0.99 |
R9472:Fsip2
|
UTSW |
2 |
82,817,285 (GRCm39) |
missense |
possibly damaging |
0.85 |
R9496:Fsip2
|
UTSW |
2 |
82,793,062 (GRCm39) |
missense |
probably benign |
|
R9523:Fsip2
|
UTSW |
2 |
82,807,972 (GRCm39) |
missense |
probably damaging |
0.99 |
R9567:Fsip2
|
UTSW |
2 |
82,798,173 (GRCm39) |
missense |
probably benign |
|
R9636:Fsip2
|
UTSW |
2 |
82,820,563 (GRCm39) |
missense |
possibly damaging |
0.52 |
R9643:Fsip2
|
UTSW |
2 |
82,821,984 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9680:Fsip2
|
UTSW |
2 |
82,819,272 (GRCm39) |
missense |
probably benign |
0.32 |
R9695:Fsip2
|
UTSW |
2 |
82,806,226 (GRCm39) |
missense |
probably benign |
|
R9705:Fsip2
|
UTSW |
2 |
82,823,634 (GRCm39) |
missense |
probably benign |
|
R9739:Fsip2
|
UTSW |
2 |
82,823,896 (GRCm39) |
missense |
possibly damaging |
0.71 |
R9751:Fsip2
|
UTSW |
2 |
82,818,241 (GRCm39) |
missense |
probably benign |
0.00 |
R9761:Fsip2
|
UTSW |
2 |
82,821,994 (GRCm39) |
missense |
probably benign |
0.00 |
R9798:Fsip2
|
UTSW |
2 |
82,810,225 (GRCm39) |
nonsense |
probably null |
|
RF003:Fsip2
|
UTSW |
2 |
82,821,865 (GRCm39) |
missense |
probably benign |
0.02 |
RF005:Fsip2
|
UTSW |
2 |
82,822,876 (GRCm39) |
missense |
probably benign |
0.04 |
RF008:Fsip2
|
UTSW |
2 |
82,808,184 (GRCm39) |
missense |
probably benign |
|
RF028:Fsip2
|
UTSW |
2 |
82,824,352 (GRCm39) |
frame shift |
probably null |
|
RF029:Fsip2
|
UTSW |
2 |
82,824,352 (GRCm39) |
frame shift |
probably null |
|
RF036:Fsip2
|
UTSW |
2 |
82,814,707 (GRCm39) |
critical splice acceptor site |
probably benign |
|
RF038:Fsip2
|
UTSW |
2 |
82,824,352 (GRCm39) |
frame shift |
probably null |
|
RF062:Fsip2
|
UTSW |
2 |
82,814,707 (GRCm39) |
critical splice acceptor site |
probably benign |
|
X0018:Fsip2
|
UTSW |
2 |
82,812,851 (GRCm39) |
nonsense |
probably null |
|
X0020:Fsip2
|
UTSW |
2 |
82,781,364 (GRCm39) |
missense |
probably damaging |
1.00 |
X0025:Fsip2
|
UTSW |
2 |
82,785,290 (GRCm39) |
missense |
possibly damaging |
0.70 |
X0027:Fsip2
|
UTSW |
2 |
82,807,122 (GRCm39) |
missense |
probably benign |
0.35 |
X0066:Fsip2
|
UTSW |
2 |
82,817,807 (GRCm39) |
missense |
possibly damaging |
0.51 |
Z1088:Fsip2
|
UTSW |
2 |
82,818,978 (GRCm39) |
missense |
possibly damaging |
0.85 |
Z1088:Fsip2
|
UTSW |
2 |
82,817,997 (GRCm39) |
missense |
possibly damaging |
0.86 |
Z1088:Fsip2
|
UTSW |
2 |
82,805,792 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1176:Fsip2
|
UTSW |
2 |
82,820,009 (GRCm39) |
missense |
probably benign |
0.02 |
Z1177:Fsip2
|
UTSW |
2 |
82,814,868 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1177:Fsip2
|
UTSW |
2 |
82,777,304 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Fsip2
|
UTSW |
2 |
82,817,547 (GRCm39) |
missense |
possibly damaging |
0.71 |
|