Other mutations in this stock |
Total: 132 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aacs |
A |
G |
5: 125,583,224 (GRCm39) |
D260G |
possibly damaging |
Het |
Aadacl4 |
T |
A |
4: 144,340,362 (GRCm39) |
L29H |
probably damaging |
Het |
Abca7 |
T |
C |
10: 79,848,022 (GRCm39) |
|
probably null |
Het |
Adgre1 |
G |
A |
17: 57,754,832 (GRCm39) |
M643I |
possibly damaging |
Het |
Adgrl2 |
A |
T |
3: 148,596,099 (GRCm39) |
M79K |
probably damaging |
Het |
Ankrd55 |
T |
A |
13: 112,459,573 (GRCm39) |
|
probably null |
Het |
Aopep |
A |
T |
13: 63,318,753 (GRCm39) |
|
probably null |
Het |
Arhgap21 |
A |
G |
2: 20,863,800 (GRCm39) |
I1257T |
probably damaging |
Het |
Arhgap26 |
T |
A |
18: 39,126,690 (GRCm39) |
|
probably benign |
Het |
Arhgap39 |
A |
G |
15: 76,622,005 (GRCm39) |
S199P |
probably damaging |
Het |
Arhgef5 |
A |
G |
6: 43,249,762 (GRCm39) |
D171G |
probably benign |
Het |
Atp7a |
T |
C |
X: 105,163,980 (GRCm39) |
V1305A |
probably damaging |
Het |
B3gnt3 |
T |
A |
8: 72,145,578 (GRCm39) |
R263S |
probably benign |
Het |
B9d1 |
A |
C |
11: 61,398,497 (GRCm39) |
D59A |
probably benign |
Het |
Bag2 |
A |
T |
1: 33,787,357 (GRCm39) |
I55N |
probably benign |
Het |
Bank1 |
T |
C |
3: 135,990,004 (GRCm39) |
I29V |
probably benign |
Het |
Bbs2 |
A |
T |
8: 94,815,743 (GRCm39) |
D174E |
probably damaging |
Het |
Bmp8b |
T |
C |
4: 123,009,030 (GRCm39) |
W203R |
probably damaging |
Het |
Cacnb2 |
A |
T |
2: 14,986,151 (GRCm39) |
E359D |
possibly damaging |
Het |
Camp |
T |
A |
9: 109,676,651 (GRCm39) |
|
probably null |
Het |
Casp4 |
C |
T |
9: 5,328,580 (GRCm39) |
|
probably benign |
Het |
Ccdc110 |
A |
T |
8: 46,395,944 (GRCm39) |
T612S |
probably benign |
Het |
Cd209b |
T |
A |
8: 3,976,640 (GRCm39) |
|
probably null |
Het |
Cemip |
T |
C |
7: 83,632,461 (GRCm39) |
D367G |
probably damaging |
Het |
Cers5 |
T |
A |
15: 99,644,960 (GRCm39) |
N131I |
probably damaging |
Het |
Cfhr4 |
T |
G |
1: 139,702,301 (GRCm39) |
D61A |
probably damaging |
Het |
Chd5 |
T |
G |
4: 152,445,129 (GRCm39) |
V370G |
probably damaging |
Het |
Cipc |
C |
A |
12: 86,999,531 (GRCm39) |
Q20K |
probably benign |
Het |
Cnr2 |
T |
A |
4: 135,644,512 (GRCm39) |
F197I |
possibly damaging |
Het |
Col7a1 |
G |
A |
9: 108,804,287 (GRCm39) |
G2233S |
unknown |
Het |
Dcdc2b |
T |
A |
4: 129,505,060 (GRCm39) |
I125F |
possibly damaging |
Het |
Ddi2 |
A |
G |
4: 141,411,713 (GRCm39) |
S400P |
probably benign |
Het |
Ddx31 |
C |
A |
2: 28,794,696 (GRCm39) |
T664K |
probably benign |
Het |
Dhx30 |
C |
A |
9: 109,929,992 (GRCm39) |
G35C |
probably damaging |
Het |
Dmxl2 |
G |
A |
9: 54,318,937 (GRCm39) |
T1576I |
probably damaging |
Het |
Dnah1 |
T |
C |
14: 31,017,280 (GRCm39) |
Y1510C |
probably damaging |
Het |
Dock10 |
C |
A |
1: 80,583,953 (GRCm39) |
G163C |
probably damaging |
Het |
Edar |
T |
C |
10: 58,457,146 (GRCm39) |
N144S |
probably benign |
Het |
Elavl2 |
T |
A |
4: 91,196,915 (GRCm39) |
E54D |
possibly damaging |
Het |
Enam |
T |
G |
5: 88,650,173 (GRCm39) |
S561A |
probably benign |
Het |
Ercc5 |
C |
A |
1: 44,206,031 (GRCm39) |
H315N |
possibly damaging |
Het |
Esp31 |
A |
G |
17: 38,955,552 (GRCm39) |
E65G |
possibly damaging |
Het |
Faap100 |
T |
C |
11: 120,262,939 (GRCm39) |
I806M |
probably benign |
Het |
Fbxw21 |
T |
C |
9: 108,974,731 (GRCm39) |
Y263C |
probably damaging |
Het |
Fsip2 |
T |
A |
2: 82,811,837 (GRCm39) |
S2719T |
possibly damaging |
Het |
Fv1 |
T |
C |
4: 147,953,875 (GRCm39) |
V147A |
probably benign |
Het |
Gal |
T |
C |
19: 3,461,590 (GRCm39) |
E65G |
probably benign |
Het |
Galnt2l |
A |
G |
8: 123,807,343 (GRCm39) |
|
probably benign |
Het |
Galnt6 |
T |
C |
15: 100,614,059 (GRCm39) |
T81A |
probably benign |
Het |
Gcc2 |
A |
G |
10: 58,106,261 (GRCm39) |
E399G |
probably damaging |
Het |
Gfi1b |
A |
T |
2: 28,500,114 (GRCm39) |
C306S |
probably damaging |
Het |
Gm10654 |
T |
A |
8: 71,384,496 (GRCm39) |
|
noncoding transcript |
Het |
Gm4953 |
T |
A |
1: 158,995,929 (GRCm39) |
|
noncoding transcript |
Het |
Gorasp2 |
T |
C |
2: 70,518,683 (GRCm39) |
|
probably benign |
Het |
Gse1 |
T |
C |
8: 121,295,205 (GRCm39) |
|
probably benign |
Het |
H2-D1 |
A |
G |
17: 35,484,973 (GRCm39) |
E278G |
probably damaging |
Het |
Herc2 |
T |
C |
7: 55,877,640 (GRCm39) |
L4569P |
probably damaging |
Het |
Hgs |
T |
A |
11: 120,368,028 (GRCm39) |
S246T |
probably damaging |
Het |
Hs2st1 |
T |
C |
3: 144,170,843 (GRCm39) |
T110A |
probably benign |
Het |
Hydin |
A |
G |
8: 111,322,070 (GRCm39) |
Y4574C |
probably benign |
Het |
Ighv1-23 |
C |
A |
12: 114,728,372 (GRCm39) |
V17F |
possibly damaging |
Het |
Ighv8-14 |
A |
T |
12: 115,772,185 (GRCm39) |
|
noncoding transcript |
Het |
Igsf21 |
C |
T |
4: 139,761,934 (GRCm39) |
R248H |
probably benign |
Het |
Il22b |
T |
C |
10: 118,130,894 (GRCm39) |
M1V |
probably null |
Het |
Il23r |
T |
C |
6: 67,400,545 (GRCm39) |
N595S |
probably benign |
Het |
Il5ra |
G |
T |
6: 106,692,629 (GRCm39) |
P372Q |
probably damaging |
Het |
Inppl1 |
A |
G |
7: 101,481,516 (GRCm39) |
V222A |
possibly damaging |
Het |
Ints10 |
T |
C |
8: 69,279,964 (GRCm39) |
V697A |
probably damaging |
Het |
Isg15 |
T |
A |
4: 156,284,217 (GRCm39) |
T104S |
probably benign |
Het |
Kif11 |
A |
G |
19: 37,406,385 (GRCm39) |
T983A |
probably benign |
Het |
Kif3b |
A |
T |
2: 153,159,212 (GRCm39) |
K338* |
probably null |
Het |
Kpna2 |
T |
A |
11: 106,881,545 (GRCm39) |
I362F |
probably damaging |
Het |
Lama2 |
G |
A |
10: 27,014,923 (GRCm39) |
T1595M |
probably damaging |
Het |
Lrrc36 |
A |
G |
8: 106,153,567 (GRCm39) |
T126A |
probably benign |
Het |
Lrrk1 |
T |
A |
7: 65,945,202 (GRCm39) |
D604V |
probably damaging |
Het |
Map7d1 |
T |
C |
4: 126,130,484 (GRCm39) |
K409E |
probably damaging |
Het |
Mast2 |
T |
C |
4: 116,210,254 (GRCm39) |
T110A |
probably benign |
Het |
Micall2 |
G |
A |
5: 139,702,580 (GRCm39) |
T221M |
probably damaging |
Het |
Morc2b |
T |
A |
17: 33,356,351 (GRCm39) |
N474Y |
probably damaging |
Het |
Myo1e |
T |
A |
9: 70,250,378 (GRCm39) |
M528K |
probably benign |
Het |
Nlrp1c-ps |
G |
T |
11: 71,151,195 (GRCm39) |
|
noncoding transcript |
Het |
Nostrin |
T |
C |
2: 68,991,486 (GRCm39) |
S160P |
possibly damaging |
Het |
Nup133 |
T |
C |
8: 124,653,870 (GRCm39) |
R530G |
possibly damaging |
Het |
Or2f2 |
T |
A |
6: 42,767,138 (GRCm39) |
L55H |
probably damaging |
Het |
Or5p64 |
T |
C |
7: 107,855,244 (GRCm39) |
I34V |
possibly damaging |
Het |
Or8c16 |
A |
G |
9: 38,130,392 (GRCm39) |
E91G |
probably damaging |
Het |
Pabpc4l |
A |
T |
3: 46,400,597 (GRCm39) |
M349K |
possibly damaging |
Het |
Pah |
G |
A |
10: 87,406,129 (GRCm39) |
G256S |
probably benign |
Het |
Pigk |
T |
C |
3: 152,445,841 (GRCm39) |
S151P |
probably damaging |
Het |
Plcd4 |
A |
C |
1: 74,603,572 (GRCm39) |
T658P |
possibly damaging |
Het |
Pld4 |
A |
T |
12: 112,730,951 (GRCm39) |
S178C |
probably benign |
Het |
Polr1a |
G |
A |
6: 71,886,213 (GRCm39) |
E23K |
possibly damaging |
Het |
Pomt1 |
T |
C |
2: 32,131,691 (GRCm39) |
S127P |
probably damaging |
Het |
Pon2 |
A |
G |
6: 5,269,029 (GRCm39) |
V215A |
possibly damaging |
Het |
Ppp3cb |
A |
T |
14: 20,559,508 (GRCm39) |
M416K |
probably damaging |
Het |
Prdm1 |
A |
T |
10: 44,318,048 (GRCm39) |
N273K |
possibly damaging |
Het |
Prg4 |
T |
A |
1: 150,331,574 (GRCm39) |
|
probably benign |
Het |
Prkn |
G |
T |
17: 11,059,359 (GRCm39) |
|
probably benign |
Het |
Ptch1 |
G |
A |
13: 63,670,866 (GRCm39) |
T888M |
probably damaging |
Het |
Pusl1 |
T |
G |
4: 155,975,899 (GRCm39) |
|
probably benign |
Het |
Rapgef6 |
A |
T |
11: 54,513,143 (GRCm39) |
E122D |
probably damaging |
Het |
Rif1 |
C |
T |
2: 52,000,530 (GRCm39) |
T1328I |
probably damaging |
Het |
Rngtt |
T |
G |
4: 33,500,292 (GRCm39) |
|
probably null |
Het |
Runx2 |
G |
A |
17: 45,125,079 (GRCm39) |
P80L |
probably damaging |
Het |
Samd1 |
A |
G |
8: 84,725,618 (GRCm39) |
|
probably benign |
Het |
Scamp5 |
A |
T |
9: 57,358,735 (GRCm39) |
F14I |
probably damaging |
Het |
Shank3 |
C |
T |
15: 89,388,547 (GRCm39) |
R380C |
probably damaging |
Het |
Shisal2a |
T |
C |
4: 108,234,658 (GRCm39) |
T70A |
probably benign |
Het |
Slc1a4 |
C |
A |
11: 20,282,166 (GRCm39) |
A103S |
probably damaging |
Het |
Slc39a14 |
A |
G |
14: 70,547,371 (GRCm39) |
V325A |
probably benign |
Het |
Slc5a9 |
C |
A |
4: 111,748,941 (GRCm39) |
|
probably null |
Het |
Spata6l |
G |
A |
19: 28,874,903 (GRCm39) |
|
probably benign |
Het |
Spta1 |
T |
A |
1: 174,013,213 (GRCm39) |
S375T |
probably damaging |
Het |
Sval1 |
A |
G |
6: 41,932,378 (GRCm39) |
N76S |
probably benign |
Het |
Synpo |
C |
T |
18: 60,762,936 (GRCm39) |
|
probably benign |
Het |
Sytl5 |
C |
T |
X: 9,781,841 (GRCm39) |
P181L |
possibly damaging |
Het |
Tacc1 |
A |
G |
8: 25,672,622 (GRCm39) |
M111T |
possibly damaging |
Het |
Tec |
T |
C |
5: 72,913,694 (GRCm39) |
D613G |
probably benign |
Het |
Tecpr2 |
C |
T |
12: 110,897,921 (GRCm39) |
T391I |
possibly damaging |
Het |
Thop1 |
G |
A |
10: 80,909,125 (GRCm39) |
G52D |
probably damaging |
Het |
Tmco5 |
T |
A |
2: 116,722,689 (GRCm39) |
V270D |
possibly damaging |
Het |
Ttn |
C |
T |
2: 76,556,973 (GRCm39) |
E28265K |
possibly damaging |
Het |
Tuft1 |
T |
C |
3: 94,542,750 (GRCm39) |
D72G |
probably damaging |
Het |
Tyrp1 |
C |
T |
4: 80,769,144 (GRCm39) |
|
probably benign |
Het |
Usp9y |
T |
C |
Y: 1,308,041 (GRCm39) |
D2265G |
probably damaging |
Het |
Vmn2r104 |
G |
A |
17: 20,250,288 (GRCm39) |
A661V |
probably benign |
Het |
Vwa5a |
A |
T |
9: 38,649,268 (GRCm39) |
N672I |
probably benign |
Het |
Wdr95 |
A |
T |
5: 149,535,157 (GRCm39) |
K772* |
probably null |
Het |
Ybx1 |
T |
C |
4: 119,140,010 (GRCm39) |
T106A |
probably benign |
Het |
Ypel3 |
T |
C |
7: 126,376,961 (GRCm39) |
S14P |
probably benign |
Het |
Zfp518a |
T |
A |
19: 40,903,972 (GRCm39) |
S1300R |
probably benign |
Het |
Zscan5b |
A |
T |
7: 6,242,189 (GRCm39) |
*469Y |
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 |
R4908:Dnah2
|
UTSW |
11 |
69,411,973 (GRCm39) |
missense |
probably benign |
0.00 |
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 |
|