Other mutations in this stock |
Total: 85 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aars2 |
T |
A |
17: 45,819,887 (GRCm39) |
Y221* |
probably null |
Het |
AC166344.1 |
T |
A |
14: 43,158,245 (GRCm39) |
F97I |
|
Het |
Ankmy2 |
T |
C |
12: 36,246,311 (GRCm39) |
S412P |
probably benign |
Het |
Ap1s3 |
T |
C |
1: 79,586,919 (GRCm39) |
T144A |
probably benign |
Het |
Armh2 |
T |
C |
13: 24,925,489 (GRCm39) |
S78P |
probably benign |
Het |
Asb3 |
T |
A |
11: 30,948,501 (GRCm39) |
L59* |
probably null |
Het |
Birc2 |
A |
C |
9: 7,818,762 (GRCm39) |
F610V |
probably damaging |
Het |
Camk4 |
G |
A |
18: 33,240,996 (GRCm39) |
|
probably null |
Het |
Ccdc162 |
A |
G |
10: 41,549,855 (GRCm39) |
S343P |
probably benign |
Het |
Ccnk |
T |
A |
12: 108,152,734 (GRCm39) |
L17Q |
probably damaging |
Het |
Cd59b |
G |
A |
2: 103,914,792 (GRCm39) |
W63* |
probably null |
Het |
Chrm3 |
C |
T |
13: 9,927,837 (GRCm39) |
V400I |
probably benign |
Het |
Crb1 |
C |
A |
1: 139,171,105 (GRCm39) |
V762F |
probably damaging |
Het |
Cspp1 |
C |
T |
1: 10,159,161 (GRCm39) |
T529I |
possibly damaging |
Het |
Cttnbp2 |
A |
G |
6: 18,448,446 (GRCm39) |
I71T |
possibly damaging |
Het |
Cyb561 |
C |
A |
11: 105,826,393 (GRCm39) |
G90V |
probably damaging |
Het |
Cyld |
T |
A |
8: 89,471,520 (GRCm39) |
D804E |
possibly damaging |
Het |
Ddx31 |
G |
A |
2: 28,738,318 (GRCm39) |
V160I |
probably benign |
Het |
Dgkg |
T |
C |
16: 22,319,132 (GRCm39) |
D643G |
probably damaging |
Het |
Dnah12 |
G |
A |
14: 26,500,869 (GRCm39) |
|
probably null |
Het |
Dnah12 |
T |
G |
14: 26,523,370 (GRCm39) |
I1953S |
probably damaging |
Het |
Dnah7b |
T |
C |
1: 46,178,870 (GRCm39) |
W848R |
probably damaging |
Het |
Dnah7c |
C |
T |
1: 46,572,368 (GRCm39) |
T947M |
probably damaging |
Het |
Dnmt3c |
C |
A |
2: 153,556,872 (GRCm39) |
|
probably null |
Het |
Dsp |
A |
T |
13: 38,363,049 (GRCm39) |
Y443F |
probably damaging |
Het |
Espl1 |
T |
A |
15: 102,227,959 (GRCm39) |
C1603* |
probably null |
Het |
Faiml |
G |
T |
9: 99,116,496 (GRCm39) |
R65S |
probably benign |
Het |
Gfpt2 |
T |
C |
11: 49,695,782 (GRCm39) |
I4T |
probably damaging |
Het |
Gm10376 |
T |
A |
14: 42,867,950 (GRCm39) |
M179L |
probably benign |
Het |
Gm4302 |
T |
A |
10: 100,177,589 (GRCm39) |
M291K |
unknown |
Het |
Gnb1l |
T |
A |
16: 18,363,918 (GRCm39) |
D154E |
probably benign |
Het |
Igkv10-94 |
T |
C |
6: 68,681,727 (GRCm39) |
R38G |
possibly damaging |
Het |
Inmt |
A |
T |
6: 55,148,013 (GRCm39) |
Y205* |
probably null |
Het |
Krba1 |
A |
G |
6: 48,393,233 (GRCm39) |
Q1049R |
probably benign |
Het |
Lpxn |
T |
A |
19: 12,810,683 (GRCm39) |
C376S |
probably damaging |
Het |
Lrrc52 |
T |
A |
1: 167,294,019 (GRCm39) |
I89F |
probably damaging |
Het |
Map9 |
A |
T |
3: 82,270,765 (GRCm39) |
T110S |
probably benign |
Het |
Mccc1 |
T |
C |
3: 36,049,967 (GRCm39) |
Y75C |
probably damaging |
Het |
Mff |
T |
A |
1: 82,724,812 (GRCm39) |
L203* |
probably null |
Het |
Micall1 |
C |
A |
15: 78,993,624 (GRCm39) |
D47E |
unknown |
Het |
Mink1 |
T |
C |
11: 70,494,329 (GRCm39) |
F243S |
probably damaging |
Het |
Mlycd |
C |
T |
8: 120,129,216 (GRCm39) |
R228W |
probably damaging |
Het |
Msr1 |
A |
T |
8: 40,042,465 (GRCm39) |
V370E |
possibly damaging |
Het |
Naip6 |
T |
C |
13: 100,436,927 (GRCm39) |
E532G |
probably damaging |
Het |
Nepn |
G |
A |
10: 52,267,815 (GRCm39) |
C27Y |
probably damaging |
Het |
Ninl |
T |
C |
2: 150,797,524 (GRCm39) |
H592R |
probably benign |
Het |
Nr4a2 |
A |
G |
2: 57,002,261 (GRCm39) |
M64T |
possibly damaging |
Het |
Oprm1 |
A |
T |
10: 6,780,203 (GRCm39) |
I171F |
possibly damaging |
Het |
Or4g16 |
T |
A |
2: 111,137,365 (GRCm39) |
F272I |
probably benign |
Het |
Or5p60 |
T |
C |
7: 107,723,781 (GRCm39) |
K230E |
probably damaging |
Het |
Pcbp1 |
A |
T |
6: 86,502,488 (GRCm39) |
M137K |
possibly damaging |
Het |
Pcf11 |
A |
T |
7: 92,306,524 (GRCm39) |
S1215T |
probably benign |
Het |
Pdlim5 |
A |
T |
3: 142,017,683 (GRCm39) |
|
probably null |
Het |
Pecam1 |
T |
C |
11: 106,579,857 (GRCm39) |
I402V |
probably damaging |
Het |
Pex12 |
T |
C |
11: 83,188,468 (GRCm39) |
T176A |
probably benign |
Het |
Phf3 |
T |
C |
1: 30,870,190 (GRCm39) |
K286R |
possibly damaging |
Het |
Pik3ap1 |
T |
A |
19: 41,320,760 (GRCm39) |
D153V |
probably damaging |
Het |
Pkhd1l1 |
T |
A |
15: 44,448,374 (GRCm39) |
|
probably null |
Het |
Plekhn1 |
A |
G |
4: 156,307,792 (GRCm39) |
V378A |
probably benign |
Het |
Pramel26 |
A |
T |
4: 143,537,233 (GRCm39) |
L366Q |
probably damaging |
Het |
Ptprm |
A |
T |
17: 67,251,283 (GRCm39) |
D531E |
possibly damaging |
Het |
Pum2 |
A |
T |
12: 8,778,952 (GRCm39) |
Q508L |
possibly damaging |
Het |
Rad54l |
A |
G |
4: 115,963,027 (GRCm39) |
S324P |
probably damaging |
Het |
Recql5 |
C |
T |
11: 115,821,498 (GRCm39) |
|
probably null |
Het |
Reln |
A |
T |
5: 22,181,594 (GRCm39) |
V1763D |
possibly damaging |
Het |
Rp1 |
T |
C |
1: 4,418,391 (GRCm39) |
N907S |
possibly damaging |
Het |
Scaf11 |
T |
A |
15: 96,318,209 (GRCm39) |
N452Y |
possibly damaging |
Het |
Scgb2b3 |
T |
A |
7: 31,059,639 (GRCm39) |
H45L |
possibly damaging |
Het |
Sim1 |
A |
G |
10: 50,772,023 (GRCm39) |
T11A |
probably damaging |
Het |
Slc5a12 |
T |
A |
2: 110,447,059 (GRCm39) |
M189K |
possibly damaging |
Het |
Slco2b1 |
C |
T |
7: 99,344,270 (GRCm39) |
G10S |
probably null |
Het |
Speer1j |
C |
T |
5: 11,555,198 (GRCm39) |
P83S |
probably damaging |
Het |
Stxbp3 |
A |
G |
3: 108,708,071 (GRCm39) |
L410P |
probably damaging |
Het |
Sugct |
T |
C |
13: 17,476,594 (GRCm39) |
N297D |
probably benign |
Het |
Syne1 |
A |
G |
10: 5,183,409 (GRCm39) |
I4132T |
probably benign |
Het |
Teddm1b |
A |
T |
1: 153,750,912 (GRCm39) |
L240F |
probably damaging |
Het |
Tlr5 |
C |
A |
1: 182,803,088 (GRCm39) |
D797E |
possibly damaging |
Het |
Tmprss13 |
G |
T |
9: 45,249,643 (GRCm39) |
G327C |
probably damaging |
Het |
Tnrc18 |
G |
T |
5: 142,773,572 (GRCm39) |
A419D |
|
Het |
Ttc28 |
T |
C |
5: 111,427,873 (GRCm39) |
Y1790H |
probably damaging |
Het |
Vmn1r125 |
T |
G |
7: 21,006,327 (GRCm39) |
M75R |
probably damaging |
Het |
Vwa3a |
T |
A |
7: 120,372,253 (GRCm39) |
D276E |
possibly damaging |
Het |
Wdfy3 |
C |
T |
5: 102,063,303 (GRCm39) |
V1322M |
probably damaging |
Het |
Wdr11 |
T |
C |
7: 129,229,830 (GRCm39) |
S872P |
possibly damaging |
Het |
Zc3h13 |
T |
C |
14: 75,559,161 (GRCm39) |
S357P |
unknown |
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 |
22,650,758 (GRCm39) |
nonsense |
probably null |
|
R7231:Asxl3
|
UTSW |
18 |
22,650,597 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|