Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
A |
T |
11: 9,244,175 (GRCm39) |
T2013S |
probably benign |
Het |
Ablim3 |
A |
G |
18: 61,938,135 (GRCm39) |
|
probably null |
Het |
Acvrl1 |
T |
A |
15: 101,034,104 (GRCm39) |
C206* |
probably null |
Het |
Adamts15 |
C |
A |
9: 30,817,454 (GRCm39) |
R541S |
probably damaging |
Het |
Add3 |
A |
G |
19: 53,221,577 (GRCm39) |
I230V |
probably benign |
Het |
Ankrd27 |
A |
G |
7: 35,327,871 (GRCm39) |
D742G |
possibly damaging |
Het |
Atp2b2 |
G |
A |
6: 113,742,693 (GRCm39) |
T798M |
possibly damaging |
Het |
Car12 |
T |
C |
9: 66,659,599 (GRCm39) |
I208T |
probably damaging |
Het |
Cgn |
T |
A |
3: 94,680,502 (GRCm39) |
Q600L |
probably damaging |
Het |
Cgnl1 |
C |
T |
9: 71,539,927 (GRCm39) |
A1106T |
probably benign |
Het |
Cmtr2 |
T |
C |
8: 110,949,178 (GRCm39) |
V496A |
probably benign |
Het |
Cplx4 |
C |
A |
18: 66,090,123 (GRCm39) |
D99Y |
probably damaging |
Het |
Cyfip2 |
T |
C |
11: 46,114,963 (GRCm39) |
T915A |
probably benign |
Het |
Cyp4a32 |
T |
C |
4: 115,466,894 (GRCm39) |
L193P |
probably damaging |
Het |
Dennd5b |
C |
T |
6: 148,946,102 (GRCm39) |
R503Q |
probably damaging |
Het |
Depdc5 |
C |
A |
5: 33,059,209 (GRCm39) |
Q303K |
possibly damaging |
Het |
Dlx1 |
T |
A |
2: 71,362,840 (GRCm39) |
M249K |
possibly damaging |
Het |
Dnah10 |
A |
T |
5: 124,890,892 (GRCm39) |
E3218V |
probably benign |
Het |
Dnah9 |
T |
C |
11: 65,856,473 (GRCm39) |
D2896G |
probably damaging |
Het |
Dtx4 |
C |
A |
19: 12,447,022 (GRCm39) |
G557* |
probably null |
Het |
Eps8l2 |
A |
G |
7: 140,940,305 (GRCm39) |
N512D |
probably damaging |
Het |
Fam20a |
T |
C |
11: 109,612,201 (GRCm39) |
D114G |
possibly damaging |
Het |
Fbln1 |
T |
C |
15: 85,090,353 (GRCm39) |
S7P |
unknown |
Het |
Fli1 |
T |
C |
9: 32,335,484 (GRCm39) |
E316G |
probably damaging |
Het |
Fmn2 |
CCCTCCTCTCCCTGGAATGGGAATACCTCCCCCACCTCCTCTCCCTGGAATGGGAATACCTCCCCCACCTCCTCTCCCTGGAATGGGAATATCTCCCCTACCTCCTCTCCCTGGAATGGGAATACCTCC |
CCCTCCTCTCCCTGGAATGGGAATACCTCCCCCACCTCCTCTCCCTGGAATGGGAATATCTCCCCTACCTCCTCTCCCTGGAATGGGAATACCTCC |
1: 174,436,769 (GRCm39) |
|
probably benign |
Het |
Haus8 |
G |
A |
8: 71,705,781 (GRCm39) |
T302I |
probably benign |
Het |
Hmcn1 |
T |
C |
1: 150,514,627 (GRCm39) |
I3582V |
probably benign |
Het |
Hnrnpul1 |
G |
A |
7: 25,447,842 (GRCm39) |
Q161* |
probably null |
Het |
Hsf4 |
C |
T |
8: 105,998,779 (GRCm39) |
A223V |
probably damaging |
Het |
Ighg2c |
A |
G |
12: 113,251,636 (GRCm39) |
W164R |
|
Het |
Isl1 |
A |
G |
13: 116,439,826 (GRCm39) |
V174A |
probably benign |
Het |
Itih4 |
A |
T |
14: 30,618,571 (GRCm39) |
I661F |
probably benign |
Het |
Klhl14 |
A |
T |
18: 21,785,193 (GRCm39) |
L78Q |
probably damaging |
Het |
L3mbtl3 |
T |
A |
10: 26,215,180 (GRCm39) |
I177F |
unknown |
Het |
Lingo3 |
T |
A |
10: 80,670,938 (GRCm39) |
T331S |
possibly damaging |
Het |
Lrrc36 |
T |
C |
8: 106,187,689 (GRCm39) |
V535A |
possibly damaging |
Het |
Mapk8ip2 |
T |
G |
15: 89,342,279 (GRCm39) |
S497A |
probably benign |
Het |
Mbip |
A |
G |
12: 56,384,547 (GRCm39) |
|
probably null |
Het |
Nelfa |
C |
T |
5: 34,056,169 (GRCm39) |
G498D |
probably damaging |
Het |
Nherf2 |
C |
T |
17: 24,869,078 (GRCm39) |
R16H |
probably damaging |
Het |
Nlrc5 |
T |
A |
8: 95,248,433 (GRCm39) |
|
probably null |
Het |
Or2ag2b |
A |
T |
7: 106,417,650 (GRCm39) |
Y120F |
probably damaging |
Het |
Or4f59 |
A |
T |
2: 111,872,711 (GRCm39) |
V222D |
probably damaging |
Het |
Or56a3 |
T |
C |
7: 104,734,994 (GRCm39) |
S24P |
possibly damaging |
Het |
Or7e171-ps1 |
T |
A |
9: 19,852,855 (GRCm39) |
T294S |
unknown |
Het |
Pde2a |
A |
G |
7: 101,155,160 (GRCm39) |
Y567C |
probably damaging |
Het |
Pdia4 |
A |
T |
6: 47,777,891 (GRCm39) |
F367Y |
probably benign |
Het |
Pkdrej |
C |
A |
15: 85,700,389 (GRCm39) |
C1849F |
possibly damaging |
Het |
Plekhj1 |
T |
G |
10: 80,633,492 (GRCm39) |
T52P |
probably damaging |
Het |
Ppp2r5d |
A |
T |
17: 46,994,986 (GRCm39) |
Y572N |
probably benign |
Het |
Prkcq |
T |
A |
2: 11,295,262 (GRCm39) |
Y570* |
probably null |
Het |
Ptpn3 |
T |
A |
4: 57,245,062 (GRCm39) |
D226V |
probably damaging |
Het |
Rab1b |
A |
G |
19: 5,155,229 (GRCm39) |
S22P |
probably damaging |
Het |
Ralgapa1 |
A |
G |
12: 55,650,976 (GRCm39) |
S2060P |
probably damaging |
Het |
Rnf148 |
G |
T |
6: 23,654,890 (GRCm39) |
S35R |
probably benign |
Het |
Runx2 |
G |
A |
17: 45,125,079 (GRCm39) |
P80L |
probably damaging |
Het |
Samd15 |
T |
A |
12: 87,247,818 (GRCm39) |
S168T |
possibly damaging |
Het |
Slc26a4 |
T |
A |
12: 31,597,945 (GRCm39) |
N167I |
probably damaging |
Het |
Slc39a1 |
C |
A |
3: 90,159,097 (GRCm39) |
H141Q |
probably benign |
Het |
Snx21 |
T |
C |
2: 164,628,121 (GRCm39) |
S46P |
probably benign |
Het |
Strip2 |
A |
G |
6: 29,944,486 (GRCm39) |
S657G |
probably damaging |
Het |
Stxbp3 |
G |
A |
3: 108,708,125 (GRCm39) |
P392L |
probably damaging |
Het |
Suclg1 |
G |
A |
6: 73,240,954 (GRCm39) |
R161H |
probably benign |
Het |
Tas1r3 |
T |
C |
4: 155,947,283 (GRCm39) |
Y134C |
probably damaging |
Het |
Tgif1 |
T |
A |
17: 71,153,168 (GRCm39) |
Q114L |
probably damaging |
Het |
Tll2 |
A |
G |
19: 41,074,673 (GRCm39) |
F964L |
probably benign |
Het |
Tmem181a |
T |
C |
17: 6,348,195 (GRCm39) |
S247P |
possibly damaging |
Het |
Trav23 |
A |
T |
14: 54,215,025 (GRCm39) |
R79S |
probably damaging |
Het |
Trf |
C |
A |
9: 103,102,347 (GRCm39) |
C177F |
probably damaging |
Het |
Triml1 |
T |
C |
8: 43,589,408 (GRCm39) |
Y260C |
probably benign |
Het |
Tulp4 |
T |
C |
17: 6,286,510 (GRCm39) |
F1513L |
probably benign |
Het |
Umodl1 |
G |
A |
17: 31,205,090 (GRCm39) |
V562I |
probably damaging |
Het |
Ush2a |
A |
G |
1: 188,491,960 (GRCm39) |
K3083R |
possibly damaging |
Het |
Vmn1r74 |
A |
T |
7: 11,580,888 (GRCm39) |
I63F |
probably benign |
Het |
Vmn2r38 |
C |
T |
7: 9,100,637 (GRCm39) |
C43Y |
possibly damaging |
Het |
Vmn2r50 |
A |
T |
7: 9,787,010 (GRCm39) |
N32K |
probably benign |
Het |
Vps13d |
A |
G |
4: 144,784,032 (GRCm39) |
V3914A |
|
Het |
Vwa5b2 |
A |
G |
16: 20,422,878 (GRCm39) |
T984A |
probably benign |
Het |
Zc3h3 |
C |
T |
15: 75,712,231 (GRCm39) |
V77M |
probably damaging |
Het |
Zfp397 |
A |
T |
18: 24,093,415 (GRCm39) |
H300L |
probably damaging |
Het |
Zfp950 |
G |
A |
19: 61,107,650 (GRCm39) |
R478C |
probably benign |
Het |
|
Other mutations in Asxl3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00429:Asxl3
|
APN |
18 |
22,658,280 (GRCm39) |
missense |
probably benign |
0.41 |
IGL00510:Asxl3
|
APN |
18 |
22,656,622 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00864:Asxl3
|
APN |
18 |
22,655,503 (GRCm39) |
missense |
probably benign |
0.06 |
IGL01074:Asxl3
|
APN |
18 |
22,655,902 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01305:Asxl3
|
APN |
18 |
22,649,503 (GRCm39) |
missense |
probably benign |
0.06 |
IGL01313:Asxl3
|
APN |
18 |
22,650,516 (GRCm39) |
missense |
probably benign |
0.41 |
IGL01349:Asxl3
|
APN |
18 |
22,657,294 (GRCm39) |
missense |
probably benign |
0.28 |
IGL01529:Asxl3
|
APN |
18 |
22,650,712 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01574:Asxl3
|
APN |
18 |
22,656,621 (GRCm39) |
missense |
probably benign |
0.06 |
IGL01583:Asxl3
|
APN |
18 |
22,649,654 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01619:Asxl3
|
APN |
18 |
22,656,385 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01720:Asxl3
|
APN |
18 |
22,658,382 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01816:Asxl3
|
APN |
18 |
22,655,545 (GRCm39) |
missense |
probably benign |
0.10 |
IGL01828:Asxl3
|
APN |
18 |
22,658,615 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL01903:Asxl3
|
APN |
18 |
22,567,633 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01906:Asxl3
|
APN |
18 |
22,655,338 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01962:Asxl3
|
APN |
18 |
22,655,502 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01991:Asxl3
|
APN |
18 |
22,649,219 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02064:Asxl3
|
APN |
18 |
22,657,401 (GRCm39) |
missense |
possibly damaging |
0.59 |
IGL02187:Asxl3
|
APN |
18 |
22,658,035 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02219:Asxl3
|
APN |
18 |
22,586,683 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL02309:Asxl3
|
APN |
18 |
22,655,510 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02478:Asxl3
|
APN |
18 |
22,656,070 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL02506:Asxl3
|
APN |
18 |
22,585,456 (GRCm39) |
missense |
probably benign |
0.19 |
IGL02660:Asxl3
|
APN |
18 |
22,657,402 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02828:Asxl3
|
APN |
18 |
22,657,718 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL02863:Asxl3
|
APN |
18 |
22,656,541 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03001:Asxl3
|
APN |
18 |
22,650,455 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03143:Asxl3
|
APN |
18 |
22,656,031 (GRCm39) |
missense |
probably benign |
0.43 |
ANU22:Asxl3
|
UTSW |
18 |
22,649,503 (GRCm39) |
missense |
probably benign |
0.06 |
BB001:Asxl3
|
UTSW |
18 |
22,658,602 (GRCm39) |
missense |
probably damaging |
0.98 |
BB011:Asxl3
|
UTSW |
18 |
22,658,602 (GRCm39) |
missense |
probably damaging |
0.98 |
R0145:Asxl3
|
UTSW |
18 |
22,586,662 (GRCm39) |
missense |
probably damaging |
1.00 |
R0201:Asxl3
|
UTSW |
18 |
22,656,211 (GRCm39) |
missense |
probably benign |
|
R0207:Asxl3
|
UTSW |
18 |
22,544,553 (GRCm39) |
splice site |
probably benign |
|
R0230:Asxl3
|
UTSW |
18 |
22,585,383 (GRCm39) |
splice site |
probably benign |
|
R0242:Asxl3
|
UTSW |
18 |
22,649,738 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0242:Asxl3
|
UTSW |
18 |
22,649,738 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0344:Asxl3
|
UTSW |
18 |
22,650,668 (GRCm39) |
missense |
probably benign |
0.00 |
R0519:Asxl3
|
UTSW |
18 |
22,656,577 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0520:Asxl3
|
UTSW |
18 |
22,656,043 (GRCm39) |
missense |
probably damaging |
0.96 |
R0548:Asxl3
|
UTSW |
18 |
22,654,849 (GRCm39) |
splice site |
probably benign |
|
R0626:Asxl3
|
UTSW |
18 |
22,655,937 (GRCm39) |
missense |
probably benign |
0.02 |
R0711:Asxl3
|
UTSW |
18 |
22,657,508 (GRCm39) |
missense |
probably benign |
0.01 |
R0744:Asxl3
|
UTSW |
18 |
22,649,097 (GRCm39) |
missense |
probably damaging |
1.00 |
R0833:Asxl3
|
UTSW |
18 |
22,649,097 (GRCm39) |
missense |
probably damaging |
1.00 |
R1035:Asxl3
|
UTSW |
18 |
22,658,106 (GRCm39) |
missense |
probably damaging |
1.00 |
R1170:Asxl3
|
UTSW |
18 |
22,657,564 (GRCm39) |
missense |
probably benign |
0.00 |
R1372:Asxl3
|
UTSW |
18 |
22,543,066 (GRCm39) |
missense |
probably benign |
0.00 |
R1440:Asxl3
|
UTSW |
18 |
22,658,281 (GRCm39) |
missense |
probably benign |
0.13 |
R1463:Asxl3
|
UTSW |
18 |
22,649,810 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1471:Asxl3
|
UTSW |
18 |
22,649,411 (GRCm39) |
missense |
probably damaging |
1.00 |
R1618:Asxl3
|
UTSW |
18 |
22,650,044 (GRCm39) |
missense |
probably damaging |
1.00 |
R1720:Asxl3
|
UTSW |
18 |
22,585,492 (GRCm39) |
missense |
probably damaging |
1.00 |
R1819:Asxl3
|
UTSW |
18 |
22,655,433 (GRCm39) |
missense |
probably damaging |
1.00 |
R1824:Asxl3
|
UTSW |
18 |
22,655,125 (GRCm39) |
missense |
probably damaging |
1.00 |
R1851:Asxl3
|
UTSW |
18 |
22,650,796 (GRCm39) |
missense |
probably damaging |
0.97 |
R1989:Asxl3
|
UTSW |
18 |
22,585,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R2041:Asxl3
|
UTSW |
18 |
22,656,508 (GRCm39) |
missense |
probably benign |
0.02 |
R2174:Asxl3
|
UTSW |
18 |
22,586,701 (GRCm39) |
missense |
possibly damaging |
0.76 |
R2175:Asxl3
|
UTSW |
18 |
22,649,652 (GRCm39) |
missense |
probably benign |
|
R2443:Asxl3
|
UTSW |
18 |
22,544,596 (GRCm39) |
missense |
probably benign |
0.12 |
R2907:Asxl3
|
UTSW |
18 |
22,650,330 (GRCm39) |
missense |
possibly damaging |
0.56 |
R4246:Asxl3
|
UTSW |
18 |
22,658,557 (GRCm39) |
missense |
probably damaging |
1.00 |
R4254:Asxl3
|
UTSW |
18 |
22,657,423 (GRCm39) |
missense |
possibly damaging |
0.58 |
R4441:Asxl3
|
UTSW |
18 |
22,657,290 (GRCm39) |
missense |
probably damaging |
0.97 |
R4660:Asxl3
|
UTSW |
18 |
22,649,534 (GRCm39) |
missense |
probably benign |
0.00 |
R4661:Asxl3
|
UTSW |
18 |
22,649,534 (GRCm39) |
missense |
probably benign |
0.00 |
R4674:Asxl3
|
UTSW |
18 |
22,650,795 (GRCm39) |
missense |
probably damaging |
1.00 |
R4749:Asxl3
|
UTSW |
18 |
22,649,826 (GRCm39) |
missense |
probably damaging |
0.99 |
R4817:Asxl3
|
UTSW |
18 |
22,658,511 (GRCm39) |
missense |
probably damaging |
0.97 |
R4935:Asxl3
|
UTSW |
18 |
22,656,369 (GRCm39) |
missense |
probably benign |
0.06 |
R5062:Asxl3
|
UTSW |
18 |
22,655,775 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5064:Asxl3
|
UTSW |
18 |
22,649,076 (GRCm39) |
missense |
probably benign |
0.00 |
R5065:Asxl3
|
UTSW |
18 |
22,658,356 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5066:Asxl3
|
UTSW |
18 |
22,658,356 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5067:Asxl3
|
UTSW |
18 |
22,658,356 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5133:Asxl3
|
UTSW |
18 |
22,649,765 (GRCm39) |
missense |
probably damaging |
1.00 |
R5174:Asxl3
|
UTSW |
18 |
22,656,172 (GRCm39) |
missense |
probably benign |
0.45 |
R5183:Asxl3
|
UTSW |
18 |
22,658,356 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5294:Asxl3
|
UTSW |
18 |
22,649,496 (GRCm39) |
missense |
possibly damaging |
0.77 |
R5416:Asxl3
|
UTSW |
18 |
22,657,551 (GRCm39) |
missense |
probably damaging |
1.00 |
R5587:Asxl3
|
UTSW |
18 |
22,658,304 (GRCm39) |
missense |
probably benign |
0.28 |
R5873:Asxl3
|
UTSW |
18 |
22,649,142 (GRCm39) |
missense |
probably benign |
0.04 |
R6240:Asxl3
|
UTSW |
18 |
22,598,565 (GRCm39) |
missense |
probably damaging |
1.00 |
R6242:Asxl3
|
UTSW |
18 |
22,655,433 (GRCm39) |
missense |
probably damaging |
1.00 |
R6316:Asxl3
|
UTSW |
18 |
22,655,839 (GRCm39) |
missense |
probably damaging |
1.00 |
R6348:Asxl3
|
UTSW |
18 |
22,650,330 (GRCm39) |
missense |
possibly damaging |
0.56 |
R6518:Asxl3
|
UTSW |
18 |
22,649,397 (GRCm39) |
missense |
probably damaging |
0.96 |
R6605:Asxl3
|
UTSW |
18 |
22,650,134 (GRCm39) |
nonsense |
probably null |
|
R6704:Asxl3
|
UTSW |
18 |
22,650,362 (GRCm39) |
missense |
probably benign |
0.00 |
R6706:Asxl3
|
UTSW |
18 |
22,586,666 (GRCm39) |
missense |
probably damaging |
1.00 |
R6786:Asxl3
|
UTSW |
18 |
22,658,497 (GRCm39) |
missense |
probably damaging |
1.00 |
R6799:Asxl3
|
UTSW |
18 |
22,598,457 (GRCm39) |
nonsense |
probably null |
|
R6811:Asxl3
|
UTSW |
18 |
22,655,968 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6817:Asxl3
|
UTSW |
18 |
22,656,637 (GRCm39) |
missense |
probably benign |
0.00 |
R6830:Asxl3
|
UTSW |
18 |
22,658,445 (GRCm39) |
missense |
probably benign |
0.45 |
R6957:Asxl3
|
UTSW |
18 |
22,655,148 (GRCm39) |
missense |
probably damaging |
1.00 |
R7015:Asxl3
|
UTSW |
18 |
22,656,978 (GRCm39) |
missense |
probably benign |
0.00 |
R7058:Asxl3
|
UTSW |
18 |
22,650,731 (GRCm39) |
missense |
probably damaging |
1.00 |
R7135:Asxl3
|
UTSW |
18 |
22,650,759 (GRCm39) |
missense |
probably damaging |
1.00 |
R7135:Asxl3
|
UTSW |
18 |
22,650,758 (GRCm39) |
nonsense |
probably null |
|
R7231:Asxl3
|
UTSW |
18 |
22,544,556 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7431:Asxl3
|
UTSW |
18 |
22,650,010 (GRCm39) |
missense |
probably damaging |
1.00 |
R7851:Asxl3
|
UTSW |
18 |
22,650,279 (GRCm39) |
missense |
possibly damaging |
0.62 |
R7871:Asxl3
|
UTSW |
18 |
22,657,281 (GRCm39) |
missense |
not run |
|
R7880:Asxl3
|
UTSW |
18 |
22,655,208 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7924:Asxl3
|
UTSW |
18 |
22,658,602 (GRCm39) |
missense |
probably damaging |
0.98 |
R8061:Asxl3
|
UTSW |
18 |
22,657,300 (GRCm39) |
missense |
possibly damaging |
0.62 |
R8115:Asxl3
|
UTSW |
18 |
22,650,642 (GRCm39) |
missense |
probably damaging |
0.99 |
R8174:Asxl3
|
UTSW |
18 |
22,650,800 (GRCm39) |
missense |
probably benign |
0.02 |
R8303:Asxl3
|
UTSW |
18 |
22,657,473 (GRCm39) |
missense |
probably benign |
|
R8360:Asxl3
|
UTSW |
18 |
22,649,174 (GRCm39) |
missense |
probably benign |
|
R8547:Asxl3
|
UTSW |
18 |
22,655,829 (GRCm39) |
missense |
probably benign |
0.04 |
R8699:Asxl3
|
UTSW |
18 |
22,567,664 (GRCm39) |
missense |
probably benign |
0.02 |
R8774:Asxl3
|
UTSW |
18 |
22,657,101 (GRCm39) |
missense |
probably damaging |
0.99 |
R8774-TAIL:Asxl3
|
UTSW |
18 |
22,657,101 (GRCm39) |
missense |
probably damaging |
0.99 |
R8867:Asxl3
|
UTSW |
18 |
22,649,547 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8915:Asxl3
|
UTSW |
18 |
22,657,763 (GRCm39) |
missense |
probably benign |
0.00 |
R8954:Asxl3
|
UTSW |
18 |
22,650,807 (GRCm39) |
missense |
probably damaging |
1.00 |
R9031:Asxl3
|
UTSW |
18 |
22,657,401 (GRCm39) |
missense |
probably damaging |
0.96 |
R9047:Asxl3
|
UTSW |
18 |
22,585,471 (GRCm39) |
missense |
probably damaging |
1.00 |
R9047:Asxl3
|
UTSW |
18 |
22,585,465 (GRCm39) |
missense |
probably damaging |
1.00 |
R9135:Asxl3
|
UTSW |
18 |
22,657,481 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9135:Asxl3
|
UTSW |
18 |
22,649,670 (GRCm39) |
missense |
probably damaging |
0.99 |
R9210:Asxl3
|
UTSW |
18 |
22,655,389 (GRCm39) |
missense |
probably benign |
0.15 |
R9212:Asxl3
|
UTSW |
18 |
22,655,389 (GRCm39) |
missense |
probably benign |
0.15 |
R9285:Asxl3
|
UTSW |
18 |
22,654,989 (GRCm39) |
missense |
probably damaging |
1.00 |
R9572:Asxl3
|
UTSW |
18 |
22,649,112 (GRCm39) |
missense |
probably benign |
0.25 |
R9707:Asxl3
|
UTSW |
18 |
22,656,304 (GRCm39) |
missense |
probably benign |
0.01 |
R9768:Asxl3
|
UTSW |
18 |
22,650,101 (GRCm39) |
missense |
probably benign |
0.00 |
R9784:Asxl3
|
UTSW |
18 |
22,650,311 (GRCm39) |
missense |
probably benign |
|
Z1088:Asxl3
|
UTSW |
18 |
22,649,829 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Asxl3
|
UTSW |
18 |
22,655,277 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Asxl3
|
UTSW |
18 |
22,656,648 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Asxl3
|
UTSW |
18 |
22,649,396 (GRCm39) |
missense |
probably benign |
0.00 |
|