Other mutations in this stock |
Total: 82 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
T |
G |
11: 9,242,080 (GRCm39) |
D1314E |
probably benign |
Het |
Abcb1a |
A |
T |
5: 8,724,707 (GRCm39) |
R47W |
probably benign |
Het |
Abcc6 |
T |
C |
7: 45,629,184 (GRCm39) |
N1354S |
probably damaging |
Het |
Abracl |
T |
C |
10: 17,887,444 (GRCm39) |
Y61C |
probably damaging |
Het |
Adamtsl1 |
A |
G |
4: 86,208,027 (GRCm39) |
T633A |
probably benign |
Het |
Agap3 |
G |
A |
5: 24,681,439 (GRCm39) |
|
probably benign |
Het |
Ago4 |
A |
T |
4: 126,400,904 (GRCm39) |
M647K |
probably damaging |
Het |
Akap7 |
G |
T |
10: 25,155,676 (GRCm39) |
S72R |
unknown |
Het |
Arhgef12 |
A |
G |
9: 42,885,870 (GRCm39) |
L1251S |
possibly damaging |
Het |
Astn2 |
A |
T |
4: 66,322,164 (GRCm39) |
V145E |
unknown |
Het |
Atxn2l |
A |
T |
7: 126,097,393 (GRCm39) |
S304R |
probably damaging |
Het |
Cd226 |
A |
T |
18: 89,287,155 (GRCm39) |
I318F |
probably damaging |
Het |
Cep250 |
C |
T |
2: 155,812,042 (GRCm39) |
A446V |
unknown |
Het |
Cfap65 |
A |
T |
1: 74,958,510 (GRCm39) |
|
probably benign |
Het |
Cfap96 |
T |
G |
8: 46,415,403 (GRCm39) |
D201A |
probably benign |
Het |
Chtf8 |
A |
G |
8: 107,613,640 (GRCm39) |
V18A |
probably benign |
Het |
Cit |
G |
T |
5: 116,074,896 (GRCm39) |
E683* |
probably null |
Het |
Ckmt2 |
T |
C |
13: 92,007,337 (GRCm39) |
R286G |
probably damaging |
Het |
Clec4a2 |
T |
A |
6: 123,116,218 (GRCm39) |
W128R |
probably damaging |
Het |
Clec4n |
T |
G |
6: 123,212,447 (GRCm39) |
S88A |
probably damaging |
Het |
Cndp2 |
G |
A |
18: 84,699,121 (GRCm39) |
A48V |
probably benign |
Het |
Csmd1 |
T |
C |
8: 16,273,286 (GRCm39) |
T849A |
probably benign |
Het |
Cts3 |
A |
T |
13: 61,715,235 (GRCm39) |
Y199* |
probably null |
Het |
Dag1 |
A |
T |
9: 108,085,734 (GRCm39) |
L469* |
probably null |
Het |
Dclre1c |
T |
C |
2: 3,439,125 (GRCm39) |
V225A |
|
Het |
Dedd |
A |
G |
1: 171,166,409 (GRCm39) |
D115G |
probably damaging |
Het |
Eif2ak3 |
T |
A |
6: 70,860,704 (GRCm39) |
W427R |
probably damaging |
Het |
Fbln2 |
T |
A |
6: 91,210,473 (GRCm39) |
V139D |
probably damaging |
Het |
Fbn1 |
A |
T |
2: 125,223,985 (GRCm39) |
M588K |
possibly damaging |
Het |
Gm17019 |
A |
T |
5: 15,081,113 (GRCm39) |
Y109* |
probably null |
Het |
Gm32742 |
T |
A |
9: 51,056,015 (GRCm39) |
N1255Y |
probably damaging |
Het |
Gm5431 |
T |
A |
11: 48,779,600 (GRCm39) |
K441* |
probably null |
Het |
Golga2 |
A |
G |
2: 32,196,079 (GRCm39) |
D898G |
|
Het |
Gramd4 |
G |
A |
15: 85,975,525 (GRCm39) |
R39H |
probably benign |
Het |
Gucy1a2 |
A |
G |
9: 3,634,553 (GRCm39) |
N199S |
probably damaging |
Het |
Heyl |
G |
A |
4: 123,139,885 (GRCm39) |
R148H |
probably damaging |
Het |
Ifi208 |
A |
T |
1: 173,523,400 (GRCm39) |
M557L |
probably benign |
Het |
Igf2r |
A |
G |
17: 12,958,238 (GRCm39) |
V145A |
probably damaging |
Het |
Ighv1-4 |
A |
T |
12: 114,450,879 (GRCm39) |
Y76* |
probably null |
Het |
Ikzf4 |
T |
C |
10: 128,468,487 (GRCm39) |
D664G |
unknown |
Het |
Il1a |
T |
A |
2: 129,146,715 (GRCm39) |
Y126F |
possibly damaging |
Het |
Lmf2 |
C |
A |
15: 89,239,771 (GRCm39) |
|
probably benign |
Het |
Lyst |
T |
C |
13: 13,808,827 (GRCm39) |
S166P |
probably damaging |
Het |
Mgat5 |
A |
C |
1: 127,294,197 (GRCm39) |
T180P |
probably benign |
Het |
Mical2 |
A |
C |
7: 111,870,589 (GRCm39) |
K26T |
possibly damaging |
Het |
Mov10 |
G |
T |
3: 104,711,659 (GRCm39) |
Y209* |
probably null |
Het |
Nol8 |
T |
C |
13: 49,815,475 (GRCm39) |
Y528H |
probably benign |
Het |
Numa1 |
T |
A |
7: 101,641,869 (GRCm39) |
S106T |
possibly damaging |
Het |
Or1e1d-ps1 |
A |
T |
11: 73,819,167 (GRCm39) |
E39V |
probably damaging |
Het |
Or4c124 |
G |
A |
2: 89,156,474 (GRCm39) |
Q17* |
probably null |
Het |
Or5b107 |
A |
G |
19: 13,142,396 (GRCm39) |
N6S |
probably damaging |
Het |
Or7g27 |
A |
G |
9: 19,250,026 (GRCm39) |
H90R |
probably benign |
Het |
Pcdhb14 |
A |
G |
18: 37,582,091 (GRCm39) |
N399S |
probably damaging |
Het |
Plcl2 |
T |
A |
17: 50,918,032 (GRCm39) |
S944T |
probably benign |
Het |
Pml |
A |
T |
9: 58,127,660 (GRCm39) |
I695N |
probably benign |
Het |
Ppard |
G |
T |
17: 28,505,349 (GRCm39) |
R12L |
unknown |
Het |
Ppip5k1 |
C |
T |
2: 121,158,125 (GRCm39) |
|
probably null |
Het |
Ppp1r3g |
T |
C |
13: 36,152,621 (GRCm39) |
S14P |
probably benign |
Het |
Pramel55 |
A |
G |
5: 95,951,623 (GRCm39) |
Y470C |
probably damaging |
Het |
Prrc2b |
C |
A |
2: 32,103,764 (GRCm39) |
R1081S |
probably damaging |
Het |
Rasgrp2 |
A |
T |
19: 6,454,438 (GRCm39) |
E160D |
possibly damaging |
Het |
Rb1cc1 |
G |
A |
1: 6,333,073 (GRCm39) |
V1331I |
probably damaging |
Het |
Rnd3 |
A |
T |
2: 51,022,413 (GRCm39) |
S210T |
probably benign |
Het |
Scaf11 |
T |
C |
15: 96,312,764 (GRCm39) |
T1426A |
probably benign |
Het |
Sin3b |
C |
T |
8: 73,460,034 (GRCm39) |
T207I |
possibly damaging |
Het |
Slc26a7 |
A |
T |
4: 14,593,873 (GRCm39) |
Y81N |
probably damaging |
Het |
Slc28a3 |
C |
T |
13: 58,724,581 (GRCm39) |
M224I |
probably benign |
Het |
Slc30a1 |
T |
C |
1: 191,639,342 (GRCm39) |
I75T |
probably damaging |
Het |
Slc6a21 |
T |
A |
7: 44,929,674 (GRCm39) |
|
probably benign |
Het |
Slco2a1 |
T |
A |
9: 102,945,243 (GRCm39) |
L206Q |
probably damaging |
Het |
Spata31d1e |
A |
G |
13: 59,890,828 (GRCm39) |
S331P |
probably benign |
Het |
Sptbn1 |
A |
G |
11: 30,104,356 (GRCm39) |
V116A |
probably damaging |
Het |
Syngap1 |
G |
A |
17: 27,181,095 (GRCm39) |
D1008N |
probably damaging |
Het |
Syt11 |
T |
C |
3: 88,669,643 (GRCm39) |
D83G |
probably benign |
Het |
Syt14 |
G |
A |
1: 192,584,131 (GRCm39) |
T428I |
probably damaging |
Het |
Taf15 |
T |
A |
11: 83,395,085 (GRCm39) |
Y338* |
probably null |
Het |
Tfap4 |
A |
T |
16: 4,365,183 (GRCm39) |
M253K |
possibly damaging |
Het |
Tnr |
T |
C |
1: 159,713,680 (GRCm39) |
S703P |
possibly damaging |
Het |
Trrap |
G |
A |
5: 144,767,830 (GRCm39) |
D2577N |
probably benign |
Het |
Uqcc6 |
A |
T |
10: 82,458,588 (GRCm39) |
M21K |
probably benign |
Het |
Wdr20 |
C |
T |
12: 110,759,597 (GRCm39) |
S161L |
possibly damaging |
Het |
Zfp503 |
C |
A |
14: 22,037,418 (GRCm39) |
V62L |
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 |
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 |
105,008,227 (GRCm39) |
unclassified |
probably benign |
|
R4895:Efcab3
|
UTSW |
11 |
104,640,496 (GRCm39) |
missense |
probably damaging |
1.00 |
R4895:Efcab3
|
UTSW |
11 |
104,611,112 (GRCm39) |
missense |
probably benign |
0.16 |
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 |
104,601,539 (GRCm39) |
missense |
probably benign |
0.01 |
R7211:Efcab3
|
UTSW |
11 |
104,615,435 (GRCm39) |
critical splice donor site |
probably null |
|
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 |
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 |
|
|