Other mutations in this stock |
Total: 105 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3300002I08Rik |
T |
C |
2: 150,153,122 (GRCm39) |
N88D |
possibly damaging |
Het |
4933430I17Rik |
A |
G |
4: 62,460,916 (GRCm39) |
I264V |
probably benign |
Het |
Abcc8 |
A |
G |
7: 45,787,429 (GRCm39) |
F591L |
probably benign |
Het |
Abr |
G |
T |
11: 76,310,658 (GRCm39) |
T810K |
probably damaging |
Het |
Abracl |
T |
C |
10: 17,894,631 (GRCm39) |
E6G |
unknown |
Het |
Adamts3 |
A |
T |
5: 89,834,750 (GRCm39) |
Y871N |
probably damaging |
Het |
Akap13 |
T |
C |
7: 75,354,275 (GRCm39) |
Y80H |
probably benign |
Het |
Alas1 |
A |
G |
9: 106,115,840 (GRCm39) |
|
probably null |
Het |
Anapc1 |
A |
C |
2: 128,517,633 (GRCm39) |
L337R |
possibly damaging |
Het |
Apaf1 |
T |
C |
10: 90,915,816 (GRCm39) |
Y24C |
probably damaging |
Het |
Arhgef16 |
A |
G |
4: 154,365,432 (GRCm39) |
V561A |
possibly damaging |
Het |
Brsk2 |
A |
G |
7: 141,546,852 (GRCm39) |
T432A |
probably benign |
Het |
C1rl |
T |
A |
6: 124,485,802 (GRCm39) |
V391E |
probably damaging |
Het |
Caps2 |
A |
T |
10: 112,036,637 (GRCm39) |
H399L |
probably benign |
Het |
Ccdc43 |
C |
A |
11: 102,577,207 (GRCm39) |
K199N |
probably benign |
Het |
Ccdc7a |
G |
T |
8: 129,555,774 (GRCm39) |
P1198T |
unknown |
Het |
Cct7 |
A |
G |
6: 85,444,625 (GRCm39) |
Y423C |
possibly damaging |
Het |
Cep112 |
A |
G |
11: 108,648,514 (GRCm39) |
T783A |
probably damaging |
Het |
Cep250 |
A |
G |
2: 155,833,459 (GRCm39) |
T1795A |
probably benign |
Het |
Clasp1 |
T |
G |
1: 118,431,560 (GRCm39) |
S397A |
possibly damaging |
Het |
Clock |
A |
C |
5: 76,377,227 (GRCm39) |
F691V |
possibly damaging |
Het |
Cmklr1 |
A |
G |
5: 113,752,341 (GRCm39) |
V220A |
probably benign |
Het |
Coro2b |
A |
T |
9: 62,335,291 (GRCm39) |
Y298* |
probably null |
Het |
Cspg4b |
A |
T |
13: 113,455,649 (GRCm39) |
N565I |
|
Het |
Cyp2t4 |
G |
A |
7: 26,854,717 (GRCm39) |
V66M |
possibly damaging |
Het |
Dlk2 |
G |
A |
17: 46,613,432 (GRCm39) |
G186D |
probably damaging |
Het |
Dok1 |
T |
C |
6: 83,009,972 (GRCm39) |
K46E |
probably damaging |
Het |
Dok3 |
A |
G |
13: 55,672,186 (GRCm39) |
I164T |
probably benign |
Het |
Ercc5 |
T |
A |
1: 44,207,041 (GRCm39) |
D651E |
probably damaging |
Het |
Erp27 |
T |
C |
6: 136,885,066 (GRCm39) |
K244R |
probably benign |
Het |
Fhip1a |
G |
A |
3: 85,580,559 (GRCm39) |
Q549* |
probably null |
Het |
Flvcr2 |
T |
C |
12: 85,793,954 (GRCm39) |
V110A |
possibly damaging |
Het |
Gsta3 |
T |
C |
1: 21,320,060 (GRCm39) |
L22P |
probably damaging |
Het |
Hdac5 |
T |
C |
11: 102,093,522 (GRCm39) |
T493A |
probably benign |
Het |
Hivep2 |
T |
A |
10: 14,005,523 (GRCm39) |
I707N |
probably benign |
Het |
Hmox1 |
A |
G |
8: 75,823,544 (GRCm39) |
N71D |
probably benign |
Het |
Hnrnpr |
G |
T |
4: 136,063,615 (GRCm39) |
V342F |
probably damaging |
Het |
Ifi44 |
T |
C |
3: 151,438,108 (GRCm39) |
D393G |
probably damaging |
Het |
Ighv1-82 |
A |
T |
12: 115,916,566 (GRCm39) |
F9I |
probably damaging |
Het |
Kalrn |
A |
G |
16: 33,854,864 (GRCm39) |
S1999P |
probably damaging |
Het |
Kcnq2 |
A |
G |
2: 180,776,753 (GRCm39) |
S45P |
probably benign |
Het |
Krt77 |
A |
T |
15: 101,769,779 (GRCm39) |
Y364N |
probably damaging |
Het |
Kti12 |
T |
C |
4: 108,705,476 (GRCm39) |
V130A |
probably benign |
Het |
Lama2 |
T |
C |
10: 27,100,015 (GRCm39) |
E830G |
probably benign |
Het |
Lrrn1 |
T |
A |
6: 107,545,505 (GRCm39) |
H434Q |
probably benign |
Het |
Med13 |
A |
T |
11: 86,179,801 (GRCm39) |
N1382K |
probably benign |
Het |
Mrpl42 |
A |
G |
10: 95,332,684 (GRCm39) |
|
probably null |
Het |
Mtor |
A |
G |
4: 148,569,103 (GRCm39) |
D1140G |
probably benign |
Het |
Mtrr |
A |
G |
13: 68,720,755 (GRCm39) |
I280T |
probably benign |
Het |
Myh4 |
A |
T |
11: 67,139,290 (GRCm39) |
I536F |
probably damaging |
Het |
Myh4 |
T |
A |
11: 67,141,129 (GRCm39) |
N730K |
probably damaging |
Het |
Nat10 |
A |
C |
2: 103,563,364 (GRCm39) |
L545R |
probably damaging |
Het |
Nav3 |
T |
A |
10: 109,520,015 (GRCm39) |
D2356V |
probably damaging |
Het |
Nbea |
A |
T |
3: 55,937,366 (GRCm39) |
S748R |
probably damaging |
Het |
Nlrp1a |
T |
C |
11: 70,998,488 (GRCm39) |
T904A |
probably benign |
Het |
Nod2 |
A |
T |
8: 89,397,050 (GRCm39) |
N820I |
probably damaging |
Het |
Nptx1 |
A |
G |
11: 119,433,381 (GRCm39) |
V406A |
probably damaging |
Het |
Nrdc |
T |
A |
4: 108,901,863 (GRCm39) |
I644K |
probably benign |
Het |
Or4e1 |
T |
C |
14: 52,700,873 (GRCm39) |
I198V |
probably benign |
Het |
Ostf1 |
T |
A |
19: 18,573,735 (GRCm39) |
I38F |
probably benign |
Het |
Pacc1 |
G |
A |
1: 191,082,004 (GRCm39) |
R337Q |
probably damaging |
Het |
Pde4b |
G |
T |
4: 102,462,183 (GRCm39) |
D605Y |
probably damaging |
Het |
Pde4d |
A |
G |
13: 109,397,196 (GRCm39) |
T3A |
|
Het |
Pknox1 |
A |
G |
17: 31,822,183 (GRCm39) |
I317V |
probably damaging |
Het |
Plekhh2 |
A |
G |
17: 84,918,240 (GRCm39) |
N1283S |
probably benign |
Het |
Ppp3cb |
G |
A |
14: 20,573,868 (GRCm39) |
A289V |
probably damaging |
Het |
Prag1 |
A |
G |
8: 36,607,208 (GRCm39) |
D983G |
probably damaging |
Het |
Psmd13 |
C |
T |
7: 140,478,455 (GRCm39) |
T62M |
|
Het |
Rab42 |
C |
T |
4: 132,029,890 (GRCm39) |
V111I |
|
Het |
Rabl2 |
T |
A |
15: 89,474,631 (GRCm39) |
|
probably null |
Het |
Rapgef6 |
T |
A |
11: 54,582,169 (GRCm39) |
S1365R |
probably damaging |
Het |
Rassf4 |
G |
T |
6: 116,617,265 (GRCm39) |
H247N |
possibly damaging |
Het |
Rbfox1 |
A |
G |
16: 7,227,573 (GRCm39) |
T363A |
probably benign |
Het |
Rbmyf9 |
T |
A |
Y: 3,774,888 (GRCm39) |
F28L |
probably damaging |
Het |
Sbf1 |
T |
C |
15: 89,184,742 (GRCm39) |
D1091G |
probably damaging |
Het |
Scaper |
A |
G |
9: 55,593,275 (GRCm39) |
V454A |
probably benign |
Het |
Selenbp2 |
G |
A |
3: 94,607,352 (GRCm39) |
D258N |
probably benign |
Het |
Sirpa |
A |
T |
2: 129,457,555 (GRCm39) |
I210F |
probably damaging |
Het |
Skint4 |
T |
C |
4: 112,015,236 (GRCm39) |
S434P |
probably benign |
Het |
Slc26a5 |
G |
A |
5: 22,016,337 (GRCm39) |
Q682* |
probably null |
Het |
Slco4a1 |
C |
T |
2: 180,115,943 (GRCm39) |
S693F |
possibly damaging |
Het |
Smpd3 |
A |
G |
8: 106,992,119 (GRCm39) |
F145L |
probably benign |
Het |
Son |
CATGGACTCCCAGATGTTAGCAACTAGCTCTATGGACTCCCAGATGTTAGCAACTAGCTCTATGGACTCCCAGATGTTAGCAACCAGCAGTATGGACTCCCAGATGTTAGCAACCAGCAGTATGGACTCCCAGATGTTAGCAACCAGCTCCATGGACTCCCAGATGTTAGCAAC |
CATGGACTCCCAGATGTTAGCAACTAGCTCTATGGACTCCCAGATGTTAGCAACCAGCAGTATGGACTCCCAGATGTTAGCAACCAGCAGTATGGACTCCCAGATGTTAGCAACCAGCTCCATGGACTCCCAGATGTTAGCAAC |
16: 91,453,579 (GRCm39) |
|
probably benign |
Het |
Spata31d1c |
A |
T |
13: 65,184,040 (GRCm39) |
L527F |
probably damaging |
Het |
Srd5a3 |
A |
G |
5: 76,297,794 (GRCm39) |
N199D |
probably benign |
Het |
Stard9 |
C |
G |
2: 120,534,564 (GRCm39) |
P3607R |
probably damaging |
Het |
Sytl1 |
A |
G |
4: 132,986,291 (GRCm39) |
|
probably null |
Het |
Tas2r126 |
A |
G |
6: 42,412,307 (GRCm39) |
H280R |
probably null |
Het |
Tcf4 |
C |
T |
18: 69,652,944 (GRCm39) |
|
probably benign |
Het |
Tlcd2 |
A |
G |
11: 75,359,112 (GRCm39) |
T28A |
probably damaging |
Het |
Tm7sf3 |
C |
T |
6: 146,525,179 (GRCm39) |
D89N |
possibly damaging |
Het |
Tmem119 |
A |
G |
5: 113,933,267 (GRCm39) |
L178P |
probably damaging |
Het |
Tmprss7 |
T |
C |
16: 45,484,564 (GRCm39) |
D532G |
probably benign |
Het |
Tnfaip8l3 |
A |
G |
9: 53,934,777 (GRCm39) |
I66T |
probably benign |
Het |
Tor1b |
A |
G |
2: 30,843,185 (GRCm39) |
Y50C |
probably damaging |
Het |
Tpp2 |
T |
A |
1: 44,017,648 (GRCm39) |
S751T |
probably benign |
Het |
Tpra1 |
T |
C |
6: 88,887,221 (GRCm39) |
V193A |
probably benign |
Het |
Trip12 |
A |
T |
1: 84,735,215 (GRCm39) |
V932E |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,777,104 (GRCm39) |
T1479S |
unknown |
Het |
Unc13c |
A |
T |
9: 73,392,220 (GRCm39) |
V2044D |
probably damaging |
Het |
Usp25 |
T |
G |
16: 76,852,076 (GRCm39) |
V197G |
probably damaging |
Het |
Vmn2r34 |
A |
G |
7: 7,675,366 (GRCm39) |
V674A |
probably benign |
Het |
Zfp7 |
T |
C |
15: 76,775,484 (GRCm39) |
S509P |
probably damaging |
Het |
Zfp821 |
A |
G |
8: 110,447,856 (GRCm39) |
T66A |
probably damaging |
Het |
Zfp97 |
T |
A |
17: 17,365,930 (GRCm39) |
N476K |
possibly damaging |
Het |
|
Other mutations in Atp10b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00944:Atp10b
|
APN |
11 |
43,092,988 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01385:Atp10b
|
APN |
11 |
43,125,256 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01524:Atp10b
|
APN |
11 |
43,150,672 (GRCm39) |
missense |
probably benign |
0.18 |
IGL01575:Atp10b
|
APN |
11 |
43,063,548 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01588:Atp10b
|
APN |
11 |
43,063,548 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01590:Atp10b
|
APN |
11 |
43,063,548 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01832:Atp10b
|
APN |
11 |
43,125,262 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01927:Atp10b
|
APN |
11 |
43,150,231 (GRCm39) |
splice site |
probably benign |
|
IGL01933:Atp10b
|
APN |
11 |
43,085,457 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02182:Atp10b
|
APN |
11 |
43,139,774 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02215:Atp10b
|
APN |
11 |
43,085,492 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02216:Atp10b
|
APN |
11 |
43,150,616 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02973:Atp10b
|
APN |
11 |
43,088,336 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03012:Atp10b
|
APN |
11 |
43,085,482 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03106:Atp10b
|
APN |
11 |
43,138,304 (GRCm39) |
missense |
probably benign |
0.32 |
IGL03123:Atp10b
|
APN |
11 |
43,044,110 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03202:Atp10b
|
APN |
11 |
43,125,268 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03339:Atp10b
|
APN |
11 |
43,121,442 (GRCm39) |
missense |
probably null |
0.71 |
R0053:Atp10b
|
UTSW |
11 |
43,107,391 (GRCm39) |
splice site |
probably benign |
|
R0053:Atp10b
|
UTSW |
11 |
43,107,391 (GRCm39) |
splice site |
probably benign |
|
R0098:Atp10b
|
UTSW |
11 |
43,080,431 (GRCm39) |
missense |
probably benign |
0.00 |
R0098:Atp10b
|
UTSW |
11 |
43,080,431 (GRCm39) |
missense |
probably benign |
0.00 |
R0281:Atp10b
|
UTSW |
11 |
43,044,131 (GRCm39) |
missense |
probably benign |
0.00 |
R0379:Atp10b
|
UTSW |
11 |
43,145,141 (GRCm39) |
missense |
probably benign |
0.05 |
R0380:Atp10b
|
UTSW |
11 |
43,116,424 (GRCm39) |
missense |
probably damaging |
1.00 |
R0470:Atp10b
|
UTSW |
11 |
43,093,866 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1355:Atp10b
|
UTSW |
11 |
43,042,482 (GRCm39) |
nonsense |
probably null |
|
R1368:Atp10b
|
UTSW |
11 |
43,092,981 (GRCm39) |
missense |
probably damaging |
1.00 |
R1370:Atp10b
|
UTSW |
11 |
43,042,482 (GRCm39) |
nonsense |
probably null |
|
R1413:Atp10b
|
UTSW |
11 |
43,121,391 (GRCm39) |
missense |
probably benign |
0.00 |
R1502:Atp10b
|
UTSW |
11 |
43,121,174 (GRCm39) |
missense |
probably damaging |
1.00 |
R1530:Atp10b
|
UTSW |
11 |
43,088,351 (GRCm39) |
missense |
probably benign |
0.03 |
R1596:Atp10b
|
UTSW |
11 |
43,126,594 (GRCm39) |
missense |
probably damaging |
1.00 |
R1675:Atp10b
|
UTSW |
11 |
43,116,475 (GRCm39) |
missense |
probably damaging |
1.00 |
R1880:Atp10b
|
UTSW |
11 |
43,150,259 (GRCm39) |
missense |
probably damaging |
1.00 |
R1938:Atp10b
|
UTSW |
11 |
43,121,245 (GRCm39) |
missense |
probably benign |
0.00 |
R1986:Atp10b
|
UTSW |
11 |
43,063,595 (GRCm39) |
missense |
probably benign |
0.12 |
R2081:Atp10b
|
UTSW |
11 |
43,092,955 (GRCm39) |
missense |
probably damaging |
1.00 |
R2083:Atp10b
|
UTSW |
11 |
43,103,250 (GRCm39) |
missense |
probably benign |
0.24 |
R2159:Atp10b
|
UTSW |
11 |
43,042,680 (GRCm39) |
missense |
possibly damaging |
0.81 |
R2255:Atp10b
|
UTSW |
11 |
43,125,207 (GRCm39) |
missense |
probably damaging |
1.00 |
R2259:Atp10b
|
UTSW |
11 |
43,080,440 (GRCm39) |
missense |
probably damaging |
1.00 |
R2259:Atp10b
|
UTSW |
11 |
43,063,572 (GRCm39) |
missense |
probably damaging |
1.00 |
R3741:Atp10b
|
UTSW |
11 |
43,126,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R3942:Atp10b
|
UTSW |
11 |
43,063,581 (GRCm39) |
missense |
probably damaging |
1.00 |
R3971:Atp10b
|
UTSW |
11 |
43,107,339 (GRCm39) |
missense |
probably damaging |
1.00 |
R4007:Atp10b
|
UTSW |
11 |
43,150,679 (GRCm39) |
missense |
probably benign |
0.04 |
R4050:Atp10b
|
UTSW |
11 |
43,150,363 (GRCm39) |
missense |
probably benign |
0.00 |
R4078:Atp10b
|
UTSW |
11 |
43,044,110 (GRCm39) |
missense |
probably benign |
0.01 |
R4567:Atp10b
|
UTSW |
11 |
43,088,384 (GRCm39) |
missense |
probably benign |
0.03 |
R4651:Atp10b
|
UTSW |
11 |
43,085,472 (GRCm39) |
missense |
probably damaging |
1.00 |
R4652:Atp10b
|
UTSW |
11 |
43,085,472 (GRCm39) |
missense |
probably damaging |
1.00 |
R4667:Atp10b
|
UTSW |
11 |
43,138,345 (GRCm39) |
missense |
probably damaging |
1.00 |
R4720:Atp10b
|
UTSW |
11 |
43,093,949 (GRCm39) |
missense |
probably benign |
|
R4987:Atp10b
|
UTSW |
11 |
43,042,440 (GRCm39) |
utr 5 prime |
probably benign |
|
R5232:Atp10b
|
UTSW |
11 |
43,093,006 (GRCm39) |
missense |
probably damaging |
1.00 |
R5233:Atp10b
|
UTSW |
11 |
43,121,387 (GRCm39) |
missense |
probably benign |
0.06 |
R5281:Atp10b
|
UTSW |
11 |
43,145,163 (GRCm39) |
missense |
probably damaging |
0.97 |
R5307:Atp10b
|
UTSW |
11 |
43,103,302 (GRCm39) |
missense |
probably damaging |
1.00 |
R5460:Atp10b
|
UTSW |
11 |
43,121,282 (GRCm39) |
missense |
probably benign |
0.00 |
R5518:Atp10b
|
UTSW |
11 |
43,042,463 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5659:Atp10b
|
UTSW |
11 |
43,136,252 (GRCm39) |
missense |
probably damaging |
1.00 |
R5688:Atp10b
|
UTSW |
11 |
43,092,000 (GRCm39) |
missense |
probably benign |
0.00 |
R5735:Atp10b
|
UTSW |
11 |
43,042,601 (GRCm39) |
missense |
probably benign |
0.00 |
R6153:Atp10b
|
UTSW |
11 |
43,145,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R6251:Atp10b
|
UTSW |
11 |
43,126,573 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6259:Atp10b
|
UTSW |
11 |
43,092,065 (GRCm39) |
missense |
probably benign |
0.24 |
R6394:Atp10b
|
UTSW |
11 |
43,116,464 (GRCm39) |
missense |
probably damaging |
1.00 |
R6492:Atp10b
|
UTSW |
11 |
43,109,784 (GRCm39) |
missense |
probably damaging |
1.00 |
R6769:Atp10b
|
UTSW |
11 |
43,094,079 (GRCm39) |
critical splice donor site |
probably null |
|
R6771:Atp10b
|
UTSW |
11 |
43,094,079 (GRCm39) |
critical splice donor site |
probably null |
|
R6775:Atp10b
|
UTSW |
11 |
43,113,040 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7134:Atp10b
|
UTSW |
11 |
43,136,291 (GRCm39) |
missense |
probably damaging |
1.00 |
R7322:Atp10b
|
UTSW |
11 |
43,103,374 (GRCm39) |
missense |
probably damaging |
1.00 |
R7367:Atp10b
|
UTSW |
11 |
43,138,328 (GRCm39) |
missense |
probably damaging |
1.00 |
R7538:Atp10b
|
UTSW |
11 |
43,116,373 (GRCm39) |
missense |
probably benign |
0.04 |
R7708:Atp10b
|
UTSW |
11 |
43,092,970 (GRCm39) |
missense |
probably damaging |
1.00 |
R7787:Atp10b
|
UTSW |
11 |
43,150,700 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8145:Atp10b
|
UTSW |
11 |
43,092,949 (GRCm39) |
missense |
probably damaging |
1.00 |
R8406:Atp10b
|
UTSW |
11 |
43,093,984 (GRCm39) |
missense |
probably benign |
0.00 |
R8503:Atp10b
|
UTSW |
11 |
43,113,066 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8542:Atp10b
|
UTSW |
11 |
43,121,208 (GRCm39) |
missense |
probably benign |
0.18 |
R8744:Atp10b
|
UTSW |
11 |
43,121,177 (GRCm39) |
missense |
probably damaging |
1.00 |
R8815:Atp10b
|
UTSW |
11 |
43,093,978 (GRCm39) |
missense |
possibly damaging |
0.63 |
R8833:Atp10b
|
UTSW |
11 |
43,112,986 (GRCm39) |
missense |
probably damaging |
1.00 |
R8880:Atp10b
|
UTSW |
11 |
43,106,811 (GRCm39) |
missense |
probably benign |
|
R8989:Atp10b
|
UTSW |
11 |
43,136,269 (GRCm39) |
nonsense |
probably null |
|
R8998:Atp10b
|
UTSW |
11 |
43,150,726 (GRCm39) |
makesense |
probably null |
|
R9255:Atp10b
|
UTSW |
11 |
43,107,148 (GRCm39) |
missense |
probably damaging |
1.00 |
R9281:Atp10b
|
UTSW |
11 |
43,116,458 (GRCm39) |
missense |
probably benign |
0.11 |
R9345:Atp10b
|
UTSW |
11 |
43,094,024 (GRCm39) |
missense |
probably damaging |
0.99 |
R9357:Atp10b
|
UTSW |
11 |
43,150,711 (GRCm39) |
missense |
probably benign |
0.18 |
R9393:Atp10b
|
UTSW |
11 |
43,063,608 (GRCm39) |
missense |
probably damaging |
1.00 |
R9644:Atp10b
|
UTSW |
11 |
43,042,659 (GRCm39) |
missense |
probably damaging |
1.00 |
R9747:Atp10b
|
UTSW |
11 |
43,088,339 (GRCm39) |
missense |
probably benign |
|
Z1177:Atp10b
|
UTSW |
11 |
43,044,176 (GRCm39) |
missense |
probably benign |
0.05 |
|