Other mutations in this stock |
Total: 90 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8b |
A |
G |
11: 109,838,003 (GRCm39) |
V1145A |
probably benign |
Het |
Ank1 |
T |
C |
8: 23,589,011 (GRCm39) |
M562T |
probably benign |
Het |
Atn1 |
A |
T |
6: 124,722,211 (GRCm39) |
S881T |
probably benign |
Het |
B3galt1 |
C |
T |
2: 67,949,059 (GRCm39) |
T258I |
probably benign |
Het |
Bahcc1 |
C |
T |
11: 120,167,591 (GRCm39) |
L1331F |
probably benign |
Het |
Capn12 |
G |
A |
7: 28,582,628 (GRCm39) |
V168M |
probably damaging |
Het |
Card14 |
T |
C |
11: 119,216,930 (GRCm39) |
V338A |
possibly damaging |
Het |
Cd27 |
T |
C |
6: 125,213,432 (GRCm39) |
|
probably benign |
Het |
Cd37 |
A |
G |
7: 44,888,109 (GRCm39) |
L37P |
probably damaging |
Het |
Cd96 |
A |
G |
16: 45,919,385 (GRCm39) |
L212P |
probably damaging |
Het |
Cep152 |
A |
G |
2: 125,444,778 (GRCm39) |
M456T |
possibly damaging |
Het |
Ces3b |
G |
A |
8: 105,811,619 (GRCm39) |
R45H |
probably benign |
Het |
Cfap54 |
T |
G |
10: 92,837,685 (GRCm39) |
T1072P |
probably damaging |
Het |
Chodl |
A |
T |
16: 78,738,659 (GRCm39) |
M172L |
possibly damaging |
Het |
Cilp2 |
A |
G |
8: 70,339,108 (GRCm39) |
S47P |
probably damaging |
Het |
Clasrp |
T |
C |
7: 19,318,232 (GRCm39) |
I596V |
unknown |
Het |
Clcn2 |
C |
T |
16: 20,530,930 (GRCm39) |
V267I |
probably damaging |
Het |
Cntln |
T |
A |
4: 84,806,936 (GRCm39) |
D139E |
probably damaging |
Het |
Cyp2j12 |
A |
C |
4: 95,994,685 (GRCm39) |
N379K |
probably damaging |
Het |
Defb21 |
T |
C |
2: 152,416,704 (GRCm39) |
V60A |
possibly damaging |
Het |
Dnajc16 |
G |
T |
4: 141,494,018 (GRCm39) |
S543* |
probably null |
Het |
Efcab12 |
G |
T |
6: 115,800,664 (GRCm39) |
H120N |
probably benign |
Het |
Efcab3 |
AACTCTA |
AA |
11: 104,806,253 (GRCm39) |
|
probably null |
Het |
Efl1 |
G |
A |
7: 82,412,161 (GRCm39) |
G850D |
probably benign |
Het |
Efna1 |
T |
C |
3: 89,183,635 (GRCm39) |
M64V |
probably benign |
Het |
Eif2ak3 |
T |
C |
6: 70,870,003 (GRCm39) |
W897R |
probably damaging |
Het |
Eif2ak4 |
T |
A |
2: 118,258,513 (GRCm39) |
F621Y |
probably damaging |
Het |
Erbin |
C |
A |
13: 103,975,966 (GRCm39) |
E643* |
probably null |
Het |
Esr1 |
G |
A |
10: 4,807,176 (GRCm39) |
W364* |
probably null |
Het |
Fam171a2 |
T |
C |
11: 102,330,861 (GRCm39) |
E206G |
possibly damaging |
Het |
Fam90a1a |
T |
C |
8: 22,451,429 (GRCm39) |
F97L |
probably benign |
Het |
Fap |
A |
T |
2: 62,378,165 (GRCm39) |
F181I |
probably benign |
Het |
Fem1b |
T |
C |
9: 62,704,916 (GRCm39) |
N115D |
probably damaging |
Het |
Gal3st2b |
G |
T |
1: 93,868,653 (GRCm39) |
A295S |
probably benign |
Het |
Galnt10 |
G |
A |
11: 57,674,681 (GRCm39) |
|
probably benign |
Het |
Gcfc2 |
T |
C |
6: 81,909,879 (GRCm39) |
V224A |
probably damaging |
Het |
Gh |
T |
C |
11: 106,191,634 (GRCm39) |
E136G |
probably damaging |
Het |
Gjd3 |
C |
T |
11: 98,873,325 (GRCm39) |
C173Y |
probably damaging |
Het |
Gm12695 |
T |
A |
4: 96,651,046 (GRCm39) |
M136L |
probably benign |
Het |
Gnas |
A |
G |
2: 174,141,277 (GRCm39) |
E482G |
unknown |
Het |
Gpa33 |
T |
C |
1: 165,980,351 (GRCm39) |
L138P |
probably damaging |
Het |
Hlf |
T |
C |
11: 90,236,714 (GRCm39) |
D181G |
probably damaging |
Het |
Irgm1 |
A |
G |
11: 48,756,698 (GRCm39) |
L387S |
probably benign |
Het |
Kctd1 |
T |
C |
18: 15,102,745 (GRCm39) |
E812G |
possibly damaging |
Het |
Klra2 |
T |
C |
6: 131,205,214 (GRCm39) |
E209G |
probably benign |
Het |
Klra3 |
C |
T |
6: 130,312,732 (GRCm39) |
V11M |
probably benign |
Het |
Klrh1 |
G |
T |
6: 129,745,084 (GRCm39) |
H171N |
probably benign |
Het |
Kmt2c |
T |
C |
5: 25,503,885 (GRCm39) |
S3808G |
probably benign |
Het |
Krtap24-1 |
A |
C |
16: 88,408,888 (GRCm39) |
S79R |
probably benign |
Het |
Limch1 |
T |
A |
5: 67,190,475 (GRCm39) |
H759Q |
probably benign |
Het |
Map3k4 |
A |
G |
17: 12,490,433 (GRCm39) |
Y333H |
probably benign |
Het |
Mmel1 |
A |
G |
4: 154,974,091 (GRCm39) |
Y377C |
probably damaging |
Het |
Ms4a14 |
A |
T |
19: 11,281,113 (GRCm39) |
Y482N |
possibly damaging |
Het |
Myo9b |
A |
G |
8: 71,801,675 (GRCm39) |
S1277G |
probably benign |
Het |
Nab1 |
T |
C |
1: 52,529,667 (GRCm39) |
T77A |
possibly damaging |
Het |
Obsl1 |
T |
C |
1: 75,482,841 (GRCm39) |
S10G |
probably benign |
Het |
Odc1 |
A |
G |
12: 17,598,329 (GRCm39) |
T157A |
possibly damaging |
Het |
Or2a5 |
T |
G |
6: 42,873,964 (GRCm39) |
L193R |
probably damaging |
Het |
Or8b52 |
T |
C |
9: 38,576,780 (GRCm39) |
D120G |
probably damaging |
Het |
Peg10 |
CCACATCAGGATCCACATCAGGATGCACATCAGCATCAGGATCCCCATCAGGATGCACATCAGGATCCACATCAGGATGCACATCAG |
CCACATCAGGATCCACATCAGGATGCACATCAG |
6: 4,756,398 (GRCm39) |
|
probably benign |
Het |
Plpp1 |
T |
A |
13: 112,943,057 (GRCm39) |
|
probably benign |
Het |
Prdm13 |
G |
A |
4: 21,679,125 (GRCm39) |
A455V |
possibly damaging |
Het |
Ptpn13 |
A |
T |
5: 103,739,101 (GRCm39) |
Y2289F |
probably damaging |
Het |
Ptpn18 |
G |
T |
1: 34,498,966 (GRCm39) |
R21L |
probably benign |
Het |
Ptprd |
A |
G |
4: 75,916,736 (GRCm39) |
|
probably null |
Het |
Rcn3 |
G |
T |
7: 44,733,095 (GRCm39) |
D258E |
probably damaging |
Het |
Ro60 |
C |
T |
1: 143,641,170 (GRCm39) |
|
probably null |
Het |
Rsf1 |
GCG |
GCGACGGCGCCG |
7: 97,229,114 (GRCm39) |
|
probably benign |
Het |
Sacs |
T |
A |
14: 61,429,895 (GRCm39) |
H651Q |
probably benign |
Het |
Sacs |
T |
C |
14: 61,448,702 (GRCm39) |
S3583P |
probably damaging |
Het |
Scel |
A |
G |
14: 103,829,807 (GRCm39) |
N463S |
possibly damaging |
Het |
Serpinb2 |
A |
T |
1: 107,443,284 (GRCm39) |
I28F |
possibly damaging |
Het |
Sin3b |
A |
G |
8: 73,473,131 (GRCm39) |
K484E |
probably benign |
Het |
Snrnp48 |
T |
A |
13: 38,400,397 (GRCm39) |
V168D |
probably damaging |
Het |
Snx18 |
T |
G |
13: 113,754,931 (GRCm39) |
M1L |
probably benign |
Het |
Spata31h1 |
T |
C |
10: 82,131,295 (GRCm39) |
N572D |
probably benign |
Het |
Srcap |
T |
A |
7: 127,158,204 (GRCm39) |
N2693K |
unknown |
Het |
Stim1 |
A |
G |
7: 102,078,014 (GRCm39) |
D172G |
|
Het |
Stip1 |
A |
T |
19: 7,002,687 (GRCm39) |
L414H |
probably damaging |
Het |
Sun1 |
A |
G |
5: 139,209,390 (GRCm39) |
H40R |
probably damaging |
Het |
Sva |
T |
A |
6: 42,019,182 (GRCm39) |
D117E |
possibly damaging |
Het |
Syne2 |
A |
G |
12: 75,943,444 (GRCm39) |
D321G |
probably damaging |
Het |
Trim45 |
A |
G |
3: 100,835,394 (GRCm39) |
D459G |
probably damaging |
Het |
Ttc6 |
G |
A |
12: 57,697,790 (GRCm39) |
W43* |
probably null |
Het |
Ugt2b35 |
A |
G |
5: 87,152,780 (GRCm39) |
T317A |
possibly damaging |
Het |
Usp32 |
C |
T |
11: 84,916,370 (GRCm39) |
R858Q |
probably damaging |
Het |
Vmn2r53 |
G |
T |
7: 12,334,752 (GRCm39) |
Q303K |
probably benign |
Het |
Yeats2 |
T |
C |
16: 19,969,312 (GRCm39) |
|
probably null |
Het |
Zfp804a |
A |
G |
2: 82,088,747 (GRCm39) |
N859D |
probably benign |
Het |
Zscan10 |
A |
T |
17: 23,824,580 (GRCm39) |
Q12L |
possibly damaging |
Het |
|
Other mutations in Celsr1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00392:Celsr1
|
APN |
15 |
85,815,546 (GRCm39) |
missense |
probably benign |
0.04 |
IGL00519:Celsr1
|
APN |
15 |
85,915,037 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00909:Celsr1
|
APN |
15 |
85,806,436 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01303:Celsr1
|
APN |
15 |
85,914,692 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01726:Celsr1
|
APN |
15 |
85,810,391 (GRCm39) |
missense |
probably benign |
0.35 |
IGL01910:Celsr1
|
APN |
15 |
85,814,096 (GRCm39) |
missense |
probably benign |
|
IGL01931:Celsr1
|
APN |
15 |
85,791,861 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01952:Celsr1
|
APN |
15 |
85,847,424 (GRCm39) |
missense |
probably benign |
0.35 |
IGL02090:Celsr1
|
APN |
15 |
85,791,922 (GRCm39) |
missense |
possibly damaging |
0.49 |
IGL02191:Celsr1
|
APN |
15 |
85,863,205 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL02372:Celsr1
|
APN |
15 |
85,814,108 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02413:Celsr1
|
APN |
15 |
85,915,427 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL02478:Celsr1
|
APN |
15 |
85,825,337 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL02507:Celsr1
|
APN |
15 |
85,784,889 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL02508:Celsr1
|
APN |
15 |
85,914,818 (GRCm39) |
nonsense |
probably null |
|
IGL02899:Celsr1
|
APN |
15 |
85,915,927 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02939:Celsr1
|
APN |
15 |
85,785,673 (GRCm39) |
missense |
probably benign |
|
IGL03212:Celsr1
|
APN |
15 |
85,814,878 (GRCm39) |
missense |
probably benign |
0.04 |
P0028:Celsr1
|
UTSW |
15 |
85,806,436 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4305001:Celsr1
|
UTSW |
15 |
85,785,138 (GRCm39) |
missense |
possibly damaging |
0.87 |
PIT4480001:Celsr1
|
UTSW |
15 |
85,916,615 (GRCm39) |
missense |
probably damaging |
0.99 |
R0018:Celsr1
|
UTSW |
15 |
85,915,243 (GRCm39) |
missense |
possibly damaging |
0.47 |
R0018:Celsr1
|
UTSW |
15 |
85,915,243 (GRCm39) |
missense |
possibly damaging |
0.47 |
R0038:Celsr1
|
UTSW |
15 |
85,813,620 (GRCm39) |
missense |
possibly damaging |
0.65 |
R0057:Celsr1
|
UTSW |
15 |
85,914,963 (GRCm39) |
missense |
probably benign |
0.02 |
R0060:Celsr1
|
UTSW |
15 |
85,806,399 (GRCm39) |
missense |
probably damaging |
0.98 |
R0060:Celsr1
|
UTSW |
15 |
85,806,399 (GRCm39) |
missense |
probably damaging |
0.98 |
R0279:Celsr1
|
UTSW |
15 |
85,787,065 (GRCm39) |
missense |
probably benign |
0.00 |
R0570:Celsr1
|
UTSW |
15 |
85,787,566 (GRCm39) |
missense |
probably benign |
0.18 |
R0611:Celsr1
|
UTSW |
15 |
85,816,524 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0731:Celsr1
|
UTSW |
15 |
85,785,798 (GRCm39) |
missense |
probably benign |
|
R0792:Celsr1
|
UTSW |
15 |
85,815,477 (GRCm39) |
missense |
probably benign |
0.02 |
R0943:Celsr1
|
UTSW |
15 |
85,787,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R0989:Celsr1
|
UTSW |
15 |
85,915,480 (GRCm39) |
missense |
probably benign |
0.39 |
R1118:Celsr1
|
UTSW |
15 |
85,916,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R1237:Celsr1
|
UTSW |
15 |
85,788,175 (GRCm39) |
missense |
probably benign |
0.01 |
R1239:Celsr1
|
UTSW |
15 |
85,863,347 (GRCm39) |
missense |
probably damaging |
0.99 |
R1405:Celsr1
|
UTSW |
15 |
85,789,635 (GRCm39) |
splice site |
probably null |
|
R1405:Celsr1
|
UTSW |
15 |
85,789,635 (GRCm39) |
splice site |
probably null |
|
R1522:Celsr1
|
UTSW |
15 |
85,815,477 (GRCm39) |
missense |
probably benign |
0.02 |
R1662:Celsr1
|
UTSW |
15 |
85,915,263 (GRCm39) |
missense |
probably damaging |
1.00 |
R1673:Celsr1
|
UTSW |
15 |
85,816,658 (GRCm39) |
missense |
probably benign |
0.00 |
R1795:Celsr1
|
UTSW |
15 |
85,914,524 (GRCm39) |
missense |
probably damaging |
0.99 |
R1799:Celsr1
|
UTSW |
15 |
85,916,886 (GRCm39) |
missense |
probably damaging |
1.00 |
R1858:Celsr1
|
UTSW |
15 |
85,916,960 (GRCm39) |
missense |
probably damaging |
1.00 |
R2040:Celsr1
|
UTSW |
15 |
85,917,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R2050:Celsr1
|
UTSW |
15 |
85,914,748 (GRCm39) |
missense |
probably benign |
0.02 |
R2131:Celsr1
|
UTSW |
15 |
85,847,424 (GRCm39) |
missense |
probably benign |
0.35 |
R2132:Celsr1
|
UTSW |
15 |
85,916,168 (GRCm39) |
missense |
possibly damaging |
0.91 |
R2189:Celsr1
|
UTSW |
15 |
85,863,431 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2192:Celsr1
|
UTSW |
15 |
85,800,924 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4213:Celsr1
|
UTSW |
15 |
85,916,008 (GRCm39) |
missense |
probably damaging |
1.00 |
R4356:Celsr1
|
UTSW |
15 |
85,863,028 (GRCm39) |
missense |
probably damaging |
1.00 |
R4414:Celsr1
|
UTSW |
15 |
85,812,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R4414:Celsr1
|
UTSW |
15 |
85,847,334 (GRCm39) |
missense |
probably benign |
0.00 |
R4416:Celsr1
|
UTSW |
15 |
85,812,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R4645:Celsr1
|
UTSW |
15 |
85,800,957 (GRCm39) |
missense |
probably benign |
0.35 |
R4666:Celsr1
|
UTSW |
15 |
85,914,695 (GRCm39) |
missense |
probably damaging |
1.00 |
R4687:Celsr1
|
UTSW |
15 |
85,816,661 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4735:Celsr1
|
UTSW |
15 |
85,790,230 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4804:Celsr1
|
UTSW |
15 |
85,822,154 (GRCm39) |
missense |
possibly damaging |
0.49 |
R4995:Celsr1
|
UTSW |
15 |
85,822,112 (GRCm39) |
missense |
probably damaging |
0.99 |
R5070:Celsr1
|
UTSW |
15 |
85,823,335 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5218:Celsr1
|
UTSW |
15 |
85,816,585 (GRCm39) |
missense |
probably damaging |
1.00 |
R5280:Celsr1
|
UTSW |
15 |
85,814,747 (GRCm39) |
missense |
probably benign |
|
R5310:Celsr1
|
UTSW |
15 |
85,810,423 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5388:Celsr1
|
UTSW |
15 |
85,809,719 (GRCm39) |
missense |
probably damaging |
0.99 |
R5484:Celsr1
|
UTSW |
15 |
85,815,483 (GRCm39) |
missense |
probably benign |
0.00 |
R5639:Celsr1
|
UTSW |
15 |
85,914,968 (GRCm39) |
missense |
probably damaging |
1.00 |
R5758:Celsr1
|
UTSW |
15 |
85,825,465 (GRCm39) |
missense |
probably benign |
0.27 |
R5778:Celsr1
|
UTSW |
15 |
85,917,156 (GRCm39) |
missense |
probably damaging |
1.00 |
R5893:Celsr1
|
UTSW |
15 |
85,788,215 (GRCm39) |
missense |
probably benign |
0.02 |
R5915:Celsr1
|
UTSW |
15 |
85,914,550 (GRCm39) |
missense |
probably damaging |
0.96 |
R5915:Celsr1
|
UTSW |
15 |
85,822,176 (GRCm39) |
missense |
probably benign |
|
R5932:Celsr1
|
UTSW |
15 |
85,916,905 (GRCm39) |
missense |
probably damaging |
1.00 |
R5950:Celsr1
|
UTSW |
15 |
85,916,701 (GRCm39) |
missense |
probably damaging |
1.00 |
R5975:Celsr1
|
UTSW |
15 |
85,803,239 (GRCm39) |
splice site |
probably null |
|
R6050:Celsr1
|
UTSW |
15 |
85,814,812 (GRCm39) |
missense |
probably benign |
0.00 |
R6117:Celsr1
|
UTSW |
15 |
85,816,612 (GRCm39) |
missense |
probably benign |
0.04 |
R6178:Celsr1
|
UTSW |
15 |
85,785,222 (GRCm39) |
missense |
probably benign |
0.08 |
R6186:Celsr1
|
UTSW |
15 |
85,805,394 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6212:Celsr1
|
UTSW |
15 |
85,800,888 (GRCm39) |
missense |
probably benign |
0.25 |
R6307:Celsr1
|
UTSW |
15 |
85,812,531 (GRCm39) |
missense |
probably benign |
|
R6320:Celsr1
|
UTSW |
15 |
85,785,160 (GRCm39) |
missense |
probably benign |
0.13 |
R6349:Celsr1
|
UTSW |
15 |
85,915,885 (GRCm39) |
missense |
probably damaging |
1.00 |
R6478:Celsr1
|
UTSW |
15 |
85,809,719 (GRCm39) |
missense |
probably damaging |
0.99 |
R6504:Celsr1
|
UTSW |
15 |
85,863,121 (GRCm39) |
missense |
probably benign |
0.07 |
R6607:Celsr1
|
UTSW |
15 |
85,847,486 (GRCm39) |
missense |
probably benign |
|
R6615:Celsr1
|
UTSW |
15 |
85,786,315 (GRCm39) |
critical splice donor site |
probably null |
|
R6661:Celsr1
|
UTSW |
15 |
85,803,135 (GRCm39) |
missense |
probably damaging |
1.00 |
R6722:Celsr1
|
UTSW |
15 |
85,790,115 (GRCm39) |
critical splice donor site |
probably null |
|
R6743:Celsr1
|
UTSW |
15 |
85,791,799 (GRCm39) |
missense |
probably damaging |
0.96 |
R6746:Celsr1
|
UTSW |
15 |
85,915,696 (GRCm39) |
missense |
probably damaging |
1.00 |
R6772:Celsr1
|
UTSW |
15 |
85,914,983 (GRCm39) |
missense |
probably benign |
|
R6838:Celsr1
|
UTSW |
15 |
85,823,395 (GRCm39) |
missense |
probably benign |
|
R6886:Celsr1
|
UTSW |
15 |
85,915,855 (GRCm39) |
missense |
probably benign |
0.00 |
R7030:Celsr1
|
UTSW |
15 |
85,789,679 (GRCm39) |
missense |
probably damaging |
0.99 |
R7060:Celsr1
|
UTSW |
15 |
85,916,856 (GRCm39) |
missense |
probably benign |
0.07 |
R7080:Celsr1
|
UTSW |
15 |
85,816,652 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7325:Celsr1
|
UTSW |
15 |
85,917,209 (GRCm39) |
missense |
probably damaging |
0.99 |
R7357:Celsr1
|
UTSW |
15 |
85,914,715 (GRCm39) |
missense |
probably benign |
0.00 |
R7371:Celsr1
|
UTSW |
15 |
85,914,875 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7446:Celsr1
|
UTSW |
15 |
85,791,874 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7465:Celsr1
|
UTSW |
15 |
85,917,593 (GRCm39) |
missense |
probably benign |
|
R7491:Celsr1
|
UTSW |
15 |
85,916,719 (GRCm39) |
missense |
possibly damaging |
0.78 |
R7639:Celsr1
|
UTSW |
15 |
85,814,073 (GRCm39) |
missense |
probably benign |
0.00 |
R7685:Celsr1
|
UTSW |
15 |
85,862,933 (GRCm39) |
nonsense |
probably null |
|
R7741:Celsr1
|
UTSW |
15 |
85,863,303 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7768:Celsr1
|
UTSW |
15 |
85,816,610 (GRCm39) |
missense |
probably benign |
|
R7974:Celsr1
|
UTSW |
15 |
85,915,231 (GRCm39) |
missense |
probably damaging |
1.00 |
R7977:Celsr1
|
UTSW |
15 |
85,917,194 (GRCm39) |
missense |
probably damaging |
1.00 |
R7987:Celsr1
|
UTSW |
15 |
85,917,194 (GRCm39) |
missense |
probably damaging |
1.00 |
R8073:Celsr1
|
UTSW |
15 |
85,823,356 (GRCm39) |
missense |
probably benign |
0.00 |
R8099:Celsr1
|
UTSW |
15 |
85,915,801 (GRCm39) |
missense |
probably damaging |
0.99 |
R8190:Celsr1
|
UTSW |
15 |
85,787,090 (GRCm39) |
missense |
probably damaging |
0.99 |
R8210:Celsr1
|
UTSW |
15 |
85,863,436 (GRCm39) |
missense |
probably benign |
0.00 |
R8289:Celsr1
|
UTSW |
15 |
85,917,286 (GRCm39) |
nonsense |
probably null |
|
R8290:Celsr1
|
UTSW |
15 |
85,917,286 (GRCm39) |
nonsense |
probably null |
|
R8292:Celsr1
|
UTSW |
15 |
85,791,819 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8328:Celsr1
|
UTSW |
15 |
85,806,445 (GRCm39) |
missense |
probably benign |
0.00 |
R8330:Celsr1
|
UTSW |
15 |
85,816,501 (GRCm39) |
missense |
probably damaging |
0.99 |
R8333:Celsr1
|
UTSW |
15 |
85,915,615 (GRCm39) |
missense |
possibly damaging |
0.65 |
R8352:Celsr1
|
UTSW |
15 |
85,917,286 (GRCm39) |
nonsense |
probably null |
|
R8384:Celsr1
|
UTSW |
15 |
85,917,286 (GRCm39) |
nonsense |
probably null |
|
R8452:Celsr1
|
UTSW |
15 |
85,917,286 (GRCm39) |
nonsense |
probably null |
|
R8463:Celsr1
|
UTSW |
15 |
85,914,415 (GRCm39) |
missense |
probably damaging |
1.00 |
R8479:Celsr1
|
UTSW |
15 |
85,917,286 (GRCm39) |
nonsense |
probably null |
|
R8480:Celsr1
|
UTSW |
15 |
85,917,286 (GRCm39) |
nonsense |
probably null |
|
R8493:Celsr1
|
UTSW |
15 |
85,822,207 (GRCm39) |
missense |
possibly damaging |
0.67 |
R8498:Celsr1
|
UTSW |
15 |
85,823,306 (GRCm39) |
missense |
probably benign |
0.01 |
R8506:Celsr1
|
UTSW |
15 |
85,917,286 (GRCm39) |
nonsense |
probably null |
|
R8771:Celsr1
|
UTSW |
15 |
85,788,175 (GRCm39) |
missense |
probably benign |
0.01 |
R8891:Celsr1
|
UTSW |
15 |
85,822,194 (GRCm39) |
missense |
probably benign |
0.01 |
R8905:Celsr1
|
UTSW |
15 |
85,788,269 (GRCm39) |
intron |
probably benign |
|
R8979:Celsr1
|
UTSW |
15 |
85,847,340 (GRCm39) |
missense |
probably damaging |
0.96 |
R9069:Celsr1
|
UTSW |
15 |
85,914,772 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9115:Celsr1
|
UTSW |
15 |
85,803,217 (GRCm39) |
missense |
probably damaging |
1.00 |
R9194:Celsr1
|
UTSW |
15 |
85,917,286 (GRCm39) |
nonsense |
probably null |
|
R9196:Celsr1
|
UTSW |
15 |
85,917,286 (GRCm39) |
nonsense |
probably null |
|
R9198:Celsr1
|
UTSW |
15 |
85,917,286 (GRCm39) |
nonsense |
probably null |
|
R9200:Celsr1
|
UTSW |
15 |
85,917,286 (GRCm39) |
nonsense |
probably null |
|
R9201:Celsr1
|
UTSW |
15 |
85,917,286 (GRCm39) |
nonsense |
probably null |
|
R9202:Celsr1
|
UTSW |
15 |
85,917,286 (GRCm39) |
nonsense |
probably null |
|
R9203:Celsr1
|
UTSW |
15 |
85,917,286 (GRCm39) |
nonsense |
probably null |
|
R9222:Celsr1
|
UTSW |
15 |
85,815,471 (GRCm39) |
missense |
possibly damaging |
0.68 |
R9236:Celsr1
|
UTSW |
15 |
85,915,051 (GRCm39) |
missense |
probably damaging |
1.00 |
R9384:Celsr1
|
UTSW |
15 |
85,917,286 (GRCm39) |
nonsense |
probably null |
|
R9386:Celsr1
|
UTSW |
15 |
85,863,231 (GRCm39) |
missense |
probably damaging |
1.00 |
R9400:Celsr1
|
UTSW |
15 |
85,917,286 (GRCm39) |
nonsense |
probably null |
|
R9401:Celsr1
|
UTSW |
15 |
85,917,286 (GRCm39) |
nonsense |
probably null |
|
R9415:Celsr1
|
UTSW |
15 |
85,917,286 (GRCm39) |
nonsense |
probably null |
|
R9428:Celsr1
|
UTSW |
15 |
85,815,549 (GRCm39) |
missense |
possibly damaging |
0.64 |
R9435:Celsr1
|
UTSW |
15 |
85,806,535 (GRCm39) |
splice site |
probably benign |
|
R9493:Celsr1
|
UTSW |
15 |
85,785,346 (GRCm39) |
missense |
probably damaging |
0.98 |
R9495:Celsr1
|
UTSW |
15 |
85,917,286 (GRCm39) |
nonsense |
probably null |
|
R9499:Celsr1
|
UTSW |
15 |
85,917,286 (GRCm39) |
nonsense |
probably null |
|
R9607:Celsr1
|
UTSW |
15 |
85,915,229 (GRCm39) |
missense |
|
|
R9673:Celsr1
|
UTSW |
15 |
85,917,286 (GRCm39) |
nonsense |
probably null |
|
Z1176:Celsr1
|
UTSW |
15 |
85,847,301 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1177:Celsr1
|
UTSW |
15 |
85,863,052 (GRCm39) |
missense |
probably damaging |
1.00 |
|