Other mutations in this stock |
Total: 82 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933434E20Rik |
T |
C |
3: 90,058,653 (GRCm38) |
|
probably null |
Het |
A630095N17Rik |
G |
A |
1: 75,232,031 (GRCm38) |
T15I |
unknown |
Het |
Actr1b |
A |
G |
1: 36,709,819 (GRCm38) |
V12A |
probably benign |
Het |
Add1 |
A |
G |
5: 34,619,353 (GRCm38) |
T473A |
possibly damaging |
Het |
Akap11 |
A |
T |
14: 78,513,888 (GRCm38) |
V353E |
|
Het |
Alcam |
G |
A |
16: 52,452,519 (GRCm38) |
|
probably benign |
Het |
Alpi |
A |
G |
1: 87,099,647 (GRCm38) |
|
probably null |
Het |
Ap3s2 |
A |
G |
7: 79,916,031 (GRCm38) |
F49S |
probably damaging |
Het |
Arpc1a |
A |
G |
5: 145,101,076 (GRCm38) |
K174E |
probably benign |
Het |
Bbox1 |
A |
T |
2: 110,265,498 (GRCm38) |
S374T |
probably damaging |
Het |
Bean1 |
CT |
C |
8: 104,182,032 (GRCm38) |
|
probably null |
Het |
Bltp2 |
T |
C |
11: 78,267,115 (GRCm38) |
S368P |
possibly damaging |
Het |
Bmp2k |
A |
G |
5: 97,057,012 (GRCm38) |
N402S |
probably benign |
Het |
Bmper |
C |
A |
9: 23,375,630 (GRCm38) |
A284D |
probably benign |
Het |
Bnip5 |
G |
A |
17: 28,905,324 (GRCm38) |
R335W |
probably damaging |
Het |
Bpifb2 |
A |
T |
2: 153,881,196 (GRCm38) |
H124L |
possibly damaging |
Het |
Bsn |
C |
T |
9: 108,112,250 (GRCm38) |
R2101Q |
probably damaging |
Het |
Cacng1 |
T |
A |
11: 107,716,192 (GRCm38) |
D67V |
probably damaging |
Het |
Catsperg1 |
A |
G |
7: 29,195,478 (GRCm38) |
S565P |
probably damaging |
Het |
Cep126 |
C |
T |
9: 8,101,778 (GRCm38) |
E252K |
probably damaging |
Het |
Cep55 |
G |
A |
19: 38,069,936 (GRCm38) |
E326K |
probably damaging |
Het |
Cfap58 |
T |
A |
19: 47,974,625 (GRCm38) |
Y491* |
probably null |
Het |
Cpeb2 |
T |
C |
5: 43,277,505 (GRCm38) |
S747P |
|
Het |
Cryz |
T |
A |
3: 154,606,520 (GRCm38) |
S85T |
probably benign |
Het |
D2hgdh |
T |
C |
1: 93,838,078 (GRCm38) |
V367A |
probably damaging |
Het |
Dgkh |
T |
C |
14: 78,599,043 (GRCm38) |
N703S |
probably benign |
Het |
Dnah11 |
T |
C |
12: 117,903,176 (GRCm38) |
S4077G |
probably benign |
Het |
Dnah14 |
A |
G |
1: 181,752,139 (GRCm38) |
H3079R |
probably damaging |
Het |
Dnmt3b |
A |
G |
2: 153,684,450 (GRCm38) |
D804G |
probably damaging |
Het |
Ell2 |
A |
G |
13: 75,750,035 (GRCm38) |
E143G |
probably damaging |
Het |
Exoc2 |
A |
G |
13: 30,822,630 (GRCm38) |
|
probably null |
Het |
Fahd2a |
A |
T |
2: 127,440,456 (GRCm38) |
I131N |
probably damaging |
Het |
Fer1l5 |
A |
G |
1: 36,421,608 (GRCm38) |
N1976D |
possibly damaging |
Het |
Flt1 |
A |
G |
5: 147,594,595 (GRCm38) |
S853P |
probably damaging |
Het |
Frg2f1 |
C |
T |
4: 119,530,793 (GRCm38) |
V170I |
probably benign |
Het |
Gcn1 |
G |
A |
5: 115,581,804 (GRCm38) |
V373M |
probably benign |
Het |
Gm19965 |
A |
G |
1: 116,821,872 (GRCm38) |
T428A |
unknown |
Het |
Gm4792 |
A |
G |
10: 94,293,868 (GRCm38) |
I124T |
unknown |
Het |
Grik2 |
A |
T |
10: 49,113,522 (GRCm38) |
C804S |
probably benign |
Het |
Heatr6 |
T |
A |
11: 83,781,391 (GRCm38) |
I1075N |
probably damaging |
Het |
Hunk |
G |
A |
16: 90,453,700 (GRCm38) |
A211T |
probably damaging |
Het |
Ighe |
T |
C |
12: 113,271,356 (GRCm38) |
I395V |
probably damaging |
Het |
Ino80e |
A |
T |
7: 126,857,312 (GRCm38) |
S104T |
probably damaging |
Het |
Inpp4a |
A |
G |
1: 37,369,453 (GRCm38) |
Y305C |
probably benign |
Het |
Insrr |
T |
A |
3: 87,804,531 (GRCm38) |
|
probably null |
Het |
Itgae |
T |
G |
11: 73,140,678 (GRCm38) |
D1073E |
possibly damaging |
Het |
Klf11 |
G |
T |
12: 24,655,142 (GRCm38) |
|
probably null |
Het |
Lrguk |
A |
T |
6: 34,029,695 (GRCm38) |
K80M |
probably benign |
Het |
Map2 |
A |
T |
1: 66,415,458 (GRCm38) |
D1169V |
probably damaging |
Het |
Mpst |
G |
T |
15: 78,413,526 (GRCm38) |
C248F |
probably damaging |
Het |
Myo9a |
C |
A |
9: 59,895,244 (GRCm38) |
Q2005K |
probably benign |
Het |
Nfatc4 |
C |
T |
14: 55,831,964 (GRCm38) |
T649I |
probably benign |
Het |
Nmt1 |
A |
G |
11: 103,046,400 (GRCm38) |
R88G |
probably benign |
Het |
Nqo1 |
G |
A |
8: 107,403,097 (GRCm38) |
|
probably benign |
Het |
Nudt2 |
T |
G |
4: 41,477,576 (GRCm38) |
M19R |
probably benign |
Het |
Or10a49 |
T |
A |
7: 108,868,269 (GRCm38) |
K295M |
probably damaging |
Het |
Or12d2 |
T |
A |
17: 37,313,631 (GRCm38) |
Y251F |
probably benign |
Het |
Or9q2 |
C |
T |
19: 13,795,162 (GRCm38) |
V150M |
probably benign |
Het |
P2ry1 |
T |
A |
3: 61,004,088 (GRCm38) |
I216N |
probably damaging |
Het |
Pcx |
T |
A |
19: 4,619,561 (GRCm38) |
L823* |
probably null |
Het |
Pkhd1 |
A |
G |
1: 20,549,756 (GRCm38) |
V880A |
probably damaging |
Het |
Plcb1 |
A |
T |
2: 135,344,276 (GRCm38) |
N721I |
probably damaging |
Het |
Prdm15 |
T |
C |
16: 97,821,846 (GRCm38) |
K269E |
possibly damaging |
Het |
Prl7b1 |
A |
G |
13: 27,602,013 (GRCm38) |
V224A |
possibly damaging |
Het |
Reln |
A |
G |
5: 21,929,127 (GRCm38) |
V2601A |
probably benign |
Het |
Rspo4 |
G |
A |
2: 151,873,073 (GRCm38) |
R210Q |
unknown |
Het |
Slc7a5 |
A |
T |
8: 121,888,423 (GRCm38) |
D228E |
probably benign |
Het |
Spopfm2 |
T |
A |
3: 94,176,202 (GRCm38) |
K101* |
probably null |
Het |
Tas2r115 |
A |
G |
6: 132,737,251 (GRCm38) |
S246P |
probably damaging |
Het |
Tenm4 |
A |
G |
7: 96,774,146 (GRCm38) |
Y716C |
probably damaging |
Het |
Tgfb3 |
T |
C |
12: 86,062,149 (GRCm38) |
K269E |
possibly damaging |
Het |
Thoc6 |
A |
G |
17: 23,670,867 (GRCm38) |
I27T |
probably benign |
Het |
Tigd5 |
G |
A |
15: 75,909,899 (GRCm38) |
G37S |
probably benign |
Het |
Tmem259 |
C |
T |
10: 79,979,672 (GRCm38) |
D102N |
possibly damaging |
Het |
Tpo |
T |
G |
12: 30,092,590 (GRCm38) |
I712L |
probably benign |
Het |
Ttn |
G |
A |
2: 76,870,548 (GRCm38) |
T21M |
possibly damaging |
Het |
Utp20 |
A |
T |
10: 88,820,710 (GRCm38) |
|
probably null |
Het |
Xrcc5 |
A |
G |
1: 72,312,589 (GRCm38) |
D106G |
probably damaging |
Het |
Xrn1 |
T |
A |
9: 95,979,141 (GRCm38) |
F451L |
probably benign |
Het |
Zar1l |
T |
A |
5: 150,517,738 (GRCm38) |
D141V |
probably damaging |
Het |
Zfp27 |
A |
T |
7: 29,895,899 (GRCm38) |
C214S |
possibly damaging |
Het |
Znfx1 |
A |
T |
2: 167,038,824 (GRCm38) |
C1211S |
probably damaging |
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 |
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 |
|
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 |
|