Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1810062G17Rik |
G |
A |
3: 36,481,806 (GRCm38) |
G74S |
unknown |
Het |
Aimp1 |
A |
T |
3: 132,667,492 (GRCm38) |
L229Q |
probably benign |
Het |
Arhgef6 |
T |
C |
X: 57,299,505 (GRCm38) |
T52A |
possibly damaging |
Het |
Aste1 |
C |
A |
9: 105,403,502 (GRCm38) |
H25Q |
probably damaging |
Het |
Atp13a1 |
G |
A |
8: 69,791,360 (GRCm38) |
G36R |
possibly damaging |
Het |
Bahcc1 |
T |
C |
11: 120,272,778 (GRCm38) |
V634A |
probably damaging |
Het |
Bltp1 |
T |
G |
3: 36,928,551 (GRCm38) |
N788K |
probably benign |
Het |
C1s1 |
A |
T |
6: 124,537,394 (GRCm38) |
Y168N |
probably damaging |
Het |
Camsap2 |
T |
C |
1: 136,274,868 (GRCm38) |
S612G |
probably damaging |
Het |
Cdh23 |
C |
A |
10: 60,314,227 (GRCm38) |
R2611L |
probably damaging |
Het |
Cfap20dc |
A |
T |
14: 8,511,021 (GRCm38) |
F464L |
probably damaging |
Het |
Cilp2 |
A |
G |
8: 69,881,694 (GRCm38) |
Y885H |
probably damaging |
Het |
Dhrs3 |
C |
T |
4: 144,927,188 (GRCm38) |
T227I |
possibly damaging |
Het |
Dnah3 |
T |
G |
7: 120,095,177 (GRCm38) |
M1L |
probably benign |
Het |
Ehbp1l1 |
A |
G |
19: 5,719,283 (GRCm38) |
I664T |
probably benign |
Het |
Eif4e |
C |
T |
3: 138,555,458 (GRCm38) |
T171I |
probably benign |
Het |
Elfn1 |
C |
T |
5: 139,973,316 (GRCm38) |
R692W |
probably damaging |
Het |
Eps8l3 |
T |
A |
3: 107,879,372 (GRCm38) |
M1K |
probably null |
Het |
Evi5 |
C |
A |
5: 107,813,545 (GRCm38) |
|
probably null |
Het |
Fancd2 |
A |
T |
6: 113,593,291 (GRCm38) |
D1401V |
probably damaging |
Het |
Fat2 |
G |
A |
11: 55,253,827 (GRCm38) |
R4074C |
probably damaging |
Het |
Fkbp4 |
A |
T |
6: 128,435,802 (GRCm38) |
V55E |
probably benign |
Het |
Fnip1 |
A |
G |
11: 54,482,503 (GRCm38) |
D180G |
probably damaging |
Het |
Galc |
A |
G |
12: 98,254,230 (GRCm38) |
F126S |
possibly damaging |
Het |
Gdf7 |
C |
T |
12: 8,301,729 (GRCm38) |
V69M |
unknown |
Het |
Glis2 |
A |
G |
16: 4,608,711 (GRCm38) |
E22G |
probably damaging |
Het |
H2bc3 |
G |
A |
13: 23,747,128 (GRCm38) |
V112M |
possibly damaging |
Het |
Hps4 |
T |
A |
5: 112,369,476 (GRCm38) |
V243E |
probably damaging |
Het |
Ighe |
T |
A |
12: 113,271,488 (GRCm38) |
I351F |
unknown |
Het |
Irak4 |
A |
T |
15: 94,551,806 (GRCm38) |
R55S |
probably damaging |
Het |
Itpr2 |
G |
A |
6: 146,227,524 (GRCm38) |
|
probably null |
Het |
Katnip |
A |
G |
7: 125,872,956 (GRCm38) |
I1544M |
possibly damaging |
Het |
Kirrel3 |
T |
C |
9: 34,939,198 (GRCm38) |
Y41H |
probably damaging |
Het |
Krr1 |
A |
G |
10: 111,975,569 (GRCm38) |
E56G |
possibly damaging |
Het |
Lgi1 |
G |
A |
19: 38,301,235 (GRCm38) |
V250I |
probably damaging |
Het |
Lipf |
A |
G |
19: 33,973,546 (GRCm38) |
N306D |
probably benign |
Het |
Lman2l |
C |
T |
1: 36,445,181 (GRCm38) |
W18* |
probably null |
Het |
Lztfl1 |
T |
A |
9: 123,702,186 (GRCm38) |
N239I |
possibly damaging |
Het |
Mief1 |
T |
C |
15: 80,247,925 (GRCm38) |
S66P |
possibly damaging |
Het |
Mmp8 |
C |
A |
9: 7,567,534 (GRCm38) |
S465* |
probably null |
Het |
Muc2 |
A |
T |
7: 141,700,875 (GRCm38) |
T208S |
probably damaging |
Het |
Myh8 |
A |
T |
11: 67,297,164 (GRCm38) |
K921* |
probably null |
Het |
Myh9 |
T |
C |
15: 77,771,947 (GRCm38) |
E1121G |
probably benign |
Het |
Nbn |
T |
C |
4: 15,969,393 (GRCm38) |
S213P |
probably damaging |
Het |
Nol10 |
A |
G |
12: 17,416,101 (GRCm38) |
E499G |
probably benign |
Het |
Nxn |
T |
C |
11: 76,398,801 (GRCm38) |
E87G |
probably damaging |
Het |
Or14c40 |
A |
G |
7: 86,664,603 (GRCm38) |
T314A |
probably benign |
Het |
Or51f2 |
T |
A |
7: 102,877,685 (GRCm38) |
C188* |
probably null |
Het |
Or8g23 |
T |
C |
9: 39,060,099 (GRCm38) |
H189R |
probably benign |
Het |
Pds5b |
CATTTATTTATTTATTTATTTATTTATTTATTTATTTAT |
CATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTAT |
5: 150,775,354 (GRCm38) |
|
probably benign |
Het |
Pigk |
A |
G |
3: 152,766,514 (GRCm38) |
I354M |
probably damaging |
Het |
Pigl |
T |
A |
11: 62,458,682 (GRCm38) |
C75S |
probably damaging |
Het |
Pm20d1 |
T |
A |
1: 131,812,114 (GRCm38) |
I400N |
probably benign |
Het |
Prkg2 |
T |
A |
5: 99,024,805 (GRCm38) |
H17L |
probably benign |
Het |
Psmd1 |
T |
A |
1: 86,075,997 (GRCm38) |
L168Q |
probably damaging |
Het |
Rab3gap2 |
A |
T |
1: 185,278,281 (GRCm38) |
H1136L |
possibly damaging |
Het |
Rb1 |
T |
C |
14: 73,294,993 (GRCm38) |
T134A |
probably benign |
Het |
Rims1 |
T |
C |
1: 22,296,996 (GRCm38) |
E1024G |
probably damaging |
Het |
Rrp12 |
A |
G |
19: 41,872,937 (GRCm38) |
V977A |
probably benign |
Het |
Rusc2 |
C |
T |
4: 43,415,212 (GRCm38) |
P173S |
probably benign |
Het |
Selenov |
A |
T |
7: 28,288,022 (GRCm38) |
D310E |
probably damaging |
Het |
Serpina3f |
T |
A |
12: 104,217,323 (GRCm38) |
L148Q |
probably damaging |
Het |
Slc10a1 |
C |
T |
12: 80,960,447 (GRCm38) |
V187I |
probably benign |
Het |
Spsb2 |
A |
G |
6: 124,810,376 (GRCm38) |
K258E |
probably damaging |
Het |
Tas2r105 |
A |
C |
6: 131,687,402 (GRCm38) |
V21G |
probably benign |
Het |
Tmem229b-ps |
T |
A |
10: 53,475,199 (GRCm38) |
|
noncoding transcript |
Het |
Tnrc6a |
C |
G |
7: 123,171,046 (GRCm38) |
H686Q |
probably benign |
Het |
Trpc2 |
T |
A |
7: 102,094,573 (GRCm38) |
F715L |
probably benign |
Het |
Ube2t |
T |
A |
1: 134,969,298 (GRCm38) |
I56N |
probably benign |
Het |
Ubr4 |
T |
C |
4: 139,480,652 (GRCm38) |
Y4915H |
possibly damaging |
Het |
Usp32 |
T |
A |
11: 85,040,004 (GRCm38) |
E533D |
probably damaging |
Het |
Vipr2 |
T |
G |
12: 116,122,810 (GRCm38) |
|
probably null |
Het |
Vmn1r15 |
A |
G |
6: 57,258,284 (GRCm38) |
T46A |
probably benign |
Het |
Vmn1r203 |
T |
G |
13: 22,524,447 (GRCm38) |
S133A |
possibly damaging |
Het |
Vmn1r215 |
T |
G |
13: 23,076,208 (GRCm38) |
N139K |
probably damaging |
Het |
Vmn1r232 |
C |
T |
17: 20,913,339 (GRCm38) |
R333H |
probably benign |
Het |
Wdr20rt |
C |
A |
12: 65,227,214 (GRCm38) |
H311N |
possibly damaging |
Het |
Zranb1 |
T |
C |
7: 132,966,696 (GRCm38) |
|
probably null |
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 |
R1764:Dnah2
|
UTSW |
11 |
69,423,543 (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 |
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 |
|