Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933407L21Rik |
A |
G |
1: 85,858,972 (GRCm39) |
|
probably benign |
Het |
Ahcy |
T |
C |
2: 154,910,888 (GRCm39) |
N27D |
probably damaging |
Het |
Akap9 |
T |
G |
5: 4,011,013 (GRCm39) |
L572R |
probably damaging |
Het |
Akna |
A |
G |
4: 63,296,850 (GRCm39) |
S909P |
probably damaging |
Het |
Atr |
A |
G |
9: 95,744,845 (GRCm39) |
E54G |
probably benign |
Het |
Baz2b |
A |
G |
2: 59,744,255 (GRCm39) |
S1417P |
probably benign |
Het |
Colgalt2 |
A |
G |
1: 152,276,094 (GRCm39) |
Y69C |
probably damaging |
Het |
Comp |
A |
G |
8: 70,828,711 (GRCm39) |
E181G |
probably damaging |
Het |
Dcaf10 |
T |
A |
4: 45,370,409 (GRCm39) |
S326T |
probably damaging |
Het |
Dscam |
T |
C |
16: 96,631,256 (GRCm39) |
E253G |
probably benign |
Het |
Dysf |
C |
A |
6: 84,074,697 (GRCm39) |
D499E |
probably damaging |
Het |
Epha1 |
G |
T |
6: 42,349,155 (GRCm39) |
T36K |
probably benign |
Het |
Ewsr1 |
A |
T |
11: 5,033,541 (GRCm39) |
D210E |
unknown |
Het |
Fabp3 |
C |
T |
4: 130,206,180 (GRCm39) |
T57I |
probably benign |
Het |
Fndc1 |
T |
A |
17: 7,991,111 (GRCm39) |
R862* |
probably null |
Het |
Gbp8 |
T |
C |
5: 105,178,707 (GRCm39) |
K203E |
possibly damaging |
Het |
Gigyf2 |
T |
A |
1: 87,292,970 (GRCm39) |
L79* |
probably null |
Het |
Gm8220 |
T |
A |
14: 44,523,152 (GRCm39) |
|
probably benign |
Het |
Gm9755 |
A |
T |
8: 67,966,929 (GRCm39) |
|
noncoding transcript |
Het |
Il6 |
T |
C |
5: 30,223,042 (GRCm39) |
Y120H |
probably damaging |
Het |
Kcnma1 |
T |
C |
14: 23,853,270 (GRCm39) |
T2A |
probably damaging |
Het |
Mroh9 |
T |
C |
1: 162,852,061 (GRCm39) |
Y876C |
probably benign |
Het |
Plekhh2 |
A |
G |
17: 84,878,548 (GRCm39) |
Y601C |
probably damaging |
Het |
Rabgap1l |
G |
T |
1: 160,281,353 (GRCm39) |
Q623K |
probably damaging |
Het |
Rad9a |
G |
A |
19: 4,250,560 (GRCm39) |
R85C |
probably damaging |
Het |
Rhox2c |
A |
C |
X: 36,635,351 (GRCm39) |
Q4H |
probably benign |
Het |
Rlig1 |
T |
C |
10: 100,414,243 (GRCm39) |
I139V |
probably benign |
Het |
Slain2 |
T |
A |
5: 73,114,927 (GRCm39) |
L386* |
probably null |
Het |
Slc4a7 |
A |
G |
14: 14,796,073 (GRCm38) |
|
probably null |
Het |
Slco1c1 |
T |
C |
6: 141,510,242 (GRCm39) |
C582R |
probably damaging |
Het |
Sulf1 |
A |
G |
1: 12,906,517 (GRCm39) |
N520D |
probably benign |
Het |
Tbc1d7 |
A |
G |
13: 43,323,325 (GRCm39) |
V22A |
probably damaging |
Het |
Tmprss6 |
A |
G |
15: 78,327,910 (GRCm39) |
V612A |
probably damaging |
Het |
Trpv2 |
A |
G |
11: 62,483,627 (GRCm39) |
E488G |
probably benign |
Het |
Ttn |
T |
A |
2: 76,585,168 (GRCm39) |
I22042F |
probably damaging |
Het |
Uspl1 |
A |
G |
5: 149,146,566 (GRCm39) |
Y439C |
probably damaging |
Het |
Vwf |
A |
G |
6: 125,661,054 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Rapgef2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00488:Rapgef2
|
APN |
3 |
78,999,332 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL01024:Rapgef2
|
APN |
3 |
78,977,445 (GRCm39) |
missense |
probably benign |
0.43 |
IGL01448:Rapgef2
|
APN |
3 |
79,011,269 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01448:Rapgef2
|
APN |
3 |
78,976,244 (GRCm39) |
missense |
probably benign |
|
IGL01928:Rapgef2
|
APN |
3 |
79,011,270 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01973:Rapgef2
|
APN |
3 |
78,999,116 (GRCm39) |
splice site |
probably null |
|
IGL02015:Rapgef2
|
APN |
3 |
78,999,371 (GRCm39) |
splice site |
probably benign |
|
IGL02498:Rapgef2
|
APN |
3 |
78,974,060 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02631:Rapgef2
|
APN |
3 |
78,990,533 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL02835:Rapgef2
|
APN |
3 |
79,000,293 (GRCm39) |
splice site |
probably benign |
|
IGL02887:Rapgef2
|
APN |
3 |
78,976,187 (GRCm39) |
splice site |
probably benign |
|
IGL03030:Rapgef2
|
APN |
3 |
78,981,614 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03035:Rapgef2
|
APN |
3 |
79,001,731 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03222:Rapgef2
|
APN |
3 |
78,995,302 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03227:Rapgef2
|
APN |
3 |
78,999,920 (GRCm39) |
splice site |
probably benign |
|
IGL03326:Rapgef2
|
APN |
3 |
78,999,140 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL03335:Rapgef2
|
APN |
3 |
79,006,492 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03384:Rapgef2
|
APN |
3 |
78,990,853 (GRCm39) |
missense |
probably damaging |
1.00 |
Bulge
|
UTSW |
3 |
78,986,439 (GRCm39) |
missense |
probably benign |
0.01 |
Hai_phat
|
UTSW |
3 |
78,993,266 (GRCm39) |
missense |
probably damaging |
1.00 |
R0022:Rapgef2
|
UTSW |
3 |
78,995,207 (GRCm39) |
missense |
probably damaging |
1.00 |
R0022:Rapgef2
|
UTSW |
3 |
78,995,207 (GRCm39) |
missense |
probably damaging |
1.00 |
R0038:Rapgef2
|
UTSW |
3 |
78,976,703 (GRCm39) |
missense |
probably benign |
0.00 |
R0117:Rapgef2
|
UTSW |
3 |
78,986,484 (GRCm39) |
missense |
probably benign |
0.00 |
R0225:Rapgef2
|
UTSW |
3 |
79,011,412 (GRCm39) |
missense |
probably damaging |
0.99 |
R0723:Rapgef2
|
UTSW |
3 |
78,986,481 (GRCm39) |
missense |
probably benign |
0.20 |
R0788:Rapgef2
|
UTSW |
3 |
79,006,502 (GRCm39) |
missense |
possibly damaging |
0.59 |
R1311:Rapgef2
|
UTSW |
3 |
78,990,854 (GRCm39) |
missense |
probably benign |
0.12 |
R1374:Rapgef2
|
UTSW |
3 |
78,995,275 (GRCm39) |
missense |
probably benign |
0.08 |
R1507:Rapgef2
|
UTSW |
3 |
78,988,600 (GRCm39) |
splice site |
probably benign |
|
R1523:Rapgef2
|
UTSW |
3 |
79,000,056 (GRCm39) |
missense |
probably damaging |
1.00 |
R1753:Rapgef2
|
UTSW |
3 |
78,996,098 (GRCm39) |
missense |
possibly damaging |
0.65 |
R1759:Rapgef2
|
UTSW |
3 |
78,974,038 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1766:Rapgef2
|
UTSW |
3 |
79,000,010 (GRCm39) |
missense |
probably damaging |
1.00 |
R2436:Rapgef2
|
UTSW |
3 |
78,996,079 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3033:Rapgef2
|
UTSW |
3 |
78,981,613 (GRCm39) |
critical splice donor site |
probably null |
|
R3766:Rapgef2
|
UTSW |
3 |
78,996,057 (GRCm39) |
missense |
probably benign |
0.01 |
R4118:Rapgef2
|
UTSW |
3 |
78,976,194 (GRCm39) |
critical splice donor site |
probably null |
|
R4416:Rapgef2
|
UTSW |
3 |
78,976,364 (GRCm39) |
nonsense |
probably null |
|
R4722:Rapgef2
|
UTSW |
3 |
78,976,480 (GRCm39) |
missense |
probably benign |
0.00 |
R4780:Rapgef2
|
UTSW |
3 |
79,077,076 (GRCm39) |
splice site |
probably benign |
|
R4825:Rapgef2
|
UTSW |
3 |
78,990,534 (GRCm39) |
missense |
probably benign |
0.03 |
R4861:Rapgef2
|
UTSW |
3 |
78,981,743 (GRCm39) |
missense |
probably benign |
0.01 |
R4861:Rapgef2
|
UTSW |
3 |
78,981,743 (GRCm39) |
missense |
probably benign |
0.01 |
R4900:Rapgef2
|
UTSW |
3 |
78,981,670 (GRCm39) |
missense |
probably benign |
0.02 |
R4943:Rapgef2
|
UTSW |
3 |
78,971,854 (GRCm39) |
missense |
probably benign |
0.00 |
R5291:Rapgef2
|
UTSW |
3 |
78,977,366 (GRCm39) |
missense |
possibly damaging |
0.64 |
R5369:Rapgef2
|
UTSW |
3 |
78,976,739 (GRCm39) |
missense |
probably benign |
0.00 |
R5413:Rapgef2
|
UTSW |
3 |
78,995,173 (GRCm39) |
missense |
probably damaging |
1.00 |
R5561:Rapgef2
|
UTSW |
3 |
78,995,950 (GRCm39) |
critical splice donor site |
probably null |
|
R5568:Rapgef2
|
UTSW |
3 |
79,011,308 (GRCm39) |
missense |
probably damaging |
1.00 |
R5642:Rapgef2
|
UTSW |
3 |
79,002,157 (GRCm39) |
missense |
probably damaging |
1.00 |
R5783:Rapgef2
|
UTSW |
3 |
78,995,300 (GRCm39) |
missense |
probably benign |
0.00 |
R6041:Rapgef2
|
UTSW |
3 |
78,976,469 (GRCm39) |
missense |
probably benign |
0.00 |
R6193:Rapgef2
|
UTSW |
3 |
78,976,751 (GRCm39) |
missense |
possibly damaging |
0.48 |
R6324:Rapgef2
|
UTSW |
3 |
78,986,439 (GRCm39) |
missense |
probably benign |
0.01 |
R6551:Rapgef2
|
UTSW |
3 |
79,122,342 (GRCm39) |
splice site |
probably null |
|
R6688:Rapgef2
|
UTSW |
3 |
78,976,435 (GRCm39) |
missense |
probably benign |
0.03 |
R6908:Rapgef2
|
UTSW |
3 |
79,011,370 (GRCm39) |
missense |
probably benign |
0.01 |
R6913:Rapgef2
|
UTSW |
3 |
78,993,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R6933:Rapgef2
|
UTSW |
3 |
78,993,266 (GRCm39) |
missense |
probably damaging |
1.00 |
R7086:Rapgef2
|
UTSW |
3 |
78,993,353 (GRCm39) |
missense |
probably benign |
0.08 |
R7106:Rapgef2
|
UTSW |
3 |
78,973,915 (GRCm39) |
missense |
probably benign |
|
R7228:Rapgef2
|
UTSW |
3 |
78,976,525 (GRCm39) |
missense |
probably benign |
0.03 |
R7242:Rapgef2
|
UTSW |
3 |
78,995,210 (GRCm39) |
nonsense |
probably null |
|
R7257:Rapgef2
|
UTSW |
3 |
78,989,934 (GRCm39) |
missense |
probably damaging |
0.99 |
R7322:Rapgef2
|
UTSW |
3 |
79,053,130 (GRCm39) |
start codon destroyed |
probably null |
0.02 |
R7443:Rapgef2
|
UTSW |
3 |
78,988,531 (GRCm39) |
missense |
probably damaging |
1.00 |
R7450:Rapgef2
|
UTSW |
3 |
79,080,366 (GRCm39) |
missense |
probably benign |
0.01 |
R7472:Rapgef2
|
UTSW |
3 |
78,976,580 (GRCm39) |
missense |
probably benign |
0.45 |
R7884:Rapgef2
|
UTSW |
3 |
78,973,933 (GRCm39) |
missense |
possibly damaging |
0.49 |
R7954:Rapgef2
|
UTSW |
3 |
78,977,454 (GRCm39) |
nonsense |
probably null |
|
R7957:Rapgef2
|
UTSW |
3 |
79,122,276 (GRCm39) |
missense |
probably benign |
0.27 |
R8071:Rapgef2
|
UTSW |
3 |
79,000,343 (GRCm39) |
missense |
probably damaging |
1.00 |
R8261:Rapgef2
|
UTSW |
3 |
78,993,325 (GRCm39) |
missense |
probably benign |
0.34 |
R8268:Rapgef2
|
UTSW |
3 |
78,993,263 (GRCm39) |
missense |
probably benign |
0.12 |
R8309:Rapgef2
|
UTSW |
3 |
78,990,509 (GRCm39) |
missense |
possibly damaging |
0.65 |
R8505:Rapgef2
|
UTSW |
3 |
78,986,349 (GRCm39) |
nonsense |
probably null |
|
R8783:Rapgef2
|
UTSW |
3 |
79,005,651 (GRCm39) |
missense |
probably damaging |
1.00 |
R8897:Rapgef2
|
UTSW |
3 |
79,019,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R8965:Rapgef2
|
UTSW |
3 |
78,999,851 (GRCm39) |
missense |
probably damaging |
1.00 |
R9028:Rapgef2
|
UTSW |
3 |
78,981,651 (GRCm39) |
missense |
probably damaging |
1.00 |
R9284:Rapgef2
|
UTSW |
3 |
79,000,010 (GRCm39) |
missense |
probably damaging |
1.00 |
R9371:Rapgef2
|
UTSW |
3 |
79,082,300 (GRCm39) |
missense |
probably damaging |
1.00 |
R9479:Rapgef2
|
UTSW |
3 |
79,019,495 (GRCm39) |
missense |
probably damaging |
1.00 |
R9493:Rapgef2
|
UTSW |
3 |
79,019,495 (GRCm39) |
missense |
probably damaging |
1.00 |
R9494:Rapgef2
|
UTSW |
3 |
79,019,495 (GRCm39) |
missense |
probably damaging |
1.00 |
R9500:Rapgef2
|
UTSW |
3 |
78,974,093 (GRCm39) |
missense |
probably benign |
|
R9657:Rapgef2
|
UTSW |
3 |
78,999,191 (GRCm39) |
missense |
probably damaging |
0.99 |
|