Other mutations in this stock |
Total: 103 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1810065E05Rik |
G |
T |
11: 58,423,926 (GRCm38) |
C150F |
probably damaging |
Het |
Aagab |
T |
A |
9: 63,616,675 (GRCm38) |
|
probably null |
Het |
Abca15 |
A |
C |
7: 120,407,474 (GRCm38) |
T1654P |
probably damaging |
Het |
Abca17 |
T |
A |
17: 24,334,266 (GRCm38) |
Y157F |
probably benign |
Het |
Aftph |
A |
T |
11: 20,698,318 (GRCm38) |
L813* |
probably null |
Het |
Agap1 |
T |
C |
1: 89,837,755 (GRCm38) |
I615T |
probably damaging |
Het |
Ak3 |
T |
G |
19: 29,022,847 (GRCm38) |
Q221H |
probably benign |
Het |
Aldoa |
A |
G |
7: 126,797,642 (GRCm38) |
|
probably null |
Het |
Anxa8 |
T |
C |
14: 34,091,916 (GRCm38) |
|
probably null |
Het |
Atpsckmt |
T |
C |
15: 31,609,572 (GRCm38) |
F146L |
probably benign |
Het |
Baz2a |
A |
G |
10: 128,123,612 (GRCm38) |
D1329G |
probably damaging |
Het |
Calhm6 |
G |
T |
10: 34,127,695 (GRCm38) |
A72E |
probably damaging |
Het |
Capn9 |
G |
A |
8: 124,605,711 (GRCm38) |
G430R |
possibly damaging |
Het |
Cd55 |
C |
T |
1: 130,449,423 (GRCm38) |
V333I |
probably benign |
Het |
Cep70 |
A |
G |
9: 99,296,385 (GRCm38) |
Y512C |
probably damaging |
Het |
Cfhr2 |
T |
G |
1: 139,831,155 (GRCm38) |
R52S |
probably benign |
Het |
Clcn6 |
A |
G |
4: 148,024,137 (GRCm38) |
F145S |
possibly damaging |
Het |
Cnksr1 |
A |
G |
4: 134,229,628 (GRCm38) |
Y488H |
probably damaging |
Het |
Diablo |
A |
G |
5: 123,523,361 (GRCm38) |
V24A |
probably benign |
Het |
Dsel |
T |
C |
1: 111,859,457 (GRCm38) |
N1116S |
probably benign |
Het |
Efnb1 |
A |
G |
X: 99,147,517 (GRCm38) |
Y343C |
probably damaging |
Het |
Esco1 |
A |
G |
18: 10,574,873 (GRCm38) |
|
probably null |
Het |
Fancd2 |
A |
G |
6: 113,549,321 (GRCm38) |
N335S |
probably benign |
Het |
Flnc |
A |
G |
6: 29,448,675 (GRCm38) |
Y1304C |
probably damaging |
Het |
Fubp3 |
A |
G |
2: 31,600,557 (GRCm38) |
|
probably benign |
Het |
Gemin4 |
G |
C |
11: 76,211,050 (GRCm38) |
P962A |
probably damaging |
Het |
Gjc3 |
A |
C |
5: 137,957,546 (GRCm38) |
L159R |
probably damaging |
Het |
Gli1 |
A |
G |
10: 127,336,727 (GRCm38) |
L182P |
probably damaging |
Het |
Gm21957 |
G |
T |
7: 125,219,453 (GRCm38) |
|
noncoding transcript |
Het |
Gm28040 |
AGTG |
AGTGGCACCTTTGGTG |
1: 133,327,321 (GRCm38) |
|
probably benign |
Het |
Gm5885 |
A |
G |
6: 133,529,275 (GRCm38) |
|
noncoding transcript |
Het |
Gon4l |
A |
T |
3: 88,887,595 (GRCm38) |
T402S |
possibly damaging |
Het |
Gprasp1 |
G |
A |
X: 135,802,042 (GRCm38) |
E995K |
possibly damaging |
Het |
Gvin-ps5 |
T |
A |
7: 106,329,956 (GRCm38) |
T245S |
probably damaging |
Het |
Helb |
A |
T |
10: 120,106,021 (GRCm38) |
M254K |
possibly damaging |
Het |
Ift20 |
G |
A |
11: 78,540,034 (GRCm38) |
E68K |
probably damaging |
Het |
Igfn1 |
AGGG |
AGG |
1: 135,974,852 (GRCm38) |
|
probably benign |
Het |
Impdh2 |
A |
G |
9: 108,565,347 (GRCm38) |
E305G |
possibly damaging |
Het |
Ints7 |
T |
A |
1: 191,604,860 (GRCm38) |
C351S |
possibly damaging |
Het |
Ipo9 |
ATCCTCCTCCTCCTCCTC |
ATCCTCCTCCTCCTCCTCCTC |
1: 135,386,268 (GRCm38) |
|
probably benign |
Het |
Ipo9 |
A |
G |
1: 135,402,250 (GRCm38) |
V484A |
probably benign |
Het |
Kcnq3 |
T |
C |
15: 65,995,851 (GRCm38) |
M648V |
probably benign |
Het |
Kctd16 |
A |
G |
18: 40,259,178 (GRCm38) |
E273G |
possibly damaging |
Het |
Kif18a |
T |
A |
2: 109,333,503 (GRCm38) |
N732K |
probably benign |
Het |
Kif21b |
C |
T |
1: 136,152,264 (GRCm38) |
R513W |
probably damaging |
Het |
Klhl36 |
T |
C |
8: 119,876,772 (GRCm38) |
C589R |
possibly damaging |
Het |
Lck |
A |
G |
4: 129,548,920 (GRCm38) |
Y481H |
probably damaging |
Het |
Lmtk2 |
A |
G |
5: 144,147,615 (GRCm38) |
Y156C |
probably damaging |
Het |
Mical3 |
A |
T |
6: 121,031,134 (GRCm38) |
|
probably null |
Het |
Mki67 |
A |
G |
7: 135,695,592 (GRCm38) |
I2571T |
possibly damaging |
Het |
Mx2 |
G |
A |
16: 97,538,703 (GRCm38) |
E20K |
probably benign |
Het |
Myo10 |
A |
G |
15: 25,714,108 (GRCm38) |
E87G |
probably benign |
Het |
Myo18b |
T |
C |
5: 112,874,026 (GRCm38) |
K500R |
probably benign |
Het |
N4bp2l2 |
A |
T |
5: 150,647,536 (GRCm38) |
I458N |
probably damaging |
Het |
Nat10 |
T |
C |
2: 103,731,303 (GRCm38) |
|
probably null |
Het |
Nfasc |
G |
A |
1: 132,596,645 (GRCm38) |
P932L |
probably damaging |
Het |
Nipa1 |
C |
A |
7: 55,997,511 (GRCm38) |
|
probably null |
Het |
Nkpd1 |
A |
G |
7: 19,524,237 (GRCm38) |
Q647R |
probably damaging |
Het |
Nlrc4 |
T |
A |
17: 74,447,951 (GRCm38) |
|
probably benign |
Het |
Nmbr |
C |
A |
10: 14,770,442 (GRCm38) |
Y353* |
probably null |
Het |
Nos1ap |
T |
A |
1: 170,329,166 (GRCm38) |
D241V |
probably damaging |
Het |
Obsl1 |
G |
A |
1: 75,486,756 (GRCm38) |
T1764M |
probably benign |
Het |
Olfr1025-ps1 |
A |
G |
2: 85,918,827 (GRCm38) |
I301V |
probably null |
Het |
Optc |
A |
T |
1: 133,903,796 (GRCm38) |
|
probably null |
Het |
Or4f4b |
A |
T |
2: 111,483,630 (GRCm38) |
T95S |
probably benign |
Het |
Or5d43 |
A |
G |
2: 88,275,010 (GRCm38) |
V13A |
probably benign |
Het |
Or6c201 |
A |
G |
10: 129,133,006 (GRCm38) |
I254T |
probably benign |
Het |
Pank1 |
G |
A |
19: 34,878,980 (GRCm38) |
R33C |
possibly damaging |
Het |
Pcmtd1 |
C |
T |
1: 7,169,565 (GRCm38) |
R77C |
probably damaging |
Het |
Phkg2 |
G |
A |
7: 127,582,214 (GRCm38) |
|
probably null |
Het |
Plcb4 |
G |
A |
2: 135,976,099 (GRCm38) |
V762M |
probably damaging |
Het |
Pramel7 |
T |
A |
2: 87,489,977 (GRCm38) |
H324L |
probably damaging |
Het |
Prelp |
C |
T |
1: 133,915,131 (GRCm38) |
R92K |
probably benign |
Het |
Ptgr3 |
T |
C |
18: 84,094,543 (GRCm38) |
Y115H |
probably benign |
Het |
Rai1 |
C |
A |
11: 60,189,467 (GRCm38) |
S1452R |
possibly damaging |
Het |
Ren1 |
C |
G |
1: 133,350,778 (GRCm38) |
|
probably null |
Het |
Rev3l |
T |
C |
10: 39,848,049 (GRCm38) |
V785A |
probably benign |
Het |
Ro60 |
T |
C |
1: 143,760,034 (GRCm38) |
D458G |
probably benign |
Het |
Rufy2 |
G |
T |
10: 62,990,994 (GRCm38) |
R104L |
probably damaging |
Het |
Senp6 |
T |
A |
9: 80,123,820 (GRCm38) |
N8K |
probably damaging |
Het |
Septin4 |
A |
T |
11: 87,583,436 (GRCm38) |
Q60L |
probably benign |
Het |
Sipa1l2 |
G |
A |
8: 125,491,491 (GRCm38) |
P369L |
probably benign |
Het |
Slc43a1 |
T |
C |
2: 84,840,961 (GRCm38) |
L37P |
probably damaging |
Het |
Slf1 |
T |
A |
13: 77,049,219 (GRCm38) |
|
probably null |
Het |
Ssr2 |
T |
A |
3: 88,576,642 (GRCm38) |
|
probably benign |
Het |
Syt2 |
ACTCTCTCT |
ACTCTCTCTCT |
1: 134,746,741 (GRCm38) |
|
probably benign |
Het |
Tas2r115 |
T |
C |
6: 132,737,358 (GRCm38) |
K210R |
probably benign |
Het |
Tbx18 |
A |
G |
9: 87,715,653 (GRCm38) |
V276A |
probably damaging |
Het |
Tesl1 |
T |
A |
X: 23,907,310 (GRCm38) |
V350E |
probably benign |
Het |
Tie1 |
G |
A |
4: 118,472,811 (GRCm38) |
R1072* |
probably null |
Het |
Tm2d2 |
C |
A |
8: 25,022,658 (GRCm38) |
T174K |
probably damaging |
Het |
Tmem98 |
A |
G |
11: 80,814,332 (GRCm38) |
D82G |
possibly damaging |
Het |
Tmub2 |
A |
G |
11: 102,287,553 (GRCm38) |
E94G |
possibly damaging |
Het |
Tnnt2 |
TG |
TGG |
1: 135,846,761 (GRCm38) |
|
probably benign |
Het |
Tonsl |
A |
T |
15: 76,632,661 (GRCm38) |
I923N |
probably damaging |
Het |
Ttc21a |
G |
A |
9: 119,964,295 (GRCm38) |
V977M |
probably damaging |
Het |
Ube2ql1 |
T |
C |
13: 69,738,664 (GRCm38) |
D226G |
probably damaging |
Het |
Ubr4 |
C |
T |
4: 139,477,207 (GRCm38) |
T4810M |
probably damaging |
Het |
Wdr87-ps |
T |
C |
7: 29,531,510 (GRCm38) |
|
noncoding transcript |
Het |
Zfp408 |
A |
G |
2: 91,647,849 (GRCm38) |
|
probably benign |
Het |
Zfp473 |
T |
C |
7: 44,733,077 (GRCm38) |
T610A |
possibly damaging |
Het |
Zfp804b |
A |
G |
5: 6,772,583 (GRCm38) |
V160A |
probably benign |
Het |
Zfp960 |
A |
G |
17: 17,087,884 (GRCm38) |
T287A |
probably benign |
Het |
|
Other mutations in Dnah7b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00336:Dnah7b
|
APN |
1 |
46,142,149 (GRCm38) |
missense |
probably benign |
0.04 |
IGL00796:Dnah7b
|
APN |
1 |
46,211,337 (GRCm38) |
missense |
probably damaging |
0.96 |
IGL00825:Dnah7b
|
APN |
1 |
46,224,651 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL00910:Dnah7b
|
APN |
1 |
46,066,729 (GRCm38) |
unclassified |
probably benign |
|
IGL00950:Dnah7b
|
APN |
1 |
46,214,322 (GRCm38) |
missense |
probably benign |
0.07 |
IGL01142:Dnah7b
|
APN |
1 |
46,195,378 (GRCm38) |
critical splice donor site |
probably null |
|
IGL01350:Dnah7b
|
APN |
1 |
46,081,432 (GRCm38) |
splice site |
probably benign |
|
IGL01392:Dnah7b
|
APN |
1 |
46,126,788 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01403:Dnah7b
|
APN |
1 |
46,116,300 (GRCm38) |
splice site |
probably benign |
|
IGL01460:Dnah7b
|
APN |
1 |
46,139,704 (GRCm38) |
missense |
possibly damaging |
0.82 |
IGL01576:Dnah7b
|
APN |
1 |
46,268,653 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01693:Dnah7b
|
APN |
1 |
46,358,147 (GRCm38) |
missense |
probably benign |
0.29 |
IGL01838:Dnah7b
|
APN |
1 |
46,358,137 (GRCm38) |
nonsense |
probably null |
|
IGL01906:Dnah7b
|
APN |
1 |
46,175,453 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01960:Dnah7b
|
APN |
1 |
46,124,337 (GRCm38) |
splice site |
probably benign |
|
IGL01989:Dnah7b
|
APN |
1 |
46,289,534 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02127:Dnah7b
|
APN |
1 |
46,139,875 (GRCm38) |
missense |
probably benign |
|
IGL02213:Dnah7b
|
APN |
1 |
46,233,592 (GRCm38) |
missense |
probably damaging |
0.97 |
IGL02267:Dnah7b
|
APN |
1 |
46,226,930 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02349:Dnah7b
|
APN |
1 |
46,099,503 (GRCm38) |
nonsense |
probably null |
|
IGL02381:Dnah7b
|
APN |
1 |
46,277,120 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02473:Dnah7b
|
APN |
1 |
46,234,193 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02484:Dnah7b
|
APN |
1 |
46,195,318 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02590:Dnah7b
|
APN |
1 |
46,123,777 (GRCm38) |
missense |
probably benign |
0.02 |
IGL02655:Dnah7b
|
APN |
1 |
46,116,301 (GRCm38) |
splice site |
probably benign |
|
IGL02704:Dnah7b
|
APN |
1 |
46,142,133 (GRCm38) |
missense |
probably benign |
0.03 |
IGL02719:Dnah7b
|
APN |
1 |
46,099,608 (GRCm38) |
splice site |
probably benign |
|
IGL02745:Dnah7b
|
APN |
1 |
46,195,029 (GRCm38) |
splice site |
probably benign |
|
IGL02818:Dnah7b
|
APN |
1 |
46,290,808 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02892:Dnah7b
|
APN |
1 |
46,119,298 (GRCm38) |
missense |
possibly damaging |
0.79 |
IGL03285:Dnah7b
|
APN |
1 |
46,182,375 (GRCm38) |
missense |
probably benign |
0.00 |
IGL03354:Dnah7b
|
APN |
1 |
46,085,689 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03355:Dnah7b
|
APN |
1 |
46,119,304 (GRCm38) |
missense |
probably benign |
0.18 |
BB001:Dnah7b
|
UTSW |
1 |
46,219,430 (GRCm38) |
missense |
probably benign |
0.04 |
BB011:Dnah7b
|
UTSW |
1 |
46,219,430 (GRCm38) |
missense |
probably benign |
0.04 |
PIT4305001:Dnah7b
|
UTSW |
1 |
46,373,348 (GRCm38) |
missense |
probably damaging |
1.00 |
R0116:Dnah7b
|
UTSW |
1 |
46,213,360 (GRCm38) |
missense |
possibly damaging |
0.94 |
R0145:Dnah7b
|
UTSW |
1 |
46,223,178 (GRCm38) |
missense |
probably damaging |
1.00 |
R0230:Dnah7b
|
UTSW |
1 |
46,219,348 (GRCm38) |
missense |
probably damaging |
1.00 |
R0302:Dnah7b
|
UTSW |
1 |
46,123,777 (GRCm38) |
missense |
probably benign |
0.26 |
R0313:Dnah7b
|
UTSW |
1 |
46,207,643 (GRCm38) |
missense |
probably damaging |
1.00 |
R0317:Dnah7b
|
UTSW |
1 |
46,134,656 (GRCm38) |
missense |
probably damaging |
1.00 |
R0347:Dnah7b
|
UTSW |
1 |
46,240,944 (GRCm38) |
missense |
probably damaging |
1.00 |
R0352:Dnah7b
|
UTSW |
1 |
46,277,126 (GRCm38) |
missense |
probably damaging |
0.98 |
R0363:Dnah7b
|
UTSW |
1 |
46,236,788 (GRCm38) |
missense |
probably damaging |
0.99 |
R0379:Dnah7b
|
UTSW |
1 |
46,140,176 (GRCm38) |
missense |
probably benign |
0.00 |
R0502:Dnah7b
|
UTSW |
1 |
46,219,544 (GRCm38) |
missense |
probably damaging |
0.96 |
R0602:Dnah7b
|
UTSW |
1 |
46,324,842 (GRCm38) |
missense |
probably damaging |
1.00 |
R0631:Dnah7b
|
UTSW |
1 |
46,240,992 (GRCm38) |
missense |
probably benign |
0.02 |
R0664:Dnah7b
|
UTSW |
1 |
46,324,842 (GRCm38) |
missense |
probably damaging |
1.00 |
R0882:Dnah7b
|
UTSW |
1 |
46,340,132 (GRCm38) |
missense |
probably benign |
0.00 |
R0931:Dnah7b
|
UTSW |
1 |
46,099,612 (GRCm38) |
splice site |
probably benign |
|
R1035:Dnah7b
|
UTSW |
1 |
46,124,448 (GRCm38) |
missense |
probably benign |
|
R1147:Dnah7b
|
UTSW |
1 |
46,340,266 (GRCm38) |
missense |
probably damaging |
0.99 |
R1147:Dnah7b
|
UTSW |
1 |
46,340,266 (GRCm38) |
missense |
probably damaging |
0.99 |
R1166:Dnah7b
|
UTSW |
1 |
46,325,810 (GRCm38) |
missense |
probably damaging |
1.00 |
R1219:Dnah7b
|
UTSW |
1 |
46,340,120 (GRCm38) |
missense |
probably benign |
0.00 |
R1318:Dnah7b
|
UTSW |
1 |
46,099,509 (GRCm38) |
missense |
possibly damaging |
0.80 |
R1334:Dnah7b
|
UTSW |
1 |
46,322,335 (GRCm38) |
missense |
probably damaging |
0.99 |
R1429:Dnah7b
|
UTSW |
1 |
46,289,656 (GRCm38) |
missense |
possibly damaging |
0.84 |
R1440:Dnah7b
|
UTSW |
1 |
46,078,593 (GRCm38) |
splice site |
probably benign |
|
R1484:Dnah7b
|
UTSW |
1 |
46,137,543 (GRCm38) |
missense |
probably benign |
0.00 |
R1529:Dnah7b
|
UTSW |
1 |
46,177,281 (GRCm38) |
missense |
probably damaging |
1.00 |
R1544:Dnah7b
|
UTSW |
1 |
46,066,797 (GRCm38) |
missense |
unknown |
|
R1607:Dnah7b
|
UTSW |
1 |
46,290,646 (GRCm38) |
missense |
probably damaging |
1.00 |
R1609:Dnah7b
|
UTSW |
1 |
46,352,966 (GRCm38) |
missense |
probably damaging |
1.00 |
R1652:Dnah7b
|
UTSW |
1 |
46,175,390 (GRCm38) |
nonsense |
probably null |
|
R1681:Dnah7b
|
UTSW |
1 |
46,324,712 (GRCm38) |
nonsense |
probably null |
|
R1716:Dnah7b
|
UTSW |
1 |
46,191,783 (GRCm38) |
missense |
probably damaging |
1.00 |
R1753:Dnah7b
|
UTSW |
1 |
46,322,335 (GRCm38) |
missense |
probably damaging |
0.99 |
R1834:Dnah7b
|
UTSW |
1 |
46,233,759 (GRCm38) |
missense |
possibly damaging |
0.90 |
R1838:Dnah7b
|
UTSW |
1 |
46,277,105 (GRCm38) |
missense |
probably damaging |
1.00 |
R1838:Dnah7b
|
UTSW |
1 |
46,116,177 (GRCm38) |
missense |
probably benign |
0.04 |
R1898:Dnah7b
|
UTSW |
1 |
46,236,714 (GRCm38) |
missense |
probably benign |
0.02 |
R1962:Dnah7b
|
UTSW |
1 |
46,242,103 (GRCm38) |
missense |
possibly damaging |
0.95 |
R2001:Dnah7b
|
UTSW |
1 |
46,142,087 (GRCm38) |
missense |
possibly damaging |
0.69 |
R2049:Dnah7b
|
UTSW |
1 |
46,268,670 (GRCm38) |
missense |
probably damaging |
1.00 |
R2076:Dnah7b
|
UTSW |
1 |
46,242,321 (GRCm38) |
nonsense |
probably null |
|
R2083:Dnah7b
|
UTSW |
1 |
46,241,067 (GRCm38) |
missense |
possibly damaging |
0.90 |
R2140:Dnah7b
|
UTSW |
1 |
46,268,670 (GRCm38) |
missense |
probably damaging |
1.00 |
R2142:Dnah7b
|
UTSW |
1 |
46,268,670 (GRCm38) |
missense |
probably damaging |
1.00 |
R2165:Dnah7b
|
UTSW |
1 |
46,097,992 (GRCm38) |
splice site |
probably benign |
|
R2172:Dnah7b
|
UTSW |
1 |
46,124,512 (GRCm38) |
missense |
probably benign |
0.12 |
R2239:Dnah7b
|
UTSW |
1 |
46,201,184 (GRCm38) |
splice site |
probably benign |
|
R2247:Dnah7b
|
UTSW |
1 |
46,277,063 (GRCm38) |
missense |
probably damaging |
1.00 |
R2267:Dnah7b
|
UTSW |
1 |
46,233,915 (GRCm38) |
missense |
probably damaging |
1.00 |
R2405:Dnah7b
|
UTSW |
1 |
46,362,954 (GRCm38) |
missense |
probably benign |
0.31 |
R2509:Dnah7b
|
UTSW |
1 |
46,195,287 (GRCm38) |
missense |
probably damaging |
0.96 |
R2895:Dnah7b
|
UTSW |
1 |
46,139,741 (GRCm38) |
missense |
probably damaging |
1.00 |
R2965:Dnah7b
|
UTSW |
1 |
46,207,572 (GRCm38) |
missense |
probably damaging |
1.00 |
R3013:Dnah7b
|
UTSW |
1 |
46,188,687 (GRCm38) |
critical splice donor site |
probably null |
|
R3022:Dnah7b
|
UTSW |
1 |
46,182,423 (GRCm38) |
missense |
probably damaging |
0.99 |
R3056:Dnah7b
|
UTSW |
1 |
46,268,709 (GRCm38) |
missense |
possibly damaging |
0.95 |
R3107:Dnah7b
|
UTSW |
1 |
46,352,873 (GRCm38) |
missense |
probably benign |
0.00 |
R3735:Dnah7b
|
UTSW |
1 |
46,299,875 (GRCm38) |
missense |
probably benign |
0.05 |
R3898:Dnah7b
|
UTSW |
1 |
46,243,257 (GRCm38) |
missense |
probably damaging |
1.00 |
R3944:Dnah7b
|
UTSW |
1 |
46,137,485 (GRCm38) |
missense |
probably damaging |
1.00 |
R3983:Dnah7b
|
UTSW |
1 |
46,233,711 (GRCm38) |
missense |
possibly damaging |
0.88 |
R4041:Dnah7b
|
UTSW |
1 |
46,081,495 (GRCm38) |
missense |
probably benign |
|
R4172:Dnah7b
|
UTSW |
1 |
46,226,946 (GRCm38) |
missense |
probably damaging |
1.00 |
R4210:Dnah7b
|
UTSW |
1 |
46,137,418 (GRCm38) |
missense |
possibly damaging |
0.63 |
R4306:Dnah7b
|
UTSW |
1 |
46,221,772 (GRCm38) |
missense |
probably damaging |
0.99 |
R4391:Dnah7b
|
UTSW |
1 |
46,337,594 (GRCm38) |
splice site |
probably null |
|
R4414:Dnah7b
|
UTSW |
1 |
46,126,680 (GRCm38) |
missense |
probably benign |
0.00 |
R4495:Dnah7b
|
UTSW |
1 |
46,085,632 (GRCm38) |
missense |
probably benign |
0.00 |
R4660:Dnah7b
|
UTSW |
1 |
46,289,536 (GRCm38) |
missense |
probably damaging |
1.00 |
R4670:Dnah7b
|
UTSW |
1 |
46,078,524 (GRCm38) |
missense |
probably damaging |
1.00 |
R4675:Dnah7b
|
UTSW |
1 |
46,217,157 (GRCm38) |
missense |
possibly damaging |
0.89 |
R4685:Dnah7b
|
UTSW |
1 |
46,211,328 (GRCm38) |
missense |
probably damaging |
1.00 |
R4727:Dnah7b
|
UTSW |
1 |
46,207,656 (GRCm38) |
missense |
probably damaging |
1.00 |
R4735:Dnah7b
|
UTSW |
1 |
46,066,955 (GRCm38) |
missense |
unknown |
|
R4780:Dnah7b
|
UTSW |
1 |
46,353,014 (GRCm38) |
missense |
probably benign |
|
R4828:Dnah7b
|
UTSW |
1 |
46,128,112 (GRCm38) |
missense |
possibly damaging |
0.59 |
R4859:Dnah7b
|
UTSW |
1 |
46,356,602 (GRCm38) |
missense |
probably damaging |
1.00 |
R4865:Dnah7b
|
UTSW |
1 |
46,195,074 (GRCm38) |
missense |
probably damaging |
1.00 |
R4871:Dnah7b
|
UTSW |
1 |
46,081,444 (GRCm38) |
missense |
probably benign |
0.21 |
R4881:Dnah7b
|
UTSW |
1 |
46,201,318 (GRCm38) |
missense |
probably damaging |
1.00 |
R4902:Dnah7b
|
UTSW |
1 |
46,290,775 (GRCm38) |
missense |
probably benign |
0.04 |
R4960:Dnah7b
|
UTSW |
1 |
46,233,726 (GRCm38) |
missense |
probably benign |
|
R5000:Dnah7b
|
UTSW |
1 |
46,099,503 (GRCm38) |
nonsense |
probably null |
|
R5005:Dnah7b
|
UTSW |
1 |
46,242,028 (GRCm38) |
missense |
probably damaging |
0.99 |
R5026:Dnah7b
|
UTSW |
1 |
46,187,363 (GRCm38) |
missense |
probably damaging |
0.99 |
R5080:Dnah7b
|
UTSW |
1 |
46,182,380 (GRCm38) |
nonsense |
probably null |
|
R5174:Dnah7b
|
UTSW |
1 |
46,243,349 (GRCm38) |
missense |
possibly damaging |
0.83 |
R5178:Dnah7b
|
UTSW |
1 |
46,358,216 (GRCm38) |
missense |
possibly damaging |
0.50 |
R5244:Dnah7b
|
UTSW |
1 |
46,233,858 (GRCm38) |
missense |
probably damaging |
1.00 |
R5250:Dnah7b
|
UTSW |
1 |
46,373,354 (GRCm38) |
missense |
probably damaging |
1.00 |
R5350:Dnah7b
|
UTSW |
1 |
46,233,689 (GRCm38) |
missense |
probably benign |
0.16 |
R5380:Dnah7b
|
UTSW |
1 |
46,217,191 (GRCm38) |
missense |
probably benign |
0.18 |
R5387:Dnah7b
|
UTSW |
1 |
46,188,659 (GRCm38) |
missense |
probably damaging |
1.00 |
R5423:Dnah7b
|
UTSW |
1 |
46,358,271 (GRCm38) |
missense |
probably benign |
0.01 |
R5426:Dnah7b
|
UTSW |
1 |
46,242,206 (GRCm38) |
missense |
possibly damaging |
0.82 |
R5451:Dnah7b
|
UTSW |
1 |
46,242,019 (GRCm38) |
missense |
possibly damaging |
0.73 |
R5459:Dnah7b
|
UTSW |
1 |
46,109,312 (GRCm38) |
missense |
probably null |
|
R5479:Dnah7b
|
UTSW |
1 |
46,223,105 (GRCm38) |
missense |
probably damaging |
1.00 |
R5583:Dnah7b
|
UTSW |
1 |
46,242,199 (GRCm38) |
missense |
probably benign |
0.06 |
R5637:Dnah7b
|
UTSW |
1 |
46,356,514 (GRCm38) |
missense |
possibly damaging |
0.95 |
R5641:Dnah7b
|
UTSW |
1 |
46,268,764 (GRCm38) |
splice site |
probably null |
|
R5659:Dnah7b
|
UTSW |
1 |
46,352,849 (GRCm38) |
missense |
probably damaging |
1.00 |
R5739:Dnah7b
|
UTSW |
1 |
46,233,992 (GRCm38) |
missense |
probably damaging |
1.00 |
R5759:Dnah7b
|
UTSW |
1 |
46,277,120 (GRCm38) |
missense |
probably damaging |
1.00 |
R5821:Dnah7b
|
UTSW |
1 |
46,142,132 (GRCm38) |
missense |
possibly damaging |
0.91 |
R5874:Dnah7b
|
UTSW |
1 |
46,191,725 (GRCm38) |
missense |
probably damaging |
1.00 |
R5892:Dnah7b
|
UTSW |
1 |
46,337,593 (GRCm38) |
critical splice donor site |
probably null |
|
R5918:Dnah7b
|
UTSW |
1 |
46,221,643 (GRCm38) |
missense |
probably benign |
|
R5941:Dnah7b
|
UTSW |
1 |
46,187,290 (GRCm38) |
missense |
probably damaging |
1.00 |
R5965:Dnah7b
|
UTSW |
1 |
46,362,987 (GRCm38) |
missense |
probably damaging |
1.00 |
R5987:Dnah7b
|
UTSW |
1 |
46,119,398 (GRCm38) |
splice site |
probably null |
|
R6041:Dnah7b
|
UTSW |
1 |
46,289,645 (GRCm38) |
missense |
probably benign |
0.04 |
R6043:Dnah7b
|
UTSW |
1 |
46,139,789 (GRCm38) |
missense |
probably benign |
|
R6049:Dnah7b
|
UTSW |
1 |
46,085,602 (GRCm38) |
missense |
probably benign |
|
R6131:Dnah7b
|
UTSW |
1 |
46,253,466 (GRCm38) |
missense |
probably damaging |
1.00 |
R6168:Dnah7b
|
UTSW |
1 |
46,290,703 (GRCm38) |
missense |
probably damaging |
1.00 |
R6195:Dnah7b
|
UTSW |
1 |
46,204,269 (GRCm38) |
missense |
probably damaging |
1.00 |
R6219:Dnah7b
|
UTSW |
1 |
46,233,585 (GRCm38) |
missense |
probably benign |
0.03 |
R6226:Dnah7b
|
UTSW |
1 |
46,126,668 (GRCm38) |
missense |
probably benign |
0.01 |
R6233:Dnah7b
|
UTSW |
1 |
46,204,269 (GRCm38) |
missense |
probably damaging |
1.00 |
R6247:Dnah7b
|
UTSW |
1 |
46,225,888 (GRCm38) |
missense |
probably benign |
|
R6273:Dnah7b
|
UTSW |
1 |
46,242,316 (GRCm38) |
missense |
possibly damaging |
0.94 |
R6279:Dnah7b
|
UTSW |
1 |
46,325,886 (GRCm38) |
missense |
probably damaging |
1.00 |
R6300:Dnah7b
|
UTSW |
1 |
46,325,886 (GRCm38) |
missense |
probably damaging |
1.00 |
R6330:Dnah7b
|
UTSW |
1 |
46,340,175 (GRCm38) |
missense |
probably damaging |
1.00 |
R6476:Dnah7b
|
UTSW |
1 |
46,242,204 (GRCm38) |
nonsense |
probably null |
|
R6494:Dnah7b
|
UTSW |
1 |
46,099,431 (GRCm38) |
missense |
probably damaging |
1.00 |
R6762:Dnah7b
|
UTSW |
1 |
46,224,742 (GRCm38) |
missense |
probably benign |
0.12 |
R6800:Dnah7b
|
UTSW |
1 |
46,340,217 (GRCm38) |
missense |
possibly damaging |
0.90 |
R6838:Dnah7b
|
UTSW |
1 |
46,191,788 (GRCm38) |
missense |
probably damaging |
1.00 |
R6937:Dnah7b
|
UTSW |
1 |
46,195,120 (GRCm38) |
missense |
probably damaging |
1.00 |
R6940:Dnah7b
|
UTSW |
1 |
46,119,268 (GRCm38) |
missense |
probably benign |
0.12 |
R6969:Dnah7b
|
UTSW |
1 |
46,358,238 (GRCm38) |
missense |
probably damaging |
1.00 |
R6993:Dnah7b
|
UTSW |
1 |
46,195,139 (GRCm38) |
critical splice donor site |
probably null |
|
R7040:Dnah7b
|
UTSW |
1 |
46,236,809 (GRCm38) |
missense |
probably benign |
0.01 |
R7117:Dnah7b
|
UTSW |
1 |
46,352,813 (GRCm38) |
critical splice acceptor site |
probably null |
|
R7135:Dnah7b
|
UTSW |
1 |
46,139,710 (GRCm38) |
missense |
probably damaging |
0.99 |
R7153:Dnah7b
|
UTSW |
1 |
46,126,804 (GRCm38) |
missense |
probably benign |
0.05 |
R7189:Dnah7b
|
UTSW |
1 |
46,242,142 (GRCm38) |
missense |
probably damaging |
1.00 |
R7237:Dnah7b
|
UTSW |
1 |
46,139,966 (GRCm38) |
missense |
probably damaging |
0.98 |
R7243:Dnah7b
|
UTSW |
1 |
46,083,754 (GRCm38) |
missense |
probably benign |
|
R7244:Dnah7b
|
UTSW |
1 |
46,277,143 (GRCm38) |
missense |
probably damaging |
0.99 |
R7248:Dnah7b
|
UTSW |
1 |
46,142,085 (GRCm38) |
missense |
possibly damaging |
0.83 |
R7318:Dnah7b
|
UTSW |
1 |
46,195,372 (GRCm38) |
missense |
probably damaging |
1.00 |
R7375:Dnah7b
|
UTSW |
1 |
46,303,634 (GRCm38) |
missense |
probably damaging |
1.00 |
R7483:Dnah7b
|
UTSW |
1 |
46,175,419 (GRCm38) |
missense |
probably damaging |
1.00 |
R7486:Dnah7b
|
UTSW |
1 |
46,290,734 (GRCm38) |
missense |
probably damaging |
1.00 |
R7498:Dnah7b
|
UTSW |
1 |
46,325,765 (GRCm38) |
missense |
probably damaging |
1.00 |
R7501:Dnah7b
|
UTSW |
1 |
46,356,554 (GRCm38) |
missense |
probably damaging |
1.00 |
R7513:Dnah7b
|
UTSW |
1 |
46,124,346 (GRCm38) |
missense |
probably benign |
0.06 |
R7547:Dnah7b
|
UTSW |
1 |
46,214,413 (GRCm38) |
missense |
possibly damaging |
0.82 |
R7620:Dnah7b
|
UTSW |
1 |
46,268,634 (GRCm38) |
missense |
probably damaging |
1.00 |
R7670:Dnah7b
|
UTSW |
1 |
46,109,302 (GRCm38) |
missense |
probably benign |
|
R7676:Dnah7b
|
UTSW |
1 |
46,234,164 (GRCm38) |
nonsense |
probably null |
|
R7731:Dnah7b
|
UTSW |
1 |
46,139,745 (GRCm38) |
missense |
probably benign |
0.00 |
R7760:Dnah7b
|
UTSW |
1 |
46,201,253 (GRCm38) |
missense |
probably damaging |
1.00 |
R7768:Dnah7b
|
UTSW |
1 |
46,137,474 (GRCm38) |
missense |
probably benign |
|
R7807:Dnah7b
|
UTSW |
1 |
46,214,367 (GRCm38) |
missense |
probably benign |
|
R7895:Dnah7b
|
UTSW |
1 |
46,249,950 (GRCm38) |
missense |
probably damaging |
1.00 |
R7911:Dnah7b
|
UTSW |
1 |
46,139,678 (GRCm38) |
missense |
probably damaging |
1.00 |
R7924:Dnah7b
|
UTSW |
1 |
46,219,430 (GRCm38) |
missense |
probably benign |
0.04 |
R7944:Dnah7b
|
UTSW |
1 |
46,227,003 (GRCm38) |
missense |
probably benign |
|
R7946:Dnah7b
|
UTSW |
1 |
46,233,579 (GRCm38) |
missense |
probably damaging |
1.00 |
R7983:Dnah7b
|
UTSW |
1 |
46,243,424 (GRCm38) |
missense |
probably damaging |
1.00 |
R8012:Dnah7b
|
UTSW |
1 |
46,243,365 (GRCm38) |
missense |
probably damaging |
1.00 |
R8069:Dnah7b
|
UTSW |
1 |
46,224,706 (GRCm38) |
nonsense |
probably null |
|
R8094:Dnah7b
|
UTSW |
1 |
46,126,804 (GRCm38) |
missense |
probably benign |
0.01 |
R8137:Dnah7b
|
UTSW |
1 |
46,233,753 (GRCm38) |
missense |
probably damaging |
1.00 |
R8167:Dnah7b
|
UTSW |
1 |
46,253,511 (GRCm38) |
missense |
possibly damaging |
0.95 |
R8268:Dnah7b
|
UTSW |
1 |
46,356,576 (GRCm38) |
missense |
probably benign |
0.43 |
R8309:Dnah7b
|
UTSW |
1 |
46,139,872 (GRCm38) |
missense |
probably damaging |
1.00 |
R8313:Dnah7b
|
UTSW |
1 |
46,175,296 (GRCm38) |
missense |
possibly damaging |
0.81 |
R8410:Dnah7b
|
UTSW |
1 |
46,356,659 (GRCm38) |
critical splice donor site |
probably null |
|
R8438:Dnah7b
|
UTSW |
1 |
46,188,679 (GRCm38) |
missense |
probably damaging |
1.00 |
R8446:Dnah7b
|
UTSW |
1 |
46,290,715 (GRCm38) |
missense |
probably damaging |
1.00 |
R8471:Dnah7b
|
UTSW |
1 |
46,099,490 (GRCm38) |
missense |
possibly damaging |
0.92 |
R8551:Dnah7b
|
UTSW |
1 |
46,116,200 (GRCm38) |
missense |
possibly damaging |
0.94 |
R8711:Dnah7b
|
UTSW |
1 |
46,175,438 (GRCm38) |
missense |
probably damaging |
1.00 |
R8745:Dnah7b
|
UTSW |
1 |
46,182,464 (GRCm38) |
missense |
possibly damaging |
0.82 |
R8765:Dnah7b
|
UTSW |
1 |
46,352,999 (GRCm38) |
missense |
possibly damaging |
0.91 |
R8797:Dnah7b
|
UTSW |
1 |
46,123,646 (GRCm38) |
missense |
probably damaging |
1.00 |
R8805:Dnah7b
|
UTSW |
1 |
46,234,145 (GRCm38) |
missense |
possibly damaging |
0.90 |
R8830:Dnah7b
|
UTSW |
1 |
46,191,793 (GRCm38) |
missense |
probably damaging |
1.00 |
R8861:Dnah7b
|
UTSW |
1 |
46,241,076 (GRCm38) |
missense |
possibly damaging |
0.82 |
R8905:Dnah7b
|
UTSW |
1 |
46,253,374 (GRCm38) |
missense |
probably damaging |
0.99 |
R9009:Dnah7b
|
UTSW |
1 |
46,223,072 (GRCm38) |
missense |
probably benign |
0.00 |
R9058:Dnah7b
|
UTSW |
1 |
46,243,415 (GRCm38) |
missense |
probably damaging |
1.00 |
R9130:Dnah7b
|
UTSW |
1 |
46,134,514 (GRCm38) |
missense |
probably benign |
0.01 |
R9131:Dnah7b
|
UTSW |
1 |
46,227,020 (GRCm38) |
missense |
probably damaging |
1.00 |
R9181:Dnah7b
|
UTSW |
1 |
46,142,034 (GRCm38) |
missense |
probably damaging |
1.00 |
R9182:Dnah7b
|
UTSW |
1 |
46,290,878 (GRCm38) |
missense |
probably benign |
0.06 |
R9223:Dnah7b
|
UTSW |
1 |
46,322,260 (GRCm38) |
missense |
probably benign |
0.12 |
R9391:Dnah7b
|
UTSW |
1 |
46,233,754 (GRCm38) |
nonsense |
probably null |
|
R9392:Dnah7b
|
UTSW |
1 |
46,123,738 (GRCm38) |
nonsense |
probably null |
|
R9456:Dnah7b
|
UTSW |
1 |
46,126,793 (GRCm38) |
missense |
possibly damaging |
0.82 |
R9498:Dnah7b
|
UTSW |
1 |
46,214,404 (GRCm38) |
missense |
probably benign |
0.27 |
R9553:Dnah7b
|
UTSW |
1 |
46,225,796 (GRCm38) |
missense |
probably damaging |
0.99 |
R9598:Dnah7b
|
UTSW |
1 |
46,253,461 (GRCm38) |
missense |
possibly damaging |
0.67 |
R9653:Dnah7b
|
UTSW |
1 |
46,213,384 (GRCm38) |
missense |
possibly damaging |
0.55 |
R9781:Dnah7b
|
UTSW |
1 |
46,337,594 (GRCm38) |
splice site |
probably null |
|
RF020:Dnah7b
|
UTSW |
1 |
46,373,261 (GRCm38) |
missense |
possibly damaging |
0.84 |
V8831:Dnah7b
|
UTSW |
1 |
46,373,298 (GRCm38) |
nonsense |
probably null |
|
X0023:Dnah7b
|
UTSW |
1 |
46,303,577 (GRCm38) |
missense |
probably benign |
0.04 |
|