Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310009B15Rik |
A |
G |
1: 138,779,857 (GRCm39) |
S132P |
probably damaging |
Het |
Abcb5 |
A |
G |
12: 118,871,270 (GRCm39) |
F710L |
probably damaging |
Het |
Acsm4 |
T |
G |
7: 119,310,622 (GRCm39) |
V503G |
probably damaging |
Het |
Adam26a |
T |
A |
8: 44,021,940 (GRCm39) |
M517L |
probably benign |
Het |
Adcy10 |
C |
A |
1: 165,391,854 (GRCm39) |
L1345I |
probably damaging |
Het |
Adgrv1 |
T |
C |
13: 81,715,609 (GRCm39) |
I860V |
probably benign |
Het |
Alcam |
T |
C |
16: 52,097,257 (GRCm39) |
D333G |
probably damaging |
Het |
Amt |
C |
A |
9: 108,177,032 (GRCm39) |
F213L |
possibly damaging |
Het |
Asxl3 |
C |
A |
18: 22,655,148 (GRCm39) |
L1053I |
probably damaging |
Het |
Atxn10 |
T |
C |
15: 85,220,699 (GRCm39) |
S12P |
probably damaging |
Het |
AU021092 |
T |
C |
16: 5,030,017 (GRCm39) |
I333V |
probably benign |
Het |
Birc6 |
A |
G |
17: 74,886,486 (GRCm39) |
I577V |
probably benign |
Het |
Cadm2 |
A |
T |
16: 66,609,726 (GRCm39) |
F132I |
probably benign |
Het |
Casp3 |
T |
A |
8: 47,087,308 (GRCm39) |
V85D |
probably damaging |
Het |
Ccdc168 |
C |
T |
1: 44,096,367 (GRCm39) |
C1577Y |
probably benign |
Het |
Ccdc85a |
A |
T |
11: 28,342,944 (GRCm39) |
|
probably benign |
Het |
Cd22 |
T |
C |
7: 30,566,999 (GRCm39) |
R760G |
possibly damaging |
Het |
Cela3a |
A |
T |
4: 137,135,441 (GRCm39) |
W41R |
probably damaging |
Het |
Cep164 |
A |
G |
9: 45,683,578 (GRCm39) |
|
probably null |
Het |
Cntnap5b |
A |
G |
1: 100,202,197 (GRCm39) |
E348G |
probably benign |
Het |
Ddx20 |
C |
A |
3: 105,591,626 (GRCm39) |
K181N |
probably benign |
Het |
Dnah14 |
G |
C |
1: 181,612,740 (GRCm39) |
A3846P |
possibly damaging |
Het |
Ern1 |
A |
C |
11: 106,294,365 (GRCm39) |
I813S |
probably damaging |
Het |
Fam181a |
G |
A |
12: 103,282,773 (GRCm39) |
G226D |
probably damaging |
Het |
Fam186a |
T |
A |
15: 99,844,357 (GRCm39) |
D629V |
unknown |
Het |
Gipr |
T |
A |
7: 18,898,529 (GRCm39) |
T26S |
probably benign |
Het |
Gm3159 |
A |
G |
14: 4,398,530 (GRCm38) |
R74G |
possibly damaging |
Het |
Greb1l |
G |
A |
18: 10,558,786 (GRCm39) |
V1814I |
probably benign |
Het |
Hacd1 |
A |
T |
2: 14,049,664 (GRCm39) |
V98E |
probably damaging |
Het |
Iars1 |
T |
G |
13: 49,875,637 (GRCm39) |
F775V |
probably damaging |
Het |
Il12rb2 |
G |
A |
6: 67,269,636 (GRCm39) |
L726F |
possibly damaging |
Het |
Itih4 |
T |
C |
14: 30,614,560 (GRCm39) |
V474A |
probably damaging |
Het |
Kmt2a |
A |
C |
9: 44,731,319 (GRCm39) |
|
probably benign |
Het |
Ktn1 |
T |
A |
14: 47,904,810 (GRCm39) |
L196* |
probably null |
Het |
Lipo4 |
A |
G |
19: 33,476,767 (GRCm39) |
V327A |
probably benign |
Het |
Lratd2 |
T |
C |
15: 60,694,934 (GRCm39) |
T271A |
probably benign |
Het |
Lrit1 |
G |
C |
14: 36,782,052 (GRCm39) |
V242L |
probably damaging |
Het |
Lrp4 |
C |
A |
2: 91,317,387 (GRCm39) |
T837K |
probably damaging |
Het |
Mad1l1 |
G |
T |
5: 140,051,572 (GRCm39) |
F664L |
probably damaging |
Het |
Mecr |
A |
G |
4: 131,589,172 (GRCm39) |
T247A |
probably benign |
Het |
Msi1 |
G |
A |
5: 115,583,483 (GRCm39) |
A228T |
probably benign |
Het |
Mup5 |
T |
A |
4: 61,751,273 (GRCm39) |
N125I |
probably damaging |
Het |
Mybl2 |
C |
T |
2: 162,914,728 (GRCm39) |
S282F |
possibly damaging |
Het |
Myom2 |
G |
A |
8: 15,167,741 (GRCm39) |
A1109T |
probably null |
Het |
Nalcn |
T |
C |
14: 123,744,966 (GRCm39) |
D354G |
probably damaging |
Het |
Nckap1l |
T |
C |
15: 103,399,938 (GRCm39) |
V1040A |
possibly damaging |
Het |
Nlrp12 |
T |
A |
7: 3,271,160 (GRCm39) |
D1051V |
probably damaging |
Het |
Nudt7 |
A |
G |
8: 114,860,385 (GRCm39) |
K16R |
probably benign |
Het |
Or4b1 |
G |
T |
2: 89,979,494 (GRCm39) |
Y285* |
probably null |
Het |
Or8g29-ps1 |
A |
G |
9: 39,200,577 (GRCm39) |
V203A |
unknown |
Het |
Paqr3 |
A |
T |
5: 97,256,110 (GRCm39) |
I88K |
possibly damaging |
Het |
Parp9 |
A |
G |
16: 35,768,716 (GRCm39) |
M299V |
probably benign |
Het |
Pde4dip |
A |
T |
3: 97,731,649 (GRCm39) |
|
probably null |
Het |
Pex13 |
T |
G |
11: 23,605,628 (GRCm39) |
M201L |
probably benign |
Het |
Pfas |
C |
A |
11: 68,884,709 (GRCm39) |
V498L |
probably benign |
Het |
Phka2 |
G |
A |
X: 159,316,044 (GRCm39) |
V230I |
probably damaging |
Het |
Plec |
T |
A |
15: 76,070,414 (GRCm39) |
D932V |
probably damaging |
Het |
Qng1 |
C |
A |
13: 58,529,775 (GRCm39) |
C279F |
probably damaging |
Het |
Qsox2 |
C |
T |
2: 26,107,654 (GRCm39) |
A445T |
probably benign |
Het |
Rapgef1 |
C |
A |
2: 29,623,710 (GRCm39) |
Q820K |
possibly damaging |
Het |
Samd13 |
A |
G |
3: 146,368,424 (GRCm39) |
|
probably null |
Het |
Samm50 |
G |
T |
15: 84,082,850 (GRCm39) |
D104Y |
probably damaging |
Het |
Sbk3 |
A |
T |
7: 4,970,522 (GRCm39) |
F282L |
probably benign |
Het |
Sfmbt1 |
C |
T |
14: 30,509,546 (GRCm39) |
H342Y |
probably benign |
Het |
Sgo2b |
CCATCATCATCATCATCATCAT |
CCATCATCATCATCATCAT |
8: 64,384,489 (GRCm39) |
|
probably benign |
Het |
Slc12a2 |
T |
A |
18: 58,043,344 (GRCm39) |
L596* |
probably null |
Het |
Spata31h1 |
A |
T |
10: 82,129,620 (GRCm39) |
I1130K |
probably benign |
Het |
St8sia3 |
T |
C |
18: 64,404,853 (GRCm39) |
S377P |
probably benign |
Het |
Stmnd1 |
T |
G |
13: 46,427,375 (GRCm39) |
S28A |
probably benign |
Het |
Syne3 |
A |
T |
12: 104,920,561 (GRCm39) |
L458Q |
probably damaging |
Het |
Synm |
C |
T |
7: 67,385,848 (GRCm39) |
V163I |
probably benign |
Het |
Tbc1d23 |
A |
G |
16: 57,028,686 (GRCm39) |
C161R |
probably damaging |
Het |
Tnfrsf4 |
G |
A |
4: 156,100,625 (GRCm39) |
V215I |
probably benign |
Het |
Vars2 |
T |
G |
17: 35,977,967 (GRCm39) |
K67Q |
probably benign |
Het |
Vmn2r13 |
A |
T |
5: 109,304,753 (GRCm39) |
Y559* |
probably null |
Het |
Wdpcp |
T |
C |
11: 21,671,154 (GRCm39) |
I465T |
possibly damaging |
Het |
Zwilch |
A |
C |
9: 64,069,844 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Ascc3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00264:Ascc3
|
APN |
10 |
50,590,531 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00690:Ascc3
|
APN |
10 |
50,576,039 (GRCm39) |
nonsense |
probably null |
|
IGL00897:Ascc3
|
APN |
10 |
50,604,187 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01077:Ascc3
|
APN |
10 |
50,525,413 (GRCm39) |
splice site |
probably benign |
|
IGL01124:Ascc3
|
APN |
10 |
50,608,569 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01555:Ascc3
|
APN |
10 |
50,626,618 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02019:Ascc3
|
APN |
10 |
50,566,235 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02161:Ascc3
|
APN |
10 |
50,726,623 (GRCm39) |
nonsense |
probably null |
|
IGL02247:Ascc3
|
APN |
10 |
50,526,686 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02318:Ascc3
|
APN |
10 |
50,604,250 (GRCm39) |
nonsense |
probably null |
|
IGL02428:Ascc3
|
APN |
10 |
50,721,791 (GRCm39) |
nonsense |
probably null |
|
IGL02432:Ascc3
|
APN |
10 |
50,576,589 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02449:Ascc3
|
APN |
10 |
50,576,695 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02640:Ascc3
|
APN |
10 |
50,643,470 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL02673:Ascc3
|
APN |
10 |
50,536,769 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03144:Ascc3
|
APN |
10 |
50,643,539 (GRCm39) |
missense |
probably benign |
0.16 |
IGL03161:Ascc3
|
APN |
10 |
50,494,168 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03218:Ascc3
|
APN |
10 |
50,699,949 (GRCm39) |
missense |
possibly damaging |
0.89 |
algorithm
|
UTSW |
10 |
50,594,472 (GRCm39) |
missense |
probably damaging |
0.97 |
heuristic
|
UTSW |
10 |
50,718,289 (GRCm39) |
missense |
probably damaging |
0.99 |
network
|
UTSW |
10 |
50,630,175 (GRCm39) |
missense |
possibly damaging |
0.53 |
R0045:Ascc3
|
UTSW |
10 |
50,594,498 (GRCm39) |
nonsense |
probably null |
|
R0045:Ascc3
|
UTSW |
10 |
50,594,498 (GRCm39) |
nonsense |
probably null |
|
R0131:Ascc3
|
UTSW |
10 |
50,611,425 (GRCm39) |
missense |
probably damaging |
0.99 |
R0131:Ascc3
|
UTSW |
10 |
50,611,425 (GRCm39) |
missense |
probably damaging |
0.99 |
R0132:Ascc3
|
UTSW |
10 |
50,611,425 (GRCm39) |
missense |
probably damaging |
0.99 |
R0149:Ascc3
|
UTSW |
10 |
50,484,089 (GRCm39) |
missense |
probably benign |
0.31 |
R0165:Ascc3
|
UTSW |
10 |
50,718,223 (GRCm39) |
splice site |
probably null |
|
R0255:Ascc3
|
UTSW |
10 |
50,521,154 (GRCm39) |
missense |
probably benign |
0.00 |
R0310:Ascc3
|
UTSW |
10 |
50,625,022 (GRCm39) |
missense |
probably benign |
0.02 |
R0314:Ascc3
|
UTSW |
10 |
50,514,095 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0362:Ascc3
|
UTSW |
10 |
50,625,051 (GRCm39) |
splice site |
probably benign |
|
R0418:Ascc3
|
UTSW |
10 |
50,625,022 (GRCm39) |
missense |
probably benign |
0.02 |
R0419:Ascc3
|
UTSW |
10 |
50,625,022 (GRCm39) |
missense |
probably benign |
0.02 |
R0421:Ascc3
|
UTSW |
10 |
50,625,022 (GRCm39) |
missense |
probably benign |
0.02 |
R0480:Ascc3
|
UTSW |
10 |
50,611,348 (GRCm39) |
missense |
probably damaging |
1.00 |
R0744:Ascc3
|
UTSW |
10 |
50,721,762 (GRCm39) |
missense |
probably benign |
0.17 |
R0833:Ascc3
|
UTSW |
10 |
50,721,762 (GRCm39) |
missense |
probably benign |
0.17 |
R1231:Ascc3
|
UTSW |
10 |
50,699,756 (GRCm39) |
missense |
probably damaging |
1.00 |
R1264:Ascc3
|
UTSW |
10 |
50,518,615 (GRCm39) |
splice site |
probably benign |
|
R1302:Ascc3
|
UTSW |
10 |
50,480,890 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
R1751:Ascc3
|
UTSW |
10 |
50,594,472 (GRCm39) |
missense |
probably damaging |
0.97 |
R1767:Ascc3
|
UTSW |
10 |
50,594,472 (GRCm39) |
missense |
probably damaging |
0.97 |
R1769:Ascc3
|
UTSW |
10 |
50,576,586 (GRCm39) |
missense |
probably damaging |
1.00 |
R1840:Ascc3
|
UTSW |
10 |
50,566,257 (GRCm39) |
missense |
probably benign |
0.00 |
R1855:Ascc3
|
UTSW |
10 |
50,494,018 (GRCm39) |
missense |
probably benign |
0.01 |
R1953:Ascc3
|
UTSW |
10 |
50,721,726 (GRCm39) |
missense |
probably benign |
|
R1976:Ascc3
|
UTSW |
10 |
50,525,262 (GRCm39) |
missense |
probably damaging |
1.00 |
R2004:Ascc3
|
UTSW |
10 |
50,493,838 (GRCm39) |
missense |
probably damaging |
1.00 |
R2013:Ascc3
|
UTSW |
10 |
50,525,908 (GRCm39) |
missense |
probably damaging |
0.99 |
R2017:Ascc3
|
UTSW |
10 |
50,566,307 (GRCm39) |
missense |
probably benign |
0.00 |
R2040:Ascc3
|
UTSW |
10 |
50,604,227 (GRCm39) |
missense |
probably benign |
|
R2043:Ascc3
|
UTSW |
10 |
50,576,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R2165:Ascc3
|
UTSW |
10 |
50,597,935 (GRCm39) |
missense |
probably damaging |
1.00 |
R2226:Ascc3
|
UTSW |
10 |
50,630,148 (GRCm39) |
missense |
probably benign |
0.07 |
R2310:Ascc3
|
UTSW |
10 |
50,624,988 (GRCm39) |
missense |
probably benign |
0.15 |
R2405:Ascc3
|
UTSW |
10 |
50,607,774 (GRCm39) |
missense |
probably damaging |
1.00 |
R2424:Ascc3
|
UTSW |
10 |
50,494,297 (GRCm39) |
missense |
probably benign |
0.14 |
R3410:Ascc3
|
UTSW |
10 |
50,576,196 (GRCm39) |
missense |
probably damaging |
1.00 |
R3617:Ascc3
|
UTSW |
10 |
50,494,281 (GRCm39) |
missense |
probably benign |
0.00 |
R3771:Ascc3
|
UTSW |
10 |
50,596,814 (GRCm39) |
splice site |
probably benign |
|
R3783:Ascc3
|
UTSW |
10 |
50,604,350 (GRCm39) |
missense |
probably damaging |
1.00 |
R3891:Ascc3
|
UTSW |
10 |
50,718,289 (GRCm39) |
missense |
probably damaging |
0.99 |
R3892:Ascc3
|
UTSW |
10 |
50,718,289 (GRCm39) |
missense |
probably damaging |
0.99 |
R4435:Ascc3
|
UTSW |
10 |
50,597,981 (GRCm39) |
missense |
probably benign |
0.14 |
R4509:Ascc3
|
UTSW |
10 |
50,718,339 (GRCm39) |
missense |
probably benign |
0.00 |
R4520:Ascc3
|
UTSW |
10 |
50,536,766 (GRCm39) |
missense |
probably benign |
|
R4521:Ascc3
|
UTSW |
10 |
50,536,766 (GRCm39) |
missense |
probably benign |
|
R4522:Ascc3
|
UTSW |
10 |
50,536,766 (GRCm39) |
missense |
probably benign |
|
R4524:Ascc3
|
UTSW |
10 |
50,536,766 (GRCm39) |
missense |
probably benign |
|
R4581:Ascc3
|
UTSW |
10 |
50,587,121 (GRCm39) |
missense |
probably damaging |
1.00 |
R4701:Ascc3
|
UTSW |
10 |
50,596,760 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4704:Ascc3
|
UTSW |
10 |
50,535,110 (GRCm39) |
missense |
probably benign |
0.02 |
R4768:Ascc3
|
UTSW |
10 |
50,576,595 (GRCm39) |
missense |
probably damaging |
1.00 |
R4823:Ascc3
|
UTSW |
10 |
50,589,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R4906:Ascc3
|
UTSW |
10 |
50,625,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R4937:Ascc3
|
UTSW |
10 |
50,699,894 (GRCm39) |
missense |
probably damaging |
1.00 |
R5001:Ascc3
|
UTSW |
10 |
50,699,744 (GRCm39) |
missense |
probably damaging |
1.00 |
R5151:Ascc3
|
UTSW |
10 |
50,514,059 (GRCm39) |
missense |
probably damaging |
0.99 |
R5263:Ascc3
|
UTSW |
10 |
50,592,757 (GRCm39) |
missense |
probably benign |
0.00 |
R5302:Ascc3
|
UTSW |
10 |
50,583,873 (GRCm39) |
missense |
probably benign |
0.09 |
R5436:Ascc3
|
UTSW |
10 |
50,535,079 (GRCm39) |
missense |
probably damaging |
0.99 |
R5455:Ascc3
|
UTSW |
10 |
50,725,679 (GRCm39) |
missense |
probably benign |
0.06 |
R5474:Ascc3
|
UTSW |
10 |
50,725,634 (GRCm39) |
missense |
probably benign |
0.25 |
R5744:Ascc3
|
UTSW |
10 |
50,586,977 (GRCm39) |
missense |
probably benign |
|
R5781:Ascc3
|
UTSW |
10 |
50,514,074 (GRCm39) |
missense |
probably damaging |
1.00 |
R5850:Ascc3
|
UTSW |
10 |
50,587,049 (GRCm39) |
missense |
probably damaging |
1.00 |
R5867:Ascc3
|
UTSW |
10 |
50,718,279 (GRCm39) |
nonsense |
probably null |
|
R5868:Ascc3
|
UTSW |
10 |
50,718,279 (GRCm39) |
nonsense |
probably null |
|
R5869:Ascc3
|
UTSW |
10 |
50,718,279 (GRCm39) |
nonsense |
probably null |
|
R6031:Ascc3
|
UTSW |
10 |
50,718,279 (GRCm39) |
nonsense |
probably null |
|
R6031:Ascc3
|
UTSW |
10 |
50,718,279 (GRCm39) |
nonsense |
probably null |
|
R6032:Ascc3
|
UTSW |
10 |
50,718,279 (GRCm39) |
nonsense |
probably null |
|
R6032:Ascc3
|
UTSW |
10 |
50,718,279 (GRCm39) |
nonsense |
probably null |
|
R6109:Ascc3
|
UTSW |
10 |
50,525,343 (GRCm39) |
missense |
probably benign |
0.37 |
R6122:Ascc3
|
UTSW |
10 |
50,494,021 (GRCm39) |
missense |
probably benign |
|
R6128:Ascc3
|
UTSW |
10 |
50,526,734 (GRCm39) |
missense |
probably damaging |
1.00 |
R6351:Ascc3
|
UTSW |
10 |
50,596,769 (GRCm39) |
missense |
probably damaging |
0.99 |
R6368:Ascc3
|
UTSW |
10 |
50,576,081 (GRCm39) |
missense |
probably damaging |
1.00 |
R6369:Ascc3
|
UTSW |
10 |
50,576,081 (GRCm39) |
missense |
probably damaging |
1.00 |
R6409:Ascc3
|
UTSW |
10 |
50,721,676 (GRCm39) |
missense |
probably benign |
0.09 |
R6472:Ascc3
|
UTSW |
10 |
50,596,783 (GRCm39) |
missense |
probably benign |
0.03 |
R6474:Ascc3
|
UTSW |
10 |
50,624,932 (GRCm39) |
missense |
probably benign |
0.01 |
R6480:Ascc3
|
UTSW |
10 |
50,587,049 (GRCm39) |
missense |
probably damaging |
1.00 |
R6553:Ascc3
|
UTSW |
10 |
50,718,273 (GRCm39) |
missense |
probably benign |
0.05 |
R6572:Ascc3
|
UTSW |
10 |
50,566,343 (GRCm39) |
nonsense |
probably null |
|
R6585:Ascc3
|
UTSW |
10 |
50,718,273 (GRCm39) |
missense |
probably benign |
0.05 |
R6656:Ascc3
|
UTSW |
10 |
50,526,021 (GRCm39) |
nonsense |
probably null |
|
R6669:Ascc3
|
UTSW |
10 |
50,716,469 (GRCm39) |
missense |
probably benign |
|
R6675:Ascc3
|
UTSW |
10 |
50,626,659 (GRCm39) |
nonsense |
probably null |
|
R6790:Ascc3
|
UTSW |
10 |
50,521,808 (GRCm39) |
missense |
probably damaging |
1.00 |
R6856:Ascc3
|
UTSW |
10 |
50,625,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R6862:Ascc3
|
UTSW |
10 |
50,725,742 (GRCm39) |
missense |
probably null |
0.51 |
R6919:Ascc3
|
UTSW |
10 |
50,521,849 (GRCm39) |
nonsense |
probably null |
|
R6936:Ascc3
|
UTSW |
10 |
50,606,057 (GRCm39) |
missense |
probably damaging |
0.98 |
R6953:Ascc3
|
UTSW |
10 |
50,521,762 (GRCm39) |
missense |
probably benign |
0.00 |
R7022:Ascc3
|
UTSW |
10 |
50,592,725 (GRCm39) |
missense |
possibly damaging |
0.55 |
R7050:Ascc3
|
UTSW |
10 |
50,716,446 (GRCm39) |
missense |
probably benign |
0.43 |
R7358:Ascc3
|
UTSW |
10 |
50,590,448 (GRCm39) |
nonsense |
probably null |
|
R7479:Ascc3
|
UTSW |
10 |
50,525,895 (GRCm39) |
missense |
probably damaging |
1.00 |
R7538:Ascc3
|
UTSW |
10 |
50,721,796 (GRCm39) |
missense |
probably damaging |
1.00 |
R7838:Ascc3
|
UTSW |
10 |
50,604,393 (GRCm39) |
missense |
probably benign |
0.04 |
R8021:Ascc3
|
UTSW |
10 |
50,607,744 (GRCm39) |
missense |
probably benign |
0.02 |
R8134:Ascc3
|
UTSW |
10 |
50,643,554 (GRCm39) |
missense |
probably benign |
0.02 |
R8252:Ascc3
|
UTSW |
10 |
50,518,706 (GRCm39) |
missense |
probably benign |
|
R8348:Ascc3
|
UTSW |
10 |
50,494,173 (GRCm39) |
missense |
probably benign |
|
R8351:Ascc3
|
UTSW |
10 |
50,725,693 (GRCm39) |
missense |
probably benign |
|
R8356:Ascc3
|
UTSW |
10 |
50,526,003 (GRCm39) |
missense |
probably benign |
0.38 |
R8362:Ascc3
|
UTSW |
10 |
50,518,692 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8395:Ascc3
|
UTSW |
10 |
50,525,400 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8448:Ascc3
|
UTSW |
10 |
50,494,173 (GRCm39) |
missense |
probably benign |
|
R8957:Ascc3
|
UTSW |
10 |
50,576,208 (GRCm39) |
missense |
probably damaging |
1.00 |
R9004:Ascc3
|
UTSW |
10 |
50,718,276 (GRCm39) |
missense |
probably benign |
|
R9133:Ascc3
|
UTSW |
10 |
50,630,175 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9200:Ascc3
|
UTSW |
10 |
50,521,787 (GRCm39) |
missense |
possibly damaging |
0.55 |
R9328:Ascc3
|
UTSW |
10 |
50,535,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R9377:Ascc3
|
UTSW |
10 |
50,608,858 (GRCm39) |
missense |
possibly damaging |
0.62 |
R9412:Ascc3
|
UTSW |
10 |
50,525,230 (GRCm39) |
missense |
probably benign |
0.00 |
R9576:Ascc3
|
UTSW |
10 |
50,494,254 (GRCm39) |
missense |
possibly damaging |
0.71 |
R9796:Ascc3
|
UTSW |
10 |
50,608,801 (GRCm39) |
nonsense |
probably null |
|
X0021:Ascc3
|
UTSW |
10 |
50,576,686 (GRCm39) |
missense |
possibly damaging |
0.88 |
X0025:Ascc3
|
UTSW |
10 |
50,526,692 (GRCm39) |
missense |
probably benign |
0.00 |
X0026:Ascc3
|
UTSW |
10 |
50,608,574 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Ascc3
|
UTSW |
10 |
50,594,517 (GRCm39) |
missense |
probably benign |
|
|