Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrv1 |
C |
T |
13: 81,658,996 (GRCm39) |
V2783I |
probably benign |
Het |
Ago4 |
A |
C |
4: 126,400,635 (GRCm39) |
C693G |
probably damaging |
Het |
Apobec2 |
T |
C |
17: 48,730,153 (GRCm39) |
E171G |
probably benign |
Het |
Arhgef40 |
A |
G |
14: 52,227,556 (GRCm39) |
E434G |
probably damaging |
Het |
Bcas1 |
T |
C |
2: 170,220,806 (GRCm39) |
D324G |
probably damaging |
Het |
Bdp1 |
A |
T |
13: 100,191,713 (GRCm39) |
V1422E |
probably damaging |
Het |
Bfsp1 |
C |
T |
2: 143,669,391 (GRCm39) |
R396Q |
probably benign |
Het |
Bpifb9b |
T |
A |
2: 154,156,026 (GRCm39) |
|
probably null |
Het |
Cacna1s |
T |
A |
1: 136,029,302 (GRCm39) |
|
probably null |
Het |
Casp8 |
T |
C |
1: 58,866,377 (GRCm39) |
F126S |
probably damaging |
Het |
Cdh26 |
T |
C |
2: 178,091,614 (GRCm39) |
S58P |
probably benign |
Het |
Cds2 |
A |
G |
2: 132,140,398 (GRCm39) |
T182A |
probably damaging |
Het |
Cfap157 |
C |
T |
2: 32,669,965 (GRCm39) |
R206H |
probably benign |
Het |
Col7a1 |
G |
A |
9: 108,795,532 (GRCm39) |
G1529E |
unknown |
Het |
Crybg3 |
A |
G |
16: 59,350,782 (GRCm39) |
F2567L |
probably benign |
Het |
Cyp2e1 |
T |
C |
7: 140,354,527 (GRCm39) |
S393P |
possibly damaging |
Het |
D5Ertd579e |
A |
G |
5: 36,773,160 (GRCm39) |
Y412H |
probably damaging |
Het |
Dclk2 |
A |
T |
3: 86,732,049 (GRCm39) |
|
probably null |
Het |
Ddx50 |
A |
T |
10: 62,463,450 (GRCm39) |
C414* |
probably null |
Het |
Dip2c |
T |
A |
13: 9,671,905 (GRCm39) |
|
probably null |
Het |
Dmtn |
G |
T |
14: 70,843,159 (GRCm39) |
P283Q |
probably damaging |
Het |
Dspp |
C |
A |
5: 104,325,789 (GRCm39) |
D717E |
unknown |
Het |
Efcab11 |
T |
C |
12: 99,685,321 (GRCm39) |
D151G |
probably damaging |
Het |
Egfem1 |
T |
C |
3: 29,206,042 (GRCm39) |
V93A |
probably damaging |
Het |
Ehbp1 |
T |
C |
11: 22,096,592 (GRCm39) |
D299G |
probably benign |
Het |
Erlec1 |
A |
G |
11: 30,884,710 (GRCm39) |
Y448H |
possibly damaging |
Het |
Fer1l4 |
T |
C |
2: 155,873,220 (GRCm39) |
K1287E |
probably benign |
Het |
Fn1 |
A |
T |
1: 71,634,968 (GRCm39) |
|
probably null |
Het |
Fut8 |
G |
T |
12: 77,521,818 (GRCm39) |
A486S |
probably damaging |
Het |
Gfra1 |
A |
T |
19: 58,255,522 (GRCm39) |
S308R |
probably damaging |
Het |
Gm10764 |
A |
G |
10: 87,126,579 (GRCm39) |
|
noncoding transcript |
Het |
Gm5958 |
C |
A |
14: 100,073,189 (GRCm39) |
|
noncoding transcript |
Het |
Gm6788 |
C |
T |
19: 28,740,664 (GRCm39) |
|
noncoding transcript |
Het |
Gsdmd |
A |
G |
15: 75,736,241 (GRCm39) |
I123M |
probably benign |
Het |
H2bc13 |
A |
T |
13: 21,900,189 (GRCm39) |
V42E |
probably damaging |
Het |
Hsf4 |
A |
G |
8: 105,999,367 (GRCm39) |
E235G |
probably benign |
Het |
Ighv1-83 |
T |
C |
12: 115,927,580 (GRCm39) |
I57V |
probably benign |
Het |
Inhca |
A |
C |
9: 103,129,054 (GRCm39) |
Y235* |
probably null |
Het |
Inpp5f |
A |
T |
7: 128,286,840 (GRCm39) |
D573V |
probably damaging |
Het |
Kcnj1 |
T |
A |
9: 32,308,056 (GRCm39) |
L160Q |
probably damaging |
Het |
Kcnmb3 |
A |
T |
3: 32,526,653 (GRCm39) |
C179* |
probably null |
Het |
Lrig1 |
A |
G |
6: 94,586,700 (GRCm39) |
F659L |
probably damaging |
Het |
Lrrc3 |
T |
C |
10: 77,737,253 (GRCm39) |
D61G |
probably benign |
Het |
Marchf4 |
T |
G |
1: 72,467,938 (GRCm39) |
S365R |
probably benign |
Het |
Mccc1 |
A |
G |
3: 36,051,703 (GRCm39) |
L32S |
probably benign |
Het |
Mei4 |
A |
G |
9: 81,772,216 (GRCm39) |
T10A |
probably benign |
Het |
Meis1 |
T |
C |
11: 18,959,222 (GRCm39) |
|
probably benign |
Het |
Mllt1 |
T |
C |
17: 57,206,813 (GRCm39) |
T344A |
probably benign |
Het |
Mmp11 |
C |
T |
10: 75,761,419 (GRCm39) |
A31T |
probably damaging |
Het |
Mrps28 |
A |
G |
3: 8,947,614 (GRCm39) |
|
probably benign |
Het |
Mthfsl |
A |
C |
9: 88,597,550 (GRCm39) |
L67V |
probably damaging |
Het |
Ncaph2 |
A |
G |
15: 89,244,574 (GRCm39) |
I11V |
probably damaging |
Het |
Ncdn |
G |
A |
4: 126,643,731 (GRCm39) |
L364F |
possibly damaging |
Het |
Nfat5 |
T |
A |
8: 108,051,284 (GRCm39) |
D47E |
probably damaging |
Het |
Or51g2 |
A |
T |
7: 102,622,614 (GRCm39) |
I195N |
possibly damaging |
Het |
Or5b106 |
T |
A |
19: 13,123,355 (GRCm39) |
I223L |
possibly damaging |
Het |
Or5bw2 |
C |
T |
7: 6,573,643 (GRCm39) |
L218F |
possibly damaging |
Het |
Pcdhb3 |
A |
T |
18: 37,435,452 (GRCm39) |
I473F |
probably damaging |
Het |
Pcdhgb8 |
A |
T |
18: 37,897,191 (GRCm39) |
N754Y |
probably damaging |
Het |
Pgbd5 |
C |
A |
8: 125,097,305 (GRCm39) |
K408N |
probably benign |
Het |
Pnisr |
A |
G |
4: 21,859,330 (GRCm39) |
|
probably benign |
Het |
Poldip3 |
A |
T |
15: 83,016,776 (GRCm39) |
|
probably null |
Het |
Ppfia2 |
G |
C |
10: 106,597,978 (GRCm39) |
L180F |
probably damaging |
Het |
Psmc3 |
A |
G |
2: 90,896,317 (GRCm39) |
|
probably benign |
Het |
Rab3gap1 |
T |
A |
1: 127,816,914 (GRCm39) |
W58R |
possibly damaging |
Het |
Rere |
T |
A |
4: 150,703,601 (GRCm39) |
W1528R |
probably damaging |
Het |
Rhot1 |
A |
G |
11: 80,100,027 (GRCm39) |
|
probably benign |
Het |
Rsf1 |
T |
C |
7: 97,311,612 (GRCm39) |
S781P |
probably damaging |
Het |
Rtraf |
T |
C |
14: 19,873,784 (GRCm39) |
K5R |
probably damaging |
Het |
Rufy4 |
T |
C |
1: 74,186,822 (GRCm39) |
C537R |
probably damaging |
Het |
Ryr2 |
A |
G |
13: 11,609,872 (GRCm39) |
V753A |
probably damaging |
Het |
Ryr3 |
T |
C |
2: 112,661,530 (GRCm39) |
H1820R |
probably damaging |
Het |
Schip1 |
A |
T |
3: 68,315,818 (GRCm39) |
|
probably benign |
Het |
Scin |
T |
A |
12: 40,119,373 (GRCm39) |
I552F |
possibly damaging |
Het |
Selp |
A |
C |
1: 163,972,475 (GRCm39) |
T705P |
probably damaging |
Het |
Sh3rf3 |
A |
T |
10: 58,842,925 (GRCm39) |
D297V |
probably damaging |
Het |
Slc24a4 |
T |
A |
12: 102,231,203 (GRCm39) |
|
probably null |
Het |
Slc2a9 |
C |
A |
5: 38,574,603 (GRCm39) |
L224F |
probably benign |
Het |
Slc35e2 |
C |
A |
4: 155,700,693 (GRCm39) |
P272Q |
probably damaging |
Het |
Slf2 |
T |
G |
19: 44,960,100 (GRCm39) |
D1022E |
probably damaging |
Het |
Syne1 |
C |
T |
10: 5,007,909 (GRCm39) |
C7932Y |
probably damaging |
Het |
Tc2n |
A |
G |
12: 101,631,954 (GRCm39) |
L301P |
probably damaging |
Het |
Tchhl1 |
A |
G |
3: 93,377,623 (GRCm39) |
D109G |
possibly damaging |
Het |
Thoc7 |
T |
C |
14: 13,953,154 (GRCm38) |
I83V |
probably damaging |
Het |
Tm4sf1 |
C |
T |
3: 57,200,448 (GRCm39) |
G85S |
probably damaging |
Het |
Tmem63a |
T |
A |
1: 180,794,086 (GRCm39) |
I541N |
probably benign |
Het |
Tmpo |
A |
G |
10: 90,985,411 (GRCm39) |
V357A |
probably damaging |
Het |
Unc80 |
T |
C |
1: 66,685,709 (GRCm39) |
Y2278H |
possibly damaging |
Het |
Vmn1r26 |
A |
G |
6: 57,985,808 (GRCm39) |
F127S |
probably damaging |
Het |
Vmn2r8 |
A |
T |
5: 108,945,264 (GRCm39) |
M781K |
probably damaging |
Het |
Vps36 |
T |
G |
8: 22,708,280 (GRCm39) |
M348R |
possibly damaging |
Het |
Vps45 |
T |
C |
3: 95,926,943 (GRCm39) |
T535A |
probably damaging |
Het |
|
Other mutations in Arfgef3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00769:Arfgef3
|
APN |
10 |
18,536,352 (GRCm39) |
missense |
probably benign |
0.03 |
IGL00835:Arfgef3
|
APN |
10 |
18,537,106 (GRCm39) |
missense |
probably benign |
|
IGL00961:Arfgef3
|
APN |
10 |
18,486,985 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01400:Arfgef3
|
APN |
10 |
18,528,454 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01501:Arfgef3
|
APN |
10 |
18,476,308 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01595:Arfgef3
|
APN |
10 |
18,470,660 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01695:Arfgef3
|
APN |
10 |
18,479,167 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01774:Arfgef3
|
APN |
10 |
18,619,363 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02348:Arfgef3
|
APN |
10 |
18,467,095 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02371:Arfgef3
|
APN |
10 |
18,522,287 (GRCm39) |
missense |
probably benign |
|
IGL02400:Arfgef3
|
APN |
10 |
18,522,005 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02630:Arfgef3
|
APN |
10 |
18,537,140 (GRCm39) |
splice site |
probably benign |
|
IGL02815:Arfgef3
|
APN |
10 |
18,528,299 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03178:Arfgef3
|
APN |
10 |
18,488,973 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03182:Arfgef3
|
APN |
10 |
18,476,292 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03267:Arfgef3
|
APN |
10 |
18,467,630 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03294:Arfgef3
|
APN |
10 |
18,540,660 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03410:Arfgef3
|
APN |
10 |
18,476,238 (GRCm39) |
missense |
probably damaging |
1.00 |
Bow-wow
|
UTSW |
10 |
18,522,478 (GRCm39) |
nonsense |
probably null |
|
R0098:Arfgef3
|
UTSW |
10 |
18,465,390 (GRCm39) |
missense |
probably damaging |
1.00 |
R0098:Arfgef3
|
UTSW |
10 |
18,465,390 (GRCm39) |
missense |
probably damaging |
1.00 |
R0141:Arfgef3
|
UTSW |
10 |
18,473,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R0164:Arfgef3
|
UTSW |
10 |
18,523,663 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0164:Arfgef3
|
UTSW |
10 |
18,523,663 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0241:Arfgef3
|
UTSW |
10 |
18,474,962 (GRCm39) |
missense |
probably damaging |
1.00 |
R0334:Arfgef3
|
UTSW |
10 |
18,468,029 (GRCm39) |
missense |
probably damaging |
0.98 |
R0352:Arfgef3
|
UTSW |
10 |
18,537,135 (GRCm39) |
missense |
probably benign |
0.17 |
R0415:Arfgef3
|
UTSW |
10 |
18,488,875 (GRCm39) |
splice site |
probably benign |
|
R0417:Arfgef3
|
UTSW |
10 |
18,479,259 (GRCm39) |
missense |
probably damaging |
1.00 |
R0442:Arfgef3
|
UTSW |
10 |
18,553,563 (GRCm39) |
splice site |
probably benign |
|
R0507:Arfgef3
|
UTSW |
10 |
18,467,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R0573:Arfgef3
|
UTSW |
10 |
18,475,036 (GRCm39) |
missense |
probably damaging |
1.00 |
R0582:Arfgef3
|
UTSW |
10 |
18,487,038 (GRCm39) |
missense |
probably damaging |
1.00 |
R0609:Arfgef3
|
UTSW |
10 |
18,473,179 (GRCm39) |
missense |
probably benign |
0.31 |
R0826:Arfgef3
|
UTSW |
10 |
18,465,414 (GRCm39) |
missense |
probably damaging |
0.98 |
R0919:Arfgef3
|
UTSW |
10 |
18,465,483 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0980:Arfgef3
|
UTSW |
10 |
18,467,866 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1027:Arfgef3
|
UTSW |
10 |
18,467,123 (GRCm39) |
missense |
probably benign |
0.02 |
R1140:Arfgef3
|
UTSW |
10 |
18,473,096 (GRCm39) |
missense |
possibly damaging |
0.77 |
R1491:Arfgef3
|
UTSW |
10 |
18,522,302 (GRCm39) |
missense |
probably damaging |
1.00 |
R1493:Arfgef3
|
UTSW |
10 |
18,506,627 (GRCm39) |
missense |
probably damaging |
0.96 |
R1529:Arfgef3
|
UTSW |
10 |
18,488,970 (GRCm39) |
nonsense |
probably null |
|
R1564:Arfgef3
|
UTSW |
10 |
18,467,452 (GRCm39) |
missense |
probably damaging |
1.00 |
R1654:Arfgef3
|
UTSW |
10 |
18,500,896 (GRCm39) |
missense |
probably null |
0.15 |
R1868:Arfgef3
|
UTSW |
10 |
18,537,135 (GRCm39) |
missense |
probably benign |
0.17 |
R1876:Arfgef3
|
UTSW |
10 |
18,473,104 (GRCm39) |
missense |
probably damaging |
1.00 |
R1908:Arfgef3
|
UTSW |
10 |
18,528,511 (GRCm39) |
missense |
possibly damaging |
0.80 |
R2211:Arfgef3
|
UTSW |
10 |
18,467,993 (GRCm39) |
missense |
possibly damaging |
0.54 |
R2316:Arfgef3
|
UTSW |
10 |
18,492,701 (GRCm39) |
missense |
probably benign |
0.19 |
R2393:Arfgef3
|
UTSW |
10 |
18,473,535 (GRCm39) |
missense |
possibly damaging |
0.88 |
R2407:Arfgef3
|
UTSW |
10 |
18,553,614 (GRCm39) |
missense |
possibly damaging |
0.63 |
R3076:Arfgef3
|
UTSW |
10 |
18,479,278 (GRCm39) |
missense |
probably damaging |
0.99 |
R3077:Arfgef3
|
UTSW |
10 |
18,479,278 (GRCm39) |
missense |
probably damaging |
0.99 |
R3963:Arfgef3
|
UTSW |
10 |
18,468,025 (GRCm39) |
missense |
probably damaging |
1.00 |
R4201:Arfgef3
|
UTSW |
10 |
18,495,530 (GRCm39) |
missense |
probably benign |
0.01 |
R4241:Arfgef3
|
UTSW |
10 |
18,500,912 (GRCm39) |
missense |
probably damaging |
1.00 |
R4244:Arfgef3
|
UTSW |
10 |
18,506,168 (GRCm39) |
missense |
probably damaging |
1.00 |
R4395:Arfgef3
|
UTSW |
10 |
18,473,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R4455:Arfgef3
|
UTSW |
10 |
18,483,423 (GRCm39) |
missense |
probably benign |
0.18 |
R4480:Arfgef3
|
UTSW |
10 |
18,476,348 (GRCm39) |
missense |
probably damaging |
1.00 |
R4499:Arfgef3
|
UTSW |
10 |
18,484,091 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4589:Arfgef3
|
UTSW |
10 |
18,521,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R4635:Arfgef3
|
UTSW |
10 |
18,510,603 (GRCm39) |
missense |
probably damaging |
1.00 |
R4776:Arfgef3
|
UTSW |
10 |
18,529,995 (GRCm39) |
missense |
probably benign |
|
R4801:Arfgef3
|
UTSW |
10 |
18,467,654 (GRCm39) |
missense |
probably benign |
0.00 |
R4802:Arfgef3
|
UTSW |
10 |
18,467,654 (GRCm39) |
missense |
probably benign |
0.00 |
R4807:Arfgef3
|
UTSW |
10 |
18,522,385 (GRCm39) |
missense |
probably benign |
|
R4828:Arfgef3
|
UTSW |
10 |
18,528,441 (GRCm39) |
missense |
probably damaging |
0.99 |
R4861:Arfgef3
|
UTSW |
10 |
18,483,479 (GRCm39) |
missense |
probably benign |
0.01 |
R4861:Arfgef3
|
UTSW |
10 |
18,483,479 (GRCm39) |
missense |
probably benign |
0.01 |
R4918:Arfgef3
|
UTSW |
10 |
18,492,638 (GRCm39) |
missense |
probably damaging |
0.99 |
R4922:Arfgef3
|
UTSW |
10 |
18,467,934 (GRCm39) |
missense |
probably damaging |
0.97 |
R4929:Arfgef3
|
UTSW |
10 |
18,506,599 (GRCm39) |
missense |
probably benign |
0.00 |
R4937:Arfgef3
|
UTSW |
10 |
18,465,454 (GRCm39) |
missense |
probably damaging |
0.98 |
R5290:Arfgef3
|
UTSW |
10 |
18,476,208 (GRCm39) |
missense |
probably damaging |
1.00 |
R5410:Arfgef3
|
UTSW |
10 |
18,486,985 (GRCm39) |
missense |
probably damaging |
0.99 |
R5807:Arfgef3
|
UTSW |
10 |
18,523,546 (GRCm39) |
splice site |
probably null |
|
R5832:Arfgef3
|
UTSW |
10 |
18,506,168 (GRCm39) |
missense |
probably damaging |
1.00 |
R5887:Arfgef3
|
UTSW |
10 |
18,483,413 (GRCm39) |
nonsense |
probably null |
|
R6272:Arfgef3
|
UTSW |
10 |
18,522,711 (GRCm39) |
missense |
probably benign |
0.00 |
R6302:Arfgef3
|
UTSW |
10 |
18,528,589 (GRCm39) |
missense |
probably damaging |
0.97 |
R6397:Arfgef3
|
UTSW |
10 |
18,483,413 (GRCm39) |
nonsense |
probably null |
|
R6495:Arfgef3
|
UTSW |
10 |
18,486,950 (GRCm39) |
critical splice donor site |
probably null |
|
R6707:Arfgef3
|
UTSW |
10 |
18,496,903 (GRCm39) |
missense |
probably benign |
0.11 |
R6814:Arfgef3
|
UTSW |
10 |
18,470,767 (GRCm39) |
missense |
probably damaging |
1.00 |
R6830:Arfgef3
|
UTSW |
10 |
18,540,637 (GRCm39) |
critical splice donor site |
probably null |
|
R6870:Arfgef3
|
UTSW |
10 |
18,522,478 (GRCm39) |
nonsense |
probably null |
|
R6941:Arfgef3
|
UTSW |
10 |
18,501,203 (GRCm39) |
missense |
possibly damaging |
0.66 |
R7094:Arfgef3
|
UTSW |
10 |
18,522,187 (GRCm39) |
missense |
probably damaging |
1.00 |
R7179:Arfgef3
|
UTSW |
10 |
18,475,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R7204:Arfgef3
|
UTSW |
10 |
18,522,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R7247:Arfgef3
|
UTSW |
10 |
18,501,139 (GRCm39) |
missense |
probably benign |
0.00 |
R7249:Arfgef3
|
UTSW |
10 |
18,506,583 (GRCm39) |
missense |
possibly damaging |
0.62 |
R7318:Arfgef3
|
UTSW |
10 |
18,506,211 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7391:Arfgef3
|
UTSW |
10 |
18,522,007 (GRCm39) |
missense |
probably benign |
0.05 |
R7527:Arfgef3
|
UTSW |
10 |
18,522,377 (GRCm39) |
missense |
probably benign |
|
R7618:Arfgef3
|
UTSW |
10 |
18,522,029 (GRCm39) |
missense |
probably damaging |
1.00 |
R7779:Arfgef3
|
UTSW |
10 |
18,470,771 (GRCm39) |
missense |
probably damaging |
0.99 |
R7851:Arfgef3
|
UTSW |
10 |
18,468,034 (GRCm39) |
missense |
probably damaging |
1.00 |
R8112:Arfgef3
|
UTSW |
10 |
18,528,379 (GRCm39) |
missense |
possibly damaging |
0.96 |
R8133:Arfgef3
|
UTSW |
10 |
18,486,951 (GRCm39) |
critical splice donor site |
probably null |
|
R8242:Arfgef3
|
UTSW |
10 |
18,505,824 (GRCm39) |
missense |
probably benign |
0.25 |
R8369:Arfgef3
|
UTSW |
10 |
18,465,477 (GRCm39) |
missense |
probably benign |
0.34 |
R8396:Arfgef3
|
UTSW |
10 |
18,528,280 (GRCm39) |
critical splice donor site |
probably null |
|
R8553:Arfgef3
|
UTSW |
10 |
18,479,278 (GRCm39) |
missense |
probably damaging |
0.99 |
R8798:Arfgef3
|
UTSW |
10 |
18,522,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R8821:Arfgef3
|
UTSW |
10 |
18,528,491 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8831:Arfgef3
|
UTSW |
10 |
18,528,491 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8918:Arfgef3
|
UTSW |
10 |
18,511,453 (GRCm39) |
missense |
probably benign |
0.01 |
R8929:Arfgef3
|
UTSW |
10 |
18,479,203 (GRCm39) |
missense |
probably damaging |
1.00 |
R9001:Arfgef3
|
UTSW |
10 |
18,522,476 (GRCm39) |
missense |
probably benign |
0.32 |
R9077:Arfgef3
|
UTSW |
10 |
18,500,899 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9258:Arfgef3
|
UTSW |
10 |
18,465,387 (GRCm39) |
missense |
probably damaging |
1.00 |
R9267:Arfgef3
|
UTSW |
10 |
18,475,028 (GRCm39) |
missense |
probably damaging |
1.00 |
R9358:Arfgef3
|
UTSW |
10 |
18,492,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R9388:Arfgef3
|
UTSW |
10 |
18,505,877 (GRCm39) |
missense |
probably benign |
0.35 |
R9389:Arfgef3
|
UTSW |
10 |
18,479,271 (GRCm39) |
missense |
probably damaging |
1.00 |
R9563:Arfgef3
|
UTSW |
10 |
18,522,275 (GRCm39) |
missense |
probably damaging |
1.00 |
R9713:Arfgef3
|
UTSW |
10 |
18,528,556 (GRCm39) |
missense |
probably damaging |
1.00 |
X0026:Arfgef3
|
UTSW |
10 |
18,528,374 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Arfgef3
|
UTSW |
10 |
18,510,600 (GRCm39) |
missense |
probably benign |
0.26 |
Z1176:Arfgef3
|
UTSW |
10 |
18,484,106 (GRCm39) |
missense |
probably damaging |
0.97 |
Z1176:Arfgef3
|
UTSW |
10 |
18,467,185 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Arfgef3
|
UTSW |
10 |
18,503,376 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Arfgef3
|
UTSW |
10 |
18,483,524 (GRCm39) |
missense |
probably damaging |
1.00 |
|