Other mutations in this stock |
Total: 98 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1600012P17Rik |
C |
T |
1: 158,796,904 (GRCm39) |
|
noncoding transcript |
Het |
2300002M23Rik |
A |
G |
17: 35,878,403 (GRCm39) |
|
probably benign |
Het |
Aadat |
T |
C |
8: 60,993,140 (GRCm39) |
V360A |
probably benign |
Het |
Abcc5 |
T |
A |
16: 20,218,376 (GRCm39) |
D283V |
probably damaging |
Het |
Abraxas1 |
T |
A |
5: 100,959,886 (GRCm39) |
K155N |
probably damaging |
Het |
Acot3 |
T |
C |
12: 84,105,364 (GRCm39) |
I277T |
probably benign |
Het |
Ankrd45 |
G |
A |
1: 160,982,960 (GRCm39) |
C157Y |
probably damaging |
Het |
Apol10a |
C |
T |
15: 77,372,841 (GRCm39) |
T159I |
possibly damaging |
Het |
Arhgef11 |
G |
A |
3: 87,605,306 (GRCm39) |
V214M |
possibly damaging |
Het |
Atg13 |
A |
G |
2: 91,515,040 (GRCm39) |
S254P |
probably damaging |
Het |
Atg16l2 |
A |
G |
7: 100,946,385 (GRCm39) |
L129P |
probably damaging |
Het |
Avl9 |
T |
A |
6: 56,703,294 (GRCm39) |
V120D |
probably damaging |
Het |
Castor1 |
A |
G |
11: 4,169,004 (GRCm39) |
E57G |
possibly damaging |
Het |
Cc2d1b |
T |
C |
4: 108,485,239 (GRCm39) |
V527A |
probably benign |
Het |
Ccnl1 |
A |
G |
3: 65,854,092 (GRCm39) |
|
probably benign |
Het |
Cenpl |
T |
A |
1: 160,910,837 (GRCm39) |
D261E |
probably damaging |
Het |
Cep192 |
T |
G |
18: 67,984,803 (GRCm39) |
I1604M |
probably benign |
Het |
Cep95 |
A |
G |
11: 106,706,560 (GRCm39) |
I573V |
probably benign |
Het |
Cfap100 |
A |
G |
6: 90,389,825 (GRCm39) |
|
probably null |
Het |
Ciao3 |
A |
T |
17: 26,000,283 (GRCm39) |
H322L |
probably damaging |
Het |
Cmc1 |
T |
A |
9: 117,904,245 (GRCm39) |
M49L |
probably benign |
Het |
Cyfip2 |
G |
T |
11: 46,170,820 (GRCm39) |
N176K |
probably damaging |
Het |
Cyp2w1 |
T |
C |
5: 139,342,430 (GRCm39) |
F408L |
probably damaging |
Het |
D630045J12Rik |
G |
A |
6: 38,172,971 (GRCm39) |
S399F |
possibly damaging |
Het |
Dcbld2 |
T |
A |
16: 58,281,339 (GRCm39) |
L528Q |
probably damaging |
Het |
Dip2b |
T |
C |
15: 100,105,658 (GRCm39) |
V1138A |
probably damaging |
Het |
Dip2c |
T |
A |
13: 9,583,375 (GRCm39) |
L119Q |
probably damaging |
Het |
Dnah3 |
T |
C |
7: 119,677,169 (GRCm39) |
D444G |
possibly damaging |
Het |
Dsg1c |
A |
T |
18: 20,408,246 (GRCm39) |
N432Y |
possibly damaging |
Het |
Dst |
T |
A |
1: 34,230,228 (GRCm39) |
I2785N |
probably benign |
Het |
Dynap |
A |
T |
18: 70,374,296 (GRCm39) |
Y77N |
possibly damaging |
Het |
Eif4g3 |
T |
C |
4: 137,910,510 (GRCm39) |
L1330P |
possibly damaging |
Het |
Eif4g3 |
T |
A |
4: 137,925,408 (GRCm39) |
S1584T |
probably benign |
Het |
Enpp1 |
A |
T |
10: 24,555,146 (GRCm39) |
C67S |
probably null |
Het |
Enpp5 |
C |
T |
17: 44,392,027 (GRCm39) |
T152I |
probably damaging |
Het |
Erbb4 |
T |
C |
1: 68,383,059 (GRCm39) |
M313V |
probably damaging |
Het |
Erc2 |
T |
G |
14: 27,498,838 (GRCm39) |
L238R |
probably damaging |
Het |
Eya3 |
T |
A |
4: 132,448,698 (GRCm39) |
|
probably benign |
Het |
Farp1 |
T |
C |
14: 121,476,199 (GRCm39) |
F339L |
probably damaging |
Het |
Fsip2 |
A |
C |
2: 82,805,697 (GRCm39) |
D672A |
possibly damaging |
Het |
Gap43 |
G |
T |
16: 42,112,581 (GRCm39) |
P60Q |
probably benign |
Het |
Gpr37l1 |
T |
A |
1: 135,094,783 (GRCm39) |
I154F |
probably damaging |
Het |
Greb1 |
A |
G |
12: 16,746,329 (GRCm39) |
S1314P |
probably damaging |
Het |
Hectd4 |
A |
T |
5: 121,486,505 (GRCm39) |
M3167L |
probably benign |
Het |
Hps3 |
C |
T |
3: 20,084,574 (GRCm39) |
|
probably null |
Het |
Hps5 |
A |
G |
7: 46,436,013 (GRCm39) |
C178R |
probably benign |
Het |
Hspg2 |
T |
A |
4: 137,297,384 (GRCm39) |
|
probably benign |
Het |
Impdh2-ps |
A |
G |
8: 100,757,839 (GRCm39) |
|
noncoding transcript |
Het |
Josd2 |
T |
A |
7: 44,120,678 (GRCm39) |
N138K |
probably damaging |
Het |
Mtmr6 |
T |
G |
14: 60,529,546 (GRCm39) |
M315R |
probably damaging |
Het |
Mtrf1 |
G |
A |
14: 79,650,520 (GRCm39) |
V323M |
probably damaging |
Het |
Myo16 |
G |
T |
8: 10,423,527 (GRCm39) |
G288W |
probably damaging |
Het |
Myo18a |
T |
C |
11: 77,714,149 (GRCm39) |
Y748H |
probably damaging |
Het |
Nek1 |
A |
T |
8: 61,551,545 (GRCm39) |
N853I |
probably benign |
Het |
Npnt |
T |
G |
3: 132,610,452 (GRCm39) |
T272P |
possibly damaging |
Het |
Obi1 |
C |
T |
14: 104,747,819 (GRCm39) |
D43N |
probably damaging |
Het |
Or2ag1b |
C |
A |
7: 106,288,351 (GRCm39) |
E196* |
probably null |
Het |
Or2b6 |
T |
A |
13: 21,823,340 (GRCm39) |
M118L |
possibly damaging |
Het |
Or2y17 |
G |
A |
11: 49,232,148 (GRCm39) |
G263D |
probably benign |
Het |
Or51e1 |
T |
A |
7: 102,359,378 (GRCm39) |
I304N |
probably damaging |
Het |
Or52n2c |
G |
A |
7: 104,574,017 (GRCm39) |
T318I |
possibly damaging |
Het |
Or5a1 |
A |
G |
19: 12,097,234 (GRCm39) |
Y269H |
possibly damaging |
Het |
Pappa2 |
T |
C |
1: 158,784,582 (GRCm39) |
R143G |
probably benign |
Het |
Pappa2 |
T |
G |
1: 158,784,572 (GRCm39) |
D146A |
probably damaging |
Het |
Pcsk9 |
C |
T |
4: 106,304,353 (GRCm39) |
G496R |
probably damaging |
Het |
Pes1 |
A |
G |
11: 3,914,058 (GRCm39) |
K8E |
probably damaging |
Het |
Phlpp2 |
G |
A |
8: 110,667,052 (GRCm39) |
G1194S |
probably damaging |
Het |
Pkn1 |
A |
C |
8: 84,398,378 (GRCm39) |
V763G |
probably damaging |
Het |
Pkp2 |
C |
A |
16: 16,048,588 (GRCm39) |
A331E |
probably damaging |
Het |
Plb1 |
T |
A |
5: 32,507,023 (GRCm39) |
|
probably null |
Het |
Plxna1 |
A |
T |
6: 89,309,657 (GRCm39) |
|
probably null |
Het |
Polq |
C |
T |
16: 36,862,109 (GRCm39) |
T264M |
probably damaging |
Het |
Prkag3 |
T |
C |
1: 74,779,864 (GRCm39) |
*490W |
probably null |
Het |
Prl2c1 |
T |
C |
13: 28,041,661 (GRCm39) |
C228R |
probably damaging |
Het |
Pus7l |
T |
C |
15: 94,438,591 (GRCm39) |
S85G |
probably benign |
Het |
Rfc3 |
A |
C |
5: 151,568,241 (GRCm39) |
|
probably benign |
Het |
Riox2 |
A |
G |
16: 59,309,732 (GRCm39) |
N362S |
probably benign |
Het |
Scaper |
A |
T |
9: 55,650,932 (GRCm39) |
D904E |
probably damaging |
Het |
Scn11a |
T |
C |
9: 119,583,627 (GRCm39) |
M1663V |
probably benign |
Het |
Slc13a3 |
A |
T |
2: 165,272,209 (GRCm39) |
I278N |
possibly damaging |
Het |
Slc22a7 |
T |
C |
17: 46,745,923 (GRCm39) |
E278G |
probably damaging |
Het |
Snrnp48 |
T |
A |
13: 38,393,893 (GRCm39) |
M66K |
probably damaging |
Het |
Styk1 |
T |
G |
6: 131,277,429 (GRCm39) |
E404A |
probably damaging |
Het |
Synj1 |
T |
A |
16: 90,752,307 (GRCm39) |
H1016L |
probably benign |
Het |
Tbc1d8 |
G |
A |
1: 39,441,959 (GRCm39) |
T211I |
possibly damaging |
Het |
Tjp2 |
T |
C |
19: 24,097,475 (GRCm39) |
|
probably null |
Het |
Tmem87a |
A |
G |
2: 120,190,518 (GRCm39) |
|
probably null |
Het |
Trappc9 |
T |
G |
15: 72,808,909 (GRCm39) |
Y718S |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,641,587 (GRCm39) |
L5176Q |
possibly damaging |
Het |
Ubqlnl |
C |
T |
7: 103,798,925 (GRCm39) |
V191M |
probably benign |
Het |
Ugt2a3 |
C |
T |
5: 87,475,054 (GRCm39) |
G397R |
probably damaging |
Het |
Wdr33 |
T |
A |
18: 32,019,139 (GRCm39) |
M454K |
probably benign |
Het |
Wdtc1 |
G |
T |
4: 133,029,110 (GRCm39) |
N325K |
possibly damaging |
Het |
Whrn |
T |
C |
4: 63,336,402 (GRCm39) |
H720R |
probably damaging |
Het |
Xirp2 |
A |
T |
2: 67,349,609 (GRCm39) |
D3268V |
probably damaging |
Het |
Zc3h7a |
A |
T |
16: 10,959,573 (GRCm39) |
H793Q |
probably damaging |
Het |
Zfp518b |
C |
T |
5: 38,831,841 (GRCm39) |
A55T |
possibly damaging |
Het |
Zmynd8 |
G |
A |
2: 165,647,249 (GRCm39) |
T901M |
probably damaging |
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 |
R2118:Ash1l
|
UTSW |
3 |
88,892,602 (GRCm39) |
missense |
possibly damaging |
0.80 |
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 |
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 |
|