Other mutations in this stock |
Total: 220 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 |
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 |
Catsper2 |
TGTC |
TGTCGTC |
2: 121,228,260 (GRCm39) |
|
probably benign |
Homo |
Ccdc170 |
ACC |
ACCGCC |
10: 4,511,023 (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 |
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 |
A |
ACCCCCC |
11: 101,080,395 (GRCm39) |
|
probably benign |
Het |
Cntnap1 |
GCCCCA |
GCCCCACCCCCA |
11: 101,080,414 (GRCm39) |
|
probably benign |
Het |
Cntnap1 |
CCAGCC |
CCAGCCTCAGCC |
11: 101,080,411 (GRCm39) |
|
probably benign |
Het |
Cntnap1 |
CCCAGC |
CCCAGCACCAGC |
11: 101,080,398 (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 |
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 |
TC |
TCTAC |
2: 57,938,100 (GRCm39) |
|
probably benign |
Het |
Ermn |
CTT |
CTTGTT |
2: 57,938,092 (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 |
Fsip2 |
TTTTT |
TTTTTGTTTT |
2: 82,814,706 (GRCm39) |
|
probably benign |
Het |
Fsip2 |
TT |
TTTTTCT |
2: 82,814,709 (GRCm39) |
|
probably benign |
Het |
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 |
CTCCTC |
CTCCTCGTCCTC |
7: 30,285,787 (GRCm39) |
|
probably benign |
Het |
Kmt2b |
TCCTCC |
TCCTCCCCCTCC |
7: 30,285,785 (GRCm39) |
|
probably benign |
Het |
Kmt2b |
CCTCCT |
CCTCCTGCTCCT |
7: 30,285,798 (GRCm39) |
|
probably benign |
Het |
Kmt2b |
TCCTCC |
TCCTCCACCTCC |
7: 30,285,791 (GRCm39) |
|
probably benign |
Het |
Kmt2b |
CCTCCT |
CCTCCTACTCCT |
7: 30,285,789 (GRCm39) |
|
probably null |
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 |
AGG |
AGGGGG |
X: 94,984,433 (GRCm39) |
|
probably benign |
Het |
Las1l |
A |
AGGC |
X: 94,984,439 (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 |
GCAACA |
GCAACAACA |
X: 70,162,418 (GRCm39) |
|
probably benign |
Het |
Mamld1 |
GCA |
GCAACA |
X: 70,162,424 (GRCm39) |
|
probably benign |
Het |
Mast4 |
GGACAAGCTGTGAGTTGGGGAACCCGGGAG |
GG |
13: 102,875,755 (GRCm39) |
|
probably null |
Homo |
Mast4 |
TGG |
TGGGGGCGG |
13: 102,872,820 (GRCm39) |
|
probably benign |
Het |
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 |
TCAGGG |
TCAGGGACAGGG |
11: 6,549,756 (GRCm39) |
|
probably benign |
Het |
Nacad |
A |
ACCAGGG |
11: 6,549,749 (GRCm39) |
|
probably benign |
Het |
Nacad |
C |
CAGGGTA |
11: 6,549,763 (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 |
AGGC |
AGGCGGC |
4: 156,324,549 (GRCm39) |
|
probably benign |
Homo |
Noc2l |
CTG |
CTGGTG |
4: 156,324,555 (GRCm39) |
|
probably benign |
Het |
Nolc1 |
CAG |
CAGAAGCAGAAG |
19: 46,069,795 (GRCm39) |
|
probably benign |
Het |
Nolc1 |
AGC |
AGCAGCAGCGGC |
19: 46,069,814 (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 Dnaaf9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00556:Dnaaf9
|
APN |
2 |
130,626,377 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01093:Dnaaf9
|
APN |
2 |
130,619,156 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01111:Dnaaf9
|
APN |
2 |
130,578,518 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL01146:Dnaaf9
|
APN |
2 |
130,612,591 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01346:Dnaaf9
|
APN |
2 |
130,633,766 (GRCm39) |
splice site |
probably benign |
|
IGL01548:Dnaaf9
|
APN |
2 |
130,656,179 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02339:Dnaaf9
|
APN |
2 |
130,581,385 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02637:Dnaaf9
|
APN |
2 |
130,656,227 (GRCm39) |
intron |
probably benign |
|
IGL02926:Dnaaf9
|
APN |
2 |
130,554,286 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02978:Dnaaf9
|
APN |
2 |
130,569,082 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03126:Dnaaf9
|
APN |
2 |
130,633,915 (GRCm39) |
splice site |
probably null |
|
IGL03387:Dnaaf9
|
APN |
2 |
130,559,200 (GRCm39) |
missense |
probably damaging |
1.00 |
best_times
|
UTSW |
2 |
130,578,496 (GRCm39) |
missense |
probably damaging |
0.99 |
Hard_times
|
UTSW |
2 |
130,555,390 (GRCm39) |
missense |
probably benign |
0.16 |
worst_times
|
UTSW |
2 |
130,555,334 (GRCm39) |
missense |
probably damaging |
1.00 |
FR4304:Dnaaf9
|
UTSW |
2 |
130,612,668 (GRCm39) |
small insertion |
probably benign |
|
FR4342:Dnaaf9
|
UTSW |
2 |
130,612,662 (GRCm39) |
small insertion |
probably benign |
|
FR4589:Dnaaf9
|
UTSW |
2 |
130,612,672 (GRCm39) |
small insertion |
probably benign |
|
FR4589:Dnaaf9
|
UTSW |
2 |
130,612,665 (GRCm39) |
small insertion |
probably benign |
|
FR4737:Dnaaf9
|
UTSW |
2 |
130,612,672 (GRCm39) |
small insertion |
probably benign |
|
FR4976:Dnaaf9
|
UTSW |
2 |
130,612,673 (GRCm39) |
small insertion |
probably benign |
|
FR4976:Dnaaf9
|
UTSW |
2 |
130,612,659 (GRCm39) |
small insertion |
probably benign |
|
R0034:Dnaaf9
|
UTSW |
2 |
130,578,492 (GRCm39) |
missense |
probably damaging |
1.00 |
R0034:Dnaaf9
|
UTSW |
2 |
130,578,492 (GRCm39) |
missense |
probably damaging |
1.00 |
R0357:Dnaaf9
|
UTSW |
2 |
130,554,866 (GRCm39) |
splice site |
probably benign |
|
R0379:Dnaaf9
|
UTSW |
2 |
130,627,466 (GRCm39) |
splice site |
probably benign |
|
R0515:Dnaaf9
|
UTSW |
2 |
130,582,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R0576:Dnaaf9
|
UTSW |
2 |
130,555,390 (GRCm39) |
missense |
probably benign |
0.16 |
R0811:Dnaaf9
|
UTSW |
2 |
130,555,334 (GRCm39) |
missense |
probably damaging |
1.00 |
R0812:Dnaaf9
|
UTSW |
2 |
130,555,334 (GRCm39) |
missense |
probably damaging |
1.00 |
R1334:Dnaaf9
|
UTSW |
2 |
130,617,642 (GRCm39) |
splice site |
probably null |
|
R1485:Dnaaf9
|
UTSW |
2 |
130,590,603 (GRCm39) |
critical splice donor site |
probably null |
|
R1486:Dnaaf9
|
UTSW |
2 |
130,579,338 (GRCm39) |
missense |
probably damaging |
1.00 |
R1670:Dnaaf9
|
UTSW |
2 |
130,554,299 (GRCm39) |
missense |
probably damaging |
1.00 |
R1678:Dnaaf9
|
UTSW |
2 |
130,656,193 (GRCm39) |
missense |
probably damaging |
0.99 |
R1700:Dnaaf9
|
UTSW |
2 |
130,551,858 (GRCm39) |
missense |
probably damaging |
0.99 |
R1742:Dnaaf9
|
UTSW |
2 |
130,582,315 (GRCm39) |
splice site |
probably null |
|
R2046:Dnaaf9
|
UTSW |
2 |
130,652,837 (GRCm39) |
missense |
possibly damaging |
0.61 |
R2374:Dnaaf9
|
UTSW |
2 |
130,662,494 (GRCm39) |
missense |
probably damaging |
1.00 |
R3878:Dnaaf9
|
UTSW |
2 |
130,620,423 (GRCm39) |
missense |
possibly damaging |
0.92 |
R3907:Dnaaf9
|
UTSW |
2 |
130,578,496 (GRCm39) |
missense |
probably damaging |
0.99 |
R4467:Dnaaf9
|
UTSW |
2 |
130,609,567 (GRCm39) |
missense |
probably damaging |
0.96 |
R4931:Dnaaf9
|
UTSW |
2 |
130,583,793 (GRCm39) |
missense |
possibly damaging |
0.58 |
R5098:Dnaaf9
|
UTSW |
2 |
130,640,101 (GRCm39) |
missense |
probably damaging |
0.99 |
R5191:Dnaaf9
|
UTSW |
2 |
130,579,323 (GRCm39) |
missense |
possibly damaging |
0.68 |
R5313:Dnaaf9
|
UTSW |
2 |
130,551,188 (GRCm39) |
missense |
probably damaging |
1.00 |
R5405:Dnaaf9
|
UTSW |
2 |
130,554,380 (GRCm39) |
missense |
probably damaging |
1.00 |
R5436:Dnaaf9
|
UTSW |
2 |
130,606,419 (GRCm39) |
missense |
probably benign |
0.16 |
R5522:Dnaaf9
|
UTSW |
2 |
130,656,222 (GRCm39) |
intron |
probably benign |
|
R5783:Dnaaf9
|
UTSW |
2 |
130,581,003 (GRCm39) |
missense |
possibly damaging |
0.59 |
R5931:Dnaaf9
|
UTSW |
2 |
130,656,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R6145:Dnaaf9
|
UTSW |
2 |
130,620,393 (GRCm39) |
missense |
probably benign |
|
R6732:Dnaaf9
|
UTSW |
2 |
130,652,740 (GRCm39) |
critical splice donor site |
probably null |
|
R6938:Dnaaf9
|
UTSW |
2 |
130,617,673 (GRCm39) |
missense |
probably benign |
0.00 |
R7161:Dnaaf9
|
UTSW |
2 |
130,648,708 (GRCm39) |
missense |
unknown |
|
R7193:Dnaaf9
|
UTSW |
2 |
130,648,708 (GRCm39) |
missense |
unknown |
|
R7194:Dnaaf9
|
UTSW |
2 |
130,648,708 (GRCm39) |
missense |
unknown |
|
R7233:Dnaaf9
|
UTSW |
2 |
130,648,708 (GRCm39) |
missense |
unknown |
|
R7234:Dnaaf9
|
UTSW |
2 |
130,648,708 (GRCm39) |
missense |
unknown |
|
R7238:Dnaaf9
|
UTSW |
2 |
130,648,708 (GRCm39) |
missense |
unknown |
|
R7239:Dnaaf9
|
UTSW |
2 |
130,648,708 (GRCm39) |
missense |
unknown |
|
R7268:Dnaaf9
|
UTSW |
2 |
130,648,708 (GRCm39) |
missense |
unknown |
|
R7807:Dnaaf9
|
UTSW |
2 |
130,552,785 (GRCm39) |
missense |
probably damaging |
1.00 |
R7904:Dnaaf9
|
UTSW |
2 |
130,633,923 (GRCm39) |
splice site |
probably null |
|
R7999:Dnaaf9
|
UTSW |
2 |
130,579,372 (GRCm39) |
missense |
probably benign |
0.00 |
R8047:Dnaaf9
|
UTSW |
2 |
130,617,019 (GRCm39) |
missense |
probably damaging |
0.98 |
R8286:Dnaaf9
|
UTSW |
2 |
130,559,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R8315:Dnaaf9
|
UTSW |
2 |
130,612,655 (GRCm39) |
small deletion |
probably benign |
|
R8439:Dnaaf9
|
UTSW |
2 |
130,612,621 (GRCm39) |
missense |
probably damaging |
1.00 |
R8925:Dnaaf9
|
UTSW |
2 |
130,579,300 (GRCm39) |
nonsense |
probably null |
|
R8927:Dnaaf9
|
UTSW |
2 |
130,579,300 (GRCm39) |
nonsense |
probably null |
|
R9070:Dnaaf9
|
UTSW |
2 |
130,654,793 (GRCm39) |
missense |
possibly damaging |
0.61 |
R9367:Dnaaf9
|
UTSW |
2 |
130,581,380 (GRCm39) |
missense |
probably benign |
0.00 |
R9558:Dnaaf9
|
UTSW |
2 |
130,617,660 (GRCm39) |
missense |
probably damaging |
1.00 |
R9565:Dnaaf9
|
UTSW |
2 |
130,648,711 (GRCm39) |
missense |
unknown |
|
R9758:Dnaaf9
|
UTSW |
2 |
130,554,938 (GRCm39) |
missense |
probably damaging |
0.99 |
RF027:Dnaaf9
|
UTSW |
2 |
130,612,664 (GRCm39) |
small insertion |
probably benign |
|
RF038:Dnaaf9
|
UTSW |
2 |
130,612,664 (GRCm39) |
nonsense |
probably null |
|
RF046:Dnaaf9
|
UTSW |
2 |
130,612,654 (GRCm39) |
nonsense |
probably null |
|
RF048:Dnaaf9
|
UTSW |
2 |
130,612,654 (GRCm39) |
nonsense |
probably null |
|
Z1177:Dnaaf9
|
UTSW |
2 |
130,552,787 (GRCm39) |
missense |
probably benign |
0.04 |
|