Other mutations in this stock |
Total: 74 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca16 |
T |
G |
7: 120,023,021 (GRCm39) |
I52M |
possibly damaging |
Het |
Agbl5 |
G |
T |
5: 31,049,335 (GRCm39) |
|
probably null |
Het |
Akt2 |
T |
C |
7: 27,336,334 (GRCm39) |
|
probably benign |
Het |
Arl6ip5 |
T |
A |
6: 97,209,378 (GRCm39) |
S138T |
probably damaging |
Het |
Atp9b |
A |
G |
18: 80,952,800 (GRCm39) |
|
probably benign |
Het |
Ccdc171 |
A |
T |
4: 83,553,919 (GRCm39) |
N422Y |
probably damaging |
Het |
Ccr5 |
C |
T |
9: 123,924,951 (GRCm39) |
P185S |
possibly damaging |
Het |
Cep63 |
G |
T |
9: 102,500,759 (GRCm39) |
Q38K |
probably benign |
Het |
Cgn |
T |
C |
3: 94,682,242 (GRCm39) |
S446G |
probably benign |
Het |
Col16a1 |
T |
A |
4: 129,952,206 (GRCm39) |
|
probably benign |
Het |
Csmd1 |
T |
A |
8: 15,968,330 (GRCm39) |
Q3099L |
probably damaging |
Het |
Dcc |
G |
A |
18: 71,708,279 (GRCm39) |
T479I |
possibly damaging |
Het |
Dclre1a |
A |
G |
19: 56,535,067 (GRCm39) |
|
probably null |
Het |
Dlg1 |
T |
A |
16: 31,502,992 (GRCm39) |
C66* |
probably null |
Het |
Dnajb9 |
T |
A |
12: 44,253,987 (GRCm39) |
H140L |
probably damaging |
Het |
Dnase1 |
G |
A |
16: 3,857,413 (GRCm39) |
V237M |
probably damaging |
Het |
Dscam |
C |
A |
16: 96,456,105 (GRCm39) |
E1274D |
probably benign |
Het |
Epb41 |
T |
C |
4: 131,727,572 (GRCm39) |
H243R |
probably damaging |
Het |
Evc |
T |
A |
5: 37,473,656 (GRCm39) |
|
probably benign |
Het |
Fcgrt |
T |
A |
7: 44,752,493 (GRCm39) |
M1L |
unknown |
Het |
Flii |
T |
C |
11: 60,610,506 (GRCm39) |
|
probably null |
Het |
Gen1 |
A |
G |
12: 11,298,355 (GRCm39) |
|
probably benign |
Het |
Gm10447 |
T |
C |
11: 53,347,257 (GRCm39) |
|
probably benign |
Het |
Gm57858 |
A |
G |
3: 36,101,054 (GRCm39) |
|
probably benign |
Het |
Gm8674 |
A |
T |
13: 50,055,975 (GRCm39) |
|
noncoding transcript |
Het |
Gpr137 |
G |
C |
19: 6,916,491 (GRCm39) |
D253E |
probably damaging |
Het |
Grid2ip |
A |
T |
5: 143,343,652 (GRCm39) |
D116V |
probably benign |
Het |
Grin2c |
A |
G |
11: 115,151,554 (GRCm39) |
|
probably benign |
Het |
Havcr1 |
A |
G |
11: 46,647,051 (GRCm39) |
T162A |
possibly damaging |
Het |
Hspa1l |
A |
T |
17: 35,196,386 (GRCm39) |
T142S |
probably benign |
Het |
Ift140 |
T |
A |
17: 25,267,409 (GRCm39) |
Y602* |
probably null |
Het |
Il18 |
T |
A |
9: 50,490,575 (GRCm39) |
|
probably benign |
Het |
Ilf3 |
T |
C |
9: 21,309,266 (GRCm39) |
V474A |
probably damaging |
Het |
Inppl1 |
T |
C |
7: 101,476,664 (GRCm39) |
Y771C |
probably damaging |
Het |
Ints2 |
T |
C |
11: 86,125,575 (GRCm39) |
T542A |
probably benign |
Het |
Ipo7 |
T |
C |
7: 109,648,868 (GRCm39) |
Y714H |
probably benign |
Het |
Itgbl1 |
T |
A |
14: 124,077,997 (GRCm39) |
C162* |
probably null |
Het |
Kcp |
T |
C |
6: 29,496,926 (GRCm39) |
H561R |
possibly damaging |
Het |
Krt23 |
G |
T |
11: 99,376,613 (GRCm39) |
T181N |
probably benign |
Het |
Lrrc40 |
A |
T |
3: 157,746,108 (GRCm39) |
D61V |
probably damaging |
Het |
Lypd4 |
T |
A |
7: 24,564,691 (GRCm39) |
H149L |
probably benign |
Het |
Map3k4 |
A |
G |
17: 12,473,058 (GRCm39) |
F953L |
probably damaging |
Het |
Mctp1 |
C |
T |
13: 76,972,982 (GRCm39) |
P405S |
probably damaging |
Het |
Mfsd2a |
G |
A |
4: 122,845,632 (GRCm39) |
T173I |
possibly damaging |
Het |
Mtus1 |
T |
C |
8: 41,535,965 (GRCm39) |
T584A |
probably benign |
Het |
Nell2 |
A |
G |
15: 95,330,782 (GRCm39) |
V213A |
probably benign |
Het |
Nipsnap1 |
G |
A |
11: 4,839,957 (GRCm39) |
G226E |
probably damaging |
Het |
Nudt15 |
T |
C |
14: 73,760,824 (GRCm39) |
Y89C |
probably damaging |
Het |
Or10g7 |
T |
A |
9: 39,905,459 (GRCm39) |
S118T |
possibly damaging |
Het |
Or10h28 |
T |
A |
17: 33,488,109 (GRCm39) |
M137K |
probably damaging |
Het |
Or13p3 |
T |
A |
4: 118,566,808 (GRCm39) |
M68K |
probably benign |
Het |
Or7a37 |
T |
G |
10: 78,806,267 (GRCm39) |
S261R |
probably damaging |
Het |
Phf24 |
A |
C |
4: 42,933,891 (GRCm39) |
E91A |
probably damaging |
Het |
Plbd1 |
T |
A |
6: 136,618,165 (GRCm39) |
N17I |
possibly damaging |
Het |
Por |
C |
T |
5: 135,761,438 (GRCm39) |
S308L |
probably benign |
Het |
Prmt8 |
T |
A |
6: 127,688,837 (GRCm39) |
K178* |
probably null |
Het |
Rev3l |
A |
G |
10: 39,693,282 (GRCm39) |
N454S |
probably damaging |
Het |
Rps6ka2 |
T |
C |
17: 7,539,009 (GRCm39) |
V309A |
probably benign |
Het |
Slc15a5 |
A |
G |
6: 137,995,112 (GRCm39) |
|
probably benign |
Het |
Slc30a6 |
G |
A |
17: 74,730,198 (GRCm39) |
V363I |
probably benign |
Het |
Snf8 |
G |
A |
11: 95,930,125 (GRCm39) |
M42I |
probably benign |
Het |
Stom |
T |
C |
2: 35,215,371 (GRCm39) |
I65V |
probably benign |
Het |
Tacr3 |
C |
T |
3: 134,637,989 (GRCm39) |
T382I |
probably benign |
Het |
Tenm3 |
A |
G |
8: 48,682,010 (GRCm39) |
V2540A |
probably damaging |
Het |
Trabd |
A |
G |
15: 88,969,816 (GRCm39) |
T314A |
possibly damaging |
Het |
Tyk2 |
T |
C |
9: 21,025,486 (GRCm39) |
|
probably null |
Het |
Ube4a |
T |
C |
9: 44,856,099 (GRCm39) |
|
probably benign |
Het |
Unc80 |
A |
G |
1: 66,589,015 (GRCm39) |
H1060R |
possibly damaging |
Het |
Virma |
A |
T |
4: 11,528,626 (GRCm39) |
K1288* |
probably null |
Het |
Vmn2r100 |
A |
C |
17: 19,751,582 (GRCm39) |
I542L |
probably benign |
Het |
Vwde |
T |
C |
6: 13,187,806 (GRCm39) |
|
probably benign |
Het |
Zfc3h1 |
T |
C |
10: 115,245,018 (GRCm39) |
I797T |
possibly damaging |
Het |
Zfp74 |
C |
T |
7: 29,653,466 (GRCm39) |
|
probably benign |
Het |
Zkscan7 |
T |
A |
9: 122,717,872 (GRCm39) |
L89Q |
probably 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 |
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 |
|