Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ablim1 |
A |
T |
19: 57,204,153 (GRCm39) |
D79E |
probably benign |
Het |
Adgra2 |
A |
G |
8: 27,604,225 (GRCm39) |
K472E |
probably damaging |
Het |
Akap9 |
A |
G |
5: 4,018,737 (GRCm39) |
D1106G |
probably benign |
Het |
Arhgap35 |
T |
C |
7: 16,232,551 (GRCm39) |
E1367G |
possibly damaging |
Het |
Arsi |
A |
T |
18: 61,050,533 (GRCm39) |
Y472F |
probably benign |
Het |
Atp6v1e2 |
C |
T |
17: 87,252,135 (GRCm39) |
D88N |
probably benign |
Het |
BC061237 |
T |
A |
14: 44,743,469 (GRCm39) |
V169E |
probably damaging |
Het |
C1galt1 |
A |
G |
6: 7,866,379 (GRCm39) |
E75G |
probably benign |
Het |
C9 |
G |
A |
15: 6,519,311 (GRCm39) |
V383I |
probably benign |
Het |
Ccdc88a |
A |
G |
11: 29,432,720 (GRCm39) |
K222R |
probably benign |
Het |
Ccna2 |
T |
C |
3: 36,620,391 (GRCm39) |
S421G |
probably benign |
Het |
Cflar |
T |
G |
1: 58,779,431 (GRCm39) |
V229G |
possibly damaging |
Het |
Clcn1 |
A |
G |
6: 42,267,131 (GRCm39) |
|
probably null |
Het |
Col14a1 |
T |
A |
15: 55,315,732 (GRCm39) |
F1342L |
unknown |
Het |
Colq |
C |
T |
14: 31,251,472 (GRCm39) |
R313H |
possibly damaging |
Het |
Coro6 |
A |
G |
11: 77,359,974 (GRCm39) |
E345G |
probably damaging |
Het |
Cracd |
T |
C |
5: 77,006,681 (GRCm39) |
V1014A |
unknown |
Het |
Cyb561 |
A |
G |
11: 105,826,708 (GRCm39) |
F182L |
probably benign |
Het |
Dap3 |
A |
G |
3: 88,833,617 (GRCm39) |
S317P |
probably benign |
Het |
Dnah9 |
G |
A |
11: 65,724,941 (GRCm39) |
A4404V |
probably damaging |
Het |
Dsg4 |
A |
G |
18: 20,579,888 (GRCm39) |
E31G |
possibly damaging |
Het |
Dsn1 |
G |
A |
2: 156,843,660 (GRCm39) |
L147F |
probably damaging |
Het |
Dysf |
T |
C |
6: 84,043,990 (GRCm39) |
V277A |
probably damaging |
Het |
Eprs1 |
T |
A |
1: 185,128,327 (GRCm39) |
I569K |
probably damaging |
Het |
Erg |
T |
C |
16: 95,162,029 (GRCm39) |
N342S |
probably damaging |
Het |
Fam114a1 |
G |
A |
5: 65,166,409 (GRCm39) |
D247N |
probably damaging |
Het |
Fat2 |
A |
G |
11: 55,202,294 (GRCm39) |
V260A |
probably benign |
Het |
Foxn4 |
T |
C |
5: 114,393,628 (GRCm39) |
D497G |
probably damaging |
Het |
Fsip2 |
A |
G |
2: 82,819,629 (GRCm39) |
I5121V |
probably benign |
Het |
Gcn1 |
T |
A |
5: 115,752,461 (GRCm39) |
D2155E |
probably benign |
Het |
Glra1 |
C |
A |
11: 55,427,210 (GRCm39) |
D42Y |
probably damaging |
Het |
Gpr171 |
A |
G |
3: 59,004,887 (GRCm39) |
V296A |
probably benign |
Het |
Grid1 |
T |
A |
14: 35,302,644 (GRCm39) |
S970T |
possibly damaging |
Het |
Hcn3 |
A |
T |
3: 89,057,370 (GRCm39) |
|
probably null |
Het |
Helb |
T |
C |
10: 119,920,754 (GRCm39) |
D1063G |
probably benign |
Het |
Hsd3b3 |
G |
A |
3: 98,649,931 (GRCm39) |
P131S |
probably damaging |
Het |
Hsp90b1 |
A |
G |
10: 86,537,672 (GRCm39) |
V211A |
probably damaging |
Het |
Htr2c |
A |
G |
X: 145,976,793 (GRCm39) |
T163A |
probably benign |
Het |
Ifi208 |
T |
A |
1: 173,523,180 (GRCm39) |
D483E |
possibly damaging |
Het |
Kbtbd6 |
T |
A |
14: 79,690,727 (GRCm39) |
V474E |
possibly damaging |
Het |
Kif21b |
T |
A |
1: 136,072,487 (GRCm39) |
Y64* |
probably null |
Het |
Kirrel1 |
C |
T |
3: 86,996,458 (GRCm39) |
M380I |
probably null |
Het |
Map3k10 |
T |
C |
7: 27,357,786 (GRCm39) |
D664G |
possibly damaging |
Het |
Map3k5 |
C |
A |
10: 20,007,798 (GRCm39) |
S1201Y |
probably benign |
Het |
Mcm2 |
T |
C |
6: 88,868,973 (GRCm39) |
E293G |
possibly damaging |
Het |
Med21 |
T |
A |
6: 146,551,599 (GRCm39) |
|
probably null |
Het |
Mettl18 |
T |
C |
1: 163,824,354 (GRCm39) |
V225A |
probably benign |
Het |
Mmp10 |
A |
T |
9: 7,508,169 (GRCm39) |
I432F |
probably damaging |
Het |
Muc5b |
T |
G |
7: 141,415,185 (GRCm39) |
Y2710* |
probably null |
Het |
Neurl4 |
A |
T |
11: 69,801,894 (GRCm39) |
I1282F |
probably benign |
Het |
Nipbl |
A |
T |
15: 8,395,313 (GRCm39) |
H191Q |
possibly damaging |
Het |
Nktr |
A |
G |
9: 121,570,759 (GRCm39) |
D167G |
probably damaging |
Het |
Nrap |
A |
G |
19: 56,368,669 (GRCm39) |
I249T |
probably damaging |
Het |
Nsfl1c |
A |
G |
2: 151,351,526 (GRCm39) |
T297A |
probably benign |
Het |
Oit3 |
A |
T |
10: 59,259,904 (GRCm39) |
C500S |
probably damaging |
Het |
Or1e1 |
G |
A |
11: 73,245,322 (GRCm39) |
V248M |
probably damaging |
Het |
Or4a39 |
C |
T |
2: 89,236,599 (GRCm39) |
V275I |
probably benign |
Het |
Or4k6 |
A |
G |
14: 50,476,190 (GRCm39) |
S51P |
probably damaging |
Het |
Or5b24 |
C |
T |
19: 12,912,581 (GRCm39) |
H160Y |
probably benign |
Het |
Or5d36 |
T |
A |
2: 87,900,956 (GRCm39) |
I257L |
probably benign |
Het |
Pcnx2 |
T |
C |
8: 126,614,327 (GRCm39) |
S375G |
probably damaging |
Het |
Pgap6 |
T |
C |
17: 26,335,757 (GRCm39) |
F48S |
probably damaging |
Het |
Phf2 |
A |
T |
13: 48,975,185 (GRCm39) |
|
probably null |
Het |
Piezo1 |
A |
T |
8: 123,213,678 (GRCm39) |
M1739K |
possibly damaging |
Het |
Piezo1 |
G |
T |
8: 123,224,945 (GRCm39) |
Q654K |
probably damaging |
Het |
Pml |
C |
T |
9: 58,141,935 (GRCm39) |
R299H |
probably damaging |
Het |
Ppp3cb |
A |
T |
14: 20,574,130 (GRCm39) |
M236K |
probably damaging |
Het |
Prkch |
T |
A |
12: 73,739,734 (GRCm39) |
C203S |
probably damaging |
Het |
Prob1 |
C |
T |
18: 35,785,869 (GRCm39) |
R795H |
possibly damaging |
Het |
Prr22 |
G |
C |
17: 57,078,274 (GRCm39) |
E142D |
possibly damaging |
Het |
Prss56 |
C |
A |
1: 87,113,305 (GRCm39) |
A211E |
possibly damaging |
Het |
Qser1 |
A |
C |
2: 104,617,649 (GRCm39) |
S1054R |
probably benign |
Het |
Rhbdl2 |
T |
C |
4: 123,720,694 (GRCm39) |
|
probably null |
Het |
Rhot2 |
C |
A |
17: 26,063,248 (GRCm39) |
G19V |
probably damaging |
Het |
Rp1l1 |
C |
T |
14: 64,267,249 (GRCm39) |
T945M |
probably damaging |
Het |
Ryr3 |
T |
C |
2: 112,794,750 (GRCm39) |
T121A |
possibly damaging |
Het |
Sdad1 |
C |
T |
5: 92,452,836 (GRCm39) |
R134Q |
possibly damaging |
Het |
Secisbp2l |
C |
T |
2: 125,582,657 (GRCm39) |
G933D |
possibly damaging |
Het |
Sharpin |
T |
A |
15: 76,231,767 (GRCm39) |
D314V |
probably damaging |
Het |
Slc14a2 |
A |
T |
18: 78,198,796 (GRCm39) |
L778Q |
probably damaging |
Het |
Slc29a3 |
A |
G |
10: 60,552,105 (GRCm39) |
V313A |
probably benign |
Het |
Slc4a11 |
C |
A |
2: 130,532,787 (GRCm39) |
R222L |
probably damaging |
Het |
Slc7a10 |
C |
T |
7: 34,900,187 (GRCm39) |
P502S |
probably damaging |
Het |
Sort1 |
T |
G |
3: 108,263,639 (GRCm39) |
Y812* |
probably null |
Het |
Spata31d1b |
G |
A |
13: 59,866,172 (GRCm39) |
V1107M |
probably damaging |
Het |
Tcp10b |
G |
A |
17: 13,289,832 (GRCm39) |
|
probably null |
Het |
Tnc |
T |
C |
4: 63,913,876 (GRCm39) |
D1312G |
possibly damaging |
Het |
Tomm40l |
G |
A |
1: 171,047,131 (GRCm39) |
R296* |
probably null |
Het |
Topors |
A |
T |
4: 40,261,015 (GRCm39) |
S756R |
unknown |
Het |
Trim9 |
T |
C |
12: 70,295,047 (GRCm39) |
N688D |
probably damaging |
Het |
Ube2o |
T |
C |
11: 116,432,734 (GRCm39) |
D744G |
probably benign |
Het |
Vmn1r224 |
A |
G |
17: 20,640,013 (GRCm39) |
I197V |
probably benign |
Het |
Zc3h18 |
A |
T |
8: 123,110,382 (GRCm39) |
D77V |
probably damaging |
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 |
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 |
|