Other mutations in this stock |
Total: 89 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam19 |
T |
A |
11: 46,019,616 (GRCm39) |
C439S |
probably damaging |
Het |
Adnp2 |
T |
C |
18: 80,174,205 (GRCm39) |
Y68C |
probably damaging |
Het |
Ahctf1 |
A |
T |
1: 179,591,038 (GRCm39) |
D1247E |
probably benign |
Het |
Alms1 |
T |
A |
6: 85,606,192 (GRCm39) |
M2614K |
possibly damaging |
Het |
Alx3 |
A |
G |
3: 107,512,292 (GRCm39) |
H310R |
probably damaging |
Het |
Ambra1 |
C |
T |
2: 91,741,773 (GRCm39) |
T1016M |
probably damaging |
Het |
Ankrd35 |
A |
G |
3: 96,591,331 (GRCm39) |
E539G |
probably damaging |
Het |
Aptx |
A |
G |
4: 40,695,145 (GRCm39) |
|
probably benign |
Het |
Arsi |
C |
T |
18: 61,050,058 (GRCm39) |
R314C |
probably benign |
Het |
Atp1a3 |
T |
C |
7: 24,688,989 (GRCm39) |
|
probably benign |
Het |
Avl9 |
G |
T |
6: 56,713,468 (GRCm39) |
R242L |
probably benign |
Het |
Bicra |
G |
T |
7: 15,705,812 (GRCm39) |
T1543K |
probably benign |
Het |
Bltp2 |
T |
A |
11: 78,177,404 (GRCm39) |
V1903E |
possibly damaging |
Het |
Bzw2 |
A |
C |
12: 36,180,014 (GRCm39) |
I71S |
probably damaging |
Het |
Camk2a |
C |
T |
18: 61,093,079 (GRCm39) |
A302V |
probably damaging |
Het |
Ccdc12 |
A |
G |
9: 110,485,665 (GRCm39) |
E12G |
possibly damaging |
Het |
Cd300lb |
A |
T |
11: 114,819,164 (GRCm39) |
F19Y |
probably benign |
Het |
Clcn3 |
A |
T |
8: 61,380,330 (GRCm39) |
C535* |
probably null |
Het |
Cntnap5c |
A |
G |
17: 58,506,012 (GRCm39) |
T679A |
probably benign |
Het |
Cpsf7 |
G |
A |
19: 10,516,993 (GRCm39) |
S365N |
possibly damaging |
Het |
Cspg4b |
T |
A |
13: 113,505,310 (GRCm39) |
S2146R |
probably benign |
Het |
Cyp20a1 |
T |
C |
1: 60,426,285 (GRCm39) |
|
probably benign |
Het |
Decr2 |
A |
T |
17: 26,302,027 (GRCm39) |
N234K |
probably benign |
Het |
Def8 |
G |
A |
8: 124,183,234 (GRCm39) |
A278T |
probably damaging |
Het |
Dock1 |
T |
C |
7: 134,331,793 (GRCm39) |
|
probably benign |
Het |
Dpy19l4 |
A |
T |
4: 11,267,619 (GRCm39) |
N440K |
probably damaging |
Het |
Eprs1 |
T |
C |
1: 185,146,588 (GRCm39) |
V1206A |
probably damaging |
Het |
Exoc6b |
A |
G |
6: 84,831,681 (GRCm39) |
|
probably null |
Het |
Fam184b |
A |
G |
5: 45,712,536 (GRCm39) |
|
probably benign |
Het |
Fcho1 |
A |
T |
8: 72,161,597 (GRCm39) |
S858T |
probably damaging |
Het |
Fgfr1 |
A |
G |
8: 26,058,214 (GRCm39) |
D430G |
possibly damaging |
Het |
Fmnl3 |
T |
C |
15: 99,219,013 (GRCm39) |
T807A |
probably damaging |
Het |
Gabra5 |
T |
C |
7: 57,063,476 (GRCm39) |
Y316C |
probably damaging |
Het |
Gh |
A |
G |
11: 106,192,346 (GRCm39) |
L16P |
probably damaging |
Het |
Glipr2 |
A |
T |
4: 43,970,532 (GRCm39) |
I87F |
probably damaging |
Het |
Glrb |
T |
A |
3: 80,763,221 (GRCm39) |
I259F |
probably damaging |
Het |
Gpr63 |
T |
C |
4: 25,007,651 (GRCm39) |
L125P |
probably damaging |
Het |
Grb2 |
A |
G |
11: 115,546,251 (GRCm39) |
Y37H |
probably damaging |
Het |
Haus2 |
G |
A |
2: 120,449,449 (GRCm39) |
|
probably benign |
Het |
Hmgcr |
T |
C |
13: 96,788,653 (GRCm39) |
N749S |
probably damaging |
Het |
Igf1r |
T |
C |
7: 67,814,990 (GRCm39) |
V297A |
probably damaging |
Het |
Il12rb2 |
G |
T |
6: 67,293,270 (GRCm39) |
P69H |
probably damaging |
Het |
Ints3 |
C |
A |
3: 90,315,818 (GRCm39) |
M315I |
probably benign |
Het |
Izumo2 |
C |
T |
7: 44,364,833 (GRCm39) |
T116I |
probably benign |
Het |
Kctd19 |
A |
C |
8: 106,121,993 (GRCm39) |
Y185D |
probably damaging |
Het |
Lama4 |
A |
G |
10: 38,936,218 (GRCm39) |
N631S |
possibly damaging |
Het |
Lama5 |
T |
G |
2: 179,819,872 (GRCm39) |
|
probably null |
Het |
Lamc1 |
A |
C |
1: 153,138,185 (GRCm39) |
L223R |
probably damaging |
Het |
Lgr4 |
G |
A |
2: 109,828,010 (GRCm39) |
|
probably null |
Het |
Loxhd1 |
T |
C |
18: 77,427,196 (GRCm39) |
L398P |
probably damaging |
Het |
Mapk9 |
T |
A |
11: 49,757,866 (GRCm39) |
D103E |
possibly damaging |
Het |
Marchf6 |
T |
C |
15: 31,469,678 (GRCm39) |
|
probably benign |
Het |
Mlxipl |
G |
A |
5: 135,162,043 (GRCm39) |
|
probably benign |
Het |
Mrgbp |
C |
A |
2: 180,225,231 (GRCm39) |
D62E |
probably benign |
Het |
Mtap |
A |
T |
4: 89,070,235 (GRCm39) |
|
probably benign |
Het |
Myt1 |
G |
A |
2: 181,443,664 (GRCm39) |
G497S |
probably damaging |
Het |
Naa25 |
T |
G |
5: 121,545,247 (GRCm39) |
|
probably benign |
Het |
Nfat5 |
C |
T |
8: 108,065,707 (GRCm39) |
R156W |
probably damaging |
Het |
Nkpd1 |
T |
C |
7: 19,253,852 (GRCm39) |
C73R |
probably benign |
Het |
Nup210l |
T |
C |
3: 90,027,218 (GRCm39) |
I200T |
probably damaging |
Het |
Nvl |
C |
A |
1: 180,941,698 (GRCm39) |
D581Y |
probably damaging |
Het |
Or51a6 |
T |
C |
7: 102,604,185 (GRCm39) |
M208V |
probably benign |
Het |
Or51f2 |
T |
C |
7: 102,527,068 (GRCm39) |
V247A |
probably benign |
Het |
Or5t17 |
T |
A |
2: 86,832,710 (GRCm39) |
Y132* |
probably null |
Het |
Or8b1c |
A |
G |
9: 38,384,612 (GRCm39) |
T190A |
probably benign |
Het |
Or9q1 |
T |
C |
19: 13,805,050 (GRCm39) |
T237A |
probably damaging |
Het |
Pcdh7 |
G |
T |
5: 58,070,590 (GRCm39) |
E1089D |
probably benign |
Het |
Pik3cd |
A |
G |
4: 149,740,836 (GRCm39) |
|
probably null |
Het |
Plekhh2 |
A |
T |
17: 84,864,820 (GRCm39) |
K69N |
probably damaging |
Het |
Ptgdr2 |
G |
A |
19: 10,917,792 (GRCm39) |
C103Y |
probably damaging |
Het |
Rrad |
A |
C |
8: 105,355,299 (GRCm39) |
H236Q |
probably benign |
Het |
Rslcan18 |
C |
T |
13: 67,246,533 (GRCm39) |
A236T |
probably benign |
Het |
Ryr2 |
C |
A |
13: 11,839,265 (GRCm39) |
D503Y |
probably damaging |
Het |
Siglec1 |
T |
C |
2: 130,916,980 (GRCm39) |
T1092A |
probably benign |
Het |
Siglecf |
A |
G |
7: 43,005,350 (GRCm39) |
T437A |
probably benign |
Het |
Spta1 |
A |
T |
1: 174,032,839 (GRCm39) |
Q965H |
probably damaging |
Het |
Stk10 |
A |
T |
11: 32,539,460 (GRCm39) |
E280V |
probably benign |
Het |
Tfg |
T |
C |
16: 56,511,351 (GRCm39) |
Y326C |
possibly damaging |
Het |
Tpp2 |
T |
A |
1: 43,999,299 (GRCm39) |
S358T |
possibly damaging |
Het |
Trim25 |
G |
T |
11: 88,906,598 (GRCm39) |
V437L |
probably benign |
Het |
Ttn |
T |
C |
2: 76,574,027 (GRCm39) |
D25622G |
probably damaging |
Het |
Ube3b |
T |
A |
5: 114,536,912 (GRCm39) |
S303R |
probably benign |
Het |
Ush2a |
T |
A |
1: 188,310,688 (GRCm39) |
V2088D |
probably damaging |
Het |
Vmn2r103 |
A |
G |
17: 20,032,241 (GRCm39) |
T672A |
probably damaging |
Het |
Wdr11 |
G |
T |
7: 129,200,785 (GRCm39) |
G79C |
probably damaging |
Het |
Wdr89 |
T |
A |
12: 75,679,367 (GRCm39) |
T296S |
probably benign |
Het |
Zdhhc24 |
T |
A |
19: 4,930,402 (GRCm39) |
L179M |
possibly damaging |
Het |
Zfp981 |
T |
C |
4: 146,622,217 (GRCm39) |
C381R |
probably damaging |
Het |
Zim1 |
A |
G |
7: 6,679,947 (GRCm39) |
I572T |
probably benign |
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 |
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 |
R1829:Dnah12
|
UTSW |
14 |
26,494,980 (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 |
26,500,869 (GRCm39) |
critical splice donor site |
probably null |
|
R7135:Dnah12
|
UTSW |
14 |
26,523,370 (GRCm39) |
missense |
probably damaging |
0.99 |
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 |
|