Other mutations in this stock |
Total: 211 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700001K19Rik |
TCT |
TCTCCT |
12: 110,634,882 (GRCm39) |
|
probably benign |
Het |
A630001G21Rik |
CTGTT |
CT |
1: 85,650,856 (GRCm39) |
|
probably benign |
Homo |
Abcb11 |
C |
A |
2: 69,073,862 (GRCm39) |
R1221L |
probably damaging |
Homo |
Abcb4 |
GAAA |
G |
5: 8,946,597 (GRCm39) |
|
probably benign |
Homo |
Ahdc1 |
CT |
CTCGT |
4: 132,790,070 (GRCm39) |
|
probably benign |
Homo |
Alpk3 |
TCT |
TCTACT |
7: 80,727,510 (GRCm39) |
|
probably benign |
Het |
Amfr |
C |
G |
8: 94,731,787 (GRCm39) |
G30R |
probably damaging |
Homo |
Ankrd35 |
GC |
GCTAC |
3: 96,591,165 (GRCm39) |
|
probably benign |
Homo |
Anxa7 |
C |
T |
14: 20,519,479 (GRCm39) |
G113E |
probably damaging |
Homo |
Apc |
CAATAAAGC |
CAATAAAGCTAATAAAGC |
18: 34,415,052 (GRCm39) |
|
probably benign |
Homo |
Apol6 |
GTTT |
GTTTCTTT |
15: 76,935,642 (GRCm39) |
|
probably null |
Homo |
Arpc1b |
GGTGGC |
GGTGGCGTGGC |
5: 145,063,597 (GRCm39) |
|
probably null |
Het |
AY358078 |
C |
T |
14: 52,043,155 (GRCm39) |
S281L |
unknown |
Homo |
Blm |
ACCTGC |
ACCTGCCTGC |
7: 80,113,519 (GRCm39) |
|
probably null |
Het |
Blm |
T |
TACCA |
7: 80,113,522 (GRCm39) |
|
probably null |
Het |
Bltp1 |
TTATTAT |
TTATTATTATTATTACTATTAT |
3: 37,104,903 (GRCm39) |
|
probably benign |
Het |
Blzf1 |
TTGT |
TT |
1: 164,131,486 (GRCm39) |
|
probably null |
Homo |
Btnl10 |
A |
AAGG |
11: 58,814,757 (GRCm39) |
|
probably benign |
Homo |
Cacna1a |
ACC |
ACCGCC |
8: 85,365,349 (GRCm39) |
|
probably benign |
Het |
Cacna1a |
ACC |
ACCCCC |
8: 85,365,355 (GRCm39) |
|
probably benign |
Homo |
Catsper2 |
TTC |
TTCTTTTACTTTGTC |
2: 121,228,021 (GRCm39) |
|
probably benign |
Homo |
Ccdc170 |
ACC |
ACCTCC |
10: 4,511,023 (GRCm39) |
|
probably benign |
Het |
Ccdc170 |
AC |
ACCCC |
10: 4,511,029 (GRCm39) |
|
probably benign |
Het |
Ccdc73 |
TAAG |
T |
2: 104,822,185 (GRCm39) |
|
probably benign |
Homo |
Ccnk |
TTCCCAC |
T |
12: 108,168,766 (GRCm39) |
|
probably benign |
Het |
Cdan1 |
A |
C |
2: 120,555,452 (GRCm39) |
V763G |
probably damaging |
Het |
Cdk6 |
A |
G |
5: 3,394,211 (GRCm39) |
|
probably benign |
Het |
Cdx1 |
TGCTGC |
TGCTGCCGCTGC |
18: 61,152,946 (GRCm39) |
|
probably benign |
Het |
Cdx1 |
GCTGCT |
GCTGCTTCTGCT |
18: 61,152,950 (GRCm39) |
|
probably benign |
Het |
Cfap46 |
CCTTCT |
CCTTCTTCT |
7: 139,218,846 (GRCm39) |
|
probably benign |
Homo |
Chd4 |
GC |
GCTCCCCC |
6: 125,099,094 (GRCm39) |
|
probably benign |
Homo |
Cluh |
GAGCCT |
GAGCCTAAGCCT |
11: 74,560,350 (GRCm39) |
|
probably benign |
Het |
Cluh |
CC |
CCTGAGGC |
11: 74,560,359 (GRCm39) |
|
probably benign |
Het |
Cluh |
CCCCGAGCC |
CCCCGAGCCCGAGCC |
11: 74,560,340 (GRCm39) |
|
probably benign |
Het |
Cluh |
AGCCTG |
AGCCTGCGCCTG |
11: 74,560,345 (GRCm39) |
|
probably benign |
Het |
Cntnap1 |
GCCCCA |
GCCCCACCCCCA |
11: 101,080,408 (GRCm39) |
|
probably benign |
Het |
Cntnap1 |
CCCAGC |
CCCAGCGCCAGC |
11: 101,080,416 (GRCm39) |
|
probably benign |
Het |
Cntnap1 |
AGCCCC |
AGCCCCCGCCCC |
11: 101,080,395 (GRCm39) |
|
probably benign |
Het |
Cntnap1 |
GCCCCA |
GCCCCAACCCCA |
11: 101,080,402 (GRCm39) |
|
probably benign |
Het |
Cracdl |
T |
A |
1: 37,664,116 (GRCm39) |
E594V |
probably benign |
Homo |
Cracdl |
C |
A |
1: 37,664,117 (GRCm39) |
E594* |
probably null |
Homo |
Cul9 |
CTC |
CTCTTC |
17: 46,811,784 (GRCm39) |
|
probably benign |
Het |
Cul9 |
CTCTTC |
CTCTTCTTC |
17: 46,811,772 (GRCm39) |
|
probably benign |
Het |
Cyth2 |
C |
A |
7: 45,462,466 (GRCm39) |
S102I |
possibly damaging |
Het |
Dbr1 |
AGGAGG |
AGGAGGCGGAGG |
9: 99,465,739 (GRCm39) |
|
probably benign |
Het |
Dbr1 |
GGAGG |
GGAGGACGAGG |
9: 99,465,752 (GRCm39) |
|
probably benign |
Het |
Dennd2b |
CACCACACTGGGGCAGCCCACACTGGGGCAG |
CCCCACACTGGGGCAG |
7: 109,156,128 (GRCm39) |
|
probably benign |
Het |
Dhx8 |
GACCGA |
GACCGATACCGA |
11: 101,629,005 (GRCm39) |
|
probably benign |
Homo |
Dhx8 |
GAGACC |
GAGACCCAGACC |
11: 101,629,015 (GRCm39) |
|
probably benign |
Homo |
Dhx8 |
CGAGAC |
CGAGACGGAGAC |
11: 101,629,008 (GRCm39) |
|
probably benign |
Homo |
Dnaaf9 |
CC |
CCTGC |
2: 130,612,672 (GRCm39) |
|
probably benign |
Het |
Dnah8 |
ACTGCCCCT |
ACT |
17: 30,854,439 (GRCm39) |
|
probably benign |
Het |
Dnah8 |
CCTCCCG |
C |
17: 30,854,451 (GRCm39) |
|
probably benign |
Homo |
Dnajb5 |
AGGTG |
A |
4: 42,957,126 (GRCm39) |
|
probably null |
Het |
Dusp10 |
G |
T |
1: 183,769,253 (GRCm39) |
C73F |
probably damaging |
Homo |
E4f1 |
CCG |
CCGACG |
17: 24,674,166 (GRCm39) |
|
probably benign |
Homo |
Eif3a |
TTA |
TTATTATA |
19: 60,763,727 (GRCm39) |
|
probably benign |
Het |
Fam81b |
TTC |
TTCGTC |
13: 76,419,438 (GRCm39) |
|
probably benign |
Het |
Fbxo22 |
G |
A |
9: 55,116,666 (GRCm39) |
R56H |
probably damaging |
Het |
Fcgr1 |
CTTCT |
C |
3: 96,191,820 (GRCm39) |
|
probably null |
Het |
Fcgr1 |
T |
C |
3: 96,194,410 (GRCm39) |
D159G |
probably benign |
Homo |
Fmn1 |
CC |
CCTCCTTC |
2: 113,356,129 (GRCm39) |
|
probably benign |
Het |
Fmn1 |
CCTCCT |
CCTCCTACTCCT |
2: 113,356,123 (GRCm39) |
|
probably benign |
Het |
Fmn1 |
CC |
CCCCCTGC |
2: 113,356,126 (GRCm39) |
|
probably benign |
Het |
G530012D18Rik |
GA |
GACAGAGATA |
1: 85,504,899 (GRCm39) |
|
probably null |
Het |
Gli3 |
G |
A |
13: 15,818,942 (GRCm39) |
R248H |
probably damaging |
Het |
Gm16503 |
G |
A |
4: 147,625,710 (GRCm39) |
G68E |
unknown |
Het |
Gm19345 |
GGATGGCAGGTG |
GG |
7: 19,591,527 (GRCm39) |
|
probably null |
Het |
Gm4340 |
AGC |
AGCTGC |
10: 104,031,958 (GRCm39) |
|
probably benign |
Het |
Gm4340 |
AG |
AGCGG |
10: 104,031,961 (GRCm39) |
|
probably benign |
Het |
Gm4340 |
GCA |
GCAACA |
10: 104,031,938 (GRCm39) |
|
probably benign |
Het |
Gm6309 |
C |
T |
5: 146,104,993 (GRCm39) |
V307I |
probably benign |
Het |
Gpatch11 |
AAGAGG |
AAGAGGCAGAGG |
17: 79,149,600 (GRCm39) |
|
probably benign |
Het |
Gpatch11 |
AGGAA |
AGGAAGCGGAA |
17: 79,149,609 (GRCm39) |
|
probably benign |
Het |
Hoxa10 |
T |
A |
6: 52,211,166 (GRCm39) |
Q250L |
possibly damaging |
Homo |
Hrh1 |
T |
C |
6: 114,458,084 (GRCm39) |
I455T |
possibly damaging |
Het |
Hspa1b |
GCGCC |
GC |
17: 35,176,105 (GRCm39) |
|
probably benign |
Homo |
Iba57 |
GAAA |
GAAAAA |
11: 59,052,331 (GRCm39) |
|
probably null |
Homo |
Igf1r |
TGGAGC |
TGGAGCTGGAGAGGGAGC |
7: 67,875,929 (GRCm39) |
|
probably benign |
Het |
Il17rd |
CGG |
CGGAGG |
14: 26,804,637 (GRCm39) |
|
probably benign |
Het |
Il2 |
TGG |
TGGGGCTTGAAGCGG |
3: 37,179,977 (GRCm39) |
|
probably benign |
Het |
Il2 |
AGGTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTG |
AGCTGCTGCTGCTGCTGCTGCTGCTG |
3: 37,179,913 (GRCm39) |
|
probably benign |
Het |
Kcng4 |
G |
T |
8: 120,360,258 (GRCm39) |
Y39* |
probably null |
Homo |
Klra2 |
G |
GAAATCCACAT |
6: 131,198,815 (GRCm39) |
|
probably null |
Het |
Kmt2b |
CCTCCT |
CCTCCTTCTCCT |
7: 30,285,792 (GRCm39) |
|
probably benign |
Het |
Kmt2b |
CCTCCT |
CCTCCTGCTCCT |
7: 30,285,795 (GRCm39) |
|
probably benign |
Het |
Kmt2b |
TCCTCC |
TCCTCCCCCTCC |
7: 30,285,803 (GRCm39) |
|
probably benign |
Het |
Kmt2b |
TCCTCC |
TCCTCCCCCTCC |
7: 30,285,791 (GRCm39) |
|
probably benign |
Het |
Krt10 |
TCCTCC |
TCCTCCGCCTCC |
11: 99,280,099 (GRCm39) |
|
probably benign |
Het |
Krt10 |
TCCGCC |
TCCGCCGCC |
11: 99,277,023 (GRCm39) |
|
probably benign |
Homo |
Krt10 |
TCC |
TCCTCCACC |
11: 99,280,105 (GRCm39) |
|
probably benign |
Homo |
Krtap28-10 |
TCCCACA |
TCCCACACCCACA |
1: 83,019,844 (GRCm39) |
|
probably benign |
Homo |
Krtap4-2 |
A |
ACAC |
11: 99,525,839 (GRCm39) |
|
probably benign |
Het |
Krtap9-3 |
AC |
ACAGGTGTCGC |
11: 99,488,830 (GRCm39) |
|
probably benign |
Het |
Las1l |
AGG |
AGGGGG |
X: 94,984,427 (GRCm39) |
|
probably benign |
Het |
Las1l |
GAG |
GAGCAG |
X: 94,984,435 (GRCm39) |
|
probably benign |
Het |
Las1l |
AGG |
AGGCGG |
X: 94,984,433 (GRCm39) |
|
probably benign |
Het |
Lrit3 |
TGC |
TGCAGC |
3: 129,582,455 (GRCm39) |
|
probably benign |
Het |
Lrit3 |
AC |
ACATTC |
3: 129,597,562 (GRCm39) |
|
probably null |
Homo |
Lrit3 |
GCT |
GCTTCT |
3: 129,582,459 (GRCm39) |
|
probably benign |
Het |
Luzp1 |
A |
AGGTGGCCTCTTCAGT |
4: 136,270,507 (GRCm39) |
|
probably benign |
Het |
Mamld1 |
AGC |
AGCCGC |
X: 70,162,441 (GRCm39) |
|
probably benign |
Het |
Mamld1 |
GCA |
GCAACA |
X: 70,162,445 (GRCm39) |
|
probably benign |
Het |
Mapk8ip3 |
G |
A |
17: 25,121,093 (GRCm39) |
|
probably null |
Homo |
Mbd1 |
TGTCTGCATCTGCGTCTTCGTCTGCATCTGCATCTGCGTCTTCGTCTGCATCTGCATCTGC |
TATCTGCATCTGCGTCTTCGTCTGCATCTGCATCTGC |
18: 74,406,644 (GRCm39) |
|
probably benign |
Het |
Nat8f2 |
T |
A |
6: 85,844,668 (GRCm39) |
L231F |
possibly damaging |
Homo |
Nfxl1 |
CC |
CCGGGGAC |
5: 72,716,464 (GRCm39) |
|
probably benign |
Het |
Noc2l |
CTG |
CTGTTG |
4: 156,324,552 (GRCm39) |
|
probably benign |
Het |
Noc2l |
GGTAG |
GG |
4: 156,325,958 (GRCm39) |
|
probably benign |
Homo |
Noc2l |
GCT |
GCTTCT |
4: 156,324,551 (GRCm39) |
|
probably benign |
Het |
Nxpe5 |
C |
T |
5: 138,228,196 (GRCm39) |
|
probably benign |
Het |
Or10j2 |
GGGCTGCTTGTGGCAAT |
G |
1: 173,098,197 (GRCm39) |
|
probably null |
Het |
Or51a43 |
G |
C |
7: 103,720,499 (GRCm39) |
|
probably benign |
Homo |
Or51f2 |
CT |
CTAATTGCCTT |
7: 102,526,440 (GRCm39) |
|
probably benign |
Homo |
Or8b41 |
A |
G |
9: 38,054,484 (GRCm39) |
I13V |
probably benign |
Homo |
Or8u3-ps |
CAG |
CAGAG |
2: 85,953,104 (GRCm39) |
|
probably null |
Homo |
Osmr |
C |
CTCA |
15: 6,867,187 (GRCm39) |
|
probably null |
Homo |
Patl2 |
GC |
GCTAC |
2: 121,956,625 (GRCm39) |
|
probably null |
Het |
Patl2 |
C |
CTGA |
2: 121,956,626 (GRCm39) |
|
probably benign |
Het |
Patl2 |
CTG |
CTGTTG |
2: 121,956,617 (GRCm39) |
|
probably benign |
Het |
Pdik1l |
GTTTTTGTTTT |
GTTTTTGTTTTTTTTTTGTTTT |
4: 134,006,678 (GRCm39) |
|
probably null |
Homo |
Pdik1l |
ACCACC |
ACCACCCCCACC |
4: 134,006,817 (GRCm39) |
|
probably benign |
Het |
Phc1 |
GCTG |
GCTGCTTCTG |
6: 122,300,557 (GRCm39) |
|
probably benign |
Het |
Piezo1 |
G |
A |
8: 123,222,308 (GRCm39) |
R503W |
probably damaging |
Homo |
Pitrm1 |
TTTTA |
T |
13: 6,610,632 (GRCm39) |
|
probably benign |
Homo |
Pkdrej |
TG |
TGGGAGCG |
15: 85,703,881 (GRCm39) |
|
probably benign |
Homo |
Pla2g4e |
AGGG |
A |
2: 120,075,205 (GRCm39) |
|
probably benign |
Homo |
Plekhs1 |
AC |
ACCTCCCCCGAGCC |
19: 56,468,295 (GRCm39) |
|
probably benign |
Het |
Pnma8a |
CCTCATGATGCACCTGCTTCAACATC |
CCTCATGATGCACCTGCTTCAACATCTCATGATGCACCTGCTTCAACATC |
7: 16,695,350 (GRCm39) |
|
probably benign |
Homo |
Pnma8b |
TGGA |
T |
7: 16,679,931 (GRCm39) |
|
probably benign |
Het |
Ppp1r3f |
C |
A |
X: 7,426,575 (GRCm39) |
G562V |
probably damaging |
Homo |
Prr13 |
CTC |
CTCATC |
15: 102,370,608 (GRCm39) |
|
probably benign |
Het |
Prss41 |
CACA |
C |
17: 24,063,071 (GRCm39) |
|
probably benign |
Het |
Prtg |
GTAAC |
G |
9: 72,764,363 (GRCm39) |
|
probably benign |
Het |
Ptk2b |
C |
T |
14: 66,411,298 (GRCm39) |
R411Q |
possibly damaging |
Homo |
Ptms |
TCT |
TCTGCT |
6: 124,891,420 (GRCm39) |
|
probably benign |
Homo |
Ptms |
C |
CTTG |
6: 124,891,424 (GRCm39) |
|
probably benign |
Homo |
Ptms |
TTC |
TTCGTC |
6: 124,891,422 (GRCm39) |
|
probably benign |
Homo |
Ptpn23 |
G |
T |
9: 110,216,701 (GRCm39) |
P1052T |
probably benign |
Homo |
Rab3il1 |
C |
A |
19: 10,011,115 (GRCm39) |
A264E |
probably damaging |
Homo |
Rbm6 |
GCTGT |
G |
9: 107,659,954 (GRCm39) |
|
probably null |
Homo |
Rtbdn |
TAG |
TAGGGGCAG |
8: 85,682,790 (GRCm39) |
|
probably benign |
Het |
Rtbdn |
GGC |
GGCAGCTGC |
8: 85,682,806 (GRCm39) |
|
probably benign |
Het |
Rtbdn |
CGGC |
CGGCAGGGGC |
8: 85,682,805 (GRCm39) |
|
probably benign |
Het |
Rtbdn |
AGCG |
AGCGTCCGCG |
8: 85,682,797 (GRCm39) |
|
probably benign |
Het |
Sbp |
CAAAG |
CAAAGCTGCTGACAAAAAAG |
17: 24,164,356 (GRCm39) |
|
probably benign |
Het |
Sbp |
G |
GCTGACAACAAAGATC |
17: 24,164,363 (GRCm39) |
|
probably benign |
Het |
Setd1a |
GTGGTAGTG |
GTGGTAGTGTTGGTAGTG |
7: 127,384,484 (GRCm39) |
|
probably benign |
Het |
Sfswap |
GCCCACTC |
GCCCACTCATCCCACTC |
5: 129,646,820 (GRCm39) |
|
probably benign |
Het |
Six3 |
GGC |
GGCAGC |
17: 85,928,785 (GRCm39) |
|
probably benign |
Het |
Six3 |
GCG |
GCGCCG |
17: 85,928,786 (GRCm39) |
|
probably benign |
Het |
Six3 |
CGG |
CGGGGG |
17: 85,928,790 (GRCm39) |
|
probably benign |
Het |
Six3 |
GGC |
GGCAGC |
17: 85,928,791 (GRCm39) |
|
probably benign |
Het |
Six3 |
CGG |
CGGGGG |
17: 85,928,793 (GRCm39) |
|
probably benign |
Het |
Six3 |
CGG |
CGGGGG |
17: 85,928,796 (GRCm39) |
|
probably benign |
Het |
Slc12a1 |
ACC |
ACCTTTGGCCACAACTCC |
2: 124,996,134 (GRCm39) |
|
probably benign |
Homo |
Smarca2 |
CAGCAGCAGCAGCAGCAGCA |
CAGCAGCAGCAGCAGCAGCAGCAGCA |
19: 26,608,399 (GRCm39) |
|
probably benign |
Homo |
Spaca1 |
TCGCTC |
TCGCTCGCGCTC |
4: 34,049,836 (GRCm39) |
|
probably benign |
Het |
Spag1 |
TTC |
TTCGTC |
15: 36,197,879 (GRCm39) |
|
probably benign |
Het |
Spag17 |
AGG |
AGGCGG |
3: 99,963,573 (GRCm39) |
|
probably benign |
Het |
Srebf2 |
G |
T |
15: 82,069,536 (GRCm39) |
A693S |
probably damaging |
Homo |
Srpk2 |
T |
C |
5: 23,750,194 (GRCm39) |
|
probably null |
Homo |
Sry |
AACTGCT |
A |
Y: 2,663,195 (GRCm39) |
|
probably benign |
Het |
Sry |
GTG |
GTGTTG |
Y: 2,662,837 (GRCm39) |
|
probably benign |
Homo |
Sry |
TGG |
TGGGGG |
Y: 2,662,838 (GRCm39) |
|
probably benign |
Homo |
Stard9 |
C |
CTAAGGGACTAGTAGG |
2: 120,526,566 (GRCm39) |
|
probably benign |
Het |
Supt20 |
CAGCAG |
CAGCAGGAGCAG |
3: 54,635,079 (GRCm39) |
|
probably benign |
Het |
Supt20 |
CAGCAG |
CAGCAGAAGCAG |
3: 54,635,082 (GRCm39) |
|
probably benign |
Het |
Supt20 |
GCAGCA |
GCAGCAACAGCA |
3: 54,635,078 (GRCm39) |
|
probably benign |
Het |
Tcof1 |
GGGTA |
G |
18: 60,961,722 (GRCm39) |
|
probably benign |
Homo |
Tdpoz3 |
A |
C |
3: 93,733,981 (GRCm39) |
N219H |
probably benign |
Het |
Tesk1 |
C |
CCCCG |
4: 43,447,004 (GRCm39) |
|
probably null |
Homo |
Tob1 |
GCA |
GCAACA |
11: 94,105,290 (GRCm39) |
|
probably benign |
Het |
Tob1 |
CACA |
CACAACA |
11: 94,105,277 (GRCm39) |
|
probably benign |
Het |
Tob1 |
A |
AGCC |
11: 94,105,304 (GRCm39) |
|
probably benign |
Het |
Trav15-2-dv6-2 |
AG |
AGAGG |
14: 53,887,213 (GRCm39) |
|
probably benign |
Homo |
Trav15-2-dv6-2 |
G |
GAAA |
14: 53,887,214 (GRCm39) |
|
probably benign |
Homo |
Trim63 |
GAGT |
G |
4: 134,055,036 (GRCm39) |
|
probably benign |
Het |
Tsbp1 |
CAG |
CAGAAG |
17: 34,679,025 (GRCm39) |
|
probably benign |
Het |
Tsbp1 |
GCA |
GCATCA |
17: 34,679,042 (GRCm39) |
|
probably benign |
Het |
Tsen2 |
G |
GAGA |
6: 115,537,038 (GRCm39) |
|
probably benign |
Het |
Ttf2 |
TC |
TCCCC |
3: 100,870,476 (GRCm39) |
|
probably benign |
Homo |
Tusc1 |
ACCGCC |
ACCGCCCCCGCC |
4: 93,223,550 (GRCm39) |
|
probably benign |
Homo |
Ubqlnl |
TGAG |
T |
7: 103,799,042 (GRCm39) |
|
probably benign |
Homo |
Ubtf |
CCT |
CCTACT |
11: 102,197,774 (GRCm39) |
|
probably null |
Het |
Ubtf |
TCC |
TCCACC |
11: 102,197,776 (GRCm39) |
|
probably benign |
Het |
Vps13b |
G |
T |
15: 35,847,103 (GRCm39) |
A2629S |
probably damaging |
Homo |
Wasf3 |
G |
T |
5: 146,407,060 (GRCm39) |
R460L |
probably damaging |
Het |
Zc3h13 |
TGCGAGATG |
TGCGAGATGAGCGAGATG |
14: 75,561,039 (GRCm39) |
|
probably benign |
Homo |
Zc3h13 |
ATGTGCGAG |
ATGTGCGAGGTGTGCGAG |
14: 75,561,036 (GRCm39) |
|
probably benign |
Homo |
Zfhx3 |
GCAACA |
GCAACAACAACAACA |
8: 109,682,720 (GRCm39) |
|
probably benign |
Het |
Zfhx3 |
GCA |
GCAACAGCACCA |
8: 109,682,735 (GRCm39) |
|
probably benign |
Het |
Zfhx3 |
AGCA |
AGCAACAGACGCA |
8: 109,682,734 (GRCm39) |
|
probably benign |
Het |
Zfp111 |
TCA |
TCAACA |
7: 23,899,230 (GRCm39) |
|
probably benign |
Homo |
Zfp112 |
CATGA |
CATGATGA |
7: 23,824,832 (GRCm39) |
|
probably benign |
Homo |
Zfp26 |
C |
A |
9: 20,349,842 (GRCm39) |
A241S |
probably benign |
Homo |
Zfp282 |
CGG |
CGGGGG |
6: 47,881,724 (GRCm39) |
|
probably benign |
Het |
Zfp282 |
CGG |
CGGGGG |
6: 47,881,733 (GRCm39) |
|
probably benign |
Het |
Zfp335 |
TC |
TCCCC |
2: 164,749,404 (GRCm39) |
|
probably benign |
Het |
Zfp335 |
TCC |
TCCGCC |
2: 164,749,395 (GRCm39) |
|
probably benign |
Het |
Zfp335 |
CTC |
CTCGTC |
2: 164,749,394 (GRCm39) |
|
probably benign |
Het |
Zfp462 |
CCACC |
CCACCTCAGCCACAGTCACC |
4: 55,009,758 (GRCm39) |
|
probably benign |
Het |
Zfp462 |
ACC |
ACCTCAGCCACAGTCGCC |
4: 55,009,760 (GRCm39) |
|
probably benign |
Het |
Zfp598 |
ACCACC |
ACCACCCCCACC |
17: 24,899,750 (GRCm39) |
|
probably benign |
Het |
Zfp598 |
AC |
ACCACCGC |
17: 24,899,765 (GRCm39) |
|
probably benign |
Het |
Zfp598 |
ACCACC |
ACCACCGCCACC |
17: 24,899,756 (GRCm39) |
|
probably benign |
Het |
Zfp831 |
TCC |
TCCCCC |
2: 174,487,264 (GRCm39) |
|
probably benign |
Het |
Zfp831 |
TC |
TCCGC |
2: 174,487,276 (GRCm39) |
|
probably benign |
Het |
Zfp831 |
CTC |
CTCATC |
2: 174,487,269 (GRCm39) |
|
probably benign |
Het |
Zfp93 |
CAGGCATAG |
CAG |
7: 23,974,814 (GRCm39) |
|
probably benign |
Homo |
Zscan10 |
TGACG |
TG |
17: 23,828,419 (GRCm39) |
|
probably benign |
Homo |
|
Other mutations in Spata31h1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00090:Spata31h1
|
APN |
10 |
82,119,586 (GRCm39) |
missense |
probably benign |
0.06 |
IGL01457:Spata31h1
|
APN |
10 |
82,120,568 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01540:Spata31h1
|
APN |
10 |
82,120,016 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL02693:Spata31h1
|
APN |
10 |
82,121,092 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02867:Spata31h1
|
APN |
10 |
82,119,654 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02889:Spata31h1
|
APN |
10 |
82,119,654 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL03080:Spata31h1
|
APN |
10 |
82,119,816 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03120:Spata31h1
|
APN |
10 |
82,120,869 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL03351:Spata31h1
|
APN |
10 |
82,119,401 (GRCm39) |
utr 3 prime |
probably benign |
|
FR4449:Spata31h1
|
UTSW |
10 |
82,121,303 (GRCm39) |
frame shift |
probably null |
|
FR4548:Spata31h1
|
UTSW |
10 |
82,126,830 (GRCm39) |
small insertion |
probably benign |
|
PIT4480001:Spata31h1
|
UTSW |
10 |
82,119,586 (GRCm39) |
missense |
probably benign |
0.06 |
R0102:Spata31h1
|
UTSW |
10 |
82,119,390 (GRCm39) |
missense |
probably damaging |
1.00 |
R0312:Spata31h1
|
UTSW |
10 |
82,120,203 (GRCm39) |
missense |
probably damaging |
1.00 |
R1303:Spata31h1
|
UTSW |
10 |
82,120,390 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2039:Spata31h1
|
UTSW |
10 |
82,120,510 (GRCm39) |
missense |
probably damaging |
1.00 |
R2356:Spata31h1
|
UTSW |
10 |
82,119,789 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4740:Spata31h1
|
UTSW |
10 |
82,119,481 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4857:Spata31h1
|
UTSW |
10 |
82,119,682 (GRCm39) |
missense |
possibly damaging |
0.61 |
R5017:Spata31h1
|
UTSW |
10 |
82,132,510 (GRCm39) |
missense |
unknown |
|
R5095:Spata31h1
|
UTSW |
10 |
82,119,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R5209:Spata31h1
|
UTSW |
10 |
82,119,652 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5388:Spata31h1
|
UTSW |
10 |
82,119,561 (GRCm39) |
missense |
probably damaging |
0.99 |
R5642:Spata31h1
|
UTSW |
10 |
82,120,317 (GRCm39) |
missense |
probably damaging |
1.00 |
R5646:Spata31h1
|
UTSW |
10 |
82,119,610 (GRCm39) |
missense |
probably damaging |
0.99 |
R6188:Spata31h1
|
UTSW |
10 |
82,121,091 (GRCm39) |
missense |
probably damaging |
0.96 |
R6215:Spata31h1
|
UTSW |
10 |
82,126,946 (GRCm39) |
missense |
probably benign |
0.07 |
R6252:Spata31h1
|
UTSW |
10 |
82,119,588 (GRCm39) |
missense |
probably benign |
0.30 |
R6275:Spata31h1
|
UTSW |
10 |
82,121,202 (GRCm39) |
missense |
probably damaging |
1.00 |
R6303:Spata31h1
|
UTSW |
10 |
82,126,202 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6304:Spata31h1
|
UTSW |
10 |
82,126,202 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6313:Spata31h1
|
UTSW |
10 |
82,129,470 (GRCm39) |
missense |
probably benign |
0.00 |
R6323:Spata31h1
|
UTSW |
10 |
82,118,916 (GRCm39) |
missense |
probably benign |
0.27 |
R6374:Spata31h1
|
UTSW |
10 |
82,124,731 (GRCm39) |
unclassified |
probably benign |
|
R6407:Spata31h1
|
UTSW |
10 |
82,129,645 (GRCm39) |
missense |
probably benign |
0.16 |
R6468:Spata31h1
|
UTSW |
10 |
82,131,150 (GRCm39) |
missense |
probably benign |
0.01 |
R6490:Spata31h1
|
UTSW |
10 |
82,125,138 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6605:Spata31h1
|
UTSW |
10 |
82,131,871 (GRCm39) |
missense |
probably benign |
0.27 |
R6614:Spata31h1
|
UTSW |
10 |
82,127,482 (GRCm39) |
missense |
probably benign |
0.31 |
R6626:Spata31h1
|
UTSW |
10 |
82,128,667 (GRCm39) |
missense |
probably benign |
0.03 |
R6630:Spata31h1
|
UTSW |
10 |
82,122,906 (GRCm39) |
missense |
possibly damaging |
0.81 |
R6646:Spata31h1
|
UTSW |
10 |
82,132,664 (GRCm39) |
missense |
unknown |
|
R6723:Spata31h1
|
UTSW |
10 |
82,125,657 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6751:Spata31h1
|
UTSW |
10 |
82,119,331 (GRCm39) |
missense |
probably benign |
0.06 |
R6850:Spata31h1
|
UTSW |
10 |
82,128,888 (GRCm39) |
missense |
possibly damaging |
0.68 |
R6944:Spata31h1
|
UTSW |
10 |
82,132,056 (GRCm39) |
missense |
probably benign |
0.03 |
R6957:Spata31h1
|
UTSW |
10 |
82,129,620 (GRCm39) |
missense |
probably benign |
0.03 |
R6988:Spata31h1
|
UTSW |
10 |
82,127,733 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7069:Spata31h1
|
UTSW |
10 |
82,125,777 (GRCm39) |
missense |
probably damaging |
0.99 |
R7164:Spata31h1
|
UTSW |
10 |
82,122,063 (GRCm39) |
missense |
probably damaging |
1.00 |
R7175:Spata31h1
|
UTSW |
10 |
82,122,583 (GRCm39) |
missense |
probably damaging |
1.00 |
R7201:Spata31h1
|
UTSW |
10 |
82,127,461 (GRCm39) |
missense |
probably benign |
0.03 |
R7203:Spata31h1
|
UTSW |
10 |
82,129,248 (GRCm39) |
missense |
probably benign |
0.00 |
R7205:Spata31h1
|
UTSW |
10 |
82,125,161 (GRCm39) |
missense |
probably benign |
0.35 |
R7241:Spata31h1
|
UTSW |
10 |
82,122,876 (GRCm39) |
missense |
probably benign |
0.01 |
R7283:Spata31h1
|
UTSW |
10 |
82,127,131 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7305:Spata31h1
|
UTSW |
10 |
82,120,953 (GRCm39) |
missense |
probably benign |
0.06 |
R7358:Spata31h1
|
UTSW |
10 |
82,127,847 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7360:Spata31h1
|
UTSW |
10 |
82,132,341 (GRCm39) |
missense |
unknown |
|
R7362:Spata31h1
|
UTSW |
10 |
82,128,831 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7385:Spata31h1
|
UTSW |
10 |
82,123,729 (GRCm39) |
missense |
probably benign |
0.05 |
R7385:Spata31h1
|
UTSW |
10 |
82,123,571 (GRCm39) |
missense |
probably benign |
0.03 |
R7472:Spata31h1
|
UTSW |
10 |
82,119,421 (GRCm39) |
missense |
probably benign |
0.03 |
R7493:Spata31h1
|
UTSW |
10 |
82,152,264 (GRCm39) |
missense |
unknown |
|
R7493:Spata31h1
|
UTSW |
10 |
82,124,798 (GRCm39) |
nonsense |
probably null |
|
R7498:Spata31h1
|
UTSW |
10 |
82,127,113 (GRCm39) |
missense |
probably benign |
0.03 |
R7512:Spata31h1
|
UTSW |
10 |
82,128,469 (GRCm39) |
missense |
probably benign |
0.31 |
R7560:Spata31h1
|
UTSW |
10 |
82,120,449 (GRCm39) |
missense |
probably damaging |
1.00 |
R7591:Spata31h1
|
UTSW |
10 |
82,128,046 (GRCm39) |
missense |
probably benign |
0.16 |
R7636:Spata31h1
|
UTSW |
10 |
82,130,973 (GRCm39) |
missense |
probably benign |
0.01 |
R7640:Spata31h1
|
UTSW |
10 |
82,130,490 (GRCm39) |
missense |
probably damaging |
0.99 |
R7709:Spata31h1
|
UTSW |
10 |
82,126,366 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7790:Spata31h1
|
UTSW |
10 |
82,123,329 (GRCm39) |
missense |
probably benign |
0.06 |
R7875:Spata31h1
|
UTSW |
10 |
82,123,456 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7878:Spata31h1
|
UTSW |
10 |
82,119,856 (GRCm39) |
missense |
probably benign |
0.04 |
R7899:Spata31h1
|
UTSW |
10 |
82,118,731 (GRCm39) |
missense |
unknown |
|
R7905:Spata31h1
|
UTSW |
10 |
82,131,936 (GRCm39) |
missense |
probably benign |
0.03 |
R7975:Spata31h1
|
UTSW |
10 |
82,119,823 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7988:Spata31h1
|
UTSW |
10 |
82,131,934 (GRCm39) |
missense |
probably benign |
0.03 |
R8076:Spata31h1
|
UTSW |
10 |
82,132,520 (GRCm39) |
nonsense |
probably null |
|
R8144:Spata31h1
|
UTSW |
10 |
82,130,433 (GRCm39) |
nonsense |
probably null |
|
R8429:Spata31h1
|
UTSW |
10 |
82,125,301 (GRCm39) |
missense |
possibly damaging |
0.62 |
R8465:Spata31h1
|
UTSW |
10 |
82,152,298 (GRCm39) |
missense |
possibly damaging |
0.52 |
R8470:Spata31h1
|
UTSW |
10 |
82,126,314 (GRCm39) |
missense |
probably damaging |
1.00 |
R8509:Spata31h1
|
UTSW |
10 |
82,126,950 (GRCm39) |
missense |
probably benign |
0.01 |
R8515:Spata31h1
|
UTSW |
10 |
82,124,436 (GRCm39) |
missense |
probably benign |
0.00 |
R8672:Spata31h1
|
UTSW |
10 |
82,127,726 (GRCm39) |
missense |
probably benign |
0.01 |
R8700:Spata31h1
|
UTSW |
10 |
82,127,859 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8827:Spata31h1
|
UTSW |
10 |
82,129,617 (GRCm39) |
missense |
probably benign |
0.07 |
R8872:Spata31h1
|
UTSW |
10 |
82,128,619 (GRCm39) |
missense |
probably benign |
0.07 |
R8875:Spata31h1
|
UTSW |
10 |
82,123,476 (GRCm39) |
missense |
probably benign |
0.16 |
R8884:Spata31h1
|
UTSW |
10 |
82,119,486 (GRCm39) |
missense |
probably damaging |
0.96 |
R8906:Spata31h1
|
UTSW |
10 |
82,122,379 (GRCm39) |
missense |
probably benign |
0.02 |
R8924:Spata31h1
|
UTSW |
10 |
82,131,295 (GRCm39) |
missense |
probably benign |
0.03 |
R8949:Spata31h1
|
UTSW |
10 |
82,123,753 (GRCm39) |
missense |
probably benign |
0.00 |
R8957:Spata31h1
|
UTSW |
10 |
82,124,908 (GRCm39) |
missense |
probably benign |
0.07 |
R9042:Spata31h1
|
UTSW |
10 |
82,123,185 (GRCm39) |
missense |
probably benign |
0.08 |
R9056:Spata31h1
|
UTSW |
10 |
82,127,101 (GRCm39) |
missense |
probably benign |
0.01 |
R9062:Spata31h1
|
UTSW |
10 |
82,126,945 (GRCm39) |
missense |
probably benign |
0.03 |
R9074:Spata31h1
|
UTSW |
10 |
82,123,894 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9086:Spata31h1
|
UTSW |
10 |
82,124,577 (GRCm39) |
missense |
probably benign |
0.07 |
R9113:Spata31h1
|
UTSW |
10 |
82,131,352 (GRCm39) |
nonsense |
probably null |
|
R9119:Spata31h1
|
UTSW |
10 |
82,131,553 (GRCm39) |
missense |
probably benign |
0.03 |
R9132:Spata31h1
|
UTSW |
10 |
82,127,896 (GRCm39) |
missense |
possibly damaging |
0.85 |
R9141:Spata31h1
|
UTSW |
10 |
82,126,610 (GRCm39) |
missense |
probably damaging |
0.98 |
R9151:Spata31h1
|
UTSW |
10 |
82,120,928 (GRCm39) |
missense |
probably damaging |
0.99 |
R9155:Spata31h1
|
UTSW |
10 |
82,120,203 (GRCm39) |
missense |
probably damaging |
1.00 |
R9159:Spata31h1
|
UTSW |
10 |
82,118,524 (GRCm39) |
nonsense |
probably null |
|
R9197:Spata31h1
|
UTSW |
10 |
82,120,401 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9212:Spata31h1
|
UTSW |
10 |
82,118,979 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9245:Spata31h1
|
UTSW |
10 |
82,123,554 (GRCm39) |
missense |
probably benign |
0.10 |
R9304:Spata31h1
|
UTSW |
10 |
82,131,930 (GRCm39) |
missense |
probably benign |
0.07 |
R9309:Spata31h1
|
UTSW |
10 |
82,130,986 (GRCm39) |
missense |
probably benign |
0.00 |
R9329:Spata31h1
|
UTSW |
10 |
82,121,439 (GRCm39) |
missense |
probably benign |
0.06 |
R9356:Spata31h1
|
UTSW |
10 |
82,125,157 (GRCm39) |
missense |
possibly damaging |
0.54 |
R9423:Spata31h1
|
UTSW |
10 |
82,123,459 (GRCm39) |
missense |
possibly damaging |
0.62 |
R9426:Spata31h1
|
UTSW |
10 |
82,126,610 (GRCm39) |
missense |
probably damaging |
0.98 |
R9457:Spata31h1
|
UTSW |
10 |
82,122,573 (GRCm39) |
missense |
probably benign |
0.02 |
R9509:Spata31h1
|
UTSW |
10 |
82,132,229 (GRCm39) |
missense |
probably benign |
0.03 |
R9612:Spata31h1
|
UTSW |
10 |
82,125,453 (GRCm39) |
missense |
possibly damaging |
0.55 |
R9674:Spata31h1
|
UTSW |
10 |
82,120,030 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9726:Spata31h1
|
UTSW |
10 |
82,118,605 (GRCm39) |
missense |
unknown |
|
RF017:Spata31h1
|
UTSW |
10 |
82,126,826 (GRCm39) |
small insertion |
probably benign |
|
RF055:Spata31h1
|
UTSW |
10 |
82,126,827 (GRCm39) |
small insertion |
probably benign |
|
Z1176:Spata31h1
|
UTSW |
10 |
82,129,062 (GRCm39) |
missense |
probably benign |
0.03 |
Z1176:Spata31h1
|
UTSW |
10 |
82,125,730 (GRCm39) |
missense |
possibly damaging |
0.94 |
Z1176:Spata31h1
|
UTSW |
10 |
82,118,371 (GRCm39) |
missense |
unknown |
|
Z1177:Spata31h1
|
UTSW |
10 |
82,123,251 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Spata31h1
|
UTSW |
10 |
82,122,960 (GRCm39) |
missense |
possibly damaging |
0.85 |
Z1177:Spata31h1
|
UTSW |
10 |
82,121,632 (GRCm39) |
missense |
possibly damaging |
0.46 |
Z1177:Spata31h1
|
UTSW |
10 |
82,125,520 (GRCm39) |
nonsense |
probably null |
|
Z1187:Spata31h1
|
UTSW |
10 |
82,124,390 (GRCm39) |
small deletion |
probably benign |
|
|