Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
0610030E20Rik |
C |
T |
6: 72,324,635 (GRCm39) |
T56M |
probably damaging |
Het |
Adamtsl5 |
C |
T |
10: 80,181,372 (GRCm39) |
S36N |
probably benign |
Het |
Adgrf5 |
A |
T |
17: 43,750,704 (GRCm39) |
|
probably benign |
Het |
Ago1 |
A |
G |
4: 126,354,210 (GRCm39) |
F200S |
probably damaging |
Het |
Akr1cl |
T |
C |
1: 65,063,865 (GRCm39) |
D108G |
possibly damaging |
Het |
Aopep |
A |
G |
13: 63,208,954 (GRCm39) |
D357G |
probably benign |
Het |
Arhgef3 |
A |
T |
14: 27,123,743 (GRCm39) |
D468V |
probably benign |
Het |
Aspn |
T |
C |
13: 49,705,353 (GRCm39) |
C72R |
possibly damaging |
Het |
Baz2b |
T |
C |
2: 59,792,485 (GRCm39) |
T548A |
possibly damaging |
Het |
Birc6 |
G |
A |
17: 74,906,368 (GRCm39) |
|
probably null |
Het |
Btnl2 |
A |
T |
17: 34,577,249 (GRCm39) |
T135S |
possibly damaging |
Het |
Ccnl1 |
T |
A |
3: 65,865,282 (GRCm39) |
I90F |
possibly damaging |
Het |
Ccnt1 |
T |
C |
15: 98,463,024 (GRCm39) |
|
probably null |
Het |
Cemip |
C |
A |
7: 83,652,616 (GRCm39) |
|
probably benign |
Het |
Cfap45 |
A |
G |
1: 172,357,501 (GRCm39) |
D85G |
probably damaging |
Het |
Cfap54 |
T |
A |
10: 92,737,941 (GRCm39) |
D2319V |
unknown |
Het |
Cma1 |
T |
C |
14: 56,181,989 (GRCm39) |
M14V |
possibly damaging |
Het |
Cmtm1 |
T |
C |
8: 105,036,774 (GRCm39) |
|
probably benign |
Het |
Col27a1 |
A |
G |
4: 63,249,559 (GRCm39) |
H1738R |
unknown |
Het |
Colq |
T |
A |
14: 31,275,794 (GRCm39) |
D41V |
probably damaging |
Het |
Cubn |
T |
C |
2: 13,337,166 (GRCm39) |
T2437A |
probably benign |
Het |
Eprs1 |
A |
G |
1: 185,150,545 (GRCm39) |
Y1349C |
probably damaging |
Het |
Eps8 |
C |
T |
6: 137,505,569 (GRCm39) |
R53Q |
possibly damaging |
Het |
Fbf1 |
T |
C |
11: 116,043,594 (GRCm39) |
D405G |
probably benign |
Het |
Fen1 |
C |
T |
19: 10,177,674 (GRCm39) |
E257K |
possibly damaging |
Het |
Gstm7 |
A |
T |
3: 107,834,271 (GRCm39) |
M198K |
possibly damaging |
Het |
Hook3 |
A |
T |
8: 26,563,675 (GRCm39) |
S190T |
probably benign |
Het |
Htra4 |
A |
C |
8: 25,520,526 (GRCm39) |
|
probably null |
Het |
Ighv1-15 |
T |
C |
12: 114,621,116 (GRCm39) |
I70V |
probably benign |
Het |
Ikzf4 |
T |
A |
10: 128,470,324 (GRCm39) |
N452Y |
probably damaging |
Het |
Insyn2a |
T |
G |
7: 134,519,427 (GRCm39) |
K368Q |
probably damaging |
Het |
Iqcf5 |
T |
A |
9: 106,393,020 (GRCm39) |
N92K |
possibly damaging |
Het |
Itk |
A |
G |
11: 46,246,661 (GRCm39) |
Y186H |
probably damaging |
Het |
Klhdc10 |
T |
C |
6: 30,446,690 (GRCm39) |
S282P |
probably benign |
Het |
Klhl18 |
T |
A |
9: 110,305,577 (GRCm39) |
E29V |
possibly damaging |
Het |
Ky |
T |
C |
9: 102,402,614 (GRCm39) |
S140P |
probably damaging |
Het |
Lmntd2 |
T |
C |
7: 140,793,550 (GRCm39) |
E112G |
unknown |
Het |
Lrrc36 |
C |
A |
8: 106,178,718 (GRCm39) |
D304E |
possibly damaging |
Het |
Macf1 |
A |
T |
4: 123,400,273 (GRCm39) |
F674Y |
probably damaging |
Het |
Notch1 |
C |
T |
2: 26,361,013 (GRCm39) |
D1111N |
probably benign |
Het |
Osbpl8 |
T |
G |
10: 111,107,941 (GRCm39) |
N312K |
possibly damaging |
Het |
Otogl |
C |
T |
10: 107,731,637 (GRCm39) |
C168Y |
probably damaging |
Het |
Phldb2 |
T |
G |
16: 45,645,934 (GRCm39) |
T171P |
probably benign |
Het |
Ppef2 |
A |
T |
5: 92,386,841 (GRCm39) |
F365L |
probably benign |
Het |
Repin1 |
G |
T |
6: 48,574,279 (GRCm39) |
E403* |
probably null |
Het |
Ryr1 |
G |
A |
7: 28,795,596 (GRCm39) |
T1105I |
probably benign |
Het |
Sclt1 |
T |
A |
3: 41,617,889 (GRCm39) |
*29L |
probably null |
Het |
Scn11a |
T |
C |
9: 119,594,503 (GRCm39) |
K1297E |
probably damaging |
Het |
Serpinb9c |
T |
A |
13: 33,334,262 (GRCm39) |
Y288F |
probably benign |
Het |
Setd1a |
T |
A |
7: 127,385,366 (GRCm39) |
M691K |
probably benign |
Het |
Sftpc |
T |
C |
14: 70,760,059 (GRCm39) |
E66G |
probably damaging |
Het |
Spata31h1 |
T |
C |
10: 82,131,934 (GRCm39) |
I359V |
probably benign |
Het |
Thnsl2 |
T |
C |
6: 71,118,303 (GRCm39) |
T42A |
probably benign |
Het |
Tram1 |
T |
C |
1: 13,640,199 (GRCm39) |
D285G |
probably benign |
Het |
Ttn |
G |
A |
2: 76,675,374 (GRCm39) |
P11137L |
unknown |
Het |
Ttn |
C |
A |
2: 76,727,103 (GRCm39) |
V5821F |
unknown |
Het |
Ttn |
A |
T |
2: 76,566,584 (GRCm39) |
I28103K |
probably damaging |
Het |
Usp38 |
T |
A |
8: 81,740,945 (GRCm39) |
M41L |
probably benign |
Het |
Zcwpw1 |
T |
G |
5: 137,815,753 (GRCm39) |
Y419D |
possibly damaging |
Het |
Zfp407 |
G |
A |
18: 84,577,525 (GRCm39) |
A1196V |
possibly damaging |
Het |
Zfp446 |
T |
A |
7: 12,712,970 (GRCm39) |
S103T |
possibly damaging |
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 |
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 |
R9486:Dnah14
|
UTSW |
1 |
181,508,494 (GRCm39) |
missense |
possibly damaging |
0.68 |
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 |
|