Other mutations in this stock |
Total: 113 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aars1 |
A |
T |
8: 111,769,338 (GRCm39) |
D287V |
probably damaging |
Het |
Abca12 |
A |
G |
1: 71,334,188 (GRCm39) |
C1105R |
probably benign |
Het |
Abca8b |
T |
A |
11: 109,833,167 (GRCm39) |
N1178Y |
probably damaging |
Het |
Abhd12 |
A |
G |
2: 150,685,318 (GRCm39) |
L189P |
probably damaging |
Het |
Acap2 |
G |
T |
16: 30,929,752 (GRCm39) |
N435K |
probably damaging |
Het |
Adam6b |
G |
T |
12: 113,453,545 (GRCm39) |
G121C |
probably damaging |
Het |
Adgrb1 |
C |
A |
15: 74,452,435 (GRCm39) |
C200* |
probably null |
Het |
Agbl5 |
T |
C |
5: 31,060,408 (GRCm39) |
S730P |
possibly damaging |
Het |
Ahsg |
G |
A |
16: 22,711,078 (GRCm39) |
|
probably benign |
Het |
Aldh9a1 |
A |
T |
1: 167,189,423 (GRCm39) |
K390N |
probably benign |
Het |
Alpk2 |
T |
A |
18: 65,427,165 (GRCm39) |
H1857L |
possibly damaging |
Het |
Apip |
T |
A |
2: 102,919,007 (GRCm39) |
N102K |
probably benign |
Het |
Asxl2 |
T |
C |
12: 3,507,125 (GRCm39) |
S106P |
probably damaging |
Het |
Atp2b2 |
G |
T |
6: 113,750,329 (GRCm39) |
R677S |
probably damaging |
Het |
Barhl1 |
A |
C |
2: 28,799,857 (GRCm39) |
M256R |
probably damaging |
Het |
Cacnb2 |
A |
T |
2: 14,990,775 (GRCm39) |
Q619L |
possibly damaging |
Het |
Ccdc137 |
C |
T |
11: 120,349,038 (GRCm39) |
P23L |
probably benign |
Het |
Cdh11 |
A |
T |
8: 103,361,273 (GRCm39) |
N688K |
possibly damaging |
Het |
Cdh18 |
C |
T |
15: 23,173,938 (GRCm39) |
P51S |
probably damaging |
Het |
Cdin1 |
G |
T |
2: 115,473,173 (GRCm39) |
R101L |
possibly damaging |
Het |
Cfhr1 |
A |
T |
1: 139,481,338 (GRCm39) |
Y181N |
probably damaging |
Het |
Chmp3 |
A |
G |
6: 71,537,923 (GRCm39) |
D50G |
probably benign |
Het |
Crem |
T |
C |
18: 3,295,037 (GRCm39) |
|
probably null |
Het |
Cyb561a3 |
G |
A |
19: 10,559,757 (GRCm39) |
W27* |
probably null |
Het |
Cyp2d12 |
C |
A |
15: 82,442,257 (GRCm39) |
N297K |
possibly damaging |
Het |
Dclk2 |
C |
T |
3: 86,712,946 (GRCm39) |
R503Q |
possibly damaging |
Het |
Dsp |
T |
G |
13: 38,377,171 (GRCm39) |
L1652R |
probably damaging |
Het |
Dstyk |
G |
A |
1: 132,377,333 (GRCm39) |
S66N |
probably benign |
Het |
Ehhadh |
T |
C |
16: 21,580,928 (GRCm39) |
E688G |
probably damaging |
Het |
Emsy |
G |
T |
7: 98,251,937 (GRCm39) |
H688N |
possibly damaging |
Het |
Emsy |
T |
A |
7: 98,251,936 (GRCm39) |
H688L |
possibly damaging |
Het |
Endod1 |
A |
G |
9: 14,268,222 (GRCm39) |
L421P |
probably damaging |
Het |
Fam222b |
C |
T |
11: 78,045,861 (GRCm39) |
P346L |
probably damaging |
Het |
Fam3c |
G |
A |
6: 22,309,436 (GRCm39) |
R182W |
probably damaging |
Het |
Gck |
T |
C |
11: 5,860,984 (GRCm39) |
D29G |
probably damaging |
Het |
Gm10320 |
C |
A |
13: 98,626,207 (GRCm39) |
R59L |
probably damaging |
Het |
Gm21798 |
C |
T |
15: 64,689,675 (GRCm39) |
|
probably benign |
Het |
Gm9376 |
A |
G |
14: 118,504,957 (GRCm39) |
T130A |
possibly damaging |
Het |
Gpr153 |
T |
A |
4: 152,366,849 (GRCm39) |
I334N |
possibly damaging |
Het |
Greb1l |
T |
C |
18: 10,509,314 (GRCm39) |
L542P |
probably damaging |
Het |
H2-T15 |
G |
T |
17: 36,368,896 (GRCm39) |
F61L |
probably damaging |
Het |
Hacl1 |
T |
C |
14: 31,362,491 (GRCm39) |
E52G |
probably benign |
Het |
Ice2 |
A |
G |
9: 69,314,635 (GRCm39) |
Y128C |
probably damaging |
Het |
Ikzf2 |
T |
A |
1: 69,581,446 (GRCm39) |
I121L |
probably benign |
Het |
Ipcef1 |
C |
T |
10: 6,869,900 (GRCm39) |
A167T |
probably benign |
Het |
Jakmip2 |
T |
A |
18: 43,715,145 (GRCm39) |
D127V |
possibly damaging |
Het |
Jph4 |
T |
C |
14: 55,352,368 (GRCm39) |
T122A |
probably damaging |
Het |
Kcns2 |
A |
G |
15: 34,838,949 (GRCm39) |
E104G |
probably damaging |
Het |
Lars2 |
A |
C |
9: 123,260,982 (GRCm39) |
R384S |
probably benign |
Het |
Lsmem1 |
T |
A |
12: 40,235,407 (GRCm39) |
H3L |
possibly damaging |
Het |
Lsmem1 |
G |
T |
12: 40,235,408 (GRCm39) |
H3N |
possibly damaging |
Het |
Ly6g2 |
T |
G |
15: 75,088,605 (GRCm39) |
|
probably null |
Het |
Mfhas1 |
A |
C |
8: 36,057,222 (GRCm39) |
S566R |
probably benign |
Het |
Mfhas1 |
C |
G |
8: 36,057,402 (GRCm39) |
R626G |
probably benign |
Het |
Mgam |
A |
G |
6: 40,643,826 (GRCm39) |
T585A |
probably damaging |
Het |
Mmp25 |
T |
C |
17: 23,858,997 (GRCm39) |
K185E |
probably benign |
Het |
Mtch1 |
T |
C |
17: 29,557,750 (GRCm39) |
I243V |
probably damaging |
Het |
Mtcp1 |
A |
T |
X: 74,455,271 (GRCm39) |
Y25* |
probably null |
Het |
Mybl2 |
A |
G |
2: 162,901,503 (GRCm39) |
T35A |
probably benign |
Het |
Myh11 |
T |
C |
16: 14,041,744 (GRCm39) |
E736G |
probably damaging |
Het |
Myh2 |
T |
C |
11: 67,067,385 (GRCm39) |
I224T |
probably damaging |
Het |
Mymx |
T |
C |
17: 45,912,759 (GRCm39) |
|
probably benign |
Het |
Nek10 |
A |
G |
14: 14,863,454 (GRCm38) |
|
probably null |
Het |
Nsd1 |
A |
T |
13: 55,394,182 (GRCm39) |
K697N |
probably damaging |
Het |
Nynrin |
A |
G |
14: 56,110,404 (GRCm39) |
D1837G |
possibly damaging |
Het |
Or14j4 |
G |
A |
17: 37,921,168 (GRCm39) |
T158I |
probably benign |
Het |
Or2ag2b |
A |
G |
7: 106,418,214 (GRCm39) |
H308R |
probably benign |
Het |
Or52s1 |
A |
T |
7: 102,861,093 (GRCm39) |
T9S |
probably benign |
Het |
Or5p81 |
T |
A |
7: 108,266,851 (GRCm39) |
I76N |
probably benign |
Het |
Or6k4 |
T |
A |
1: 173,964,760 (GRCm39) |
I150N |
probably benign |
Het |
Pgap6 |
T |
C |
17: 26,341,194 (GRCm39) |
Y766H |
probably damaging |
Het |
Phf19 |
T |
C |
2: 34,801,781 (GRCm39) |
T10A |
probably benign |
Het |
Pkd1 |
A |
T |
17: 24,784,558 (GRCm39) |
H368L |
probably benign |
Het |
Plscr2 |
A |
G |
9: 92,172,808 (GRCm39) |
R156G |
probably damaging |
Het |
Ppp1r42 |
G |
A |
1: 10,070,311 (GRCm39) |
R61C |
probably benign |
Het |
Pptc7 |
T |
G |
5: 122,451,679 (GRCm39) |
V45G |
probably damaging |
Het |
Prlhr |
G |
A |
19: 60,455,867 (GRCm39) |
T233I |
probably damaging |
Het |
Prr23a4 |
T |
A |
9: 98,785,446 (GRCm39) |
I37N |
possibly damaging |
Het |
Reps1 |
C |
T |
10: 17,983,462 (GRCm39) |
T435I |
probably damaging |
Het |
Ret |
T |
A |
6: 118,130,912 (GRCm39) |
T1084S |
probably damaging |
Het |
Rgl2 |
T |
A |
17: 34,152,595 (GRCm39) |
M402K |
probably benign |
Het |
Rp2 |
A |
G |
X: 20,243,154 (GRCm39) |
K43R |
probably benign |
Het |
Rundc3b |
A |
T |
5: 8,629,117 (GRCm39) |
W95R |
probably damaging |
Het |
Samd9l |
T |
C |
6: 3,375,107 (GRCm39) |
D718G |
possibly damaging |
Het |
Scnn1b |
G |
A |
7: 121,502,068 (GRCm39) |
R242H |
probably benign |
Het |
Smad4 |
G |
T |
18: 73,774,965 (GRCm39) |
Q445K |
probably benign |
Het |
Smchd1 |
G |
T |
17: 71,677,332 (GRCm39) |
P1486T |
probably damaging |
Het |
Snx25 |
G |
T |
8: 46,488,669 (GRCm39) |
N895K |
possibly damaging |
Het |
Sox2 |
A |
G |
3: 34,704,890 (GRCm39) |
D109G |
probably damaging |
Het |
Stfa2 |
A |
T |
16: 36,225,564 (GRCm39) |
N38K |
probably damaging |
Het |
Stfa2 |
C |
A |
16: 36,225,573 (GRCm39) |
E35D |
possibly damaging |
Het |
Stfa3 |
A |
G |
16: 36,271,023 (GRCm39) |
L87P |
probably damaging |
Het |
Strbp |
T |
C |
2: 37,530,921 (GRCm39) |
D111G |
possibly damaging |
Het |
Supt20 |
C |
A |
3: 54,635,079 (GRCm39) |
|
probably benign |
Het |
Svep1 |
A |
G |
4: 58,096,310 (GRCm39) |
Y1437H |
possibly damaging |
Het |
Tbx4 |
T |
A |
11: 85,802,746 (GRCm39) |
|
probably null |
Het |
Tmem117 |
A |
T |
15: 94,992,432 (GRCm39) |
N364I |
probably damaging |
Het |
Trat1 |
T |
C |
16: 48,581,742 (GRCm39) |
E45G |
probably damaging |
Het |
Trpc2 |
G |
A |
7: 101,733,326 (GRCm39) |
D92N |
probably damaging |
Het |
Trpm1 |
G |
A |
7: 63,876,530 (GRCm39) |
D528N |
probably damaging |
Het |
Ttll9 |
A |
G |
2: 152,842,156 (GRCm39) |
S337G |
possibly damaging |
Het |
Utrn |
A |
T |
10: 12,351,018 (GRCm39) |
I355N |
probably damaging |
Het |
Vangl1 |
A |
G |
3: 102,070,782 (GRCm39) |
S385P |
probably benign |
Het |
Vmn1r209 |
A |
G |
13: 22,990,409 (GRCm39) |
S94P |
possibly damaging |
Het |
Vmn2r28 |
T |
A |
7: 5,496,810 (GRCm39) |
Q14L |
probably benign |
Het |
Vps45 |
A |
G |
3: 95,954,557 (GRCm39) |
|
probably null |
Het |
Wdr48 |
T |
C |
9: 119,733,396 (GRCm39) |
V81A |
probably benign |
Het |
Xpnpep2 |
A |
G |
X: 47,214,230 (GRCm39) |
N476S |
probably benign |
Het |
Zbtb41 |
A |
T |
1: 139,374,660 (GRCm39) |
K707* |
probably null |
Het |
Zfp442 |
A |
C |
2: 150,250,983 (GRCm39) |
C306W |
probably damaging |
Het |
Zfp811 |
T |
C |
17: 33,017,116 (GRCm39) |
N307S |
possibly damaging |
Het |
Zfp976 |
A |
G |
7: 42,265,735 (GRCm39) |
W17R |
probably damaging |
Het |
Zyg11b |
T |
C |
4: 108,123,290 (GRCm39) |
T226A |
possibly damaging |
Het |
|
Other mutations in Dnah12 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01412:Dnah12
|
APN |
14 |
26,492,962 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01602:Dnah12
|
APN |
14 |
26,431,430 (GRCm39) |
splice site |
probably benign |
|
IGL01681:Dnah12
|
APN |
14 |
26,443,315 (GRCm39) |
missense |
probably benign |
|
IGL02082:Dnah12
|
APN |
14 |
26,428,317 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL02140:Dnah12
|
APN |
14 |
26,437,732 (GRCm39) |
missense |
probably benign |
0.20 |
IGL02170:Dnah12
|
APN |
14 |
26,495,069 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02174:Dnah12
|
APN |
14 |
26,428,072 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02367:Dnah12
|
APN |
14 |
26,430,316 (GRCm39) |
missense |
probably benign |
0.30 |
IGL02418:Dnah12
|
APN |
14 |
26,495,679 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03039:Dnah12
|
APN |
14 |
26,445,667 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03066:Dnah12
|
APN |
14 |
26,418,553 (GRCm39) |
missense |
probably benign |
0.06 |
drippings
|
UTSW |
14 |
26,576,761 (GRCm39) |
missense |
probably damaging |
1.00 |
grueben
|
UTSW |
14 |
26,600,036 (GRCm39) |
missense |
probably damaging |
1.00 |
BB010:Dnah12
|
UTSW |
14 |
26,488,072 (GRCm39) |
missense |
probably benign |
0.00 |
BB020:Dnah12
|
UTSW |
14 |
26,488,072 (GRCm39) |
missense |
probably benign |
0.00 |
F5770:Dnah12
|
UTSW |
14 |
26,495,050 (GRCm39) |
missense |
possibly damaging |
0.95 |
FR4304:Dnah12
|
UTSW |
14 |
26,571,342 (GRCm39) |
missense |
probably damaging |
1.00 |
FR4340:Dnah12
|
UTSW |
14 |
26,571,342 (GRCm39) |
missense |
probably damaging |
1.00 |
FR4342:Dnah12
|
UTSW |
14 |
26,571,342 (GRCm39) |
missense |
probably damaging |
1.00 |
FR4589:Dnah12
|
UTSW |
14 |
26,571,342 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03055:Dnah12
|
UTSW |
14 |
26,594,697 (GRCm39) |
missense |
probably damaging |
1.00 |
LCD18:Dnah12
|
UTSW |
14 |
26,571,342 (GRCm39) |
missense |
probably damaging |
1.00 |
R0003:Dnah12
|
UTSW |
14 |
26,494,601 (GRCm39) |
missense |
probably damaging |
1.00 |
R0110:Dnah12
|
UTSW |
14 |
26,520,856 (GRCm39) |
missense |
probably damaging |
1.00 |
R0302:Dnah12
|
UTSW |
14 |
26,521,956 (GRCm39) |
missense |
probably damaging |
1.00 |
R0355:Dnah12
|
UTSW |
14 |
26,427,272 (GRCm39) |
splice site |
probably null |
|
R0364:Dnah12
|
UTSW |
14 |
26,445,628 (GRCm39) |
missense |
probably benign |
0.10 |
R0469:Dnah12
|
UTSW |
14 |
26,520,856 (GRCm39) |
missense |
probably damaging |
1.00 |
R0558:Dnah12
|
UTSW |
14 |
26,430,465 (GRCm39) |
missense |
probably benign |
0.00 |
R0709:Dnah12
|
UTSW |
14 |
26,606,222 (GRCm39) |
splice site |
probably benign |
|
R0734:Dnah12
|
UTSW |
14 |
26,521,970 (GRCm39) |
missense |
probably benign |
0.00 |
R1273:Dnah12
|
UTSW |
14 |
26,460,375 (GRCm39) |
nonsense |
probably null |
|
R1496:Dnah12
|
UTSW |
14 |
26,431,403 (GRCm39) |
missense |
probably benign |
|
R1503:Dnah12
|
UTSW |
14 |
26,495,649 (GRCm39) |
missense |
probably damaging |
1.00 |
R1535:Dnah12
|
UTSW |
14 |
26,538,279 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1608:Dnah12
|
UTSW |
14 |
26,488,147 (GRCm39) |
missense |
probably damaging |
1.00 |
R1682:Dnah12
|
UTSW |
14 |
26,500,840 (GRCm39) |
missense |
possibly damaging |
0.71 |
R1758:Dnah12
|
UTSW |
14 |
26,488,071 (GRCm39) |
missense |
probably benign |
0.02 |
R1826:Dnah12
|
UTSW |
14 |
26,432,174 (GRCm39) |
missense |
probably benign |
0.01 |
R1829:Dnah12
|
UTSW |
14 |
26,522,032 (GRCm39) |
missense |
probably damaging |
1.00 |
R1862:Dnah12
|
UTSW |
14 |
26,430,412 (GRCm39) |
missense |
probably benign |
0.30 |
R1862:Dnah12
|
UTSW |
14 |
26,418,553 (GRCm39) |
missense |
probably benign |
0.06 |
R1913:Dnah12
|
UTSW |
14 |
26,514,221 (GRCm39) |
splice site |
probably null |
|
R1933:Dnah12
|
UTSW |
14 |
26,455,650 (GRCm39) |
missense |
probably damaging |
0.98 |
R2006:Dnah12
|
UTSW |
14 |
26,536,416 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2045:Dnah12
|
UTSW |
14 |
26,503,485 (GRCm39) |
missense |
probably null |
1.00 |
R2113:Dnah12
|
UTSW |
14 |
26,488,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R2125:Dnah12
|
UTSW |
14 |
26,445,613 (GRCm39) |
nonsense |
probably null |
|
R2126:Dnah12
|
UTSW |
14 |
26,445,613 (GRCm39) |
nonsense |
probably null |
|
R2207:Dnah12
|
UTSW |
14 |
26,503,744 (GRCm39) |
missense |
probably damaging |
0.99 |
R2213:Dnah12
|
UTSW |
14 |
26,460,485 (GRCm39) |
missense |
probably benign |
0.06 |
R2511:Dnah12
|
UTSW |
14 |
26,491,907 (GRCm39) |
missense |
possibly damaging |
0.65 |
R2875:Dnah12
|
UTSW |
14 |
26,598,907 (GRCm39) |
missense |
probably benign |
0.05 |
R2875:Dnah12
|
UTSW |
14 |
26,414,625 (GRCm39) |
missense |
probably benign |
0.04 |
R3551:Dnah12
|
UTSW |
14 |
26,492,929 (GRCm39) |
missense |
probably benign |
0.01 |
R3713:Dnah12
|
UTSW |
14 |
26,534,747 (GRCm39) |
missense |
probably benign |
|
R3729:Dnah12
|
UTSW |
14 |
26,427,220 (GRCm39) |
missense |
probably benign |
0.02 |
R3799:Dnah12
|
UTSW |
14 |
26,492,880 (GRCm39) |
missense |
probably damaging |
1.00 |
R3846:Dnah12
|
UTSW |
14 |
26,431,366 (GRCm39) |
missense |
probably benign |
0.00 |
R3892:Dnah12
|
UTSW |
14 |
26,578,573 (GRCm39) |
missense |
probably benign |
0.03 |
R3921:Dnah12
|
UTSW |
14 |
26,493,008 (GRCm39) |
missense |
probably damaging |
1.00 |
R3940:Dnah12
|
UTSW |
14 |
26,444,754 (GRCm39) |
missense |
probably benign |
|
R4065:Dnah12
|
UTSW |
14 |
26,492,405 (GRCm39) |
missense |
probably benign |
0.02 |
R4113:Dnah12
|
UTSW |
14 |
26,414,722 (GRCm39) |
missense |
probably damaging |
0.98 |
R4249:Dnah12
|
UTSW |
14 |
26,430,341 (GRCm39) |
missense |
possibly damaging |
0.70 |
R4259:Dnah12
|
UTSW |
14 |
26,520,883 (GRCm39) |
missense |
probably benign |
0.01 |
R4260:Dnah12
|
UTSW |
14 |
26,520,883 (GRCm39) |
missense |
probably benign |
0.01 |
R4348:Dnah12
|
UTSW |
14 |
26,536,498 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4457:Dnah12
|
UTSW |
14 |
26,537,464 (GRCm39) |
missense |
probably damaging |
1.00 |
R4490:Dnah12
|
UTSW |
14 |
26,455,758 (GRCm39) |
missense |
possibly damaging |
0.67 |
R4491:Dnah12
|
UTSW |
14 |
26,455,758 (GRCm39) |
missense |
possibly damaging |
0.67 |
R4494:Dnah12
|
UTSW |
14 |
26,593,812 (GRCm39) |
missense |
probably damaging |
0.99 |
R4523:Dnah12
|
UTSW |
14 |
26,598,915 (GRCm39) |
missense |
possibly damaging |
0.83 |
R4523:Dnah12
|
UTSW |
14 |
26,491,979 (GRCm39) |
missense |
probably damaging |
0.97 |
R4546:Dnah12
|
UTSW |
14 |
26,494,971 (GRCm39) |
missense |
probably damaging |
1.00 |
R4584:Dnah12
|
UTSW |
14 |
26,494,551 (GRCm39) |
missense |
probably damaging |
1.00 |
R4624:Dnah12
|
UTSW |
14 |
26,456,913 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4689:Dnah12
|
UTSW |
14 |
26,427,994 (GRCm39) |
missense |
probably benign |
0.00 |
R4727:Dnah12
|
UTSW |
14 |
26,594,274 (GRCm39) |
missense |
probably damaging |
1.00 |
R4732:Dnah12
|
UTSW |
14 |
26,503,741 (GRCm39) |
missense |
probably damaging |
1.00 |
R4733:Dnah12
|
UTSW |
14 |
26,503,741 (GRCm39) |
missense |
probably damaging |
1.00 |
R4851:Dnah12
|
UTSW |
14 |
26,437,784 (GRCm39) |
nonsense |
probably null |
|
R4879:Dnah12
|
UTSW |
14 |
26,439,201 (GRCm39) |
critical splice donor site |
probably null |
|
R4893:Dnah12
|
UTSW |
14 |
26,431,325 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4915:Dnah12
|
UTSW |
14 |
26,455,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R4927:Dnah12
|
UTSW |
14 |
26,583,762 (GRCm39) |
nonsense |
probably null |
|
R4939:Dnah12
|
UTSW |
14 |
26,613,481 (GRCm39) |
missense |
probably damaging |
1.00 |
R4962:Dnah12
|
UTSW |
14 |
26,437,855 (GRCm39) |
missense |
probably benign |
0.00 |
R5011:Dnah12
|
UTSW |
14 |
26,431,326 (GRCm39) |
missense |
probably benign |
0.03 |
R5013:Dnah12
|
UTSW |
14 |
26,431,326 (GRCm39) |
missense |
probably benign |
0.03 |
R5043:Dnah12
|
UTSW |
14 |
26,606,147 (GRCm39) |
missense |
probably damaging |
1.00 |
R5049:Dnah12
|
UTSW |
14 |
26,456,852 (GRCm39) |
missense |
probably benign |
0.09 |
R5122:Dnah12
|
UTSW |
14 |
26,439,155 (GRCm39) |
missense |
probably benign |
0.00 |
R5135:Dnah12
|
UTSW |
14 |
26,492,434 (GRCm39) |
missense |
probably damaging |
0.99 |
R5149:Dnah12
|
UTSW |
14 |
26,572,883 (GRCm39) |
nonsense |
probably null |
|
R5154:Dnah12
|
UTSW |
14 |
26,571,320 (GRCm39) |
missense |
probably benign |
0.12 |
R5206:Dnah12
|
UTSW |
14 |
26,491,942 (GRCm39) |
missense |
probably damaging |
1.00 |
R5307:Dnah12
|
UTSW |
14 |
26,414,641 (GRCm39) |
missense |
possibly damaging |
0.49 |
R5330:Dnah12
|
UTSW |
14 |
26,495,787 (GRCm39) |
missense |
probably damaging |
1.00 |
R5335:Dnah12
|
UTSW |
14 |
26,601,695 (GRCm39) |
missense |
probably damaging |
1.00 |
R5339:Dnah12
|
UTSW |
14 |
26,536,494 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5354:Dnah12
|
UTSW |
14 |
26,496,299 (GRCm39) |
splice site |
probably null |
|
R5389:Dnah12
|
UTSW |
14 |
26,456,904 (GRCm39) |
missense |
probably damaging |
1.00 |
R5434:Dnah12
|
UTSW |
14 |
26,581,256 (GRCm39) |
missense |
probably damaging |
1.00 |
R5466:Dnah12
|
UTSW |
14 |
26,493,007 (GRCm39) |
missense |
probably damaging |
1.00 |
R5655:Dnah12
|
UTSW |
14 |
26,431,424 (GRCm39) |
missense |
probably benign |
0.01 |
R5681:Dnah12
|
UTSW |
14 |
26,537,452 (GRCm39) |
missense |
probably benign |
0.32 |
R5824:Dnah12
|
UTSW |
14 |
26,492,475 (GRCm39) |
critical splice donor site |
probably null |
|
R5863:Dnah12
|
UTSW |
14 |
26,576,878 (GRCm39) |
missense |
probably damaging |
1.00 |
R5890:Dnah12
|
UTSW |
14 |
26,428,039 (GRCm39) |
missense |
probably benign |
0.09 |
R5912:Dnah12
|
UTSW |
14 |
26,491,965 (GRCm39) |
nonsense |
probably null |
|
R5916:Dnah12
|
UTSW |
14 |
26,428,073 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5941:Dnah12
|
UTSW |
14 |
26,428,022 (GRCm39) |
missense |
probably benign |
0.00 |
R5987:Dnah12
|
UTSW |
14 |
26,608,828 (GRCm39) |
missense |
possibly damaging |
0.54 |
R5992:Dnah12
|
UTSW |
14 |
26,418,496 (GRCm39) |
missense |
probably benign |
0.04 |
R6132:Dnah12
|
UTSW |
14 |
26,439,066 (GRCm39) |
missense |
probably damaging |
1.00 |
R6136:Dnah12
|
UTSW |
14 |
26,597,227 (GRCm39) |
missense |
probably damaging |
0.99 |
R6158:Dnah12
|
UTSW |
14 |
26,495,642 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6183:Dnah12
|
UTSW |
14 |
26,583,726 (GRCm39) |
missense |
probably damaging |
1.00 |
R6191:Dnah12
|
UTSW |
14 |
26,431,412 (GRCm39) |
missense |
probably benign |
0.03 |
R6235:Dnah12
|
UTSW |
14 |
26,576,761 (GRCm39) |
missense |
probably damaging |
1.00 |
R6277:Dnah12
|
UTSW |
14 |
26,492,439 (GRCm39) |
missense |
probably damaging |
1.00 |
R6332:Dnah12
|
UTSW |
14 |
26,439,129 (GRCm39) |
missense |
probably damaging |
0.99 |
R6334:Dnah12
|
UTSW |
14 |
26,427,989 (GRCm39) |
missense |
possibly damaging |
0.51 |
R6443:Dnah12
|
UTSW |
14 |
26,600,008 (GRCm39) |
missense |
probably benign |
0.06 |
R6480:Dnah12
|
UTSW |
14 |
26,594,412 (GRCm39) |
missense |
probably damaging |
1.00 |
R6530:Dnah12
|
UTSW |
14 |
26,456,865 (GRCm39) |
missense |
probably damaging |
1.00 |
R6678:Dnah12
|
UTSW |
14 |
26,456,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R6709:Dnah12
|
UTSW |
14 |
26,594,706 (GRCm39) |
missense |
probably damaging |
1.00 |
R6724:Dnah12
|
UTSW |
14 |
26,518,180 (GRCm39) |
missense |
probably benign |
0.02 |
R6745:Dnah12
|
UTSW |
14 |
26,428,383 (GRCm39) |
missense |
probably damaging |
0.99 |
R6788:Dnah12
|
UTSW |
14 |
26,523,470 (GRCm39) |
missense |
probably damaging |
0.99 |
R6894:Dnah12
|
UTSW |
14 |
26,456,904 (GRCm39) |
missense |
probably damaging |
1.00 |
R6912:Dnah12
|
UTSW |
14 |
26,600,036 (GRCm39) |
missense |
probably damaging |
1.00 |
R6982:Dnah12
|
UTSW |
14 |
26,521,033 (GRCm39) |
splice site |
probably null |
|
R7001:Dnah12
|
UTSW |
14 |
26,601,681 (GRCm39) |
missense |
probably damaging |
0.99 |
R7002:Dnah12
|
UTSW |
14 |
26,598,955 (GRCm39) |
missense |
probably damaging |
1.00 |
R7017:Dnah12
|
UTSW |
14 |
26,456,835 (GRCm39) |
missense |
probably benign |
|
R7107:Dnah12
|
UTSW |
14 |
26,500,869 (GRCm39) |
critical splice donor site |
probably null |
|
R7108:Dnah12
|
UTSW |
14 |
26,500,869 (GRCm39) |
critical splice donor site |
probably null |
|
R7121:Dnah12
|
UTSW |
14 |
26,500,869 (GRCm39) |
critical splice donor site |
probably null |
|
R7122:Dnah12
|
UTSW |
14 |
26,500,869 (GRCm39) |
critical splice donor site |
probably null |
|
R7135:Dnah12
|
UTSW |
14 |
26,523,370 (GRCm39) |
missense |
probably damaging |
0.99 |
R7135:Dnah12
|
UTSW |
14 |
26,500,869 (GRCm39) |
critical splice donor site |
probably null |
|
R7150:Dnah12
|
UTSW |
14 |
26,583,689 (GRCm39) |
missense |
probably damaging |
0.99 |
R7188:Dnah12
|
UTSW |
14 |
26,536,370 (GRCm39) |
missense |
probably benign |
0.04 |
R7201:Dnah12
|
UTSW |
14 |
26,536,579 (GRCm39) |
missense |
probably benign |
0.08 |
R7202:Dnah12
|
UTSW |
14 |
26,500,869 (GRCm39) |
critical splice donor site |
probably null |
|
R7204:Dnah12
|
UTSW |
14 |
26,503,442 (GRCm39) |
missense |
probably damaging |
0.99 |
R7204:Dnah12
|
UTSW |
14 |
26,500,869 (GRCm39) |
critical splice donor site |
probably null |
|
R7205:Dnah12
|
UTSW |
14 |
26,500,869 (GRCm39) |
critical splice donor site |
probably null |
|
R7206:Dnah12
|
UTSW |
14 |
26,500,869 (GRCm39) |
critical splice donor site |
probably null |
|
R7219:Dnah12
|
UTSW |
14 |
26,576,837 (GRCm39) |
missense |
probably damaging |
0.99 |
R7337:Dnah12
|
UTSW |
14 |
26,488,534 (GRCm39) |
splice site |
probably null |
|
R7339:Dnah12
|
UTSW |
14 |
26,594,277 (GRCm39) |
missense |
probably benign |
|
R7363:Dnah12
|
UTSW |
14 |
26,445,766 (GRCm39) |
missense |
probably benign |
|
R7426:Dnah12
|
UTSW |
14 |
26,445,781 (GRCm39) |
missense |
probably benign |
0.01 |
R7472:Dnah12
|
UTSW |
14 |
26,578,592 (GRCm39) |
missense |
probably benign |
0.01 |
R7579:Dnah12
|
UTSW |
14 |
26,492,460 (GRCm39) |
missense |
probably benign |
0.05 |
R7655:Dnah12
|
UTSW |
14 |
26,581,273 (GRCm39) |
missense |
probably benign |
0.21 |
R7656:Dnah12
|
UTSW |
14 |
26,581,273 (GRCm39) |
missense |
probably benign |
0.21 |
R7694:Dnah12
|
UTSW |
14 |
26,503,337 (GRCm39) |
missense |
probably damaging |
1.00 |
R7730:Dnah12
|
UTSW |
14 |
26,507,890 (GRCm39) |
missense |
probably damaging |
1.00 |
R7837:Dnah12
|
UTSW |
14 |
26,518,176 (GRCm39) |
missense |
probably benign |
0.01 |
R7855:Dnah12
|
UTSW |
14 |
26,551,286 (GRCm39) |
missense |
probably benign |
0.14 |
R7870:Dnah12
|
UTSW |
14 |
26,578,486 (GRCm39) |
missense |
probably benign |
0.00 |
R7920:Dnah12
|
UTSW |
14 |
26,578,499 (GRCm39) |
missense |
possibly damaging |
0.58 |
R7933:Dnah12
|
UTSW |
14 |
26,488,072 (GRCm39) |
missense |
probably benign |
0.00 |
R7956:Dnah12
|
UTSW |
14 |
26,430,427 (GRCm39) |
missense |
probably damaging |
0.96 |
R8192:Dnah12
|
UTSW |
14 |
26,428,036 (GRCm39) |
missense |
probably benign |
|
R8263:Dnah12
|
UTSW |
14 |
26,613,421 (GRCm39) |
missense |
noncoding transcript |
|
R8287:Dnah12
|
UTSW |
14 |
26,534,560 (GRCm39) |
missense |
probably benign |
|
R8336:Dnah12
|
UTSW |
14 |
26,432,220 (GRCm39) |
missense |
probably benign |
0.01 |
R8362:Dnah12
|
UTSW |
14 |
26,576,788 (GRCm39) |
missense |
probably damaging |
1.00 |
R8392:Dnah12
|
UTSW |
14 |
26,607,869 (GRCm39) |
missense |
probably benign |
|
R8458:Dnah12
|
UTSW |
14 |
26,548,849 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8481:Dnah12
|
UTSW |
14 |
26,575,753 (GRCm39) |
missense |
probably benign |
0.02 |
R8551:Dnah12
|
UTSW |
14 |
26,496,227 (GRCm39) |
missense |
probably damaging |
0.97 |
R8669:Dnah12
|
UTSW |
14 |
26,552,582 (GRCm39) |
splice site |
probably benign |
|
R8698:Dnah12
|
UTSW |
14 |
26,428,418 (GRCm39) |
missense |
probably benign |
0.02 |
R8709:Dnah12
|
UTSW |
14 |
26,414,757 (GRCm39) |
missense |
probably benign |
0.00 |
R8778:Dnah12
|
UTSW |
14 |
26,455,718 (GRCm39) |
missense |
probably benign |
0.29 |
R9049:Dnah12
|
UTSW |
14 |
26,443,275 (GRCm39) |
missense |
probably benign |
0.00 |
R9087:Dnah12
|
UTSW |
14 |
26,546,503 (GRCm39) |
missense |
probably damaging |
1.00 |
R9099:Dnah12
|
UTSW |
14 |
26,492,325 (GRCm39) |
missense |
probably benign |
0.31 |
R9153:Dnah12
|
UTSW |
14 |
26,536,569 (GRCm39) |
missense |
probably damaging |
1.00 |
R9177:Dnah12
|
UTSW |
14 |
26,571,255 (GRCm39) |
missense |
possibly damaging |
0.84 |
R9214:Dnah12
|
UTSW |
14 |
26,445,060 (GRCm39) |
missense |
probably benign |
0.02 |
R9268:Dnah12
|
UTSW |
14 |
26,571,255 (GRCm39) |
missense |
possibly damaging |
0.84 |
R9274:Dnah12
|
UTSW |
14 |
26,537,374 (GRCm39) |
missense |
probably benign |
0.00 |
R9293:Dnah12
|
UTSW |
14 |
26,495,016 (GRCm39) |
missense |
probably benign |
|
R9322:Dnah12
|
UTSW |
14 |
26,492,934 (GRCm39) |
missense |
possibly damaging |
0.75 |
R9353:Dnah12
|
UTSW |
14 |
26,578,507 (GRCm39) |
missense |
probably damaging |
1.00 |
R9506:Dnah12
|
UTSW |
14 |
26,514,168 (GRCm39) |
missense |
probably benign |
0.00 |
R9518:Dnah12
|
UTSW |
14 |
26,495,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R9524:Dnah12
|
UTSW |
14 |
26,572,494 (GRCm39) |
missense |
probably null |
0.91 |
R9562:Dnah12
|
UTSW |
14 |
26,597,281 (GRCm39) |
missense |
possibly damaging |
0.58 |
R9565:Dnah12
|
UTSW |
14 |
26,597,281 (GRCm39) |
missense |
possibly damaging |
0.58 |
R9573:Dnah12
|
UTSW |
14 |
26,414,619 (GRCm39) |
missense |
probably benign |
|
R9581:Dnah12
|
UTSW |
14 |
26,491,985 (GRCm39) |
missense |
probably damaging |
1.00 |
R9689:Dnah12
|
UTSW |
14 |
26,590,871 (GRCm39) |
missense |
probably null |
1.00 |
R9727:Dnah12
|
UTSW |
14 |
26,523,510 (GRCm39) |
nonsense |
probably null |
|
V7580:Dnah12
|
UTSW |
14 |
26,495,050 (GRCm39) |
missense |
possibly damaging |
0.95 |
V7581:Dnah12
|
UTSW |
14 |
26,495,050 (GRCm39) |
missense |
possibly damaging |
0.95 |
X0018:Dnah12
|
UTSW |
14 |
26,536,437 (GRCm39) |
missense |
probably damaging |
1.00 |
X0027:Dnah12
|
UTSW |
14 |
26,538,245 (GRCm39) |
missense |
probably damaging |
1.00 |
X0065:Dnah12
|
UTSW |
14 |
26,536,602 (GRCm39) |
missense |
possibly damaging |
0.93 |
Z1177:Dnah12
|
UTSW |
14 |
26,597,172 (GRCm39) |
missense |
probably damaging |
1.00 |
|