Other mutations in this stock |
Total: 100 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adat3 |
C |
T |
10: 80,442,234 (GRCm39) |
A24V |
probably benign |
Het |
Agbl1 |
A |
T |
7: 76,239,241 (GRCm39) |
E832D |
unknown |
Het |
Akap8l |
G |
A |
17: 32,554,545 (GRCm39) |
S347L |
probably benign |
Het |
Ankmy1 |
G |
T |
1: 92,804,379 (GRCm39) |
A868E |
probably damaging |
Het |
Ankrd49 |
A |
T |
9: 14,693,837 (GRCm39) |
L110* |
probably null |
Het |
Aoc3 |
A |
G |
11: 101,228,229 (GRCm39) |
T679A |
probably damaging |
Het |
Ap1s3 |
A |
G |
1: 79,592,018 (GRCm39) |
Y111H |
probably damaging |
Het |
Arnt |
T |
A |
3: 95,402,659 (GRCm39) |
N777K |
probably damaging |
Het |
Atp4b |
A |
T |
8: 13,436,732 (GRCm39) |
M260K |
probably benign |
Het |
Bcl2l15 |
A |
T |
3: 103,740,729 (GRCm39) |
D65V |
probably damaging |
Het |
Bicdl1 |
G |
T |
5: 115,801,845 (GRCm39) |
S340* |
probably null |
Het |
Ccdc15 |
T |
C |
9: 37,226,574 (GRCm39) |
R467G |
probably benign |
Het |
Ccdc68 |
T |
A |
18: 70,102,084 (GRCm39) |
M327K |
possibly damaging |
Het |
Ccdc83 |
T |
C |
7: 89,873,138 (GRCm39) |
T406A |
probably benign |
Het |
Ccnf |
A |
T |
17: 24,468,232 (GRCm39) |
V55D |
probably damaging |
Het |
Cdcp3 |
C |
A |
7: 130,830,562 (GRCm39) |
P332Q |
probably damaging |
Het |
Cldn12 |
A |
G |
5: 5,558,008 (GRCm39) |
F140L |
probably benign |
Het |
Copb1 |
A |
C |
7: 113,844,720 (GRCm39) |
I213S |
possibly damaging |
Het |
Cps1 |
G |
A |
1: 67,179,016 (GRCm39) |
G76D |
probably damaging |
Het |
Ctrc |
A |
G |
4: 141,567,627 (GRCm39) |
W159R |
probably damaging |
Het |
Cul4a |
C |
T |
8: 13,190,279 (GRCm39) |
T572M |
possibly damaging |
Het |
Cyp2c40 |
A |
T |
19: 39,796,050 (GRCm39) |
Y109* |
probably null |
Het |
Dcc |
A |
G |
18: 71,553,317 (GRCm39) |
Y780H |
probably benign |
Het |
Dctn1 |
C |
T |
6: 83,166,887 (GRCm39) |
A283V |
possibly damaging |
Het |
Dio1 |
T |
C |
4: 107,154,874 (GRCm39) |
D134G |
probably benign |
Het |
Dlg5 |
A |
T |
14: 24,198,390 (GRCm39) |
D1514E |
probably benign |
Het |
Dlg5 |
A |
T |
14: 24,227,907 (GRCm39) |
L338Q |
probably damaging |
Het |
Dlgap2 |
A |
T |
8: 14,879,952 (GRCm39) |
K767N |
probably damaging |
Het |
Dst |
A |
T |
1: 34,313,270 (GRCm39) |
I4346F |
probably benign |
Het |
Dzip1l |
T |
C |
9: 99,543,065 (GRCm39) |
F507L |
probably benign |
Het |
Erich2 |
A |
T |
2: 70,362,109 (GRCm39) |
D300V |
probably damaging |
Het |
Fam114a2 |
C |
T |
11: 57,404,515 (GRCm39) |
G83D |
probably damaging |
Het |
Fam131a |
C |
T |
16: 20,520,444 (GRCm39) |
A299V |
probably benign |
Het |
Fbln2 |
A |
G |
6: 91,247,143 (GRCm39) |
|
probably null |
Het |
Fbn2 |
T |
C |
18: 58,204,912 (GRCm39) |
D1177G |
possibly damaging |
Het |
Fbxl6 |
T |
C |
15: 76,422,113 (GRCm39) |
|
probably null |
Het |
Frem3 |
A |
T |
8: 81,339,965 (GRCm39) |
I753F |
probably damaging |
Het |
Gfra1 |
A |
G |
19: 58,288,744 (GRCm39) |
S234P |
probably damaging |
Het |
Gtse1 |
T |
A |
15: 85,752,901 (GRCm39) |
S339T |
probably benign |
Het |
Hdgfl3 |
T |
C |
7: 81,550,106 (GRCm39) |
N76S |
probably benign |
Het |
Herc6 |
A |
G |
6: 57,558,089 (GRCm39) |
E23G |
probably benign |
Het |
Hid1 |
T |
A |
11: 115,245,545 (GRCm39) |
H420L |
probably damaging |
Het |
Igsf21 |
G |
A |
4: 139,755,049 (GRCm39) |
T440I |
probably benign |
Het |
Ikzf4 |
T |
A |
10: 128,468,451 (GRCm39) |
H676L |
unknown |
Het |
Il18r1 |
A |
G |
1: 40,520,140 (GRCm39) |
E177G |
probably benign |
Het |
Iqch |
A |
G |
9: 63,415,599 (GRCm39) |
Y558H |
possibly damaging |
Het |
Kif11 |
A |
T |
19: 37,399,072 (GRCm39) |
N752I |
possibly damaging |
Het |
Kntc1 |
T |
A |
5: 123,925,019 (GRCm39) |
C1111S |
possibly damaging |
Het |
Krtap9-5 |
A |
G |
11: 99,839,800 (GRCm39) |
K167R |
unknown |
Het |
Lgalsl2 |
C |
T |
7: 5,362,440 (GRCm39) |
R24C |
probably benign |
Het |
Lipe |
G |
T |
7: 25,080,036 (GRCm39) |
T704K |
probably benign |
Het |
Lrrc32 |
A |
T |
7: 98,147,414 (GRCm39) |
I65F |
possibly damaging |
Het |
Mogs |
C |
T |
6: 83,093,188 (GRCm39) |
H179Y |
probably damaging |
Het |
Mtnr1b |
A |
T |
9: 15,774,590 (GRCm39) |
Y156* |
probably null |
Het |
Mtus1 |
T |
C |
8: 41,537,590 (GRCm39) |
H42R |
probably benign |
Het |
Mx2 |
T |
A |
16: 97,346,918 (GRCm39) |
D128E |
probably benign |
Het |
Myof |
A |
T |
19: 37,939,939 (GRCm39) |
L829* |
probably null |
Het |
Naip6 |
T |
C |
13: 100,420,359 (GRCm39) |
K1304E |
probably benign |
Het |
Neo1 |
A |
C |
9: 58,791,826 (GRCm39) |
S1307R |
probably benign |
Het |
Nipbl |
A |
T |
15: 8,359,779 (GRCm39) |
D1475E |
probably benign |
Het |
Nlrp9b |
T |
A |
7: 19,757,875 (GRCm39) |
F371I |
probably damaging |
Het |
Nrip1 |
A |
T |
16: 76,088,338 (GRCm39) |
M1073K |
probably damaging |
Het |
Obox6 |
T |
C |
7: 15,567,863 (GRCm39) |
N195D |
probably damaging |
Het |
Or13a18 |
T |
A |
7: 140,190,091 (GRCm39) |
I4K |
probably benign |
Het |
Or1j18 |
T |
A |
2: 36,624,650 (GRCm39) |
F106I |
probably benign |
Het |
Or5ac24 |
A |
T |
16: 59,165,687 (GRCm39) |
C126S |
probably damaging |
Het |
Or5b99 |
C |
T |
19: 12,976,922 (GRCm39) |
H191Y |
probably benign |
Het |
Or5p64 |
C |
A |
7: 107,855,045 (GRCm39) |
C100F |
probably damaging |
Het |
Pax7 |
T |
C |
4: 139,511,880 (GRCm39) |
K232E |
probably benign |
Het |
Phldb3 |
C |
T |
7: 24,310,689 (GRCm39) |
|
probably benign |
Het |
Pkd1l1 |
C |
A |
11: 8,915,148 (GRCm39) |
V131L |
|
Het |
Ppp2r5a |
A |
G |
1: 191,128,532 (GRCm39) |
S28P |
probably benign |
Het |
Prl8a1 |
A |
G |
13: 27,758,068 (GRCm39) |
S214P |
probably damaging |
Het |
Prmt2 |
A |
T |
10: 76,056,838 (GRCm39) |
C228* |
probably null |
Het |
Prpf8 |
C |
T |
11: 75,399,738 (GRCm39) |
R2266* |
probably null |
Het |
Rabl6 |
A |
G |
2: 25,474,153 (GRCm39) |
S648P |
unknown |
Het |
Ralgapb |
T |
A |
2: 158,285,275 (GRCm39) |
D591E |
probably benign |
Het |
Rprd1a |
A |
G |
18: 24,639,889 (GRCm39) |
|
probably null |
Het |
Rsu1 |
T |
C |
2: 13,221,686 (GRCm39) |
R165G |
probably damaging |
Het |
Samd8 |
A |
G |
14: 21,842,491 (GRCm39) |
E334G |
probably benign |
Het |
Scn9a |
T |
A |
2: 66,364,561 (GRCm39) |
Q804L |
probably damaging |
Het |
Sez6 |
A |
G |
11: 77,864,711 (GRCm39) |
D557G |
probably benign |
Het |
Sgsm1 |
A |
T |
5: 113,427,501 (GRCm39) |
|
probably null |
Het |
Slc17a3 |
T |
A |
13: 24,039,832 (GRCm39) |
M290K |
|
Het |
Snd1 |
T |
A |
6: 28,531,449 (GRCm39) |
V330E |
probably benign |
Het |
Tceanc2 |
T |
C |
4: 107,022,852 (GRCm39) |
K45R |
probably damaging |
Het |
Tg |
A |
T |
15: 66,568,437 (GRCm39) |
I1375F |
probably benign |
Het |
Tmem116 |
T |
A |
5: 121,633,124 (GRCm39) |
I357K |
|
Het |
Tmem39a |
G |
T |
16: 38,408,658 (GRCm39) |
R407L |
possibly damaging |
Het |
Tmem74 |
A |
T |
15: 43,730,761 (GRCm39) |
M94K |
probably benign |
Het |
Tpp1 |
C |
T |
7: 105,398,751 (GRCm39) |
C226Y |
probably damaging |
Het |
Trbv21 |
T |
C |
6: 41,179,861 (GRCm39) |
I59T |
not run |
Het |
Trim11 |
A |
G |
11: 58,869,463 (GRCm39) |
D133G |
probably benign |
Het |
Uaca |
G |
A |
9: 60,753,282 (GRCm39) |
V76I |
probably damaging |
Het |
Ugt2a3 |
A |
G |
5: 87,475,539 (GRCm39) |
|
probably null |
Het |
Vmn2r104 |
G |
T |
17: 20,249,737 (GRCm39) |
H845N |
probably benign |
Het |
Wdr24 |
T |
C |
17: 26,045,101 (GRCm39) |
Y279H |
probably damaging |
Het |
Zbtb46 |
A |
G |
2: 181,065,512 (GRCm39) |
S213P |
probably benign |
Het |
Zdhhc13 |
C |
A |
7: 48,461,103 (GRCm39) |
Y346* |
probably null |
Het |
Zfp280b |
A |
T |
10: 75,875,075 (GRCm39) |
H318L |
probably 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 |
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 |
|