Other mutations in this stock |
Total: 87 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700020L24Rik |
T |
C |
11: 83,331,190 (GRCm39) |
S31P |
possibly damaging |
Het |
4933430I17Rik |
T |
A |
4: 62,457,109 (GRCm39) |
L143M |
possibly damaging |
Het |
Abca13 |
T |
C |
11: 9,259,013 (GRCm39) |
|
probably benign |
Het |
Abcg5 |
T |
A |
17: 84,978,575 (GRCm39) |
E294D |
probably benign |
Het |
Abi3bp |
T |
C |
16: 56,298,227 (GRCm39) |
|
probably benign |
Het |
Adamts8 |
T |
C |
9: 30,854,359 (GRCm39) |
F76S |
probably damaging |
Het |
Agpat3 |
T |
C |
10: 78,113,918 (GRCm39) |
R257G |
probably damaging |
Het |
Ahctf1 |
C |
A |
1: 179,597,017 (GRCm39) |
R43L |
probably damaging |
Het |
AI593442 |
T |
C |
9: 52,588,993 (GRCm39) |
T195A |
probably benign |
Het |
Aipl1 |
A |
T |
11: 71,920,195 (GRCm39) |
L291Q |
possibly damaging |
Het |
Ambn |
T |
A |
5: 88,608,617 (GRCm39) |
|
probably benign |
Het |
Arap2 |
G |
A |
5: 62,864,028 (GRCm39) |
T532I |
probably damaging |
Het |
Arg1 |
T |
C |
10: 24,796,621 (GRCm39) |
N69D |
possibly damaging |
Het |
Arhgef10 |
A |
G |
8: 14,984,820 (GRCm39) |
D200G |
probably damaging |
Het |
Arhgef38 |
T |
C |
3: 132,866,514 (GRCm39) |
K208E |
probably benign |
Het |
Asb4 |
A |
T |
6: 5,390,687 (GRCm39) |
T27S |
probably benign |
Het |
Car12 |
T |
C |
9: 66,621,174 (GRCm39) |
V15A |
probably benign |
Het |
Cdc20b |
A |
G |
13: 113,215,232 (GRCm39) |
I267V |
probably benign |
Het |
Cdh1 |
A |
G |
8: 107,390,842 (GRCm39) |
I653V |
probably benign |
Het |
Cenpe |
T |
A |
3: 134,952,645 (GRCm39) |
M1445K |
possibly damaging |
Het |
Cfap43 |
T |
C |
19: 47,758,877 (GRCm39) |
E932G |
probably damaging |
Het |
Cfhr1 |
G |
C |
1: 139,478,642 (GRCm39) |
Q243E |
probably benign |
Het |
Cnih2 |
C |
A |
19: 5,148,276 (GRCm39) |
A6S |
possibly damaging |
Het |
Cntnap1 |
G |
T |
11: 101,079,483 (GRCm39) |
M1240I |
probably benign |
Het |
Cntrl |
T |
C |
2: 35,051,977 (GRCm39) |
S1050P |
probably benign |
Het |
Cyp2a12 |
A |
G |
7: 26,736,071 (GRCm39) |
*493W |
probably null |
Het |
Dbx2 |
A |
C |
15: 95,522,681 (GRCm39) |
L342R |
probably damaging |
Het |
Dmd |
G |
C |
X: 83,356,089 (GRCm39) |
A2257P |
probably benign |
Het |
Dnajb2 |
T |
C |
1: 75,214,121 (GRCm39) |
W30R |
probably damaging |
Het |
Ecel1 |
A |
G |
1: 87,075,997 (GRCm39) |
S727P |
probably damaging |
Het |
Ednrb |
T |
A |
14: 104,059,204 (GRCm39) |
D274V |
probably benign |
Het |
Fam78b |
G |
A |
1: 166,906,278 (GRCm39) |
V146M |
probably damaging |
Het |
Fancd2 |
A |
G |
6: 113,537,035 (GRCm39) |
|
probably benign |
Het |
Fbxw14 |
T |
C |
9: 109,103,692 (GRCm39) |
|
probably benign |
Het |
Gimap4 |
G |
T |
6: 48,667,905 (GRCm39) |
C92F |
probably benign |
Het |
Gm10033 |
A |
C |
8: 69,824,942 (GRCm39) |
|
noncoding transcript |
Het |
Gm5828 |
A |
G |
1: 16,840,199 (GRCm39) |
|
noncoding transcript |
Het |
Gnpat |
T |
C |
8: 125,603,680 (GRCm39) |
V186A |
probably damaging |
Het |
Gnptab |
T |
C |
10: 88,272,260 (GRCm39) |
S967P |
probably benign |
Het |
Ikbkb |
T |
C |
8: 23,157,233 (GRCm39) |
|
probably benign |
Het |
Il1rap |
A |
T |
16: 26,529,315 (GRCm39) |
H379L |
probably damaging |
Het |
Ints12 |
T |
C |
3: 132,814,921 (GRCm39) |
V376A |
probably damaging |
Het |
Kalrn |
C |
T |
16: 34,152,600 (GRCm39) |
S309N |
possibly damaging |
Het |
Kel |
T |
A |
6: 41,666,234 (GRCm39) |
I471L |
probably benign |
Het |
Klhl25 |
T |
C |
7: 75,516,480 (GRCm39) |
V462A |
probably damaging |
Het |
Ksr1 |
A |
T |
11: 78,936,019 (GRCm39) |
M77K |
probably benign |
Het |
Leo1 |
T |
A |
9: 75,353,094 (GRCm39) |
N212K |
probably damaging |
Het |
Ltbp1 |
T |
A |
17: 75,617,154 (GRCm39) |
V1031E |
possibly damaging |
Het |
Ltbr |
A |
G |
6: 125,286,440 (GRCm39) |
S249P |
probably benign |
Het |
Mast4 |
A |
G |
13: 102,890,713 (GRCm39) |
V855A |
probably damaging |
Het |
Mdga2 |
T |
A |
12: 66,915,526 (GRCm39) |
E43V |
probably damaging |
Het |
Mmaa |
A |
T |
8: 79,994,588 (GRCm39) |
L406* |
probably null |
Het |
Mtcl2 |
T |
C |
2: 156,875,245 (GRCm39) |
E835G |
probably damaging |
Het |
Nlrp12 |
A |
T |
7: 3,290,079 (GRCm39) |
N144K |
probably damaging |
Het |
Nlrp6 |
T |
C |
7: 140,506,357 (GRCm39) |
V766A |
probably benign |
Het |
Or4f61 |
C |
A |
2: 111,922,675 (GRCm39) |
V124L |
probably benign |
Het |
Or5h18 |
A |
G |
16: 58,848,178 (GRCm39) |
F31L |
possibly damaging |
Het |
Pabpc4l |
T |
C |
3: 46,401,276 (GRCm39) |
T123A |
probably benign |
Het |
Pappa2 |
T |
C |
1: 158,684,836 (GRCm39) |
T768A |
probably damaging |
Het |
Pde6d |
A |
G |
1: 86,473,524 (GRCm39) |
F91L |
probably benign |
Het |
Ppp1r13l |
A |
G |
7: 19,105,346 (GRCm39) |
M373V |
possibly damaging |
Het |
Prss37 |
G |
A |
6: 40,492,294 (GRCm39) |
R186* |
probably null |
Het |
Psg16 |
C |
A |
7: 16,824,548 (GRCm39) |
H111N |
probably benign |
Het |
Psg20 |
T |
A |
7: 18,414,947 (GRCm39) |
Y316F |
probably benign |
Het |
Psmd1 |
T |
A |
1: 86,006,422 (GRCm39) |
S263T |
possibly damaging |
Het |
Rai14 |
A |
G |
15: 10,575,252 (GRCm39) |
F569L |
probably benign |
Het |
Rbpms2 |
T |
A |
9: 65,558,229 (GRCm39) |
D116E |
probably damaging |
Het |
Rgs20 |
A |
G |
1: 4,987,113 (GRCm39) |
|
probably benign |
Het |
Rnf114 |
T |
C |
2: 167,352,803 (GRCm39) |
L101P |
probably damaging |
Het |
Rnf168 |
T |
G |
16: 32,097,036 (GRCm39) |
L37R |
probably damaging |
Het |
Rpe |
T |
C |
1: 66,754,387 (GRCm39) |
M153T |
probably damaging |
Het |
Sap18 |
T |
A |
14: 58,036,011 (GRCm39) |
S66T |
probably damaging |
Het |
Slc2a13 |
A |
G |
15: 91,400,679 (GRCm39) |
V181A |
probably damaging |
Het |
Spag17 |
A |
G |
3: 99,956,556 (GRCm39) |
E884G |
possibly damaging |
Het |
Sycn |
T |
C |
7: 28,240,713 (GRCm39) |
S127P |
probably damaging |
Het |
Tas2r106 |
A |
T |
6: 131,655,317 (GRCm39) |
L178H |
probably damaging |
Het |
Tas2r117 |
T |
A |
6: 132,780,129 (GRCm39) |
I89K |
probably damaging |
Het |
Tep1 |
C |
A |
14: 51,093,029 (GRCm39) |
|
probably null |
Het |
Tex14 |
T |
C |
11: 87,410,569 (GRCm39) |
|
probably benign |
Het |
Tll1 |
T |
C |
8: 64,538,591 (GRCm39) |
E351G |
probably benign |
Het |
Tmem44 |
T |
A |
16: 30,366,262 (GRCm39) |
K55* |
probably null |
Het |
Trak1 |
T |
A |
9: 121,302,063 (GRCm39) |
*940R |
probably null |
Het |
Vmn1r200 |
C |
T |
13: 22,579,353 (GRCm39) |
T43I |
probably damaging |
Het |
Wars2 |
T |
C |
3: 99,123,883 (GRCm39) |
V248A |
probably benign |
Het |
Wfdc6b |
C |
T |
2: 164,459,363 (GRCm39) |
R142C |
probably benign |
Het |
Zfp729a |
A |
T |
13: 67,769,613 (GRCm39) |
|
probably null |
Het |
Zfp759 |
C |
A |
13: 67,287,578 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Ash1l |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00094:Ash1l
|
APN |
3 |
88,889,019 (GRCm39) |
missense |
probably benign |
0.19 |
IGL00819:Ash1l
|
APN |
3 |
88,915,043 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL00939:Ash1l
|
APN |
3 |
88,942,543 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01064:Ash1l
|
APN |
3 |
88,979,791 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01066:Ash1l
|
APN |
3 |
88,891,942 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01087:Ash1l
|
APN |
3 |
88,971,209 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01293:Ash1l
|
APN |
3 |
88,890,836 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01541:Ash1l
|
APN |
3 |
88,973,572 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01863:Ash1l
|
APN |
3 |
88,892,813 (GRCm39) |
nonsense |
probably null |
|
IGL02326:Ash1l
|
APN |
3 |
88,873,364 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02407:Ash1l
|
APN |
3 |
88,979,855 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02419:Ash1l
|
APN |
3 |
88,892,872 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02422:Ash1l
|
APN |
3 |
88,976,386 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02494:Ash1l
|
APN |
3 |
88,973,525 (GRCm39) |
nonsense |
probably null |
|
IGL02727:Ash1l
|
APN |
3 |
88,930,344 (GRCm39) |
missense |
probably benign |
|
IGL02732:Ash1l
|
APN |
3 |
88,873,535 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02817:Ash1l
|
APN |
3 |
88,892,108 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02887:Ash1l
|
APN |
3 |
88,891,488 (GRCm39) |
missense |
probably benign |
0.11 |
IGL03224:Ash1l
|
APN |
3 |
88,942,575 (GRCm39) |
splice site |
probably benign |
|
IGL03253:Ash1l
|
APN |
3 |
88,891,981 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03327:Ash1l
|
APN |
3 |
88,930,390 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03398:Ash1l
|
APN |
3 |
88,914,527 (GRCm39) |
missense |
probably benign |
0.01 |
3-1:Ash1l
|
UTSW |
3 |
88,873,633 (GRCm39) |
missense |
probably benign |
|
BB008:Ash1l
|
UTSW |
3 |
88,950,848 (GRCm39) |
missense |
probably damaging |
1.00 |
BB018:Ash1l
|
UTSW |
3 |
88,950,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R0068:Ash1l
|
UTSW |
3 |
88,914,624 (GRCm39) |
missense |
probably benign |
0.17 |
R0068:Ash1l
|
UTSW |
3 |
88,914,624 (GRCm39) |
missense |
probably benign |
0.17 |
R0239:Ash1l
|
UTSW |
3 |
88,974,529 (GRCm39) |
missense |
possibly damaging |
0.49 |
R0239:Ash1l
|
UTSW |
3 |
88,974,529 (GRCm39) |
missense |
possibly damaging |
0.49 |
R0395:Ash1l
|
UTSW |
3 |
88,965,896 (GRCm39) |
missense |
probably damaging |
1.00 |
R0477:Ash1l
|
UTSW |
3 |
88,890,766 (GRCm39) |
missense |
probably benign |
0.41 |
R0528:Ash1l
|
UTSW |
3 |
88,889,584 (GRCm39) |
missense |
probably benign |
|
R0543:Ash1l
|
UTSW |
3 |
88,971,085 (GRCm39) |
splice site |
probably null |
|
R0855:Ash1l
|
UTSW |
3 |
88,961,761 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1147:Ash1l
|
UTSW |
3 |
88,892,194 (GRCm39) |
missense |
possibly damaging |
0.72 |
R1147:Ash1l
|
UTSW |
3 |
88,892,194 (GRCm39) |
missense |
possibly damaging |
0.72 |
R1163:Ash1l
|
UTSW |
3 |
88,942,570 (GRCm39) |
critical splice donor site |
probably null |
|
R1196:Ash1l
|
UTSW |
3 |
88,890,623 (GRCm39) |
missense |
probably damaging |
0.99 |
R1419:Ash1l
|
UTSW |
3 |
88,892,204 (GRCm39) |
missense |
probably damaging |
0.99 |
R1445:Ash1l
|
UTSW |
3 |
88,914,659 (GRCm39) |
missense |
probably benign |
0.02 |
R1466:Ash1l
|
UTSW |
3 |
88,959,372 (GRCm39) |
missense |
probably damaging |
1.00 |
R1466:Ash1l
|
UTSW |
3 |
88,959,372 (GRCm39) |
missense |
probably damaging |
1.00 |
R1480:Ash1l
|
UTSW |
3 |
88,892,359 (GRCm39) |
missense |
probably damaging |
1.00 |
R1506:Ash1l
|
UTSW |
3 |
88,965,806 (GRCm39) |
missense |
probably damaging |
0.99 |
R1537:Ash1l
|
UTSW |
3 |
88,979,783 (GRCm39) |
missense |
probably damaging |
0.99 |
R1584:Ash1l
|
UTSW |
3 |
88,959,372 (GRCm39) |
missense |
probably damaging |
1.00 |
R1669:Ash1l
|
UTSW |
3 |
88,974,549 (GRCm39) |
critical splice donor site |
probably null |
|
R1713:Ash1l
|
UTSW |
3 |
88,983,531 (GRCm39) |
missense |
probably damaging |
1.00 |
R1780:Ash1l
|
UTSW |
3 |
88,873,291 (GRCm39) |
missense |
probably benign |
|
R1793:Ash1l
|
UTSW |
3 |
88,977,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R1881:Ash1l
|
UTSW |
3 |
88,888,862 (GRCm39) |
missense |
probably benign |
0.00 |
R1909:Ash1l
|
UTSW |
3 |
88,891,835 (GRCm39) |
missense |
probably benign |
0.29 |
R1938:Ash1l
|
UTSW |
3 |
88,891,729 (GRCm39) |
missense |
probably damaging |
0.98 |
R2035:Ash1l
|
UTSW |
3 |
88,973,624 (GRCm39) |
missense |
probably benign |
0.00 |
R2070:Ash1l
|
UTSW |
3 |
88,873,510 (GRCm39) |
missense |
probably damaging |
1.00 |
R2071:Ash1l
|
UTSW |
3 |
88,873,510 (GRCm39) |
missense |
probably damaging |
1.00 |
R2114:Ash1l
|
UTSW |
3 |
88,890,571 (GRCm39) |
missense |
probably benign |
0.00 |
R2116:Ash1l
|
UTSW |
3 |
88,890,571 (GRCm39) |
missense |
probably benign |
0.00 |
R2143:Ash1l
|
UTSW |
3 |
88,892,726 (GRCm39) |
missense |
probably benign |
0.09 |
R2164:Ash1l
|
UTSW |
3 |
88,892,726 (GRCm39) |
missense |
probably benign |
0.09 |
R2210:Ash1l
|
UTSW |
3 |
88,973,605 (GRCm39) |
missense |
probably damaging |
1.00 |
R2247:Ash1l
|
UTSW |
3 |
88,914,674 (GRCm39) |
missense |
possibly damaging |
0.77 |
R2303:Ash1l
|
UTSW |
3 |
88,933,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R2860:Ash1l
|
UTSW |
3 |
88,961,785 (GRCm39) |
missense |
probably damaging |
1.00 |
R2861:Ash1l
|
UTSW |
3 |
88,961,785 (GRCm39) |
missense |
probably damaging |
1.00 |
R3104:Ash1l
|
UTSW |
3 |
88,961,693 (GRCm39) |
missense |
probably damaging |
1.00 |
R4133:Ash1l
|
UTSW |
3 |
88,889,567 (GRCm39) |
missense |
probably benign |
0.00 |
R4164:Ash1l
|
UTSW |
3 |
88,889,273 (GRCm39) |
missense |
probably damaging |
0.97 |
R4270:Ash1l
|
UTSW |
3 |
88,889,347 (GRCm39) |
missense |
probably benign |
0.26 |
R4271:Ash1l
|
UTSW |
3 |
88,889,347 (GRCm39) |
missense |
probably benign |
0.26 |
R4287:Ash1l
|
UTSW |
3 |
88,973,722 (GRCm39) |
missense |
probably damaging |
0.99 |
R4409:Ash1l
|
UTSW |
3 |
88,914,506 (GRCm39) |
missense |
probably damaging |
0.99 |
R4459:Ash1l
|
UTSW |
3 |
88,873,541 (GRCm39) |
missense |
probably damaging |
0.99 |
R4487:Ash1l
|
UTSW |
3 |
88,892,622 (GRCm39) |
missense |
possibly damaging |
0.65 |
R4674:Ash1l
|
UTSW |
3 |
88,979,783 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4739:Ash1l
|
UTSW |
3 |
88,890,152 (GRCm39) |
missense |
probably benign |
0.19 |
R4927:Ash1l
|
UTSW |
3 |
88,892,641 (GRCm39) |
missense |
probably damaging |
1.00 |
R5000:Ash1l
|
UTSW |
3 |
88,965,941 (GRCm39) |
missense |
probably damaging |
1.00 |
R5016:Ash1l
|
UTSW |
3 |
88,889,630 (GRCm39) |
missense |
probably damaging |
1.00 |
R5055:Ash1l
|
UTSW |
3 |
88,930,519 (GRCm39) |
critical splice donor site |
probably null |
|
R5081:Ash1l
|
UTSW |
3 |
88,892,024 (GRCm39) |
missense |
probably damaging |
1.00 |
R5082:Ash1l
|
UTSW |
3 |
88,873,541 (GRCm39) |
missense |
probably damaging |
0.99 |
R5090:Ash1l
|
UTSW |
3 |
88,960,184 (GRCm39) |
missense |
probably damaging |
1.00 |
R5113:Ash1l
|
UTSW |
3 |
88,973,582 (GRCm39) |
missense |
probably damaging |
0.99 |
R5408:Ash1l
|
UTSW |
3 |
88,889,701 (GRCm39) |
missense |
probably damaging |
1.00 |
R5452:Ash1l
|
UTSW |
3 |
88,892,183 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5487:Ash1l
|
UTSW |
3 |
88,888,733 (GRCm39) |
missense |
probably benign |
0.17 |
R5610:Ash1l
|
UTSW |
3 |
88,930,492 (GRCm39) |
missense |
probably damaging |
1.00 |
R5624:Ash1l
|
UTSW |
3 |
88,892,916 (GRCm39) |
missense |
probably damaging |
1.00 |
R5682:Ash1l
|
UTSW |
3 |
88,914,914 (GRCm39) |
missense |
probably damaging |
0.99 |
R5712:Ash1l
|
UTSW |
3 |
88,959,297 (GRCm39) |
missense |
probably damaging |
0.99 |
R5719:Ash1l
|
UTSW |
3 |
88,965,933 (GRCm39) |
missense |
probably damaging |
1.00 |
R5719:Ash1l
|
UTSW |
3 |
88,961,805 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5839:Ash1l
|
UTSW |
3 |
88,890,658 (GRCm39) |
missense |
probably damaging |
0.99 |
R5859:Ash1l
|
UTSW |
3 |
88,976,300 (GRCm39) |
missense |
probably damaging |
1.00 |
R5877:Ash1l
|
UTSW |
3 |
88,888,891 (GRCm39) |
missense |
probably benign |
0.00 |
R5940:Ash1l
|
UTSW |
3 |
88,891,343 (GRCm39) |
missense |
probably damaging |
0.96 |
R6026:Ash1l
|
UTSW |
3 |
88,892,326 (GRCm39) |
missense |
probably damaging |
1.00 |
R6027:Ash1l
|
UTSW |
3 |
88,892,326 (GRCm39) |
missense |
probably damaging |
1.00 |
R6029:Ash1l
|
UTSW |
3 |
88,892,326 (GRCm39) |
missense |
probably damaging |
1.00 |
R6033:Ash1l
|
UTSW |
3 |
88,892,326 (GRCm39) |
missense |
probably damaging |
1.00 |
R6033:Ash1l
|
UTSW |
3 |
88,892,326 (GRCm39) |
missense |
probably damaging |
1.00 |
R6034:Ash1l
|
UTSW |
3 |
88,892,326 (GRCm39) |
missense |
probably damaging |
1.00 |
R6034:Ash1l
|
UTSW |
3 |
88,892,326 (GRCm39) |
missense |
probably damaging |
1.00 |
R6035:Ash1l
|
UTSW |
3 |
88,892,326 (GRCm39) |
missense |
probably damaging |
1.00 |
R6035:Ash1l
|
UTSW |
3 |
88,892,326 (GRCm39) |
missense |
probably damaging |
1.00 |
R6089:Ash1l
|
UTSW |
3 |
88,960,450 (GRCm39) |
nonsense |
probably null |
|
R6110:Ash1l
|
UTSW |
3 |
88,892,436 (GRCm39) |
missense |
probably damaging |
1.00 |
R6168:Ash1l
|
UTSW |
3 |
88,960,080 (GRCm39) |
nonsense |
probably null |
|
R6200:Ash1l
|
UTSW |
3 |
88,977,834 (GRCm39) |
missense |
probably damaging |
1.00 |
R6290:Ash1l
|
UTSW |
3 |
88,890,068 (GRCm39) |
nonsense |
probably null |
|
R6331:Ash1l
|
UTSW |
3 |
88,915,172 (GRCm39) |
missense |
probably benign |
0.00 |
R6425:Ash1l
|
UTSW |
3 |
88,891,087 (GRCm39) |
missense |
probably damaging |
0.99 |
R6540:Ash1l
|
UTSW |
3 |
88,892,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R6568:Ash1l
|
UTSW |
3 |
88,959,344 (GRCm39) |
missense |
probably benign |
0.09 |
R6828:Ash1l
|
UTSW |
3 |
88,983,420 (GRCm39) |
missense |
probably benign |
0.00 |
R6843:Ash1l
|
UTSW |
3 |
88,892,695 (GRCm39) |
missense |
probably damaging |
1.00 |
R6894:Ash1l
|
UTSW |
3 |
88,890,298 (GRCm39) |
missense |
probably benign |
0.00 |
R6976:Ash1l
|
UTSW |
3 |
88,888,964 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7038:Ash1l
|
UTSW |
3 |
88,889,978 (GRCm39) |
missense |
probably benign |
0.00 |
R7073:Ash1l
|
UTSW |
3 |
88,892,647 (GRCm39) |
missense |
probably damaging |
1.00 |
R7133:Ash1l
|
UTSW |
3 |
88,890,764 (GRCm39) |
frame shift |
probably null |
|
R7150:Ash1l
|
UTSW |
3 |
88,984,381 (GRCm39) |
missense |
probably damaging |
1.00 |
R7205:Ash1l
|
UTSW |
3 |
88,873,259 (GRCm39) |
missense |
probably benign |
0.00 |
R7254:Ash1l
|
UTSW |
3 |
88,977,816 (GRCm39) |
missense |
probably damaging |
1.00 |
R7272:Ash1l
|
UTSW |
3 |
88,961,941 (GRCm39) |
splice site |
probably null |
|
R7288:Ash1l
|
UTSW |
3 |
88,873,199 (GRCm39) |
start gained |
probably benign |
|
R7319:Ash1l
|
UTSW |
3 |
88,888,694 (GRCm39) |
missense |
probably benign |
0.19 |
R7341:Ash1l
|
UTSW |
3 |
88,889,066 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7342:Ash1l
|
UTSW |
3 |
88,873,304 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7454:Ash1l
|
UTSW |
3 |
88,891,172 (GRCm39) |
missense |
probably benign |
0.16 |
R7677:Ash1l
|
UTSW |
3 |
88,950,500 (GRCm39) |
missense |
probably damaging |
1.00 |
R7822:Ash1l
|
UTSW |
3 |
88,914,571 (GRCm39) |
missense |
probably benign |
|
R7857:Ash1l
|
UTSW |
3 |
88,891,616 (GRCm39) |
nonsense |
probably null |
|
R7889:Ash1l
|
UTSW |
3 |
88,873,345 (GRCm39) |
missense |
probably benign |
0.00 |
R7898:Ash1l
|
UTSW |
3 |
88,890,932 (GRCm39) |
missense |
possibly damaging |
0.54 |
R7931:Ash1l
|
UTSW |
3 |
88,950,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R7937:Ash1l
|
UTSW |
3 |
88,977,624 (GRCm39) |
nonsense |
probably null |
|
R7973:Ash1l
|
UTSW |
3 |
88,960,164 (GRCm39) |
missense |
probably benign |
|
R8119:Ash1l
|
UTSW |
3 |
88,942,734 (GRCm39) |
missense |
probably damaging |
1.00 |
R8157:Ash1l
|
UTSW |
3 |
88,971,014 (GRCm39) |
critical splice donor site |
probably null |
|
R8162:Ash1l
|
UTSW |
3 |
88,977,553 (GRCm39) |
missense |
probably damaging |
0.99 |
R8194:Ash1l
|
UTSW |
3 |
88,960,062 (GRCm39) |
missense |
probably damaging |
1.00 |
R8306:Ash1l
|
UTSW |
3 |
88,873,259 (GRCm39) |
missense |
probably benign |
0.00 |
R8497:Ash1l
|
UTSW |
3 |
88,914,951 (GRCm39) |
missense |
probably benign |
0.02 |
R8558:Ash1l
|
UTSW |
3 |
88,891,713 (GRCm39) |
missense |
probably damaging |
0.96 |
R8744:Ash1l
|
UTSW |
3 |
88,965,890 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8923:Ash1l
|
UTSW |
3 |
88,892,974 (GRCm39) |
missense |
possibly damaging |
0.51 |
R8969:Ash1l
|
UTSW |
3 |
88,873,598 (GRCm39) |
missense |
possibly damaging |
0.52 |
R8970:Ash1l
|
UTSW |
3 |
88,976,307 (GRCm39) |
missense |
probably benign |
0.00 |
R9002:Ash1l
|
UTSW |
3 |
88,888,715 (GRCm39) |
missense |
probably benign |
0.17 |
R9023:Ash1l
|
UTSW |
3 |
88,892,576 (GRCm39) |
missense |
probably damaging |
1.00 |
R9032:Ash1l
|
UTSW |
3 |
88,891,529 (GRCm39) |
missense |
probably benign |
0.00 |
R9032:Ash1l
|
UTSW |
3 |
88,889,294 (GRCm39) |
missense |
probably benign |
0.19 |
R9049:Ash1l
|
UTSW |
3 |
88,914,671 (GRCm39) |
missense |
probably benign |
|
R9085:Ash1l
|
UTSW |
3 |
88,891,529 (GRCm39) |
missense |
probably benign |
0.00 |
R9085:Ash1l
|
UTSW |
3 |
88,889,294 (GRCm39) |
missense |
probably benign |
0.19 |
R9130:Ash1l
|
UTSW |
3 |
88,965,848 (GRCm39) |
nonsense |
probably null |
|
R9149:Ash1l
|
UTSW |
3 |
88,914,530 (GRCm39) |
missense |
probably benign |
|
R9294:Ash1l
|
UTSW |
3 |
88,890,297 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9365:Ash1l
|
UTSW |
3 |
88,889,207 (GRCm39) |
missense |
possibly damaging |
0.63 |
R9450:Ash1l
|
UTSW |
3 |
88,915,139 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9542:Ash1l
|
UTSW |
3 |
88,950,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R9558:Ash1l
|
UTSW |
3 |
88,889,521 (GRCm39) |
missense |
probably benign |
0.02 |
R9572:Ash1l
|
UTSW |
3 |
88,960,188 (GRCm39) |
missense |
probably damaging |
1.00 |
R9688:Ash1l
|
UTSW |
3 |
88,892,024 (GRCm39) |
missense |
probably damaging |
1.00 |
R9736:Ash1l
|
UTSW |
3 |
88,891,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R9765:Ash1l
|
UTSW |
3 |
88,930,500 (GRCm39) |
missense |
probably damaging |
1.00 |
R9789:Ash1l
|
UTSW |
3 |
88,873,373 (GRCm39) |
missense |
probably benign |
|
X0017:Ash1l
|
UTSW |
3 |
88,891,892 (GRCm39) |
missense |
probably benign |
0.45 |
X0019:Ash1l
|
UTSW |
3 |
88,977,863 (GRCm39) |
missense |
probably damaging |
1.00 |
X0021:Ash1l
|
UTSW |
3 |
88,890,511 (GRCm39) |
missense |
probably benign |
0.10 |
Z1088:Ash1l
|
UTSW |
3 |
88,890,016 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Ash1l
|
UTSW |
3 |
88,950,524 (GRCm39) |
missense |
probably damaging |
1.00 |
|