Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ap5z1 |
G |
A |
5: 142,456,213 (GRCm39) |
R344H |
probably damaging |
Het |
Ccdc38 |
C |
T |
10: 93,418,296 (GRCm39) |
|
probably benign |
Het |
Cd47 |
T |
C |
16: 49,714,543 (GRCm39) |
L184P |
probably damaging |
Het |
Cps1 |
T |
C |
1: 67,269,440 (GRCm39) |
S1480P |
probably damaging |
Het |
Cyp2a4 |
A |
G |
7: 26,012,348 (GRCm39) |
D377G |
probably damaging |
Het |
Ddb1 |
G |
A |
19: 10,585,682 (GRCm39) |
G132D |
probably damaging |
Het |
Dlgap2 |
T |
C |
8: 14,881,228 (GRCm39) |
|
probably benign |
Het |
Epg5 |
A |
G |
18: 78,024,541 (GRCm39) |
D1132G |
probably benign |
Het |
Fam184b |
T |
C |
5: 45,712,485 (GRCm39) |
E511G |
probably benign |
Het |
Fbn1 |
T |
A |
2: 125,188,354 (GRCm39) |
D1495V |
probably damaging |
Het |
Gpatch1 |
A |
T |
7: 34,991,187 (GRCm39) |
L619Q |
probably damaging |
Het |
Inpp4b |
T |
G |
8: 82,470,445 (GRCm39) |
|
probably null |
Het |
Kifc1 |
T |
C |
17: 34,102,849 (GRCm39) |
R192G |
probably benign |
Het |
Klhl30 |
C |
T |
1: 91,288,798 (GRCm39) |
T519M |
probably damaging |
Het |
Klhl8 |
A |
C |
5: 104,011,049 (GRCm39) |
L516R |
probably damaging |
Het |
Meikin |
T |
A |
11: 54,289,270 (GRCm39) |
|
probably benign |
Het |
Mlph |
T |
A |
1: 90,869,425 (GRCm39) |
S476T |
probably damaging |
Het |
Neb |
T |
C |
2: 52,133,401 (GRCm39) |
Y3379C |
probably damaging |
Het |
Nfxl1 |
G |
A |
5: 72,681,488 (GRCm39) |
T681I |
probably benign |
Het |
Nhsl3 |
A |
G |
4: 129,116,082 (GRCm39) |
S849P |
possibly damaging |
Het |
Obox1 |
A |
T |
7: 15,289,426 (GRCm39) |
|
probably benign |
Het |
Oplah |
G |
A |
15: 76,190,755 (GRCm39) |
R31C |
probably damaging |
Het |
Polb |
T |
C |
8: 23,143,073 (GRCm39) |
|
probably benign |
Het |
Ppfibp2 |
A |
G |
7: 107,285,195 (GRCm39) |
|
probably benign |
Het |
Prr12 |
A |
G |
7: 44,695,642 (GRCm39) |
S1275P |
unknown |
Het |
Ptcd3 |
C |
A |
6: 71,885,637 (GRCm39) |
E30* |
probably null |
Het |
Ranbp2 |
T |
C |
10: 58,321,715 (GRCm39) |
|
probably benign |
Het |
Rbpms2 |
ACTGCTGCTGCTGCTGC |
ACTGCTGCTGCTGCTGCTGC |
9: 65,558,948 (GRCm39) |
|
probably benign |
Het |
Rims1 |
G |
A |
1: 22,367,172 (GRCm39) |
T1176M |
probably damaging |
Het |
Ripor2 |
T |
C |
13: 24,857,095 (GRCm39) |
|
probably null |
Het |
Sae1 |
A |
G |
7: 16,112,333 (GRCm39) |
I60T |
probably damaging |
Het |
Tenm2 |
T |
C |
11: 35,899,281 (GRCm39) |
T2626A |
probably benign |
Het |
Trrap |
A |
G |
5: 144,783,428 (GRCm39) |
Q3419R |
probably damaging |
Het |
Vill |
C |
A |
9: 118,890,562 (GRCm39) |
N158K |
probably benign |
Het |
Zbtb14 |
A |
G |
17: 69,694,575 (GRCm39) |
N91S |
probably damaging |
Het |
Zfp248 |
A |
G |
6: 118,410,334 (GRCm39) |
L25P |
probably damaging |
Het |
Zmym1 |
T |
A |
4: 126,943,404 (GRCm39) |
K230I |
probably damaging |
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 |
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 |
R4743:Rapgef2
|
UTSW |
3 |
79,080,375 (GRCm39) |
missense |
probably damaging |
0.99 |
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 |
|