Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930449I24Rik |
T |
A |
5: 146,441,752 (GRCm39) |
S300T |
possibly damaging |
Het |
A2ml1 |
A |
C |
6: 128,535,400 (GRCm39) |
V770G |
probably damaging |
Het |
Abca6 |
A |
G |
11: 110,110,475 (GRCm39) |
I558T |
probably benign |
Het |
Abhd17c |
C |
A |
7: 83,759,870 (GRCm39) |
G295W |
probably damaging |
Het |
Actn3 |
G |
A |
19: 4,921,703 (GRCm39) |
A159V |
probably damaging |
Het |
Adgrv1 |
A |
T |
13: 81,705,199 (GRCm39) |
F1537Y |
probably damaging |
Het |
Agbl1 |
G |
T |
7: 76,069,628 (GRCm39) |
V373F |
possibly damaging |
Het |
Aldh1a1 |
A |
T |
19: 20,620,279 (GRCm39) |
E485D |
probably benign |
Het |
Amdhd2 |
A |
G |
17: 24,377,282 (GRCm39) |
|
probably null |
Het |
Armc3 |
A |
G |
2: 19,206,622 (GRCm39) |
D15G |
probably damaging |
Het |
Atp2b2 |
A |
G |
6: 113,737,611 (GRCm39) |
L921P |
probably damaging |
Het |
Btbd16 |
A |
G |
7: 130,386,038 (GRCm39) |
N88S |
probably benign |
Het |
Capn10 |
T |
A |
1: 92,865,756 (GRCm39) |
C77* |
probably null |
Het |
Caskin1 |
T |
C |
17: 24,715,970 (GRCm39) |
|
probably null |
Het |
Catsper4 |
T |
C |
4: 133,941,117 (GRCm39) |
D254G |
probably benign |
Het |
Catsperg1 |
T |
C |
7: 28,884,465 (GRCm39) |
D958G |
probably damaging |
Het |
Ccar2 |
T |
G |
14: 70,377,100 (GRCm39) |
K787Q |
probably benign |
Het |
Ccdc191 |
C |
T |
16: 43,728,998 (GRCm39) |
T244I |
probably benign |
Het |
Cd33 |
A |
T |
7: 43,179,699 (GRCm39) |
L243Q |
possibly damaging |
Het |
Cdc37 |
T |
C |
9: 21,061,143 (GRCm39) |
Y4C |
probably damaging |
Het |
Cenpe |
T |
G |
3: 134,945,541 (GRCm39) |
N1018K |
probably benign |
Het |
Crocc |
G |
A |
4: 140,744,407 (GRCm39) |
R1830C |
probably damaging |
Het |
Csmd1 |
T |
C |
8: 15,967,392 (GRCm39) |
D3157G |
probably damaging |
Het |
Dhx57 |
C |
T |
17: 80,580,477 (GRCm39) |
V492M |
probably damaging |
Het |
Dnhd1 |
C |
T |
7: 105,342,928 (GRCm39) |
T1424I |
possibly damaging |
Het |
Dsc3 |
C |
T |
18: 20,101,411 (GRCm39) |
A661T |
probably benign |
Het |
F930015N05Rik |
A |
G |
11: 64,326,229 (GRCm39) |
|
probably benign |
Het |
Fbxo34 |
C |
A |
14: 47,767,563 (GRCm39) |
R308S |
probably damaging |
Het |
Gm10608 |
CAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA |
CAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA |
9: 118,989,784 (GRCm39) |
|
probably benign |
Het |
Gm11595 |
A |
T |
11: 99,663,327 (GRCm39) |
C118S |
unknown |
Het |
Gm9742 |
A |
T |
13: 8,085,011 (GRCm39) |
|
noncoding transcript |
Het |
Gmeb2 |
G |
A |
2: 180,900,842 (GRCm39) |
A185V |
probably benign |
Het |
Gpr15 |
A |
G |
16: 58,538,618 (GRCm39) |
V157A |
possibly damaging |
Het |
Gpr3 |
C |
T |
4: 132,937,932 (GRCm39) |
A247T |
probably damaging |
Het |
Grin2b |
A |
C |
6: 135,755,698 (GRCm39) |
S539A |
probably benign |
Het |
Hmbs |
T |
C |
9: 44,252,004 (GRCm39) |
T92A |
probably benign |
Het |
Inpp4a |
A |
G |
1: 37,406,000 (GRCm39) |
M173V |
probably benign |
Het |
Irx4 |
T |
A |
13: 73,413,595 (GRCm39) |
S22T |
probably benign |
Het |
Jph3 |
C |
T |
8: 122,511,881 (GRCm39) |
A623V |
probably benign |
Het |
Kif1b |
G |
A |
4: 149,272,097 (GRCm39) |
S1568L |
possibly damaging |
Het |
Ksr1 |
G |
A |
11: 78,924,139 (GRCm39) |
S361L |
probably damaging |
Het |
Lyst |
T |
G |
13: 13,809,847 (GRCm39) |
Y506D |
probably damaging |
Het |
Mctp1 |
A |
G |
13: 76,972,941 (GRCm39) |
D648G |
probably damaging |
Het |
Megf8 |
T |
C |
7: 25,064,007 (GRCm39) |
S2788P |
possibly damaging |
Het |
Mfsd2b |
T |
A |
12: 4,917,659 (GRCm39) |
Y129F |
probably benign |
Het |
Mindy4 |
T |
C |
6: 55,195,250 (GRCm39) |
S155P |
probably benign |
Het |
Mospd4 |
A |
G |
18: 46,598,731 (GRCm39) |
|
noncoding transcript |
Het |
Myo18b |
A |
T |
5: 112,978,944 (GRCm39) |
L1223Q |
probably damaging |
Het |
Nckipsd |
A |
G |
9: 108,688,932 (GRCm39) |
T156A |
probably benign |
Het |
Ndst1 |
G |
A |
18: 60,824,280 (GRCm39) |
T799I |
probably benign |
Het |
Npffr2 |
A |
T |
5: 89,715,924 (GRCm39) |
I84F |
probably damaging |
Het |
Nphp3 |
G |
A |
9: 103,885,442 (GRCm39) |
V167M |
probably damaging |
Het |
Nup107 |
C |
A |
10: 117,610,380 (GRCm39) |
R354L |
possibly damaging |
Het |
Olfml2a |
T |
C |
2: 38,831,699 (GRCm39) |
C93R |
probably damaging |
Het |
Or12e10 |
A |
G |
2: 87,640,685 (GRCm39) |
I174V |
probably benign |
Het |
Or1e25 |
C |
G |
11: 73,493,631 (GRCm39) |
S75C |
possibly damaging |
Het |
Or5l14 |
A |
T |
2: 87,793,176 (GRCm39) |
V20D |
probably benign |
Het |
Pappa |
T |
A |
4: 65,215,494 (GRCm39) |
L1134M |
probably damaging |
Het |
Plscr4 |
T |
G |
9: 92,370,683 (GRCm39) |
F217V |
possibly damaging |
Het |
Pnpla8 |
T |
A |
12: 44,354,840 (GRCm39) |
Y667N |
probably benign |
Het |
Polg |
A |
G |
7: 79,114,676 (GRCm39) |
L95P |
probably damaging |
Het |
Psg20 |
T |
G |
7: 18,416,643 (GRCm39) |
I158L |
probably damaging |
Het |
Pwwp2a |
A |
G |
11: 43,596,145 (GRCm39) |
S437G |
probably benign |
Het |
Rdx |
A |
G |
9: 51,981,032 (GRCm39) |
M305V |
possibly damaging |
Het |
Rinl |
A |
G |
7: 28,496,168 (GRCm39) |
E383G |
probably damaging |
Het |
Ror1 |
A |
G |
4: 100,299,290 (GRCm39) |
M888V |
probably benign |
Het |
Rps12 |
A |
T |
10: 23,662,776 (GRCm39) |
I22K |
possibly damaging |
Het |
Rtca |
C |
A |
3: 116,291,323 (GRCm39) |
R219L |
possibly damaging |
Het |
Ryr2 |
G |
A |
13: 11,727,081 (GRCm39) |
P2427S |
probably damaging |
Het |
Slc10a6 |
A |
G |
5: 103,756,922 (GRCm39) |
Y281H |
probably benign |
Het |
Slc39a11 |
A |
G |
11: 113,260,629 (GRCm39) |
S176P |
probably benign |
Het |
Slfn10-ps |
A |
G |
11: 82,921,168 (GRCm39) |
|
noncoding transcript |
Het |
Spef2 |
T |
C |
15: 9,729,747 (GRCm39) |
T124A |
possibly damaging |
Het |
Sult2a4 |
G |
T |
7: 13,649,185 (GRCm39) |
P207Q |
probably damaging |
Het |
Tas1r3 |
G |
A |
4: 155,944,927 (GRCm39) |
R765C |
probably damaging |
Het |
Tcstv1a |
T |
C |
13: 120,355,282 (GRCm39) |
T117A |
probably damaging |
Het |
Tha1 |
A |
G |
11: 117,760,600 (GRCm39) |
V208A |
probably damaging |
Het |
Tmbim4 |
T |
A |
10: 120,060,658 (GRCm39) |
I215N |
probably damaging |
Het |
Tmem202 |
T |
A |
9: 59,427,483 (GRCm39) |
I122F |
probably benign |
Het |
Tomm70a |
T |
C |
16: 56,942,234 (GRCm39) |
S4P |
unknown |
Het |
Tpcn2 |
A |
G |
7: 144,827,712 (GRCm39) |
|
probably benign |
Het |
Trim36 |
A |
T |
18: 46,345,404 (GRCm39) |
F10I |
probably benign |
Het |
Usp30 |
A |
G |
5: 114,249,224 (GRCm39) |
E176G |
probably damaging |
Het |
Usp8 |
T |
G |
2: 126,579,495 (GRCm39) |
|
probably null |
Het |
Vmn1r32 |
T |
A |
6: 66,530,533 (GRCm39) |
Y81F |
probably benign |
Het |
Vps36 |
G |
T |
8: 22,708,305 (GRCm39) |
|
probably null |
Het |
Wdr87-ps |
T |
C |
7: 29,236,565 (GRCm39) |
|
noncoding transcript |
Het |
Wnt3 |
A |
G |
11: 103,703,474 (GRCm39) |
H319R |
possibly damaging |
Het |
Zfp319 |
A |
T |
8: 96,050,391 (GRCm39) |
|
probably benign |
Het |
Zfp408 |
T |
C |
2: 91,475,519 (GRCm39) |
E545G |
probably damaging |
Het |
Zfp799 |
C |
T |
17: 33,038,472 (GRCm39) |
R598Q |
possibly damaging |
Het |
Zfp831 |
T |
C |
2: 174,489,917 (GRCm39) |
V1228A |
probably benign |
Het |
Zfp938 |
T |
C |
10: 82,061,876 (GRCm39) |
D248G |
probably benign |
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 |
R1695:Dnah2
|
UTSW |
11 |
69,405,517 (GRCm39) |
missense |
possibly damaging |
0.74 |
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 |
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 |
|