Other mutations in this stock |
Total: 95 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930522L14Rik |
A |
G |
5: 109,736,789 (GRCm38) |
V401A |
probably benign |
Het |
Abca7 |
G |
T |
10: 80,008,950 (GRCm38) |
W1502L |
probably damaging |
Het |
Adcy7 |
A |
G |
8: 88,308,840 (GRCm38) |
E124G |
probably benign |
Het |
Aif1l |
G |
A |
2: 31,965,106 (GRCm38) |
E66K |
probably benign |
Het |
Aldh8a1 |
A |
T |
10: 21,395,493 (GRCm38) |
M373L |
probably benign |
Het |
Alg6 |
T |
C |
4: 99,741,578 (GRCm38) |
Y131H |
probably benign |
Het |
Arhgef6 |
T |
C |
X: 57,338,562 (GRCm38) |
M5V |
probably benign |
Het |
Arrdc4 |
A |
T |
7: 68,741,874 (GRCm38) |
I215K |
probably damaging |
Het |
Asb4 |
A |
G |
6: 5,390,798 (GRCm38) |
|
probably null |
Het |
Astn1 |
T |
C |
1: 158,504,251 (GRCm38) |
I305T |
probably benign |
Het |
Atp5f1b |
T |
A |
10: 128,084,080 (GRCm38) |
|
probably benign |
Het |
Atp8a1 |
C |
A |
5: 67,631,567 (GRCm38) |
M1044I |
probably benign |
Het |
Atp9b |
C |
T |
18: 80,909,591 (GRCm38) |
|
probably null |
Het |
Brd10 |
T |
A |
19: 29,719,160 (GRCm38) |
T978S |
possibly damaging |
Het |
Btaf1 |
A |
G |
19: 36,951,118 (GRCm38) |
H113R |
probably benign |
Het |
C87436 |
G |
T |
6: 86,453,612 (GRCm38) |
C338F |
possibly damaging |
Het |
Casz1 |
T |
C |
4: 148,942,900 (GRCm38) |
|
probably benign |
Het |
Cbr3 |
T |
A |
16: 93,690,482 (GRCm38) |
H184Q |
probably damaging |
Het |
Cct8l1 |
T |
C |
5: 25,517,099 (GRCm38) |
S271P |
possibly damaging |
Het |
Cdc34 |
G |
T |
10: 79,685,338 (GRCm38) |
|
probably null |
Het |
Cdc34 |
A |
G |
10: 79,685,340 (GRCm38) |
K77R |
probably benign |
Het |
Cdh20 |
A |
G |
1: 104,934,345 (GRCm38) |
|
probably benign |
Het |
Celsr3 |
A |
G |
9: 108,828,958 (GRCm38) |
E880G |
probably damaging |
Het |
Cers1 |
T |
G |
8: 70,321,491 (GRCm38) |
|
probably null |
Het |
Cntn5 |
T |
C |
9: 9,673,983 (GRCm38) |
I705V |
probably benign |
Het |
Dennd4c |
T |
A |
4: 86,803,010 (GRCm38) |
D636E |
probably damaging |
Het |
Dnah11 |
T |
C |
12: 118,190,825 (GRCm38) |
E240G |
probably benign |
Het |
Dpysl3 |
T |
C |
18: 43,363,518 (GRCm38) |
E151G |
probably damaging |
Het |
Efcab9 |
T |
G |
11: 32,524,457 (GRCm38) |
T9P |
possibly damaging |
Het |
Eif4g2 |
A |
T |
7: 111,074,487 (GRCm38) |
F725Y |
probably damaging |
Het |
Epha6 |
T |
A |
16: 59,775,728 (GRCm38) |
I867F |
probably null |
Het |
Erbin |
T |
C |
13: 103,843,451 (GRCm38) |
|
probably benign |
Het |
Evi5l |
A |
G |
8: 4,203,560 (GRCm38) |
E468G |
probably damaging |
Het |
Filip1l |
C |
T |
16: 57,570,038 (GRCm38) |
R330W |
probably damaging |
Het |
Fmo3 |
C |
T |
1: 162,958,573 (GRCm38) |
V283M |
possibly damaging |
Het |
Gabarapl1 |
A |
T |
6: 129,533,518 (GRCm38) |
K24N |
possibly damaging |
Het |
Gigyf1 |
C |
T |
5: 137,522,508 (GRCm38) |
|
probably benign |
Het |
Gm5581 |
T |
A |
6: 131,181,399 (GRCm38) |
|
noncoding transcript |
Het |
Gon4l |
G |
T |
3: 88,892,599 (GRCm38) |
K850N |
probably damaging |
Het |
Igf2bp3 |
C |
T |
6: 49,109,046 (GRCm38) |
R233H |
probably damaging |
Het |
Iqcf4 |
G |
A |
9: 106,568,694 (GRCm38) |
R85C |
probably benign |
Het |
Kalrn |
C |
T |
16: 34,212,873 (GRCm38) |
R473Q |
probably damaging |
Het |
Lmod2 |
T |
A |
6: 24,603,377 (GRCm38) |
V117E |
probably damaging |
Het |
Mapk11 |
A |
G |
15: 89,144,391 (GRCm38) |
|
probably null |
Het |
Mcm3 |
G |
A |
1: 20,805,879 (GRCm38) |
R664C |
probably damaging |
Het |
Mex3d |
A |
G |
10: 80,386,936 (GRCm38) |
M162T |
probably benign |
Het |
Mrgprb3 |
A |
G |
7: 48,643,023 (GRCm38) |
I260T |
probably benign |
Het |
Ncor2 |
G |
T |
5: 125,028,615 (GRCm38) |
A1637D |
possibly damaging |
Het |
Nedd4 |
T |
A |
9: 72,730,907 (GRCm38) |
D441E |
probably damaging |
Het |
Nek5 |
A |
T |
8: 22,109,912 (GRCm38) |
C194S |
probably damaging |
Het |
Nos1ap |
T |
C |
1: 170,318,878 (GRCm38) |
D369G |
possibly damaging |
Het |
Ntrk1 |
G |
T |
3: 87,780,084 (GRCm38) |
T681K |
probably damaging |
Het |
Or13a24 |
T |
C |
7: 140,574,470 (GRCm38) |
W106R |
probably damaging |
Het |
Or4f14 |
A |
G |
2: 111,912,181 (GRCm38) |
F250L |
possibly damaging |
Het |
Otogl |
C |
T |
10: 107,899,461 (GRCm38) |
W154* |
probably null |
Het |
Pcdh20 |
T |
C |
14: 88,469,184 (GRCm38) |
T227A |
possibly damaging |
Het |
Pcdhb17 |
T |
C |
18: 37,487,271 (GRCm38) |
S705P |
probably damaging |
Het |
Piezo2 |
T |
C |
18: 63,124,642 (GRCm38) |
H335R |
possibly damaging |
Het |
Pkn2 |
T |
C |
3: 142,793,854 (GRCm38) |
Q954R |
probably damaging |
Het |
Pramel23 |
C |
A |
4: 143,698,270 (GRCm38) |
C201F |
probably benign |
Het |
Prkcq |
G |
A |
2: 11,232,631 (GRCm38) |
V74M |
probably damaging |
Het |
Prkrip1 |
A |
T |
5: 136,189,635 (GRCm38) |
|
probably null |
Het |
Pttg1ip2 |
A |
T |
5: 5,478,943 (GRCm38) |
I24N |
possibly damaging |
Het |
Rb1cc1 |
A |
G |
1: 6,214,680 (GRCm38) |
|
probably benign |
Het |
Rbm5 |
A |
T |
9: 107,767,564 (GRCm38) |
Y11* |
probably null |
Het |
Rsf1 |
CG |
CGACGGCGGTG |
7: 97,579,908 (GRCm38) |
|
probably benign |
Het |
Ryr3 |
C |
A |
2: 112,860,460 (GRCm38) |
V1082L |
probably damaging |
Het |
Scart2 |
A |
G |
7: 140,297,265 (GRCm38) |
E831G |
probably benign |
Het |
Sel1l3 |
C |
A |
5: 53,170,447 (GRCm38) |
E497* |
probably null |
Het |
Serpina6 |
A |
T |
12: 103,653,923 (GRCm38) |
I189N |
probably damaging |
Het |
Serpinb11 |
A |
T |
1: 107,376,802 (GRCm38) |
T166S |
probably benign |
Het |
Skint7 |
T |
C |
4: 111,982,073 (GRCm38) |
L188S |
probably benign |
Het |
Slc25a45 |
C |
T |
19: 5,884,930 (GRCm38) |
A269V |
probably damaging |
Het |
Sltm |
A |
G |
9: 70,561,800 (GRCm38) |
T114A |
probably benign |
Het |
Sned1 |
G |
A |
1: 93,281,654 (GRCm38) |
V830M |
possibly damaging |
Het |
Spen |
C |
A |
4: 141,472,950 (GRCm38) |
V2766L |
probably damaging |
Het |
Srgap2 |
T |
A |
1: 131,319,537 (GRCm38) |
I445F |
possibly damaging |
Het |
Stox2 |
A |
T |
8: 47,194,016 (GRCm38) |
Y200* |
probably null |
Het |
Strada |
C |
A |
11: 106,164,184 (GRCm38) |
R384L |
probably damaging |
Het |
Tctn2 |
G |
A |
5: 124,619,031 (GRCm38) |
|
noncoding transcript |
Het |
Tgfbr3l |
G |
T |
8: 4,249,282 (GRCm38) |
R461L |
probably benign |
Het |
Tmem65 |
A |
G |
15: 58,790,149 (GRCm38) |
|
probably benign |
Het |
Tpst1 |
G |
T |
5: 130,114,502 (GRCm38) |
V294F |
possibly damaging |
Het |
Trim23 |
A |
G |
13: 104,198,618 (GRCm38) |
Y384C |
probably damaging |
Het |
Ube3b |
C |
G |
5: 114,404,617 (GRCm38) |
L512V |
possibly damaging |
Het |
Ubxn4 |
T |
A |
1: 128,256,179 (GRCm38) |
V92E |
probably damaging |
Het |
Vmn2r57 |
A |
T |
7: 41,400,643 (GRCm38) |
C561S |
probably damaging |
Het |
Vwa8 |
A |
G |
14: 78,908,195 (GRCm38) |
D104G |
probably damaging |
Het |
Wdr25 |
T |
A |
12: 109,026,438 (GRCm38) |
L73* |
probably null |
Het |
Wnt9a |
G |
A |
11: 59,330,902 (GRCm38) |
A209T |
probably benign |
Het |
Zcchc17 |
A |
C |
4: 130,329,595 (GRCm38) |
C133G |
probably damaging |
Het |
Zdhhc18 |
T |
A |
4: 133,608,676 (GRCm38) |
M375L |
probably benign |
Het |
Zfhx3 |
T |
C |
8: 108,951,644 (GRCm38) |
F3109L |
probably benign |
Het |
Zfp202 |
T |
A |
9: 40,210,466 (GRCm38) |
D286E |
probably benign |
Het |
Zzef1 |
T |
C |
11: 72,893,332 (GRCm38) |
L2021P |
probably benign |
Het |
|
Other mutations in Dnah2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00087:Dnah2
|
APN |
11 |
69,492,672 (GRCm38) |
missense |
possibly damaging |
0.93 |
IGL00418:Dnah2
|
APN |
11 |
69,495,066 (GRCm38) |
splice site |
probably benign |
|
IGL00772:Dnah2
|
APN |
11 |
69,451,257 (GRCm38) |
missense |
probably damaging |
0.97 |
IGL00819:Dnah2
|
APN |
11 |
69,473,350 (GRCm38) |
critical splice donor site |
probably null |
|
IGL00827:Dnah2
|
APN |
11 |
69,448,457 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01060:Dnah2
|
APN |
11 |
69,478,092 (GRCm38) |
missense |
possibly damaging |
0.86 |
IGL01340:Dnah2
|
APN |
11 |
69,493,184 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL01349:Dnah2
|
APN |
11 |
69,475,606 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL01413:Dnah2
|
APN |
11 |
69,432,964 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL01451:Dnah2
|
APN |
11 |
69,474,191 (GRCm38) |
splice site |
probably benign |
|
IGL01480:Dnah2
|
APN |
11 |
69,458,371 (GRCm38) |
missense |
possibly damaging |
0.91 |
IGL01537:Dnah2
|
APN |
11 |
69,516,080 (GRCm38) |
missense |
probably benign |
0.17 |
IGL01592:Dnah2
|
APN |
11 |
69,431,087 (GRCm38) |
missense |
probably benign |
0.14 |
IGL01612:Dnah2
|
APN |
11 |
69,465,063 (GRCm38) |
splice site |
probably benign |
|
IGL01667:Dnah2
|
APN |
11 |
69,544,395 (GRCm38) |
missense |
probably benign |
|
IGL01667:Dnah2
|
APN |
11 |
69,520,941 (GRCm38) |
missense |
probably damaging |
0.98 |
IGL01691:Dnah2
|
APN |
11 |
69,539,443 (GRCm38) |
missense |
probably benign |
|
IGL02019:Dnah2
|
APN |
11 |
69,474,285 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02039:Dnah2
|
APN |
11 |
69,499,212 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02076:Dnah2
|
APN |
11 |
69,422,559 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL02085:Dnah2
|
APN |
11 |
69,458,185 (GRCm38) |
missense |
probably benign |
0.07 |
IGL02158:Dnah2
|
APN |
11 |
69,458,123 (GRCm38) |
missense |
probably benign |
|
IGL02381:Dnah2
|
APN |
11 |
69,446,292 (GRCm38) |
missense |
probably benign |
0.25 |
IGL02681:Dnah2
|
APN |
11 |
69,452,933 (GRCm38) |
missense |
probably benign |
0.40 |
IGL02957:Dnah2
|
APN |
11 |
69,448,507 (GRCm38) |
missense |
possibly damaging |
0.96 |
IGL02961:Dnah2
|
APN |
11 |
69,518,414 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02969:Dnah2
|
APN |
11 |
69,521,187 (GRCm38) |
missense |
possibly damaging |
0.80 |
IGL03117:Dnah2
|
APN |
11 |
69,436,291 (GRCm38) |
splice site |
probably benign |
|
IGL03120:Dnah2
|
APN |
11 |
69,421,848 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03183:Dnah2
|
APN |
11 |
69,458,488 (GRCm38) |
missense |
possibly damaging |
0.94 |
IGL03197:Dnah2
|
APN |
11 |
69,459,263 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03263:Dnah2
|
APN |
11 |
69,529,381 (GRCm38) |
critical splice donor site |
probably null |
|
IGL03333:Dnah2
|
APN |
11 |
69,495,123 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03338:Dnah2
|
APN |
11 |
69,496,577 (GRCm38) |
missense |
probably benign |
0.13 |
argyrios
|
UTSW |
11 |
69,516,590 (GRCm38) |
missense |
possibly damaging |
0.47 |
Aureus
|
UTSW |
11 |
69,429,348 (GRCm38) |
missense |
probably damaging |
1.00 |
platinum
|
UTSW |
11 |
69,458,042 (GRCm38) |
missense |
probably damaging |
0.96 |
R0334_dnah2_144
|
UTSW |
11 |
69,436,836 (GRCm38) |
missense |
probably damaging |
1.00 |
R2150_dnah2_212
|
UTSW |
11 |
69,515,761 (GRCm38) |
missense |
probably benign |
0.14 |
BB005:Dnah2
|
UTSW |
11 |
69,430,835 (GRCm38) |
missense |
probably damaging |
0.98 |
BB015:Dnah2
|
UTSW |
11 |
69,430,835 (GRCm38) |
missense |
probably damaging |
0.98 |
E0370:Dnah2
|
UTSW |
11 |
69,515,615 (GRCm38) |
splice site |
probably null |
|
P0026:Dnah2
|
UTSW |
11 |
69,464,947 (GRCm38) |
missense |
probably damaging |
1.00 |
R0133:Dnah2
|
UTSW |
11 |
69,421,009 (GRCm38) |
missense |
probably damaging |
1.00 |
R0190:Dnah2
|
UTSW |
11 |
69,435,249 (GRCm38) |
missense |
probably damaging |
1.00 |
R0334:Dnah2
|
UTSW |
11 |
69,436,836 (GRCm38) |
missense |
probably damaging |
1.00 |
R0359:Dnah2
|
UTSW |
11 |
69,529,531 (GRCm38) |
missense |
probably benign |
0.00 |
R0386:Dnah2
|
UTSW |
11 |
69,447,861 (GRCm38) |
missense |
probably damaging |
1.00 |
R0414:Dnah2
|
UTSW |
11 |
69,499,238 (GRCm38) |
missense |
probably benign |
0.26 |
R0427:Dnah2
|
UTSW |
11 |
69,452,879 (GRCm38) |
missense |
probably damaging |
0.99 |
R0433:Dnah2
|
UTSW |
11 |
69,459,288 (GRCm38) |
missense |
probably damaging |
1.00 |
R0442:Dnah2
|
UTSW |
11 |
69,448,542 (GRCm38) |
missense |
probably damaging |
1.00 |
R0462:Dnah2
|
UTSW |
11 |
69,459,201 (GRCm38) |
missense |
probably damaging |
1.00 |
R0463:Dnah2
|
UTSW |
11 |
69,423,126 (GRCm38) |
missense |
probably damaging |
1.00 |
R0611:Dnah2
|
UTSW |
11 |
69,499,194 (GRCm38) |
missense |
probably damaging |
1.00 |
R0626:Dnah2
|
UTSW |
11 |
69,477,683 (GRCm38) |
missense |
probably benign |
0.07 |
R0924:Dnah2
|
UTSW |
11 |
69,421,308 (GRCm38) |
missense |
probably damaging |
1.00 |
R0968:Dnah2
|
UTSW |
11 |
69,448,519 (GRCm38) |
missense |
possibly damaging |
0.67 |
R1066:Dnah2
|
UTSW |
11 |
69,447,819 (GRCm38) |
missense |
probably damaging |
1.00 |
R1183:Dnah2
|
UTSW |
11 |
69,446,648 (GRCm38) |
missense |
possibly damaging |
0.95 |
R1184:Dnah2
|
UTSW |
11 |
69,499,190 (GRCm38) |
missense |
probably damaging |
1.00 |
R1186:Dnah2
|
UTSW |
11 |
69,515,700 (GRCm38) |
missense |
probably damaging |
0.99 |
R1453:Dnah2
|
UTSW |
11 |
69,451,050 (GRCm38) |
missense |
probably damaging |
0.99 |
R1498:Dnah2
|
UTSW |
11 |
69,520,667 (GRCm38) |
splice site |
probably null |
|
R1538:Dnah2
|
UTSW |
11 |
69,477,202 (GRCm38) |
missense |
probably benign |
0.17 |
R1574:Dnah2
|
UTSW |
11 |
69,514,688 (GRCm38) |
missense |
probably benign |
0.26 |
R1574:Dnah2
|
UTSW |
11 |
69,514,688 (GRCm38) |
missense |
probably benign |
0.26 |
R1590:Dnah2
|
UTSW |
11 |
69,521,198 (GRCm38) |
missense |
probably benign |
0.00 |
R1590:Dnah2
|
UTSW |
11 |
69,422,754 (GRCm38) |
critical splice donor site |
probably null |
|
R1655:Dnah2
|
UTSW |
11 |
69,473,854 (GRCm38) |
missense |
probably damaging |
1.00 |
R1695:Dnah2
|
UTSW |
11 |
69,514,691 (GRCm38) |
missense |
possibly damaging |
0.74 |
R1726:Dnah2
|
UTSW |
11 |
69,497,889 (GRCm38) |
missense |
probably damaging |
1.00 |
R1815:Dnah2
|
UTSW |
11 |
69,475,574 (GRCm38) |
missense |
probably damaging |
1.00 |
R1822:Dnah2
|
UTSW |
11 |
69,514,804 (GRCm38) |
missense |
probably damaging |
1.00 |
R1859:Dnah2
|
UTSW |
11 |
69,437,886 (GRCm38) |
missense |
probably damaging |
0.99 |
R1911:Dnah2
|
UTSW |
11 |
69,515,752 (GRCm38) |
missense |
possibly damaging |
0.64 |
R1913:Dnah2
|
UTSW |
11 |
69,464,930 (GRCm38) |
missense |
probably damaging |
1.00 |
R1981:Dnah2
|
UTSW |
11 |
69,474,325 (GRCm38) |
missense |
probably damaging |
1.00 |
R2010:Dnah2
|
UTSW |
11 |
69,458,358 (GRCm38) |
critical splice donor site |
probably null |
|
R2016:Dnah2
|
UTSW |
11 |
69,437,070 (GRCm38) |
missense |
probably damaging |
0.97 |
R2017:Dnah2
|
UTSW |
11 |
69,437,070 (GRCm38) |
missense |
probably damaging |
0.97 |
R2044:Dnah2
|
UTSW |
11 |
69,524,240 (GRCm38) |
missense |
probably benign |
0.14 |
R2077:Dnah2
|
UTSW |
11 |
69,496,606 (GRCm38) |
missense |
possibly damaging |
0.73 |
R2096:Dnah2
|
UTSW |
11 |
69,455,916 (GRCm38) |
missense |
probably damaging |
0.98 |
R2099:Dnah2
|
UTSW |
11 |
69,493,237 (GRCm38) |
missense |
probably damaging |
1.00 |
R2127:Dnah2
|
UTSW |
11 |
69,458,185 (GRCm38) |
missense |
probably benign |
0.02 |
R2128:Dnah2
|
UTSW |
11 |
69,458,185 (GRCm38) |
missense |
probably benign |
0.02 |
R2146:Dnah2
|
UTSW |
11 |
69,515,761 (GRCm38) |
missense |
probably benign |
0.14 |
R2147:Dnah2
|
UTSW |
11 |
69,515,761 (GRCm38) |
missense |
probably benign |
0.14 |
R2150:Dnah2
|
UTSW |
11 |
69,515,761 (GRCm38) |
missense |
probably benign |
0.14 |
R2404:Dnah2
|
UTSW |
11 |
69,437,221 (GRCm38) |
missense |
probably damaging |
0.99 |
R2510:Dnah2
|
UTSW |
11 |
69,524,206 (GRCm38) |
nonsense |
probably null |
|
R2517:Dnah2
|
UTSW |
11 |
69,516,644 (GRCm38) |
missense |
probably damaging |
1.00 |
R3014:Dnah2
|
UTSW |
11 |
69,430,478 (GRCm38) |
missense |
probably benign |
|
R3741:Dnah2
|
UTSW |
11 |
69,448,469 (GRCm38) |
missense |
probably damaging |
1.00 |
R3814:Dnah2
|
UTSW |
11 |
69,492,650 (GRCm38) |
splice site |
probably null |
|
R3872:Dnah2
|
UTSW |
11 |
69,429,348 (GRCm38) |
missense |
probably damaging |
1.00 |
R3873:Dnah2
|
UTSW |
11 |
69,429,348 (GRCm38) |
missense |
probably damaging |
1.00 |
R3874:Dnah2
|
UTSW |
11 |
69,429,348 (GRCm38) |
missense |
probably damaging |
1.00 |
R3875:Dnah2
|
UTSW |
11 |
69,429,348 (GRCm38) |
missense |
probably damaging |
1.00 |
R3881:Dnah2
|
UTSW |
11 |
69,451,347 (GRCm38) |
missense |
possibly damaging |
0.94 |
R3953:Dnah2
|
UTSW |
11 |
69,454,103 (GRCm38) |
missense |
probably damaging |
1.00 |
R3956:Dnah2
|
UTSW |
11 |
69,484,021 (GRCm38) |
missense |
probably benign |
0.00 |
R4501:Dnah2
|
UTSW |
11 |
69,477,659 (GRCm38) |
missense |
probably benign |
|
R4515:Dnah2
|
UTSW |
11 |
69,465,631 (GRCm38) |
missense |
possibly damaging |
0.61 |
R4612:Dnah2
|
UTSW |
11 |
69,483,367 (GRCm38) |
missense |
possibly damaging |
0.93 |
R4625:Dnah2
|
UTSW |
11 |
69,463,661 (GRCm38) |
missense |
probably damaging |
1.00 |
R4627:Dnah2
|
UTSW |
11 |
69,465,376 (GRCm38) |
missense |
probably damaging |
1.00 |
R4642:Dnah2
|
UTSW |
11 |
69,496,559 (GRCm38) |
missense |
probably benign |
0.00 |
R4683:Dnah2
|
UTSW |
11 |
69,458,942 (GRCm38) |
missense |
probably damaging |
1.00 |
R4698:Dnah2
|
UTSW |
11 |
69,498,532 (GRCm38) |
missense |
probably damaging |
1.00 |
R4710:Dnah2
|
UTSW |
11 |
69,478,077 (GRCm38) |
missense |
probably damaging |
1.00 |
R4712:Dnah2
|
UTSW |
11 |
69,516,590 (GRCm38) |
missense |
possibly damaging |
0.47 |
R4713:Dnah2
|
UTSW |
11 |
69,476,688 (GRCm38) |
missense |
probably damaging |
1.00 |
R4717:Dnah2
|
UTSW |
11 |
69,429,357 (GRCm38) |
missense |
probably benign |
0.00 |
R4740:Dnah2
|
UTSW |
11 |
69,458,042 (GRCm38) |
missense |
probably damaging |
0.96 |
R4780:Dnah2
|
UTSW |
11 |
69,473,871 (GRCm38) |
missense |
probably damaging |
0.97 |
R4825:Dnah2
|
UTSW |
11 |
69,423,205 (GRCm38) |
missense |
probably damaging |
1.00 |
R4864:Dnah2
|
UTSW |
11 |
69,422,590 (GRCm38) |
missense |
probably damaging |
0.98 |
R4868:Dnah2
|
UTSW |
11 |
69,463,648 (GRCm38) |
missense |
probably damaging |
1.00 |
R4879:Dnah2
|
UTSW |
11 |
69,476,691 (GRCm38) |
missense |
probably damaging |
1.00 |
R4908:Dnah2
|
UTSW |
11 |
69,521,147 (GRCm38) |
missense |
probably benign |
0.00 |
R4911:Dnah2
|
UTSW |
11 |
69,499,104 (GRCm38) |
critical splice donor site |
probably null |
|
R4954:Dnah2
|
UTSW |
11 |
69,539,496 (GRCm38) |
missense |
possibly damaging |
0.61 |
R4962:Dnah2
|
UTSW |
11 |
69,455,973 (GRCm38) |
nonsense |
probably null |
|
R5015:Dnah2
|
UTSW |
11 |
69,497,882 (GRCm38) |
missense |
possibly damaging |
0.89 |
R5049:Dnah2
|
UTSW |
11 |
69,448,166 (GRCm38) |
missense |
probably damaging |
1.00 |
R5055:Dnah2
|
UTSW |
11 |
69,520,773 (GRCm38) |
missense |
possibly damaging |
0.67 |
R5153:Dnah2
|
UTSW |
11 |
69,520,933 (GRCm38) |
missense |
possibly damaging |
0.84 |
R5155:Dnah2
|
UTSW |
11 |
69,422,536 (GRCm38) |
missense |
probably damaging |
1.00 |
R5186:Dnah2
|
UTSW |
11 |
69,435,884 (GRCm38) |
missense |
probably damaging |
1.00 |
R5187:Dnah2
|
UTSW |
11 |
69,458,920 (GRCm38) |
missense |
probably benign |
0.15 |
R5208:Dnah2
|
UTSW |
11 |
69,458,920 (GRCm38) |
missense |
probably benign |
0.15 |
R5252:Dnah2
|
UTSW |
11 |
69,529,469 (GRCm38) |
missense |
probably damaging |
0.98 |
R5296:Dnah2
|
UTSW |
11 |
69,458,920 (GRCm38) |
missense |
probably benign |
0.15 |
R5298:Dnah2
|
UTSW |
11 |
69,458,920 (GRCm38) |
missense |
probably benign |
0.15 |
R5299:Dnah2
|
UTSW |
11 |
69,458,920 (GRCm38) |
missense |
probably benign |
0.15 |
R5301:Dnah2
|
UTSW |
11 |
69,458,920 (GRCm38) |
missense |
probably benign |
0.15 |
R5324:Dnah2
|
UTSW |
11 |
69,457,993 (GRCm38) |
missense |
probably benign |
0.07 |
R5350:Dnah2
|
UTSW |
11 |
69,516,036 (GRCm38) |
missense |
possibly damaging |
0.48 |
R5377:Dnah2
|
UTSW |
11 |
69,421,848 (GRCm38) |
missense |
probably damaging |
1.00 |
R5393:Dnah2
|
UTSW |
11 |
69,500,857 (GRCm38) |
missense |
probably benign |
|
R5421:Dnah2
|
UTSW |
11 |
69,435,636 (GRCm38) |
missense |
probably damaging |
1.00 |
R5452:Dnah2
|
UTSW |
11 |
69,524,383 (GRCm38) |
missense |
probably damaging |
1.00 |
R5461:Dnah2
|
UTSW |
11 |
69,473,351 (GRCm38) |
critical splice donor site |
probably null |
|
R5474:Dnah2
|
UTSW |
11 |
69,458,920 (GRCm38) |
missense |
probably benign |
0.15 |
R5476:Dnah2
|
UTSW |
11 |
69,458,920 (GRCm38) |
missense |
probably benign |
0.15 |
R5477:Dnah2
|
UTSW |
11 |
69,458,920 (GRCm38) |
missense |
probably benign |
0.15 |
R5510:Dnah2
|
UTSW |
11 |
69,458,920 (GRCm38) |
missense |
probably benign |
0.15 |
R5527:Dnah2
|
UTSW |
11 |
69,437,188 (GRCm38) |
nonsense |
probably null |
|
R5566:Dnah2
|
UTSW |
11 |
69,516,569 (GRCm38) |
nonsense |
probably null |
|
R5587:Dnah2
|
UTSW |
11 |
69,437,242 (GRCm38) |
missense |
probably damaging |
1.00 |
R5628:Dnah2
|
UTSW |
11 |
69,458,920 (GRCm38) |
missense |
probably benign |
0.15 |
R5688:Dnah2
|
UTSW |
11 |
69,458,920 (GRCm38) |
missense |
probably benign |
0.15 |
R5690:Dnah2
|
UTSW |
11 |
69,491,544 (GRCm38) |
missense |
probably benign |
0.15 |
R5711:Dnah2
|
UTSW |
11 |
69,435,390 (GRCm38) |
missense |
probably damaging |
1.00 |
R5735:Dnah2
|
UTSW |
11 |
69,430,817 (GRCm38) |
missense |
possibly damaging |
0.93 |
R5826:Dnah2
|
UTSW |
11 |
69,458,920 (GRCm38) |
missense |
probably benign |
0.15 |
R5913:Dnah2
|
UTSW |
11 |
69,448,430 (GRCm38) |
missense |
probably damaging |
1.00 |
R5914:Dnah2
|
UTSW |
11 |
69,458,920 (GRCm38) |
missense |
probably benign |
0.15 |
R5960:Dnah2
|
UTSW |
11 |
69,458,920 (GRCm38) |
missense |
probably benign |
0.15 |
R5961:Dnah2
|
UTSW |
11 |
69,458,920 (GRCm38) |
missense |
probably benign |
0.15 |
R5961:Dnah2
|
UTSW |
11 |
69,431,148 (GRCm38) |
missense |
probably damaging |
1.00 |
R5977:Dnah2
|
UTSW |
11 |
69,520,881 (GRCm38) |
missense |
possibly damaging |
0.79 |
R6020:Dnah2
|
UTSW |
11 |
69,500,839 (GRCm38) |
missense |
probably benign |
|
R6036:Dnah2
|
UTSW |
11 |
69,458,920 (GRCm38) |
missense |
probably benign |
0.15 |
R6036:Dnah2
|
UTSW |
11 |
69,458,920 (GRCm38) |
missense |
probably benign |
0.15 |
R6050:Dnah2
|
UTSW |
11 |
69,458,920 (GRCm38) |
missense |
probably benign |
0.15 |
R6086:Dnah2
|
UTSW |
11 |
69,516,008 (GRCm38) |
missense |
probably benign |
0.30 |
R6115:Dnah2
|
UTSW |
11 |
69,446,649 (GRCm38) |
missense |
probably damaging |
1.00 |
R6123:Dnah2
|
UTSW |
11 |
69,518,359 (GRCm38) |
missense |
probably benign |
0.29 |
R6159:Dnah2
|
UTSW |
11 |
69,458,920 (GRCm38) |
missense |
probably benign |
0.15 |
R6159:Dnah2
|
UTSW |
11 |
69,458,542 (GRCm38) |
missense |
probably damaging |
1.00 |
R6163:Dnah2
|
UTSW |
11 |
69,520,903 (GRCm38) |
nonsense |
probably null |
|
R6171:Dnah2
|
UTSW |
11 |
69,423,042 (GRCm38) |
missense |
probably damaging |
1.00 |
R6263:Dnah2
|
UTSW |
11 |
69,457,412 (GRCm38) |
missense |
probably damaging |
1.00 |
R6298:Dnah2
|
UTSW |
11 |
69,491,641 (GRCm38) |
missense |
probably benign |
0.25 |
R6352:Dnah2
|
UTSW |
11 |
69,448,227 (GRCm38) |
missense |
probably damaging |
1.00 |
R6399:Dnah2
|
UTSW |
11 |
69,458,518 (GRCm38) |
missense |
probably damaging |
0.98 |
R6466:Dnah2
|
UTSW |
11 |
69,539,415 (GRCm38) |
missense |
probably benign |
|
R6478:Dnah2
|
UTSW |
11 |
69,516,010 (GRCm38) |
missense |
probably benign |
0.01 |
R6516:Dnah2
|
UTSW |
11 |
69,465,386 (GRCm38) |
missense |
probably benign |
0.34 |
R6538:Dnah2
|
UTSW |
11 |
69,437,197 (GRCm38) |
missense |
possibly damaging |
0.87 |
R6802:Dnah2
|
UTSW |
11 |
69,423,690 (GRCm38) |
missense |
probably damaging |
1.00 |
R6861:Dnah2
|
UTSW |
11 |
69,455,963 (GRCm38) |
missense |
possibly damaging |
0.64 |
R6869:Dnah2
|
UTSW |
11 |
69,429,471 (GRCm38) |
missense |
probably damaging |
1.00 |
R6894:Dnah2
|
UTSW |
11 |
69,484,260 (GRCm38) |
missense |
probably benign |
0.12 |
R6935:Dnah2
|
UTSW |
11 |
69,421,741 (GRCm38) |
missense |
probably damaging |
1.00 |
R7017:Dnah2
|
UTSW |
11 |
69,491,547 (GRCm38) |
nonsense |
probably null |
|
R7073:Dnah2
|
UTSW |
11 |
69,430,492 (GRCm38) |
nonsense |
probably null |
|
R7111:Dnah2
|
UTSW |
11 |
69,446,753 (GRCm38) |
splice site |
probably null |
|
R7125:Dnah2
|
UTSW |
11 |
69,436,182 (GRCm38) |
missense |
probably damaging |
0.99 |
R7137:Dnah2
|
UTSW |
11 |
69,491,555 (GRCm38) |
missense |
probably damaging |
1.00 |
R7190:Dnah2
|
UTSW |
11 |
69,549,097 (GRCm38) |
splice site |
probably null |
|
R7214:Dnah2
|
UTSW |
11 |
69,431,109 (GRCm38) |
missense |
probably damaging |
1.00 |
R7227:Dnah2
|
UTSW |
11 |
69,421,396 (GRCm38) |
missense |
probably damaging |
0.99 |
R7238:Dnah2
|
UTSW |
11 |
69,459,146 (GRCm38) |
critical splice donor site |
probably null |
|
R7256:Dnah2
|
UTSW |
11 |
69,431,094 (GRCm38) |
missense |
probably damaging |
1.00 |
R7267:Dnah2
|
UTSW |
11 |
69,500,817 (GRCm38) |
missense |
probably damaging |
1.00 |
R7420:Dnah2
|
UTSW |
11 |
69,478,797 (GRCm38) |
missense |
possibly damaging |
0.94 |
R7421:Dnah2
|
UTSW |
11 |
69,492,805 (GRCm38) |
missense |
probably benign |
0.25 |
R7437:Dnah2
|
UTSW |
11 |
69,498,627 (GRCm38) |
missense |
probably damaging |
1.00 |
R7461:Dnah2
|
UTSW |
11 |
69,548,990 (GRCm38) |
critical splice donor site |
probably null |
|
R7473:Dnah2
|
UTSW |
11 |
69,491,658 (GRCm38) |
missense |
probably damaging |
0.99 |
R7528:Dnah2
|
UTSW |
11 |
69,500,796 (GRCm38) |
missense |
probably damaging |
0.99 |
R7613:Dnah2
|
UTSW |
11 |
69,548,990 (GRCm38) |
critical splice donor site |
probably null |
|
R7615:Dnah2
|
UTSW |
11 |
69,435,304 (GRCm38) |
missense |
probably damaging |
0.99 |
R7626:Dnah2
|
UTSW |
11 |
69,498,685 (GRCm38) |
missense |
probably damaging |
0.99 |
R7745:Dnah2
|
UTSW |
11 |
69,451,318 (GRCm38) |
nonsense |
probably null |
|
R7764:Dnah2
|
UTSW |
11 |
69,458,158 (GRCm38) |
missense |
probably benign |
0.29 |
R7793:Dnah2
|
UTSW |
11 |
69,495,214 (GRCm38) |
missense |
probably benign |
0.00 |
R7819:Dnah2
|
UTSW |
11 |
69,516,593 (GRCm38) |
missense |
probably benign |
0.01 |
R7881:Dnah2
|
UTSW |
11 |
69,431,238 (GRCm38) |
missense |
probably damaging |
1.00 |
R7900:Dnah2
|
UTSW |
11 |
69,518,428 (GRCm38) |
missense |
probably damaging |
1.00 |
R7916:Dnah2
|
UTSW |
11 |
69,421,148 (GRCm38) |
critical splice acceptor site |
probably null |
|
R7921:Dnah2
|
UTSW |
11 |
69,520,834 (GRCm38) |
missense |
probably benign |
|
R7928:Dnah2
|
UTSW |
11 |
69,430,835 (GRCm38) |
missense |
probably damaging |
0.98 |
R7937:Dnah2
|
UTSW |
11 |
69,517,685 (GRCm38) |
nonsense |
probably null |
|
R7995:Dnah2
|
UTSW |
11 |
69,520,737 (GRCm38) |
missense |
possibly damaging |
0.77 |
R8202:Dnah2
|
UTSW |
11 |
69,478,823 (GRCm38) |
missense |
probably benign |
0.00 |
R8208:Dnah2
|
UTSW |
11 |
69,520,852 (GRCm38) |
missense |
probably benign |
0.05 |
R8215:Dnah2
|
UTSW |
11 |
69,435,367 (GRCm38) |
missense |
probably damaging |
1.00 |
R8279:Dnah2
|
UTSW |
11 |
69,475,573 (GRCm38) |
missense |
probably damaging |
1.00 |
R8338:Dnah2
|
UTSW |
11 |
69,487,296 (GRCm38) |
missense |
probably damaging |
1.00 |
R8348:Dnah2
|
UTSW |
11 |
69,429,447 (GRCm38) |
missense |
possibly damaging |
0.95 |
R8405:Dnah2
|
UTSW |
11 |
69,458,463 (GRCm38) |
missense |
probably damaging |
1.00 |
R8407:Dnah2
|
UTSW |
11 |
69,459,278 (GRCm38) |
missense |
probably benign |
0.00 |
R8493:Dnah2
|
UTSW |
11 |
69,452,978 (GRCm38) |
missense |
probably damaging |
1.00 |
R8673:Dnah2
|
UTSW |
11 |
69,514,697 (GRCm38) |
missense |
probably benign |
0.23 |
R8725:Dnah2
|
UTSW |
11 |
69,524,179 (GRCm38) |
missense |
probably damaging |
1.00 |
R8727:Dnah2
|
UTSW |
11 |
69,524,179 (GRCm38) |
missense |
probably damaging |
1.00 |
R8730:Dnah2
|
UTSW |
11 |
69,493,261 (GRCm38) |
missense |
possibly damaging |
0.73 |
R8804:Dnah2
|
UTSW |
11 |
69,465,685 (GRCm38) |
missense |
probably benign |
0.01 |
R8876:Dnah2
|
UTSW |
11 |
69,491,522 (GRCm38) |
missense |
probably damaging |
1.00 |
R8894:Dnah2
|
UTSW |
11 |
69,492,222 (GRCm38) |
missense |
probably benign |
0.01 |
R8938:Dnah2
|
UTSW |
11 |
69,437,928 (GRCm38) |
missense |
probably damaging |
0.99 |
R9044:Dnah2
|
UTSW |
11 |
69,529,421 (GRCm38) |
missense |
probably benign |
|
R9085:Dnah2
|
UTSW |
11 |
69,429,398 (GRCm38) |
missense |
possibly damaging |
0.69 |
R9110:Dnah2
|
UTSW |
11 |
69,544,382 (GRCm38) |
missense |
probably benign |
|
R9156:Dnah2
|
UTSW |
11 |
69,422,861 (GRCm38) |
missense |
|
|
R9251:Dnah2
|
UTSW |
11 |
69,515,793 (GRCm38) |
missense |
probably damaging |
1.00 |
R9258:Dnah2
|
UTSW |
11 |
69,477,253 (GRCm38) |
missense |
probably damaging |
1.00 |
R9279:Dnah2
|
UTSW |
11 |
69,518,278 (GRCm38) |
missense |
probably benign |
0.01 |
R9318:Dnah2
|
UTSW |
11 |
69,484,329 (GRCm38) |
missense |
probably benign |
0.07 |
R9321:Dnah2
|
UTSW |
11 |
69,448,113 (GRCm38) |
critical splice donor site |
probably null |
|
R9350:Dnah2
|
UTSW |
11 |
69,493,247 (GRCm38) |
missense |
probably benign |
0.10 |
R9358:Dnah2
|
UTSW |
11 |
69,515,766 (GRCm38) |
missense |
probably damaging |
0.99 |
R9417:Dnah2
|
UTSW |
11 |
69,436,164 (GRCm38) |
missense |
probably damaging |
1.00 |
R9420:Dnah2
|
UTSW |
11 |
69,478,116 (GRCm38) |
missense |
probably benign |
0.09 |
R9438:Dnah2
|
UTSW |
11 |
69,473,394 (GRCm38) |
missense |
probably damaging |
1.00 |
R9469:Dnah2
|
UTSW |
11 |
69,431,070 (GRCm38) |
missense |
probably damaging |
1.00 |
R9487:Dnah2
|
UTSW |
11 |
69,515,791 (GRCm38) |
missense |
possibly damaging |
0.47 |
R9495:Dnah2
|
UTSW |
11 |
69,454,382 (GRCm38) |
missense |
possibly damaging |
0.89 |
R9579:Dnah2
|
UTSW |
11 |
69,477,215 (GRCm38) |
missense |
probably damaging |
1.00 |
R9608:Dnah2
|
UTSW |
11 |
69,454,062 (GRCm38) |
missense |
probably null |
1.00 |
R9651:Dnah2
|
UTSW |
11 |
69,450,998 (GRCm38) |
critical splice donor site |
probably null |
|
R9662:Dnah2
|
UTSW |
11 |
69,452,937 (GRCm38) |
missense |
probably benign |
|
RF004:Dnah2
|
UTSW |
11 |
69,437,187 (GRCm38) |
missense |
probably benign |
0.24 |
U24488:Dnah2
|
UTSW |
11 |
69,483,822 (GRCm38) |
missense |
probably damaging |
0.99 |
X0021:Dnah2
|
UTSW |
11 |
69,448,562 (GRCm38) |
missense |
possibly damaging |
0.81 |
Z1088:Dnah2
|
UTSW |
11 |
69,430,793 (GRCm38) |
missense |
probably damaging |
1.00 |
Z1176:Dnah2
|
UTSW |
11 |
69,421,821 (GRCm38) |
missense |
possibly damaging |
0.46 |
Z1176:Dnah2
|
UTSW |
11 |
69,516,523 (GRCm38) |
missense |
probably damaging |
1.00 |
Z1176:Dnah2
|
UTSW |
11 |
69,516,481 (GRCm38) |
missense |
probably damaging |
1.00 |
Z1176:Dnah2
|
UTSW |
11 |
69,498,667 (GRCm38) |
missense |
probably benign |
0.12 |
Z1176:Dnah2
|
UTSW |
11 |
69,487,054 (GRCm38) |
missense |
possibly damaging |
0.46 |
Z1176:Dnah2
|
UTSW |
11 |
69,451,120 (GRCm38) |
missense |
probably benign |
|
Z1177:Dnah2
|
UTSW |
11 |
69,544,557 (GRCm38) |
critical splice acceptor site |
probably null |
|
Z1177:Dnah2
|
UTSW |
11 |
69,463,453 (GRCm38) |
missense |
possibly damaging |
0.63 |
|