Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
T |
A |
3: 137,773,986 (GRCm39) |
D1058E |
probably damaging |
Het |
4933405L10Rik |
A |
T |
8: 106,435,563 (GRCm39) |
|
probably null |
Het |
Adamtsl3 |
T |
A |
7: 82,114,907 (GRCm39) |
|
probably benign |
Het |
Afdn |
C |
T |
17: 14,072,698 (GRCm39) |
P874S |
probably damaging |
Het |
Ankrd6 |
G |
A |
4: 32,815,326 (GRCm39) |
A391V |
probably damaging |
Het |
Arhgef28 |
T |
G |
13: 98,067,762 (GRCm39) |
T1388P |
probably damaging |
Het |
BC005537 |
T |
C |
13: 24,989,923 (GRCm39) |
F129L |
probably damaging |
Het |
Celf2 |
A |
G |
2: 6,726,226 (GRCm39) |
|
probably null |
Het |
Chid1 |
C |
T |
7: 141,076,590 (GRCm39) |
V325I |
probably benign |
Het |
Cnn3 |
T |
A |
3: 121,243,633 (GRCm39) |
D31E |
probably benign |
Het |
Col12a1 |
G |
A |
9: 79,559,317 (GRCm39) |
P1857L |
probably damaging |
Het |
Cpeb1 |
T |
A |
7: 81,001,618 (GRCm39) |
R430W |
probably benign |
Het |
Daw1 |
T |
C |
1: 83,169,059 (GRCm39) |
|
probably benign |
Het |
Dcaf13 |
A |
G |
15: 39,001,484 (GRCm39) |
Y264C |
probably damaging |
Het |
Dnah6 |
T |
C |
6: 73,064,585 (GRCm39) |
I2666V |
probably damaging |
Het |
Dnai2 |
A |
C |
11: 114,645,158 (GRCm39) |
D531A |
probably benign |
Het |
Dock10 |
A |
T |
1: 80,501,692 (GRCm39) |
F1833I |
probably damaging |
Het |
Efhd2 |
C |
T |
4: 141,587,183 (GRCm39) |
A200T |
probably damaging |
Het |
Epb41l5 |
T |
A |
1: 119,551,641 (GRCm39) |
|
probably benign |
Het |
Ermp1 |
A |
G |
19: 29,608,788 (GRCm39) |
Y164H |
possibly damaging |
Het |
Gkn2 |
T |
C |
6: 87,350,401 (GRCm39) |
|
probably benign |
Het |
Golgb1 |
A |
T |
16: 36,739,152 (GRCm39) |
Q2497L |
probably damaging |
Het |
Gzme |
A |
T |
14: 56,355,196 (GRCm39) |
M245K |
probably damaging |
Het |
Iars2 |
A |
T |
1: 185,054,585 (GRCm39) |
|
probably benign |
Het |
Icosl |
T |
A |
10: 77,909,775 (GRCm39) |
V240D |
probably damaging |
Het |
Igsf3 |
T |
C |
3: 101,334,709 (GRCm39) |
M262T |
probably benign |
Het |
Ing3 |
G |
T |
6: 21,971,236 (GRCm39) |
E336* |
probably null |
Het |
Kat2a |
A |
T |
11: 100,597,297 (GRCm39) |
V625E |
probably damaging |
Het |
Ksr1 |
A |
G |
11: 78,929,073 (GRCm39) |
|
probably benign |
Het |
Lypd8 |
A |
T |
11: 58,277,583 (GRCm39) |
M122L |
probably benign |
Het |
Mdfi |
A |
T |
17: 48,143,855 (GRCm39) |
|
probably benign |
Het |
Med13 |
A |
G |
11: 86,192,179 (GRCm39) |
|
probably benign |
Het |
Msh6 |
C |
T |
17: 88,294,112 (GRCm39) |
R956C |
probably damaging |
Het |
Myo15b |
A |
G |
11: 115,774,664 (GRCm39) |
E670G |
probably damaging |
Het |
Myo1d |
A |
G |
11: 80,375,158 (GRCm39) |
L972P |
probably damaging |
Het |
Or4s2b |
A |
G |
2: 88,509,018 (GRCm39) |
D266G |
probably damaging |
Het |
Or51ai2 |
G |
A |
7: 103,587,024 (GRCm39) |
A146T |
probably benign |
Het |
Or7g12 |
T |
A |
9: 18,899,447 (GRCm39) |
N54K |
probably benign |
Het |
Pde8b |
C |
G |
13: 95,244,325 (GRCm39) |
S143T |
possibly damaging |
Het |
Pias4 |
G |
T |
10: 80,993,364 (GRCm39) |
|
probably benign |
Het |
Prkca |
A |
G |
11: 107,872,480 (GRCm39) |
Y427H |
probably benign |
Het |
Psg25 |
G |
A |
7: 18,263,485 (GRCm39) |
Q113* |
probably null |
Het |
Rab3gap2 |
T |
A |
1: 184,982,123 (GRCm39) |
S392T |
probably damaging |
Het |
Scrib |
A |
G |
15: 75,938,756 (GRCm39) |
|
probably benign |
Het |
Sdk2 |
A |
G |
11: 113,793,970 (GRCm39) |
|
probably benign |
Het |
Serpinb1c |
T |
A |
13: 33,070,266 (GRCm39) |
|
probably benign |
Het |
Serpinb9f |
T |
A |
13: 33,511,904 (GRCm39) |
W136R |
probably damaging |
Het |
Skic3 |
C |
T |
13: 76,331,010 (GRCm39) |
P1480L |
probably damaging |
Het |
Skint10 |
C |
A |
4: 112,573,102 (GRCm39) |
|
probably benign |
Het |
Slc25a13 |
T |
C |
6: 6,117,128 (GRCm39) |
T196A |
probably damaging |
Het |
Slc26a5 |
T |
C |
5: 22,052,230 (GRCm39) |
H33R |
probably damaging |
Het |
Slc27a6 |
T |
C |
18: 58,731,829 (GRCm39) |
|
probably benign |
Het |
Slitrk6 |
A |
T |
14: 110,987,251 (GRCm39) |
Y819N |
probably damaging |
Het |
Spata46 |
C |
T |
1: 170,139,603 (GRCm39) |
Q201* |
probably null |
Het |
Sptbn1 |
A |
T |
11: 30,064,739 (GRCm39) |
V1920E |
probably damaging |
Het |
Taf6l |
A |
G |
19: 8,755,881 (GRCm39) |
F256L |
probably benign |
Het |
Tmco3 |
T |
A |
8: 13,342,039 (GRCm39) |
N104K |
probably damaging |
Het |
Tmem200c |
A |
G |
17: 69,149,249 (GRCm39) |
T611A |
probably damaging |
Het |
Tmem202 |
T |
G |
9: 59,432,655 (GRCm39) |
Y24S |
probably damaging |
Het |
Tpp1 |
A |
G |
7: 105,398,626 (GRCm39) |
L230P |
probably damaging |
Het |
Trim56 |
C |
T |
5: 137,141,846 (GRCm39) |
E557K |
probably benign |
Het |
Trrap |
C |
T |
5: 144,790,309 (GRCm39) |
L3590F |
probably damaging |
Het |
Tulp4 |
A |
G |
17: 6,189,387 (GRCm39) |
T70A |
possibly damaging |
Het |
Vcp |
G |
C |
4: 42,986,201 (GRCm39) |
A297G |
probably benign |
Het |
Vwf |
T |
A |
6: 125,603,234 (GRCm39) |
H861Q |
probably benign |
Het |
Wdr64 |
T |
C |
1: 175,599,751 (GRCm39) |
I536T |
probably benign |
Het |
Zfp850 |
T |
C |
7: 27,689,698 (GRCm39) |
N170S |
probably benign |
Het |
Zfp87 |
G |
A |
13: 74,524,544 (GRCm39) |
|
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 |
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 |
22,650,597 (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 |
|