Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4931406B18Rik |
G |
A |
7: 43,150,571 (GRCm39) |
T67I |
possibly damaging |
Het |
Abca5 |
A |
T |
11: 110,197,106 (GRCm39) |
M524K |
probably benign |
Het |
Aco2 |
G |
A |
15: 81,779,597 (GRCm39) |
V134I |
probably benign |
Het |
Acsf2 |
C |
T |
11: 94,461,206 (GRCm39) |
M323I |
probably benign |
Het |
Acvr1 |
T |
C |
2: 58,337,585 (GRCm39) |
D499G |
probably benign |
Het |
Armc5 |
G |
A |
7: 127,839,597 (GRCm39) |
C305Y |
probably damaging |
Het |
Astl |
T |
C |
2: 127,198,306 (GRCm39) |
I286T |
probably benign |
Het |
Atp8a2 |
G |
A |
14: 60,249,859 (GRCm39) |
S544L |
probably benign |
Het |
Bbs7 |
G |
T |
3: 36,659,853 (GRCm39) |
A194E |
probably benign |
Het |
Brca2 |
A |
G |
5: 150,465,207 (GRCm39) |
D1657G |
probably damaging |
Het |
Cfap46 |
G |
A |
7: 139,219,616 (GRCm39) |
S1283L |
probably benign |
Het |
Creld2 |
T |
C |
15: 88,704,200 (GRCm39) |
S64P |
probably damaging |
Het |
Crtc1 |
T |
C |
8: 70,850,961 (GRCm39) |
E217G |
probably damaging |
Het |
Cyp2d26 |
C |
T |
15: 82,675,320 (GRCm39) |
V345M |
probably benign |
Het |
Cyp2j11 |
T |
C |
4: 96,183,108 (GRCm39) |
M487V |
probably benign |
Het |
Dnah12 |
T |
C |
14: 26,600,036 (GRCm39) |
I3692T |
probably damaging |
Het |
Dtnb |
A |
T |
12: 3,698,221 (GRCm39) |
|
probably null |
Het |
Erf |
T |
C |
7: 24,944,003 (GRCm39) |
T443A |
possibly damaging |
Het |
Ermp1 |
T |
A |
19: 29,594,011 (GRCm39) |
I720F |
probably benign |
Het |
Fam83b |
T |
A |
9: 76,398,214 (GRCm39) |
E963V |
probably damaging |
Het |
Fat1 |
T |
A |
8: 45,504,060 (GRCm39) |
S4463T |
probably benign |
Het |
Fbxw27 |
T |
A |
9: 109,617,148 (GRCm39) |
K118* |
probably null |
Het |
Fcgbp |
A |
T |
7: 27,789,129 (GRCm39) |
Y565F |
probably benign |
Het |
Garre1 |
A |
G |
7: 33,945,093 (GRCm39) |
S384P |
probably benign |
Het |
Gm128 |
A |
T |
3: 95,147,740 (GRCm39) |
S185T |
probably benign |
Het |
Gm6309 |
C |
T |
5: 146,105,640 (GRCm39) |
E175K |
probably damaging |
Het |
Gpatch2l |
G |
A |
12: 86,290,958 (GRCm39) |
R47H |
probably damaging |
Het |
Gprin2 |
T |
C |
14: 33,916,597 (GRCm39) |
Y391C |
probably damaging |
Het |
Hexa |
T |
C |
9: 59,447,221 (GRCm39) |
L72P |
probably damaging |
Het |
Il31ra |
T |
A |
13: 112,685,998 (GRCm39) |
D124V |
probably damaging |
Het |
Kdm2a |
C |
T |
19: 4,372,529 (GRCm39) |
A939T |
probably benign |
Het |
Kif16b |
A |
G |
2: 142,542,019 (GRCm39) |
|
probably benign |
Het |
Kndc1 |
A |
T |
7: 139,490,194 (GRCm39) |
D232V |
probably damaging |
Het |
Lrrc37a |
T |
G |
11: 103,348,369 (GRCm39) |
R2775S |
unknown |
Het |
Luc7l3 |
C |
T |
11: 94,200,462 (GRCm39) |
R52H |
probably damaging |
Het |
Mapk15 |
A |
T |
15: 75,865,747 (GRCm39) |
R13S |
probably damaging |
Het |
Mdga2 |
G |
T |
12: 66,552,889 (GRCm39) |
Q187K |
probably benign |
Het |
Mfsd2b |
G |
A |
12: 4,920,611 (GRCm39) |
Q69* |
probably null |
Het |
Mlph |
A |
T |
1: 90,873,342 (GRCm39) |
D551V |
probably damaging |
Het |
Mup5 |
A |
T |
4: 61,752,806 (GRCm39) |
F72L |
probably benign |
Het |
Narf |
T |
C |
11: 121,129,287 (GRCm39) |
S24P |
probably benign |
Het |
Ncapg2 |
A |
G |
12: 116,390,202 (GRCm39) |
I384V |
probably benign |
Het |
Neo1 |
T |
C |
9: 58,824,335 (GRCm39) |
T698A |
probably benign |
Het |
Nox3 |
A |
G |
17: 3,736,198 (GRCm39) |
S143P |
probably damaging |
Het |
Nrros |
T |
C |
16: 31,981,057 (GRCm39) |
R24G |
probably null |
Het |
Or10ak9 |
T |
A |
4: 118,726,335 (GRCm39) |
M119K |
probably damaging |
Het |
Or6b1 |
T |
C |
6: 42,815,736 (GRCm39) |
V307A |
probably benign |
Het |
Pde9a |
T |
C |
17: 31,685,386 (GRCm39) |
S347P |
possibly damaging |
Het |
Pitpnm3 |
T |
C |
11: 71,961,222 (GRCm39) |
D315G |
probably benign |
Het |
Plaat5 |
A |
G |
19: 7,616,830 (GRCm39) |
|
probably benign |
Het |
Plekha6 |
C |
T |
1: 133,200,273 (GRCm39) |
A284V |
probably benign |
Het |
Plekhg2 |
A |
G |
7: 28,059,684 (GRCm39) |
V1215A |
probably benign |
Het |
Ppif |
C |
A |
14: 25,698,711 (GRCm39) |
A144E |
probably damaging |
Het |
Ppp1r10 |
T |
C |
17: 36,240,453 (GRCm39) |
V581A |
possibly damaging |
Het |
Prr12 |
A |
G |
7: 44,698,269 (GRCm39) |
|
probably benign |
Het |
Rfx6 |
T |
C |
10: 51,599,949 (GRCm39) |
V565A |
probably benign |
Het |
Rsrc1 |
C |
T |
3: 66,901,982 (GRCm39) |
P44L |
unknown |
Het |
Saxo2 |
A |
G |
7: 82,284,402 (GRCm39) |
V152A |
possibly damaging |
Het |
Sdk2 |
T |
C |
11: 113,793,946 (GRCm39) |
D86G |
probably benign |
Het |
Shroom3 |
A |
T |
5: 93,090,876 (GRCm39) |
M1128L |
probably benign |
Het |
Smok2a |
C |
A |
17: 13,444,543 (GRCm39) |
T40K |
probably benign |
Het |
Tatdn1 |
C |
T |
15: 58,793,118 (GRCm39) |
|
probably null |
Het |
Tbc1d2 |
C |
A |
4: 46,649,712 (GRCm39) |
G108V |
probably damaging |
Het |
Tbck |
T |
C |
3: 132,392,703 (GRCm39) |
I48T |
possibly damaging |
Het |
Tm7sf3 |
A |
G |
6: 146,527,601 (GRCm39) |
F75S |
possibly damaging |
Het |
Tmx4 |
T |
C |
2: 134,440,719 (GRCm39) |
D245G |
probably benign |
Het |
Trim68 |
A |
T |
7: 102,333,675 (GRCm39) |
D2E |
probably damaging |
Het |
Trps1 |
T |
A |
15: 50,685,694 (GRCm39) |
Q157L |
possibly damaging |
Het |
Ttc22 |
A |
G |
4: 106,495,800 (GRCm39) |
T385A |
probably benign |
Het |
Ubap2l |
A |
T |
3: 89,946,155 (GRCm39) |
F150I |
possibly damaging |
Het |
Ube2u |
C |
T |
4: 100,389,352 (GRCm39) |
R105W |
probably damaging |
Het |
Ubr4 |
G |
A |
4: 139,185,545 (GRCm39) |
|
probably null |
Het |
Unc5b |
A |
G |
10: 60,666,871 (GRCm39) |
L25P |
probably benign |
Het |
Usp38 |
A |
G |
8: 81,719,958 (GRCm39) |
S424P |
probably damaging |
Het |
Vmn1r222 |
T |
A |
13: 23,416,374 (GRCm39) |
S280C |
probably benign |
Het |
Vmn1r59 |
A |
T |
7: 5,457,599 (GRCm39) |
F54I |
probably benign |
Het |
Vmn2r-ps117 |
T |
A |
17: 19,047,464 (GRCm39) |
C536S |
probably damaging |
Het |
Zkscan2 |
A |
C |
7: 123,099,196 (GRCm39) |
|
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 |
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 |
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 |
|