Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2ml1 |
A |
G |
6: 128,546,942 (GRCm39) |
F396L |
probably damaging |
Het |
Abca13 |
T |
C |
11: 9,240,621 (GRCm39) |
I828T |
possibly damaging |
Het |
Ace3 |
A |
T |
11: 105,896,219 (GRCm39) |
T722S |
probably benign |
Het |
Acot2 |
A |
G |
12: 84,039,426 (GRCm39) |
T312A |
probably benign |
Het |
Adra2a |
A |
G |
19: 54,035,963 (GRCm39) |
I440V |
probably damaging |
Het |
Arhgap22 |
T |
A |
14: 33,073,303 (GRCm39) |
M4K |
probably benign |
Het |
Atp8b3 |
C |
T |
10: 80,366,821 (GRCm39) |
C259Y |
probably damaging |
Het |
Bcl2 |
T |
A |
1: 106,471,109 (GRCm39) |
Y199F |
probably benign |
Het |
Brca1 |
A |
T |
11: 101,414,520 (GRCm39) |
C1205S |
probably benign |
Het |
Col7a1 |
T |
C |
9: 108,811,396 (GRCm39) |
V2743A |
unknown |
Het |
Crybg1 |
A |
G |
10: 43,880,145 (GRCm39) |
|
probably benign |
Het |
Cyp2c40 |
T |
A |
19: 39,755,808 (GRCm39) |
H502L |
probably benign |
Het |
Cyp2c40 |
A |
T |
19: 39,796,050 (GRCm39) |
Y109* |
probably null |
Het |
Cyp4a29 |
T |
C |
4: 115,106,916 (GRCm39) |
M191T |
probably damaging |
Het |
Dcaf1 |
A |
G |
9: 106,735,916 (GRCm39) |
R955G |
possibly damaging |
Het |
Dcaf4 |
G |
T |
12: 83,582,726 (GRCm39) |
A274S |
probably damaging |
Het |
Dlx1 |
A |
G |
2: 71,362,828 (GRCm39) |
H245R |
probably damaging |
Het |
Dock10 |
A |
T |
1: 80,479,452 (GRCm39) |
V2167D |
unknown |
Het |
Epyc |
A |
G |
10: 97,511,697 (GRCm39) |
Q230R |
probably benign |
Het |
Etnk1 |
G |
A |
6: 143,130,310 (GRCm39) |
R143H |
probably damaging |
Het |
Fhip2b |
T |
C |
14: 70,826,479 (GRCm39) |
D203G |
probably benign |
Het |
Fmo2 |
T |
C |
1: 162,708,292 (GRCm39) |
E281G |
probably damaging |
Het |
Gm2042 |
T |
A |
12: 87,925,963 (GRCm39) |
Y304N |
possibly damaging |
Het |
Hecw2 |
T |
C |
1: 53,852,466 (GRCm39) |
D1551G |
probably damaging |
Het |
Hgd |
A |
T |
16: 37,413,811 (GRCm39) |
D91V |
probably benign |
Het |
Hspa12a |
A |
G |
19: 58,797,891 (GRCm39) |
F276L |
probably benign |
Het |
Ifitm10 |
C |
T |
7: 141,909,812 (GRCm39) |
V95M |
probably damaging |
Het |
Ints3 |
G |
A |
3: 90,313,579 (GRCm39) |
R350* |
probably null |
Het |
Kdm4c |
T |
A |
4: 74,252,966 (GRCm39) |
I511K |
probably benign |
Het |
Kif27 |
A |
G |
13: 58,492,348 (GRCm39) |
S264P |
probably damaging |
Het |
L1td1 |
A |
G |
4: 98,624,899 (GRCm39) |
T365A |
probably benign |
Het |
Ltbp2 |
T |
A |
12: 84,878,648 (GRCm39) |
T304S |
possibly damaging |
Het |
Mamdc4 |
T |
A |
2: 25,455,164 (GRCm39) |
Y962F |
probably benign |
Het |
Map3k4 |
C |
T |
17: 12,489,860 (GRCm39) |
A524T |
probably damaging |
Het |
Mfsd8 |
C |
T |
3: 40,789,627 (GRCm39) |
R140H |
probably damaging |
Het |
Mmp3 |
A |
G |
9: 7,451,256 (GRCm39) |
I331V |
possibly damaging |
Het |
Mpdz |
T |
A |
4: 81,254,043 (GRCm39) |
I1030F |
probably damaging |
Het |
Mtx1 |
A |
T |
3: 89,120,163 (GRCm39) |
C62S |
|
Het |
Muc20 |
A |
T |
16: 32,615,248 (GRCm39) |
V43E |
possibly damaging |
Het |
Naa25 |
A |
G |
5: 121,577,958 (GRCm39) |
E955G |
probably damaging |
Het |
Nelfcd |
A |
G |
2: 174,268,635 (GRCm39) |
Y562C |
probably damaging |
Het |
Nsd2 |
T |
A |
5: 34,018,493 (GRCm39) |
M509K |
probably benign |
Het |
Obscn |
T |
C |
11: 58,918,272 (GRCm39) |
T207A |
|
Het |
Or1ad1 |
T |
A |
11: 50,875,691 (GRCm39) |
H54Q |
possibly damaging |
Het |
Or4a39 |
C |
T |
2: 89,236,959 (GRCm39) |
V155M |
possibly damaging |
Het |
Or4k5 |
T |
A |
14: 50,385,672 (GRCm39) |
I220L |
probably benign |
Het |
Osbpl11 |
A |
T |
16: 33,006,283 (GRCm39) |
N37I |
possibly damaging |
Het |
Pcdh9 |
A |
G |
14: 93,797,956 (GRCm39) |
S1032P |
possibly damaging |
Het |
Pde6b |
T |
A |
5: 108,551,241 (GRCm39) |
I175N |
probably damaging |
Het |
Pfkl |
T |
A |
10: 77,824,184 (GRCm39) |
M735L |
probably benign |
Het |
Pkp4 |
T |
C |
2: 59,138,722 (GRCm39) |
V324A |
probably benign |
Het |
Ptprb |
T |
A |
10: 116,155,494 (GRCm39) |
C462* |
probably null |
Het |
Rasal3 |
T |
C |
17: 32,617,910 (GRCm39) |
N221S |
probably benign |
Het |
Reep1 |
A |
T |
6: 71,684,969 (GRCm39) |
I6F |
probably benign |
Het |
Rhobtb1 |
T |
A |
10: 69,106,621 (GRCm39) |
F457L |
probably damaging |
Het |
Ryr1 |
T |
C |
7: 28,777,965 (GRCm39) |
N2184S |
probably benign |
Het |
Scn11a |
T |
G |
9: 119,624,774 (GRCm39) |
H516P |
possibly damaging |
Het |
Sipa1l1 |
T |
C |
12: 82,404,139 (GRCm39) |
|
probably null |
Het |
Slc17a7 |
A |
G |
7: 44,821,606 (GRCm39) |
N381S |
possibly damaging |
Het |
Slc38a3 |
C |
T |
9: 107,536,322 (GRCm39) |
V25M |
probably benign |
Het |
Spag1 |
T |
G |
15: 36,181,954 (GRCm39) |
D37E |
probably damaging |
Het |
Spib |
G |
T |
7: 44,178,815 (GRCm39) |
D114E |
possibly damaging |
Het |
Tpx2 |
A |
T |
2: 152,726,933 (GRCm39) |
Y400F |
probably damaging |
Het |
Trhde |
A |
G |
10: 114,532,014 (GRCm39) |
I362T |
possibly damaging |
Het |
Usp17ld |
C |
T |
7: 102,899,381 (GRCm39) |
G517E |
probably benign |
Het |
Vmn1r22 |
A |
T |
6: 57,877,404 (GRCm39) |
M191K |
probably damaging |
Het |
Wdr6 |
G |
A |
9: 108,453,182 (GRCm39) |
R234C |
probably damaging |
Het |
Zdhhc22 |
C |
T |
12: 87,030,398 (GRCm39) |
M183I |
probably benign |
Het |
Zfp1007 |
C |
A |
5: 109,824,062 (GRCm39) |
G463* |
probably null |
Het |
Zfp949 |
C |
A |
9: 88,452,182 (GRCm39) |
T584N |
probably benign |
Het |
|
Other mutations in Dnah14 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01086:Dnah14
|
APN |
1 |
181,579,611 (GRCm39) |
missense |
probably benign |
0.17 |
IGL01764:Dnah14
|
APN |
1 |
181,572,342 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03218:Dnah14
|
APN |
1 |
181,582,834 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03290:Dnah14
|
APN |
1 |
181,591,543 (GRCm39) |
splice site |
probably benign |
|
IGL03384:Dnah14
|
APN |
1 |
181,573,514 (GRCm39) |
missense |
probably benign |
0.03 |
R0009:Dnah14
|
UTSW |
1 |
181,596,972 (GRCm39) |
splice site |
probably benign |
|
R0125:Dnah14
|
UTSW |
1 |
181,579,628 (GRCm39) |
missense |
probably damaging |
0.99 |
R0579:Dnah14
|
UTSW |
1 |
181,572,312 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0973:Dnah14
|
UTSW |
1 |
181,579,710 (GRCm39) |
missense |
probably damaging |
1.00 |
R0973:Dnah14
|
UTSW |
1 |
181,579,710 (GRCm39) |
missense |
probably damaging |
1.00 |
R0974:Dnah14
|
UTSW |
1 |
181,579,710 (GRCm39) |
missense |
probably damaging |
1.00 |
R1609:Dnah14
|
UTSW |
1 |
181,577,742 (GRCm39) |
missense |
probably damaging |
0.97 |
R1860:Dnah14
|
UTSW |
1 |
181,591,525 (GRCm39) |
missense |
probably damaging |
1.00 |
R2050:Dnah14
|
UTSW |
1 |
181,580,127 (GRCm39) |
missense |
probably damaging |
1.00 |
R2974:Dnah14
|
UTSW |
1 |
181,582,806 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4715:Dnah14
|
UTSW |
1 |
181,584,788 (GRCm39) |
missense |
probably damaging |
1.00 |
R5076:Dnah14
|
UTSW |
1 |
181,584,799 (GRCm39) |
missense |
probably benign |
0.01 |
R5424:Dnah14
|
UTSW |
1 |
181,590,875 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5808:Dnah14
|
UTSW |
1 |
181,568,724 (GRCm39) |
missense |
possibly damaging |
0.72 |
R5997:Dnah14
|
UTSW |
1 |
181,597,670 (GRCm39) |
missense |
probably benign |
0.00 |
R6052:Dnah14
|
UTSW |
1 |
181,494,052 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6061:Dnah14
|
UTSW |
1 |
181,536,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R6089:Dnah14
|
UTSW |
1 |
181,577,719 (GRCm39) |
missense |
probably damaging |
1.00 |
R6092:Dnah14
|
UTSW |
1 |
181,449,398 (GRCm39) |
missense |
probably benign |
0.13 |
R6145:Dnah14
|
UTSW |
1 |
181,493,982 (GRCm39) |
missense |
probably benign |
0.00 |
R6163:Dnah14
|
UTSW |
1 |
181,493,926 (GRCm39) |
missense |
probably benign |
0.33 |
R6246:Dnah14
|
UTSW |
1 |
181,508,453 (GRCm39) |
missense |
probably benign |
0.00 |
R6302:Dnah14
|
UTSW |
1 |
181,428,771 (GRCm39) |
missense |
possibly damaging |
0.96 |
R6306:Dnah14
|
UTSW |
1 |
181,412,589 (GRCm39) |
frame shift |
probably null |
|
R6326:Dnah14
|
UTSW |
1 |
181,611,121 (GRCm39) |
missense |
probably damaging |
1.00 |
R6348:Dnah14
|
UTSW |
1 |
181,454,285 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6367:Dnah14
|
UTSW |
1 |
181,582,951 (GRCm39) |
splice site |
probably null |
|
R6376:Dnah14
|
UTSW |
1 |
181,433,459 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6389:Dnah14
|
UTSW |
1 |
181,478,767 (GRCm39) |
critical splice donor site |
probably null |
|
R6433:Dnah14
|
UTSW |
1 |
181,479,222 (GRCm39) |
missense |
probably damaging |
0.99 |
R6454:Dnah14
|
UTSW |
1 |
181,611,270 (GRCm39) |
missense |
probably damaging |
1.00 |
R6476:Dnah14
|
UTSW |
1 |
181,572,333 (GRCm39) |
missense |
probably benign |
0.26 |
R6523:Dnah14
|
UTSW |
1 |
181,471,186 (GRCm39) |
missense |
probably benign |
0.00 |
R6529:Dnah14
|
UTSW |
1 |
181,494,034 (GRCm39) |
missense |
probably damaging |
0.98 |
R6538:Dnah14
|
UTSW |
1 |
181,412,550 (GRCm39) |
missense |
unknown |
|
R6546:Dnah14
|
UTSW |
1 |
181,566,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R6752:Dnah14
|
UTSW |
1 |
181,421,017 (GRCm39) |
missense |
probably benign |
0.07 |
R6762:Dnah14
|
UTSW |
1 |
181,584,824 (GRCm39) |
missense |
probably damaging |
1.00 |
R6786:Dnah14
|
UTSW |
1 |
181,468,970 (GRCm39) |
missense |
probably benign |
0.21 |
R6849:Dnah14
|
UTSW |
1 |
181,636,510 (GRCm39) |
missense |
probably benign |
0.00 |
R6877:Dnah14
|
UTSW |
1 |
181,455,997 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6912:Dnah14
|
UTSW |
1 |
181,577,748 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6919:Dnah14
|
UTSW |
1 |
181,412,631 (GRCm39) |
missense |
probably benign |
0.04 |
R6924:Dnah14
|
UTSW |
1 |
181,455,517 (GRCm39) |
missense |
probably benign |
0.04 |
R6957:Dnah14
|
UTSW |
1 |
181,612,740 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6980:Dnah14
|
UTSW |
1 |
181,475,795 (GRCm39) |
missense |
probably benign |
0.00 |
R7018:Dnah14
|
UTSW |
1 |
181,454,509 (GRCm39) |
missense |
possibly damaging |
0.55 |
R7046:Dnah14
|
UTSW |
1 |
181,450,568 (GRCm39) |
missense |
probably benign |
0.01 |
R7058:Dnah14
|
UTSW |
1 |
181,525,614 (GRCm39) |
missense |
probably benign |
0.00 |
R7068:Dnah14
|
UTSW |
1 |
181,597,355 (GRCm39) |
missense |
probably benign |
0.35 |
R7115:Dnah14
|
UTSW |
1 |
181,547,710 (GRCm39) |
missense |
probably damaging |
1.00 |
R7130:Dnah14
|
UTSW |
1 |
181,573,523 (GRCm39) |
nonsense |
probably null |
|
R7165:Dnah14
|
UTSW |
1 |
181,532,100 (GRCm39) |
missense |
probably benign |
0.00 |
R7169:Dnah14
|
UTSW |
1 |
181,529,930 (GRCm39) |
missense |
probably benign |
0.00 |
R7184:Dnah14
|
UTSW |
1 |
181,532,094 (GRCm39) |
nonsense |
probably null |
|
R7232:Dnah14
|
UTSW |
1 |
181,584,928 (GRCm39) |
missense |
probably damaging |
1.00 |
R7260:Dnah14
|
UTSW |
1 |
181,534,309 (GRCm39) |
missense |
probably damaging |
0.99 |
R7276:Dnah14
|
UTSW |
1 |
181,513,372 (GRCm39) |
missense |
probably benign |
0.41 |
R7290:Dnah14
|
UTSW |
1 |
181,455,739 (GRCm39) |
missense |
probably benign |
0.20 |
R7314:Dnah14
|
UTSW |
1 |
181,612,819 (GRCm39) |
splice site |
probably null |
|
R7326:Dnah14
|
UTSW |
1 |
181,425,968 (GRCm39) |
missense |
probably benign |
0.02 |
R7336:Dnah14
|
UTSW |
1 |
181,625,299 (GRCm39) |
missense |
probably damaging |
0.96 |
R7363:Dnah14
|
UTSW |
1 |
181,518,089 (GRCm39) |
splice site |
probably null |
|
R7371:Dnah14
|
UTSW |
1 |
181,454,450 (GRCm39) |
missense |
probably benign |
0.05 |
R7376:Dnah14
|
UTSW |
1 |
181,590,967 (GRCm39) |
missense |
probably benign |
0.03 |
R7418:Dnah14
|
UTSW |
1 |
181,444,307 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7473:Dnah14
|
UTSW |
1 |
181,579,704 (GRCm39) |
missense |
probably damaging |
0.99 |
R7514:Dnah14
|
UTSW |
1 |
181,455,632 (GRCm39) |
missense |
probably damaging |
0.96 |
R7555:Dnah14
|
UTSW |
1 |
181,597,619 (GRCm39) |
missense |
probably benign |
0.26 |
R7641:Dnah14
|
UTSW |
1 |
181,535,098 (GRCm39) |
missense |
probably benign |
0.01 |
R7663:Dnah14
|
UTSW |
1 |
181,579,720 (GRCm39) |
splice site |
probably null |
|
R7674:Dnah14
|
UTSW |
1 |
181,535,098 (GRCm39) |
missense |
probably benign |
0.01 |
R7680:Dnah14
|
UTSW |
1 |
181,513,365 (GRCm39) |
missense |
probably benign |
0.15 |
R7709:Dnah14
|
UTSW |
1 |
181,530,049 (GRCm39) |
critical splice donor site |
probably null |
|
R7842:Dnah14
|
UTSW |
1 |
181,455,463 (GRCm39) |
missense |
probably damaging |
0.99 |
R7861:Dnah14
|
UTSW |
1 |
181,444,324 (GRCm39) |
missense |
probably damaging |
1.00 |
R7988:Dnah14
|
UTSW |
1 |
181,611,139 (GRCm39) |
missense |
probably damaging |
0.97 |
R8016:Dnah14
|
UTSW |
1 |
181,475,876 (GRCm39) |
missense |
probably benign |
0.05 |
R8042:Dnah14
|
UTSW |
1 |
181,471,196 (GRCm39) |
critical splice donor site |
probably null |
|
R8071:Dnah14
|
UTSW |
1 |
181,443,459 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8086:Dnah14
|
UTSW |
1 |
181,593,797 (GRCm39) |
missense |
probably damaging |
1.00 |
R8095:Dnah14
|
UTSW |
1 |
181,633,597 (GRCm39) |
nonsense |
probably null |
|
R8139:Dnah14
|
UTSW |
1 |
181,582,853 (GRCm39) |
missense |
probably damaging |
1.00 |
R8176:Dnah14
|
UTSW |
1 |
181,484,598 (GRCm39) |
missense |
probably damaging |
0.96 |
R8193:Dnah14
|
UTSW |
1 |
181,515,770 (GRCm39) |
missense |
probably damaging |
1.00 |
R8197:Dnah14
|
UTSW |
1 |
181,517,666 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8209:Dnah14
|
UTSW |
1 |
181,623,110 (GRCm39) |
missense |
possibly damaging |
0.69 |
R8226:Dnah14
|
UTSW |
1 |
181,623,110 (GRCm39) |
missense |
possibly damaging |
0.69 |
R8251:Dnah14
|
UTSW |
1 |
181,492,430 (GRCm39) |
missense |
probably damaging |
1.00 |
R8264:Dnah14
|
UTSW |
1 |
181,572,357 (GRCm39) |
missense |
probably damaging |
0.99 |
R8284:Dnah14
|
UTSW |
1 |
181,601,376 (GRCm39) |
missense |
probably benign |
0.03 |
R8289:Dnah14
|
UTSW |
1 |
181,543,780 (GRCm39) |
nonsense |
probably null |
|
R8323:Dnah14
|
UTSW |
1 |
181,532,109 (GRCm39) |
missense |
probably benign |
0.01 |
R8442:Dnah14
|
UTSW |
1 |
181,568,849 (GRCm39) |
missense |
probably damaging |
0.97 |
R8458:Dnah14
|
UTSW |
1 |
181,633,577 (GRCm39) |
missense |
|
|
R8507:Dnah14
|
UTSW |
1 |
181,468,979 (GRCm39) |
missense |
probably benign |
0.02 |
R8509:Dnah14
|
UTSW |
1 |
181,642,220 (GRCm39) |
missense |
|
|
R8520:Dnah14
|
UTSW |
1 |
181,481,203 (GRCm39) |
missense |
probably damaging |
1.00 |
R8530:Dnah14
|
UTSW |
1 |
181,492,511 (GRCm39) |
missense |
probably damaging |
1.00 |
R8703:Dnah14
|
UTSW |
1 |
181,493,576 (GRCm39) |
nonsense |
probably null |
|
R8710:Dnah14
|
UTSW |
1 |
181,517,876 (GRCm39) |
missense |
probably benign |
0.04 |
R8752:Dnah14
|
UTSW |
1 |
181,455,581 (GRCm39) |
missense |
probably benign |
0.00 |
R8792:Dnah14
|
UTSW |
1 |
181,642,189 (GRCm39) |
missense |
|
|
R8797:Dnah14
|
UTSW |
1 |
181,465,412 (GRCm39) |
missense |
probably benign |
0.19 |
R8821:Dnah14
|
UTSW |
1 |
181,619,569 (GRCm39) |
nonsense |
probably null |
|
R8834:Dnah14
|
UTSW |
1 |
181,444,315 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8913:Dnah14
|
UTSW |
1 |
181,553,063 (GRCm39) |
missense |
probably benign |
0.01 |
R8925:Dnah14
|
UTSW |
1 |
181,508,321 (GRCm39) |
missense |
probably damaging |
1.00 |
R8927:Dnah14
|
UTSW |
1 |
181,508,321 (GRCm39) |
missense |
probably damaging |
1.00 |
R8934:Dnah14
|
UTSW |
1 |
181,450,288 (GRCm39) |
missense |
possibly damaging |
0.84 |
R9090:Dnah14
|
UTSW |
1 |
181,597,325 (GRCm39) |
missense |
probably benign |
0.33 |
R9169:Dnah14
|
UTSW |
1 |
181,433,381 (GRCm39) |
missense |
probably benign |
0.06 |
R9199:Dnah14
|
UTSW |
1 |
181,478,566 (GRCm39) |
missense |
possibly damaging |
0.50 |
R9212:Dnah14
|
UTSW |
1 |
181,628,852 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9213:Dnah14
|
UTSW |
1 |
181,444,205 (GRCm39) |
critical splice donor site |
probably null |
|
R9271:Dnah14
|
UTSW |
1 |
181,597,325 (GRCm39) |
missense |
probably benign |
0.33 |
R9282:Dnah14
|
UTSW |
1 |
181,642,077 (GRCm39) |
missense |
|
|
R9350:Dnah14
|
UTSW |
1 |
181,562,369 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9358:Dnah14
|
UTSW |
1 |
181,536,598 (GRCm39) |
missense |
probably benign |
0.01 |
R9436:Dnah14
|
UTSW |
1 |
181,508,348 (GRCm39) |
missense |
probably damaging |
1.00 |
R9484:Dnah14
|
UTSW |
1 |
181,625,311 (GRCm39) |
missense |
probably benign |
0.01 |
R9484:Dnah14
|
UTSW |
1 |
181,517,773 (GRCm39) |
missense |
probably benign |
0.45 |
R9546:Dnah14
|
UTSW |
1 |
181,420,992 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9547:Dnah14
|
UTSW |
1 |
181,420,992 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9578:Dnah14
|
UTSW |
1 |
181,502,007 (GRCm39) |
missense |
probably benign |
0.16 |
R9654:Dnah14
|
UTSW |
1 |
181,593,904 (GRCm39) |
missense |
probably benign |
0.01 |
R9681:Dnah14
|
UTSW |
1 |
181,562,414 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9683:Dnah14
|
UTSW |
1 |
181,426,509 (GRCm39) |
missense |
probably benign |
0.01 |
R9687:Dnah14
|
UTSW |
1 |
181,425,978 (GRCm39) |
missense |
probably benign |
0.01 |
R9718:Dnah14
|
UTSW |
1 |
181,450,544 (GRCm39) |
missense |
probably benign |
0.08 |
R9751:Dnah14
|
UTSW |
1 |
181,619,610 (GRCm39) |
missense |
probably damaging |
1.00 |
R9757:Dnah14
|
UTSW |
1 |
181,513,349 (GRCm39) |
missense |
probably benign |
0.03 |
RF007:Dnah14
|
UTSW |
1 |
181,513,374 (GRCm39) |
missense |
probably benign |
0.00 |
RF012:Dnah14
|
UTSW |
1 |
181,455,463 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1176:Dnah14
|
UTSW |
1 |
181,584,916 (GRCm39) |
missense |
possibly damaging |
0.83 |
Z1177:Dnah14
|
UTSW |
1 |
181,517,885 (GRCm39) |
missense |
probably benign |
0.03 |
Z1177:Dnah14
|
UTSW |
1 |
181,593,869 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Dnah14
|
UTSW |
1 |
181,590,899 (GRCm39) |
missense |
probably damaging |
1.00 |
|