Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700097O09Rik |
A |
T |
12: 55,106,295 (GRCm39) |
S143T |
probably benign |
Het |
9030624G23Rik |
A |
T |
12: 24,094,724 (GRCm39) |
M149K |
unknown |
Het |
Aadacl4fm4 |
A |
T |
4: 144,396,913 (GRCm39) |
I273K |
possibly damaging |
Het |
Agpat3 |
T |
A |
10: 78,119,034 (GRCm39) |
I187F |
probably benign |
Het |
Ahcyl1 |
C |
T |
3: 107,576,467 (GRCm39) |
A332T |
probably damaging |
Het |
Aldh3b3 |
A |
G |
19: 4,014,871 (GRCm39) |
I123V |
possibly damaging |
Het |
Ap5z1 |
T |
A |
5: 142,456,313 (GRCm39) |
|
probably null |
Het |
Apob |
A |
T |
12: 8,061,933 (GRCm39) |
I3472F |
probably benign |
Het |
Arhgef33 |
C |
T |
17: 80,680,914 (GRCm39) |
P685S |
probably benign |
Het |
Arhgef4 |
T |
C |
1: 34,845,478 (GRCm39) |
I130T |
probably damaging |
Het |
Arnt2 |
A |
T |
7: 83,954,406 (GRCm39) |
F263I |
probably benign |
Het |
Bbof1 |
A |
G |
12: 84,466,763 (GRCm39) |
R177G |
probably damaging |
Het |
Bbs2 |
C |
A |
8: 94,807,764 (GRCm39) |
G372W |
probably damaging |
Het |
Blmh |
T |
A |
11: 76,836,721 (GRCm39) |
|
probably null |
Het |
Ccdc30 |
A |
T |
4: 119,209,910 (GRCm39) |
|
probably null |
Het |
Cdca7l |
G |
T |
12: 117,837,467 (GRCm39) |
L219F |
probably damaging |
Het |
Cenpu |
C |
A |
8: 47,015,499 (GRCm39) |
A138E |
probably benign |
Het |
Cfap65 |
T |
A |
1: 74,972,321 (GRCm39) |
T13S |
probably benign |
Het |
Clasp2 |
A |
G |
9: 113,733,016 (GRCm39) |
M951V |
probably benign |
Het |
Clca4a |
A |
G |
3: 144,674,166 (GRCm39) |
S190P |
probably benign |
Het |
Clcn4 |
A |
G |
7: 7,298,167 (GRCm39) |
V74A |
probably benign |
Het |
Cntln |
C |
T |
4: 84,981,561 (GRCm39) |
T913M |
possibly damaging |
Het |
Cntnap4 |
T |
A |
8: 113,478,829 (GRCm39) |
V185E |
probably damaging |
Het |
Col26a1 |
C |
T |
5: 136,777,031 (GRCm39) |
|
probably null |
Het |
Ctcf |
A |
T |
8: 106,390,690 (GRCm39) |
Q99L |
possibly damaging |
Het |
Dgke |
T |
C |
11: 88,931,682 (GRCm39) |
Q524R |
probably damaging |
Het |
Dhrs7 |
A |
T |
12: 72,699,234 (GRCm39) |
|
probably null |
Het |
Dnah7b |
T |
C |
1: 46,289,110 (GRCm39) |
Y2969H |
probably damaging |
Het |
Dync1h1 |
T |
G |
12: 110,582,891 (GRCm39) |
I358S |
probably damaging |
Het |
Efcab3 |
A |
C |
11: 105,008,150 (GRCm39) |
D410A |
probably benign |
Het |
Emilin2 |
T |
C |
17: 71,580,908 (GRCm39) |
D606G |
probably benign |
Het |
Ermard |
C |
T |
17: 15,283,875 (GRCm39) |
T622I |
possibly damaging |
Het |
Exo1 |
A |
G |
1: 175,728,562 (GRCm39) |
D542G |
probably benign |
Het |
Fgd5 |
A |
T |
6: 91,964,262 (GRCm39) |
D165V |
probably benign |
Het |
Gdap1 |
T |
C |
1: 17,231,368 (GRCm39) |
W238R |
probably damaging |
Het |
Gm11096 |
T |
G |
17: 81,749,328 (GRCm39) |
I7M |
unknown |
Het |
Gm40460 |
ACCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG |
ACCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG |
7: 141,794,450 (GRCm39) |
|
probably benign |
Het |
Gmppb |
A |
T |
9: 107,927,770 (GRCm39) |
M175L |
probably benign |
Het |
Gorasp2 |
G |
A |
2: 70,514,442 (GRCm39) |
S273N |
probably benign |
Het |
Gtf3c1 |
T |
C |
7: 125,271,994 (GRCm39) |
M642V |
possibly damaging |
Het |
Hmx2 |
T |
A |
7: 131,157,600 (GRCm39) |
L238Q |
probably damaging |
Het |
Kif13b |
A |
G |
14: 64,973,598 (GRCm39) |
D316G |
probably damaging |
Het |
Kmt2c |
A |
G |
5: 25,578,174 (GRCm39) |
S701P |
possibly damaging |
Het |
Lama4 |
T |
A |
10: 38,964,325 (GRCm39) |
N1332K |
probably damaging |
Het |
Lrp2 |
T |
C |
2: 69,288,823 (GRCm39) |
D3681G |
probably damaging |
Het |
Maml3 |
G |
T |
3: 51,605,143 (GRCm39) |
P722Q |
probably damaging |
Het |
Mier2 |
C |
A |
10: 79,377,719 (GRCm39) |
|
probably benign |
Het |
Ms4a15 |
A |
T |
19: 10,956,694 (GRCm39) |
|
probably null |
Het |
Msh5 |
T |
C |
17: 35,263,355 (GRCm39) |
M158V |
probably benign |
Het |
Nova2 |
A |
T |
7: 18,676,270 (GRCm39) |
K136I |
|
Het |
Npm1 |
A |
T |
11: 33,106,001 (GRCm39) |
|
probably null |
Het |
Nr4a3 |
T |
A |
4: 48,051,390 (GRCm39) |
M48K |
probably benign |
Het |
Nrap |
T |
G |
19: 56,342,584 (GRCm39) |
T806P |
probably benign |
Het |
Ntf3 |
G |
A |
6: 126,079,203 (GRCm39) |
T101M |
probably benign |
Het |
Or2aj4 |
G |
A |
16: 19,385,472 (GRCm39) |
R54* |
probably null |
Het |
Paxbp1 |
T |
A |
16: 90,822,166 (GRCm39) |
D648V |
probably damaging |
Het |
Pcdhb18 |
T |
A |
18: 37,623,520 (GRCm39) |
D283E |
probably benign |
Het |
Phrf1 |
C |
A |
7: 140,839,288 (GRCm39) |
Q828K |
unknown |
Het |
Pigq |
A |
T |
17: 26,156,299 (GRCm39) |
I43N |
probably benign |
Het |
Pou6f2 |
G |
T |
13: 18,300,033 (GRCm39) |
T542K |
|
Het |
Ppfibp2 |
T |
A |
7: 107,320,524 (GRCm39) |
|
probably null |
Het |
Rab1b |
A |
T |
19: 5,150,524 (GRCm39) |
M163K |
probably benign |
Het |
Reck |
T |
C |
4: 43,890,970 (GRCm39) |
V36A |
probably benign |
Het |
Resp18 |
C |
T |
1: 75,254,846 (GRCm39) |
D36N |
probably null |
Het |
Rint1 |
A |
C |
5: 24,005,720 (GRCm39) |
H134P |
probably damaging |
Het |
Rps19 |
A |
T |
7: 24,587,764 (GRCm39) |
K77M |
possibly damaging |
Het |
Sec24b |
A |
T |
3: 129,789,598 (GRCm39) |
S808T |
probably benign |
Het |
Sema4c |
A |
C |
1: 36,592,199 (GRCm39) |
V216G |
probably damaging |
Het |
Septin10 |
T |
A |
10: 59,016,871 (GRCm39) |
T218S |
probably benign |
Het |
Septin3 |
A |
T |
15: 82,170,020 (GRCm39) |
H182L |
probably benign |
Het |
Sipa1 |
A |
G |
19: 5,702,690 (GRCm39) |
S836P |
probably benign |
Het |
Slc9a5 |
A |
G |
8: 106,089,998 (GRCm39) |
K652R |
probably damaging |
Het |
Slco5a1 |
T |
A |
1: 13,059,927 (GRCm39) |
I265F |
possibly damaging |
Het |
Snapc5 |
T |
A |
9: 64,086,614 (GRCm39) |
M1K |
probably null |
Het |
Snx5 |
T |
A |
2: 144,095,740 (GRCm39) |
D307V |
possibly damaging |
Het |
Srebf2 |
A |
T |
15: 82,061,441 (GRCm39) |
M381L |
probably benign |
Het |
Ssh2 |
G |
C |
11: 77,345,452 (GRCm39) |
E1146Q |
probably benign |
Het |
Suco |
A |
T |
1: 161,672,937 (GRCm39) |
|
probably null |
Het |
Tanc2 |
T |
A |
11: 105,812,651 (GRCm39) |
L1365Q |
probably damaging |
Het |
Tas1r3 |
A |
G |
4: 155,947,005 (GRCm39) |
L200P |
probably damaging |
Het |
Thbs2 |
T |
G |
17: 14,896,483 (GRCm39) |
D802A |
probably damaging |
Het |
Trav3-1 |
G |
A |
14: 52,818,550 (GRCm39) |
V75M |
probably benign |
Het |
Trim9 |
G |
A |
12: 70,301,961 (GRCm39) |
P559L |
probably benign |
Het |
Trpc6 |
G |
A |
9: 8,655,219 (GRCm39) |
G683D |
probably damaging |
Het |
Unc5b |
C |
A |
10: 60,615,509 (GRCm39) |
V164L |
possibly damaging |
Het |
Usf3 |
A |
T |
16: 44,036,565 (GRCm39) |
R348S |
possibly damaging |
Het |
Vmn1r236 |
T |
C |
17: 21,507,728 (GRCm39) |
V282A |
possibly damaging |
Het |
Vmn2r1 |
A |
G |
3: 63,997,130 (GRCm39) |
E262G |
possibly damaging |
Het |
Xirp2 |
A |
G |
2: 67,339,841 (GRCm39) |
E694G |
probably damaging |
Het |
Xpo4 |
T |
A |
14: 57,840,048 (GRCm39) |
H572L |
probably benign |
Het |
Zfhx4 |
A |
G |
3: 5,307,259 (GRCm39) |
T162A |
probably benign |
Het |
Zfp110 |
T |
A |
7: 12,571,020 (GRCm39) |
H59Q |
possibly damaging |
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 |
R0611:Ralgapa1
|
UTSW |
12 |
55,842,483 (GRCm39) |
missense |
probably damaging |
0.99 |
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 |
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 |
|