Other mutations in this stock |
Total: 99 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110059G10Rik |
T |
A |
9: 122,778,008 (GRCm39) |
I79L |
probably benign |
Het |
Ablim2 |
C |
T |
5: 35,959,766 (GRCm39) |
R73C |
possibly damaging |
Het |
Acaa1a |
G |
A |
9: 119,177,772 (GRCm39) |
S218N |
probably benign |
Het |
Acsm5 |
A |
T |
7: 119,137,314 (GRCm39) |
I377F |
probably damaging |
Het |
Ahnak2 |
T |
C |
12: 112,741,706 (GRCm39) |
T789A |
probably benign |
Het |
Ak9 |
A |
T |
10: 41,296,678 (GRCm39) |
T1475S |
unknown |
Het |
AU040320 |
A |
T |
4: 126,747,081 (GRCm39) |
N1028Y |
probably damaging |
Het |
Bahcc1 |
T |
A |
11: 120,178,580 (GRCm39) |
S2380T |
probably benign |
Het |
Cadps |
A |
G |
14: 12,536,386 (GRCm38) |
Y525H |
probably damaging |
Het |
Casp8ap2 |
A |
G |
4: 32,639,905 (GRCm39) |
T320A |
possibly damaging |
Het |
Ccdc138 |
A |
G |
10: 58,380,817 (GRCm39) |
N483D |
possibly damaging |
Het |
Ccdc39 |
G |
A |
3: 33,893,242 (GRCm39) |
|
probably null |
Het |
Cd300c2 |
T |
C |
11: 114,887,772 (GRCm39) |
N210S |
probably damaging |
Het |
Cd84 |
A |
G |
1: 171,700,432 (GRCm39) |
D183G |
probably damaging |
Het |
Cep95 |
C |
T |
11: 106,702,172 (GRCm39) |
P390S |
probably damaging |
Het |
Chd9 |
A |
T |
8: 91,741,877 (GRCm39) |
H1622L |
possibly damaging |
Het |
Cilp |
C |
A |
9: 65,185,302 (GRCm39) |
Q466K |
probably benign |
Het |
Cinp |
T |
A |
12: 110,850,487 (GRCm39) |
T5S |
probably damaging |
Het |
Clec4a2 |
T |
C |
6: 123,119,462 (GRCm39) |
L238S |
probably damaging |
Het |
Cntrob |
T |
C |
11: 69,211,732 (GRCm39) |
Y164C |
probably damaging |
Het |
Col6a3 |
A |
G |
1: 90,735,246 (GRCm39) |
L1408P |
probably damaging |
Het |
Cul3 |
G |
A |
1: 80,258,632 (GRCm39) |
S468L |
possibly damaging |
Het |
Dnah11 |
T |
A |
12: 118,090,618 (GRCm39) |
D1081V |
probably benign |
Het |
Efna3 |
C |
G |
3: 89,222,805 (GRCm39) |
R185P |
probably damaging |
Het |
F5 |
A |
T |
1: 164,039,389 (GRCm39) |
I2000F |
probably damaging |
Het |
Fancm |
G |
A |
12: 65,141,645 (GRCm39) |
G422E |
probably benign |
Het |
Gcnt2 |
A |
T |
13: 41,014,210 (GRCm39) |
D127V |
probably damaging |
Het |
Gm21798 |
G |
T |
15: 64,689,618 (GRCm39) |
|
probably benign |
Het |
Gramd1a |
A |
C |
7: 30,838,292 (GRCm39) |
S320R |
probably benign |
Het |
Grn |
T |
C |
11: 102,327,344 (GRCm39) |
|
probably benign |
Het |
Helq |
A |
T |
5: 100,910,507 (GRCm39) |
|
probably null |
Het |
Herc2 |
A |
G |
7: 55,827,660 (GRCm39) |
I2914V |
probably benign |
Het |
Hnrnph1 |
T |
C |
11: 50,269,237 (GRCm39) |
V27A |
probably damaging |
Het |
Hs1bp3 |
G |
T |
12: 8,374,007 (GRCm39) |
G182C |
probably damaging |
Het |
Idnk |
C |
T |
13: 58,311,267 (GRCm39) |
P78L |
probably benign |
Het |
Il10ra |
T |
C |
9: 45,166,919 (GRCm39) |
D544G |
probably benign |
Het |
Inpp5e |
T |
C |
2: 26,290,918 (GRCm39) |
D383G |
probably damaging |
Het |
Jak1 |
A |
T |
4: 101,036,911 (GRCm39) |
V243D |
probably damaging |
Het |
Kcnma1 |
A |
T |
14: 23,359,220 (GRCm39) |
S1036T |
probably damaging |
Het |
Kif26a |
G |
A |
12: 112,123,776 (GRCm39) |
C127Y |
probably damaging |
Het |
Kif2c |
T |
C |
4: 117,023,608 (GRCm39) |
E368G |
probably damaging |
Het |
Lasp1 |
T |
A |
11: 97,724,530 (GRCm39) |
|
probably null |
Het |
Lcor |
T |
A |
19: 41,572,601 (GRCm39) |
V452D |
probably benign |
Het |
Lrrtm1 |
C |
G |
6: 77,221,661 (GRCm39) |
H373D |
probably benign |
Het |
Matr3 |
T |
A |
18: 35,705,754 (GRCm39) |
D226E |
probably damaging |
Het |
Mmp17 |
G |
A |
5: 129,682,730 (GRCm39) |
W456* |
probably null |
Het |
Mpp4 |
T |
C |
1: 59,164,748 (GRCm39) |
E463G |
probably damaging |
Het |
Myh6 |
A |
C |
14: 55,194,419 (GRCm39) |
F737V |
probably damaging |
Het |
Nars2 |
T |
A |
7: 96,672,948 (GRCm39) |
D271E |
probably benign |
Het |
Nav2 |
A |
G |
7: 49,254,258 (GRCm39) |
E2352G |
probably damaging |
Het |
Nckap1 |
A |
G |
2: 80,353,718 (GRCm39) |
|
probably null |
Het |
Nckap5 |
A |
T |
1: 125,955,324 (GRCm39) |
S477R |
probably damaging |
Het |
Nek11 |
T |
G |
9: 105,175,488 (GRCm39) |
I319L |
probably benign |
Het |
Neto2 |
A |
G |
8: 86,396,393 (GRCm39) |
I84T |
probably damaging |
Het |
Nlrp9a |
A |
T |
7: 26,250,369 (GRCm39) |
I45F |
probably damaging |
Het |
Numa1 |
G |
A |
7: 101,662,012 (GRCm39) |
R548H |
probably damaging |
Het |
Or10a5 |
A |
C |
7: 106,635,364 (GRCm39) |
M1L |
probably benign |
Het |
Or14c39 |
A |
C |
7: 86,344,395 (GRCm39) |
I244L |
probably benign |
Het |
Or2ag1b |
A |
T |
7: 106,288,740 (GRCm39) |
L66H |
probably damaging |
Het |
Or4c10 |
A |
T |
2: 89,760,923 (GRCm39) |
M257L |
probably benign |
Het |
Or4c100 |
T |
A |
2: 88,356,254 (GRCm39) |
I109N |
probably damaging |
Het |
Or4k36 |
T |
A |
2: 111,146,574 (GRCm39) |
F250Y |
probably benign |
Het |
Or7g25 |
A |
G |
9: 19,160,149 (GRCm39) |
V182A |
probably benign |
Het |
Or9m1 |
A |
T |
2: 87,733,533 (GRCm39) |
N162K |
probably damaging |
Het |
Pcdhb16 |
T |
A |
18: 37,612,894 (GRCm39) |
|
probably null |
Het |
Pdcd10 |
T |
C |
3: 75,448,553 (GRCm39) |
T4A |
probably damaging |
Het |
Pgc |
A |
T |
17: 48,039,819 (GRCm39) |
Y71F |
probably damaging |
Het |
Phlpp1 |
G |
A |
1: 106,317,481 (GRCm39) |
G1234E |
probably damaging |
Het |
Prr27 |
T |
C |
5: 87,990,888 (GRCm39) |
F167L |
probably benign |
Het |
Prrc2b |
T |
A |
2: 32,116,330 (GRCm39) |
S1421T |
possibly damaging |
Het |
Pxmp2 |
A |
G |
5: 110,431,518 (GRCm39) |
V75A |
probably benign |
Het |
Pygl |
A |
T |
12: 70,243,807 (GRCm39) |
M545K |
probably null |
Het |
Ranbp9 |
A |
G |
13: 43,574,733 (GRCm39) |
Y412H |
possibly damaging |
Het |
Rcc1 |
A |
G |
4: 132,065,064 (GRCm39) |
V140A |
probably damaging |
Het |
Reln |
A |
G |
5: 22,184,718 (GRCm39) |
V1599A |
probably benign |
Het |
Rhebl1 |
A |
T |
15: 98,776,903 (GRCm39) |
D122E |
probably damaging |
Het |
Rock2 |
C |
T |
12: 17,009,492 (GRCm39) |
L676F |
probably benign |
Het |
Scn9a |
A |
T |
2: 66,357,087 (GRCm39) |
D1062E |
probably benign |
Het |
Sec63 |
T |
C |
10: 42,681,186 (GRCm39) |
I390T |
probably damaging |
Het |
Slc10a6 |
T |
C |
5: 103,754,493 (GRCm39) |
E346G |
probably benign |
Het |
Slc12a3 |
G |
A |
8: 95,075,216 (GRCm39) |
V737M |
possibly damaging |
Het |
Slc12a8 |
T |
C |
16: 33,426,629 (GRCm39) |
|
probably null |
Het |
Slc25a38 |
T |
A |
9: 119,949,354 (GRCm39) |
I102N |
probably damaging |
Het |
Spg7 |
T |
A |
8: 123,807,394 (GRCm39) |
V390E |
probably damaging |
Het |
Tbc1d20 |
T |
C |
2: 152,144,228 (GRCm39) |
V75A |
probably benign |
Het |
Tesk1 |
T |
A |
4: 43,445,555 (GRCm39) |
C243* |
probably null |
Het |
Ttk |
T |
A |
9: 83,725,739 (GRCm39) |
N220K |
possibly damaging |
Het |
Ttll5 |
A |
G |
12: 85,965,948 (GRCm39) |
E651G |
probably benign |
Het |
Tubd1 |
T |
C |
11: 86,457,879 (GRCm39) |
Y426H |
probably damaging |
Het |
Uba6 |
T |
C |
5: 86,288,293 (GRCm39) |
|
silent |
Het |
Ube2ql1 |
G |
A |
13: 69,852,289 (GRCm39) |
R263W |
probably damaging |
Het |
Vmn2r117 |
C |
T |
17: 23,678,812 (GRCm39) |
G804D |
probably damaging |
Het |
Vmn2r25 |
C |
T |
6: 123,805,406 (GRCm39) |
E484K |
probably benign |
Het |
Vmn2r4 |
T |
A |
3: 64,296,476 (GRCm39) |
I770F |
possibly damaging |
Het |
Vmn2r82 |
G |
A |
10: 79,214,589 (GRCm39) |
V191M |
probably benign |
Het |
Zbtb45 |
C |
T |
7: 12,742,037 (GRCm39) |
V74M |
probably damaging |
Het |
Zfp366 |
T |
C |
13: 99,370,609 (GRCm39) |
V443A |
possibly damaging |
Het |
Zfyve1 |
A |
T |
12: 83,598,345 (GRCm39) |
C628S |
probably damaging |
Het |
Zfyve26 |
A |
T |
12: 79,296,469 (GRCm39) |
|
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 |
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 |
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 |
|