Other mutations in this stock |
Total: 96 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts20 |
A |
G |
15: 94,253,243 (GRCm39) |
C377R |
probably damaging |
Het |
Adgrv1 |
T |
C |
13: 81,677,132 (GRCm39) |
K1180E |
probably benign |
Het |
Ankle1 |
A |
G |
8: 71,860,562 (GRCm39) |
T340A |
probably benign |
Het |
Armc2 |
A |
T |
10: 41,839,663 (GRCm39) |
L434Q |
probably damaging |
Het |
Atm |
C |
T |
9: 53,412,269 (GRCm39) |
E960K |
probably benign |
Het |
Bend5 |
G |
T |
4: 111,272,436 (GRCm39) |
R22L |
probably benign |
Het |
Cacng6 |
C |
T |
7: 3,479,020 (GRCm39) |
T133I |
probably damaging |
Het |
Cep120 |
G |
A |
18: 53,873,208 (GRCm39) |
T41I |
probably damaging |
Het |
Ciz1 |
T |
C |
2: 32,257,477 (GRCm39) |
L174P |
probably damaging |
Het |
Cmah |
G |
A |
13: 24,612,880 (GRCm39) |
D26N |
probably benign |
Het |
Cnot1 |
A |
C |
8: 96,452,781 (GRCm39) |
D2098E |
probably damaging |
Het |
Cnot10 |
A |
C |
9: 114,455,504 (GRCm39) |
S207R |
probably damaging |
Het |
Col14a1 |
A |
G |
15: 55,271,160 (GRCm39) |
T638A |
unknown |
Het |
Coro1a |
T |
C |
7: 126,301,194 (GRCm39) |
E102G |
probably damaging |
Het |
Ddx27 |
A |
C |
2: 166,869,684 (GRCm39) |
D373A |
probably benign |
Het |
Defb38 |
A |
T |
8: 19,073,483 (GRCm39) |
Y63* |
probably null |
Het |
Dhx37 |
A |
G |
5: 125,498,166 (GRCm39) |
V681A |
probably damaging |
Het |
Dmxl1 |
T |
A |
18: 50,011,884 (GRCm39) |
L1347H |
probably damaging |
Het |
Dnmt3l |
C |
A |
10: 77,899,130 (GRCm39) |
L110I |
probably damaging |
Het |
Gcn1 |
A |
T |
5: 115,736,884 (GRCm39) |
M1276L |
probably benign |
Het |
Gfus |
A |
G |
15: 75,797,991 (GRCm39) |
F223S |
probably damaging |
Het |
Gm10277 |
TC |
T |
11: 77,676,828 (GRCm39) |
|
probably null |
Het |
Gm12790 |
G |
A |
4: 101,824,848 (GRCm39) |
T140I |
possibly damaging |
Het |
Golga3 |
A |
T |
5: 110,335,261 (GRCm39) |
M192L |
probably damaging |
Het |
H2-T22 |
A |
T |
17: 36,349,949 (GRCm39) |
|
probably null |
Het |
Hectd2 |
C |
A |
19: 36,591,824 (GRCm39) |
T675K |
probably damaging |
Het |
Hinfp |
T |
C |
9: 44,210,912 (GRCm39) |
N116S |
probably damaging |
Het |
Hoatz |
A |
G |
9: 51,012,384 (GRCm39) |
S79P |
possibly damaging |
Het |
Hs6st3 |
T |
A |
14: 120,106,699 (GRCm39) |
L369Q |
probably damaging |
Het |
Ift74 |
A |
G |
4: 94,515,496 (GRCm39) |
T138A |
probably benign |
Het |
Ipo7 |
T |
A |
7: 109,650,325 (GRCm39) |
Y792N |
probably damaging |
Het |
Jak1 |
A |
T |
4: 101,036,872 (GRCm39) |
I256N |
probably damaging |
Het |
Kcnd2 |
T |
A |
6: 21,216,431 (GRCm39) |
L45Q |
probably damaging |
Het |
Klhl3 |
A |
T |
13: 58,166,805 (GRCm39) |
V342E |
probably damaging |
Het |
Krt28 |
A |
C |
11: 99,255,943 (GRCm39) |
S439A |
probably benign |
Het |
L3mbtl1 |
T |
A |
2: 162,801,990 (GRCm39) |
|
probably null |
Het |
Lrch1 |
G |
A |
14: 75,022,971 (GRCm39) |
P634L |
probably damaging |
Het |
Lrp1 |
C |
T |
10: 127,412,362 (GRCm39) |
W1314* |
probably null |
Het |
Lrwd1 |
T |
A |
5: 136,159,332 (GRCm39) |
Y431F |
probably damaging |
Het |
Lyst |
A |
G |
13: 13,810,286 (GRCm39) |
E652G |
probably damaging |
Het |
Mageb3 |
A |
G |
2: 121,785,033 (GRCm39) |
V223A |
probably damaging |
Het |
Map1b |
G |
T |
13: 99,567,152 (GRCm39) |
S1856R |
unknown |
Het |
Mecom |
T |
A |
3: 30,019,607 (GRCm39) |
Q759L |
probably damaging |
Het |
Mfsd6 |
T |
A |
1: 52,700,134 (GRCm39) |
R671S |
probably benign |
Het |
Mllt10 |
A |
G |
2: 18,167,380 (GRCm39) |
N435S |
probably benign |
Het |
Mta2 |
T |
C |
19: 8,920,880 (GRCm39) |
I27T |
probably damaging |
Het |
Ndufab1 |
A |
G |
7: 121,700,987 (GRCm39) |
L20P |
probably benign |
Het |
Nfatc2ip |
T |
A |
7: 125,984,280 (GRCm39) |
Y371F |
probably damaging |
Het |
Nhlrc1 |
A |
C |
13: 47,167,661 (GRCm39) |
S199A |
probably benign |
Het |
Nipa1 |
G |
T |
7: 55,635,273 (GRCm39) |
N113K |
possibly damaging |
Het |
Nlgn1 |
T |
A |
3: 26,187,414 (GRCm39) |
N157I |
probably damaging |
Het |
Nlrp1a |
T |
A |
11: 71,005,326 (GRCm39) |
K630* |
probably null |
Het |
Nmi |
T |
C |
2: 51,838,719 (GRCm39) |
T272A |
probably benign |
Het |
Nr1i3 |
T |
A |
1: 171,046,163 (GRCm39) |
L181Q |
probably damaging |
Het |
Nrxn1 |
A |
T |
17: 91,011,705 (GRCm39) |
I308K |
probably damaging |
Het |
Nup50l |
A |
T |
6: 96,141,841 (GRCm39) |
V401E |
probably damaging |
Het |
Or14a256 |
T |
C |
7: 86,265,286 (GRCm39) |
D189G |
probably benign |
Het |
Or52z15 |
T |
C |
7: 103,332,519 (GRCm39) |
I188T |
probably damaging |
Het |
Or5al7 |
A |
T |
2: 85,993,073 (GRCm39) |
Y73* |
probably null |
Het |
Or8g50 |
T |
A |
9: 39,648,600 (GRCm39) |
M163K |
probably damaging |
Het |
Osgin2 |
G |
A |
4: 16,008,648 (GRCm39) |
T51M |
probably damaging |
Het |
Pkd1l2 |
T |
A |
8: 117,757,461 (GRCm39) |
T1526S |
possibly damaging |
Het |
Pkhd1l1 |
G |
T |
15: 44,432,878 (GRCm39) |
A3378S |
probably damaging |
Het |
Plg |
A |
T |
17: 12,603,364 (GRCm39) |
D90V |
probably damaging |
Het |
Plppr3 |
A |
T |
10: 79,701,572 (GRCm39) |
D423E |
probably benign |
Het |
Prpf8 |
T |
C |
11: 75,378,547 (GRCm39) |
V66A |
possibly damaging |
Het |
Psg19 |
A |
T |
7: 18,528,180 (GRCm39) |
Y188N |
probably damaging |
Het |
Ptgs1 |
C |
A |
2: 36,127,708 (GRCm39) |
S89* |
probably null |
Het |
Ptx3 |
T |
A |
3: 66,132,187 (GRCm39) |
I236N |
probably damaging |
Het |
Pygm |
A |
G |
19: 6,436,438 (GRCm39) |
N100S |
probably damaging |
Het |
Reps1 |
A |
G |
10: 18,000,668 (GRCm39) |
E760G |
probably damaging |
Het |
Rgs7 |
T |
A |
1: 174,918,639 (GRCm39) |
N235I |
probably damaging |
Het |
Rgsl1 |
T |
A |
1: 153,693,295 (GRCm39) |
M629L |
probably benign |
Het |
Rrh |
T |
C |
3: 129,604,336 (GRCm39) |
I288M |
probably damaging |
Het |
Sctr |
A |
T |
1: 119,959,312 (GRCm39) |
D70V |
probably damaging |
Het |
Sec11c |
A |
T |
18: 65,933,720 (GRCm39) |
T9S |
probably benign |
Het |
Spty2d1 |
C |
T |
7: 46,645,933 (GRCm39) |
G570D |
probably damaging |
Het |
Stx1b |
T |
C |
7: 127,410,077 (GRCm39) |
E153G |
probably damaging |
Het |
Synm |
G |
A |
7: 67,383,343 (GRCm39) |
R1440W |
probably benign |
Het |
Tcof1 |
T |
C |
18: 60,965,857 (GRCm39) |
E415G |
possibly damaging |
Het |
Tgfb1i1 |
G |
A |
7: 127,851,977 (GRCm39) |
R353H |
probably damaging |
Het |
Thbs3 |
T |
C |
3: 89,126,699 (GRCm39) |
F271S |
probably damaging |
Het |
Tlr5 |
T |
C |
1: 182,803,194 (GRCm39) |
W833R |
probably damaging |
Het |
Tmem132b |
A |
G |
5: 125,699,615 (GRCm39) |
E92G |
probably damaging |
Het |
Tmem221 |
T |
C |
8: 72,010,472 (GRCm39) |
Y133C |
probably damaging |
Het |
Tmem229b-ps |
A |
G |
10: 53,351,552 (GRCm39) |
|
noncoding transcript |
Het |
Tnxb |
T |
C |
17: 34,891,201 (GRCm39) |
C515R |
probably damaging |
Het |
Trp53rka |
T |
A |
2: 165,333,415 (GRCm39) |
N158I |
probably damaging |
Het |
Usp20 |
T |
A |
2: 30,906,317 (GRCm39) |
C562S |
probably damaging |
Het |
Usp31 |
C |
T |
7: 121,247,919 (GRCm39) |
V1175M |
probably benign |
Het |
Veph1 |
G |
T |
3: 65,964,610 (GRCm39) |
N806K |
probably benign |
Het |
Vmn1r223 |
G |
T |
13: 23,433,832 (GRCm39) |
C142F |
probably damaging |
Het |
Vmn2r80 |
A |
T |
10: 79,030,558 (GRCm39) |
S795C |
probably benign |
Het |
Wdr41 |
A |
G |
13: 95,151,537 (GRCm39) |
|
probably null |
Het |
Zfp617 |
A |
T |
8: 72,686,009 (GRCm39) |
H113L |
probably benign |
Het |
Zfp715 |
T |
A |
7: 42,947,370 (GRCm39) |
R863S |
possibly 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 |
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 |
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 |
|