Other mutations in this stock |
Total: 27 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam3 |
T |
C |
8: 25,184,227 (GRCm39) |
D591G |
probably benign |
Het |
Aqp4 |
T |
A |
18: 15,526,617 (GRCm39) |
E288V |
possibly damaging |
Het |
Astn2 |
T |
C |
4: 65,562,943 (GRCm39) |
Y894C |
probably damaging |
Het |
Bahd1 |
C |
T |
2: 118,746,887 (GRCm39) |
P169S |
probably damaging |
Het |
Dennd4c |
AGGAGCTCCTGGAGC |
AGGAGC |
4: 86,743,557 (GRCm39) |
|
probably benign |
Het |
Dnah6 |
T |
C |
6: 73,150,333 (GRCm39) |
D810G |
probably benign |
Het |
Dst |
T |
C |
1: 34,191,366 (GRCm39) |
I222T |
probably damaging |
Het |
Eif4g3 |
A |
T |
4: 137,830,721 (GRCm39) |
T159S |
probably damaging |
Het |
Ercc5 |
A |
G |
1: 44,219,734 (GRCm39) |
E1002G |
possibly damaging |
Het |
Gm5414 |
T |
C |
15: 101,533,044 (GRCm39) |
E461G |
probably damaging |
Het |
Heatr5a |
A |
T |
12: 51,997,821 (GRCm39) |
C359* |
probably null |
Het |
Ift88 |
G |
A |
14: 57,715,501 (GRCm39) |
D515N |
probably damaging |
Het |
Kmt2a |
A |
G |
9: 44,733,160 (GRCm39) |
|
probably benign |
Het |
Lypd8 |
T |
C |
11: 58,275,453 (GRCm39) |
Y63H |
probably damaging |
Het |
Mcm3 |
A |
T |
1: 20,878,992 (GRCm39) |
Y594N |
probably damaging |
Het |
Myo9b |
G |
A |
8: 71,786,981 (GRCm39) |
R721Q |
probably benign |
Het |
Naip1 |
T |
C |
13: 100,568,966 (GRCm39) |
M322V |
probably benign |
Het |
Neurl2 |
T |
C |
2: 164,674,975 (GRCm39) |
E129G |
probably benign |
Het |
Nr2f2 |
A |
G |
7: 70,007,810 (GRCm39) |
V71A |
possibly damaging |
Het |
Rab36 |
G |
A |
10: 74,880,328 (GRCm39) |
V63I |
probably damaging |
Het |
Rap1gap2 |
C |
A |
11: 74,298,148 (GRCm39) |
A491S |
possibly damaging |
Het |
Selenbp1 |
T |
C |
3: 94,845,351 (GRCm39) |
V149A |
probably benign |
Het |
Smg9 |
A |
G |
7: 24,115,949 (GRCm39) |
D280G |
probably damaging |
Het |
Tlr1 |
T |
C |
5: 65,082,912 (GRCm39) |
D555G |
probably damaging |
Het |
Tomm70a |
G |
A |
16: 56,942,388 (GRCm39) |
G55D |
probably damaging |
Het |
Tpte |
T |
A |
8: 22,810,888 (GRCm39) |
S182T |
possibly damaging |
Het |
Zfp58 |
T |
C |
13: 67,639,741 (GRCm39) |
E250G |
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 |
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 |
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 |
|