Other mutations in this stock |
Total: 82 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A630089N07Rik |
C |
T |
16: 97,867,651 (GRCm39) |
A104T |
probably damaging |
Het |
Abhd18 |
T |
A |
3: 40,884,627 (GRCm39) |
L222Q |
probably damaging |
Het |
Adam30 |
C |
T |
3: 98,070,348 (GRCm39) |
T727M |
possibly damaging |
Het |
Adh6b |
A |
T |
3: 138,058,729 (GRCm39) |
Q137L |
probably damaging |
Het |
Alpl |
C |
T |
4: 137,475,127 (GRCm39) |
V269I |
probably benign |
Het |
Ang2 |
C |
T |
14: 51,432,996 (GRCm39) |
G129S |
probably benign |
Het |
Atp6v0a1 |
A |
T |
11: 100,920,015 (GRCm39) |
H216L |
possibly damaging |
Het |
BC030500 |
C |
T |
8: 59,366,049 (GRCm39) |
T61I |
unknown |
Het |
Brpf1 |
T |
G |
6: 113,293,491 (GRCm39) |
L520R |
probably damaging |
Het |
Btbd10 |
A |
G |
7: 112,927,626 (GRCm39) |
I243T |
possibly damaging |
Het |
Bub1 |
C |
A |
2: 127,646,139 (GRCm39) |
C947F |
probably damaging |
Het |
C4b |
T |
C |
17: 34,953,459 (GRCm39) |
E1008G |
probably damaging |
Het |
Ccdc40 |
A |
G |
11: 119,155,323 (GRCm39) |
T1188A |
probably benign |
Het |
Cdcp3 |
A |
G |
7: 130,875,485 (GRCm39) |
T1770A |
unknown |
Het |
Cnn1 |
G |
T |
9: 22,010,557 (GRCm39) |
|
probably benign |
Het |
Colgalt2 |
T |
C |
1: 152,360,662 (GRCm39) |
M233T |
probably damaging |
Het |
Cox15 |
A |
T |
19: 43,735,181 (GRCm39) |
C195* |
probably null |
Het |
Cped1 |
A |
T |
6: 22,059,941 (GRCm39) |
R202S |
possibly damaging |
Het |
Dact2 |
A |
T |
17: 14,417,146 (GRCm39) |
C351* |
probably null |
Het |
Dbnl |
A |
G |
11: 5,738,582 (GRCm39) |
N8S |
probably benign |
Het |
Depdc1a |
T |
A |
3: 159,228,356 (GRCm39) |
N369K |
probably benign |
Het |
Dscaml1 |
T |
A |
9: 45,341,759 (GRCm39) |
Y57N |
probably benign |
Het |
Eif2b3 |
A |
G |
4: 116,927,944 (GRCm39) |
T388A |
probably benign |
Het |
Eif4h |
A |
C |
5: 134,654,393 (GRCm39) |
|
probably null |
Het |
Elf1 |
C |
T |
14: 79,810,667 (GRCm39) |
Q288* |
probably null |
Het |
Fbxl5 |
A |
T |
5: 43,908,362 (GRCm39) |
|
probably benign |
Het |
Fgl2 |
C |
T |
5: 21,580,677 (GRCm39) |
R340* |
probably null |
Het |
Fut4 |
T |
C |
9: 14,662,082 (GRCm39) |
D404G |
probably damaging |
Het |
Glmn |
G |
A |
5: 107,718,152 (GRCm39) |
P255L |
probably benign |
Het |
Gm14322 |
C |
T |
2: 177,411,481 (GRCm39) |
T97I |
probably benign |
Het |
Gm44511 |
C |
A |
6: 128,797,997 (GRCm39) |
C32F |
probably damaging |
Het |
Gm5478 |
A |
G |
15: 101,553,871 (GRCm39) |
F247S |
probably damaging |
Het |
Golgb1 |
T |
A |
16: 36,739,563 (GRCm39) |
M2675K |
probably damaging |
Het |
Hectd1 |
T |
C |
12: 51,849,000 (GRCm39) |
D368G |
possibly damaging |
Het |
Hnrnpul2 |
A |
G |
19: 8,798,064 (GRCm39) |
N140S |
probably benign |
Het |
Htr4 |
A |
T |
18: 62,561,209 (GRCm39) |
I157L |
probably damaging |
Het |
Igf2bp3 |
G |
T |
6: 49,086,009 (GRCm39) |
|
probably benign |
Het |
Kcnma1 |
T |
G |
14: 23,436,332 (GRCm39) |
M790L |
probably benign |
Het |
Kcnv1 |
G |
A |
15: 44,977,999 (GRCm39) |
S13L |
unknown |
Het |
Kctd20 |
C |
T |
17: 29,184,025 (GRCm39) |
R312* |
probably null |
Het |
Kdm3b |
T |
A |
18: 34,960,435 (GRCm39) |
I1340N |
probably damaging |
Het |
Kdm6b |
A |
G |
11: 69,292,919 (GRCm39) |
F1286L |
unknown |
Het |
Knl1 |
T |
A |
2: 118,899,524 (GRCm39) |
F408L |
probably benign |
Het |
Lypd5 |
G |
T |
7: 24,053,101 (GRCm39) |
G253W |
probably damaging |
Het |
Mea1 |
A |
G |
17: 46,992,614 (GRCm39) |
T21A |
probably benign |
Het |
Metrnl |
A |
G |
11: 121,606,842 (GRCm39) |
E299G |
possibly damaging |
Het |
Mindy4 |
T |
A |
6: 55,256,055 (GRCm39) |
|
probably benign |
Het |
Muc5ac |
C |
T |
7: 141,363,481 (GRCm39) |
|
probably benign |
Het |
Nbn |
G |
A |
4: 15,963,911 (GRCm39) |
S104N |
probably damaging |
Het |
Nxpe2 |
A |
T |
9: 48,238,073 (GRCm39) |
F61I |
probably benign |
Het |
Or6c1b |
T |
C |
10: 129,273,334 (GRCm39) |
Y218H |
probably benign |
Het |
Or6c70 |
T |
A |
10: 129,710,092 (GRCm39) |
D178V |
probably damaging |
Het |
Pcdhb20 |
C |
T |
18: 37,638,437 (GRCm39) |
A321V |
probably damaging |
Het |
Pgr |
C |
A |
9: 8,901,544 (GRCm39) |
P359Q |
probably damaging |
Het |
Pi4k2b |
G |
A |
5: 52,908,031 (GRCm39) |
V157I |
probably benign |
Het |
Piezo2 |
C |
T |
18: 63,242,956 (GRCm39) |
S621N |
probably benign |
Het |
Plekhm1 |
A |
C |
11: 103,258,444 (GRCm39) |
F1031L |
probably damaging |
Het |
Pltp |
A |
G |
2: 164,696,301 (GRCm39) |
S124P |
probably damaging |
Het |
Polr3gl |
T |
A |
3: 96,487,154 (GRCm39) |
E177V |
probably benign |
Het |
Pstk |
G |
T |
7: 130,973,024 (GRCm39) |
R41L |
possibly damaging |
Het |
Ptprk |
C |
A |
10: 28,442,541 (GRCm39) |
|
probably benign |
Het |
Rasgrp1 |
T |
C |
2: 117,119,158 (GRCm39) |
E493G |
probably benign |
Het |
Rtn3 |
A |
G |
19: 7,434,726 (GRCm39) |
L422P |
probably benign |
Het |
Rusc2 |
C |
T |
4: 43,401,351 (GRCm39) |
|
probably benign |
Het |
Sbno2 |
A |
G |
10: 79,911,090 (GRCm39) |
F6S |
probably benign |
Het |
Sh2d4a |
A |
G |
8: 68,798,695 (GRCm39) |
Y348C |
probably damaging |
Het |
Sh3rf3 |
A |
G |
10: 58,939,992 (GRCm39) |
|
probably null |
Het |
Sipa1l2 |
T |
C |
8: 126,177,125 (GRCm39) |
E1163G |
probably benign |
Het |
Strip1 |
G |
C |
3: 107,521,964 (GRCm39) |
A738G |
probably damaging |
Het |
Tdrkh |
C |
T |
3: 94,333,299 (GRCm39) |
R255C |
probably benign |
Het |
Tex11 |
C |
T |
X: 100,059,191 (GRCm39) |
V190I |
possibly damaging |
Het |
Tln1 |
A |
T |
4: 43,555,911 (GRCm39) |
M101K |
possibly damaging |
Het |
Trav6-2 |
A |
C |
14: 52,905,028 (GRCm39) |
|
probably benign |
Het |
Tspan11 |
A |
T |
6: 127,900,674 (GRCm39) |
I82F |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,779,320 (GRCm39) |
K1233E |
unknown |
Het |
U2af2 |
T |
A |
7: 5,070,432 (GRCm39) |
|
probably benign |
Het |
Usp29 |
A |
T |
7: 6,965,917 (GRCm39) |
S587C |
probably damaging |
Het |
Vmn1r235 |
A |
T |
17: 21,482,056 (GRCm39) |
Q127L |
probably damaging |
Het |
Vmn1r65 |
C |
A |
7: 6,011,503 (GRCm39) |
A244S |
probably damaging |
Het |
Vmn2r18 |
A |
G |
5: 151,508,462 (GRCm39) |
S221P |
probably damaging |
Het |
Zfp229 |
T |
C |
17: 21,964,828 (GRCm39) |
S353P |
probably damaging |
Het |
Zpld2 |
T |
C |
4: 133,930,150 (GRCm39) |
K52E |
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 |
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 |
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 |
|