Other mutations in this stock |
Total: 83 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam1b |
T |
A |
5: 121,638,970 (GRCm39) |
T692S |
probably benign |
Het |
Adgrf3 |
T |
A |
5: 30,408,553 (GRCm39) |
N75I |
probably benign |
Het |
Adgrg5 |
A |
G |
8: 95,664,373 (GRCm39) |
M328V |
probably damaging |
Het |
Adk |
A |
G |
14: 21,431,668 (GRCm39) |
D286G |
probably benign |
Het |
Ankrd28 |
T |
A |
14: 31,429,201 (GRCm39) |
D917V |
probably damaging |
Het |
Appl2 |
C |
T |
10: 83,457,446 (GRCm39) |
D141N |
probably damaging |
Het |
Arfgef2 |
T |
C |
2: 166,706,632 (GRCm39) |
V952A |
probably damaging |
Het |
Arpc2 |
T |
A |
1: 74,287,391 (GRCm39) |
H70Q |
probably damaging |
Het |
Bpifa5 |
T |
C |
2: 154,009,580 (GRCm39) |
L261P |
probably damaging |
Het |
Brca1 |
G |
T |
11: 101,415,281 (GRCm39) |
T951K |
probably damaging |
Het |
Ccdc73 |
A |
T |
2: 104,822,450 (GRCm39) |
S800C |
probably damaging |
Het |
Cdh15 |
C |
G |
8: 123,588,755 (GRCm39) |
D276E |
probably benign |
Het |
Cfap119 |
A |
G |
7: 127,186,745 (GRCm39) |
|
probably null |
Het |
Cfap418 |
T |
A |
4: 10,874,644 (GRCm39) |
D10E |
probably damaging |
Het |
Cfh |
T |
C |
1: 140,030,575 (GRCm39) |
I551V |
probably damaging |
Het |
Chd7 |
T |
A |
4: 8,833,960 (GRCm39) |
L1238Q |
probably damaging |
Het |
Chd9 |
T |
G |
8: 91,728,410 (GRCm39) |
F1275L |
probably damaging |
Het |
Chrnb3 |
A |
G |
8: 27,883,728 (GRCm39) |
Y155C |
probably damaging |
Het |
Cltc |
C |
A |
11: 86,591,886 (GRCm39) |
|
probably null |
Het |
Ctsll3 |
T |
A |
13: 60,948,791 (GRCm39) |
N55Y |
probably damaging |
Het |
Cysltr2 |
T |
C |
14: 73,267,321 (GRCm39) |
M130V |
probably benign |
Het |
Daglb |
T |
C |
5: 143,480,361 (GRCm39) |
M455T |
probably benign |
Het |
Dbn1 |
A |
G |
13: 55,624,521 (GRCm39) |
S343P |
probably benign |
Het |
Dusp6 |
T |
A |
10: 99,099,555 (GRCm39) |
M1K |
probably null |
Het |
Eif3m |
T |
C |
2: 104,847,298 (GRCm39) |
E12G |
probably damaging |
Het |
Epha2 |
T |
C |
4: 141,033,828 (GRCm39) |
V29A |
possibly damaging |
Het |
Farp2 |
T |
A |
1: 93,488,047 (GRCm39) |
N91K |
probably damaging |
Het |
Ferd3l |
C |
A |
12: 33,978,971 (GRCm39) |
S161R |
probably benign |
Het |
Fgd2 |
A |
T |
17: 29,587,219 (GRCm39) |
D315V |
possibly damaging |
Het |
Fhip2a |
T |
C |
19: 57,367,603 (GRCm39) |
W337R |
probably damaging |
Het |
Fstl4 |
T |
A |
11: 53,056,705 (GRCm39) |
|
probably null |
Het |
Grm5 |
A |
G |
7: 87,685,311 (GRCm39) |
D476G |
possibly damaging |
Het |
Gtf3c3 |
C |
T |
1: 54,456,937 (GRCm39) |
A488T |
probably damaging |
Het |
Hdlbp |
A |
G |
1: 93,364,922 (GRCm39) |
L115P |
probably damaging |
Het |
Hk2 |
T |
A |
6: 82,721,932 (GRCm39) |
N136Y |
probably damaging |
Het |
Hs2st1 |
G |
T |
3: 144,140,415 (GRCm39) |
A302E |
probably benign |
Het |
Htr7 |
T |
C |
19: 35,947,136 (GRCm39) |
N293D |
probably benign |
Het |
Ikbkb |
T |
A |
8: 23,163,496 (GRCm39) |
E271D |
probably benign |
Het |
Il5ra |
A |
T |
6: 106,715,335 (GRCm39) |
Y166* |
probably null |
Het |
Il9r |
T |
A |
11: 32,143,227 (GRCm39) |
H244L |
probably benign |
Het |
Itih4 |
T |
C |
14: 30,613,456 (GRCm39) |
|
probably null |
Het |
Kirrel1 |
C |
T |
3: 86,996,458 (GRCm39) |
M380I |
probably null |
Het |
Large1 |
A |
T |
8: 73,544,710 (GRCm39) |
D689E |
probably damaging |
Het |
Limk2 |
A |
G |
11: 3,303,275 (GRCm39) |
|
probably null |
Het |
Med15 |
A |
G |
16: 17,540,644 (GRCm39) |
F34S |
probably damaging |
Het |
Mprip |
C |
T |
11: 59,643,357 (GRCm39) |
T505I |
probably damaging |
Het |
Mtor |
T |
A |
4: 148,623,364 (GRCm39) |
N2071K |
probably benign |
Het |
Muc16 |
A |
G |
9: 18,408,729 (GRCm39) |
L2522P |
probably damaging |
Het |
Myd88 |
A |
T |
9: 119,166,908 (GRCm39) |
|
probably null |
Het |
Myo7a |
A |
C |
7: 97,741,703 (GRCm39) |
F484V |
possibly damaging |
Het |
Nme1 |
A |
C |
11: 93,851,593 (GRCm39) |
L81R |
probably benign |
Het |
Ntn4 |
T |
A |
10: 93,569,464 (GRCm39) |
|
probably null |
Het |
Or2y13 |
T |
C |
11: 49,415,162 (GRCm39) |
V204A |
probably benign |
Het |
Or4p19 |
T |
C |
2: 88,242,444 (GRCm39) |
D186G |
probably damaging |
Het |
Or51l4 |
A |
T |
7: 103,404,131 (GRCm39) |
Y220* |
probably null |
Het |
Otogl |
T |
G |
10: 107,649,878 (GRCm39) |
N1159T |
probably damaging |
Het |
Pabpc6 |
G |
A |
17: 9,887,003 (GRCm39) |
T516I |
probably benign |
Het |
Pcdh1 |
C |
T |
18: 38,335,921 (GRCm39) |
R238H |
probably damaging |
Het |
Pex5l |
T |
A |
3: 33,008,531 (GRCm39) |
N151I |
probably benign |
Het |
Plekha7 |
T |
C |
7: 115,727,920 (GRCm39) |
N980S |
probably damaging |
Het |
Reg4 |
C |
T |
3: 98,143,677 (GRCm39) |
T157I |
probably benign |
Het |
Rev3l |
A |
T |
10: 39,700,612 (GRCm39) |
E1703V |
probably damaging |
Het |
Rev3l |
G |
T |
10: 39,700,611 (GRCm39) |
E1703* |
probably null |
Het |
Rsf1 |
GCG |
GCGACG |
7: 97,229,114 (GRCm39) |
|
probably benign |
Het |
Saal1 |
T |
C |
7: 46,342,340 (GRCm39) |
K368E |
probably damaging |
Het |
Scn9a |
C |
T |
2: 66,335,220 (GRCm39) |
W1245* |
probably null |
Het |
Slc38a11 |
T |
A |
2: 65,147,315 (GRCm39) |
L387F |
probably damaging |
Het |
Sned1 |
G |
A |
1: 93,209,376 (GRCm39) |
V830M |
possibly damaging |
Het |
Sptb |
C |
A |
12: 76,667,641 (GRCm39) |
V819L |
probably benign |
Het |
Sptbn1 |
T |
C |
11: 30,086,124 (GRCm39) |
T1195A |
probably benign |
Het |
Ssna1 |
C |
A |
2: 25,162,024 (GRCm39) |
V57F |
possibly damaging |
Het |
Stk32a |
G |
T |
18: 43,446,485 (GRCm39) |
E312* |
probably null |
Het |
Synpo |
A |
G |
18: 60,736,459 (GRCm39) |
F496L |
probably benign |
Het |
Syt15 |
C |
T |
14: 33,944,858 (GRCm39) |
T135M |
probably benign |
Het |
Tm9sf4 |
A |
G |
2: 153,032,832 (GRCm39) |
E246G |
probably benign |
Het |
Trim44 |
T |
C |
2: 102,187,830 (GRCm39) |
M308V |
possibly damaging |
Het |
Unc119b |
T |
A |
5: 115,272,885 (GRCm39) |
K29* |
probably null |
Het |
Vim |
T |
A |
2: 13,584,921 (GRCm39) |
D367E |
probably benign |
Het |
Virma |
T |
A |
4: 11,494,814 (GRCm39) |
N38K |
probably damaging |
Het |
Vmn1r228 |
A |
T |
17: 20,996,560 (GRCm39) |
D319E |
possibly damaging |
Het |
Vmn2r32 |
T |
A |
7: 7,466,991 (GRCm39) |
I846F |
probably benign |
Het |
Vps13b |
T |
C |
15: 35,576,667 (GRCm39) |
V1025A |
probably benign |
Het |
Vps13c |
G |
T |
9: 67,879,357 (GRCm39) |
E566* |
probably null |
Het |
|
Other mutations in Dnah2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00087:Dnah2
|
APN |
11 |
69,383,498 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL00418:Dnah2
|
APN |
11 |
69,385,892 (GRCm39) |
splice site |
probably benign |
|
IGL00772:Dnah2
|
APN |
11 |
69,342,083 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL00819:Dnah2
|
APN |
11 |
69,364,176 (GRCm39) |
critical splice donor site |
probably null |
|
IGL00827:Dnah2
|
APN |
11 |
69,339,283 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01060:Dnah2
|
APN |
11 |
69,368,918 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL01340:Dnah2
|
APN |
11 |
69,384,010 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01349:Dnah2
|
APN |
11 |
69,366,432 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01413:Dnah2
|
APN |
11 |
69,323,790 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01451:Dnah2
|
APN |
11 |
69,365,017 (GRCm39) |
splice site |
probably benign |
|
IGL01480:Dnah2
|
APN |
11 |
69,349,197 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL01537:Dnah2
|
APN |
11 |
69,406,906 (GRCm39) |
missense |
probably benign |
0.17 |
IGL01592:Dnah2
|
APN |
11 |
69,321,913 (GRCm39) |
missense |
probably benign |
0.14 |
IGL01612:Dnah2
|
APN |
11 |
69,355,889 (GRCm39) |
splice site |
probably benign |
|
IGL01667:Dnah2
|
APN |
11 |
69,435,221 (GRCm39) |
missense |
probably benign |
|
IGL01667:Dnah2
|
APN |
11 |
69,411,767 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01691:Dnah2
|
APN |
11 |
69,430,269 (GRCm39) |
missense |
probably benign |
|
IGL02019:Dnah2
|
APN |
11 |
69,365,111 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02039:Dnah2
|
APN |
11 |
69,390,038 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02076:Dnah2
|
APN |
11 |
69,313,385 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02085:Dnah2
|
APN |
11 |
69,349,011 (GRCm39) |
missense |
probably benign |
0.07 |
IGL02158:Dnah2
|
APN |
11 |
69,348,949 (GRCm39) |
missense |
probably benign |
|
IGL02381:Dnah2
|
APN |
11 |
69,337,118 (GRCm39) |
missense |
probably benign |
0.25 |
IGL02681:Dnah2
|
APN |
11 |
69,343,759 (GRCm39) |
missense |
probably benign |
0.40 |
IGL02957:Dnah2
|
APN |
11 |
69,339,333 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL02961:Dnah2
|
APN |
11 |
69,409,240 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02969:Dnah2
|
APN |
11 |
69,412,013 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL03117:Dnah2
|
APN |
11 |
69,327,117 (GRCm39) |
splice site |
probably benign |
|
IGL03120:Dnah2
|
APN |
11 |
69,312,674 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03183:Dnah2
|
APN |
11 |
69,349,314 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL03197:Dnah2
|
APN |
11 |
69,350,089 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03263:Dnah2
|
APN |
11 |
69,420,207 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03333:Dnah2
|
APN |
11 |
69,385,949 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03338:Dnah2
|
APN |
11 |
69,387,403 (GRCm39) |
missense |
probably benign |
0.13 |
argyrios
|
UTSW |
11 |
69,407,416 (GRCm39) |
missense |
possibly damaging |
0.47 |
Aureus
|
UTSW |
11 |
69,320,174 (GRCm39) |
missense |
probably damaging |
1.00 |
platinum
|
UTSW |
11 |
69,348,868 (GRCm39) |
missense |
probably damaging |
0.96 |
R0334_dnah2_144
|
UTSW |
11 |
69,327,662 (GRCm39) |
missense |
probably damaging |
1.00 |
R2150_dnah2_212
|
UTSW |
11 |
69,406,587 (GRCm39) |
missense |
probably benign |
0.14 |
BB005:Dnah2
|
UTSW |
11 |
69,321,661 (GRCm39) |
missense |
probably damaging |
0.98 |
BB015:Dnah2
|
UTSW |
11 |
69,321,661 (GRCm39) |
missense |
probably damaging |
0.98 |
E0370:Dnah2
|
UTSW |
11 |
69,406,441 (GRCm39) |
splice site |
probably null |
|
P0026:Dnah2
|
UTSW |
11 |
69,355,773 (GRCm39) |
missense |
probably damaging |
1.00 |
R0133:Dnah2
|
UTSW |
11 |
69,311,835 (GRCm39) |
missense |
probably damaging |
1.00 |
R0190:Dnah2
|
UTSW |
11 |
69,326,075 (GRCm39) |
missense |
probably damaging |
1.00 |
R0334:Dnah2
|
UTSW |
11 |
69,327,662 (GRCm39) |
missense |
probably damaging |
1.00 |
R0359:Dnah2
|
UTSW |
11 |
69,420,357 (GRCm39) |
missense |
probably benign |
0.00 |
R0386:Dnah2
|
UTSW |
11 |
69,338,687 (GRCm39) |
missense |
probably damaging |
1.00 |
R0414:Dnah2
|
UTSW |
11 |
69,390,064 (GRCm39) |
missense |
probably benign |
0.26 |
R0427:Dnah2
|
UTSW |
11 |
69,343,705 (GRCm39) |
missense |
probably damaging |
0.99 |
R0433:Dnah2
|
UTSW |
11 |
69,350,114 (GRCm39) |
missense |
probably damaging |
1.00 |
R0442:Dnah2
|
UTSW |
11 |
69,339,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R0462:Dnah2
|
UTSW |
11 |
69,350,027 (GRCm39) |
missense |
probably damaging |
1.00 |
R0463:Dnah2
|
UTSW |
11 |
69,313,952 (GRCm39) |
missense |
probably damaging |
1.00 |
R0611:Dnah2
|
UTSW |
11 |
69,390,020 (GRCm39) |
missense |
probably damaging |
1.00 |
R0626:Dnah2
|
UTSW |
11 |
69,368,509 (GRCm39) |
missense |
probably benign |
0.07 |
R0924:Dnah2
|
UTSW |
11 |
69,312,134 (GRCm39) |
missense |
probably damaging |
1.00 |
R0968:Dnah2
|
UTSW |
11 |
69,339,345 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1066:Dnah2
|
UTSW |
11 |
69,338,645 (GRCm39) |
missense |
probably damaging |
1.00 |
R1183:Dnah2
|
UTSW |
11 |
69,337,474 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1184:Dnah2
|
UTSW |
11 |
69,390,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R1186:Dnah2
|
UTSW |
11 |
69,406,526 (GRCm39) |
missense |
probably damaging |
0.99 |
R1453:Dnah2
|
UTSW |
11 |
69,341,876 (GRCm39) |
missense |
probably damaging |
0.99 |
R1498:Dnah2
|
UTSW |
11 |
69,411,493 (GRCm39) |
splice site |
probably null |
|
R1538:Dnah2
|
UTSW |
11 |
69,368,028 (GRCm39) |
missense |
probably benign |
0.17 |
R1574:Dnah2
|
UTSW |
11 |
69,405,514 (GRCm39) |
missense |
probably benign |
0.26 |
R1574:Dnah2
|
UTSW |
11 |
69,405,514 (GRCm39) |
missense |
probably benign |
0.26 |
R1590:Dnah2
|
UTSW |
11 |
69,412,024 (GRCm39) |
missense |
probably benign |
0.00 |
R1590:Dnah2
|
UTSW |
11 |
69,313,580 (GRCm39) |
critical splice donor site |
probably null |
|
R1655:Dnah2
|
UTSW |
11 |
69,364,680 (GRCm39) |
missense |
probably damaging |
1.00 |
R1726:Dnah2
|
UTSW |
11 |
69,388,715 (GRCm39) |
missense |
probably damaging |
1.00 |
R1764:Dnah2
|
UTSW |
11 |
69,314,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R1815:Dnah2
|
UTSW |
11 |
69,366,400 (GRCm39) |
missense |
probably damaging |
1.00 |
R1822:Dnah2
|
UTSW |
11 |
69,405,630 (GRCm39) |
missense |
probably damaging |
1.00 |
R1859:Dnah2
|
UTSW |
11 |
69,328,712 (GRCm39) |
missense |
probably damaging |
0.99 |
R1911:Dnah2
|
UTSW |
11 |
69,406,578 (GRCm39) |
missense |
possibly damaging |
0.64 |
R1913:Dnah2
|
UTSW |
11 |
69,355,756 (GRCm39) |
missense |
probably damaging |
1.00 |
R1981:Dnah2
|
UTSW |
11 |
69,365,151 (GRCm39) |
missense |
probably damaging |
1.00 |
R2010:Dnah2
|
UTSW |
11 |
69,349,184 (GRCm39) |
critical splice donor site |
probably null |
|
R2016:Dnah2
|
UTSW |
11 |
69,327,896 (GRCm39) |
missense |
probably damaging |
0.97 |
R2017:Dnah2
|
UTSW |
11 |
69,327,896 (GRCm39) |
missense |
probably damaging |
0.97 |
R2044:Dnah2
|
UTSW |
11 |
69,415,066 (GRCm39) |
missense |
probably benign |
0.14 |
R2077:Dnah2
|
UTSW |
11 |
69,387,432 (GRCm39) |
missense |
possibly damaging |
0.73 |
R2096:Dnah2
|
UTSW |
11 |
69,346,742 (GRCm39) |
missense |
probably damaging |
0.98 |
R2099:Dnah2
|
UTSW |
11 |
69,384,063 (GRCm39) |
missense |
probably damaging |
1.00 |
R2127:Dnah2
|
UTSW |
11 |
69,349,011 (GRCm39) |
missense |
probably benign |
0.02 |
R2128:Dnah2
|
UTSW |
11 |
69,349,011 (GRCm39) |
missense |
probably benign |
0.02 |
R2146:Dnah2
|
UTSW |
11 |
69,406,587 (GRCm39) |
missense |
probably benign |
0.14 |
R2147:Dnah2
|
UTSW |
11 |
69,406,587 (GRCm39) |
missense |
probably benign |
0.14 |
R2150:Dnah2
|
UTSW |
11 |
69,406,587 (GRCm39) |
missense |
probably benign |
0.14 |
R2404:Dnah2
|
UTSW |
11 |
69,328,047 (GRCm39) |
missense |
probably damaging |
0.99 |
R2510:Dnah2
|
UTSW |
11 |
69,415,032 (GRCm39) |
nonsense |
probably null |
|
R2517:Dnah2
|
UTSW |
11 |
69,407,470 (GRCm39) |
missense |
probably damaging |
1.00 |
R3014:Dnah2
|
UTSW |
11 |
69,321,304 (GRCm39) |
missense |
probably benign |
|
R3741:Dnah2
|
UTSW |
11 |
69,339,295 (GRCm39) |
missense |
probably damaging |
1.00 |
R3814:Dnah2
|
UTSW |
11 |
69,383,476 (GRCm39) |
splice site |
probably null |
|
R3872:Dnah2
|
UTSW |
11 |
69,320,174 (GRCm39) |
missense |
probably damaging |
1.00 |
R3873:Dnah2
|
UTSW |
11 |
69,320,174 (GRCm39) |
missense |
probably damaging |
1.00 |
R3874:Dnah2
|
UTSW |
11 |
69,320,174 (GRCm39) |
missense |
probably damaging |
1.00 |
R3875:Dnah2
|
UTSW |
11 |
69,320,174 (GRCm39) |
missense |
probably damaging |
1.00 |
R3881:Dnah2
|
UTSW |
11 |
69,342,173 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3953:Dnah2
|
UTSW |
11 |
69,344,929 (GRCm39) |
missense |
probably damaging |
1.00 |
R3956:Dnah2
|
UTSW |
11 |
69,374,847 (GRCm39) |
missense |
probably benign |
0.00 |
R4501:Dnah2
|
UTSW |
11 |
69,368,485 (GRCm39) |
missense |
probably benign |
|
R4515:Dnah2
|
UTSW |
11 |
69,356,457 (GRCm39) |
missense |
possibly damaging |
0.61 |
R4612:Dnah2
|
UTSW |
11 |
69,374,193 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4625:Dnah2
|
UTSW |
11 |
69,354,487 (GRCm39) |
missense |
probably damaging |
1.00 |
R4627:Dnah2
|
UTSW |
11 |
69,356,202 (GRCm39) |
missense |
probably damaging |
1.00 |
R4642:Dnah2
|
UTSW |
11 |
69,387,385 (GRCm39) |
missense |
probably benign |
0.00 |
R4683:Dnah2
|
UTSW |
11 |
69,349,768 (GRCm39) |
missense |
probably damaging |
1.00 |
R4698:Dnah2
|
UTSW |
11 |
69,389,358 (GRCm39) |
missense |
probably damaging |
1.00 |
R4710:Dnah2
|
UTSW |
11 |
69,368,903 (GRCm39) |
missense |
probably damaging |
1.00 |
R4712:Dnah2
|
UTSW |
11 |
69,407,416 (GRCm39) |
missense |
possibly damaging |
0.47 |
R4713:Dnah2
|
UTSW |
11 |
69,367,514 (GRCm39) |
missense |
probably damaging |
1.00 |
R4717:Dnah2
|
UTSW |
11 |
69,320,183 (GRCm39) |
missense |
probably benign |
0.00 |
R4740:Dnah2
|
UTSW |
11 |
69,348,868 (GRCm39) |
missense |
probably damaging |
0.96 |
R4780:Dnah2
|
UTSW |
11 |
69,364,697 (GRCm39) |
missense |
probably damaging |
0.97 |
R4825:Dnah2
|
UTSW |
11 |
69,314,031 (GRCm39) |
missense |
probably damaging |
1.00 |
R4864:Dnah2
|
UTSW |
11 |
69,313,416 (GRCm39) |
missense |
probably damaging |
0.98 |
R4868:Dnah2
|
UTSW |
11 |
69,354,474 (GRCm39) |
missense |
probably damaging |
1.00 |
R4879:Dnah2
|
UTSW |
11 |
69,367,517 (GRCm39) |
missense |
probably damaging |
1.00 |
R4908:Dnah2
|
UTSW |
11 |
69,411,973 (GRCm39) |
missense |
probably benign |
0.00 |
R4911:Dnah2
|
UTSW |
11 |
69,389,930 (GRCm39) |
critical splice donor site |
probably null |
|
R4954:Dnah2
|
UTSW |
11 |
69,430,322 (GRCm39) |
missense |
possibly damaging |
0.61 |
R4962:Dnah2
|
UTSW |
11 |
69,346,799 (GRCm39) |
nonsense |
probably null |
|
R5015:Dnah2
|
UTSW |
11 |
69,388,708 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5049:Dnah2
|
UTSW |
11 |
69,338,992 (GRCm39) |
missense |
probably damaging |
1.00 |
R5055:Dnah2
|
UTSW |
11 |
69,411,599 (GRCm39) |
missense |
possibly damaging |
0.67 |
R5153:Dnah2
|
UTSW |
11 |
69,411,759 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5155:Dnah2
|
UTSW |
11 |
69,313,362 (GRCm39) |
missense |
probably damaging |
1.00 |
R5186:Dnah2
|
UTSW |
11 |
69,326,710 (GRCm39) |
missense |
probably damaging |
1.00 |
R5187:Dnah2
|
UTSW |
11 |
69,349,746 (GRCm39) |
missense |
probably benign |
0.15 |
R5208:Dnah2
|
UTSW |
11 |
69,349,746 (GRCm39) |
missense |
probably benign |
0.15 |
R5252:Dnah2
|
UTSW |
11 |
69,420,295 (GRCm39) |
missense |
probably damaging |
0.98 |
R5296:Dnah2
|
UTSW |
11 |
69,349,746 (GRCm39) |
missense |
probably benign |
0.15 |
R5298:Dnah2
|
UTSW |
11 |
69,349,746 (GRCm39) |
missense |
probably benign |
0.15 |
R5299:Dnah2
|
UTSW |
11 |
69,349,746 (GRCm39) |
missense |
probably benign |
0.15 |
R5301:Dnah2
|
UTSW |
11 |
69,349,746 (GRCm39) |
missense |
probably benign |
0.15 |
R5324:Dnah2
|
UTSW |
11 |
69,348,819 (GRCm39) |
missense |
probably benign |
0.07 |
R5350:Dnah2
|
UTSW |
11 |
69,406,862 (GRCm39) |
missense |
possibly damaging |
0.48 |
R5377:Dnah2
|
UTSW |
11 |
69,312,674 (GRCm39) |
missense |
probably damaging |
1.00 |
R5393:Dnah2
|
UTSW |
11 |
69,391,683 (GRCm39) |
missense |
probably benign |
|
R5421:Dnah2
|
UTSW |
11 |
69,326,462 (GRCm39) |
missense |
probably damaging |
1.00 |
R5452:Dnah2
|
UTSW |
11 |
69,415,209 (GRCm39) |
missense |
probably damaging |
1.00 |
R5461:Dnah2
|
UTSW |
11 |
69,364,177 (GRCm39) |
critical splice donor site |
probably null |
|
R5474:Dnah2
|
UTSW |
11 |
69,349,746 (GRCm39) |
missense |
probably benign |
0.15 |
R5476:Dnah2
|
UTSW |
11 |
69,349,746 (GRCm39) |
missense |
probably benign |
0.15 |
R5477:Dnah2
|
UTSW |
11 |
69,349,746 (GRCm39) |
missense |
probably benign |
0.15 |
R5510:Dnah2
|
UTSW |
11 |
69,349,746 (GRCm39) |
missense |
probably benign |
0.15 |
R5527:Dnah2
|
UTSW |
11 |
69,328,014 (GRCm39) |
nonsense |
probably null |
|
R5566:Dnah2
|
UTSW |
11 |
69,407,395 (GRCm39) |
nonsense |
probably null |
|
R5587:Dnah2
|
UTSW |
11 |
69,328,068 (GRCm39) |
missense |
probably damaging |
1.00 |
R5628:Dnah2
|
UTSW |
11 |
69,349,746 (GRCm39) |
missense |
probably benign |
0.15 |
R5688:Dnah2
|
UTSW |
11 |
69,349,746 (GRCm39) |
missense |
probably benign |
0.15 |
R5690:Dnah2
|
UTSW |
11 |
69,382,370 (GRCm39) |
missense |
probably benign |
0.15 |
R5711:Dnah2
|
UTSW |
11 |
69,326,216 (GRCm39) |
missense |
probably damaging |
1.00 |
R5735:Dnah2
|
UTSW |
11 |
69,321,643 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5826:Dnah2
|
UTSW |
11 |
69,349,746 (GRCm39) |
missense |
probably benign |
0.15 |
R5913:Dnah2
|
UTSW |
11 |
69,339,256 (GRCm39) |
missense |
probably damaging |
1.00 |
R5914:Dnah2
|
UTSW |
11 |
69,349,746 (GRCm39) |
missense |
probably benign |
0.15 |
R5960:Dnah2
|
UTSW |
11 |
69,349,746 (GRCm39) |
missense |
probably benign |
0.15 |
R5961:Dnah2
|
UTSW |
11 |
69,349,746 (GRCm39) |
missense |
probably benign |
0.15 |
R5961:Dnah2
|
UTSW |
11 |
69,321,974 (GRCm39) |
missense |
probably damaging |
1.00 |
R5977:Dnah2
|
UTSW |
11 |
69,411,707 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6020:Dnah2
|
UTSW |
11 |
69,391,665 (GRCm39) |
missense |
probably benign |
|
R6036:Dnah2
|
UTSW |
11 |
69,349,746 (GRCm39) |
missense |
probably benign |
0.15 |
R6036:Dnah2
|
UTSW |
11 |
69,349,746 (GRCm39) |
missense |
probably benign |
0.15 |
R6050:Dnah2
|
UTSW |
11 |
69,349,746 (GRCm39) |
missense |
probably benign |
0.15 |
R6086:Dnah2
|
UTSW |
11 |
69,406,834 (GRCm39) |
missense |
probably benign |
0.30 |
R6115:Dnah2
|
UTSW |
11 |
69,337,475 (GRCm39) |
missense |
probably damaging |
1.00 |
R6123:Dnah2
|
UTSW |
11 |
69,409,185 (GRCm39) |
missense |
probably benign |
0.29 |
R6159:Dnah2
|
UTSW |
11 |
69,349,746 (GRCm39) |
missense |
probably benign |
0.15 |
R6159:Dnah2
|
UTSW |
11 |
69,349,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R6163:Dnah2
|
UTSW |
11 |
69,411,729 (GRCm39) |
nonsense |
probably null |
|
R6171:Dnah2
|
UTSW |
11 |
69,313,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R6263:Dnah2
|
UTSW |
11 |
69,348,238 (GRCm39) |
missense |
probably damaging |
1.00 |
R6298:Dnah2
|
UTSW |
11 |
69,382,467 (GRCm39) |
missense |
probably benign |
0.25 |
R6352:Dnah2
|
UTSW |
11 |
69,339,053 (GRCm39) |
missense |
probably damaging |
1.00 |
R6399:Dnah2
|
UTSW |
11 |
69,349,344 (GRCm39) |
missense |
probably damaging |
0.98 |
R6466:Dnah2
|
UTSW |
11 |
69,430,241 (GRCm39) |
missense |
probably benign |
|
R6478:Dnah2
|
UTSW |
11 |
69,406,836 (GRCm39) |
missense |
probably benign |
0.01 |
R6516:Dnah2
|
UTSW |
11 |
69,356,212 (GRCm39) |
missense |
probably benign |
0.34 |
R6538:Dnah2
|
UTSW |
11 |
69,328,023 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6802:Dnah2
|
UTSW |
11 |
69,314,516 (GRCm39) |
missense |
probably damaging |
1.00 |
R6861:Dnah2
|
UTSW |
11 |
69,346,789 (GRCm39) |
missense |
possibly damaging |
0.64 |
R6869:Dnah2
|
UTSW |
11 |
69,320,297 (GRCm39) |
missense |
probably damaging |
1.00 |
R6894:Dnah2
|
UTSW |
11 |
69,375,086 (GRCm39) |
missense |
probably benign |
0.12 |
R6935:Dnah2
|
UTSW |
11 |
69,312,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R7017:Dnah2
|
UTSW |
11 |
69,382,373 (GRCm39) |
nonsense |
probably null |
|
R7073:Dnah2
|
UTSW |
11 |
69,321,318 (GRCm39) |
nonsense |
probably null |
|
R7111:Dnah2
|
UTSW |
11 |
69,337,579 (GRCm39) |
splice site |
probably null |
|
R7125:Dnah2
|
UTSW |
11 |
69,327,008 (GRCm39) |
missense |
probably damaging |
0.99 |
R7137:Dnah2
|
UTSW |
11 |
69,382,381 (GRCm39) |
missense |
probably damaging |
1.00 |
R7190:Dnah2
|
UTSW |
11 |
69,439,923 (GRCm39) |
splice site |
probably null |
|
R7214:Dnah2
|
UTSW |
11 |
69,321,935 (GRCm39) |
missense |
probably damaging |
1.00 |
R7227:Dnah2
|
UTSW |
11 |
69,312,222 (GRCm39) |
missense |
probably damaging |
0.99 |
R7238:Dnah2
|
UTSW |
11 |
69,349,972 (GRCm39) |
critical splice donor site |
probably null |
|
R7256:Dnah2
|
UTSW |
11 |
69,321,920 (GRCm39) |
missense |
probably damaging |
1.00 |
R7267:Dnah2
|
UTSW |
11 |
69,391,643 (GRCm39) |
missense |
probably damaging |
1.00 |
R7420:Dnah2
|
UTSW |
11 |
69,369,623 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7421:Dnah2
|
UTSW |
11 |
69,383,631 (GRCm39) |
missense |
probably benign |
0.25 |
R7437:Dnah2
|
UTSW |
11 |
69,389,453 (GRCm39) |
missense |
probably damaging |
1.00 |
R7461:Dnah2
|
UTSW |
11 |
69,439,816 (GRCm39) |
critical splice donor site |
probably null |
|
R7473:Dnah2
|
UTSW |
11 |
69,382,484 (GRCm39) |
missense |
probably damaging |
0.99 |
R7528:Dnah2
|
UTSW |
11 |
69,391,622 (GRCm39) |
missense |
probably damaging |
0.99 |
R7613:Dnah2
|
UTSW |
11 |
69,439,816 (GRCm39) |
critical splice donor site |
probably null |
|
R7615:Dnah2
|
UTSW |
11 |
69,326,130 (GRCm39) |
missense |
probably damaging |
0.99 |
R7626:Dnah2
|
UTSW |
11 |
69,389,511 (GRCm39) |
missense |
probably damaging |
0.99 |
R7745:Dnah2
|
UTSW |
11 |
69,342,144 (GRCm39) |
nonsense |
probably null |
|
R7764:Dnah2
|
UTSW |
11 |
69,348,984 (GRCm39) |
missense |
probably benign |
0.29 |
R7793:Dnah2
|
UTSW |
11 |
69,386,040 (GRCm39) |
missense |
probably benign |
0.00 |
R7819:Dnah2
|
UTSW |
11 |
69,407,419 (GRCm39) |
missense |
probably benign |
0.01 |
R7881:Dnah2
|
UTSW |
11 |
69,322,064 (GRCm39) |
missense |
probably damaging |
1.00 |
R7900:Dnah2
|
UTSW |
11 |
69,409,254 (GRCm39) |
missense |
probably damaging |
1.00 |
R7916:Dnah2
|
UTSW |
11 |
69,311,974 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7921:Dnah2
|
UTSW |
11 |
69,411,660 (GRCm39) |
missense |
probably benign |
|
R7928:Dnah2
|
UTSW |
11 |
69,321,661 (GRCm39) |
missense |
probably damaging |
0.98 |
R7937:Dnah2
|
UTSW |
11 |
69,408,511 (GRCm39) |
nonsense |
probably null |
|
R7995:Dnah2
|
UTSW |
11 |
69,411,563 (GRCm39) |
missense |
possibly damaging |
0.77 |
R8202:Dnah2
|
UTSW |
11 |
69,369,649 (GRCm39) |
missense |
probably benign |
0.00 |
R8208:Dnah2
|
UTSW |
11 |
69,411,678 (GRCm39) |
missense |
probably benign |
0.05 |
R8215:Dnah2
|
UTSW |
11 |
69,326,193 (GRCm39) |
missense |
probably damaging |
1.00 |
R8279:Dnah2
|
UTSW |
11 |
69,366,399 (GRCm39) |
missense |
probably damaging |
1.00 |
R8338:Dnah2
|
UTSW |
11 |
69,378,122 (GRCm39) |
missense |
probably damaging |
1.00 |
R8348:Dnah2
|
UTSW |
11 |
69,320,273 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8405:Dnah2
|
UTSW |
11 |
69,349,289 (GRCm39) |
missense |
probably damaging |
1.00 |
R8407:Dnah2
|
UTSW |
11 |
69,350,104 (GRCm39) |
missense |
probably benign |
0.00 |
R8493:Dnah2
|
UTSW |
11 |
69,343,804 (GRCm39) |
missense |
probably damaging |
1.00 |
R8673:Dnah2
|
UTSW |
11 |
69,405,523 (GRCm39) |
missense |
probably benign |
0.23 |
R8725:Dnah2
|
UTSW |
11 |
69,415,005 (GRCm39) |
missense |
probably damaging |
1.00 |
R8727:Dnah2
|
UTSW |
11 |
69,415,005 (GRCm39) |
missense |
probably damaging |
1.00 |
R8730:Dnah2
|
UTSW |
11 |
69,384,087 (GRCm39) |
missense |
possibly damaging |
0.73 |
R8804:Dnah2
|
UTSW |
11 |
69,356,511 (GRCm39) |
missense |
probably benign |
0.01 |
R8876:Dnah2
|
UTSW |
11 |
69,382,348 (GRCm39) |
missense |
probably damaging |
1.00 |
R8894:Dnah2
|
UTSW |
11 |
69,383,048 (GRCm39) |
missense |
probably benign |
0.01 |
R8938:Dnah2
|
UTSW |
11 |
69,328,754 (GRCm39) |
missense |
probably damaging |
0.99 |
R9044:Dnah2
|
UTSW |
11 |
69,420,247 (GRCm39) |
missense |
probably benign |
|
R9085:Dnah2
|
UTSW |
11 |
69,320,224 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9110:Dnah2
|
UTSW |
11 |
69,435,208 (GRCm39) |
missense |
probably benign |
|
R9156:Dnah2
|
UTSW |
11 |
69,313,687 (GRCm39) |
missense |
|
|
R9251:Dnah2
|
UTSW |
11 |
69,406,619 (GRCm39) |
missense |
probably damaging |
1.00 |
R9258:Dnah2
|
UTSW |
11 |
69,368,079 (GRCm39) |
missense |
probably damaging |
1.00 |
R9279:Dnah2
|
UTSW |
11 |
69,409,104 (GRCm39) |
missense |
probably benign |
0.01 |
R9318:Dnah2
|
UTSW |
11 |
69,375,155 (GRCm39) |
missense |
probably benign |
0.07 |
R9321:Dnah2
|
UTSW |
11 |
69,338,939 (GRCm39) |
critical splice donor site |
probably null |
|
R9350:Dnah2
|
UTSW |
11 |
69,384,073 (GRCm39) |
missense |
probably benign |
0.10 |
R9358:Dnah2
|
UTSW |
11 |
69,406,592 (GRCm39) |
missense |
probably damaging |
0.99 |
R9417:Dnah2
|
UTSW |
11 |
69,326,990 (GRCm39) |
missense |
probably damaging |
1.00 |
R9420:Dnah2
|
UTSW |
11 |
69,368,942 (GRCm39) |
missense |
probably benign |
0.09 |
R9438:Dnah2
|
UTSW |
11 |
69,364,220 (GRCm39) |
missense |
probably damaging |
1.00 |
R9469:Dnah2
|
UTSW |
11 |
69,321,896 (GRCm39) |
missense |
probably damaging |
1.00 |
R9487:Dnah2
|
UTSW |
11 |
69,406,617 (GRCm39) |
missense |
possibly damaging |
0.47 |
R9495:Dnah2
|
UTSW |
11 |
69,345,208 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9579:Dnah2
|
UTSW |
11 |
69,368,041 (GRCm39) |
missense |
probably damaging |
1.00 |
R9608:Dnah2
|
UTSW |
11 |
69,344,888 (GRCm39) |
missense |
probably null |
1.00 |
R9651:Dnah2
|
UTSW |
11 |
69,341,824 (GRCm39) |
critical splice donor site |
probably null |
|
R9662:Dnah2
|
UTSW |
11 |
69,343,763 (GRCm39) |
missense |
probably benign |
|
RF004:Dnah2
|
UTSW |
11 |
69,328,013 (GRCm39) |
missense |
probably benign |
0.24 |
U24488:Dnah2
|
UTSW |
11 |
69,374,648 (GRCm39) |
missense |
probably damaging |
0.99 |
X0021:Dnah2
|
UTSW |
11 |
69,339,388 (GRCm39) |
missense |
possibly damaging |
0.81 |
Z1088:Dnah2
|
UTSW |
11 |
69,321,619 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Dnah2
|
UTSW |
11 |
69,312,647 (GRCm39) |
missense |
possibly damaging |
0.46 |
Z1176:Dnah2
|
UTSW |
11 |
69,407,349 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Dnah2
|
UTSW |
11 |
69,407,307 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Dnah2
|
UTSW |
11 |
69,389,493 (GRCm39) |
missense |
probably benign |
0.12 |
Z1176:Dnah2
|
UTSW |
11 |
69,377,880 (GRCm39) |
missense |
possibly damaging |
0.46 |
Z1176:Dnah2
|
UTSW |
11 |
69,341,946 (GRCm39) |
missense |
probably benign |
|
Z1177:Dnah2
|
UTSW |
11 |
69,435,383 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1177:Dnah2
|
UTSW |
11 |
69,354,279 (GRCm39) |
missense |
possibly damaging |
0.63 |
|