Other mutations in this stock |
Total: 125 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930432E11Rik |
C |
T |
7: 29,260,710 (GRCm39) |
|
noncoding transcript |
Het |
Abcb11 |
A |
G |
2: 69,115,627 (GRCm39) |
I579T |
probably damaging |
Het |
Abcc9 |
T |
C |
6: 142,627,830 (GRCm39) |
N400S |
probably benign |
Het |
Adarb2 |
T |
C |
13: 8,781,855 (GRCm39) |
L577P |
probably damaging |
Het |
Agt |
A |
C |
8: 125,283,852 (GRCm39) |
N422K |
probably damaging |
Het |
Ahnak |
A |
T |
19: 8,990,766 (GRCm39) |
K4017* |
probably null |
Het |
Akap13 |
C |
A |
7: 75,397,494 (GRCm39) |
Q2575K |
probably damaging |
Het |
Aldh3a2 |
A |
T |
11: 61,144,541 (GRCm39) |
I339K |
probably damaging |
Het |
Alox15 |
G |
T |
11: 70,236,450 (GRCm39) |
Y483* |
probably null |
Het |
Ampd1 |
A |
T |
3: 103,006,913 (GRCm39) |
I713F |
probably damaging |
Het |
Amph |
A |
T |
13: 19,297,286 (GRCm39) |
E344V |
possibly damaging |
Het |
Arhgef18 |
T |
C |
8: 3,436,959 (GRCm39) |
Y250H |
probably damaging |
Het |
Arid5b |
A |
G |
10: 67,932,807 (GRCm39) |
S1032P |
probably damaging |
Het |
Armc8 |
C |
A |
9: 99,387,741 (GRCm39) |
L393F |
probably damaging |
Het |
Bpnt1 |
A |
G |
1: 185,077,623 (GRCm39) |
|
probably null |
Het |
Cachd1 |
G |
A |
4: 100,845,418 (GRCm39) |
R970H |
probably damaging |
Het |
Cd207 |
T |
C |
6: 83,652,738 (GRCm39) |
T131A |
probably benign |
Het |
Cd83 |
G |
A |
13: 43,951,009 (GRCm39) |
V54I |
probably benign |
Het |
Cfap43 |
T |
C |
19: 47,752,115 (GRCm39) |
K1086E |
probably benign |
Het |
Cfap65 |
A |
T |
1: 74,941,328 (GRCm39) |
V1837E |
probably benign |
Het |
Clcnka |
T |
A |
4: 141,123,917 (GRCm39) |
H89L |
probably benign |
Het |
Cnga4 |
T |
C |
7: 105,054,182 (GRCm39) |
I50T |
possibly damaging |
Het |
Cog5 |
A |
G |
12: 31,887,358 (GRCm39) |
|
probably benign |
Het |
Col11a2 |
T |
A |
17: 34,278,322 (GRCm39) |
|
probably null |
Het |
Col28a1 |
T |
G |
6: 8,175,291 (GRCm39) |
I186L |
possibly damaging |
Het |
Col4a2 |
T |
A |
8: 11,481,252 (GRCm39) |
M808K |
probably benign |
Het |
Copb2 |
A |
G |
9: 98,445,528 (GRCm39) |
|
probably benign |
Het |
Dbnl |
G |
A |
11: 5,745,441 (GRCm39) |
|
probably benign |
Het |
Dbx2 |
T |
C |
15: 95,552,493 (GRCm39) |
T51A |
possibly damaging |
Het |
Dcp1a |
A |
T |
14: 30,224,842 (GRCm39) |
M123L |
probably damaging |
Het |
Ddx42 |
T |
A |
11: 106,123,659 (GRCm39) |
F217I |
probably benign |
Het |
Dlc1 |
T |
C |
8: 37,325,205 (GRCm39) |
T367A |
probably benign |
Het |
Dmgdh |
A |
T |
13: 93,888,863 (GRCm39) |
T834S |
probably benign |
Het |
Dnase1l2 |
C |
A |
17: 24,660,056 (GRCm39) |
V271L |
possibly damaging |
Het |
Dsc1 |
T |
C |
18: 20,229,114 (GRCm39) |
Y392C |
probably damaging |
Het |
Edn1 |
T |
C |
13: 42,458,718 (GRCm39) |
|
probably benign |
Het |
Efcab3 |
G |
A |
11: 104,611,327 (GRCm39) |
D390N |
probably benign |
Het |
Eps8l3 |
T |
C |
3: 107,792,126 (GRCm39) |
L351P |
probably damaging |
Het |
F12 |
G |
A |
13: 55,570,296 (GRCm39) |
|
probably benign |
Het |
Fam47e |
T |
C |
5: 92,726,317 (GRCm39) |
|
probably benign |
Het |
Fcrl5 |
C |
A |
3: 87,349,320 (GRCm39) |
Q32K |
probably benign |
Het |
Fndc1 |
C |
T |
17: 7,960,505 (GRCm39) |
V1637I |
possibly damaging |
Het |
Foxg1 |
G |
T |
12: 49,431,350 (GRCm39) |
|
probably benign |
Het |
Frrs1 |
A |
T |
3: 116,696,070 (GRCm39) |
I530F |
possibly damaging |
Het |
Galnt5 |
A |
T |
2: 57,889,097 (GRCm39) |
K232N |
probably benign |
Het |
Ggt5 |
G |
A |
10: 75,438,482 (GRCm39) |
V68M |
probably damaging |
Het |
Gm16519 |
T |
C |
17: 71,236,101 (GRCm39) |
C17R |
probably benign |
Het |
Gm17535 |
A |
G |
9: 3,035,804 (GRCm39) |
Y224C |
probably null |
Het |
Gm9631 |
T |
G |
11: 121,836,455 (GRCm39) |
D28A |
probably damaging |
Het |
Gpx2 |
T |
C |
12: 76,842,087 (GRCm39) |
I21M |
probably benign |
Het |
H2-Q2 |
T |
G |
17: 35,564,661 (GRCm39) |
D354E |
probably damaging |
Het |
Icam2 |
A |
T |
11: 106,271,717 (GRCm39) |
I71K |
probably damaging |
Het |
Il12a |
T |
C |
3: 68,605,223 (GRCm39) |
|
probably benign |
Het |
Insm2 |
C |
G |
12: 55,647,225 (GRCm39) |
A323G |
probably benign |
Het |
Itga1 |
T |
C |
13: 115,104,835 (GRCm39) |
T1064A |
probably benign |
Het |
Itgad |
T |
A |
7: 127,773,176 (GRCm39) |
V11E |
possibly damaging |
Het |
Kctd15 |
C |
T |
7: 34,344,306 (GRCm39) |
S115N |
probably damaging |
Het |
Klra5 |
A |
G |
6: 129,880,527 (GRCm39) |
W124R |
probably damaging |
Het |
Kng2 |
T |
A |
16: 22,806,486 (GRCm39) |
D571V |
probably benign |
Het |
Kpna6 |
A |
T |
4: 129,544,583 (GRCm39) |
F380I |
probably benign |
Het |
Lipo3 |
A |
T |
19: 33,762,169 (GRCm39) |
Y109* |
probably null |
Het |
Lrrc37 |
T |
A |
11: 103,503,986 (GRCm39) |
K485* |
probably null |
Het |
Man2a2 |
T |
C |
7: 80,012,945 (GRCm39) |
H540R |
possibly damaging |
Het |
Map2k4 |
T |
C |
11: 65,603,101 (GRCm39) |
E188G |
probably damaging |
Het |
Mast4 |
T |
C |
13: 102,895,252 (GRCm39) |
|
probably benign |
Het |
Mbtd1 |
A |
G |
11: 93,796,038 (GRCm39) |
D25G |
probably damaging |
Het |
Med13 |
T |
A |
11: 86,221,915 (GRCm39) |
Q238L |
possibly damaging |
Het |
Mmachc |
A |
G |
4: 116,560,851 (GRCm39) |
Y215H |
probably damaging |
Het |
Mtor |
T |
A |
4: 148,568,811 (GRCm39) |
Y1110* |
probably null |
Het |
Nek2 |
A |
G |
1: 191,554,331 (GRCm39) |
N57D |
probably damaging |
Het |
Nek7 |
ACCCC |
ACCC |
1: 138,443,431 (GRCm39) |
|
probably null |
Het |
Neo1 |
G |
T |
9: 58,838,317 (GRCm39) |
T489K |
probably damaging |
Het |
Neu1 |
T |
A |
17: 35,153,736 (GRCm39) |
Y387N |
probably damaging |
Het |
Nfasc |
A |
T |
1: 132,536,176 (GRCm39) |
C586* |
probably null |
Het |
Nle1 |
G |
A |
11: 82,795,671 (GRCm39) |
L259F |
probably damaging |
Het |
Nrde2 |
G |
A |
12: 100,110,105 (GRCm39) |
Q309* |
probably null |
Het |
Nufip2 |
C |
T |
11: 77,577,279 (GRCm39) |
H76Y |
probably benign |
Het |
Or10ak16 |
A |
C |
4: 118,750,687 (GRCm39) |
T136P |
probably damaging |
Het |
Or2y13 |
A |
T |
11: 49,415,405 (GRCm39) |
N285I |
probably damaging |
Het |
Or4k6 |
A |
T |
14: 50,476,096 (GRCm39) |
I82N |
probably damaging |
Het |
Or52e18 |
A |
T |
7: 104,609,018 (GRCm39) |
I307N |
probably benign |
Het |
Or52r1c |
T |
C |
7: 102,735,358 (GRCm39) |
F206S |
probably damaging |
Het |
Or9s18 |
A |
T |
13: 65,300,877 (GRCm39) |
I280F |
probably damaging |
Het |
Pcdhb5 |
A |
G |
18: 37,454,675 (GRCm39) |
T352A |
probably benign |
Het |
Pcdhb7 |
A |
T |
18: 37,476,442 (GRCm39) |
D526V |
probably damaging |
Het |
Phkg1 |
A |
T |
5: 129,893,394 (GRCm39) |
|
probably null |
Het |
Plg |
C |
T |
17: 12,637,623 (GRCm39) |
T744M |
probably damaging |
Het |
Plxnd1 |
A |
C |
6: 115,935,660 (GRCm39) |
|
probably benign |
Het |
Poglut1 |
A |
T |
16: 38,349,837 (GRCm39) |
I312N |
probably damaging |
Het |
Ppp1r16a |
C |
T |
15: 76,574,999 (GRCm39) |
|
probably benign |
Het |
Ppt1 |
A |
G |
4: 122,737,892 (GRCm39) |
M77V |
probably benign |
Het |
Pramel26 |
A |
C |
4: 143,539,155 (GRCm39) |
S113A |
possibly damaging |
Het |
Pramel5 |
G |
T |
4: 143,998,190 (GRCm39) |
T351N |
probably damaging |
Het |
Psmb4 |
G |
A |
3: 94,792,275 (GRCm39) |
R216C |
probably benign |
Het |
Ptprd |
T |
C |
4: 76,002,640 (GRCm39) |
T699A |
probably damaging |
Het |
Retreg3 |
A |
T |
11: 100,989,455 (GRCm39) |
|
probably benign |
Het |
Sanbr |
C |
T |
11: 23,525,491 (GRCm39) |
R716H |
probably damaging |
Het |
Scaper |
G |
A |
9: 55,665,340 (GRCm39) |
A389V |
probably damaging |
Het |
Serinc5 |
G |
A |
13: 92,825,245 (GRCm39) |
D225N |
possibly damaging |
Het |
Slco1a1 |
T |
G |
6: 141,871,480 (GRCm39) |
|
probably benign |
Het |
Snapc1 |
C |
T |
12: 74,021,806 (GRCm39) |
R81C |
probably damaging |
Het |
Sod3 |
A |
T |
5: 52,525,421 (GRCm39) |
D40V |
probably benign |
Het |
Sorcs3 |
C |
A |
19: 48,194,734 (GRCm39) |
A39E |
probably benign |
Het |
Spon1 |
A |
T |
7: 113,639,056 (GRCm39) |
T761S |
probably benign |
Het |
Syde2 |
A |
G |
3: 145,720,004 (GRCm39) |
|
probably null |
Het |
Synm |
T |
A |
7: 67,408,916 (GRCm39) |
D154V |
probably benign |
Het |
Synpo2 |
T |
C |
3: 122,908,098 (GRCm39) |
E406G |
probably damaging |
Het |
Tcea3 |
T |
A |
4: 135,975,382 (GRCm39) |
L8* |
probably null |
Het |
Tec |
G |
A |
5: 72,980,840 (GRCm39) |
L33F |
probably damaging |
Het |
Tex15 |
T |
A |
8: 34,072,354 (GRCm39) |
S2634T |
possibly damaging |
Het |
Tg |
T |
A |
15: 66,601,475 (GRCm39) |
Y162N |
probably damaging |
Het |
Tmem8b |
G |
A |
4: 43,690,123 (GRCm39) |
V853I |
probably benign |
Het |
Togaram1 |
A |
G |
12: 65,068,240 (GRCm39) |
K1748E |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,728,822 (GRCm39) |
|
probably benign |
Het |
Usp36 |
C |
T |
11: 118,163,847 (GRCm39) |
D234N |
probably damaging |
Het |
Usp40 |
G |
A |
1: 87,906,244 (GRCm39) |
P664S |
probably benign |
Het |
Vmn1r54 |
T |
A |
6: 90,246,635 (GRCm39) |
L183H |
probably benign |
Het |
Vmn1r58 |
T |
G |
7: 5,413,676 (GRCm39) |
I185L |
probably benign |
Het |
Wnt8a |
A |
T |
18: 34,680,618 (GRCm39) |
R328W |
probably benign |
Het |
Yars1 |
A |
G |
4: 129,107,732 (GRCm39) |
|
probably benign |
Het |
Zbtb49 |
A |
C |
5: 38,358,018 (GRCm39) |
M745R |
probably damaging |
Het |
Zeb1 |
T |
G |
18: 5,759,027 (GRCm39) |
F162V |
probably damaging |
Het |
Zfp369 |
A |
T |
13: 65,445,362 (GRCm39) |
H835L |
probably damaging |
Het |
Zic5 |
A |
G |
14: 122,701,351 (GRCm39) |
V460A |
unknown |
Het |
Zp3 |
A |
G |
5: 136,013,210 (GRCm39) |
N181D |
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 |
FR4340:Dnah8
|
UTSW |
17 |
30,854,437 (GRCm39) |
small deletion |
probably benign |
|
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 |
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 |
|
|