Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8a |
T |
A |
11: 109,921,714 (GRCm39) |
M1447L |
probably benign |
Het |
Adam30 |
G |
A |
3: 98,070,257 (GRCm39) |
V697I |
probably benign |
Het |
Adamts12 |
A |
G |
15: 11,277,452 (GRCm39) |
N689D |
probably benign |
Het |
Adamts15 |
T |
C |
9: 30,813,906 (GRCm39) |
K753R |
probably benign |
Het |
Adra2a |
T |
C |
19: 54,034,835 (GRCm39) |
F64L |
probably damaging |
Het |
Ankub1 |
A |
G |
3: 57,580,345 (GRCm39) |
L104P |
probably damaging |
Het |
Arel1 |
A |
G |
12: 84,988,719 (GRCm39) |
V10A |
probably benign |
Het |
Atad2 |
A |
T |
15: 57,962,047 (GRCm39) |
N1165K |
probably benign |
Het |
Atp6v0d2 |
T |
A |
4: 19,880,060 (GRCm39) |
D279V |
probably benign |
Het |
Cadps |
A |
T |
14: 12,616,099 (GRCm38) |
D310E |
probably damaging |
Het |
Caskin2 |
T |
C |
11: 115,695,615 (GRCm39) |
I249V |
possibly damaging |
Het |
Cdh23 |
T |
C |
10: 60,212,620 (GRCm39) |
N1598S |
probably benign |
Het |
Cep250 |
A |
T |
2: 155,834,682 (GRCm39) |
Q2202H |
probably benign |
Het |
Ces5a |
T |
A |
8: 94,261,311 (GRCm39) |
T35S |
probably damaging |
Het |
Cnot11 |
G |
A |
1: 39,579,020 (GRCm39) |
W295* |
probably null |
Het |
Cntnap5a |
G |
T |
1: 116,149,619 (GRCm39) |
W565L |
probably damaging |
Het |
Dgka |
T |
C |
10: 128,569,468 (GRCm39) |
E148G |
probably damaging |
Het |
Erbin |
G |
A |
13: 103,998,834 (GRCm39) |
T184I |
probably damaging |
Het |
Fam20c |
G |
T |
5: 138,793,309 (GRCm39) |
G477W |
probably damaging |
Het |
Fan1 |
T |
A |
7: 64,022,234 (GRCm39) |
N340Y |
probably damaging |
Het |
Fgfr4 |
T |
C |
13: 55,309,262 (GRCm39) |
V433A |
probably benign |
Het |
Gal3st1 |
A |
T |
11: 3,948,093 (GRCm39) |
Q100L |
possibly damaging |
Het |
Gfra2 |
T |
C |
14: 71,163,380 (GRCm39) |
F221S |
probably damaging |
Het |
Gm19965 |
G |
A |
1: 116,748,921 (GRCm39) |
V201M |
|
Het |
Gnb1l |
A |
T |
16: 18,382,806 (GRCm39) |
T282S |
probably benign |
Het |
Gpr171 |
A |
T |
3: 59,005,147 (GRCm39) |
N209K |
probably benign |
Het |
Greb1 |
G |
A |
12: 16,761,739 (GRCm39) |
T547I |
probably damaging |
Het |
Ifi214 |
A |
T |
1: 173,357,097 (GRCm39) |
V2E |
probably benign |
Het |
Ighv1-71 |
T |
C |
12: 115,706,267 (GRCm39) |
M1V |
probably null |
Het |
Itm2b |
C |
T |
14: 73,605,785 (GRCm39) |
G67D |
probably damaging |
Het |
Kif21a |
A |
T |
15: 90,851,432 (GRCm39) |
C995* |
probably null |
Het |
Kifc2 |
A |
T |
15: 76,544,904 (GRCm39) |
Y13F |
probably damaging |
Het |
Lamb1 |
T |
A |
12: 31,315,595 (GRCm39) |
V59D |
probably benign |
Het |
Lhx1 |
A |
T |
11: 84,412,703 (GRCm39) |
D163E |
probably damaging |
Het |
Lrrc1 |
A |
T |
9: 77,365,121 (GRCm39) |
Y187N |
probably benign |
Het |
Map3k1 |
C |
A |
13: 111,904,645 (GRCm39) |
V380F |
probably damaging |
Het |
Mapk11 |
T |
C |
15: 89,028,511 (GRCm39) |
D283G |
probably damaging |
Het |
Mccc2 |
G |
T |
13: 100,091,207 (GRCm39) |
A430D |
probably damaging |
Het |
Mest |
A |
G |
6: 30,747,158 (GRCm39) |
N340S |
unknown |
Het |
Mms22l |
T |
C |
4: 24,517,139 (GRCm39) |
L340P |
probably benign |
Het |
Mrnip |
A |
G |
11: 50,087,808 (GRCm39) |
Y110C |
possibly damaging |
Het |
Mtmr4 |
A |
G |
11: 87,502,063 (GRCm39) |
T706A |
probably benign |
Het |
Muc21 |
G |
A |
17: 35,929,761 (GRCm39) |
A1475V |
unknown |
Het |
Ncstn |
A |
G |
1: 171,900,373 (GRCm39) |
F234S |
probably benign |
Het |
Nrp1 |
T |
C |
8: 129,202,777 (GRCm39) |
|
probably null |
Het |
Nup37 |
T |
G |
10: 88,010,356 (GRCm39) |
C217G |
probably damaging |
Het |
Or8g22 |
A |
G |
9: 38,958,694 (GRCm39) |
L7P |
unknown |
Het |
Pdzrn3 |
T |
C |
6: 101,128,206 (GRCm39) |
N820S |
probably benign |
Het |
Pgap1 |
A |
T |
1: 54,587,225 (GRCm39) |
F117Y |
possibly damaging |
Het |
Phip |
A |
T |
9: 82,753,346 (GRCm39) |
F1799L |
possibly damaging |
Het |
Ppm1f |
T |
A |
16: 16,728,819 (GRCm39) |
F74I |
probably benign |
Het |
Prpf8 |
C |
A |
11: 75,384,783 (GRCm39) |
N775K |
possibly damaging |
Het |
Ptdss2 |
T |
C |
7: 140,731,693 (GRCm39) |
I167T |
possibly damaging |
Het |
Ptpn18 |
G |
A |
1: 34,501,892 (GRCm39) |
|
probably null |
Het |
Rbl2 |
C |
A |
8: 91,841,669 (GRCm39) |
A955D |
probably benign |
Het |
Rgl1 |
A |
G |
1: 152,420,146 (GRCm39) |
S366P |
possibly damaging |
Het |
Rit2 |
A |
T |
18: 31,376,221 (GRCm39) |
M38K |
possibly damaging |
Het |
Robo1 |
A |
G |
16: 72,801,408 (GRCm39) |
M1011V |
probably benign |
Het |
Senp6 |
A |
T |
9: 80,043,797 (GRCm39) |
E809D |
probably benign |
Het |
Stard3 |
G |
A |
11: 98,269,045 (GRCm39) |
|
probably null |
Het |
Taar3 |
T |
G |
10: 23,826,298 (GRCm39) |
Y281* |
probably null |
Het |
Tacc2 |
G |
T |
7: 130,331,103 (GRCm39) |
K352N |
probably benign |
Het |
Tamalin |
G |
A |
15: 101,129,419 (GRCm39) |
S234N |
probably damaging |
Het |
Tasor |
T |
A |
14: 27,160,610 (GRCm39) |
I124N |
probably damaging |
Het |
Tdpoz4 |
G |
A |
3: 93,704,155 (GRCm39) |
V151I |
not run |
Het |
Tenm2 |
A |
G |
11: 35,914,298 (GRCm39) |
L2413P |
probably damaging |
Het |
Tgm6 |
T |
C |
2: 129,983,110 (GRCm39) |
V233A |
probably damaging |
Het |
Tlx3 |
G |
A |
11: 33,153,514 (GRCm39) |
|
probably benign |
Het |
Tmem94 |
G |
T |
11: 115,677,082 (GRCm39) |
R118L |
possibly damaging |
Het |
Trim23 |
C |
A |
13: 104,323,941 (GRCm39) |
H133Q |
probably damaging |
Het |
Unc80 |
A |
T |
1: 66,640,356 (GRCm39) |
D1421V |
probably damaging |
Het |
Vmn1r172 |
A |
G |
7: 23,360,048 (GRCm39) |
N311S |
unknown |
Het |
Vps25 |
T |
A |
11: 101,149,775 (GRCm39) |
L153Q |
probably damaging |
Het |
Wbp1l |
G |
T |
19: 46,611,876 (GRCm39) |
|
probably benign |
Het |
Ythdc2 |
A |
G |
18: 44,970,558 (GRCm39) |
I291V |
possibly damaging |
Het |
Zfp2 |
A |
G |
11: 50,791,570 (GRCm39) |
C158R |
probably damaging |
Het |
Zfp786 |
G |
A |
6: 47,796,929 (GRCm39) |
P670S |
probably damaging |
Het |
Zfp827 |
G |
A |
8: 79,916,442 (GRCm39) |
R339H |
possibly damaging |
Het |
Zmym6 |
C |
T |
4: 127,017,294 (GRCm39) |
A1025V |
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 |
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 |
|