Other mutations in this stock |
Total: 113 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aars1 |
A |
T |
8: 111,042,706 (GRCm38) |
D287V |
probably damaging |
Het |
Abca12 |
A |
G |
1: 71,295,029 (GRCm38) |
C1105R |
probably benign |
Het |
Abca8b |
T |
A |
11: 109,942,341 (GRCm38) |
N1178Y |
probably damaging |
Het |
Abhd12 |
A |
G |
2: 150,843,398 (GRCm38) |
L189P |
probably damaging |
Het |
Acap2 |
G |
T |
16: 31,110,934 (GRCm38) |
N435K |
probably damaging |
Het |
Adam6b |
G |
T |
12: 113,489,925 (GRCm38) |
G121C |
probably damaging |
Het |
Adgrb1 |
C |
A |
15: 74,580,586 (GRCm38) |
C200* |
probably null |
Het |
Agbl5 |
T |
C |
5: 30,903,064 (GRCm38) |
S730P |
possibly damaging |
Het |
Ahsg |
G |
A |
16: 22,892,328 (GRCm38) |
|
probably benign |
Het |
Aldh9a1 |
A |
T |
1: 167,361,854 (GRCm38) |
K390N |
probably benign |
Het |
Alpk2 |
T |
A |
18: 65,294,094 (GRCm38) |
H1857L |
possibly damaging |
Het |
Apip |
T |
A |
2: 103,088,662 (GRCm38) |
N102K |
probably benign |
Het |
Asxl2 |
T |
C |
12: 3,457,125 (GRCm38) |
S106P |
probably damaging |
Het |
Atp2b2 |
G |
T |
6: 113,773,368 (GRCm38) |
R677S |
probably damaging |
Het |
Barhl1 |
A |
C |
2: 28,909,845 (GRCm38) |
M256R |
probably damaging |
Het |
Cacnb2 |
A |
T |
2: 14,985,964 (GRCm38) |
Q619L |
possibly damaging |
Het |
Ccdc137 |
C |
T |
11: 120,458,212 (GRCm38) |
P23L |
probably benign |
Het |
Cdh11 |
A |
T |
8: 102,634,641 (GRCm38) |
N688K |
possibly damaging |
Het |
Cdh18 |
C |
T |
15: 23,173,852 (GRCm38) |
P51S |
probably damaging |
Het |
Cdin1 |
G |
T |
2: 115,642,692 (GRCm38) |
R101L |
possibly damaging |
Het |
Cfhr1 |
A |
T |
1: 139,553,600 (GRCm38) |
Y181N |
probably damaging |
Het |
Chmp3 |
A |
G |
6: 71,560,939 (GRCm38) |
D50G |
probably benign |
Het |
Crem |
T |
C |
18: 3,295,037 (GRCm38) |
|
probably null |
Het |
Cyb561a3 |
G |
A |
19: 10,582,393 (GRCm38) |
W27* |
probably null |
Het |
Cyp2d12 |
C |
A |
15: 82,558,056 (GRCm38) |
N297K |
possibly damaging |
Het |
Dclk2 |
C |
T |
3: 86,805,639 (GRCm38) |
R503Q |
possibly damaging |
Het |
Dsp |
T |
G |
13: 38,193,195 (GRCm38) |
L1652R |
probably damaging |
Het |
Dstyk |
G |
A |
1: 132,449,595 (GRCm38) |
S66N |
probably benign |
Het |
Ehhadh |
T |
C |
16: 21,762,178 (GRCm38) |
E688G |
probably damaging |
Het |
Emsy |
G |
T |
7: 98,602,730 (GRCm38) |
H688N |
possibly damaging |
Het |
Emsy |
T |
A |
7: 98,602,729 (GRCm38) |
H688L |
possibly damaging |
Het |
Endod1 |
A |
G |
9: 14,356,926 (GRCm38) |
L421P |
probably damaging |
Het |
Fam222b |
C |
T |
11: 78,155,035 (GRCm38) |
P346L |
probably damaging |
Het |
Fam3c |
G |
A |
6: 22,309,437 (GRCm38) |
R182W |
probably damaging |
Het |
Gck |
T |
C |
11: 5,910,984 (GRCm38) |
D29G |
probably damaging |
Het |
Gm10320 |
C |
A |
13: 98,489,699 (GRCm38) |
R59L |
probably damaging |
Het |
Gm11127 |
G |
T |
17: 36,058,004 (GRCm38) |
F61L |
probably damaging |
Het |
Gm21798 |
C |
T |
15: 64,817,826 (GRCm38) |
|
probably benign |
Het |
Gm9376 |
A |
G |
14: 118,267,545 (GRCm38) |
T130A |
possibly damaging |
Het |
Gpr153 |
T |
A |
4: 152,282,392 (GRCm38) |
I334N |
possibly damaging |
Het |
Greb1l |
T |
C |
18: 10,509,314 (GRCm38) |
L542P |
probably damaging |
Het |
Hacl1 |
T |
C |
14: 31,640,534 (GRCm38) |
E52G |
probably benign |
Het |
Ice2 |
A |
G |
9: 69,407,353 (GRCm38) |
Y128C |
probably damaging |
Het |
Ikzf2 |
T |
A |
1: 69,542,287 (GRCm38) |
I121L |
probably benign |
Het |
Ipcef1 |
C |
T |
10: 6,919,900 (GRCm38) |
A167T |
probably benign |
Het |
Jakmip2 |
T |
A |
18: 43,582,080 (GRCm38) |
D127V |
possibly damaging |
Het |
Jph4 |
T |
C |
14: 55,114,911 (GRCm38) |
T122A |
probably damaging |
Het |
Kcns2 |
A |
G |
15: 34,838,803 (GRCm38) |
E104G |
probably damaging |
Het |
Lars2 |
A |
C |
9: 123,431,917 (GRCm38) |
R384S |
probably benign |
Het |
Lsmem1 |
G |
T |
12: 40,185,409 (GRCm38) |
H3N |
possibly damaging |
Het |
Lsmem1 |
T |
A |
12: 40,185,408 (GRCm38) |
H3L |
possibly damaging |
Het |
Ly6g2 |
T |
G |
15: 75,216,756 (GRCm38) |
|
probably null |
Het |
Mfhas1 |
C |
G |
8: 35,590,248 (GRCm38) |
R626G |
probably benign |
Het |
Mfhas1 |
A |
C |
8: 35,590,068 (GRCm38) |
S566R |
probably benign |
Het |
Mgam |
A |
G |
6: 40,666,892 (GRCm38) |
T585A |
probably damaging |
Het |
Mmp25 |
T |
C |
17: 23,640,023 (GRCm38) |
K185E |
probably benign |
Het |
Mtch1 |
T |
C |
17: 29,338,776 (GRCm38) |
I243V |
probably damaging |
Het |
Mtcp1 |
A |
T |
X: 75,411,665 (GRCm38) |
Y25* |
probably null |
Het |
Mybl2 |
A |
G |
2: 163,059,583 (GRCm38) |
T35A |
probably benign |
Het |
Myh11 |
T |
C |
16: 14,223,880 (GRCm38) |
E736G |
probably damaging |
Het |
Myh2 |
T |
C |
11: 67,176,559 (GRCm38) |
I224T |
probably damaging |
Het |
Mymx |
T |
C |
17: 45,601,833 (GRCm38) |
|
probably benign |
Het |
Nek10 |
A |
G |
14: 14,863,454 (GRCm38) |
|
probably null |
Het |
Nsd1 |
A |
T |
13: 55,246,369 (GRCm38) |
K697N |
probably damaging |
Het |
Nynrin |
A |
G |
14: 55,872,947 (GRCm38) |
D1837G |
possibly damaging |
Het |
Or14j4 |
G |
A |
17: 37,610,277 (GRCm38) |
T158I |
probably benign |
Het |
Or2ag2b |
A |
G |
7: 106,819,007 (GRCm38) |
H308R |
probably benign |
Het |
Or52s1 |
A |
T |
7: 103,211,886 (GRCm38) |
T9S |
probably benign |
Het |
Or5p81 |
T |
A |
7: 108,667,644 (GRCm38) |
I76N |
probably benign |
Het |
Or6k4 |
T |
A |
1: 174,137,194 (GRCm38) |
I150N |
probably benign |
Het |
Pgap6 |
T |
C |
17: 26,122,220 (GRCm38) |
Y766H |
probably damaging |
Het |
Phf19 |
T |
C |
2: 34,911,769 (GRCm38) |
T10A |
probably benign |
Het |
Pkd1 |
A |
T |
17: 24,565,584 (GRCm38) |
H368L |
probably benign |
Het |
Plscr2 |
A |
G |
9: 92,290,755 (GRCm38) |
R156G |
probably damaging |
Het |
Ppp1r42 |
G |
A |
1: 10,000,086 (GRCm38) |
R61C |
probably benign |
Het |
Pptc7 |
T |
G |
5: 122,313,616 (GRCm38) |
V45G |
probably damaging |
Het |
Prlhr |
G |
A |
19: 60,467,429 (GRCm38) |
T233I |
probably damaging |
Het |
Prr23a4 |
T |
A |
9: 98,903,393 (GRCm38) |
I37N |
possibly damaging |
Het |
Reps1 |
C |
T |
10: 18,107,714 (GRCm38) |
T435I |
probably damaging |
Het |
Ret |
T |
A |
6: 118,153,951 (GRCm38) |
T1084S |
probably damaging |
Het |
Rgl2 |
T |
A |
17: 33,933,621 (GRCm38) |
M402K |
probably benign |
Het |
Rp2 |
A |
G |
X: 20,376,915 (GRCm38) |
K43R |
probably benign |
Het |
Rundc3b |
A |
T |
5: 8,579,117 (GRCm38) |
W95R |
probably damaging |
Het |
Samd9l |
T |
C |
6: 3,375,107 (GRCm38) |
D718G |
possibly damaging |
Het |
Scnn1b |
G |
A |
7: 121,902,845 (GRCm38) |
R242H |
probably benign |
Het |
Smad4 |
G |
T |
18: 73,641,894 (GRCm38) |
Q445K |
probably benign |
Het |
Smchd1 |
G |
T |
17: 71,370,337 (GRCm38) |
P1486T |
probably damaging |
Het |
Snx25 |
G |
T |
8: 46,035,632 (GRCm38) |
N895K |
possibly damaging |
Het |
Sox2 |
A |
G |
3: 34,650,741 (GRCm38) |
D109G |
probably damaging |
Het |
Stfa2 |
A |
T |
16: 36,405,202 (GRCm38) |
N38K |
probably damaging |
Het |
Stfa2 |
C |
A |
16: 36,405,211 (GRCm38) |
E35D |
possibly damaging |
Het |
Stfa3 |
A |
G |
16: 36,450,661 (GRCm38) |
L87P |
probably damaging |
Het |
Strbp |
T |
C |
2: 37,640,909 (GRCm38) |
D111G |
possibly damaging |
Het |
Supt20 |
C |
A |
3: 54,727,658 (GRCm38) |
|
probably benign |
Het |
Svep1 |
A |
G |
4: 58,096,310 (GRCm38) |
Y1437H |
possibly damaging |
Het |
Tbx4 |
T |
A |
11: 85,911,920 (GRCm38) |
|
probably null |
Het |
Tmem117 |
A |
T |
15: 95,094,551 (GRCm38) |
N364I |
probably damaging |
Het |
Trat1 |
T |
C |
16: 48,761,379 (GRCm38) |
E45G |
probably damaging |
Het |
Trpc2 |
G |
A |
7: 102,084,119 (GRCm38) |
D92N |
probably damaging |
Het |
Trpm1 |
G |
A |
7: 64,226,782 (GRCm38) |
D528N |
probably damaging |
Het |
Ttll9 |
A |
G |
2: 153,000,236 (GRCm38) |
S337G |
possibly damaging |
Het |
Utrn |
A |
T |
10: 12,475,274 (GRCm38) |
I355N |
probably damaging |
Het |
Vangl1 |
A |
G |
3: 102,163,466 (GRCm38) |
S385P |
probably benign |
Het |
Vmn1r209 |
A |
G |
13: 22,806,239 (GRCm38) |
S94P |
possibly damaging |
Het |
Vmn2r28 |
T |
A |
7: 5,493,811 (GRCm38) |
Q14L |
probably benign |
Het |
Vps45 |
A |
G |
3: 96,047,245 (GRCm38) |
|
probably null |
Het |
Wdr48 |
T |
C |
9: 119,904,330 (GRCm38) |
V81A |
probably benign |
Het |
Xpnpep2 |
A |
G |
X: 48,125,353 (GRCm38) |
N476S |
probably benign |
Het |
Zbtb41 |
A |
T |
1: 139,446,922 (GRCm38) |
K707* |
probably null |
Het |
Zfp442 |
A |
C |
2: 150,409,063 (GRCm38) |
C306W |
probably damaging |
Het |
Zfp811 |
T |
C |
17: 32,798,142 (GRCm38) |
N307S |
possibly damaging |
Het |
Zfp976 |
A |
G |
7: 42,616,311 (GRCm38) |
W17R |
probably damaging |
Het |
Zyg11b |
T |
C |
4: 108,266,093 (GRCm38) |
T226A |
possibly damaging |
Het |
|
Other mutations in Dnah12 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01412:Dnah12
|
APN |
14 |
26,771,005 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01602:Dnah12
|
APN |
14 |
26,710,275 (GRCm38) |
splice site |
probably benign |
|
IGL01681:Dnah12
|
APN |
14 |
26,722,160 (GRCm38) |
missense |
probably benign |
|
IGL02082:Dnah12
|
APN |
14 |
26,707,162 (GRCm38) |
missense |
possibly damaging |
0.79 |
IGL02140:Dnah12
|
APN |
14 |
26,716,577 (GRCm38) |
missense |
probably benign |
0.20 |
IGL02170:Dnah12
|
APN |
14 |
26,773,112 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL02174:Dnah12
|
APN |
14 |
26,706,917 (GRCm38) |
missense |
probably benign |
0.00 |
IGL02367:Dnah12
|
APN |
14 |
26,709,161 (GRCm38) |
missense |
probably benign |
0.30 |
IGL02418:Dnah12
|
APN |
14 |
26,773,722 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03039:Dnah12
|
APN |
14 |
26,724,512 (GRCm38) |
missense |
probably benign |
0.02 |
IGL03066:Dnah12
|
APN |
14 |
26,697,398 (GRCm38) |
missense |
probably benign |
0.06 |
drippings
|
UTSW |
14 |
26,854,804 (GRCm38) |
missense |
probably damaging |
1.00 |
grueben
|
UTSW |
14 |
26,878,079 (GRCm38) |
missense |
probably damaging |
1.00 |
BB010:Dnah12
|
UTSW |
14 |
26,766,115 (GRCm38) |
missense |
probably benign |
0.00 |
BB020:Dnah12
|
UTSW |
14 |
26,766,115 (GRCm38) |
missense |
probably benign |
0.00 |
F5770:Dnah12
|
UTSW |
14 |
26,773,093 (GRCm38) |
missense |
possibly damaging |
0.95 |
FR4304:Dnah12
|
UTSW |
14 |
26,849,385 (GRCm38) |
missense |
probably damaging |
1.00 |
FR4340:Dnah12
|
UTSW |
14 |
26,849,385 (GRCm38) |
missense |
probably damaging |
1.00 |
FR4342:Dnah12
|
UTSW |
14 |
26,849,385 (GRCm38) |
missense |
probably damaging |
1.00 |
FR4589:Dnah12
|
UTSW |
14 |
26,849,385 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03055:Dnah12
|
UTSW |
14 |
26,872,740 (GRCm38) |
missense |
probably damaging |
1.00 |
LCD18:Dnah12
|
UTSW |
14 |
26,849,385 (GRCm38) |
missense |
probably damaging |
1.00 |
R0003:Dnah12
|
UTSW |
14 |
26,772,644 (GRCm38) |
missense |
probably damaging |
1.00 |
R0110:Dnah12
|
UTSW |
14 |
26,798,899 (GRCm38) |
missense |
probably damaging |
1.00 |
R0302:Dnah12
|
UTSW |
14 |
26,799,999 (GRCm38) |
missense |
probably damaging |
1.00 |
R0355:Dnah12
|
UTSW |
14 |
26,706,117 (GRCm38) |
splice site |
probably null |
|
R0364:Dnah12
|
UTSW |
14 |
26,724,473 (GRCm38) |
missense |
probably benign |
0.10 |
R0469:Dnah12
|
UTSW |
14 |
26,798,899 (GRCm38) |
missense |
probably damaging |
1.00 |
R0558:Dnah12
|
UTSW |
14 |
26,709,310 (GRCm38) |
missense |
probably benign |
0.00 |
R0709:Dnah12
|
UTSW |
14 |
26,884,265 (GRCm38) |
splice site |
probably benign |
|
R0734:Dnah12
|
UTSW |
14 |
26,800,013 (GRCm38) |
missense |
probably benign |
0.00 |
R1273:Dnah12
|
UTSW |
14 |
26,739,220 (GRCm38) |
nonsense |
probably null |
|
R1496:Dnah12
|
UTSW |
14 |
26,710,248 (GRCm38) |
missense |
probably benign |
|
R1503:Dnah12
|
UTSW |
14 |
26,773,692 (GRCm38) |
missense |
probably damaging |
1.00 |
R1535:Dnah12
|
UTSW |
14 |
26,816,322 (GRCm38) |
missense |
possibly damaging |
0.91 |
R1608:Dnah12
|
UTSW |
14 |
26,766,190 (GRCm38) |
missense |
probably damaging |
1.00 |
R1682:Dnah12
|
UTSW |
14 |
26,778,883 (GRCm38) |
missense |
possibly damaging |
0.71 |
R1758:Dnah12
|
UTSW |
14 |
26,766,114 (GRCm38) |
missense |
probably benign |
0.02 |
R1826:Dnah12
|
UTSW |
14 |
26,711,019 (GRCm38) |
missense |
probably benign |
0.01 |
R1829:Dnah12
|
UTSW |
14 |
26,773,023 (GRCm38) |
missense |
probably damaging |
1.00 |
R1862:Dnah12
|
UTSW |
14 |
26,709,257 (GRCm38) |
missense |
probably benign |
0.30 |
R1862:Dnah12
|
UTSW |
14 |
26,697,398 (GRCm38) |
missense |
probably benign |
0.06 |
R1913:Dnah12
|
UTSW |
14 |
26,792,264 (GRCm38) |
splice site |
probably null |
|
R1933:Dnah12
|
UTSW |
14 |
26,734,495 (GRCm38) |
missense |
probably damaging |
0.98 |
R2006:Dnah12
|
UTSW |
14 |
26,814,459 (GRCm38) |
missense |
possibly damaging |
0.95 |
R2045:Dnah12
|
UTSW |
14 |
26,781,528 (GRCm38) |
missense |
probably null |
1.00 |
R2113:Dnah12
|
UTSW |
14 |
26,766,141 (GRCm38) |
missense |
probably damaging |
1.00 |
R2125:Dnah12
|
UTSW |
14 |
26,724,458 (GRCm38) |
nonsense |
probably null |
|
R2126:Dnah12
|
UTSW |
14 |
26,724,458 (GRCm38) |
nonsense |
probably null |
|
R2207:Dnah12
|
UTSW |
14 |
26,781,787 (GRCm38) |
missense |
probably damaging |
0.99 |
R2213:Dnah12
|
UTSW |
14 |
26,739,330 (GRCm38) |
missense |
probably benign |
0.06 |
R2511:Dnah12
|
UTSW |
14 |
26,769,950 (GRCm38) |
missense |
possibly damaging |
0.65 |
R2875:Dnah12
|
UTSW |
14 |
26,876,950 (GRCm38) |
missense |
probably benign |
0.05 |
R2875:Dnah12
|
UTSW |
14 |
26,693,470 (GRCm38) |
missense |
probably benign |
0.04 |
R3551:Dnah12
|
UTSW |
14 |
26,770,972 (GRCm38) |
missense |
probably benign |
0.01 |
R3713:Dnah12
|
UTSW |
14 |
26,812,790 (GRCm38) |
missense |
probably benign |
|
R3729:Dnah12
|
UTSW |
14 |
26,706,065 (GRCm38) |
missense |
probably benign |
0.02 |
R3799:Dnah12
|
UTSW |
14 |
26,770,923 (GRCm38) |
missense |
probably damaging |
1.00 |
R3846:Dnah12
|
UTSW |
14 |
26,710,211 (GRCm38) |
missense |
probably benign |
0.00 |
R3892:Dnah12
|
UTSW |
14 |
26,856,616 (GRCm38) |
missense |
probably benign |
0.03 |
R3921:Dnah12
|
UTSW |
14 |
26,771,051 (GRCm38) |
missense |
probably damaging |
1.00 |
R3940:Dnah12
|
UTSW |
14 |
26,723,599 (GRCm38) |
missense |
probably benign |
|
R4065:Dnah12
|
UTSW |
14 |
26,770,448 (GRCm38) |
missense |
probably benign |
0.02 |
R4113:Dnah12
|
UTSW |
14 |
26,693,567 (GRCm38) |
missense |
probably damaging |
0.98 |
R4249:Dnah12
|
UTSW |
14 |
26,709,186 (GRCm38) |
missense |
possibly damaging |
0.70 |
R4259:Dnah12
|
UTSW |
14 |
26,798,926 (GRCm38) |
missense |
probably benign |
0.01 |
R4260:Dnah12
|
UTSW |
14 |
26,798,926 (GRCm38) |
missense |
probably benign |
0.01 |
R4348:Dnah12
|
UTSW |
14 |
26,814,541 (GRCm38) |
missense |
possibly damaging |
0.94 |
R4457:Dnah12
|
UTSW |
14 |
26,815,507 (GRCm38) |
missense |
probably damaging |
1.00 |
R4490:Dnah12
|
UTSW |
14 |
26,734,603 (GRCm38) |
missense |
possibly damaging |
0.67 |
R4491:Dnah12
|
UTSW |
14 |
26,734,603 (GRCm38) |
missense |
possibly damaging |
0.67 |
R4494:Dnah12
|
UTSW |
14 |
26,871,855 (GRCm38) |
missense |
probably damaging |
0.99 |
R4523:Dnah12
|
UTSW |
14 |
26,876,958 (GRCm38) |
missense |
possibly damaging |
0.83 |
R4523:Dnah12
|
UTSW |
14 |
26,770,022 (GRCm38) |
missense |
probably damaging |
0.97 |
R4546:Dnah12
|
UTSW |
14 |
26,773,014 (GRCm38) |
missense |
probably damaging |
1.00 |
R4584:Dnah12
|
UTSW |
14 |
26,772,594 (GRCm38) |
missense |
probably damaging |
1.00 |
R4624:Dnah12
|
UTSW |
14 |
26,735,758 (GRCm38) |
missense |
possibly damaging |
0.82 |
R4689:Dnah12
|
UTSW |
14 |
26,706,839 (GRCm38) |
missense |
probably benign |
0.00 |
R4727:Dnah12
|
UTSW |
14 |
26,872,317 (GRCm38) |
missense |
probably damaging |
1.00 |
R4732:Dnah12
|
UTSW |
14 |
26,781,784 (GRCm38) |
missense |
probably damaging |
1.00 |
R4733:Dnah12
|
UTSW |
14 |
26,781,784 (GRCm38) |
missense |
probably damaging |
1.00 |
R4851:Dnah12
|
UTSW |
14 |
26,716,629 (GRCm38) |
nonsense |
probably null |
|
R4879:Dnah12
|
UTSW |
14 |
26,718,046 (GRCm38) |
critical splice donor site |
probably null |
|
R4893:Dnah12
|
UTSW |
14 |
26,710,170 (GRCm38) |
missense |
possibly damaging |
0.66 |
R4915:Dnah12
|
UTSW |
14 |
26,734,570 (GRCm38) |
missense |
probably damaging |
1.00 |
R4927:Dnah12
|
UTSW |
14 |
26,861,805 (GRCm38) |
nonsense |
probably null |
|
R4939:Dnah12
|
UTSW |
14 |
26,891,524 (GRCm38) |
missense |
probably damaging |
1.00 |
R4962:Dnah12
|
UTSW |
14 |
26,716,700 (GRCm38) |
missense |
probably benign |
0.00 |
R5011:Dnah12
|
UTSW |
14 |
26,710,171 (GRCm38) |
missense |
probably benign |
0.03 |
R5013:Dnah12
|
UTSW |
14 |
26,710,171 (GRCm38) |
missense |
probably benign |
0.03 |
R5043:Dnah12
|
UTSW |
14 |
26,884,190 (GRCm38) |
missense |
probably damaging |
1.00 |
R5049:Dnah12
|
UTSW |
14 |
26,735,697 (GRCm38) |
missense |
probably benign |
0.09 |
R5122:Dnah12
|
UTSW |
14 |
26,718,000 (GRCm38) |
missense |
probably benign |
0.00 |
R5135:Dnah12
|
UTSW |
14 |
26,770,477 (GRCm38) |
missense |
probably damaging |
0.99 |
R5149:Dnah12
|
UTSW |
14 |
26,850,926 (GRCm38) |
nonsense |
probably null |
|
R5154:Dnah12
|
UTSW |
14 |
26,849,363 (GRCm38) |
missense |
probably benign |
0.12 |
R5206:Dnah12
|
UTSW |
14 |
26,769,985 (GRCm38) |
missense |
probably damaging |
1.00 |
R5307:Dnah12
|
UTSW |
14 |
26,693,486 (GRCm38) |
missense |
possibly damaging |
0.49 |
R5330:Dnah12
|
UTSW |
14 |
26,773,830 (GRCm38) |
missense |
probably damaging |
1.00 |
R5335:Dnah12
|
UTSW |
14 |
26,879,738 (GRCm38) |
missense |
probably damaging |
1.00 |
R5339:Dnah12
|
UTSW |
14 |
26,814,537 (GRCm38) |
missense |
possibly damaging |
0.83 |
R5354:Dnah12
|
UTSW |
14 |
26,774,342 (GRCm38) |
splice site |
probably null |
|
R5389:Dnah12
|
UTSW |
14 |
26,735,749 (GRCm38) |
missense |
probably damaging |
1.00 |
R5434:Dnah12
|
UTSW |
14 |
26,859,299 (GRCm38) |
missense |
probably damaging |
1.00 |
R5466:Dnah12
|
UTSW |
14 |
26,771,050 (GRCm38) |
missense |
probably damaging |
1.00 |
R5655:Dnah12
|
UTSW |
14 |
26,710,269 (GRCm38) |
missense |
probably benign |
0.01 |
R5681:Dnah12
|
UTSW |
14 |
26,815,495 (GRCm38) |
missense |
probably benign |
0.32 |
R5824:Dnah12
|
UTSW |
14 |
26,770,518 (GRCm38) |
critical splice donor site |
probably null |
|
R5863:Dnah12
|
UTSW |
14 |
26,854,921 (GRCm38) |
missense |
probably damaging |
1.00 |
R5890:Dnah12
|
UTSW |
14 |
26,706,884 (GRCm38) |
missense |
probably benign |
0.09 |
R5912:Dnah12
|
UTSW |
14 |
26,770,008 (GRCm38) |
nonsense |
probably null |
|
R5916:Dnah12
|
UTSW |
14 |
26,706,918 (GRCm38) |
missense |
possibly damaging |
0.92 |
R5941:Dnah12
|
UTSW |
14 |
26,706,867 (GRCm38) |
missense |
probably benign |
0.00 |
R5987:Dnah12
|
UTSW |
14 |
26,886,871 (GRCm38) |
missense |
possibly damaging |
0.54 |
R5992:Dnah12
|
UTSW |
14 |
26,697,341 (GRCm38) |
missense |
probably benign |
0.04 |
R6132:Dnah12
|
UTSW |
14 |
26,717,911 (GRCm38) |
missense |
probably damaging |
1.00 |
R6136:Dnah12
|
UTSW |
14 |
26,875,270 (GRCm38) |
missense |
probably damaging |
0.99 |
R6158:Dnah12
|
UTSW |
14 |
26,773,685 (GRCm38) |
missense |
possibly damaging |
0.95 |
R6183:Dnah12
|
UTSW |
14 |
26,861,769 (GRCm38) |
missense |
probably damaging |
1.00 |
R6191:Dnah12
|
UTSW |
14 |
26,710,257 (GRCm38) |
missense |
probably benign |
0.03 |
R6235:Dnah12
|
UTSW |
14 |
26,854,804 (GRCm38) |
missense |
probably damaging |
1.00 |
R6277:Dnah12
|
UTSW |
14 |
26,770,482 (GRCm38) |
missense |
probably damaging |
1.00 |
R6332:Dnah12
|
UTSW |
14 |
26,717,974 (GRCm38) |
missense |
probably damaging |
0.99 |
R6334:Dnah12
|
UTSW |
14 |
26,706,834 (GRCm38) |
missense |
possibly damaging |
0.51 |
R6443:Dnah12
|
UTSW |
14 |
26,878,051 (GRCm38) |
missense |
probably benign |
0.06 |
R6480:Dnah12
|
UTSW |
14 |
26,872,455 (GRCm38) |
missense |
probably damaging |
1.00 |
R6530:Dnah12
|
UTSW |
14 |
26,735,710 (GRCm38) |
missense |
probably damaging |
1.00 |
R6678:Dnah12
|
UTSW |
14 |
26,735,692 (GRCm38) |
missense |
probably damaging |
1.00 |
R6709:Dnah12
|
UTSW |
14 |
26,872,749 (GRCm38) |
missense |
probably damaging |
1.00 |
R6724:Dnah12
|
UTSW |
14 |
26,796,223 (GRCm38) |
missense |
probably benign |
0.02 |
R6745:Dnah12
|
UTSW |
14 |
26,707,228 (GRCm38) |
missense |
probably damaging |
0.99 |
R6788:Dnah12
|
UTSW |
14 |
26,801,513 (GRCm38) |
missense |
probably damaging |
0.99 |
R6894:Dnah12
|
UTSW |
14 |
26,735,749 (GRCm38) |
missense |
probably damaging |
1.00 |
R6912:Dnah12
|
UTSW |
14 |
26,878,079 (GRCm38) |
missense |
probably damaging |
1.00 |
R6982:Dnah12
|
UTSW |
14 |
26,799,076 (GRCm38) |
splice site |
probably null |
|
R7001:Dnah12
|
UTSW |
14 |
26,879,724 (GRCm38) |
missense |
probably damaging |
0.99 |
R7002:Dnah12
|
UTSW |
14 |
26,876,998 (GRCm38) |
missense |
probably damaging |
1.00 |
R7017:Dnah12
|
UTSW |
14 |
26,735,680 (GRCm38) |
missense |
probably benign |
|
R7107:Dnah12
|
UTSW |
14 |
26,778,912 (GRCm38) |
critical splice donor site |
probably null |
|
R7108:Dnah12
|
UTSW |
14 |
26,778,912 (GRCm38) |
critical splice donor site |
probably null |
|
R7121:Dnah12
|
UTSW |
14 |
26,778,912 (GRCm38) |
critical splice donor site |
probably null |
|
R7122:Dnah12
|
UTSW |
14 |
26,778,912 (GRCm38) |
critical splice donor site |
probably null |
|
R7135:Dnah12
|
UTSW |
14 |
26,801,413 (GRCm38) |
missense |
probably damaging |
0.99 |
R7135:Dnah12
|
UTSW |
14 |
26,778,912 (GRCm38) |
critical splice donor site |
probably null |
|
R7150:Dnah12
|
UTSW |
14 |
26,861,732 (GRCm38) |
missense |
probably damaging |
0.99 |
R7188:Dnah12
|
UTSW |
14 |
26,814,413 (GRCm38) |
missense |
probably benign |
0.04 |
R7201:Dnah12
|
UTSW |
14 |
26,814,622 (GRCm38) |
missense |
probably benign |
0.08 |
R7202:Dnah12
|
UTSW |
14 |
26,778,912 (GRCm38) |
critical splice donor site |
probably null |
|
R7204:Dnah12
|
UTSW |
14 |
26,781,485 (GRCm38) |
missense |
probably damaging |
0.99 |
R7204:Dnah12
|
UTSW |
14 |
26,778,912 (GRCm38) |
critical splice donor site |
probably null |
|
R7205:Dnah12
|
UTSW |
14 |
26,778,912 (GRCm38) |
critical splice donor site |
probably null |
|
R7206:Dnah12
|
UTSW |
14 |
26,778,912 (GRCm38) |
critical splice donor site |
probably null |
|
R7219:Dnah12
|
UTSW |
14 |
26,854,880 (GRCm38) |
missense |
probably damaging |
0.99 |
R7337:Dnah12
|
UTSW |
14 |
26,766,577 (GRCm38) |
splice site |
probably null |
|
R7339:Dnah12
|
UTSW |
14 |
26,872,320 (GRCm38) |
missense |
probably benign |
|
R7363:Dnah12
|
UTSW |
14 |
26,724,611 (GRCm38) |
missense |
probably benign |
|
R7426:Dnah12
|
UTSW |
14 |
26,724,626 (GRCm38) |
missense |
probably benign |
0.01 |
R7472:Dnah12
|
UTSW |
14 |
26,856,635 (GRCm38) |
missense |
probably benign |
0.01 |
R7579:Dnah12
|
UTSW |
14 |
26,770,503 (GRCm38) |
missense |
probably benign |
0.05 |
R7655:Dnah12
|
UTSW |
14 |
26,859,316 (GRCm38) |
missense |
probably benign |
0.21 |
R7656:Dnah12
|
UTSW |
14 |
26,859,316 (GRCm38) |
missense |
probably benign |
0.21 |
R7694:Dnah12
|
UTSW |
14 |
26,781,380 (GRCm38) |
missense |
probably damaging |
1.00 |
R7730:Dnah12
|
UTSW |
14 |
26,785,933 (GRCm38) |
missense |
probably damaging |
1.00 |
R7837:Dnah12
|
UTSW |
14 |
26,796,219 (GRCm38) |
missense |
probably benign |
0.01 |
R7855:Dnah12
|
UTSW |
14 |
26,829,329 (GRCm38) |
missense |
probably benign |
0.14 |
R7870:Dnah12
|
UTSW |
14 |
26,856,529 (GRCm38) |
missense |
probably benign |
0.00 |
R7920:Dnah12
|
UTSW |
14 |
26,856,542 (GRCm38) |
missense |
possibly damaging |
0.58 |
R7933:Dnah12
|
UTSW |
14 |
26,766,115 (GRCm38) |
missense |
probably benign |
0.00 |
R7956:Dnah12
|
UTSW |
14 |
26,709,272 (GRCm38) |
missense |
probably damaging |
0.96 |
R8192:Dnah12
|
UTSW |
14 |
26,706,881 (GRCm38) |
missense |
probably benign |
|
R8263:Dnah12
|
UTSW |
14 |
26,891,464 (GRCm38) |
missense |
noncoding transcript |
|
R8287:Dnah12
|
UTSW |
14 |
26,812,603 (GRCm38) |
missense |
probably benign |
|
R8336:Dnah12
|
UTSW |
14 |
26,711,065 (GRCm38) |
missense |
probably benign |
0.01 |
R8362:Dnah12
|
UTSW |
14 |
26,854,831 (GRCm38) |
missense |
probably damaging |
1.00 |
R8392:Dnah12
|
UTSW |
14 |
26,885,912 (GRCm38) |
missense |
probably benign |
|
R8458:Dnah12
|
UTSW |
14 |
26,826,892 (GRCm38) |
critical splice acceptor site |
probably null |
|
R8481:Dnah12
|
UTSW |
14 |
26,853,796 (GRCm38) |
missense |
probably benign |
0.02 |
R8551:Dnah12
|
UTSW |
14 |
26,774,270 (GRCm38) |
missense |
probably damaging |
0.97 |
R8669:Dnah12
|
UTSW |
14 |
26,830,625 (GRCm38) |
splice site |
probably benign |
|
R8698:Dnah12
|
UTSW |
14 |
26,707,263 (GRCm38) |
missense |
probably benign |
0.02 |
R8709:Dnah12
|
UTSW |
14 |
26,693,602 (GRCm38) |
missense |
probably benign |
0.00 |
R8778:Dnah12
|
UTSW |
14 |
26,734,563 (GRCm38) |
missense |
probably benign |
0.29 |
R9049:Dnah12
|
UTSW |
14 |
26,722,120 (GRCm38) |
missense |
probably benign |
0.00 |
R9087:Dnah12
|
UTSW |
14 |
26,824,546 (GRCm38) |
missense |
probably damaging |
1.00 |
R9099:Dnah12
|
UTSW |
14 |
26,770,368 (GRCm38) |
missense |
probably benign |
0.31 |
R9153:Dnah12
|
UTSW |
14 |
26,814,612 (GRCm38) |
missense |
probably damaging |
1.00 |
R9177:Dnah12
|
UTSW |
14 |
26,849,298 (GRCm38) |
missense |
possibly damaging |
0.84 |
R9214:Dnah12
|
UTSW |
14 |
26,723,905 (GRCm38) |
missense |
probably benign |
0.02 |
R9268:Dnah12
|
UTSW |
14 |
26,849,298 (GRCm38) |
missense |
possibly damaging |
0.84 |
R9274:Dnah12
|
UTSW |
14 |
26,815,417 (GRCm38) |
missense |
probably benign |
0.00 |
R9293:Dnah12
|
UTSW |
14 |
26,773,059 (GRCm38) |
missense |
probably benign |
|
R9322:Dnah12
|
UTSW |
14 |
26,770,977 (GRCm38) |
missense |
possibly damaging |
0.75 |
R9353:Dnah12
|
UTSW |
14 |
26,856,550 (GRCm38) |
missense |
probably damaging |
1.00 |
R9506:Dnah12
|
UTSW |
14 |
26,792,211 (GRCm38) |
missense |
probably benign |
0.00 |
R9518:Dnah12
|
UTSW |
14 |
26,773,756 (GRCm38) |
missense |
probably damaging |
1.00 |
R9524:Dnah12
|
UTSW |
14 |
26,850,537 (GRCm38) |
missense |
probably null |
0.91 |
R9562:Dnah12
|
UTSW |
14 |
26,875,324 (GRCm38) |
missense |
possibly damaging |
0.58 |
R9565:Dnah12
|
UTSW |
14 |
26,875,324 (GRCm38) |
missense |
possibly damaging |
0.58 |
R9573:Dnah12
|
UTSW |
14 |
26,693,464 (GRCm38) |
missense |
probably benign |
|
R9581:Dnah12
|
UTSW |
14 |
26,770,028 (GRCm38) |
missense |
probably damaging |
1.00 |
R9689:Dnah12
|
UTSW |
14 |
26,868,914 (GRCm38) |
missense |
probably null |
1.00 |
R9727:Dnah12
|
UTSW |
14 |
26,801,553 (GRCm38) |
nonsense |
probably null |
|
V7580:Dnah12
|
UTSW |
14 |
26,773,093 (GRCm38) |
missense |
possibly damaging |
0.95 |
V7581:Dnah12
|
UTSW |
14 |
26,773,093 (GRCm38) |
missense |
possibly damaging |
0.95 |
X0018:Dnah12
|
UTSW |
14 |
26,814,480 (GRCm38) |
missense |
probably damaging |
1.00 |
X0027:Dnah12
|
UTSW |
14 |
26,816,288 (GRCm38) |
missense |
probably damaging |
1.00 |
X0065:Dnah12
|
UTSW |
14 |
26,814,645 (GRCm38) |
missense |
possibly damaging |
0.93 |
Z1177:Dnah12
|
UTSW |
14 |
26,875,215 (GRCm38) |
missense |
probably damaging |
1.00 |
|