Other mutations in this stock |
Total: 111 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2210408I21Rik |
C |
T |
13: 77,418,039 (GRCm39) |
T741I |
possibly damaging |
Het |
Aadacl4fm2 |
A |
T |
4: 144,281,976 (GRCm39) |
I272K |
probably damaging |
Het |
Acot3 |
A |
T |
12: 84,100,347 (GRCm39) |
Q41L |
probably damaging |
Het |
Actl7b |
G |
A |
4: 56,740,165 (GRCm39) |
Q398* |
probably null |
Het |
Adgrb2 |
C |
A |
4: 129,886,417 (GRCm39) |
Q186K |
probably damaging |
Het |
Akr1a1 |
A |
G |
4: 116,495,171 (GRCm39) |
|
probably null |
Het |
Ap3s2 |
A |
T |
7: 79,530,238 (GRCm39) |
F192L |
probably damaging |
Het |
Apobr |
T |
G |
7: 126,184,151 (GRCm39) |
|
probably null |
Het |
Arhgap5 |
A |
G |
12: 52,566,128 (GRCm39) |
N1033S |
probably damaging |
Het |
Arid3c |
G |
T |
4: 41,725,947 (GRCm39) |
R219S |
probably damaging |
Het |
Bves |
C |
T |
10: 45,223,961 (GRCm39) |
T207M |
probably damaging |
Het |
Cacna1d |
T |
C |
14: 29,788,013 (GRCm39) |
K1619R |
probably damaging |
Het |
Caps2 |
A |
T |
10: 112,026,883 (GRCm39) |
D223V |
possibly damaging |
Het |
Cd3g |
A |
C |
9: 44,885,640 (GRCm39) |
L35R |
probably damaging |
Het |
Cdh23 |
A |
T |
10: 60,359,315 (GRCm39) |
V261E |
probably benign |
Het |
Cfap54 |
T |
G |
10: 92,846,882 (GRCm39) |
T1028P |
probably damaging |
Het |
Ch25h |
C |
A |
19: 34,451,686 (GRCm39) |
V281L |
probably benign |
Het |
Cip2a |
A |
C |
16: 48,837,849 (GRCm39) |
I850L |
probably benign |
Het |
Clu |
G |
T |
14: 66,218,354 (GRCm39) |
V405L |
possibly damaging |
Het |
Col6a3 |
A |
T |
1: 90,757,935 (GRCm39) |
H6Q |
probably damaging |
Het |
Cps1 |
G |
A |
1: 67,207,533 (GRCm39) |
|
probably null |
Het |
Ctr9 |
T |
C |
7: 110,654,870 (GRCm39) |
S1134P |
unknown |
Het |
Cts7 |
C |
T |
13: 61,500,624 (GRCm39) |
G308S |
probably damaging |
Het |
Cyp2c39 |
C |
A |
19: 39,555,335 (GRCm39) |
T385K |
probably damaging |
Het |
Dennd5a |
A |
T |
7: 109,517,919 (GRCm39) |
D596E |
probably benign |
Het |
Disc1 |
T |
A |
8: 125,851,349 (GRCm39) |
I413K |
probably benign |
Het |
Dll3 |
C |
T |
7: 27,993,922 (GRCm39) |
G505D |
probably damaging |
Het |
Dnah3 |
A |
G |
7: 119,677,794 (GRCm39) |
W377R |
probably damaging |
Het |
Dop1b |
A |
G |
16: 93,596,814 (GRCm39) |
D1792G |
probably damaging |
Het |
Dpep3 |
T |
A |
8: 106,700,325 (GRCm39) |
R460S |
probably benign |
Het |
Ebf4 |
A |
G |
2: 130,200,751 (GRCm39) |
N302S |
probably damaging |
Het |
Egflam |
T |
C |
15: 7,319,396 (GRCm39) |
E194G |
possibly damaging |
Het |
Ep400 |
A |
T |
5: 110,841,174 (GRCm39) |
|
probably benign |
Het |
Ercc6 |
T |
C |
14: 32,248,133 (GRCm39) |
M228T |
probably damaging |
Het |
Fbxo9 |
T |
C |
9: 77,994,529 (GRCm39) |
T264A |
probably damaging |
Het |
Fcrl5 |
C |
A |
3: 87,364,721 (GRCm39) |
P486T |
possibly damaging |
Het |
Fyb1 |
T |
C |
15: 6,609,960 (GRCm39) |
F178L |
probably damaging |
Het |
Gaa |
T |
A |
11: 119,171,286 (GRCm39) |
I646N |
probably damaging |
Het |
Gm5431 |
A |
T |
11: 48,785,853 (GRCm39) |
V174E |
possibly damaging |
Het |
Gnpat |
T |
G |
8: 125,613,691 (GRCm39) |
|
probably null |
Het |
Gucy1a2 |
G |
T |
9: 3,759,622 (GRCm39) |
R476I |
probably benign |
Het |
Hars1 |
A |
G |
18: 36,904,156 (GRCm39) |
L241P |
probably damaging |
Het |
Haus5 |
G |
A |
7: 30,357,328 (GRCm39) |
Q399* |
probably null |
Het |
Hephl1 |
T |
C |
9: 14,970,542 (GRCm39) |
E984G |
probably damaging |
Het |
Hmces |
C |
T |
6: 87,898,574 (GRCm39) |
Q132* |
probably null |
Het |
Hsp90b1 |
G |
T |
10: 86,530,389 (GRCm39) |
T490K |
probably damaging |
Het |
Idh2 |
T |
G |
7: 79,748,906 (GRCm39) |
E125A |
probably damaging |
Het |
Ipo13 |
G |
T |
4: 117,761,719 (GRCm39) |
H465Q |
probably benign |
Het |
Isca2 |
C |
A |
12: 84,820,393 (GRCm39) |
T31K |
probably damaging |
Het |
Itga9 |
T |
C |
9: 118,527,529 (GRCm39) |
V560A |
probably benign |
Het |
Jhy |
G |
A |
9: 40,822,453 (GRCm39) |
Q562* |
probably null |
Het |
Kcnj5 |
A |
G |
9: 32,233,865 (GRCm39) |
I150T |
probably damaging |
Het |
Kmt2a |
A |
G |
9: 44,752,918 (GRCm39) |
I1419T |
unknown |
Het |
Lix1 |
T |
C |
17: 17,666,320 (GRCm39) |
F160L |
possibly damaging |
Het |
Lonrf2 |
G |
A |
1: 38,852,357 (GRCm39) |
P165S |
probably benign |
Het |
Map4k1 |
A |
T |
7: 28,688,777 (GRCm39) |
Q276L |
possibly damaging |
Het |
Mmp9 |
G |
A |
2: 164,791,342 (GRCm39) |
G171S |
probably damaging |
Het |
Mvp |
C |
A |
7: 126,594,907 (GRCm39) |
|
probably null |
Het |
Mylk3 |
T |
A |
8: 86,091,460 (GRCm39) |
E115V |
probably damaging |
Het |
Nebl |
T |
A |
2: 17,393,565 (GRCm39) |
T603S |
probably damaging |
Het |
Nudt15 |
T |
C |
14: 73,760,776 (GRCm39) |
D105G |
probably benign |
Het |
Or12j2 |
A |
C |
7: 139,915,912 (GRCm39) |
T46P |
possibly damaging |
Het |
Or2w1b |
G |
A |
13: 21,300,476 (GRCm39) |
V205I |
probably benign |
Het |
Or51b6 |
T |
A |
7: 103,555,906 (GRCm39) |
W87R |
probably damaging |
Het |
Or52i2 |
G |
T |
7: 102,319,369 (GRCm39) |
V81L |
probably damaging |
Het |
Or52l1 |
A |
T |
7: 104,829,967 (GRCm39) |
H199Q |
probably damaging |
Het |
Or8g2b |
A |
G |
9: 39,751,581 (GRCm39) |
M284V |
probably benign |
Het |
Osbpl9 |
A |
T |
4: 108,923,415 (GRCm39) |
C495S |
probably damaging |
Het |
Pamr1 |
A |
G |
2: 102,471,197 (GRCm39) |
T507A |
probably benign |
Het |
Pcdhb9 |
T |
A |
18: 37,536,380 (GRCm39) |
C791* |
probably null |
Het |
Pcgf6 |
T |
C |
19: 47,038,957 (GRCm39) |
E101G |
probably damaging |
Het |
Pdgfrl |
A |
T |
8: 41,438,831 (GRCm39) |
I256F |
probably benign |
Het |
Pdzd7 |
T |
C |
19: 45,033,950 (GRCm39) |
R45G |
possibly damaging |
Het |
Pecr |
C |
T |
1: 72,316,568 (GRCm39) |
V46I |
possibly damaging |
Het |
Pgr |
A |
G |
9: 8,922,715 (GRCm39) |
|
probably null |
Het |
Pik3c2a |
A |
T |
7: 116,017,162 (GRCm39) |
Y198* |
probably null |
Het |
Pp2d1 |
T |
A |
17: 53,822,338 (GRCm39) |
M243L |
possibly damaging |
Het |
Ppp1r1a |
T |
A |
15: 103,441,919 (GRCm39) |
I50L |
possibly damaging |
Het |
Proc |
T |
C |
18: 32,260,459 (GRCm39) |
D222G |
probably benign |
Het |
Ptprq |
T |
A |
10: 107,370,560 (GRCm39) |
R2044* |
probably null |
Het |
Ranbp2 |
T |
C |
10: 58,296,341 (GRCm39) |
V326A |
probably benign |
Het |
Reep6 |
T |
A |
10: 80,169,815 (GRCm39) |
F122I |
possibly damaging |
Het |
Rubcn |
C |
A |
16: 32,663,471 (GRCm39) |
R388S |
probably damaging |
Het |
Rusc1 |
A |
G |
3: 88,996,600 (GRCm39) |
L62P |
probably damaging |
Het |
Satb2 |
T |
C |
1: 56,889,448 (GRCm39) |
N423S |
probably damaging |
Het |
Scart1 |
G |
T |
7: 139,800,522 (GRCm39) |
C101F |
probably damaging |
Het |
Serpinb9d |
A |
G |
13: 33,384,731 (GRCm39) |
K236R |
probably benign |
Het |
Slc4a7 |
A |
G |
14: 14,765,709 (GRCm38) |
R680G |
probably benign |
Het |
Slitrk1 |
T |
A |
14: 109,150,528 (GRCm39) |
Y61F |
probably benign |
Het |
Son |
A |
G |
16: 91,457,114 (GRCm39) |
|
probably benign |
Het |
Sparc |
T |
A |
11: 55,286,602 (GRCm39) |
|
probably null |
Het |
Spon2 |
A |
G |
5: 33,373,729 (GRCm39) |
F194S |
probably damaging |
Het |
Spta1 |
A |
G |
1: 174,068,608 (GRCm39) |
E2136G |
probably damaging |
Het |
Stat4 |
T |
C |
1: 52,146,084 (GRCm39) |
S746P |
probably damaging |
Het |
Stk31 |
T |
A |
6: 49,446,238 (GRCm39) |
S958R |
probably benign |
Het |
Stom |
T |
A |
2: 35,205,929 (GRCm39) |
I267F |
probably damaging |
Het |
Stx12 |
A |
T |
4: 132,585,788 (GRCm39) |
D197E |
probably damaging |
Het |
Taok3 |
A |
T |
5: 117,393,991 (GRCm39) |
N588I |
possibly damaging |
Het |
Tgs1 |
A |
G |
4: 3,598,658 (GRCm39) |
D657G |
probably damaging |
Het |
Trim6 |
A |
G |
7: 103,882,044 (GRCm39) |
T432A |
probably damaging |
Het |
Trim72 |
C |
G |
7: 127,603,757 (GRCm39) |
C34W |
probably damaging |
Het |
Trpc4ap |
A |
T |
2: 155,499,664 (GRCm39) |
I286N |
probably benign |
Het |
Ttn |
A |
G |
2: 76,693,905 (GRCm39) |
V321A |
possibly damaging |
Het |
Utp4 |
T |
A |
8: 107,645,352 (GRCm39) |
I583N |
probably damaging |
Het |
Wdfy2 |
G |
T |
14: 63,181,546 (GRCm39) |
M225I |
probably benign |
Het |
Wfdc1 |
A |
G |
8: 120,407,776 (GRCm39) |
T134A |
probably benign |
Het |
Wnt9b |
A |
G |
11: 103,622,954 (GRCm39) |
S150P |
probably damaging |
Het |
Zbtb46 |
A |
T |
2: 181,053,477 (GRCm39) |
F412I |
probably damaging |
Het |
Zc3h15 |
G |
A |
2: 83,491,492 (GRCm39) |
R240H |
probably benign |
Het |
Zfp11 |
A |
T |
5: 129,733,737 (GRCm39) |
Y575N |
probably benign |
Het |
Zfp687 |
T |
C |
3: 94,919,200 (GRCm39) |
M191V |
probably benign |
Het |
|
Other mutations in Efcab3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00897:Efcab3
|
APN |
11 |
104,990,847 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01308:Efcab3
|
APN |
11 |
104,611,523 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01483:Efcab3
|
APN |
11 |
104,630,173 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01695:Efcab3
|
APN |
11 |
104,626,889 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01860:Efcab3
|
APN |
11 |
104,581,747 (GRCm39) |
missense |
probably benign |
0.16 |
IGL01981:Efcab3
|
APN |
11 |
104,612,258 (GRCm39) |
intron |
probably benign |
|
IGL01984:Efcab3
|
APN |
11 |
104,629,134 (GRCm39) |
missense |
probably benign |
0.20 |
IGL02023:Efcab3
|
APN |
11 |
104,612,258 (GRCm39) |
intron |
probably benign |
|
IGL02252:Efcab3
|
APN |
11 |
104,644,753 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL02886:Efcab3
|
APN |
11 |
104,986,700 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL03116:Efcab3
|
APN |
11 |
104,612,359 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03141:Efcab3
|
APN |
11 |
104,986,696 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03242:Efcab3
|
APN |
11 |
104,997,230 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03274:Efcab3
|
APN |
11 |
104,611,919 (GRCm39) |
missense |
probably benign |
0.03 |
IGL03408:Efcab3
|
APN |
11 |
104,601,447 (GRCm39) |
missense |
probably benign |
0.03 |
PIT4812001:Efcab3
|
UTSW |
11 |
104,990,805 (GRCm39) |
missense |
probably null |
0.00 |
R0018:Efcab3
|
UTSW |
11 |
104,612,378 (GRCm39) |
critical splice donor site |
probably null |
|
R0068:Efcab3
|
UTSW |
11 |
104,611,648 (GRCm39) |
missense |
probably benign |
0.29 |
R0350:Efcab3
|
UTSW |
11 |
104,581,706 (GRCm39) |
missense |
probably benign |
0.03 |
R0388:Efcab3
|
UTSW |
11 |
105,000,227 (GRCm39) |
missense |
possibly damaging |
0.61 |
R0646:Efcab3
|
UTSW |
11 |
104,611,327 (GRCm39) |
missense |
probably benign |
0.03 |
R0668:Efcab3
|
UTSW |
11 |
104,611,318 (GRCm39) |
missense |
probably benign |
0.16 |
R0715:Efcab3
|
UTSW |
11 |
104,611,706 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0944:Efcab3
|
UTSW |
11 |
104,601,556 (GRCm39) |
splice site |
probably null |
|
R1330:Efcab3
|
UTSW |
11 |
104,637,116 (GRCm39) |
missense |
possibly damaging |
0.84 |
R1440:Efcab3
|
UTSW |
11 |
104,999,581 (GRCm39) |
splice site |
probably benign |
|
R1508:Efcab3
|
UTSW |
11 |
104,601,503 (GRCm39) |
missense |
probably benign |
0.03 |
R1540:Efcab3
|
UTSW |
11 |
104,999,726 (GRCm39) |
missense |
probably benign |
0.07 |
R1643:Efcab3
|
UTSW |
11 |
104,589,804 (GRCm39) |
missense |
probably benign |
0.16 |
R1651:Efcab3
|
UTSW |
11 |
104,611,492 (GRCm39) |
missense |
probably benign |
0.03 |
R1665:Efcab3
|
UTSW |
11 |
104,611,940 (GRCm39) |
missense |
probably benign |
0.07 |
R1702:Efcab3
|
UTSW |
11 |
104,581,832 (GRCm39) |
missense |
probably benign |
0.03 |
R1779:Efcab3
|
UTSW |
11 |
104,611,765 (GRCm39) |
missense |
probably benign |
0.15 |
R1813:Efcab3
|
UTSW |
11 |
104,611,514 (GRCm39) |
missense |
probably benign |
0.07 |
R1818:Efcab3
|
UTSW |
11 |
104,612,333 (GRCm39) |
missense |
probably benign |
0.10 |
R1896:Efcab3
|
UTSW |
11 |
104,611,514 (GRCm39) |
missense |
probably benign |
0.07 |
R1969:Efcab3
|
UTSW |
11 |
104,637,090 (GRCm39) |
missense |
probably damaging |
1.00 |
R2029:Efcab3
|
UTSW |
11 |
104,990,851 (GRCm39) |
missense |
probably damaging |
0.99 |
R2139:Efcab3
|
UTSW |
11 |
104,642,737 (GRCm39) |
missense |
possibly damaging |
0.53 |
R2165:Efcab3
|
UTSW |
11 |
104,642,688 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2359:Efcab3
|
UTSW |
11 |
104,630,106 (GRCm39) |
missense |
possibly damaging |
0.80 |
R2394:Efcab3
|
UTSW |
11 |
104,629,121 (GRCm39) |
missense |
probably benign |
0.17 |
R2401:Efcab3
|
UTSW |
11 |
104,963,144 (GRCm39) |
critical splice donor site |
probably null |
|
R2406:Efcab3
|
UTSW |
11 |
104,611,457 (GRCm39) |
missense |
probably benign |
0.03 |
R2570:Efcab3
|
UTSW |
11 |
104,624,490 (GRCm39) |
missense |
probably damaging |
1.00 |
R3795:Efcab3
|
UTSW |
11 |
104,624,501 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3901:Efcab3
|
UTSW |
11 |
104,974,713 (GRCm39) |
missense |
possibly damaging |
0.68 |
R4244:Efcab3
|
UTSW |
11 |
105,002,629 (GRCm39) |
missense |
probably damaging |
1.00 |
R4352:Efcab3
|
UTSW |
11 |
104,630,140 (GRCm39) |
missense |
probably null |
0.25 |
R4359:Efcab3
|
UTSW |
11 |
104,624,547 (GRCm39) |
splice site |
probably null |
|
R4424:Efcab3
|
UTSW |
11 |
104,626,940 (GRCm39) |
critical splice donor site |
probably null |
|
R4895:Efcab3
|
UTSW |
11 |
104,611,112 (GRCm39) |
missense |
probably benign |
0.16 |
R4895:Efcab3
|
UTSW |
11 |
105,008,227 (GRCm39) |
unclassified |
probably benign |
|
R4895:Efcab3
|
UTSW |
11 |
104,640,496 (GRCm39) |
missense |
probably damaging |
1.00 |
R5006:Efcab3
|
UTSW |
11 |
104,620,503 (GRCm39) |
splice site |
probably null |
|
R5066:Efcab3
|
UTSW |
11 |
104,611,490 (GRCm39) |
missense |
probably benign |
0.03 |
R5316:Efcab3
|
UTSW |
11 |
104,967,286 (GRCm39) |
missense |
possibly damaging |
0.80 |
R5329:Efcab3
|
UTSW |
11 |
104,644,632 (GRCm39) |
splice site |
probably null |
|
R5405:Efcab3
|
UTSW |
11 |
104,612,018 (GRCm39) |
missense |
probably benign |
0.07 |
R5814:Efcab3
|
UTSW |
11 |
104,626,940 (GRCm39) |
critical splice donor site |
probably benign |
|
R5888:Efcab3
|
UTSW |
11 |
104,612,227 (GRCm39) |
splice site |
probably benign |
|
R5910:Efcab3
|
UTSW |
11 |
104,581,760 (GRCm39) |
missense |
probably benign |
0.01 |
R5975:Efcab3
|
UTSW |
11 |
104,578,375 (GRCm39) |
start gained |
probably benign |
|
R6019:Efcab3
|
UTSW |
11 |
104,933,728 (GRCm39) |
critical splice donor site |
probably null |
|
R6028:Efcab3
|
UTSW |
11 |
104,660,481 (GRCm39) |
critical splice donor site |
probably null |
|
R6048:Efcab3
|
UTSW |
11 |
104,835,259 (GRCm39) |
missense |
unknown |
|
R6059:Efcab3
|
UTSW |
11 |
104,927,595 (GRCm39) |
missense |
probably benign |
0.03 |
R6147:Efcab3
|
UTSW |
11 |
104,858,566 (GRCm39) |
missense |
unknown |
|
R6176:Efcab3
|
UTSW |
11 |
104,683,383 (GRCm39) |
missense |
probably benign |
0.16 |
R6181:Efcab3
|
UTSW |
11 |
104,722,159 (GRCm39) |
missense |
probably benign |
0.25 |
R6196:Efcab3
|
UTSW |
11 |
104,746,386 (GRCm39) |
missense |
probably benign |
0.07 |
R6245:Efcab3
|
UTSW |
11 |
104,675,834 (GRCm39) |
missense |
probably benign |
0.03 |
R6262:Efcab3
|
UTSW |
11 |
104,784,579 (GRCm39) |
missense |
probably benign |
0.24 |
R6263:Efcab3
|
UTSW |
11 |
104,810,312 (GRCm39) |
missense |
unknown |
|
R6277:Efcab3
|
UTSW |
11 |
104,901,148 (GRCm39) |
missense |
possibly damaging |
0.49 |
R6338:Efcab3
|
UTSW |
11 |
104,734,034 (GRCm39) |
nonsense |
probably null |
|
R6355:Efcab3
|
UTSW |
11 |
104,896,511 (GRCm39) |
missense |
probably benign |
0.29 |
R6356:Efcab3
|
UTSW |
11 |
104,784,533 (GRCm39) |
missense |
probably benign |
0.19 |
R6365:Efcab3
|
UTSW |
11 |
104,815,412 (GRCm39) |
missense |
unknown |
|
R6378:Efcab3
|
UTSW |
11 |
104,999,620 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6391:Efcab3
|
UTSW |
11 |
104,885,143 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6494:Efcab3
|
UTSW |
11 |
104,990,845 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6556:Efcab3
|
UTSW |
11 |
104,899,077 (GRCm39) |
missense |
probably null |
0.03 |
R6573:Efcab3
|
UTSW |
11 |
104,971,461 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6604:Efcab3
|
UTSW |
11 |
104,589,772 (GRCm39) |
nonsense |
probably null |
|
R6605:Efcab3
|
UTSW |
11 |
104,890,107 (GRCm39) |
splice site |
probably null |
|
R6634:Efcab3
|
UTSW |
11 |
104,784,609 (GRCm39) |
missense |
probably benign |
0.17 |
R6723:Efcab3
|
UTSW |
11 |
105,007,906 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6851:Efcab3
|
UTSW |
11 |
104,896,521 (GRCm39) |
missense |
probably benign |
0.03 |
R6862:Efcab3
|
UTSW |
11 |
104,612,284 (GRCm39) |
nonsense |
probably null |
|
R6949:Efcab3
|
UTSW |
11 |
104,799,896 (GRCm39) |
missense |
probably damaging |
1.00 |
R6970:Efcab3
|
UTSW |
11 |
104,667,182 (GRCm39) |
missense |
probably benign |
0.03 |
R7014:Efcab3
|
UTSW |
11 |
104,584,248 (GRCm39) |
missense |
probably benign |
0.03 |
R7097:Efcab3
|
UTSW |
11 |
104,899,787 (GRCm39) |
missense |
possibly damaging |
0.68 |
R7122:Efcab3
|
UTSW |
11 |
104,899,787 (GRCm39) |
missense |
possibly damaging |
0.68 |
R7124:Efcab3
|
UTSW |
11 |
104,629,100 (GRCm39) |
missense |
probably benign |
0.17 |
R7146:Efcab3
|
UTSW |
11 |
104,913,764 (GRCm39) |
missense |
probably benign |
0.03 |
R7146:Efcab3
|
UTSW |
11 |
104,858,578 (GRCm39) |
missense |
unknown |
|
R7154:Efcab3
|
UTSW |
11 |
104,589,966 (GRCm39) |
splice site |
probably null |
|
R7175:Efcab3
|
UTSW |
11 |
104,838,237 (GRCm39) |
missense |
unknown |
|
R7189:Efcab3
|
UTSW |
11 |
104,986,690 (GRCm39) |
missense |
probably benign |
|
R7198:Efcab3
|
UTSW |
11 |
104,642,711 (GRCm39) |
missense |
probably benign |
0.15 |
R7211:Efcab3
|
UTSW |
11 |
104,615,435 (GRCm39) |
critical splice donor site |
probably null |
|
R7211:Efcab3
|
UTSW |
11 |
104,601,539 (GRCm39) |
missense |
probably benign |
0.01 |
R7216:Efcab3
|
UTSW |
11 |
104,771,375 (GRCm39) |
missense |
possibly damaging |
0.49 |
R7221:Efcab3
|
UTSW |
11 |
104,791,432 (GRCm39) |
missense |
probably benign |
0.36 |
R7233:Efcab3
|
UTSW |
11 |
104,730,669 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7236:Efcab3
|
UTSW |
11 |
104,790,093 (GRCm39) |
missense |
probably benign |
0.10 |
R7262:Efcab3
|
UTSW |
11 |
104,745,432 (GRCm39) |
critical splice donor site |
probably null |
|
R7289:Efcab3
|
UTSW |
11 |
104,929,184 (GRCm39) |
missense |
probably benign |
0.24 |
R7323:Efcab3
|
UTSW |
11 |
104,920,837 (GRCm39) |
missense |
probably benign |
0.07 |
R7378:Efcab3
|
UTSW |
11 |
104,605,528 (GRCm39) |
missense |
probably benign |
0.03 |
R7388:Efcab3
|
UTSW |
11 |
104,611,871 (GRCm39) |
missense |
probably damaging |
0.97 |
R7390:Efcab3
|
UTSW |
11 |
104,615,411 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7411:Efcab3
|
UTSW |
11 |
104,890,549 (GRCm39) |
missense |
probably benign |
0.10 |
R7468:Efcab3
|
UTSW |
11 |
104,640,526 (GRCm39) |
missense |
probably benign |
0.17 |
R7483:Efcab3
|
UTSW |
11 |
105,000,112 (GRCm39) |
missense |
probably benign |
0.39 |
R7497:Efcab3
|
UTSW |
11 |
104,653,516 (GRCm39) |
critical splice donor site |
probably null |
|
R7612:Efcab3
|
UTSW |
11 |
104,999,647 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7620:Efcab3
|
UTSW |
11 |
104,722,969 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7638:Efcab3
|
UTSW |
11 |
104,927,625 (GRCm39) |
missense |
probably benign |
0.03 |
R7661:Efcab3
|
UTSW |
11 |
104,617,503 (GRCm39) |
missense |
probably benign |
0.03 |
R7667:Efcab3
|
UTSW |
11 |
104,642,737 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7682:Efcab3
|
UTSW |
11 |
104,855,174 (GRCm39) |
splice site |
probably null |
|
R7708:Efcab3
|
UTSW |
11 |
104,855,397 (GRCm39) |
missense |
unknown |
|
R7719:Efcab3
|
UTSW |
11 |
105,002,674 (GRCm39) |
missense |
probably benign |
0.14 |
R7721:Efcab3
|
UTSW |
11 |
104,615,366 (GRCm39) |
nonsense |
probably null |
|
R7735:Efcab3
|
UTSW |
11 |
104,962,465 (GRCm39) |
missense |
probably benign |
|
R7747:Efcab3
|
UTSW |
11 |
104,733,429 (GRCm39) |
missense |
probably damaging |
0.96 |
R7840:Efcab3
|
UTSW |
11 |
104,624,539 (GRCm39) |
missense |
probably benign |
0.07 |
R7846:Efcab3
|
UTSW |
11 |
104,605,571 (GRCm39) |
critical splice donor site |
probably null |
|
R7893:Efcab3
|
UTSW |
11 |
104,870,186 (GRCm39) |
missense |
unknown |
|
R7895:Efcab3
|
UTSW |
11 |
105,008,150 (GRCm39) |
missense |
probably benign |
0.29 |
R7897:Efcab3
|
UTSW |
11 |
104,889,061 (GRCm39) |
missense |
probably benign |
0.24 |
R7936:Efcab3
|
UTSW |
11 |
104,890,524 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7936:Efcab3
|
UTSW |
11 |
104,937,385 (GRCm39) |
critical splice donor site |
probably null |
|
R7959:Efcab3
|
UTSW |
11 |
104,933,627 (GRCm39) |
missense |
probably damaging |
0.96 |
R8031:Efcab3
|
UTSW |
11 |
104,772,295 (GRCm39) |
missense |
possibly damaging |
0.49 |
R8041:Efcab3
|
UTSW |
11 |
104,810,305 (GRCm39) |
missense |
unknown |
|
R8054:Efcab3
|
UTSW |
11 |
104,621,226 (GRCm39) |
missense |
probably benign |
0.07 |
R8056:Efcab3
|
UTSW |
11 |
104,799,896 (GRCm39) |
missense |
probably damaging |
0.98 |
R8061:Efcab3
|
UTSW |
11 |
104,997,275 (GRCm39) |
missense |
probably benign |
0.00 |
R8088:Efcab3
|
UTSW |
11 |
104,889,072 (GRCm39) |
missense |
probably benign |
0.10 |
R8112:Efcab3
|
UTSW |
11 |
104,841,026 (GRCm39) |
missense |
unknown |
|
R8116:Efcab3
|
UTSW |
11 |
105,002,677 (GRCm39) |
missense |
possibly damaging |
0.65 |
R8340:Efcab3
|
UTSW |
11 |
104,876,856 (GRCm39) |
missense |
unknown |
|
R8405:Efcab3
|
UTSW |
11 |
104,612,024 (GRCm39) |
missense |
probably benign |
0.02 |
R8413:Efcab3
|
UTSW |
11 |
104,811,135 (GRCm39) |
missense |
unknown |
|
R8472:Efcab3
|
UTSW |
11 |
104,709,463 (GRCm39) |
missense |
probably benign |
0.07 |
R8549:Efcab3
|
UTSW |
11 |
104,890,521 (GRCm39) |
missense |
probably damaging |
0.99 |
R8699:Efcab3
|
UTSW |
11 |
104,672,072 (GRCm39) |
missense |
probably benign |
0.03 |
R8711:Efcab3
|
UTSW |
11 |
104,743,371 (GRCm39) |
missense |
probably benign |
0.03 |
R8732:Efcab3
|
UTSW |
11 |
104,695,100 (GRCm39) |
missense |
probably benign |
0.03 |
R8745:Efcab3
|
UTSW |
11 |
104,749,304 (GRCm39) |
missense |
possibly damaging |
0.57 |
R8806:Efcab3
|
UTSW |
11 |
104,928,695 (GRCm39) |
missense |
probably benign |
0.07 |
R8810:Efcab3
|
UTSW |
11 |
104,805,721 (GRCm39) |
missense |
unknown |
|
R8845:Efcab3
|
UTSW |
11 |
104,899,787 (GRCm39) |
missense |
possibly damaging |
0.68 |
R8870:Efcab3
|
UTSW |
11 |
104,791,500 (GRCm39) |
missense |
probably benign |
0.07 |
R8872:Efcab3
|
UTSW |
11 |
104,760,880 (GRCm39) |
missense |
probably benign |
0.19 |
R8879:Efcab3
|
UTSW |
11 |
104,581,781 (GRCm39) |
missense |
probably benign |
0.03 |
R8924:Efcab3
|
UTSW |
11 |
104,806,253 (GRCm39) |
frame shift |
probably null |
|
R8954:Efcab3
|
UTSW |
11 |
104,909,525 (GRCm39) |
critical splice donor site |
probably null |
|
R8960:Efcab3
|
UTSW |
11 |
104,820,772 (GRCm39) |
splice site |
probably benign |
|
R8975:Efcab3
|
UTSW |
11 |
104,954,415 (GRCm39) |
missense |
probably benign |
0.17 |
R8988:Efcab3
|
UTSW |
11 |
104,911,352 (GRCm39) |
missense |
probably benign |
0.07 |
R8998:Efcab3
|
UTSW |
11 |
104,640,477 (GRCm39) |
missense |
probably benign |
0.09 |
R8999:Efcab3
|
UTSW |
11 |
104,640,477 (GRCm39) |
missense |
probably benign |
0.09 |
R9002:Efcab3
|
UTSW |
11 |
104,920,822 (GRCm39) |
missense |
probably damaging |
0.99 |
R9012:Efcab3
|
UTSW |
11 |
104,711,347 (GRCm39) |
critical splice donor site |
probably null |
|
R9036:Efcab3
|
UTSW |
11 |
104,927,601 (GRCm39) |
missense |
probably benign |
0.03 |
R9037:Efcab3
|
UTSW |
11 |
104,803,791 (GRCm39) |
missense |
unknown |
|
R9059:Efcab3
|
UTSW |
11 |
104,642,689 (GRCm39) |
missense |
possibly damaging |
0.73 |
R9066:Efcab3
|
UTSW |
11 |
104,631,688 (GRCm39) |
intron |
probably benign |
|
R9122:Efcab3
|
UTSW |
11 |
104,856,605 (GRCm39) |
missense |
unknown |
|
R9125:Efcab3
|
UTSW |
11 |
104,736,360 (GRCm39) |
missense |
probably damaging |
1.00 |
R9127:Efcab3
|
UTSW |
11 |
104,741,407 (GRCm39) |
missense |
probably benign |
0.07 |
R9171:Efcab3
|
UTSW |
11 |
104,800,708 (GRCm39) |
missense |
probably benign |
0.36 |
R9219:Efcab3
|
UTSW |
11 |
104,836,691 (GRCm39) |
missense |
unknown |
|
R9224:Efcab3
|
UTSW |
11 |
104,661,801 (GRCm39) |
missense |
probably benign |
0.07 |
R9235:Efcab3
|
UTSW |
11 |
104,907,987 (GRCm39) |
missense |
probably benign |
0.19 |
R9294:Efcab3
|
UTSW |
11 |
104,722,126 (GRCm39) |
missense |
probably benign |
0.24 |
R9318:Efcab3
|
UTSW |
11 |
104,856,648 (GRCm39) |
critical splice donor site |
probably null |
|
R9322:Efcab3
|
UTSW |
11 |
104,765,199 (GRCm39) |
missense |
probably benign |
0.36 |
R9361:Efcab3
|
UTSW |
11 |
104,896,524 (GRCm39) |
missense |
probably benign |
0.03 |
R9408:Efcab3
|
UTSW |
11 |
104,621,255 (GRCm39) |
critical splice donor site |
probably null |
|
R9434:Efcab3
|
UTSW |
11 |
104,899,863 (GRCm39) |
missense |
probably benign |
0.24 |
R9477:Efcab3
|
UTSW |
11 |
104,836,698 (GRCm39) |
missense |
unknown |
|
R9658:Efcab3
|
UTSW |
11 |
104,611,120 (GRCm39) |
missense |
probably benign |
0.03 |
R9719:Efcab3
|
UTSW |
11 |
104,867,912 (GRCm39) |
missense |
unknown |
|
R9751:Efcab3
|
UTSW |
11 |
104,783,911 (GRCm39) |
missense |
probably benign |
0.19 |
R9763:Efcab3
|
UTSW |
11 |
104,890,485 (GRCm39) |
missense |
possibly damaging |
0.89 |
X0026:Efcab3
|
UTSW |
11 |
105,007,937 (GRCm39) |
missense |
probably benign |
0.03 |
X0026:Efcab3
|
UTSW |
11 |
104,611,801 (GRCm39) |
missense |
probably benign |
0.07 |
Z1088:Efcab3
|
UTSW |
11 |
104,642,728 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1176:Efcab3
|
UTSW |
11 |
104,990,872 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Efcab3
|
UTSW |
11 |
104,892,793 (GRCm39) |
missense |
probably benign |
0.29 |
Z1176:Efcab3
|
UTSW |
11 |
104,999,598 (GRCm39) |
nonsense |
probably null |
|
Z1177:Efcab3
|
UTSW |
11 |
104,711,344 (GRCm39) |
missense |
probably benign |
0.03 |
Z1177:Efcab3
|
UTSW |
11 |
104,630,164 (GRCm39) |
nonsense |
probably null |
|
Z1177:Efcab3
|
UTSW |
11 |
104,814,845 (GRCm39) |
missense |
unknown |
|
|