Other mutations in this stock |
Total: 87 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2410002F23Rik |
G |
T |
7: 43,900,435 (GRCm39) |
R113S |
probably benign |
Het |
Ackr2 |
A |
T |
9: 121,738,026 (GRCm39) |
I134F |
probably damaging |
Het |
Actr3b |
T |
A |
5: 26,036,709 (GRCm39) |
I174N |
possibly damaging |
Het |
Akap9 |
T |
A |
5: 4,094,847 (GRCm39) |
S2214T |
possibly damaging |
Het |
Arhgef12 |
C |
A |
9: 42,890,768 (GRCm39) |
R986L |
possibly damaging |
Het |
Brap |
G |
T |
5: 121,801,422 (GRCm39) |
S59I |
possibly damaging |
Het |
Btnl1 |
C |
T |
17: 34,598,578 (GRCm39) |
H65Y |
probably damaging |
Het |
C1s2 |
T |
C |
6: 124,612,004 (GRCm39) |
T121A |
probably damaging |
Het |
Capn1 |
T |
A |
19: 6,064,388 (GRCm39) |
Y37F |
probably benign |
Het |
Ccdc39 |
T |
C |
3: 33,869,650 (GRCm39) |
K726E |
probably damaging |
Het |
Cd300lb |
G |
A |
11: 114,816,865 (GRCm39) |
S195F |
probably damaging |
Het |
Cenpf |
T |
C |
1: 189,411,264 (GRCm39) |
K307E |
probably damaging |
Het |
Chodl |
A |
C |
16: 78,738,251 (GRCm39) |
N73T |
possibly damaging |
Het |
Cimip2c |
G |
A |
5: 30,637,851 (GRCm39) |
G66E |
probably damaging |
Het |
Crnn |
A |
T |
3: 93,055,747 (GRCm39) |
M178L |
probably benign |
Het |
Cyp4a12b |
A |
G |
4: 115,290,110 (GRCm39) |
D221G |
probably damaging |
Het |
Dipk2a |
A |
T |
9: 94,406,498 (GRCm39) |
I303N |
probably damaging |
Het |
Dmxl2 |
A |
G |
9: 54,301,097 (GRCm39) |
V2338A |
probably benign |
Het |
Dnah9 |
G |
T |
11: 65,928,411 (GRCm39) |
P2086Q |
probably damaging |
Het |
Dsg2 |
A |
G |
18: 20,725,346 (GRCm39) |
I486V |
probably benign |
Het |
E2f8 |
A |
G |
7: 48,524,855 (GRCm39) |
S265P |
probably damaging |
Het |
Eif1b |
A |
G |
9: 120,323,296 (GRCm39) |
D52G |
probably benign |
Het |
Etl4 |
A |
T |
2: 20,790,153 (GRCm39) |
T602S |
probably benign |
Het |
Exoc3l2 |
A |
T |
7: 19,223,059 (GRCm39) |
|
probably benign |
Het |
Fbxl6 |
C |
A |
15: 76,421,173 (GRCm39) |
V297F |
probably damaging |
Het |
Fgr |
T |
A |
4: 132,725,786 (GRCm39) |
N398K |
probably benign |
Het |
G3bp1 |
A |
G |
11: 55,379,986 (GRCm39) |
R107G |
probably damaging |
Het |
Gp2 |
A |
T |
7: 119,052,155 (GRCm39) |
N186K |
probably benign |
Het |
Hbs1l |
T |
A |
10: 21,217,831 (GRCm39) |
L249* |
probably null |
Het |
Hmgcs2 |
T |
A |
3: 98,204,337 (GRCm39) |
L246* |
probably null |
Het |
Hsp90ab1 |
G |
T |
17: 45,880,254 (GRCm39) |
H96Q |
probably benign |
Het |
Ibtk |
C |
T |
9: 85,588,603 (GRCm39) |
V1078I |
probably benign |
Het |
Ltn1 |
T |
C |
16: 87,212,530 (GRCm39) |
D677G |
probably benign |
Het |
Lyst |
C |
T |
13: 13,887,405 (GRCm39) |
T3078I |
possibly damaging |
Het |
Mamdc4 |
A |
G |
2: 25,459,402 (GRCm39) |
F199S |
probably damaging |
Het |
Megf6 |
G |
T |
4: 154,261,578 (GRCm39) |
V68L |
probably benign |
Het |
Mki67 |
G |
A |
7: 135,299,592 (GRCm39) |
T1814I |
probably damaging |
Het |
Msantd5l |
T |
A |
11: 51,145,264 (GRCm39) |
I108F |
possibly damaging |
Het |
Mttp |
A |
T |
3: 137,800,763 (GRCm39) |
F766I |
probably benign |
Het |
Nbl1 |
T |
A |
4: 138,810,915 (GRCm39) |
|
probably null |
Het |
Nmrk1 |
T |
A |
19: 18,618,802 (GRCm39) |
L118Q |
probably damaging |
Het |
Nopchap1 |
C |
T |
10: 83,201,656 (GRCm39) |
S143L |
probably damaging |
Het |
Oog3 |
A |
T |
4: 143,886,082 (GRCm39) |
L172H |
probably damaging |
Het |
Or2y11 |
T |
G |
11: 49,443,260 (GRCm39) |
S229A |
probably damaging |
Het |
Osbpl1a |
T |
G |
18: 12,892,457 (GRCm39) |
Q332P |
probably damaging |
Het |
Pik3cg |
A |
G |
12: 32,243,709 (GRCm39) |
F921L |
possibly damaging |
Het |
Plch2 |
T |
C |
4: 155,069,054 (GRCm39) |
S1086G |
possibly damaging |
Het |
Plekha5 |
A |
G |
6: 140,369,942 (GRCm39) |
T18A |
possibly damaging |
Het |
Pogz |
T |
A |
3: 94,786,276 (GRCm39) |
S955T |
probably benign |
Het |
Pot1b |
A |
T |
17: 55,960,413 (GRCm39) |
I639N |
probably benign |
Het |
Prkdc |
T |
C |
16: 15,505,254 (GRCm39) |
I852T |
probably benign |
Het |
Prps1l1 |
A |
G |
12: 35,035,521 (GRCm39) |
K212R |
probably benign |
Het |
Ptpn5 |
A |
G |
7: 46,735,807 (GRCm39) |
Y304H |
probably damaging |
Het |
Rgs22 |
A |
T |
15: 36,099,880 (GRCm39) |
Y278* |
probably null |
Het |
Rif1 |
GCCACCA |
GCCA |
2: 52,000,336 (GRCm39) |
|
probably benign |
Het |
Rnf213 |
T |
A |
11: 119,333,489 (GRCm39) |
Y2899* |
probably null |
Het |
Rttn |
C |
T |
18: 89,004,197 (GRCm39) |
T397I |
possibly damaging |
Het |
Sacs |
G |
T |
14: 61,410,902 (GRCm39) |
|
probably null |
Het |
Sbf2 |
G |
T |
7: 110,060,419 (GRCm39) |
Q182K |
probably damaging |
Het |
Sec14l5 |
C |
T |
16: 4,984,968 (GRCm39) |
R105* |
probably null |
Het |
Sh2b1 |
A |
T |
7: 126,071,536 (GRCm39) |
D216E |
possibly damaging |
Het |
Sh3gl3 |
A |
G |
7: 81,920,008 (GRCm39) |
N72S |
possibly damaging |
Het |
Slc12a1 |
A |
T |
2: 125,015,619 (GRCm39) |
I391F |
probably damaging |
Het |
Slc36a2 |
G |
A |
11: 55,072,381 (GRCm39) |
A77V |
probably damaging |
Het |
Smc2 |
A |
T |
4: 52,474,987 (GRCm39) |
I888L |
probably benign |
Het |
Smoc1 |
C |
T |
12: 81,197,450 (GRCm39) |
T194M |
probably damaging |
Het |
Sorcs1 |
C |
T |
19: 50,666,630 (GRCm39) |
G93R |
probably benign |
Het |
Sox30 |
T |
G |
11: 45,882,595 (GRCm39) |
F542V |
probably damaging |
Het |
Svep1 |
A |
G |
4: 58,206,030 (GRCm39) |
V116A |
possibly damaging |
Het |
Synj2 |
A |
G |
17: 6,063,966 (GRCm39) |
D330G |
probably benign |
Het |
Tenm3 |
A |
C |
8: 48,796,384 (GRCm39) |
S202A |
possibly damaging |
Het |
Tg |
C |
T |
15: 66,601,443 (GRCm39) |
T151I |
probably benign |
Het |
Tnfaip2 |
A |
G |
12: 111,414,527 (GRCm39) |
E361G |
probably damaging |
Het |
Tnk1 |
A |
T |
11: 69,746,009 (GRCm39) |
D305E |
probably damaging |
Het |
Tpp1 |
A |
G |
7: 105,399,177 (GRCm39) |
L133P |
probably damaging |
Het |
Trappc1 |
T |
A |
11: 69,215,243 (GRCm39) |
M41K |
probably damaging |
Het |
Tsen54 |
A |
G |
11: 115,706,549 (GRCm39) |
D9G |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,804,598 (GRCm39) |
I225F |
probably damaging |
Het |
Ube4b |
T |
C |
4: 149,457,298 (GRCm39) |
K313R |
probably benign |
Het |
Vps50 |
T |
C |
6: 3,555,379 (GRCm39) |
V425A |
probably damaging |
Het |
Wbp2 |
A |
T |
11: 115,971,445 (GRCm39) |
Y153* |
probably null |
Het |
Xrn1 |
A |
G |
9: 95,861,273 (GRCm39) |
S478G |
probably benign |
Het |
Zfp354c |
T |
C |
11: 50,707,969 (GRCm39) |
E77G |
probably benign |
Het |
Zfp462 |
T |
C |
4: 55,008,496 (GRCm39) |
M154T |
probably benign |
Het |
Zfp704 |
A |
G |
3: 9,539,585 (GRCm39) |
V255A |
probably damaging |
Het |
Zfp763 |
G |
T |
17: 33,238,752 (GRCm39) |
A131E |
probably benign |
Het |
Zfp931 |
A |
T |
2: 177,711,651 (GRCm39) |
V32E |
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 |
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 |
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 |
|