Other mutations in this stock |
Total: 103 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1810065E05Rik |
G |
T |
11: 58,314,752 (GRCm39) |
C150F |
probably damaging |
Het |
Aagab |
T |
A |
9: 63,523,957 (GRCm39) |
|
probably null |
Het |
Abca15 |
A |
C |
7: 120,006,697 (GRCm39) |
T1654P |
probably damaging |
Het |
Abca17 |
T |
A |
17: 24,553,240 (GRCm39) |
Y157F |
probably benign |
Het |
Aftph |
A |
T |
11: 20,648,318 (GRCm39) |
L813* |
probably null |
Het |
Agap1 |
T |
C |
1: 89,765,477 (GRCm39) |
I615T |
probably damaging |
Het |
Ak3 |
T |
G |
19: 29,000,247 (GRCm39) |
Q221H |
probably benign |
Het |
Aldoa |
A |
G |
7: 126,396,814 (GRCm39) |
|
probably null |
Het |
Anxa8 |
T |
C |
14: 33,813,873 (GRCm39) |
|
probably null |
Het |
Atpsckmt |
T |
C |
15: 31,609,718 (GRCm39) |
F146L |
probably benign |
Het |
Baz2a |
A |
G |
10: 127,959,481 (GRCm39) |
D1329G |
probably damaging |
Het |
Calhm6 |
G |
T |
10: 34,003,691 (GRCm39) |
A72E |
probably damaging |
Het |
Capn9 |
G |
A |
8: 125,332,450 (GRCm39) |
G430R |
possibly damaging |
Het |
Cd55 |
C |
T |
1: 130,377,160 (GRCm39) |
V333I |
probably benign |
Het |
Cep70 |
A |
G |
9: 99,178,438 (GRCm39) |
Y512C |
probably damaging |
Het |
Cfhr2 |
T |
G |
1: 139,758,893 (GRCm39) |
R52S |
probably benign |
Het |
Clcn6 |
A |
G |
4: 148,108,594 (GRCm39) |
F145S |
possibly damaging |
Het |
Cnksr1 |
A |
G |
4: 133,956,939 (GRCm39) |
Y488H |
probably damaging |
Het |
Diablo |
A |
G |
5: 123,661,424 (GRCm39) |
V24A |
probably benign |
Het |
Dsel |
T |
C |
1: 111,787,187 (GRCm39) |
N1116S |
probably benign |
Het |
Efnb1 |
A |
G |
X: 98,191,123 (GRCm39) |
Y343C |
probably damaging |
Het |
Esco1 |
A |
G |
18: 10,574,873 (GRCm39) |
|
probably null |
Het |
Fancd2 |
A |
G |
6: 113,526,282 (GRCm39) |
N335S |
probably benign |
Het |
Flnc |
A |
G |
6: 29,448,674 (GRCm39) |
Y1304C |
probably damaging |
Het |
Fubp3 |
A |
G |
2: 31,490,569 (GRCm39) |
|
probably benign |
Het |
Gemin4 |
G |
C |
11: 76,101,876 (GRCm39) |
P962A |
probably damaging |
Het |
Gjc3 |
A |
C |
5: 137,955,808 (GRCm39) |
L159R |
probably damaging |
Het |
Gli1 |
A |
G |
10: 127,172,596 (GRCm39) |
L182P |
probably damaging |
Het |
Gm21957 |
G |
T |
7: 124,818,625 (GRCm39) |
|
noncoding transcript |
Het |
Gm28040 |
AGTG |
AGTGGCACCTTTGGTG |
1: 133,255,059 (GRCm39) |
|
probably benign |
Het |
Gm5885 |
A |
G |
6: 133,506,238 (GRCm39) |
|
noncoding transcript |
Het |
Gon4l |
A |
T |
3: 88,794,902 (GRCm39) |
T402S |
possibly damaging |
Het |
Gprasp1 |
G |
A |
X: 134,702,791 (GRCm39) |
E995K |
possibly damaging |
Het |
Gvin-ps5 |
T |
A |
7: 105,929,163 (GRCm39) |
T245S |
probably damaging |
Het |
Helb |
A |
T |
10: 119,941,926 (GRCm39) |
M254K |
possibly damaging |
Het |
Ift20 |
G |
A |
11: 78,430,860 (GRCm39) |
E68K |
probably damaging |
Het |
Igfn1 |
AGGG |
AGG |
1: 135,902,590 (GRCm39) |
|
probably benign |
Het |
Impdh2 |
A |
G |
9: 108,442,546 (GRCm39) |
E305G |
possibly damaging |
Het |
Ints7 |
T |
A |
1: 191,336,972 (GRCm39) |
C351S |
possibly damaging |
Het |
Ipo9 |
ATCCTCCTCCTCCTCCTC |
ATCCTCCTCCTCCTCCTCCTC |
1: 135,314,006 (GRCm39) |
|
probably benign |
Het |
Ipo9 |
A |
G |
1: 135,329,988 (GRCm39) |
V484A |
probably benign |
Het |
Kcnq3 |
T |
C |
15: 65,867,700 (GRCm39) |
M648V |
probably benign |
Het |
Kctd16 |
A |
G |
18: 40,392,231 (GRCm39) |
E273G |
possibly damaging |
Het |
Kif18a |
T |
A |
2: 109,163,848 (GRCm39) |
N732K |
probably benign |
Het |
Kif21b |
C |
T |
1: 136,080,002 (GRCm39) |
R513W |
probably damaging |
Het |
Klhl36 |
T |
C |
8: 120,603,511 (GRCm39) |
C589R |
possibly damaging |
Het |
Lck |
A |
G |
4: 129,442,713 (GRCm39) |
Y481H |
probably damaging |
Het |
Lmtk2 |
A |
G |
5: 144,084,433 (GRCm39) |
Y156C |
probably damaging |
Het |
Mical3 |
A |
T |
6: 121,008,095 (GRCm39) |
|
probably null |
Het |
Mki67 |
A |
G |
7: 135,297,321 (GRCm39) |
I2571T |
possibly damaging |
Het |
Mx2 |
G |
A |
16: 97,339,903 (GRCm39) |
E20K |
probably benign |
Het |
Myo10 |
A |
G |
15: 25,714,194 (GRCm39) |
E87G |
probably benign |
Het |
Myo18b |
T |
C |
5: 113,021,892 (GRCm39) |
K500R |
probably benign |
Het |
N4bp2l2 |
A |
T |
5: 150,571,001 (GRCm39) |
I458N |
probably damaging |
Het |
Nat10 |
T |
C |
2: 103,561,648 (GRCm39) |
|
probably null |
Het |
Nfasc |
G |
A |
1: 132,524,383 (GRCm39) |
P932L |
probably damaging |
Het |
Nipa1 |
C |
A |
7: 55,647,259 (GRCm39) |
|
probably null |
Het |
Nkpd1 |
A |
G |
7: 19,258,162 (GRCm39) |
Q647R |
probably damaging |
Het |
Nlrc4 |
T |
A |
17: 74,754,946 (GRCm39) |
|
probably benign |
Het |
Nmbr |
C |
A |
10: 14,646,186 (GRCm39) |
Y353* |
probably null |
Het |
Nos1ap |
T |
A |
1: 170,156,735 (GRCm39) |
D241V |
probably damaging |
Het |
Obsl1 |
G |
A |
1: 75,486,756 (GRCm38) |
T1764M |
probably benign |
Het |
Optc |
A |
T |
1: 133,831,534 (GRCm39) |
|
probably null |
Het |
Or4f4b |
A |
T |
2: 111,313,975 (GRCm39) |
T95S |
probably benign |
Het |
Or5d43 |
A |
G |
2: 88,105,354 (GRCm39) |
V13A |
probably benign |
Het |
Or5m13 |
A |
G |
2: 85,749,171 (GRCm39) |
I301V |
probably null |
Het |
Or6c201 |
A |
G |
10: 128,968,875 (GRCm39) |
I254T |
probably benign |
Het |
Pank1 |
G |
A |
19: 34,856,380 (GRCm39) |
R33C |
possibly damaging |
Het |
Pcmtd1 |
C |
T |
1: 7,239,789 (GRCm39) |
R77C |
probably damaging |
Het |
Phkg2 |
G |
A |
7: 127,181,386 (GRCm39) |
|
probably null |
Het |
Plcb4 |
G |
A |
2: 135,818,019 (GRCm39) |
V762M |
probably damaging |
Het |
Pramel7 |
T |
A |
2: 87,320,321 (GRCm39) |
H324L |
probably damaging |
Het |
Prelp |
C |
T |
1: 133,842,869 (GRCm39) |
R92K |
probably benign |
Het |
Ptgr3 |
T |
C |
18: 84,112,668 (GRCm39) |
Y115H |
probably benign |
Het |
Rai1 |
C |
A |
11: 60,080,293 (GRCm39) |
S1452R |
possibly damaging |
Het |
Ren1 |
C |
G |
1: 133,278,516 (GRCm39) |
|
probably null |
Het |
Rev3l |
T |
C |
10: 39,724,045 (GRCm39) |
V785A |
probably benign |
Het |
Ro60 |
T |
C |
1: 143,635,772 (GRCm39) |
D458G |
probably benign |
Het |
Rufy2 |
G |
T |
10: 62,826,773 (GRCm39) |
R104L |
probably damaging |
Het |
Senp6 |
T |
A |
9: 80,031,102 (GRCm39) |
N8K |
probably damaging |
Het |
Septin4 |
A |
T |
11: 87,474,262 (GRCm39) |
Q60L |
probably benign |
Het |
Sipa1l2 |
G |
A |
8: 126,218,230 (GRCm39) |
P369L |
probably benign |
Het |
Slc43a1 |
T |
C |
2: 84,671,305 (GRCm39) |
L37P |
probably damaging |
Het |
Slf1 |
T |
A |
13: 77,197,338 (GRCm39) |
|
probably null |
Het |
Ssr2 |
T |
A |
3: 88,483,949 (GRCm39) |
|
probably benign |
Het |
Syt2 |
ACTCTCTCT |
ACTCTCTCTCT |
1: 134,674,479 (GRCm39) |
|
probably benign |
Het |
Tas2r115 |
T |
C |
6: 132,714,321 (GRCm39) |
K210R |
probably benign |
Het |
Tbx18 |
A |
G |
9: 87,597,706 (GRCm39) |
V276A |
probably damaging |
Het |
Tesl1 |
T |
A |
X: 23,773,549 (GRCm39) |
V350E |
probably benign |
Het |
Tie1 |
G |
A |
4: 118,330,008 (GRCm39) |
R1072* |
probably null |
Het |
Tm2d2 |
C |
A |
8: 25,512,674 (GRCm39) |
T174K |
probably damaging |
Het |
Tmem98 |
A |
G |
11: 80,705,158 (GRCm39) |
D82G |
possibly damaging |
Het |
Tmub2 |
A |
G |
11: 102,178,379 (GRCm39) |
E94G |
possibly damaging |
Het |
Tnnt2 |
TG |
TGG |
1: 135,774,499 (GRCm39) |
|
probably benign |
Het |
Tonsl |
A |
T |
15: 76,516,861 (GRCm39) |
I923N |
probably damaging |
Het |
Ttc21a |
G |
A |
9: 119,793,361 (GRCm39) |
V977M |
probably damaging |
Het |
Ube2ql1 |
T |
C |
13: 69,886,783 (GRCm39) |
D226G |
probably damaging |
Het |
Ubr4 |
C |
T |
4: 139,204,518 (GRCm39) |
T4810M |
probably damaging |
Het |
Wdr87-ps |
T |
C |
7: 29,230,935 (GRCm39) |
|
noncoding transcript |
Het |
Zfp408 |
A |
G |
2: 91,478,194 (GRCm39) |
|
probably benign |
Het |
Zfp473 |
T |
C |
7: 44,382,501 (GRCm39) |
T610A |
possibly damaging |
Het |
Zfp804b |
A |
G |
5: 6,822,583 (GRCm39) |
V160A |
probably benign |
Het |
Zfp960 |
A |
G |
17: 17,308,146 (GRCm39) |
T287A |
probably benign |
Het |
|
Other mutations in Dnah7b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00336:Dnah7b
|
APN |
1 |
46,181,309 (GRCm39) |
missense |
probably benign |
0.04 |
IGL00796:Dnah7b
|
APN |
1 |
46,250,497 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL00825:Dnah7b
|
APN |
1 |
46,263,811 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00910:Dnah7b
|
APN |
1 |
46,105,889 (GRCm39) |
unclassified |
probably benign |
|
IGL00950:Dnah7b
|
APN |
1 |
46,253,482 (GRCm39) |
missense |
probably benign |
0.07 |
IGL01142:Dnah7b
|
APN |
1 |
46,234,538 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01350:Dnah7b
|
APN |
1 |
46,120,592 (GRCm39) |
splice site |
probably benign |
|
IGL01392:Dnah7b
|
APN |
1 |
46,165,948 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01403:Dnah7b
|
APN |
1 |
46,155,460 (GRCm39) |
splice site |
probably benign |
|
IGL01460:Dnah7b
|
APN |
1 |
46,178,864 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01576:Dnah7b
|
APN |
1 |
46,307,813 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01693:Dnah7b
|
APN |
1 |
46,397,307 (GRCm39) |
missense |
probably benign |
0.29 |
IGL01838:Dnah7b
|
APN |
1 |
46,397,297 (GRCm39) |
nonsense |
probably null |
|
IGL01906:Dnah7b
|
APN |
1 |
46,214,613 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01960:Dnah7b
|
APN |
1 |
46,163,497 (GRCm39) |
splice site |
probably benign |
|
IGL01989:Dnah7b
|
APN |
1 |
46,328,694 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02127:Dnah7b
|
APN |
1 |
46,179,035 (GRCm39) |
missense |
probably benign |
|
IGL02213:Dnah7b
|
APN |
1 |
46,272,752 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02267:Dnah7b
|
APN |
1 |
46,266,090 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02349:Dnah7b
|
APN |
1 |
46,138,663 (GRCm39) |
nonsense |
probably null |
|
IGL02381:Dnah7b
|
APN |
1 |
46,316,280 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02473:Dnah7b
|
APN |
1 |
46,273,353 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02484:Dnah7b
|
APN |
1 |
46,234,478 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02590:Dnah7b
|
APN |
1 |
46,162,937 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02655:Dnah7b
|
APN |
1 |
46,155,461 (GRCm39) |
splice site |
probably benign |
|
IGL02704:Dnah7b
|
APN |
1 |
46,181,293 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02719:Dnah7b
|
APN |
1 |
46,138,768 (GRCm39) |
splice site |
probably benign |
|
IGL02745:Dnah7b
|
APN |
1 |
46,234,189 (GRCm39) |
splice site |
probably benign |
|
IGL02818:Dnah7b
|
APN |
1 |
46,329,968 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02892:Dnah7b
|
APN |
1 |
46,158,458 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL03285:Dnah7b
|
APN |
1 |
46,221,535 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03354:Dnah7b
|
APN |
1 |
46,124,849 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03355:Dnah7b
|
APN |
1 |
46,158,464 (GRCm39) |
missense |
probably benign |
0.18 |
BB001:Dnah7b
|
UTSW |
1 |
46,258,590 (GRCm39) |
missense |
probably benign |
0.04 |
BB011:Dnah7b
|
UTSW |
1 |
46,258,590 (GRCm39) |
missense |
probably benign |
0.04 |
PIT4305001:Dnah7b
|
UTSW |
1 |
46,412,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R0116:Dnah7b
|
UTSW |
1 |
46,252,520 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0145:Dnah7b
|
UTSW |
1 |
46,262,338 (GRCm39) |
missense |
probably damaging |
1.00 |
R0230:Dnah7b
|
UTSW |
1 |
46,258,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R0302:Dnah7b
|
UTSW |
1 |
46,162,937 (GRCm39) |
missense |
probably benign |
0.26 |
R0313:Dnah7b
|
UTSW |
1 |
46,246,803 (GRCm39) |
missense |
probably damaging |
1.00 |
R0317:Dnah7b
|
UTSW |
1 |
46,173,816 (GRCm39) |
missense |
probably damaging |
1.00 |
R0347:Dnah7b
|
UTSW |
1 |
46,280,104 (GRCm39) |
missense |
probably damaging |
1.00 |
R0352:Dnah7b
|
UTSW |
1 |
46,316,286 (GRCm39) |
missense |
probably damaging |
0.98 |
R0363:Dnah7b
|
UTSW |
1 |
46,275,948 (GRCm39) |
missense |
probably damaging |
0.99 |
R0379:Dnah7b
|
UTSW |
1 |
46,179,336 (GRCm39) |
missense |
probably benign |
0.00 |
R0502:Dnah7b
|
UTSW |
1 |
46,258,704 (GRCm39) |
missense |
probably damaging |
0.96 |
R0602:Dnah7b
|
UTSW |
1 |
46,364,002 (GRCm39) |
missense |
probably damaging |
1.00 |
R0631:Dnah7b
|
UTSW |
1 |
46,280,152 (GRCm39) |
missense |
probably benign |
0.02 |
R0664:Dnah7b
|
UTSW |
1 |
46,364,002 (GRCm39) |
missense |
probably damaging |
1.00 |
R0882:Dnah7b
|
UTSW |
1 |
46,379,292 (GRCm39) |
missense |
probably benign |
0.00 |
R0931:Dnah7b
|
UTSW |
1 |
46,138,772 (GRCm39) |
splice site |
probably benign |
|
R1035:Dnah7b
|
UTSW |
1 |
46,163,608 (GRCm39) |
missense |
probably benign |
|
R1147:Dnah7b
|
UTSW |
1 |
46,379,426 (GRCm39) |
missense |
probably damaging |
0.99 |
R1147:Dnah7b
|
UTSW |
1 |
46,379,426 (GRCm39) |
missense |
probably damaging |
0.99 |
R1166:Dnah7b
|
UTSW |
1 |
46,364,970 (GRCm39) |
missense |
probably damaging |
1.00 |
R1219:Dnah7b
|
UTSW |
1 |
46,379,280 (GRCm39) |
missense |
probably benign |
0.00 |
R1318:Dnah7b
|
UTSW |
1 |
46,138,669 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1334:Dnah7b
|
UTSW |
1 |
46,361,495 (GRCm39) |
missense |
probably damaging |
0.99 |
R1429:Dnah7b
|
UTSW |
1 |
46,328,816 (GRCm39) |
missense |
possibly damaging |
0.84 |
R1440:Dnah7b
|
UTSW |
1 |
46,117,753 (GRCm39) |
splice site |
probably benign |
|
R1484:Dnah7b
|
UTSW |
1 |
46,176,703 (GRCm39) |
missense |
probably benign |
0.00 |
R1529:Dnah7b
|
UTSW |
1 |
46,216,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R1544:Dnah7b
|
UTSW |
1 |
46,105,957 (GRCm39) |
missense |
unknown |
|
R1607:Dnah7b
|
UTSW |
1 |
46,329,806 (GRCm39) |
missense |
probably damaging |
1.00 |
R1609:Dnah7b
|
UTSW |
1 |
46,392,126 (GRCm39) |
missense |
probably damaging |
1.00 |
R1652:Dnah7b
|
UTSW |
1 |
46,214,550 (GRCm39) |
nonsense |
probably null |
|
R1681:Dnah7b
|
UTSW |
1 |
46,363,872 (GRCm39) |
nonsense |
probably null |
|
R1716:Dnah7b
|
UTSW |
1 |
46,230,943 (GRCm39) |
missense |
probably damaging |
1.00 |
R1753:Dnah7b
|
UTSW |
1 |
46,361,495 (GRCm39) |
missense |
probably damaging |
0.99 |
R1834:Dnah7b
|
UTSW |
1 |
46,272,919 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1838:Dnah7b
|
UTSW |
1 |
46,316,265 (GRCm39) |
missense |
probably damaging |
1.00 |
R1838:Dnah7b
|
UTSW |
1 |
46,155,337 (GRCm39) |
missense |
probably benign |
0.04 |
R1898:Dnah7b
|
UTSW |
1 |
46,275,874 (GRCm39) |
missense |
probably benign |
0.02 |
R1962:Dnah7b
|
UTSW |
1 |
46,281,263 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2001:Dnah7b
|
UTSW |
1 |
46,181,247 (GRCm39) |
missense |
possibly damaging |
0.69 |
R2049:Dnah7b
|
UTSW |
1 |
46,307,830 (GRCm39) |
missense |
probably damaging |
1.00 |
R2076:Dnah7b
|
UTSW |
1 |
46,281,481 (GRCm39) |
nonsense |
probably null |
|
R2083:Dnah7b
|
UTSW |
1 |
46,280,227 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2140:Dnah7b
|
UTSW |
1 |
46,307,830 (GRCm39) |
missense |
probably damaging |
1.00 |
R2142:Dnah7b
|
UTSW |
1 |
46,307,830 (GRCm39) |
missense |
probably damaging |
1.00 |
R2165:Dnah7b
|
UTSW |
1 |
46,137,152 (GRCm39) |
splice site |
probably benign |
|
R2172:Dnah7b
|
UTSW |
1 |
46,163,672 (GRCm39) |
missense |
probably benign |
0.12 |
R2239:Dnah7b
|
UTSW |
1 |
46,240,344 (GRCm39) |
splice site |
probably benign |
|
R2247:Dnah7b
|
UTSW |
1 |
46,316,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R2267:Dnah7b
|
UTSW |
1 |
46,273,075 (GRCm39) |
missense |
probably damaging |
1.00 |
R2405:Dnah7b
|
UTSW |
1 |
46,402,114 (GRCm39) |
missense |
probably benign |
0.31 |
R2509:Dnah7b
|
UTSW |
1 |
46,234,447 (GRCm39) |
missense |
probably damaging |
0.96 |
R2895:Dnah7b
|
UTSW |
1 |
46,178,901 (GRCm39) |
missense |
probably damaging |
1.00 |
R2965:Dnah7b
|
UTSW |
1 |
46,246,732 (GRCm39) |
missense |
probably damaging |
1.00 |
R3013:Dnah7b
|
UTSW |
1 |
46,227,847 (GRCm39) |
critical splice donor site |
probably null |
|
R3022:Dnah7b
|
UTSW |
1 |
46,221,583 (GRCm39) |
missense |
probably damaging |
0.99 |
R3056:Dnah7b
|
UTSW |
1 |
46,307,869 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3107:Dnah7b
|
UTSW |
1 |
46,392,033 (GRCm39) |
missense |
probably benign |
0.00 |
R3735:Dnah7b
|
UTSW |
1 |
46,339,035 (GRCm39) |
missense |
probably benign |
0.05 |
R3898:Dnah7b
|
UTSW |
1 |
46,282,417 (GRCm39) |
missense |
probably damaging |
1.00 |
R3944:Dnah7b
|
UTSW |
1 |
46,176,645 (GRCm39) |
missense |
probably damaging |
1.00 |
R3983:Dnah7b
|
UTSW |
1 |
46,272,871 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4041:Dnah7b
|
UTSW |
1 |
46,120,655 (GRCm39) |
missense |
probably benign |
|
R4172:Dnah7b
|
UTSW |
1 |
46,266,106 (GRCm39) |
missense |
probably damaging |
1.00 |
R4210:Dnah7b
|
UTSW |
1 |
46,176,578 (GRCm39) |
missense |
possibly damaging |
0.63 |
R4306:Dnah7b
|
UTSW |
1 |
46,260,932 (GRCm39) |
missense |
probably damaging |
0.99 |
R4391:Dnah7b
|
UTSW |
1 |
46,376,754 (GRCm39) |
splice site |
probably null |
|
R4414:Dnah7b
|
UTSW |
1 |
46,165,840 (GRCm39) |
missense |
probably benign |
0.00 |
R4495:Dnah7b
|
UTSW |
1 |
46,124,792 (GRCm39) |
missense |
probably benign |
0.00 |
R4660:Dnah7b
|
UTSW |
1 |
46,328,696 (GRCm39) |
missense |
probably damaging |
1.00 |
R4670:Dnah7b
|
UTSW |
1 |
46,117,684 (GRCm39) |
missense |
probably damaging |
1.00 |
R4675:Dnah7b
|
UTSW |
1 |
46,256,317 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4685:Dnah7b
|
UTSW |
1 |
46,250,488 (GRCm39) |
missense |
probably damaging |
1.00 |
R4727:Dnah7b
|
UTSW |
1 |
46,246,816 (GRCm39) |
missense |
probably damaging |
1.00 |
R4735:Dnah7b
|
UTSW |
1 |
46,106,115 (GRCm39) |
missense |
unknown |
|
R4780:Dnah7b
|
UTSW |
1 |
46,392,174 (GRCm39) |
missense |
probably benign |
|
R4828:Dnah7b
|
UTSW |
1 |
46,167,272 (GRCm39) |
missense |
possibly damaging |
0.59 |
R4859:Dnah7b
|
UTSW |
1 |
46,395,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R4865:Dnah7b
|
UTSW |
1 |
46,234,234 (GRCm39) |
missense |
probably damaging |
1.00 |
R4871:Dnah7b
|
UTSW |
1 |
46,120,604 (GRCm39) |
missense |
probably benign |
0.21 |
R4881:Dnah7b
|
UTSW |
1 |
46,240,478 (GRCm39) |
missense |
probably damaging |
1.00 |
R4902:Dnah7b
|
UTSW |
1 |
46,329,935 (GRCm39) |
missense |
probably benign |
0.04 |
R4960:Dnah7b
|
UTSW |
1 |
46,272,886 (GRCm39) |
missense |
probably benign |
|
R5000:Dnah7b
|
UTSW |
1 |
46,138,663 (GRCm39) |
nonsense |
probably null |
|
R5005:Dnah7b
|
UTSW |
1 |
46,281,188 (GRCm39) |
missense |
probably damaging |
0.99 |
R5026:Dnah7b
|
UTSW |
1 |
46,226,523 (GRCm39) |
missense |
probably damaging |
0.99 |
R5080:Dnah7b
|
UTSW |
1 |
46,221,540 (GRCm39) |
nonsense |
probably null |
|
R5174:Dnah7b
|
UTSW |
1 |
46,282,509 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5178:Dnah7b
|
UTSW |
1 |
46,397,376 (GRCm39) |
missense |
possibly damaging |
0.50 |
R5244:Dnah7b
|
UTSW |
1 |
46,273,018 (GRCm39) |
missense |
probably damaging |
1.00 |
R5250:Dnah7b
|
UTSW |
1 |
46,412,514 (GRCm39) |
missense |
probably damaging |
1.00 |
R5350:Dnah7b
|
UTSW |
1 |
46,272,849 (GRCm39) |
missense |
probably benign |
0.16 |
R5380:Dnah7b
|
UTSW |
1 |
46,256,351 (GRCm39) |
missense |
probably benign |
0.18 |
R5387:Dnah7b
|
UTSW |
1 |
46,227,819 (GRCm39) |
missense |
probably damaging |
1.00 |
R5423:Dnah7b
|
UTSW |
1 |
46,397,431 (GRCm39) |
missense |
probably benign |
0.01 |
R5426:Dnah7b
|
UTSW |
1 |
46,281,366 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5451:Dnah7b
|
UTSW |
1 |
46,281,179 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5459:Dnah7b
|
UTSW |
1 |
46,148,472 (GRCm39) |
missense |
probably null |
|
R5479:Dnah7b
|
UTSW |
1 |
46,262,265 (GRCm39) |
missense |
probably damaging |
1.00 |
R5583:Dnah7b
|
UTSW |
1 |
46,281,359 (GRCm39) |
missense |
probably benign |
0.06 |
R5637:Dnah7b
|
UTSW |
1 |
46,395,674 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5641:Dnah7b
|
UTSW |
1 |
46,307,924 (GRCm39) |
splice site |
probably null |
|
R5659:Dnah7b
|
UTSW |
1 |
46,392,009 (GRCm39) |
missense |
probably damaging |
1.00 |
R5739:Dnah7b
|
UTSW |
1 |
46,273,152 (GRCm39) |
missense |
probably damaging |
1.00 |
R5759:Dnah7b
|
UTSW |
1 |
46,316,280 (GRCm39) |
missense |
probably damaging |
1.00 |
R5821:Dnah7b
|
UTSW |
1 |
46,181,292 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5874:Dnah7b
|
UTSW |
1 |
46,230,885 (GRCm39) |
missense |
probably damaging |
1.00 |
R5892:Dnah7b
|
UTSW |
1 |
46,376,753 (GRCm39) |
critical splice donor site |
probably null |
|
R5918:Dnah7b
|
UTSW |
1 |
46,260,803 (GRCm39) |
missense |
probably benign |
|
R5941:Dnah7b
|
UTSW |
1 |
46,226,450 (GRCm39) |
missense |
probably damaging |
1.00 |
R5965:Dnah7b
|
UTSW |
1 |
46,402,147 (GRCm39) |
missense |
probably damaging |
1.00 |
R5987:Dnah7b
|
UTSW |
1 |
46,158,558 (GRCm39) |
splice site |
probably null |
|
R6041:Dnah7b
|
UTSW |
1 |
46,328,805 (GRCm39) |
missense |
probably benign |
0.04 |
R6043:Dnah7b
|
UTSW |
1 |
46,178,949 (GRCm39) |
missense |
probably benign |
|
R6049:Dnah7b
|
UTSW |
1 |
46,124,762 (GRCm39) |
missense |
probably benign |
|
R6131:Dnah7b
|
UTSW |
1 |
46,292,626 (GRCm39) |
missense |
probably damaging |
1.00 |
R6168:Dnah7b
|
UTSW |
1 |
46,329,863 (GRCm39) |
missense |
probably damaging |
1.00 |
R6195:Dnah7b
|
UTSW |
1 |
46,243,429 (GRCm39) |
missense |
probably damaging |
1.00 |
R6219:Dnah7b
|
UTSW |
1 |
46,272,745 (GRCm39) |
missense |
probably benign |
0.03 |
R6226:Dnah7b
|
UTSW |
1 |
46,165,828 (GRCm39) |
missense |
probably benign |
0.01 |
R6233:Dnah7b
|
UTSW |
1 |
46,243,429 (GRCm39) |
missense |
probably damaging |
1.00 |
R6247:Dnah7b
|
UTSW |
1 |
46,265,048 (GRCm39) |
missense |
probably benign |
|
R6273:Dnah7b
|
UTSW |
1 |
46,281,476 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6279:Dnah7b
|
UTSW |
1 |
46,365,046 (GRCm39) |
missense |
probably damaging |
1.00 |
R6300:Dnah7b
|
UTSW |
1 |
46,365,046 (GRCm39) |
missense |
probably damaging |
1.00 |
R6330:Dnah7b
|
UTSW |
1 |
46,379,335 (GRCm39) |
missense |
probably damaging |
1.00 |
R6476:Dnah7b
|
UTSW |
1 |
46,281,364 (GRCm39) |
nonsense |
probably null |
|
R6494:Dnah7b
|
UTSW |
1 |
46,138,591 (GRCm39) |
missense |
probably damaging |
1.00 |
R6762:Dnah7b
|
UTSW |
1 |
46,263,902 (GRCm39) |
missense |
probably benign |
0.12 |
R6800:Dnah7b
|
UTSW |
1 |
46,379,377 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6838:Dnah7b
|
UTSW |
1 |
46,230,948 (GRCm39) |
missense |
probably damaging |
1.00 |
R6937:Dnah7b
|
UTSW |
1 |
46,234,280 (GRCm39) |
missense |
probably damaging |
1.00 |
R6940:Dnah7b
|
UTSW |
1 |
46,158,428 (GRCm39) |
missense |
probably benign |
0.12 |
R6969:Dnah7b
|
UTSW |
1 |
46,397,398 (GRCm39) |
missense |
probably damaging |
1.00 |
R6993:Dnah7b
|
UTSW |
1 |
46,234,299 (GRCm39) |
critical splice donor site |
probably null |
|
R7040:Dnah7b
|
UTSW |
1 |
46,275,969 (GRCm39) |
missense |
probably benign |
0.01 |
R7117:Dnah7b
|
UTSW |
1 |
46,391,973 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7135:Dnah7b
|
UTSW |
1 |
46,178,870 (GRCm39) |
missense |
probably damaging |
0.99 |
R7153:Dnah7b
|
UTSW |
1 |
46,165,964 (GRCm39) |
missense |
probably benign |
0.05 |
R7189:Dnah7b
|
UTSW |
1 |
46,281,302 (GRCm39) |
missense |
probably damaging |
1.00 |
R7237:Dnah7b
|
UTSW |
1 |
46,179,126 (GRCm39) |
missense |
probably damaging |
0.98 |
R7243:Dnah7b
|
UTSW |
1 |
46,122,914 (GRCm39) |
missense |
probably benign |
|
R7244:Dnah7b
|
UTSW |
1 |
46,316,303 (GRCm39) |
missense |
probably damaging |
0.99 |
R7248:Dnah7b
|
UTSW |
1 |
46,181,245 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7318:Dnah7b
|
UTSW |
1 |
46,234,532 (GRCm39) |
missense |
probably damaging |
1.00 |
R7375:Dnah7b
|
UTSW |
1 |
46,342,794 (GRCm39) |
missense |
probably damaging |
1.00 |
R7483:Dnah7b
|
UTSW |
1 |
46,214,579 (GRCm39) |
missense |
probably damaging |
1.00 |
R7486:Dnah7b
|
UTSW |
1 |
46,329,894 (GRCm39) |
missense |
probably damaging |
1.00 |
R7498:Dnah7b
|
UTSW |
1 |
46,364,925 (GRCm39) |
missense |
probably damaging |
1.00 |
R7501:Dnah7b
|
UTSW |
1 |
46,395,714 (GRCm39) |
missense |
probably damaging |
1.00 |
R7513:Dnah7b
|
UTSW |
1 |
46,163,506 (GRCm39) |
missense |
probably benign |
0.06 |
R7547:Dnah7b
|
UTSW |
1 |
46,253,573 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7620:Dnah7b
|
UTSW |
1 |
46,307,794 (GRCm39) |
missense |
probably damaging |
1.00 |
R7670:Dnah7b
|
UTSW |
1 |
46,148,462 (GRCm39) |
missense |
probably benign |
|
R7676:Dnah7b
|
UTSW |
1 |
46,273,324 (GRCm39) |
nonsense |
probably null |
|
R7731:Dnah7b
|
UTSW |
1 |
46,178,905 (GRCm39) |
missense |
probably benign |
0.00 |
R7760:Dnah7b
|
UTSW |
1 |
46,240,413 (GRCm39) |
missense |
probably damaging |
1.00 |
R7768:Dnah7b
|
UTSW |
1 |
46,176,634 (GRCm39) |
missense |
probably benign |
|
R7807:Dnah7b
|
UTSW |
1 |
46,253,527 (GRCm39) |
missense |
probably benign |
|
R7895:Dnah7b
|
UTSW |
1 |
46,289,110 (GRCm39) |
missense |
probably damaging |
1.00 |
R7911:Dnah7b
|
UTSW |
1 |
46,178,838 (GRCm39) |
missense |
probably damaging |
1.00 |
R7924:Dnah7b
|
UTSW |
1 |
46,258,590 (GRCm39) |
missense |
probably benign |
0.04 |
R7944:Dnah7b
|
UTSW |
1 |
46,266,163 (GRCm39) |
missense |
probably benign |
|
R7946:Dnah7b
|
UTSW |
1 |
46,272,739 (GRCm39) |
missense |
probably damaging |
1.00 |
R7983:Dnah7b
|
UTSW |
1 |
46,282,584 (GRCm39) |
missense |
probably damaging |
1.00 |
R8012:Dnah7b
|
UTSW |
1 |
46,282,525 (GRCm39) |
missense |
probably damaging |
1.00 |
R8069:Dnah7b
|
UTSW |
1 |
46,263,866 (GRCm39) |
nonsense |
probably null |
|
R8094:Dnah7b
|
UTSW |
1 |
46,165,964 (GRCm39) |
missense |
probably benign |
0.01 |
R8137:Dnah7b
|
UTSW |
1 |
46,272,913 (GRCm39) |
missense |
probably damaging |
1.00 |
R8167:Dnah7b
|
UTSW |
1 |
46,292,671 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8268:Dnah7b
|
UTSW |
1 |
46,395,736 (GRCm39) |
missense |
probably benign |
0.43 |
R8309:Dnah7b
|
UTSW |
1 |
46,179,032 (GRCm39) |
missense |
probably damaging |
1.00 |
R8313:Dnah7b
|
UTSW |
1 |
46,214,456 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8410:Dnah7b
|
UTSW |
1 |
46,395,819 (GRCm39) |
critical splice donor site |
probably null |
|
R8438:Dnah7b
|
UTSW |
1 |
46,227,839 (GRCm39) |
missense |
probably damaging |
1.00 |
R8446:Dnah7b
|
UTSW |
1 |
46,329,875 (GRCm39) |
missense |
probably damaging |
1.00 |
R8471:Dnah7b
|
UTSW |
1 |
46,138,650 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8551:Dnah7b
|
UTSW |
1 |
46,155,360 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8711:Dnah7b
|
UTSW |
1 |
46,214,598 (GRCm39) |
missense |
probably damaging |
1.00 |
R8745:Dnah7b
|
UTSW |
1 |
46,221,624 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8765:Dnah7b
|
UTSW |
1 |
46,392,159 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8797:Dnah7b
|
UTSW |
1 |
46,162,806 (GRCm39) |
missense |
probably damaging |
1.00 |
R8805:Dnah7b
|
UTSW |
1 |
46,273,305 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8830:Dnah7b
|
UTSW |
1 |
46,230,953 (GRCm39) |
missense |
probably damaging |
1.00 |
R8861:Dnah7b
|
UTSW |
1 |
46,280,236 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8905:Dnah7b
|
UTSW |
1 |
46,292,534 (GRCm39) |
missense |
probably damaging |
0.99 |
R9009:Dnah7b
|
UTSW |
1 |
46,262,232 (GRCm39) |
missense |
probably benign |
0.00 |
R9058:Dnah7b
|
UTSW |
1 |
46,282,575 (GRCm39) |
missense |
probably damaging |
1.00 |
R9130:Dnah7b
|
UTSW |
1 |
46,173,674 (GRCm39) |
missense |
probably benign |
0.01 |
R9131:Dnah7b
|
UTSW |
1 |
46,266,180 (GRCm39) |
missense |
probably damaging |
1.00 |
R9181:Dnah7b
|
UTSW |
1 |
46,181,194 (GRCm39) |
missense |
probably damaging |
1.00 |
R9182:Dnah7b
|
UTSW |
1 |
46,330,038 (GRCm39) |
missense |
probably benign |
0.06 |
R9223:Dnah7b
|
UTSW |
1 |
46,361,420 (GRCm39) |
missense |
probably benign |
0.12 |
R9391:Dnah7b
|
UTSW |
1 |
46,272,914 (GRCm39) |
nonsense |
probably null |
|
R9392:Dnah7b
|
UTSW |
1 |
46,162,898 (GRCm39) |
nonsense |
probably null |
|
R9456:Dnah7b
|
UTSW |
1 |
46,165,953 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9498:Dnah7b
|
UTSW |
1 |
46,253,564 (GRCm39) |
missense |
probably benign |
0.27 |
R9553:Dnah7b
|
UTSW |
1 |
46,264,956 (GRCm39) |
missense |
probably damaging |
0.99 |
R9598:Dnah7b
|
UTSW |
1 |
46,292,621 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9653:Dnah7b
|
UTSW |
1 |
46,252,544 (GRCm39) |
missense |
possibly damaging |
0.55 |
R9781:Dnah7b
|
UTSW |
1 |
46,376,754 (GRCm39) |
splice site |
probably null |
|
RF020:Dnah7b
|
UTSW |
1 |
46,412,421 (GRCm39) |
missense |
possibly damaging |
0.84 |
V8831:Dnah7b
|
UTSW |
1 |
46,412,458 (GRCm39) |
nonsense |
probably null |
|
X0023:Dnah7b
|
UTSW |
1 |
46,342,737 (GRCm39) |
missense |
probably benign |
0.04 |
|