Other mutations in this stock |
Total: 125 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930432E11Rik |
C |
T |
7: 29,260,710 (GRCm39) |
|
noncoding transcript |
Het |
Abcb11 |
A |
G |
2: 69,115,627 (GRCm39) |
I579T |
probably damaging |
Het |
Abcc9 |
T |
C |
6: 142,627,830 (GRCm39) |
N400S |
probably benign |
Het |
Adarb2 |
T |
C |
13: 8,781,855 (GRCm39) |
L577P |
probably damaging |
Het |
Agt |
A |
C |
8: 125,283,852 (GRCm39) |
N422K |
probably damaging |
Het |
Ahnak |
A |
T |
19: 8,990,766 (GRCm39) |
K4017* |
probably null |
Het |
Akap13 |
C |
A |
7: 75,397,494 (GRCm39) |
Q2575K |
probably damaging |
Het |
Aldh3a2 |
A |
T |
11: 61,144,541 (GRCm39) |
I339K |
probably damaging |
Het |
Alox15 |
G |
T |
11: 70,236,450 (GRCm39) |
Y483* |
probably null |
Het |
Ampd1 |
A |
T |
3: 103,006,913 (GRCm39) |
I713F |
probably damaging |
Het |
Amph |
A |
T |
13: 19,297,286 (GRCm39) |
E344V |
possibly damaging |
Het |
Arhgef18 |
T |
C |
8: 3,436,959 (GRCm39) |
Y250H |
probably damaging |
Het |
Arid5b |
A |
G |
10: 67,932,807 (GRCm39) |
S1032P |
probably damaging |
Het |
Armc8 |
C |
A |
9: 99,387,741 (GRCm39) |
L393F |
probably damaging |
Het |
Bpnt1 |
A |
G |
1: 185,077,623 (GRCm39) |
|
probably null |
Het |
Cachd1 |
G |
A |
4: 100,845,418 (GRCm39) |
R970H |
probably damaging |
Het |
Cd207 |
T |
C |
6: 83,652,738 (GRCm39) |
T131A |
probably benign |
Het |
Cd83 |
G |
A |
13: 43,951,009 (GRCm39) |
V54I |
probably benign |
Het |
Cfap43 |
T |
C |
19: 47,752,115 (GRCm39) |
K1086E |
probably benign |
Het |
Cfap65 |
A |
T |
1: 74,941,328 (GRCm39) |
V1837E |
probably benign |
Het |
Clcnka |
T |
A |
4: 141,123,917 (GRCm39) |
H89L |
probably benign |
Het |
Cnga4 |
T |
C |
7: 105,054,182 (GRCm39) |
I50T |
possibly damaging |
Het |
Cog5 |
A |
G |
12: 31,887,358 (GRCm39) |
|
probably benign |
Het |
Col11a2 |
T |
A |
17: 34,278,322 (GRCm39) |
|
probably null |
Het |
Col28a1 |
T |
G |
6: 8,175,291 (GRCm39) |
I186L |
possibly damaging |
Het |
Col4a2 |
T |
A |
8: 11,481,252 (GRCm39) |
M808K |
probably benign |
Het |
Copb2 |
A |
G |
9: 98,445,528 (GRCm39) |
|
probably benign |
Het |
Dbnl |
G |
A |
11: 5,745,441 (GRCm39) |
|
probably benign |
Het |
Dbx2 |
T |
C |
15: 95,552,493 (GRCm39) |
T51A |
possibly damaging |
Het |
Dcp1a |
A |
T |
14: 30,224,842 (GRCm39) |
M123L |
probably damaging |
Het |
Ddx42 |
T |
A |
11: 106,123,659 (GRCm39) |
F217I |
probably benign |
Het |
Dlc1 |
T |
C |
8: 37,325,205 (GRCm39) |
T367A |
probably benign |
Het |
Dmgdh |
A |
T |
13: 93,888,863 (GRCm39) |
T834S |
probably benign |
Het |
Dnah8 |
T |
C |
17: 30,903,147 (GRCm39) |
S929P |
probably damaging |
Het |
Dnase1l2 |
C |
A |
17: 24,660,056 (GRCm39) |
V271L |
possibly damaging |
Het |
Dsc1 |
T |
C |
18: 20,229,114 (GRCm39) |
Y392C |
probably damaging |
Het |
Edn1 |
T |
C |
13: 42,458,718 (GRCm39) |
|
probably benign |
Het |
Eps8l3 |
T |
C |
3: 107,792,126 (GRCm39) |
L351P |
probably damaging |
Het |
F12 |
G |
A |
13: 55,570,296 (GRCm39) |
|
probably benign |
Het |
Fam47e |
T |
C |
5: 92,726,317 (GRCm39) |
|
probably benign |
Het |
Fcrl5 |
C |
A |
3: 87,349,320 (GRCm39) |
Q32K |
probably benign |
Het |
Fndc1 |
C |
T |
17: 7,960,505 (GRCm39) |
V1637I |
possibly damaging |
Het |
Foxg1 |
G |
T |
12: 49,431,350 (GRCm39) |
|
probably benign |
Het |
Frrs1 |
A |
T |
3: 116,696,070 (GRCm39) |
I530F |
possibly damaging |
Het |
Galnt5 |
A |
T |
2: 57,889,097 (GRCm39) |
K232N |
probably benign |
Het |
Ggt5 |
G |
A |
10: 75,438,482 (GRCm39) |
V68M |
probably damaging |
Het |
Gm16519 |
T |
C |
17: 71,236,101 (GRCm39) |
C17R |
probably benign |
Het |
Gm17535 |
A |
G |
9: 3,035,804 (GRCm39) |
Y224C |
probably null |
Het |
Gm9631 |
T |
G |
11: 121,836,455 (GRCm39) |
D28A |
probably damaging |
Het |
Gpx2 |
T |
C |
12: 76,842,087 (GRCm39) |
I21M |
probably benign |
Het |
H2-Q2 |
T |
G |
17: 35,564,661 (GRCm39) |
D354E |
probably damaging |
Het |
Icam2 |
A |
T |
11: 106,271,717 (GRCm39) |
I71K |
probably damaging |
Het |
Il12a |
T |
C |
3: 68,605,223 (GRCm39) |
|
probably benign |
Het |
Insm2 |
C |
G |
12: 55,647,225 (GRCm39) |
A323G |
probably benign |
Het |
Itga1 |
T |
C |
13: 115,104,835 (GRCm39) |
T1064A |
probably benign |
Het |
Itgad |
T |
A |
7: 127,773,176 (GRCm39) |
V11E |
possibly damaging |
Het |
Kctd15 |
C |
T |
7: 34,344,306 (GRCm39) |
S115N |
probably damaging |
Het |
Klra5 |
A |
G |
6: 129,880,527 (GRCm39) |
W124R |
probably damaging |
Het |
Kng2 |
T |
A |
16: 22,806,486 (GRCm39) |
D571V |
probably benign |
Het |
Kpna6 |
A |
T |
4: 129,544,583 (GRCm39) |
F380I |
probably benign |
Het |
Lipo3 |
A |
T |
19: 33,762,169 (GRCm39) |
Y109* |
probably null |
Het |
Lrrc37 |
T |
A |
11: 103,503,986 (GRCm39) |
K485* |
probably null |
Het |
Man2a2 |
T |
C |
7: 80,012,945 (GRCm39) |
H540R |
possibly damaging |
Het |
Map2k4 |
T |
C |
11: 65,603,101 (GRCm39) |
E188G |
probably damaging |
Het |
Mast4 |
T |
C |
13: 102,895,252 (GRCm39) |
|
probably benign |
Het |
Mbtd1 |
A |
G |
11: 93,796,038 (GRCm39) |
D25G |
probably damaging |
Het |
Med13 |
T |
A |
11: 86,221,915 (GRCm39) |
Q238L |
possibly damaging |
Het |
Mmachc |
A |
G |
4: 116,560,851 (GRCm39) |
Y215H |
probably damaging |
Het |
Mtor |
T |
A |
4: 148,568,811 (GRCm39) |
Y1110* |
probably null |
Het |
Nek2 |
A |
G |
1: 191,554,331 (GRCm39) |
N57D |
probably damaging |
Het |
Nek7 |
ACCCC |
ACCC |
1: 138,443,431 (GRCm39) |
|
probably null |
Het |
Neo1 |
G |
T |
9: 58,838,317 (GRCm39) |
T489K |
probably damaging |
Het |
Neu1 |
T |
A |
17: 35,153,736 (GRCm39) |
Y387N |
probably damaging |
Het |
Nfasc |
A |
T |
1: 132,536,176 (GRCm39) |
C586* |
probably null |
Het |
Nle1 |
G |
A |
11: 82,795,671 (GRCm39) |
L259F |
probably damaging |
Het |
Nrde2 |
G |
A |
12: 100,110,105 (GRCm39) |
Q309* |
probably null |
Het |
Nufip2 |
C |
T |
11: 77,577,279 (GRCm39) |
H76Y |
probably benign |
Het |
Or10ak16 |
A |
C |
4: 118,750,687 (GRCm39) |
T136P |
probably damaging |
Het |
Or2y13 |
A |
T |
11: 49,415,405 (GRCm39) |
N285I |
probably damaging |
Het |
Or4k6 |
A |
T |
14: 50,476,096 (GRCm39) |
I82N |
probably damaging |
Het |
Or52e18 |
A |
T |
7: 104,609,018 (GRCm39) |
I307N |
probably benign |
Het |
Or52r1c |
T |
C |
7: 102,735,358 (GRCm39) |
F206S |
probably damaging |
Het |
Or9s18 |
A |
T |
13: 65,300,877 (GRCm39) |
I280F |
probably damaging |
Het |
Pcdhb5 |
A |
G |
18: 37,454,675 (GRCm39) |
T352A |
probably benign |
Het |
Pcdhb7 |
A |
T |
18: 37,476,442 (GRCm39) |
D526V |
probably damaging |
Het |
Phkg1 |
A |
T |
5: 129,893,394 (GRCm39) |
|
probably null |
Het |
Plg |
C |
T |
17: 12,637,623 (GRCm39) |
T744M |
probably damaging |
Het |
Plxnd1 |
A |
C |
6: 115,935,660 (GRCm39) |
|
probably benign |
Het |
Poglut1 |
A |
T |
16: 38,349,837 (GRCm39) |
I312N |
probably damaging |
Het |
Ppp1r16a |
C |
T |
15: 76,574,999 (GRCm39) |
|
probably benign |
Het |
Ppt1 |
A |
G |
4: 122,737,892 (GRCm39) |
M77V |
probably benign |
Het |
Pramel26 |
A |
C |
4: 143,539,155 (GRCm39) |
S113A |
possibly damaging |
Het |
Pramel5 |
G |
T |
4: 143,998,190 (GRCm39) |
T351N |
probably damaging |
Het |
Psmb4 |
G |
A |
3: 94,792,275 (GRCm39) |
R216C |
probably benign |
Het |
Ptprd |
T |
C |
4: 76,002,640 (GRCm39) |
T699A |
probably damaging |
Het |
Retreg3 |
A |
T |
11: 100,989,455 (GRCm39) |
|
probably benign |
Het |
Sanbr |
C |
T |
11: 23,525,491 (GRCm39) |
R716H |
probably damaging |
Het |
Scaper |
G |
A |
9: 55,665,340 (GRCm39) |
A389V |
probably damaging |
Het |
Serinc5 |
G |
A |
13: 92,825,245 (GRCm39) |
D225N |
possibly damaging |
Het |
Slco1a1 |
T |
G |
6: 141,871,480 (GRCm39) |
|
probably benign |
Het |
Snapc1 |
C |
T |
12: 74,021,806 (GRCm39) |
R81C |
probably damaging |
Het |
Sod3 |
A |
T |
5: 52,525,421 (GRCm39) |
D40V |
probably benign |
Het |
Sorcs3 |
C |
A |
19: 48,194,734 (GRCm39) |
A39E |
probably benign |
Het |
Spon1 |
A |
T |
7: 113,639,056 (GRCm39) |
T761S |
probably benign |
Het |
Syde2 |
A |
G |
3: 145,720,004 (GRCm39) |
|
probably null |
Het |
Synm |
T |
A |
7: 67,408,916 (GRCm39) |
D154V |
probably benign |
Het |
Synpo2 |
T |
C |
3: 122,908,098 (GRCm39) |
E406G |
probably damaging |
Het |
Tcea3 |
T |
A |
4: 135,975,382 (GRCm39) |
L8* |
probably null |
Het |
Tec |
G |
A |
5: 72,980,840 (GRCm39) |
L33F |
probably damaging |
Het |
Tex15 |
T |
A |
8: 34,072,354 (GRCm39) |
S2634T |
possibly damaging |
Het |
Tg |
T |
A |
15: 66,601,475 (GRCm39) |
Y162N |
probably damaging |
Het |
Tmem8b |
G |
A |
4: 43,690,123 (GRCm39) |
V853I |
probably benign |
Het |
Togaram1 |
A |
G |
12: 65,068,240 (GRCm39) |
K1748E |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,728,822 (GRCm39) |
|
probably benign |
Het |
Usp36 |
C |
T |
11: 118,163,847 (GRCm39) |
D234N |
probably damaging |
Het |
Usp40 |
G |
A |
1: 87,906,244 (GRCm39) |
P664S |
probably benign |
Het |
Vmn1r54 |
T |
A |
6: 90,246,635 (GRCm39) |
L183H |
probably benign |
Het |
Vmn1r58 |
T |
G |
7: 5,413,676 (GRCm39) |
I185L |
probably benign |
Het |
Wnt8a |
A |
T |
18: 34,680,618 (GRCm39) |
R328W |
probably benign |
Het |
Yars1 |
A |
G |
4: 129,107,732 (GRCm39) |
|
probably benign |
Het |
Zbtb49 |
A |
C |
5: 38,358,018 (GRCm39) |
M745R |
probably damaging |
Het |
Zeb1 |
T |
G |
18: 5,759,027 (GRCm39) |
F162V |
probably damaging |
Het |
Zfp369 |
A |
T |
13: 65,445,362 (GRCm39) |
H835L |
probably damaging |
Het |
Zic5 |
A |
G |
14: 122,701,351 (GRCm39) |
V460A |
unknown |
Het |
Zp3 |
A |
G |
5: 136,013,210 (GRCm39) |
N181D |
possibly damaging |
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 |
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 |
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 |
|
|