Other mutations in this stock |
Total: 91 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
0610040J01Rik |
T |
C |
5: 64,056,011 (GRCm39) |
V249A |
possibly damaging |
Het |
9930111J21Rik2 |
C |
G |
11: 48,910,149 (GRCm39) |
L761F |
probably damaging |
Het |
Abca1 |
G |
A |
4: 53,090,291 (GRCm39) |
T386I |
probably damaging |
Het |
Abca14 |
T |
C |
7: 119,888,764 (GRCm39) |
Y1237H |
probably benign |
Het |
Abi3bp |
C |
T |
16: 56,471,088 (GRCm39) |
R578* |
probably null |
Het |
Abi3bp |
T |
G |
16: 56,433,566 (GRCm39) |
L550R |
probably benign |
Het |
Adamts7 |
A |
T |
9: 90,062,729 (GRCm39) |
K394N |
probably damaging |
Het |
Ahdc1 |
A |
G |
4: 132,793,220 (GRCm39) |
E1487G |
possibly damaging |
Het |
AI987944 |
T |
C |
7: 41,023,950 (GRCm39) |
E343G |
probably damaging |
Het |
Ankrd26 |
T |
A |
6: 118,500,843 (GRCm39) |
H876L |
possibly damaging |
Het |
Atg16l1 |
A |
C |
1: 87,694,737 (GRCm39) |
Q138P |
probably benign |
Het |
Atp1b1 |
G |
T |
1: 164,281,084 (GRCm39) |
T11K |
probably benign |
Het |
Calr3 |
A |
G |
8: 73,188,683 (GRCm39) |
L40S |
probably damaging |
Het |
Ccar1 |
A |
C |
10: 62,581,066 (GRCm39) |
D1119E |
unknown |
Het |
Cdan1 |
C |
A |
2: 120,551,241 (GRCm39) |
C1093F |
probably damaging |
Het |
Cdk12 |
T |
G |
11: 98,101,464 (GRCm39) |
S441A |
unknown |
Het |
Ces4a |
T |
A |
8: 105,872,746 (GRCm39) |
V333E |
probably damaging |
Het |
Cfap61 |
T |
C |
2: 146,056,600 (GRCm39) |
L1193P |
probably damaging |
Het |
Chd2 |
A |
T |
7: 73,128,416 (GRCm39) |
D856E |
probably benign |
Het |
Chil3 |
T |
C |
3: 106,071,562 (GRCm39) |
D34G |
probably benign |
Het |
Cln3 |
T |
A |
7: 126,178,390 (GRCm39) |
H211L |
probably benign |
Het |
Cpa1 |
A |
G |
6: 30,641,818 (GRCm39) |
D214G |
probably damaging |
Het |
Cttnbp2 |
T |
G |
6: 18,408,693 (GRCm39) |
D976A |
probably benign |
Het |
Dcstamp |
T |
A |
15: 39,617,708 (GRCm39) |
V39E |
probably damaging |
Het |
Dicer1 |
C |
T |
12: 104,697,297 (GRCm39) |
V87M |
possibly damaging |
Het |
Duox1 |
A |
G |
2: 122,175,194 (GRCm39) |
T1331A |
probably benign |
Het |
Elapor1 |
C |
T |
3: 108,382,359 (GRCm39) |
G270E |
probably damaging |
Het |
Fam184a |
T |
A |
10: 53,528,530 (GRCm39) |
Q29L |
probably damaging |
Het |
Fcer2a |
T |
C |
8: 3,738,557 (GRCm39) |
E60G |
possibly damaging |
Het |
Flnc |
C |
T |
6: 29,459,507 (GRCm39) |
P2536S |
probably damaging |
Het |
Fnbp1l |
A |
T |
3: 122,340,611 (GRCm39) |
M463K |
probably benign |
Het |
Garem2 |
A |
G |
5: 30,319,762 (GRCm39) |
D408G |
probably benign |
Het |
Gm6370 |
T |
A |
5: 146,430,539 (GRCm39) |
D241E |
probably benign |
Het |
Gpc3 |
T |
A |
X: 51,486,083 (GRCm39) |
I344F |
probably damaging |
Het |
Gtf2e1 |
T |
A |
16: 37,331,904 (GRCm39) |
E390D |
possibly damaging |
Het |
Hmgcs2 |
T |
A |
3: 98,198,499 (GRCm39) |
I134N |
probably damaging |
Het |
Il15ra |
T |
A |
2: 11,723,155 (GRCm39) |
|
probably null |
Het |
Ints8 |
A |
T |
4: 11,225,712 (GRCm39) |
M615K |
possibly damaging |
Het |
Irak1 |
G |
A |
X: 73,060,744 (GRCm39) |
T193I |
probably damaging |
Het |
Jmjd1c |
A |
G |
10: 67,075,242 (GRCm39) |
|
probably null |
Het |
Knstrn |
T |
A |
2: 118,661,456 (GRCm39) |
|
probably null |
Het |
Letm1 |
C |
A |
5: 33,926,830 (GRCm39) |
V156L |
possibly damaging |
Het |
Lrrc24 |
G |
A |
15: 76,607,111 (GRCm39) |
P95L |
probably damaging |
Het |
Map2k2 |
T |
C |
10: 80,955,213 (GRCm39) |
S14P |
probably damaging |
Het |
Me3 |
T |
C |
7: 89,499,589 (GRCm39) |
Y535H |
probably damaging |
Het |
Nfatc2ip |
T |
C |
7: 125,990,467 (GRCm39) |
E178G |
probably benign |
Het |
Nop56 |
T |
A |
2: 130,119,488 (GRCm39) |
I51N |
probably damaging |
Het |
Ntn4 |
C |
T |
10: 93,543,215 (GRCm39) |
R314W |
probably damaging |
Het |
Nudt5 |
A |
T |
2: 5,860,794 (GRCm39) |
I22F |
possibly damaging |
Het |
Or10a2 |
T |
A |
7: 106,673,523 (GRCm39) |
W163R |
probably damaging |
Het |
Or2m12 |
C |
T |
16: 19,105,047 (GRCm39) |
A149T |
probably benign |
Het |
Or4p23 |
C |
G |
2: 88,576,953 (GRCm39) |
G93A |
probably benign |
Het |
Pbrm1 |
A |
G |
14: 30,754,406 (GRCm39) |
D142G |
possibly damaging |
Het |
Pdcl |
A |
T |
2: 37,242,056 (GRCm39) |
N231K |
probably benign |
Het |
Pdlim2 |
C |
T |
14: 70,402,228 (GRCm39) |
R296H |
probably damaging |
Het |
Pid1 |
T |
A |
1: 84,016,159 (GRCm39) |
I69F |
probably damaging |
Het |
Pkhd1 |
A |
G |
1: 20,607,584 (GRCm39) |
S1091P |
probably benign |
Het |
Plcb4 |
T |
C |
2: 135,844,514 (GRCm39) |
I144T |
probably benign |
Het |
Plxnd1 |
T |
C |
6: 115,939,725 (GRCm39) |
N1418S |
probably benign |
Het |
Pmm1 |
T |
C |
15: 81,840,601 (GRCm39) |
T82A |
probably benign |
Het |
Prrc2b |
C |
A |
2: 32,113,476 (GRCm39) |
Q1970K |
probably damaging |
Het |
Ptprz1 |
C |
T |
6: 23,000,649 (GRCm39) |
T913M |
possibly damaging |
Het |
Rbm8a2 |
T |
C |
1: 175,806,420 (GRCm39) |
E19G |
possibly damaging |
Het |
Rgs3 |
T |
C |
4: 62,608,741 (GRCm39) |
S336P |
probably damaging |
Het |
Saxo5 |
A |
T |
8: 3,529,028 (GRCm39) |
D201V |
probably benign |
Het |
Serpina11 |
G |
T |
12: 103,952,233 (GRCm39) |
T179K |
probably damaging |
Het |
Serpina1f |
T |
C |
12: 103,659,655 (GRCm39) |
N209S |
possibly damaging |
Het |
Serpinf2 |
G |
A |
11: 75,327,588 (GRCm39) |
T159I |
probably benign |
Het |
Slc19a1 |
T |
C |
10: 76,877,758 (GRCm39) |
C98R |
possibly damaging |
Het |
Slc22a20 |
A |
T |
19: 6,021,553 (GRCm39) |
I483N |
possibly damaging |
Het |
Spata31d1d |
A |
G |
13: 59,879,435 (GRCm39) |
C34R |
possibly damaging |
Het |
Stoml2 |
G |
T |
4: 43,030,243 (GRCm39) |
Y119* |
probably null |
Het |
Susd1 |
A |
G |
4: 59,349,843 (GRCm39) |
L531P |
possibly damaging |
Het |
Timd5 |
A |
G |
11: 46,419,394 (GRCm39) |
N70S |
probably benign |
Het |
Tln1 |
C |
T |
4: 43,553,083 (GRCm39) |
|
probably null |
Het |
Tmem39b |
A |
C |
4: 129,587,716 (GRCm39) |
S32A |
probably benign |
Het |
Tmx3 |
T |
C |
18: 90,546,037 (GRCm39) |
F206S |
probably damaging |
Het |
Tnfsf14 |
T |
C |
17: 57,497,638 (GRCm39) |
D198G |
possibly damaging |
Het |
Trappc10 |
A |
G |
10: 78,034,876 (GRCm39) |
|
probably null |
Het |
Tssk2 |
A |
G |
16: 17,716,603 (GRCm39) |
D2G |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,601,985 (GRCm39) |
N18559S |
possibly damaging |
Het |
Ube3b |
G |
A |
5: 114,527,135 (GRCm39) |
V118M |
probably damaging |
Het |
Vmn1r23 |
T |
C |
6: 57,903,604 (GRCm39) |
D58G |
probably benign |
Het |
Vmn2r53 |
T |
A |
7: 12,335,366 (GRCm39) |
Y98F |
probably damaging |
Het |
Vmn2r58 |
T |
A |
7: 41,513,594 (GRCm39) |
N350Y |
probably benign |
Het |
Vmn2r82 |
A |
T |
10: 79,192,519 (GRCm39) |
H32L |
probably benign |
Het |
Wsb1 |
T |
C |
11: 79,131,212 (GRCm39) |
I395V |
probably benign |
Het |
Zbtb47 |
A |
G |
9: 121,591,703 (GRCm39) |
T8A |
possibly damaging |
Het |
Zfat |
T |
C |
15: 68,051,709 (GRCm39) |
D695G |
probably benign |
Het |
Zfp358 |
G |
T |
8: 3,546,995 (GRCm39) |
V526F |
possibly damaging |
Het |
Zmat1 |
A |
G |
X: 133,873,861 (GRCm39) |
L476P |
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 |
|
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 |
|