Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930438A08Rik |
A |
G |
11: 58,179,176 (GRCm39) |
Y170C |
probably damaging |
Het |
Adcy2 |
C |
T |
13: 69,036,161 (GRCm39) |
V167I |
probably benign |
Het |
Agl |
A |
G |
3: 116,545,825 (GRCm39) |
Y1324H |
probably damaging |
Het |
Arhgef37 |
G |
T |
18: 61,641,860 (GRCm39) |
Q170K |
probably damaging |
Het |
Asah2 |
A |
G |
19: 31,994,176 (GRCm39) |
S390P |
probably damaging |
Het |
Atp8a1 |
A |
T |
5: 67,932,068 (GRCm39) |
H240Q |
probably benign |
Het |
Btbd16 |
T |
A |
7: 130,390,557 (GRCm39) |
N151K |
probably damaging |
Het |
Ccdc73 |
T |
A |
2: 104,803,499 (GRCm39) |
|
probably benign |
Het |
Cecr2 |
G |
T |
6: 120,735,159 (GRCm39) |
M21I |
probably benign |
Het |
Ckap2l |
T |
C |
2: 129,127,636 (GRCm39) |
T181A |
probably benign |
Het |
Col4a3 |
T |
C |
1: 82,629,879 (GRCm39) |
|
probably benign |
Het |
Cplane1 |
T |
A |
15: 8,252,576 (GRCm39) |
C1933S |
probably benign |
Het |
Dnah9 |
A |
G |
11: 65,972,074 (GRCm39) |
|
probably benign |
Het |
Fat3 |
T |
C |
9: 16,286,419 (GRCm39) |
T1035A |
probably benign |
Het |
Fzd8 |
A |
G |
18: 9,212,947 (GRCm39) |
T10A |
unknown |
Het |
Gm9631 |
C |
A |
11: 121,833,328 (GRCm39) |
C636F |
probably damaging |
Het |
Gp1ba |
A |
G |
11: 70,531,614 (GRCm39) |
|
probably benign |
Het |
Gsk3a |
A |
G |
7: 24,931,134 (GRCm39) |
V277A |
probably damaging |
Het |
H2-M1 |
T |
A |
17: 36,981,120 (GRCm39) |
|
probably benign |
Het |
Hesx1 |
T |
A |
14: 26,722,809 (GRCm39) |
W45R |
probably damaging |
Het |
Il23r |
T |
A |
6: 67,463,317 (GRCm39) |
M59L |
possibly damaging |
Het |
Insc |
T |
A |
7: 114,444,312 (GRCm39) |
V433E |
probably benign |
Het |
Itga8 |
T |
C |
2: 12,196,053 (GRCm39) |
|
probably benign |
Het |
Kif13a |
T |
A |
13: 46,966,299 (GRCm39) |
E436V |
probably damaging |
Het |
Liph |
A |
G |
16: 21,814,100 (GRCm39) |
F7S |
probably benign |
Het |
Lpar2 |
T |
C |
8: 70,276,823 (GRCm39) |
V204A |
probably damaging |
Het |
Lrfn4 |
T |
A |
19: 4,662,668 (GRCm39) |
|
probably null |
Het |
Man2b2 |
A |
T |
5: 36,983,402 (GRCm39) |
D182E |
probably benign |
Het |
Mmp27 |
T |
C |
9: 7,581,156 (GRCm39) |
|
probably benign |
Het |
Mrm1 |
A |
G |
11: 84,705,639 (GRCm39) |
|
probably benign |
Het |
Mtx3 |
T |
C |
13: 92,986,869 (GRCm39) |
S271P |
probably damaging |
Het |
Myh11 |
A |
T |
16: 14,044,480 (GRCm39) |
M641K |
possibly damaging |
Het |
Necab2 |
A |
G |
8: 120,197,670 (GRCm39) |
D332G |
probably damaging |
Het |
Ngfr |
A |
G |
11: 95,465,065 (GRCm39) |
I261T |
possibly damaging |
Het |
Nrap |
T |
C |
19: 56,345,757 (GRCm39) |
E617G |
probably damaging |
Het |
Obscn |
G |
T |
11: 58,941,306 (GRCm39) |
T4505K |
probably benign |
Het |
Or8b37 |
G |
T |
9: 37,959,123 (GRCm39) |
V202L |
probably benign |
Het |
Or8b57 |
A |
G |
9: 40,003,807 (GRCm39) |
Y148H |
probably damaging |
Het |
Osbpl11 |
T |
A |
16: 33,062,100 (GRCm39) |
|
probably benign |
Het |
Otof |
A |
G |
5: 30,552,041 (GRCm39) |
V301A |
probably damaging |
Het |
Phf3 |
A |
T |
1: 30,850,919 (GRCm39) |
L1145Q |
probably damaging |
Het |
Phospho2 |
T |
A |
2: 69,626,540 (GRCm39) |
I232N |
possibly damaging |
Het |
Pomgnt2 |
T |
A |
9: 121,811,127 (GRCm39) |
K551N |
probably damaging |
Het |
Ptchd3 |
A |
G |
11: 121,721,984 (GRCm39) |
T286A |
possibly damaging |
Het |
Rnf213 |
A |
G |
11: 119,331,976 (GRCm39) |
D2396G |
probably damaging |
Het |
Sh3pxd2b |
A |
G |
11: 32,373,341 (GRCm39) |
E836G |
possibly damaging |
Het |
Simc1 |
G |
T |
13: 54,673,468 (GRCm39) |
M605I |
possibly damaging |
Het |
Slc12a3 |
G |
A |
8: 95,056,061 (GRCm39) |
E66K |
possibly damaging |
Het |
Spg11 |
T |
C |
2: 121,915,464 (GRCm39) |
N1060S |
probably benign |
Het |
Supt5 |
A |
T |
7: 28,028,462 (GRCm39) |
W178R |
probably damaging |
Het |
Tmem41a |
G |
T |
16: 21,756,740 (GRCm39) |
F126L |
probably benign |
Het |
Ube2m |
T |
A |
7: 12,771,553 (GRCm39) |
Q35L |
probably benign |
Het |
Usp33 |
A |
G |
3: 152,086,211 (GRCm39) |
D658G |
probably damaging |
Het |
Vmn2r12 |
A |
T |
5: 109,238,373 (GRCm39) |
C456S |
probably benign |
Het |
Vmn2r81 |
T |
A |
10: 79,104,434 (GRCm39) |
D352E |
probably damaging |
Het |
Zfp516 |
A |
G |
18: 83,005,388 (GRCm39) |
Y764C |
probably damaging |
Het |
Zswim7 |
A |
G |
11: 62,167,473 (GRCm39) |
|
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 |
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 |
R1711:Efcab3
|
UTSW |
11 |
104,611,514 (GRCm39) |
missense |
probably benign |
0.07 |
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 |
|
|