Other mutations in this stock |
Total: 117 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca15 |
C |
A |
7: 119,945,221 (GRCm39) |
N432K |
possibly damaging |
Het |
Abitram |
A |
G |
4: 56,804,230 (GRCm39) |
I82V |
probably null |
Het |
Adamtsl5 |
G |
A |
10: 80,180,693 (GRCm39) |
T123I |
probably benign |
Het |
Aff4 |
T |
C |
11: 53,263,702 (GRCm39) |
S241P |
probably damaging |
Het |
Agl |
A |
G |
3: 116,552,404 (GRCm39) |
L510P |
|
Het |
Aox1 |
A |
T |
1: 58,329,142 (GRCm39) |
K196* |
probably null |
Het |
Arhgef37 |
A |
G |
18: 61,637,456 (GRCm39) |
L402P |
probably damaging |
Het |
Arid4b |
T |
C |
13: 14,355,891 (GRCm39) |
|
probably null |
Het |
Atp5pb |
A |
G |
3: 105,851,118 (GRCm39) |
V193A |
probably benign |
Het |
Atp8b3 |
A |
G |
10: 80,365,463 (GRCm39) |
|
probably null |
Het |
Baz2a |
G |
T |
10: 127,951,947 (GRCm39) |
R555L |
probably damaging |
Het |
Casp4 |
G |
T |
9: 5,321,345 (GRCm39) |
S32I |
possibly damaging |
Het |
Cd300lb |
A |
G |
11: 114,819,128 (GRCm39) |
V167A |
probably damaging |
Het |
Cdc42bpg |
C |
T |
19: 6,368,428 (GRCm39) |
T1042I |
probably damaging |
Het |
Ceacam20 |
T |
C |
7: 19,704,159 (GRCm39) |
F70S |
probably damaging |
Het |
Cep162 |
C |
T |
9: 87,074,819 (GRCm39) |
V1388I |
probably damaging |
Het |
Cfap65 |
A |
G |
1: 74,959,585 (GRCm39) |
V855A |
possibly damaging |
Het |
Chil3 |
G |
T |
3: 106,063,022 (GRCm39) |
D189E |
probably benign |
Het |
Cln3 |
A |
G |
7: 126,180,912 (GRCm39) |
I43T |
probably benign |
Het |
Cntnap5a |
A |
G |
1: 116,370,110 (GRCm39) |
Q909R |
probably benign |
Het |
Ctsd |
C |
A |
7: 141,937,278 (GRCm39) |
A77S |
probably damaging |
Het |
Dnah17 |
T |
A |
11: 117,981,543 (GRCm39) |
Q1716L |
probably null |
Het |
Dock3 |
C |
A |
9: 106,772,782 (GRCm39) |
M490I |
probably benign |
Het |
Erg |
T |
C |
16: 95,260,015 (GRCm39) |
|
probably null |
Het |
Farp2 |
A |
T |
1: 93,548,950 (GRCm39) |
M1019L |
possibly damaging |
Het |
Fcgbp |
A |
G |
7: 27,785,949 (GRCm39) |
K462R |
probably benign |
Het |
Fn1 |
A |
T |
1: 71,688,384 (GRCm39) |
N173K |
probably damaging |
Het |
Fsip2 |
A |
T |
2: 82,810,441 (GRCm39) |
L2253F |
probably damaging |
Het |
Gabrd |
C |
T |
4: 155,469,970 (GRCm39) |
R413H |
possibly damaging |
Het |
Galnt5 |
A |
T |
2: 57,907,151 (GRCm39) |
D538V |
probably damaging |
Het |
Gje1 |
T |
A |
10: 14,592,223 (GRCm39) |
L186F |
probably damaging |
Het |
Gm16686 |
A |
T |
4: 88,673,563 (GRCm39) |
C89S |
unknown |
Het |
Gna15 |
G |
T |
10: 81,338,831 (GRCm39) |
A336E |
probably benign |
Het |
Golga4 |
C |
T |
9: 118,388,563 (GRCm39) |
S1895L |
probably benign |
Het |
Gon4l |
A |
T |
3: 88,814,829 (GRCm39) |
M1933L |
probably benign |
Het |
Gpr183 |
T |
C |
14: 122,192,156 (GRCm39) |
S122G |
possibly damaging |
Het |
Gtf2h4 |
G |
A |
17: 35,980,250 (GRCm39) |
T348I |
probably damaging |
Het |
Hace1 |
T |
C |
10: 45,481,636 (GRCm39) |
Y120H |
probably damaging |
Het |
Hivep2 |
C |
T |
10: 14,007,061 (GRCm39) |
H1220Y |
possibly damaging |
Het |
Hmx2 |
T |
C |
7: 131,156,232 (GRCm39) |
F66S |
probably benign |
Het |
Hoxd12 |
A |
T |
2: 74,505,569 (GRCm39) |
S47C |
possibly damaging |
Het |
Hp |
C |
A |
8: 110,301,832 (GRCm39) |
|
probably null |
Het |
Idh3a |
T |
A |
9: 54,508,492 (GRCm39) |
D355E |
probably benign |
Het |
Itga2b |
A |
T |
11: 102,347,120 (GRCm39) |
M921K |
probably benign |
Het |
Jcad |
A |
G |
18: 4,675,529 (GRCm39) |
D1097G |
probably benign |
Het |
Kdm5b |
A |
T |
1: 134,523,571 (GRCm39) |
T249S |
probably benign |
Het |
Klhl11 |
G |
T |
11: 100,355,178 (GRCm39) |
H214Q |
probably benign |
Het |
L3hypdh |
A |
T |
12: 72,131,705 (GRCm39) |
Y76N |
probably damaging |
Het |
Lama4 |
G |
T |
10: 38,921,751 (GRCm39) |
R424L |
possibly damaging |
Het |
Lepr |
A |
G |
4: 101,602,853 (GRCm39) |
I214V |
probably benign |
Het |
Lipc |
G |
T |
9: 70,709,450 (GRCm39) |
N432K |
probably benign |
Het |
Lipm |
C |
T |
19: 34,093,598 (GRCm39) |
A216V |
possibly damaging |
Het |
Lrrc23 |
A |
G |
6: 124,756,088 (GRCm39) |
S2P |
unknown |
Het |
Lyst |
T |
A |
13: 13,812,109 (GRCm39) |
D840E |
probably benign |
Het |
Mmp23 |
T |
A |
4: 155,736,041 (GRCm39) |
T204S |
probably damaging |
Het |
Mms19 |
T |
C |
19: 41,936,717 (GRCm39) |
T785A |
probably benign |
Het |
Mov10 |
A |
T |
3: 104,707,368 (GRCm39) |
|
probably null |
Het |
Mtf2 |
A |
G |
5: 108,248,836 (GRCm39) |
T383A |
probably benign |
Het |
Myo5c |
G |
A |
9: 75,158,809 (GRCm39) |
|
probably null |
Het |
Nfxl1 |
A |
T |
5: 72,681,517 (GRCm39) |
C671* |
probably null |
Het |
Npepps |
A |
G |
11: 97,103,982 (GRCm39) |
V813A |
probably benign |
Het |
Nrn1 |
C |
A |
13: 36,910,825 (GRCm39) |
W69L |
probably damaging |
Het |
Oprd1 |
A |
C |
4: 131,841,378 (GRCm39) |
D193E |
probably benign |
Het |
Or2ag1b |
T |
A |
7: 106,288,417 (GRCm39) |
I174F |
possibly damaging |
Het |
Or52p1 |
C |
T |
7: 104,267,059 (GRCm39) |
H58Y |
probably damaging |
Het |
Or55b3 |
A |
T |
7: 102,126,883 (GRCm39) |
Y65N |
probably damaging |
Het |
Or56b2j |
T |
A |
7: 104,352,796 (GRCm39) |
D7E |
probably benign |
Het |
Or6c202 |
A |
G |
10: 128,996,620 (GRCm39) |
Y78H |
possibly damaging |
Het |
Or6c209 |
T |
C |
10: 129,483,027 (GRCm39) |
I10T |
probably damaging |
Het |
Or6k6 |
A |
C |
1: 173,944,753 (GRCm39) |
F276L |
probably benign |
Het |
Pcdhac1 |
G |
T |
18: 37,225,550 (GRCm39) |
V788L |
probably benign |
Het |
Pcdhb11 |
G |
A |
18: 37,556,313 (GRCm39) |
V548M |
probably damaging |
Het |
Pde4c |
A |
T |
8: 71,201,621 (GRCm39) |
E517V |
possibly damaging |
Het |
Pdzd7 |
T |
C |
19: 45,022,086 (GRCm39) |
R521G |
possibly damaging |
Het |
Pik3c2a |
T |
A |
7: 115,972,089 (GRCm39) |
K780N |
probably damaging |
Het |
Plb1 |
T |
G |
5: 32,478,591 (GRCm39) |
|
probably null |
Het |
Plcb4 |
T |
A |
2: 135,842,139 (GRCm39) |
L1041Q |
probably benign |
Het |
Pnpla6 |
G |
A |
8: 3,566,540 (GRCm39) |
|
probably null |
Het |
Ppat |
A |
T |
5: 77,063,826 (GRCm39) |
N441K |
probably damaging |
Het |
Ppp1r1b |
G |
A |
11: 98,246,305 (GRCm39) |
A132T |
probably damaging |
Het |
Prl2c2 |
A |
C |
13: 13,172,065 (GRCm39) |
|
probably null |
Het |
Prr14 |
T |
C |
7: 127,074,458 (GRCm39) |
I330T |
probably benign |
Het |
Pycr1 |
T |
C |
11: 120,533,749 (GRCm39) |
D36G |
probably benign |
Het |
Rabep2 |
T |
A |
7: 126,037,891 (GRCm39) |
I221N |
probably damaging |
Het |
Rad23b |
A |
G |
4: 55,370,469 (GRCm39) |
D165G |
probably benign |
Het |
Reln |
G |
A |
5: 22,176,951 (GRCm39) |
T1905I |
probably damaging |
Het |
Ripor2 |
T |
C |
13: 24,878,188 (GRCm39) |
V321A |
probably benign |
Het |
Rnf43 |
A |
G |
11: 87,622,678 (GRCm39) |
D466G |
probably benign |
Het |
Rpl6 |
A |
T |
5: 121,343,655 (GRCm39) |
R63W |
possibly damaging |
Het |
S100a14 |
A |
G |
3: 90,435,511 (GRCm39) |
T102A |
probably benign |
Het |
Samd11 |
C |
A |
4: 156,333,857 (GRCm39) |
V195L |
probably benign |
Het |
Scaper |
G |
A |
9: 55,669,561 (GRCm39) |
Q372* |
probably null |
Het |
Sec14l5 |
G |
T |
16: 4,998,739 (GRCm39) |
C593F |
probably damaging |
Het |
Sema6d |
T |
C |
2: 124,496,078 (GRCm39) |
Y41H |
probably damaging |
Het |
Serac1 |
G |
A |
17: 6,119,589 (GRCm39) |
R114W |
probably damaging |
Het |
Slc12a4 |
T |
C |
8: 106,677,468 (GRCm39) |
E388G |
probably benign |
Het |
Smarcd3 |
T |
C |
5: 24,800,810 (GRCm39) |
T164A |
probably benign |
Het |
Smtn |
C |
A |
11: 3,480,249 (GRCm39) |
R324L |
probably benign |
Het |
Spata31d1c |
C |
T |
13: 65,183,175 (GRCm39) |
P239L |
probably benign |
Het |
Srcap |
T |
C |
7: 127,137,689 (GRCm39) |
V1013A |
possibly damaging |
Het |
Sv2b |
T |
C |
7: 74,773,812 (GRCm39) |
N553S |
probably damaging |
Het |
Tex35 |
T |
A |
1: 156,932,656 (GRCm39) |
N52I |
probably damaging |
Het |
Ticrr |
T |
C |
7: 79,343,734 (GRCm39) |
S1200P |
probably benign |
Het |
Tmem19 |
A |
G |
10: 115,183,604 (GRCm39) |
L125P |
probably damaging |
Het |
Trio |
A |
G |
15: 27,856,193 (GRCm39) |
V666A |
probably benign |
Het |
Ttn |
T |
C |
2: 76,747,627 (GRCm39) |
D4474G |
probably benign |
Het |
Usp43 |
A |
T |
11: 67,783,842 (GRCm39) |
S368T |
possibly damaging |
Het |
Vmn2r72 |
T |
A |
7: 85,400,348 (GRCm39) |
M234L |
probably benign |
Het |
Wdr93 |
T |
A |
7: 79,427,055 (GRCm39) |
|
probably null |
Het |
Wrap73 |
T |
A |
4: 154,240,584 (GRCm39) |
W359R |
probably damaging |
Het |
Ywhah |
A |
G |
5: 33,183,985 (GRCm39) |
I63V |
probably benign |
Het |
Zbtb7b |
G |
T |
3: 89,288,366 (GRCm39) |
P151T |
probably damaging |
Het |
Zfp318 |
A |
G |
17: 46,710,995 (GRCm39) |
N906S |
probably damaging |
Het |
Zfp423 |
C |
A |
8: 88,507,341 (GRCm39) |
C1001F |
probably damaging |
Het |
Zmym1 |
A |
G |
4: 126,943,191 (GRCm39) |
I399T |
possibly damaging |
Het |
Zmynd15 |
G |
A |
11: 70,353,014 (GRCm39) |
G296D |
probably benign |
Het |
Znfx1 |
T |
A |
2: 166,890,475 (GRCm39) |
I670F |
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 |
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 |
|
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 |
|