Other mutations in this stock |
Total: 82 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca14 |
T |
A |
7: 119,851,479 (GRCm39) |
M819K |
possibly damaging |
Het |
Adamtsl3 |
T |
G |
7: 82,178,120 (GRCm39) |
C528G |
probably damaging |
Het |
Akap9 |
A |
G |
5: 4,004,870 (GRCm39) |
K148E |
probably benign |
Het |
Akr1b1 |
A |
T |
6: 34,286,577 (GRCm39) |
D225E |
probably benign |
Het |
Alms1 |
C |
A |
6: 85,655,653 (GRCm39) |
Q2931K |
possibly damaging |
Het |
Ano3 |
T |
C |
2: 110,715,346 (GRCm39) |
K31E |
possibly damaging |
Het |
Cdc37 |
A |
G |
9: 21,053,537 (GRCm39) |
I242T |
probably damaging |
Het |
Celsr1 |
T |
A |
15: 85,816,524 (GRCm39) |
K1806N |
possibly damaging |
Het |
Clpb |
T |
A |
7: 101,436,956 (GRCm39) |
I707N |
possibly damaging |
Het |
Cntnap2 |
A |
T |
6: 47,072,483 (GRCm39) |
Y1017F |
possibly damaging |
Het |
Creb3l2 |
A |
T |
6: 37,311,416 (GRCm39) |
S458T |
probably benign |
Het |
Ctnnd2 |
C |
A |
15: 31,009,230 (GRCm39) |
T1109K |
possibly damaging |
Het |
Dcaf10 |
T |
A |
4: 45,373,011 (GRCm39) |
L425Q |
probably damaging |
Het |
Dlec1 |
A |
G |
9: 118,941,167 (GRCm39) |
E239G |
probably benign |
Het |
Dnah2 |
T |
C |
11: 69,390,020 (GRCm39) |
K742E |
probably damaging |
Het |
Dsp |
A |
T |
13: 38,371,717 (GRCm39) |
R889S |
probably damaging |
Het |
Dync1h1 |
T |
A |
12: 110,599,222 (GRCm39) |
M1859K |
probably damaging |
Het |
Efcab7 |
T |
A |
4: 99,758,886 (GRCm39) |
N361K |
probably damaging |
Het |
Eps8l2 |
T |
C |
7: 140,935,646 (GRCm39) |
V139A |
probably damaging |
Het |
Fads3 |
T |
G |
19: 10,019,200 (GRCm39) |
H35Q |
probably damaging |
Het |
Fam163b |
C |
A |
2: 27,003,583 (GRCm39) |
V24F |
probably damaging |
Het |
Gm14496 |
A |
T |
2: 181,636,904 (GRCm39) |
T121S |
probably benign |
Het |
Gm4799 |
C |
T |
10: 82,790,563 (GRCm39) |
|
noncoding transcript |
Het |
Gm7168 |
A |
T |
17: 14,169,797 (GRCm39) |
D388V |
probably benign |
Het |
Gmeb1 |
A |
T |
4: 131,953,386 (GRCm39) |
L460* |
probably null |
Het |
Gpc6 |
T |
G |
14: 118,212,430 (GRCm39) |
F534V |
probably null |
Het |
Hectd3 |
A |
G |
4: 116,853,241 (GRCm39) |
D156G |
possibly damaging |
Het |
Itga6 |
T |
C |
2: 71,650,404 (GRCm39) |
I150T |
possibly damaging |
Het |
Kansl1 |
A |
G |
11: 104,229,012 (GRCm39) |
M863T |
probably benign |
Het |
Kcnb2 |
A |
T |
1: 15,780,664 (GRCm39) |
Y512F |
probably benign |
Het |
Klhdc2 |
A |
T |
12: 69,347,053 (GRCm39) |
M73L |
probably benign |
Het |
Ktn1 |
A |
G |
14: 47,932,073 (GRCm39) |
T667A |
probably benign |
Het |
Lgsn |
A |
C |
1: 31,242,736 (GRCm39) |
I273L |
probably benign |
Het |
Lilra5 |
A |
G |
7: 4,245,232 (GRCm39) |
D292G |
probably benign |
Het |
Mrps27 |
C |
T |
13: 99,541,582 (GRCm39) |
R229C |
probably damaging |
Het |
Muc5b |
T |
G |
7: 141,416,173 (GRCm39) |
S3040A |
probably benign |
Het |
Nat14 |
T |
C |
7: 4,926,275 (GRCm39) |
S7P |
probably damaging |
Het |
Nfia |
A |
G |
4: 97,671,694 (GRCm39) |
I135V |
possibly damaging |
Het |
Nkd1 |
G |
A |
8: 89,248,944 (GRCm39) |
A30T |
probably damaging |
Het |
Nup205 |
A |
G |
6: 35,202,903 (GRCm39) |
D1370G |
probably null |
Het |
Or1j15 |
C |
G |
2: 36,459,568 (GRCm39) |
|
probably null |
Het |
Or4k15c |
G |
A |
14: 50,321,310 (GRCm39) |
T276I |
probably damaging |
Het |
Or51k2 |
T |
C |
7: 103,596,400 (GRCm39) |
L209P |
probably damaging |
Het |
Or5p79 |
T |
A |
7: 108,221,494 (GRCm39) |
N158K |
possibly damaging |
Het |
Or8s10 |
T |
C |
15: 98,336,168 (GRCm39) |
S273P |
possibly damaging |
Het |
Orc1 |
C |
T |
4: 108,459,229 (GRCm39) |
A466V |
probably benign |
Het |
Otud7a |
T |
A |
7: 63,385,638 (GRCm39) |
D367E |
possibly damaging |
Het |
Pcdhb4 |
A |
G |
18: 37,441,263 (GRCm39) |
Y191C |
probably damaging |
Het |
Pclo |
T |
C |
5: 14,762,828 (GRCm39) |
V3767A |
unknown |
Het |
Pclo |
T |
C |
5: 14,728,789 (GRCm39) |
|
probably benign |
Het |
Prmt1 |
A |
T |
7: 44,628,225 (GRCm39) |
|
probably null |
Het |
Rangrf |
T |
C |
11: 68,863,518 (GRCm39) |
S163G |
probably benign |
Het |
Rgs12 |
C |
A |
5: 35,176,804 (GRCm39) |
A65E |
probably damaging |
Het |
Rrbp1 |
T |
C |
2: 143,830,436 (GRCm39) |
N577S |
probably damaging |
Het |
Septin11 |
A |
G |
5: 93,315,393 (GRCm39) |
H374R |
probably damaging |
Het |
Serpina5 |
T |
G |
12: 104,070,046 (GRCm39) |
N314K |
probably benign |
Het |
Sgce |
T |
C |
6: 4,689,621 (GRCm39) |
D395G |
probably damaging |
Het |
Slc26a9 |
A |
T |
1: 131,690,499 (GRCm39) |
N501I |
probably damaging |
Het |
Slc9c1 |
A |
G |
16: 45,401,965 (GRCm39) |
D784G |
possibly damaging |
Het |
Snapc2 |
A |
G |
8: 4,305,676 (GRCm39) |
D207G |
probably benign |
Het |
Stard9 |
G |
T |
2: 120,529,738 (GRCm39) |
M1998I |
probably benign |
Het |
Stk38 |
A |
C |
17: 29,194,907 (GRCm39) |
F280V |
possibly damaging |
Het |
Tas2r126 |
A |
G |
6: 42,412,025 (GRCm39) |
K186R |
probably damaging |
Het |
Tdp1 |
A |
C |
12: 99,875,970 (GRCm39) |
D307A |
probably benign |
Het |
Tead2 |
A |
G |
7: 44,866,674 (GRCm39) |
D11G |
probably damaging |
Het |
Tmco4 |
C |
A |
4: 138,747,383 (GRCm39) |
L211I |
probably damaging |
Het |
Tmem183a |
A |
G |
1: 134,280,115 (GRCm39) |
F255S |
probably damaging |
Het |
Tmem87a |
C |
T |
2: 120,205,929 (GRCm39) |
G349S |
possibly damaging |
Het |
Tpte |
G |
A |
8: 22,826,549 (GRCm39) |
E377K |
possibly damaging |
Het |
Trim32 |
T |
C |
4: 65,531,893 (GRCm39) |
F150S |
possibly damaging |
Het |
Trpc7 |
T |
A |
13: 57,035,636 (GRCm39) |
K99M |
probably damaging |
Het |
Ttc22 |
A |
G |
4: 106,491,381 (GRCm39) |
K195E |
probably damaging |
Het |
Txn2 |
G |
A |
15: 77,811,917 (GRCm39) |
P7S |
probably damaging |
Het |
Ubxn2a |
G |
A |
12: 4,930,700 (GRCm39) |
T220I |
probably damaging |
Het |
Ufd1 |
A |
G |
16: 18,633,626 (GRCm39) |
N17S |
possibly damaging |
Het |
Unc13a |
A |
G |
8: 72,102,509 (GRCm39) |
S958P |
probably damaging |
Het |
Vmn1r202 |
T |
A |
13: 22,685,824 (GRCm39) |
M198L |
probably damaging |
Het |
Vmn2r84 |
G |
A |
10: 130,221,991 (GRCm39) |
A743V |
probably damaging |
Het |
Washc5 |
A |
G |
15: 59,213,007 (GRCm39) |
F891S |
probably damaging |
Het |
Zfp708 |
T |
C |
13: 67,218,375 (GRCm39) |
T495A |
probably benign |
Het |
Zfp81 |
A |
G |
17: 33,553,593 (GRCm39) |
I407T |
probably benign |
Het |
Zswim5 |
T |
C |
4: 116,843,874 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Ralgapa1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00089:Ralgapa1
|
APN |
12 |
55,769,558 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL00494:Ralgapa1
|
APN |
12 |
55,793,970 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00731:Ralgapa1
|
APN |
12 |
55,749,237 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL00851:Ralgapa1
|
APN |
12 |
55,756,360 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01133:Ralgapa1
|
APN |
12 |
55,689,144 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01133:Ralgapa1
|
APN |
12 |
55,689,133 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01354:Ralgapa1
|
APN |
12 |
55,824,101 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL01514:Ralgapa1
|
APN |
12 |
55,766,442 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02033:Ralgapa1
|
APN |
12 |
55,689,262 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL02064:Ralgapa1
|
APN |
12 |
55,754,862 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02556:Ralgapa1
|
APN |
12 |
55,689,234 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL02605:Ralgapa1
|
APN |
12 |
55,759,450 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02657:Ralgapa1
|
APN |
12 |
55,720,292 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02676:Ralgapa1
|
APN |
12 |
55,723,202 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02894:Ralgapa1
|
APN |
12 |
55,763,854 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL02944:Ralgapa1
|
APN |
12 |
55,804,736 (GRCm39) |
missense |
probably benign |
0.01 |
Anhydrous
|
UTSW |
12 |
55,842,563 (GRCm39) |
critical splice acceptor site |
probably null |
|
Aqueous
|
UTSW |
12 |
55,745,639 (GRCm39) |
missense |
probably damaging |
1.00 |
bantam
|
UTSW |
12 |
55,769,558 (GRCm39) |
critical splice donor site |
probably null |
|
Deliquescent
|
UTSW |
12 |
55,829,685 (GRCm39) |
splice site |
probably benign |
|
wickedwarlock
|
UTSW |
12 |
55,824,077 (GRCm39) |
missense |
probably null |
0.99 |
F5770:Ralgapa1
|
UTSW |
12 |
55,842,438 (GRCm39) |
splice site |
probably benign |
|
IGL03046:Ralgapa1
|
UTSW |
12 |
55,741,942 (GRCm39) |
missense |
probably damaging |
1.00 |
R0011:Ralgapa1
|
UTSW |
12 |
55,833,048 (GRCm39) |
missense |
probably damaging |
0.99 |
R0096:Ralgapa1
|
UTSW |
12 |
55,786,290 (GRCm39) |
missense |
probably damaging |
1.00 |
R0277:Ralgapa1
|
UTSW |
12 |
55,724,023 (GRCm39) |
missense |
probably damaging |
0.99 |
R0323:Ralgapa1
|
UTSW |
12 |
55,724,023 (GRCm39) |
missense |
probably damaging |
0.99 |
R0333:Ralgapa1
|
UTSW |
12 |
55,829,685 (GRCm39) |
splice site |
probably benign |
|
R0361:Ralgapa1
|
UTSW |
12 |
55,723,354 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0385:Ralgapa1
|
UTSW |
12 |
55,723,823 (GRCm39) |
missense |
probably damaging |
1.00 |
R0386:Ralgapa1
|
UTSW |
12 |
55,754,852 (GRCm39) |
missense |
probably benign |
0.03 |
R0498:Ralgapa1
|
UTSW |
12 |
55,736,576 (GRCm39) |
missense |
possibly damaging |
0.66 |
R0552:Ralgapa1
|
UTSW |
12 |
55,723,550 (GRCm39) |
missense |
probably benign |
0.27 |
R0564:Ralgapa1
|
UTSW |
12 |
55,829,670 (GRCm39) |
missense |
possibly damaging |
0.84 |
R0730:Ralgapa1
|
UTSW |
12 |
55,712,448 (GRCm39) |
missense |
probably damaging |
1.00 |
R0741:Ralgapa1
|
UTSW |
12 |
55,723,366 (GRCm39) |
missense |
probably damaging |
0.99 |
R0815:Ralgapa1
|
UTSW |
12 |
55,829,562 (GRCm39) |
splice site |
probably benign |
|
R0815:Ralgapa1
|
UTSW |
12 |
55,809,466 (GRCm39) |
nonsense |
probably null |
|
R0863:Ralgapa1
|
UTSW |
12 |
55,829,562 (GRCm39) |
splice site |
probably benign |
|
R0863:Ralgapa1
|
UTSW |
12 |
55,809,466 (GRCm39) |
nonsense |
probably null |
|
R1068:Ralgapa1
|
UTSW |
12 |
55,837,095 (GRCm39) |
critical splice donor site |
probably null |
|
R1147:Ralgapa1
|
UTSW |
12 |
55,749,265 (GRCm39) |
missense |
probably damaging |
1.00 |
R1147:Ralgapa1
|
UTSW |
12 |
55,749,265 (GRCm39) |
missense |
probably damaging |
1.00 |
R1256:Ralgapa1
|
UTSW |
12 |
55,809,446 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1343:Ralgapa1
|
UTSW |
12 |
55,754,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R1378:Ralgapa1
|
UTSW |
12 |
55,723,711 (GRCm39) |
missense |
probably damaging |
1.00 |
R1474:Ralgapa1
|
UTSW |
12 |
55,788,265 (GRCm39) |
missense |
probably benign |
0.09 |
R1494:Ralgapa1
|
UTSW |
12 |
55,731,309 (GRCm39) |
missense |
probably damaging |
0.99 |
R1593:Ralgapa1
|
UTSW |
12 |
55,817,488 (GRCm39) |
missense |
probably damaging |
1.00 |
R1607:Ralgapa1
|
UTSW |
12 |
55,788,321 (GRCm39) |
missense |
probably damaging |
1.00 |
R1681:Ralgapa1
|
UTSW |
12 |
55,809,388 (GRCm39) |
missense |
probably benign |
0.35 |
R1689:Ralgapa1
|
UTSW |
12 |
55,723,552 (GRCm39) |
missense |
possibly damaging |
0.79 |
R1714:Ralgapa1
|
UTSW |
12 |
55,689,174 (GRCm39) |
missense |
probably damaging |
1.00 |
R1832:Ralgapa1
|
UTSW |
12 |
55,804,752 (GRCm39) |
missense |
probably benign |
0.03 |
R1870:Ralgapa1
|
UTSW |
12 |
55,723,817 (GRCm39) |
missense |
possibly damaging |
0.66 |
R2040:Ralgapa1
|
UTSW |
12 |
55,833,107 (GRCm39) |
missense |
probably damaging |
1.00 |
R2043:Ralgapa1
|
UTSW |
12 |
55,723,811 (GRCm39) |
missense |
probably damaging |
0.99 |
R2046:Ralgapa1
|
UTSW |
12 |
55,741,945 (GRCm39) |
missense |
probably damaging |
1.00 |
R2109:Ralgapa1
|
UTSW |
12 |
55,822,973 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2114:Ralgapa1
|
UTSW |
12 |
55,833,134 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2115:Ralgapa1
|
UTSW |
12 |
55,833,134 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2202:Ralgapa1
|
UTSW |
12 |
55,659,585 (GRCm39) |
splice site |
probably null |
|
R2203:Ralgapa1
|
UTSW |
12 |
55,659,585 (GRCm39) |
splice site |
probably null |
|
R2233:Ralgapa1
|
UTSW |
12 |
55,763,856 (GRCm39) |
missense |
probably benign |
0.13 |
R2235:Ralgapa1
|
UTSW |
12 |
55,763,856 (GRCm39) |
missense |
probably benign |
0.13 |
R2341:Ralgapa1
|
UTSW |
12 |
55,723,909 (GRCm39) |
missense |
possibly damaging |
0.66 |
R2507:Ralgapa1
|
UTSW |
12 |
55,764,986 (GRCm39) |
missense |
probably damaging |
1.00 |
R2508:Ralgapa1
|
UTSW |
12 |
55,764,986 (GRCm39) |
missense |
probably damaging |
1.00 |
R2972:Ralgapa1
|
UTSW |
12 |
55,867,540 (GRCm39) |
missense |
possibly damaging |
0.61 |
R3160:Ralgapa1
|
UTSW |
12 |
55,756,371 (GRCm39) |
missense |
probably damaging |
1.00 |
R3162:Ralgapa1
|
UTSW |
12 |
55,756,371 (GRCm39) |
missense |
probably damaging |
1.00 |
R3401:Ralgapa1
|
UTSW |
12 |
55,705,922 (GRCm39) |
missense |
possibly damaging |
0.66 |
R3416:Ralgapa1
|
UTSW |
12 |
55,817,398 (GRCm39) |
splice site |
probably benign |
|
R3499:Ralgapa1
|
UTSW |
12 |
55,741,928 (GRCm39) |
splice site |
probably benign |
|
R3799:Ralgapa1
|
UTSW |
12 |
55,705,915 (GRCm39) |
missense |
probably damaging |
1.00 |
R3948:Ralgapa1
|
UTSW |
12 |
55,745,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R4039:Ralgapa1
|
UTSW |
12 |
55,842,486 (GRCm39) |
missense |
probably damaging |
0.99 |
R4120:Ralgapa1
|
UTSW |
12 |
55,687,429 (GRCm39) |
missense |
probably damaging |
1.00 |
R4165:Ralgapa1
|
UTSW |
12 |
55,687,429 (GRCm39) |
missense |
probably damaging |
1.00 |
R4166:Ralgapa1
|
UTSW |
12 |
55,687,429 (GRCm39) |
missense |
probably damaging |
1.00 |
R4212:Ralgapa1
|
UTSW |
12 |
55,786,115 (GRCm39) |
critical splice donor site |
probably null |
|
R4232:Ralgapa1
|
UTSW |
12 |
55,687,429 (GRCm39) |
missense |
probably damaging |
1.00 |
R4233:Ralgapa1
|
UTSW |
12 |
55,687,429 (GRCm39) |
missense |
probably damaging |
1.00 |
R4234:Ralgapa1
|
UTSW |
12 |
55,687,429 (GRCm39) |
missense |
probably damaging |
1.00 |
R4235:Ralgapa1
|
UTSW |
12 |
55,687,429 (GRCm39) |
missense |
probably damaging |
1.00 |
R4399:Ralgapa1
|
UTSW |
12 |
55,842,563 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4698:Ralgapa1
|
UTSW |
12 |
55,724,061 (GRCm39) |
splice site |
probably null |
|
R4715:Ralgapa1
|
UTSW |
12 |
55,740,243 (GRCm39) |
missense |
probably damaging |
1.00 |
R4755:Ralgapa1
|
UTSW |
12 |
55,759,533 (GRCm39) |
missense |
probably damaging |
1.00 |
R4810:Ralgapa1
|
UTSW |
12 |
55,841,778 (GRCm39) |
critical splice donor site |
probably null |
|
R4827:Ralgapa1
|
UTSW |
12 |
55,723,222 (GRCm39) |
missense |
probably damaging |
1.00 |
R4849:Ralgapa1
|
UTSW |
12 |
55,745,588 (GRCm39) |
missense |
probably damaging |
0.99 |
R4934:Ralgapa1
|
UTSW |
12 |
55,809,359 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5006:Ralgapa1
|
UTSW |
12 |
55,764,899 (GRCm39) |
missense |
probably benign |
0.02 |
R5114:Ralgapa1
|
UTSW |
12 |
55,659,508 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5140:Ralgapa1
|
UTSW |
12 |
55,712,459 (GRCm39) |
missense |
probably damaging |
1.00 |
R5140:Ralgapa1
|
UTSW |
12 |
55,822,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R5168:Ralgapa1
|
UTSW |
12 |
55,804,817 (GRCm39) |
missense |
probably benign |
0.05 |
R5407:Ralgapa1
|
UTSW |
12 |
55,723,582 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5441:Ralgapa1
|
UTSW |
12 |
55,766,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R5473:Ralgapa1
|
UTSW |
12 |
55,723,495 (GRCm39) |
missense |
probably benign |
0.41 |
R5624:Ralgapa1
|
UTSW |
12 |
55,659,523 (GRCm39) |
missense |
probably damaging |
1.00 |
R5766:Ralgapa1
|
UTSW |
12 |
55,867,551 (GRCm39) |
start codon destroyed |
probably null |
0.99 |
R5826:Ralgapa1
|
UTSW |
12 |
55,723,898 (GRCm39) |
missense |
probably damaging |
1.00 |
R5950:Ralgapa1
|
UTSW |
12 |
55,785,050 (GRCm39) |
missense |
possibly damaging |
0.58 |
R5980:Ralgapa1
|
UTSW |
12 |
55,817,401 (GRCm39) |
splice site |
probably null |
|
R6019:Ralgapa1
|
UTSW |
12 |
55,730,827 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6065:Ralgapa1
|
UTSW |
12 |
55,804,709 (GRCm39) |
critical splice donor site |
probably null |
|
R6326:Ralgapa1
|
UTSW |
12 |
55,793,931 (GRCm39) |
missense |
probably damaging |
1.00 |
R6355:Ralgapa1
|
UTSW |
12 |
55,745,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R6408:Ralgapa1
|
UTSW |
12 |
55,730,695 (GRCm39) |
nonsense |
probably null |
|
R6448:Ralgapa1
|
UTSW |
12 |
55,766,446 (GRCm39) |
missense |
probably benign |
0.14 |
R6453:Ralgapa1
|
UTSW |
12 |
55,785,104 (GRCm39) |
missense |
probably damaging |
1.00 |
R6590:Ralgapa1
|
UTSW |
12 |
55,769,558 (GRCm39) |
critical splice donor site |
probably null |
|
R6690:Ralgapa1
|
UTSW |
12 |
55,769,558 (GRCm39) |
critical splice donor site |
probably null |
|
R6738:Ralgapa1
|
UTSW |
12 |
55,809,512 (GRCm39) |
missense |
probably damaging |
1.00 |
R6836:Ralgapa1
|
UTSW |
12 |
55,651,058 (GRCm39) |
splice site |
probably null |
|
R6936:Ralgapa1
|
UTSW |
12 |
55,832,997 (GRCm39) |
missense |
probably damaging |
0.99 |
R6945:Ralgapa1
|
UTSW |
12 |
55,822,976 (GRCm39) |
missense |
possibly damaging |
0.64 |
R7028:Ralgapa1
|
UTSW |
12 |
55,804,844 (GRCm39) |
missense |
probably damaging |
1.00 |
R7075:Ralgapa1
|
UTSW |
12 |
55,867,508 (GRCm39) |
missense |
possibly damaging |
0.66 |
R7076:Ralgapa1
|
UTSW |
12 |
55,768,361 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7098:Ralgapa1
|
UTSW |
12 |
55,837,095 (GRCm39) |
critical splice donor site |
probably null |
|
R7231:Ralgapa1
|
UTSW |
12 |
55,650,976 (GRCm39) |
missense |
probably damaging |
1.00 |
R7254:Ralgapa1
|
UTSW |
12 |
55,741,978 (GRCm39) |
missense |
probably damaging |
1.00 |
R7326:Ralgapa1
|
UTSW |
12 |
55,755,789 (GRCm39) |
missense |
probably damaging |
1.00 |
R7485:Ralgapa1
|
UTSW |
12 |
55,759,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R7580:Ralgapa1
|
UTSW |
12 |
55,765,013 (GRCm39) |
missense |
probably benign |
0.00 |
R7677:Ralgapa1
|
UTSW |
12 |
55,705,928 (GRCm39) |
missense |
probably damaging |
0.96 |
R7702:Ralgapa1
|
UTSW |
12 |
55,756,341 (GRCm39) |
missense |
probably damaging |
1.00 |
R7702:Ralgapa1
|
UTSW |
12 |
55,756,340 (GRCm39) |
missense |
probably damaging |
1.00 |
R7707:Ralgapa1
|
UTSW |
12 |
55,824,077 (GRCm39) |
missense |
probably null |
0.99 |
R7723:Ralgapa1
|
UTSW |
12 |
55,788,298 (GRCm39) |
missense |
probably benign |
|
R7763:Ralgapa1
|
UTSW |
12 |
55,804,740 (GRCm39) |
missense |
probably benign |
0.28 |
R7791:Ralgapa1
|
UTSW |
12 |
55,788,304 (GRCm39) |
missense |
probably damaging |
0.97 |
R7812:Ralgapa1
|
UTSW |
12 |
55,766,413 (GRCm39) |
missense |
possibly damaging |
0.67 |
R7868:Ralgapa1
|
UTSW |
12 |
55,659,423 (GRCm39) |
missense |
probably benign |
0.00 |
R7895:Ralgapa1
|
UTSW |
12 |
55,793,934 (GRCm39) |
missense |
probably benign |
0.44 |
R7896:Ralgapa1
|
UTSW |
12 |
55,744,663 (GRCm39) |
missense |
probably benign |
0.01 |
R8004:Ralgapa1
|
UTSW |
12 |
55,749,242 (GRCm39) |
missense |
probably damaging |
0.99 |
R8094:Ralgapa1
|
UTSW |
12 |
55,829,631 (GRCm39) |
missense |
probably damaging |
0.99 |
R8213:Ralgapa1
|
UTSW |
12 |
55,769,699 (GRCm39) |
missense |
probably damaging |
0.99 |
R8307:Ralgapa1
|
UTSW |
12 |
55,788,308 (GRCm39) |
missense |
probably damaging |
0.99 |
R8423:Ralgapa1
|
UTSW |
12 |
55,705,847 (GRCm39) |
missense |
probably damaging |
0.99 |
R8462:Ralgapa1
|
UTSW |
12 |
55,723,303 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8469:Ralgapa1
|
UTSW |
12 |
55,786,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R8675:Ralgapa1
|
UTSW |
12 |
55,785,002 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8802:Ralgapa1
|
UTSW |
12 |
55,785,101 (GRCm39) |
missense |
probably damaging |
0.99 |
R8937:Ralgapa1
|
UTSW |
12 |
55,749,345 (GRCm39) |
missense |
probably damaging |
0.96 |
R8953:Ralgapa1
|
UTSW |
12 |
55,867,546 (GRCm39) |
missense |
probably damaging |
0.99 |
R8974:Ralgapa1
|
UTSW |
12 |
55,723,791 (GRCm39) |
missense |
probably benign |
|
R9011:Ralgapa1
|
UTSW |
12 |
55,652,314 (GRCm39) |
intron |
probably benign |
|
R9089:Ralgapa1
|
UTSW |
12 |
55,723,351 (GRCm39) |
missense |
probably damaging |
0.97 |
R9124:Ralgapa1
|
UTSW |
12 |
55,781,881 (GRCm39) |
missense |
probably damaging |
1.00 |
R9254:Ralgapa1
|
UTSW |
12 |
55,769,583 (GRCm39) |
missense |
probably damaging |
1.00 |
R9320:Ralgapa1
|
UTSW |
12 |
55,755,843 (GRCm39) |
missense |
possibly damaging |
0.59 |
R9379:Ralgapa1
|
UTSW |
12 |
55,769,583 (GRCm39) |
missense |
probably damaging |
1.00 |
R9446:Ralgapa1
|
UTSW |
12 |
55,754,808 (GRCm39) |
missense |
probably damaging |
0.97 |
R9684:Ralgapa1
|
UTSW |
12 |
55,659,485 (GRCm39) |
missense |
possibly damaging |
0.63 |
Z1176:Ralgapa1
|
UTSW |
12 |
55,755,865 (GRCm39) |
missense |
probably damaging |
1.00 |
|