Other mutations in this stock |
Total: 115 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930433I11Rik |
AACC |
A |
7: 40,642,479 (GRCm39) |
|
probably benign |
Het |
4930578G10Rik |
G |
T |
4: 42,761,098 (GRCm39) |
|
probably benign |
Het |
7530416G11Rik |
T |
A |
15: 85,378,508 (GRCm39) |
E45V |
unknown |
Homo |
A530064D06Rik |
GTAGGAAGCTTAG |
GTAG |
17: 48,470,549 (GRCm39) |
|
probably benign |
Homo |
Arpc1b |
CC |
CCTGGTC |
5: 145,063,602 (GRCm39) |
|
probably null |
Het |
Arrb2 |
C |
T |
11: 70,329,497 (GRCm39) |
T269M |
probably damaging |
Homo |
Bcas3 |
G |
A |
11: 85,400,323 (GRCm39) |
V431I |
probably benign |
Homo |
Blm |
ACCT |
ACCTGCCT |
7: 80,113,515 (GRCm39) |
|
probably benign |
Het |
Blm |
TCCTCCTCCTCCTCCTCCTCCTCC |
TCCTCCTCCTCCACCTCCTCCTCCTCCTCCTCCTCC |
7: 80,162,658 (GRCm39) |
|
probably benign |
Het |
Blm |
TCCTCCTCCTCCTCCTCCTCCTCC |
TCCTCCTCCTCCGCCTCCTCCTCCTCCTCCTCCTCC |
7: 80,162,655 (GRCm39) |
|
probably benign |
Het |
Bltp1 |
TATTATTAT |
TATTATTATTATTATCATTATTAT |
3: 37,104,901 (GRCm39) |
|
probably benign |
Het |
Cacna1a |
ACC |
ACCGCC |
8: 85,365,352 (GRCm39) |
|
probably benign |
Het |
Cacna1f |
AGG |
AGGCGG |
X: 7,486,306 (GRCm39) |
|
probably benign |
Het |
Calhm1 |
CTCTGTGGCTGTGGCTGTGGCTGTG |
CTCTGTGGCTGTGTCTGTGGCTGTGGCTGTGGCTGTG |
19: 47,129,690 (GRCm39) |
|
probably benign |
Het |
Casz1 |
ACCACAGCCACAGCCACAGCCAC |
ACCACAGCCACAGCCAC |
4: 149,036,759 (GRCm39) |
|
probably benign |
Homo |
Ccdc121 |
GAGAAG |
GAG |
5: 31,644,717 (GRCm39) |
|
probably benign |
Het |
Cd164 |
G |
T |
10: 41,397,922 (GRCm39) |
A59S |
probably benign |
Het |
Cd22 |
C |
T |
7: 30,577,507 (GRCm39) |
R2H |
possibly damaging |
Homo |
Cd80 |
GAA |
GAAAAA |
16: 38,306,678 (GRCm39) |
|
probably benign |
Homo |
Cimip2b |
CAGAG |
CAG |
4: 43,427,384 (GRCm39) |
|
probably null |
Homo |
Col2a1 |
C |
A |
15: 97,886,862 (GRCm39) |
|
probably null |
Het |
Col6a5 |
A |
T |
9: 105,811,373 (GRCm39) |
N715K |
unknown |
Homo |
Crygc |
A |
T |
1: 65,110,822 (GRCm39) |
F155Y |
probably benign |
Het |
Cul9 |
TCC |
TCCCCC |
17: 46,811,779 (GRCm39) |
|
probably benign |
Het |
Cyp2d11 |
T |
TGGGA |
15: 82,274,223 (GRCm39) |
|
probably null |
Homo |
Dbr1 |
AGG |
AGGAGGCGG |
9: 99,465,754 (GRCm39) |
|
probably benign |
Het |
Dennd10 |
CT |
CTTTT |
19: 60,803,059 (GRCm39) |
|
probably benign |
Homo |
Dennd2b |
CACCACACTGGGGCAGCCCACACTGGGGCAG |
CCCCACACTGGGGCAG |
7: 109,156,128 (GRCm39) |
|
probably benign |
Het |
Dnah12 |
G |
T |
14: 26,571,342 (GRCm39) |
G2817V |
probably damaging |
Homo |
Dthd1 |
C |
CTTA |
5: 63,000,369 (GRCm39) |
|
probably benign |
Homo |
Frem3 |
CT |
CTTTT |
8: 81,341,870 (GRCm39) |
|
probably benign |
Homo |
Frmpd2 |
G |
T |
14: 33,232,978 (GRCm39) |
L399F |
probably damaging |
Homo |
G530012D18Rik |
CACACAGAGAGAGAGAGAGAGAGAGA |
CA |
1: 85,504,873 (GRCm39) |
|
probably benign |
Het |
Gbp2b |
A |
G |
3: 142,309,413 (GRCm39) |
I175V |
probably benign |
Het |
Gm14393 |
T |
C |
2: 174,903,427 (GRCm39) |
E160G |
possibly damaging |
Het |
Gm16519 |
A |
AGAAC |
17: 71,236,333 (GRCm39) |
|
probably null |
Homo |
Gm4340 |
GCAG |
GCAACAG |
10: 104,031,959 (GRCm39) |
|
probably benign |
Het |
Gm4340 |
CAGAAG |
CAGAAGAAG |
10: 104,031,960 (GRCm39) |
|
probably benign |
Het |
Gm4340 |
CAG |
CAGTAG |
10: 104,031,936 (GRCm39) |
|
probably null |
Het |
Gpatch11 |
AGGAAG |
AGGAAGGGGAAG |
17: 79,149,603 (GRCm39) |
|
probably benign |
Het |
H2-Q4 |
G |
A |
17: 35,599,381 (GRCm39) |
D155N |
probably damaging |
Het |
Ifi208 |
ATGGTG |
ATG |
1: 173,505,264 (GRCm39) |
|
probably benign |
Homo |
Ighv5-9 |
C |
T |
12: 113,625,497 (GRCm39) |
S82N |
probably benign |
Homo |
Ipo9 |
TCC |
TCCCCC |
1: 135,314,007 (GRCm39) |
|
probably benign |
Het |
Ipo9 |
CTC |
CTCTTC |
1: 135,314,009 (GRCm39) |
|
probably benign |
Het |
Isg20l2 |
AAG |
AAGTAG |
3: 87,839,019 (GRCm39) |
|
probably null |
Het |
Kmt2b |
TCCTCC |
TCCTCCCCCTCC |
7: 30,285,800 (GRCm39) |
|
probably benign |
Het |
Kmt2b |
TCCTCC |
TCCTCCCCCTCC |
7: 30,285,788 (GRCm39) |
|
probably benign |
Het |
Kmt2b |
TCCTCC |
TCCTCCCCCTCC |
7: 30,285,794 (GRCm39) |
|
probably benign |
Het |
Krt10 |
CCTCCT |
CCTCCTTCTCCT |
11: 99,280,100 (GRCm39) |
|
probably benign |
Het |
Krt10 |
CAC |
CACGAC |
11: 99,277,028 (GRCm39) |
|
probably benign |
Het |
Krt10 |
ACCG |
ACCGCCG |
11: 99,277,029 (GRCm39) |
|
probably benign |
Homo |
Las1l |
TCCTC |
TCCTCTACCTC |
X: 94,984,228 (GRCm39) |
|
probably benign |
Het |
Lce1a1 |
C |
T |
3: 92,554,151 (GRCm39) |
G108S |
unknown |
Het |
Lkaaear1 |
CCAGCTCCAG |
CCAGCTCCAGCTGCAGCTCCAG |
2: 181,339,387 (GRCm39) |
|
probably benign |
Het |
Lrit3 |
CTG |
CTGTTG |
3: 129,582,457 (GRCm39) |
|
probably benign |
Het |
Mamld1 |
CAG |
CAGAAG |
X: 70,162,452 (GRCm39) |
|
probably benign |
Het |
Mapk7 |
TGCTGGCGCTGGTGCTGGCGCTGG |
TGCTGGCGCTGGCGCTGGTGCTGGCGCTGG |
11: 61,381,032 (GRCm39) |
|
probably benign |
Het |
Mast4 |
GCA |
GCAGTGTCA |
13: 102,872,825 (GRCm39) |
|
probably benign |
Homo |
Mast4 |
TTTT |
TTTTATTT |
13: 102,871,365 (GRCm39) |
|
probably null |
Het |
Med12l |
AGC |
AGCCGC |
3: 59,183,406 (GRCm39) |
|
probably benign |
Het |
Mfsd5 |
G |
A |
15: 102,189,596 (GRCm39) |
V323I |
probably benign |
Het |
Nacad |
GTC |
GTCAGGATC |
11: 6,549,761 (GRCm39) |
|
probably benign |
Het |
Naip1 |
A |
C |
13: 100,559,584 (GRCm39) |
M1140R |
probably benign |
Het |
Nbea |
TTTA |
T |
3: 55,916,633 (GRCm39) |
|
probably benign |
Homo |
Nefh |
CTCACCTGGGGACTTGGCCTC |
CTCACCTGGGGACTTGGCCTCACCTGGGGACTTGGCCTC |
11: 4,891,040 (GRCm39) |
|
probably benign |
Homo |
Nefh |
ACTTGGCCTCACCTGGGG |
ACTTGGCCTCACCTGGGGCCTTGGCCTCACCTGGGG |
11: 4,891,033 (GRCm39) |
|
probably benign |
Het |
Nefh |
GCCTCACCTGGGGACTTGGCCTC |
GCCTCACCTGGGGACTTGGCCTCACCTGGGGACTTGGCCTC |
11: 4,891,038 (GRCm39) |
|
probably benign |
Homo |
Neu1 |
TCTTCTA |
T |
17: 35,151,534 (GRCm39) |
|
probably benign |
Het |
Nutf2 |
G |
T |
8: 106,603,202 (GRCm39) |
D78Y |
probably damaging |
Het |
Or51q1 |
TCC |
TCCC |
7: 103,629,110 (GRCm39) |
|
probably null |
Het |
Or5e1 |
AT |
ATGATATT |
7: 108,354,161 (GRCm39) |
|
probably benign |
Homo |
Or5p70 |
G |
A |
7: 107,995,105 (GRCm39) |
M259I |
probably benign |
Het |
Or5p70 |
A |
G |
7: 107,995,100 (GRCm39) |
T258A |
probably benign |
Het |
Pdik1l |
ACCAC |
ACCACCCCCAC |
4: 134,006,823 (GRCm39) |
|
probably benign |
Het |
Phaf1 |
G |
A |
8: 105,967,730 (GRCm39) |
G207E |
probably benign |
Homo |
Pik3c2g |
AG |
AGAGGG |
6: 139,612,654 (GRCm39) |
|
probably null |
Homo |
Plekhs1 |
TCCAGAC |
TCCAGACCTCCCCCCAGAC |
19: 56,468,290 (GRCm39) |
|
probably benign |
Homo |
Prag1 |
C |
CAGT |
8: 36,571,040 (GRCm39) |
|
probably benign |
Homo |
Pramel16 |
G |
A |
4: 143,676,312 (GRCm39) |
T264M |
probably damaging |
Het |
Prkn |
G |
A |
17: 12,073,650 (GRCm39) |
V323M |
probably damaging |
Homo |
Raet1d |
A |
G |
10: 22,247,458 (GRCm39) |
Q178R |
probably benign |
Het |
Serac1 |
T |
A |
17: 6,121,083 (GRCm39) |
K70N |
probably damaging |
Homo |
Serpina3i |
CGG |
CGGTGG |
12: 104,231,423 (GRCm39) |
|
probably benign |
Het |
Sfswap |
ACTCAGCCC |
ACTCAGCCCCCTCAGCCC |
5: 129,646,815 (GRCm39) |
|
probably benign |
Het |
Six3 |
CGG |
CGGGGG |
17: 85,928,784 (GRCm39) |
|
probably benign |
Het |
Sp140l1 |
A |
C |
1: 85,087,072 (GRCm39) |
N6K |
probably damaging |
Het |
Speer4a1 |
C |
A |
5: 26,241,746 (GRCm39) |
E127* |
probably null |
Het |
Sry |
GCTGCTGCTGCTG |
GCTGCTGCTGCTGCTG |
Y: 2,662,824 (GRCm39) |
|
probably benign |
Het |
Tbr1 |
A |
C |
2: 61,636,691 (GRCm39) |
|
probably benign |
Het |
Tdpoz2 |
T |
TCC |
3: 93,558,922 (GRCm39) |
|
probably null |
Homo |
Tdpoz4 |
GAA |
GA |
3: 93,704,187 (GRCm39) |
|
probably null |
Het |
Tgoln1 |
AAG |
AAGCCTCAG |
6: 72,593,334 (GRCm39) |
|
probably benign |
Homo |
Tmbim7 |
C |
T |
5: 3,720,064 (GRCm39) |
R100C |
possibly damaging |
Het |
Tob1 |
CA |
CAGAA |
11: 94,105,303 (GRCm39) |
|
probably benign |
Het |
Tob1 |
AGC |
AGCCGC |
11: 94,105,280 (GRCm39) |
|
probably benign |
Het |
Tob1 |
AGC |
AGCCGC |
11: 94,105,286 (GRCm39) |
|
probably benign |
Het |
Tomm5 |
GCATCTTCC |
GCATCTTCCACATCTTCC |
4: 45,107,973 (GRCm39) |
|
probably benign |
Het |
Triobp |
TCGG |
TCGGCGG |
15: 78,877,590 (GRCm39) |
|
probably benign |
Homo |
Tsbp1 |
GC |
GCAAC |
17: 34,679,051 (GRCm39) |
|
probably benign |
Het |
Tsbp1 |
CAG |
CAGTAG |
17: 34,679,034 (GRCm39) |
|
probably null |
Het |
Tsbp1 |
GCA |
GCATCA |
17: 34,679,042 (GRCm39) |
|
probably benign |
Het |
Tsen2 |
AGG |
AGGGGG |
6: 115,537,027 (GRCm39) |
|
probably benign |
Homo |
Tsen2 |
AGG |
AGGGGG |
6: 115,537,030 (GRCm39) |
|
probably benign |
Homo |
Ubtf |
TCC |
TCCCCC |
11: 102,197,776 (GRCm39) |
|
probably benign |
Het |
Vmn2r87 |
C |
T |
10: 130,314,583 (GRCm39) |
M334I |
probably benign |
Homo |
Zc3h13 |
CGGGATGTGCG |
CGGGATGTGCGGGATGTGCG |
14: 75,561,032 (GRCm39) |
|
probably benign |
Homo |
Zfp28 |
G |
A |
7: 6,397,862 (GRCm39) |
G766R |
probably damaging |
Het |
Zfp384 |
AAGCCCAGGCCCAGGCCCAGGCCCA |
AAGCCCAGGCCCAAGCCCAGGCCCAGGCCCAGGCCCA |
6: 125,013,426 (GRCm39) |
|
probably benign |
Het |
Zfp428 |
G |
A |
7: 24,214,506 (GRCm39) |
D41N |
probably damaging |
Homo |
Zfp598 |
CCACAGGC |
CC |
17: 24,898,346 (GRCm39) |
|
probably benign |
Het |
Zfp598 |
CCACCA |
CCACCAACACCA |
17: 24,899,757 (GRCm39) |
|
probably benign |
Het |
Zfp831 |
TCC |
TCCCCC |
2: 174,487,273 (GRCm39) |
|
probably benign |
Het |
Zfp933 |
GCTT |
GCTTTTCTT |
4: 147,910,186 (GRCm39) |
|
probably null |
Homo |
Zfp936 |
G |
A |
7: 42,838,913 (GRCm39) |
G127R |
possibly damaging |
Het |
|
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 |
FR4737:Dnah8
|
UTSW |
17 |
30,854,451 (GRCm39) |
small deletion |
probably benign |
|
FR4737:Dnah8
|
UTSW |
17 |
30,854,439 (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 |
30,854,479 (GRCm39) |
missense |
unknown |
|
R1935:Dnah8
|
UTSW |
17 |
30,945,870 (GRCm39) |
splice site |
probably benign |
|
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 |
|
|