Other mutations in this stock |
Total: 210 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 |
CCCCGAGCC |
CCCCGAGCCCGAGCC |
11: 74,560,340 (GRCm39) |
|
probably benign |
Het |
Cluh |
CC |
CCTGAGGC |
11: 74,560,359 (GRCm39) |
|
probably benign |
Het |
Cluh |
GAGCCT |
GAGCCTAAGCCT |
11: 74,560,350 (GRCm39) |
|
probably benign |
Het |
Cluh |
AGCCTG |
AGCCTGCGCCTG |
11: 74,560,345 (GRCm39) |
|
probably benign |
Het |
Cntnap1 |
AGCCCC |
AGCCCCCGCCCC |
11: 101,080,395 (GRCm39) |
|
probably benign |
Het |
Cntnap1 |
CCCAGC |
CCCAGCGCCAGC |
11: 101,080,416 (GRCm39) |
|
probably benign |
Het |
Cntnap1 |
GCCCCA |
GCCCCACCCCCA |
11: 101,080,408 (GRCm39) |
|
probably benign |
Het |
Cntnap1 |
GCCCCA |
GCCCCAACCCCA |
11: 101,080,402 (GRCm39) |
|
probably benign |
Het |
Cracdl |
C |
A |
1: 37,664,117 (GRCm39) |
E594* |
probably null |
Homo |
Cracdl |
T |
A |
1: 37,664,116 (GRCm39) |
E594V |
probably benign |
Homo |
Cul9 |
CTCTTC |
CTCTTCTTC |
17: 46,811,772 (GRCm39) |
|
probably benign |
Het |
Cul9 |
CTC |
CTCTTC |
17: 46,811,784 (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 |
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 |
Spata31h1 |
TTCA |
T |
10: 82,121,303 (GRCm39) |
|
probably benign |
Homo |
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 Dnah8 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00498:Dnah8
|
APN |
17 |
30,896,150 (GRCm39) |
missense |
probably benign |
0.06 |
IGL00508:Dnah8
|
APN |
17 |
31,074,904 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00547:Dnah8
|
APN |
17 |
31,034,677 (GRCm39) |
nonsense |
probably null |
|
IGL00551:Dnah8
|
APN |
17 |
30,882,452 (GRCm39) |
nonsense |
probably null |
|
IGL00732:Dnah8
|
APN |
17 |
30,875,615 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00775:Dnah8
|
APN |
17 |
30,986,880 (GRCm39) |
nonsense |
probably null |
|
IGL00840:Dnah8
|
APN |
17 |
31,009,915 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00845:Dnah8
|
APN |
17 |
31,038,250 (GRCm39) |
critical splice donor site |
probably null |
|
IGL00953:Dnah8
|
APN |
17 |
30,925,431 (GRCm39) |
nonsense |
probably null |
|
IGL00976:Dnah8
|
APN |
17 |
31,070,684 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01395:Dnah8
|
APN |
17 |
30,854,979 (GRCm39) |
missense |
probably benign |
0.06 |
IGL01467:Dnah8
|
APN |
17 |
30,998,890 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01469:Dnah8
|
APN |
17 |
30,902,688 (GRCm39) |
splice site |
probably benign |
|
IGL01515:Dnah8
|
APN |
17 |
30,867,459 (GRCm39) |
missense |
probably benign |
|
IGL01723:Dnah8
|
APN |
17 |
30,927,445 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01837:Dnah8
|
APN |
17 |
30,970,565 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01921:Dnah8
|
APN |
17 |
30,955,115 (GRCm39) |
missense |
probably benign |
|
IGL01958:Dnah8
|
APN |
17 |
31,074,869 (GRCm39) |
splice site |
probably benign |
|
IGL01968:Dnah8
|
APN |
17 |
30,875,572 (GRCm39) |
nonsense |
probably null |
|
IGL02093:Dnah8
|
APN |
17 |
30,936,854 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02151:Dnah8
|
APN |
17 |
30,867,391 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL02182:Dnah8
|
APN |
17 |
31,013,737 (GRCm39) |
missense |
possibly damaging |
0.45 |
IGL02233:Dnah8
|
APN |
17 |
30,925,487 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02236:Dnah8
|
APN |
17 |
30,868,747 (GRCm39) |
nonsense |
probably null |
|
IGL02259:Dnah8
|
APN |
17 |
30,978,588 (GRCm39) |
missense |
probably benign |
|
IGL02263:Dnah8
|
APN |
17 |
30,948,139 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02303:Dnah8
|
APN |
17 |
30,932,021 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02341:Dnah8
|
APN |
17 |
30,966,231 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02351:Dnah8
|
APN |
17 |
30,986,785 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02358:Dnah8
|
APN |
17 |
30,986,785 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02377:Dnah8
|
APN |
17 |
31,013,770 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02390:Dnah8
|
APN |
17 |
31,049,819 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02392:Dnah8
|
APN |
17 |
31,037,025 (GRCm39) |
splice site |
probably benign |
|
IGL02414:Dnah8
|
APN |
17 |
30,919,387 (GRCm39) |
missense |
probably benign |
|
IGL02455:Dnah8
|
APN |
17 |
30,891,308 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02817:Dnah8
|
APN |
17 |
30,887,269 (GRCm39) |
missense |
probably benign |
|
IGL02831:Dnah8
|
APN |
17 |
30,931,250 (GRCm39) |
missense |
probably benign |
0.23 |
IGL02863:Dnah8
|
APN |
17 |
30,988,671 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02894:Dnah8
|
APN |
17 |
30,940,084 (GRCm39) |
nonsense |
probably null |
|
IGL02954:Dnah8
|
APN |
17 |
30,923,809 (GRCm39) |
missense |
probably benign |
0.30 |
IGL02964:Dnah8
|
APN |
17 |
30,965,735 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03080:Dnah8
|
APN |
17 |
30,937,980 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03081:Dnah8
|
APN |
17 |
30,905,347 (GRCm39) |
splice site |
probably benign |
|
IGL03086:Dnah8
|
APN |
17 |
30,961,754 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03087:Dnah8
|
APN |
17 |
31,003,118 (GRCm39) |
missense |
probably benign |
|
IGL03176:Dnah8
|
APN |
17 |
30,913,011 (GRCm39) |
missense |
probably benign |
|
IGL03191:Dnah8
|
APN |
17 |
30,945,804 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03210:Dnah8
|
APN |
17 |
31,034,639 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL03252:Dnah8
|
APN |
17 |
30,892,894 (GRCm39) |
splice site |
probably null |
|
IGL03255:Dnah8
|
APN |
17 |
30,960,355 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03288:Dnah8
|
APN |
17 |
30,891,323 (GRCm39) |
missense |
probably benign |
|
IGL03348:Dnah8
|
APN |
17 |
30,965,960 (GRCm39) |
missense |
probably damaging |
0.99 |
Alternator
|
UTSW |
17 |
30,984,609 (GRCm39) |
missense |
probably benign |
|
armature
|
UTSW |
17 |
30,927,364 (GRCm39) |
missense |
probably benign |
0.02 |
Brush
|
UTSW |
17 |
30,965,964 (GRCm39) |
missense |
probably damaging |
1.00 |
Dynos
|
UTSW |
17 |
30,934,483 (GRCm39) |
missense |
possibly damaging |
0.84 |
joule
|
UTSW |
17 |
30,932,072 (GRCm39) |
critical splice donor site |
probably null |
|
solenoid
|
UTSW |
17 |
30,960,152 (GRCm39) |
missense |
probably damaging |
1.00 |
FR4340:Dnah8
|
UTSW |
17 |
30,854,437 (GRCm39) |
small deletion |
probably benign |
|
FR4737:Dnah8
|
UTSW |
17 |
30,854,451 (GRCm39) |
small deletion |
probably benign |
|
I2288:Dnah8
|
UTSW |
17 |
30,882,428 (GRCm39) |
missense |
probably benign |
|
P0029:Dnah8
|
UTSW |
17 |
30,984,694 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4812001:Dnah8
|
UTSW |
17 |
30,927,419 (GRCm39) |
missense |
probably benign |
0.04 |
R0016:Dnah8
|
UTSW |
17 |
30,882,290 (GRCm39) |
missense |
probably benign |
|
R0035:Dnah8
|
UTSW |
17 |
30,902,595 (GRCm39) |
splice site |
probably benign |
|
R0035:Dnah8
|
UTSW |
17 |
30,902,595 (GRCm39) |
splice site |
probably benign |
|
R0062:Dnah8
|
UTSW |
17 |
30,984,685 (GRCm39) |
missense |
probably damaging |
1.00 |
R0062:Dnah8
|
UTSW |
17 |
30,984,685 (GRCm39) |
missense |
probably damaging |
1.00 |
R0087:Dnah8
|
UTSW |
17 |
30,974,093 (GRCm39) |
missense |
probably damaging |
1.00 |
R0090:Dnah8
|
UTSW |
17 |
31,003,064 (GRCm39) |
missense |
probably benign |
0.20 |
R0119:Dnah8
|
UTSW |
17 |
30,934,483 (GRCm39) |
missense |
possibly damaging |
0.84 |
R0164:Dnah8
|
UTSW |
17 |
30,967,639 (GRCm39) |
missense |
probably benign |
|
R0164:Dnah8
|
UTSW |
17 |
30,967,639 (GRCm39) |
missense |
probably benign |
|
R0184:Dnah8
|
UTSW |
17 |
30,902,657 (GRCm39) |
missense |
probably benign |
0.04 |
R0240:Dnah8
|
UTSW |
17 |
30,984,653 (GRCm39) |
missense |
probably damaging |
0.98 |
R0240:Dnah8
|
UTSW |
17 |
30,984,653 (GRCm39) |
missense |
probably damaging |
0.98 |
R0241:Dnah8
|
UTSW |
17 |
30,984,653 (GRCm39) |
missense |
probably damaging |
0.98 |
R0241:Dnah8
|
UTSW |
17 |
30,984,653 (GRCm39) |
missense |
probably damaging |
0.98 |
R0265:Dnah8
|
UTSW |
17 |
30,909,245 (GRCm39) |
missense |
probably benign |
|
R0268:Dnah8
|
UTSW |
17 |
30,988,681 (GRCm39) |
missense |
probably damaging |
1.00 |
R0282:Dnah8
|
UTSW |
17 |
30,955,130 (GRCm39) |
missense |
probably damaging |
1.00 |
R0299:Dnah8
|
UTSW |
17 |
30,934,483 (GRCm39) |
missense |
possibly damaging |
0.84 |
R0334:Dnah8
|
UTSW |
17 |
31,090,325 (GRCm39) |
missense |
probably damaging |
0.99 |
R0393:Dnah8
|
UTSW |
17 |
30,927,364 (GRCm39) |
missense |
probably benign |
0.02 |
R0423:Dnah8
|
UTSW |
17 |
30,920,955 (GRCm39) |
missense |
probably benign |
|
R0470:Dnah8
|
UTSW |
17 |
30,927,514 (GRCm39) |
splice site |
probably benign |
|
R0477:Dnah8
|
UTSW |
17 |
30,974,054 (GRCm39) |
missense |
probably damaging |
1.00 |
R0490:Dnah8
|
UTSW |
17 |
30,919,393 (GRCm39) |
missense |
probably benign |
|
R0499:Dnah8
|
UTSW |
17 |
30,934,483 (GRCm39) |
missense |
possibly damaging |
0.84 |
R0582:Dnah8
|
UTSW |
17 |
30,937,935 (GRCm39) |
missense |
probably benign |
0.01 |
R0601:Dnah8
|
UTSW |
17 |
30,927,332 (GRCm39) |
missense |
probably benign |
0.06 |
R0646:Dnah8
|
UTSW |
17 |
30,903,147 (GRCm39) |
missense |
probably damaging |
0.97 |
R0665:Dnah8
|
UTSW |
17 |
30,955,129 (GRCm39) |
missense |
probably damaging |
0.99 |
R0800:Dnah8
|
UTSW |
17 |
30,923,636 (GRCm39) |
missense |
probably benign |
|
R0843:Dnah8
|
UTSW |
17 |
31,032,069 (GRCm39) |
missense |
probably damaging |
1.00 |
R0940:Dnah8
|
UTSW |
17 |
31,022,217 (GRCm39) |
missense |
probably damaging |
1.00 |
R0964:Dnah8
|
UTSW |
17 |
30,892,894 (GRCm39) |
splice site |
probably null |
|
R1102:Dnah8
|
UTSW |
17 |
31,073,738 (GRCm39) |
splice site |
probably null |
|
R1137:Dnah8
|
UTSW |
17 |
31,074,910 (GRCm39) |
missense |
probably damaging |
1.00 |
R1342:Dnah8
|
UTSW |
17 |
30,939,974 (GRCm39) |
missense |
probably damaging |
0.99 |
R1375:Dnah8
|
UTSW |
17 |
30,956,269 (GRCm39) |
missense |
probably damaging |
1.00 |
R1377:Dnah8
|
UTSW |
17 |
31,059,596 (GRCm39) |
nonsense |
probably null |
|
R1464:Dnah8
|
UTSW |
17 |
30,914,147 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1464:Dnah8
|
UTSW |
17 |
30,914,147 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1470:Dnah8
|
UTSW |
17 |
30,966,251 (GRCm39) |
nonsense |
probably null |
|
R1470:Dnah8
|
UTSW |
17 |
30,966,251 (GRCm39) |
nonsense |
probably null |
|
R1497:Dnah8
|
UTSW |
17 |
30,971,049 (GRCm39) |
missense |
probably damaging |
1.00 |
R1513:Dnah8
|
UTSW |
17 |
30,892,862 (GRCm39) |
missense |
probably benign |
|
R1541:Dnah8
|
UTSW |
17 |
30,966,221 (GRCm39) |
missense |
probably damaging |
1.00 |
R1563:Dnah8
|
UTSW |
17 |
30,854,638 (GRCm39) |
missense |
probably benign |
0.07 |
R1634:Dnah8
|
UTSW |
17 |
30,932,072 (GRCm39) |
critical splice donor site |
probably null |
|
R1670:Dnah8
|
UTSW |
17 |
30,944,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R1710:Dnah8
|
UTSW |
17 |
31,073,914 (GRCm39) |
missense |
probably damaging |
1.00 |
R1743:Dnah8
|
UTSW |
17 |
30,988,625 (GRCm39) |
missense |
probably benign |
0.28 |
R1761:Dnah8
|
UTSW |
17 |
30,998,890 (GRCm39) |
missense |
probably damaging |
1.00 |
R1785:Dnah8
|
UTSW |
17 |
30,941,911 (GRCm39) |
missense |
probably damaging |
0.98 |
R1804:Dnah8
|
UTSW |
17 |
30,927,381 (GRCm39) |
missense |
probably benign |
0.00 |
R1808:Dnah8
|
UTSW |
17 |
30,903,160 (GRCm39) |
missense |
probably damaging |
1.00 |
R1824:Dnah8
|
UTSW |
17 |
30,950,154 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1836:Dnah8
|
UTSW |
17 |
31,093,901 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1935:Dnah8
|
UTSW |
17 |
30,945,870 (GRCm39) |
splice site |
probably benign |
|
R1935:Dnah8
|
UTSW |
17 |
30,854,479 (GRCm39) |
missense |
unknown |
|
R1940:Dnah8
|
UTSW |
17 |
30,950,181 (GRCm39) |
missense |
probably damaging |
1.00 |
R1946:Dnah8
|
UTSW |
17 |
30,931,359 (GRCm39) |
missense |
probably benign |
0.00 |
R2025:Dnah8
|
UTSW |
17 |
30,950,133 (GRCm39) |
missense |
probably damaging |
0.99 |
R2038:Dnah8
|
UTSW |
17 |
30,977,255 (GRCm39) |
missense |
probably damaging |
1.00 |
R2042:Dnah8
|
UTSW |
17 |
30,854,632 (GRCm39) |
missense |
probably benign |
0.01 |
R2148:Dnah8
|
UTSW |
17 |
30,956,232 (GRCm39) |
missense |
probably damaging |
1.00 |
R2177:Dnah8
|
UTSW |
17 |
30,872,367 (GRCm39) |
missense |
probably benign |
|
R2180:Dnah8
|
UTSW |
17 |
31,059,621 (GRCm39) |
missense |
probably benign |
0.00 |
R2262:Dnah8
|
UTSW |
17 |
30,892,809 (GRCm39) |
missense |
probably damaging |
1.00 |
R2263:Dnah8
|
UTSW |
17 |
30,892,809 (GRCm39) |
missense |
probably damaging |
1.00 |
R2328:Dnah8
|
UTSW |
17 |
31,013,718 (GRCm39) |
missense |
probably damaging |
1.00 |
R2357:Dnah8
|
UTSW |
17 |
31,093,909 (GRCm39) |
missense |
probably benign |
0.00 |
R2357:Dnah8
|
UTSW |
17 |
30,990,846 (GRCm39) |
missense |
probably benign |
|
R2360:Dnah8
|
UTSW |
17 |
30,896,178 (GRCm39) |
missense |
probably benign |
0.22 |
R2496:Dnah8
|
UTSW |
17 |
31,070,705 (GRCm39) |
missense |
probably damaging |
1.00 |
R2497:Dnah8
|
UTSW |
17 |
30,960,339 (GRCm39) |
nonsense |
probably null |
|
R2509:Dnah8
|
UTSW |
17 |
30,994,019 (GRCm39) |
missense |
probably benign |
0.02 |
R3114:Dnah8
|
UTSW |
17 |
31,052,542 (GRCm39) |
missense |
probably benign |
0.04 |
R3708:Dnah8
|
UTSW |
17 |
30,958,631 (GRCm39) |
missense |
probably damaging |
0.98 |
R3720:Dnah8
|
UTSW |
17 |
31,073,872 (GRCm39) |
missense |
probably damaging |
1.00 |
R3722:Dnah8
|
UTSW |
17 |
31,073,872 (GRCm39) |
missense |
probably damaging |
1.00 |
R3727:Dnah8
|
UTSW |
17 |
30,958,622 (GRCm39) |
nonsense |
probably null |
|
R3747:Dnah8
|
UTSW |
17 |
31,003,148 (GRCm39) |
nonsense |
probably null |
|
R3748:Dnah8
|
UTSW |
17 |
31,003,148 (GRCm39) |
nonsense |
probably null |
|
R3749:Dnah8
|
UTSW |
17 |
31,003,148 (GRCm39) |
nonsense |
probably null |
|
R3787:Dnah8
|
UTSW |
17 |
30,974,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R3790:Dnah8
|
UTSW |
17 |
31,073,872 (GRCm39) |
missense |
probably damaging |
1.00 |
R3804:Dnah8
|
UTSW |
17 |
30,889,621 (GRCm39) |
missense |
probably benign |
0.00 |
R3857:Dnah8
|
UTSW |
17 |
30,882,396 (GRCm39) |
missense |
probably damaging |
0.96 |
R3898:Dnah8
|
UTSW |
17 |
31,073,872 (GRCm39) |
missense |
probably damaging |
1.00 |
R3899:Dnah8
|
UTSW |
17 |
31,073,872 (GRCm39) |
missense |
probably damaging |
1.00 |
R3938:Dnah8
|
UTSW |
17 |
31,073,911 (GRCm39) |
missense |
probably damaging |
1.00 |
R3943:Dnah8
|
UTSW |
17 |
30,913,039 (GRCm39) |
splice site |
probably benign |
|
R4091:Dnah8
|
UTSW |
17 |
30,988,813 (GRCm39) |
missense |
probably damaging |
1.00 |
R4291:Dnah8
|
UTSW |
17 |
30,967,533 (GRCm39) |
missense |
probably benign |
|
R4326:Dnah8
|
UTSW |
17 |
30,971,066 (GRCm39) |
missense |
probably benign |
0.04 |
R4346:Dnah8
|
UTSW |
17 |
30,944,072 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4429:Dnah8
|
UTSW |
17 |
30,971,120 (GRCm39) |
missense |
probably damaging |
1.00 |
R4457:Dnah8
|
UTSW |
17 |
31,032,125 (GRCm39) |
missense |
probably benign |
|
R4475:Dnah8
|
UTSW |
17 |
30,875,959 (GRCm39) |
missense |
probably benign |
0.12 |
R4565:Dnah8
|
UTSW |
17 |
30,967,542 (GRCm39) |
missense |
probably benign |
0.00 |
R4566:Dnah8
|
UTSW |
17 |
30,967,542 (GRCm39) |
missense |
probably benign |
0.00 |
R4568:Dnah8
|
UTSW |
17 |
30,967,542 (GRCm39) |
missense |
probably benign |
0.00 |
R4573:Dnah8
|
UTSW |
17 |
30,919,380 (GRCm39) |
missense |
probably benign |
0.00 |
R4580:Dnah8
|
UTSW |
17 |
30,881,026 (GRCm39) |
missense |
probably benign |
0.00 |
R4585:Dnah8
|
UTSW |
17 |
30,970,541 (GRCm39) |
missense |
probably benign |
0.01 |
R4611:Dnah8
|
UTSW |
17 |
30,903,211 (GRCm39) |
missense |
probably damaging |
1.00 |
R4720:Dnah8
|
UTSW |
17 |
30,902,608 (GRCm39) |
missense |
probably benign |
0.08 |
R4721:Dnah8
|
UTSW |
17 |
30,944,140 (GRCm39) |
missense |
probably damaging |
1.00 |
R4727:Dnah8
|
UTSW |
17 |
31,070,721 (GRCm39) |
missense |
probably damaging |
1.00 |
R4731:Dnah8
|
UTSW |
17 |
30,994,035 (GRCm39) |
missense |
probably null |
0.02 |
R4732:Dnah8
|
UTSW |
17 |
30,994,035 (GRCm39) |
missense |
probably null |
0.02 |
R4733:Dnah8
|
UTSW |
17 |
30,994,035 (GRCm39) |
missense |
probably null |
0.02 |
R4798:Dnah8
|
UTSW |
17 |
30,967,542 (GRCm39) |
missense |
probably benign |
0.00 |
R4814:Dnah8
|
UTSW |
17 |
30,986,898 (GRCm39) |
missense |
probably damaging |
1.00 |
R4892:Dnah8
|
UTSW |
17 |
30,967,542 (GRCm39) |
missense |
probably benign |
0.00 |
R4894:Dnah8
|
UTSW |
17 |
30,967,542 (GRCm39) |
missense |
probably benign |
0.00 |
R4900:Dnah8
|
UTSW |
17 |
30,965,949 (GRCm39) |
missense |
probably damaging |
1.00 |
R4901:Dnah8
|
UTSW |
17 |
31,059,688 (GRCm39) |
critical splice donor site |
probably null |
|
R4913:Dnah8
|
UTSW |
17 |
31,038,113 (GRCm39) |
missense |
probably damaging |
0.99 |
R4931:Dnah8
|
UTSW |
17 |
30,967,542 (GRCm39) |
missense |
probably benign |
0.00 |
R4932:Dnah8
|
UTSW |
17 |
30,967,542 (GRCm39) |
missense |
probably benign |
0.00 |
R4933:Dnah8
|
UTSW |
17 |
30,967,542 (GRCm39) |
missense |
probably benign |
0.00 |
R4942:Dnah8
|
UTSW |
17 |
30,948,116 (GRCm39) |
missense |
probably benign |
|
R4969:Dnah8
|
UTSW |
17 |
30,941,988 (GRCm39) |
missense |
probably damaging |
1.00 |
R4975:Dnah8
|
UTSW |
17 |
30,875,959 (GRCm39) |
missense |
probably benign |
0.12 |
R4977:Dnah8
|
UTSW |
17 |
30,882,275 (GRCm39) |
missense |
probably benign |
0.00 |
R5001:Dnah8
|
UTSW |
17 |
31,006,159 (GRCm39) |
missense |
probably damaging |
1.00 |
R5011:Dnah8
|
UTSW |
17 |
30,967,542 (GRCm39) |
missense |
probably benign |
0.00 |
R5013:Dnah8
|
UTSW |
17 |
30,967,542 (GRCm39) |
missense |
probably benign |
0.00 |
R5014:Dnah8
|
UTSW |
17 |
30,967,542 (GRCm39) |
missense |
probably benign |
0.00 |
R5024:Dnah8
|
UTSW |
17 |
30,955,070 (GRCm39) |
missense |
probably damaging |
1.00 |
R5075:Dnah8
|
UTSW |
17 |
30,967,542 (GRCm39) |
missense |
probably benign |
0.00 |
R5075:Dnah8
|
UTSW |
17 |
31,019,505 (GRCm39) |
missense |
probably damaging |
1.00 |
R5075:Dnah8
|
UTSW |
17 |
30,958,731 (GRCm39) |
critical splice donor site |
probably null |
|
R5112:Dnah8
|
UTSW |
17 |
30,950,012 (GRCm39) |
missense |
probably benign |
0.02 |
R5121:Dnah8
|
UTSW |
17 |
31,029,327 (GRCm39) |
missense |
probably benign |
0.14 |
R5138:Dnah8
|
UTSW |
17 |
30,984,571 (GRCm39) |
missense |
probably damaging |
0.99 |
R5151:Dnah8
|
UTSW |
17 |
30,931,269 (GRCm39) |
missense |
probably benign |
0.06 |
R5191:Dnah8
|
UTSW |
17 |
30,965,739 (GRCm39) |
missense |
probably damaging |
1.00 |
R5238:Dnah8
|
UTSW |
17 |
31,009,891 (GRCm39) |
missense |
probably damaging |
1.00 |
R5260:Dnah8
|
UTSW |
17 |
30,919,393 (GRCm39) |
missense |
probably benign |
|
R5358:Dnah8
|
UTSW |
17 |
30,965,928 (GRCm39) |
missense |
probably damaging |
1.00 |
R5403:Dnah8
|
UTSW |
17 |
30,967,542 (GRCm39) |
missense |
probably benign |
0.00 |
R5404:Dnah8
|
UTSW |
17 |
30,967,542 (GRCm39) |
missense |
probably benign |
0.00 |
R5482:Dnah8
|
UTSW |
17 |
31,019,521 (GRCm39) |
missense |
probably damaging |
0.96 |
R5489:Dnah8
|
UTSW |
17 |
31,009,930 (GRCm39) |
missense |
probably damaging |
1.00 |
R5513:Dnah8
|
UTSW |
17 |
30,971,890 (GRCm39) |
missense |
probably damaging |
0.99 |
R5635:Dnah8
|
UTSW |
17 |
30,925,360 (GRCm39) |
missense |
probably benign |
0.00 |
R5640:Dnah8
|
UTSW |
17 |
31,022,082 (GRCm39) |
missense |
probably damaging |
1.00 |
R5649:Dnah8
|
UTSW |
17 |
31,019,561 (GRCm39) |
missense |
probably benign |
0.13 |
R5662:Dnah8
|
UTSW |
17 |
30,956,307 (GRCm39) |
missense |
probably damaging |
1.00 |
R5673:Dnah8
|
UTSW |
17 |
31,022,235 (GRCm39) |
missense |
probably damaging |
1.00 |
R5677:Dnah8
|
UTSW |
17 |
30,967,542 (GRCm39) |
missense |
probably benign |
0.00 |
R5699:Dnah8
|
UTSW |
17 |
31,029,298 (GRCm39) |
missense |
probably benign |
0.22 |
R5737:Dnah8
|
UTSW |
17 |
30,967,542 (GRCm39) |
missense |
probably benign |
0.00 |
R5738:Dnah8
|
UTSW |
17 |
30,967,542 (GRCm39) |
missense |
probably benign |
0.00 |
R5739:Dnah8
|
UTSW |
17 |
30,937,981 (GRCm39) |
missense |
probably benign |
0.00 |
R5766:Dnah8
|
UTSW |
17 |
30,909,235 (GRCm39) |
missense |
probably benign |
0.01 |
R5790:Dnah8
|
UTSW |
17 |
31,093,978 (GRCm39) |
missense |
probably damaging |
0.98 |
R5848:Dnah8
|
UTSW |
17 |
30,947,165 (GRCm39) |
missense |
possibly damaging |
0.69 |
R5854:Dnah8
|
UTSW |
17 |
31,013,737 (GRCm39) |
missense |
possibly damaging |
0.45 |
R5885:Dnah8
|
UTSW |
17 |
31,013,691 (GRCm39) |
missense |
probably damaging |
1.00 |
R5886:Dnah8
|
UTSW |
17 |
31,013,691 (GRCm39) |
missense |
probably damaging |
1.00 |
R5887:Dnah8
|
UTSW |
17 |
31,013,691 (GRCm39) |
missense |
probably damaging |
1.00 |
R5899:Dnah8
|
UTSW |
17 |
30,875,659 (GRCm39) |
missense |
probably benign |
0.32 |
R5979:Dnah8
|
UTSW |
17 |
31,034,638 (GRCm39) |
nonsense |
probably null |
|
R5986:Dnah8
|
UTSW |
17 |
31,070,604 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5999:Dnah8
|
UTSW |
17 |
30,882,279 (GRCm39) |
missense |
probably benign |
0.32 |
R6042:Dnah8
|
UTSW |
17 |
30,966,239 (GRCm39) |
missense |
probably damaging |
1.00 |
R6175:Dnah8
|
UTSW |
17 |
30,967,542 (GRCm39) |
missense |
probably benign |
0.00 |
R6181:Dnah8
|
UTSW |
17 |
30,967,542 (GRCm39) |
missense |
probably benign |
0.00 |
R6237:Dnah8
|
UTSW |
17 |
30,966,828 (GRCm39) |
nonsense |
probably null |
|
R6239:Dnah8
|
UTSW |
17 |
31,029,333 (GRCm39) |
missense |
probably damaging |
0.99 |
R6337:Dnah8
|
UTSW |
17 |
30,967,542 (GRCm39) |
missense |
probably benign |
0.00 |
R6365:Dnah8
|
UTSW |
17 |
30,967,542 (GRCm39) |
missense |
probably benign |
0.00 |
R6416:Dnah8
|
UTSW |
17 |
30,984,609 (GRCm39) |
missense |
probably benign |
|
R6443:Dnah8
|
UTSW |
17 |
30,990,859 (GRCm39) |
missense |
probably benign |
0.10 |
R6478:Dnah8
|
UTSW |
17 |
30,967,542 (GRCm39) |
missense |
probably benign |
0.00 |
R6479:Dnah8
|
UTSW |
17 |
30,967,542 (GRCm39) |
missense |
probably benign |
0.00 |
R6480:Dnah8
|
UTSW |
17 |
30,967,542 (GRCm39) |
missense |
probably benign |
0.00 |
R6481:Dnah8
|
UTSW |
17 |
30,967,542 (GRCm39) |
missense |
probably benign |
0.00 |
R6533:Dnah8
|
UTSW |
17 |
30,965,964 (GRCm39) |
missense |
probably damaging |
1.00 |
R6606:Dnah8
|
UTSW |
17 |
30,967,542 (GRCm39) |
missense |
probably benign |
0.00 |
R6608:Dnah8
|
UTSW |
17 |
30,967,542 (GRCm39) |
missense |
probably benign |
0.00 |
R6610:Dnah8
|
UTSW |
17 |
30,967,542 (GRCm39) |
missense |
probably benign |
0.00 |
R6675:Dnah8
|
UTSW |
17 |
30,967,542 (GRCm39) |
missense |
probably benign |
0.00 |
R6723:Dnah8
|
UTSW |
17 |
30,967,542 (GRCm39) |
missense |
probably benign |
0.00 |
R6724:Dnah8
|
UTSW |
17 |
30,967,542 (GRCm39) |
missense |
probably benign |
0.00 |
R6754:Dnah8
|
UTSW |
17 |
30,967,542 (GRCm39) |
missense |
probably benign |
0.00 |
R6755:Dnah8
|
UTSW |
17 |
30,967,542 (GRCm39) |
missense |
probably benign |
0.00 |
R6759:Dnah8
|
UTSW |
17 |
30,882,266 (GRCm39) |
splice site |
probably null |
|
R6765:Dnah8
|
UTSW |
17 |
30,967,542 (GRCm39) |
missense |
probably benign |
0.00 |
R6766:Dnah8
|
UTSW |
17 |
30,967,542 (GRCm39) |
missense |
probably benign |
0.00 |
R6778:Dnah8
|
UTSW |
17 |
30,854,640 (GRCm39) |
missense |
probably benign |
0.00 |
R6781:Dnah8
|
UTSW |
17 |
30,984,698 (GRCm39) |
frame shift |
probably null |
|
R6788:Dnah8
|
UTSW |
17 |
30,867,439 (GRCm39) |
missense |
probably benign |
0.14 |
R6814:Dnah8
|
UTSW |
17 |
30,981,653 (GRCm39) |
missense |
probably damaging |
1.00 |
R6825:Dnah8
|
UTSW |
17 |
30,960,147 (GRCm39) |
missense |
probably damaging |
1.00 |
R6838:Dnah8
|
UTSW |
17 |
30,929,525 (GRCm39) |
missense |
probably damaging |
1.00 |
R6872:Dnah8
|
UTSW |
17 |
30,981,653 (GRCm39) |
missense |
probably damaging |
1.00 |
R6877:Dnah8
|
UTSW |
17 |
30,965,933 (GRCm39) |
missense |
probably damaging |
1.00 |
R6944:Dnah8
|
UTSW |
17 |
31,013,633 (GRCm39) |
missense |
probably benign |
0.09 |
R6982:Dnah8
|
UTSW |
17 |
30,986,899 (GRCm39) |
missense |
probably benign |
0.03 |
R6984:Dnah8
|
UTSW |
17 |
30,958,712 (GRCm39) |
missense |
probably damaging |
1.00 |
R6987:Dnah8
|
UTSW |
17 |
30,881,065 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6988:Dnah8
|
UTSW |
17 |
30,862,249 (GRCm39) |
missense |
probably damaging |
1.00 |
R7099:Dnah8
|
UTSW |
17 |
30,923,698 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7106:Dnah8
|
UTSW |
17 |
30,960,152 (GRCm39) |
missense |
probably damaging |
1.00 |
R7112:Dnah8
|
UTSW |
17 |
31,090,366 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7146:Dnah8
|
UTSW |
17 |
30,988,618 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7146:Dnah8
|
UTSW |
17 |
30,863,591 (GRCm39) |
missense |
probably benign |
0.01 |
R7309:Dnah8
|
UTSW |
17 |
31,093,988 (GRCm39) |
missense |
probably damaging |
1.00 |
R7324:Dnah8
|
UTSW |
17 |
31,003,099 (GRCm39) |
missense |
probably benign |
0.01 |
R7373:Dnah8
|
UTSW |
17 |
30,986,939 (GRCm39) |
critical splice donor site |
probably null |
|
R7423:Dnah8
|
UTSW |
17 |
30,923,743 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7430:Dnah8
|
UTSW |
17 |
30,925,363 (GRCm39) |
missense |
probably damaging |
0.98 |
R7450:Dnah8
|
UTSW |
17 |
31,006,165 (GRCm39) |
missense |
probably damaging |
0.99 |
R7580:Dnah8
|
UTSW |
17 |
30,994,077 (GRCm39) |
missense |
probably damaging |
0.98 |
R7604:Dnah8
|
UTSW |
17 |
31,032,069 (GRCm39) |
missense |
probably damaging |
1.00 |
R7635:Dnah8
|
UTSW |
17 |
31,004,081 (GRCm39) |
missense |
probably damaging |
1.00 |
R7646:Dnah8
|
UTSW |
17 |
30,868,651 (GRCm39) |
missense |
probably benign |
0.00 |
R7685:Dnah8
|
UTSW |
17 |
30,876,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R7793:Dnah8
|
UTSW |
17 |
31,074,918 (GRCm39) |
missense |
probably benign |
0.20 |
R7827:Dnah8
|
UTSW |
17 |
30,979,841 (GRCm39) |
frame shift |
probably null |
|
R7866:Dnah8
|
UTSW |
17 |
31,093,901 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7877:Dnah8
|
UTSW |
17 |
30,882,348 (GRCm39) |
missense |
probably benign |
|
R7891:Dnah8
|
UTSW |
17 |
30,931,263 (GRCm39) |
missense |
probably benign |
0.09 |
R7977:Dnah8
|
UTSW |
17 |
30,963,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R7987:Dnah8
|
UTSW |
17 |
30,963,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R8025:Dnah8
|
UTSW |
17 |
30,960,311 (GRCm39) |
nonsense |
probably null |
|
R8076:Dnah8
|
UTSW |
17 |
31,003,127 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8170:Dnah8
|
UTSW |
17 |
30,892,797 (GRCm39) |
missense |
probably damaging |
1.00 |
R8199:Dnah8
|
UTSW |
17 |
31,090,393 (GRCm39) |
missense |
probably benign |
0.06 |
R8253:Dnah8
|
UTSW |
17 |
30,979,841 (GRCm39) |
frame shift |
probably null |
|
R8270:Dnah8
|
UTSW |
17 |
31,059,687 (GRCm39) |
missense |
probably damaging |
1.00 |
R8291:Dnah8
|
UTSW |
17 |
30,984,701 (GRCm39) |
missense |
probably damaging |
1.00 |
R8334:Dnah8
|
UTSW |
17 |
30,988,805 (GRCm39) |
missense |
probably benign |
0.12 |
R8348:Dnah8
|
UTSW |
17 |
30,892,814 (GRCm39) |
missense |
probably benign |
|
R8348:Dnah8
|
UTSW |
17 |
30,955,121 (GRCm39) |
missense |
probably damaging |
0.96 |
R8354:Dnah8
|
UTSW |
17 |
30,862,234 (GRCm39) |
missense |
probably benign |
0.17 |
R8355:Dnah8
|
UTSW |
17 |
30,914,152 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8439:Dnah8
|
UTSW |
17 |
30,979,841 (GRCm39) |
frame shift |
probably null |
|
R8448:Dnah8
|
UTSW |
17 |
30,892,814 (GRCm39) |
missense |
probably benign |
|
R8459:Dnah8
|
UTSW |
17 |
30,944,221 (GRCm39) |
critical splice donor site |
probably null |
|
R8462:Dnah8
|
UTSW |
17 |
30,875,603 (GRCm39) |
missense |
probably damaging |
1.00 |
R8506:Dnah8
|
UTSW |
17 |
30,940,108 (GRCm39) |
missense |
probably benign |
|
R8524:Dnah8
|
UTSW |
17 |
30,934,472 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8555:Dnah8
|
UTSW |
17 |
30,940,084 (GRCm39) |
nonsense |
probably null |
|
R8698:Dnah8
|
UTSW |
17 |
31,094,009 (GRCm39) |
missense |
probably damaging |
1.00 |
R8719:Dnah8
|
UTSW |
17 |
30,960,289 (GRCm39) |
missense |
probably damaging |
0.97 |
R8778:Dnah8
|
UTSW |
17 |
30,979,841 (GRCm39) |
frame shift |
probably null |
|
R8781:Dnah8
|
UTSW |
17 |
30,944,078 (GRCm39) |
missense |
probably damaging |
1.00 |
R8821:Dnah8
|
UTSW |
17 |
31,013,712 (GRCm39) |
missense |
probably damaging |
1.00 |
R8864:Dnah8
|
UTSW |
17 |
30,981,616 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8885:Dnah8
|
UTSW |
17 |
30,927,286 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8983:Dnah8
|
UTSW |
17 |
31,070,628 (GRCm39) |
missense |
probably damaging |
0.98 |
R8994:Dnah8
|
UTSW |
17 |
31,009,807 (GRCm39) |
missense |
probably benign |
0.05 |
R9031:Dnah8
|
UTSW |
17 |
30,956,401 (GRCm39) |
missense |
probably damaging |
1.00 |
R9068:Dnah8
|
UTSW |
17 |
30,975,729 (GRCm39) |
missense |
possibly damaging |
0.63 |
R9225:Dnah8
|
UTSW |
17 |
30,854,647 (GRCm39) |
missense |
probably benign |
0.01 |
R9280:Dnah8
|
UTSW |
17 |
31,004,071 (GRCm39) |
missense |
possibly damaging |
0.52 |
R9291:Dnah8
|
UTSW |
17 |
30,944,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R9314:Dnah8
|
UTSW |
17 |
30,990,857 (GRCm39) |
missense |
probably benign |
|
R9347:Dnah8
|
UTSW |
17 |
30,927,333 (GRCm39) |
missense |
probably benign |
0.00 |
R9393:Dnah8
|
UTSW |
17 |
30,872,361 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9415:Dnah8
|
UTSW |
17 |
31,029,297 (GRCm39) |
missense |
probably benign |
0.02 |
R9458:Dnah8
|
UTSW |
17 |
31,049,777 (GRCm39) |
missense |
probably damaging |
1.00 |
R9465:Dnah8
|
UTSW |
17 |
30,979,841 (GRCm39) |
frame shift |
probably null |
|
R9518:Dnah8
|
UTSW |
17 |
30,979,841 (GRCm39) |
frame shift |
probably null |
|
R9524:Dnah8
|
UTSW |
17 |
30,979,841 (GRCm39) |
frame shift |
probably null |
|
R9564:Dnah8
|
UTSW |
17 |
30,932,021 (GRCm39) |
missense |
probably benign |
0.07 |
R9587:Dnah8
|
UTSW |
17 |
30,979,841 (GRCm39) |
frame shift |
probably null |
|
R9599:Dnah8
|
UTSW |
17 |
30,979,841 (GRCm39) |
frame shift |
probably null |
|
R9641:Dnah8
|
UTSW |
17 |
30,932,029 (GRCm39) |
missense |
probably benign |
0.13 |
R9674:Dnah8
|
UTSW |
17 |
30,998,112 (GRCm39) |
missense |
possibly damaging |
0.84 |
R9679:Dnah8
|
UTSW |
17 |
31,037,115 (GRCm39) |
missense |
probably benign |
|
R9789:Dnah8
|
UTSW |
17 |
30,980,104 (GRCm39) |
critical splice donor site |
probably null |
|
RF027:Dnah8
|
UTSW |
17 |
30,854,450 (GRCm39) |
frame shift |
probably null |
|
X0001:Dnah8
|
UTSW |
17 |
30,967,654 (GRCm39) |
missense |
probably damaging |
1.00 |
X0013:Dnah8
|
UTSW |
17 |
31,038,160 (GRCm39) |
missense |
possibly damaging |
0.71 |
Z1176:Dnah8
|
UTSW |
17 |
30,867,514 (GRCm39) |
missense |
probably benign |
|
Z1177:Dnah8
|
UTSW |
17 |
30,932,069 (GRCm39) |
missense |
probably null |
1.00 |
Z1177:Dnah8
|
UTSW |
17 |
30,913,007 (GRCm39) |
missense |
probably benign |
|
|