Other mutations in this stock |
Total: 85 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700067K01Rik |
C |
A |
8: 84,729,733 (GRCm39) |
|
probably benign |
Het |
Aadacl3 |
C |
T |
4: 144,190,130 (GRCm39) |
W57* |
probably null |
Het |
Abca2 |
G |
T |
2: 25,337,417 (GRCm39) |
|
probably null |
Het |
Abca3 |
A |
G |
17: 24,593,373 (GRCm39) |
I257V |
probably benign |
Het |
Adamts2 |
A |
G |
11: 50,666,963 (GRCm39) |
D420G |
probably damaging |
Het |
Adamts5 |
A |
G |
16: 85,696,135 (GRCm39) |
F341L |
probably damaging |
Het |
Ahnak |
T |
A |
19: 8,991,062 (GRCm39) |
D4115E |
probably damaging |
Het |
Arhgap20 |
T |
C |
9: 51,751,751 (GRCm39) |
S365P |
possibly damaging |
Het |
Atrn |
G |
A |
2: 130,822,054 (GRCm39) |
V916I |
probably benign |
Het |
Blmh |
T |
C |
11: 76,856,651 (GRCm39) |
V82A |
probably damaging |
Het |
C1ra |
A |
T |
6: 124,490,664 (GRCm39) |
Y19F |
probably benign |
Het |
Cactin |
A |
G |
10: 81,159,067 (GRCm39) |
E306G |
probably damaging |
Het |
Clca4b |
T |
C |
3: 144,631,110 (GRCm39) |
E250G |
probably benign |
Het |
Col17a1 |
A |
T |
19: 47,654,317 (GRCm39) |
S647T |
possibly damaging |
Het |
Cope |
T |
A |
8: 70,759,181 (GRCm39) |
D74E |
probably damaging |
Het |
Dsg1c |
T |
C |
18: 20,403,435 (GRCm39) |
I198T |
probably damaging |
Het |
Elfn2 |
T |
C |
15: 78,557,434 (GRCm39) |
N371S |
probably damaging |
Het |
Elmo2 |
G |
T |
2: 165,146,839 (GRCm39) |
A246D |
probably benign |
Het |
Ewsr1 |
A |
T |
11: 5,035,935 (GRCm39) |
M187K |
possibly damaging |
Het |
Faap100 |
A |
T |
11: 120,265,114 (GRCm39) |
S587R |
possibly damaging |
Het |
Fam234b |
C |
T |
6: 135,186,247 (GRCm39) |
S85L |
probably benign |
Het |
Fanca |
A |
T |
8: 124,033,169 (GRCm39) |
S292R |
probably benign |
Het |
Fanci |
G |
A |
7: 79,093,711 (GRCm39) |
C1021Y |
probably damaging |
Het |
Fhod3 |
T |
C |
18: 25,245,640 (GRCm39) |
I1230T |
probably benign |
Het |
Fmo5 |
T |
C |
3: 97,536,456 (GRCm39) |
L27S |
probably damaging |
Het |
Fmo9 |
A |
G |
1: 166,502,031 (GRCm39) |
V147A |
probably null |
Het |
Fnbp4 |
A |
G |
2: 90,583,301 (GRCm39) |
Y309C |
probably damaging |
Het |
Foxb1 |
T |
C |
9: 69,666,844 (GRCm39) |
T229A |
probably benign |
Het |
Gapvd1 |
A |
G |
2: 34,618,552 (GRCm39) |
Y274H |
probably damaging |
Het |
Gbp8 |
T |
C |
5: 105,165,541 (GRCm39) |
|
probably null |
Het |
Gcn1 |
T |
A |
5: 115,730,480 (GRCm39) |
L888Q |
probably damaging |
Het |
Gm17490 |
T |
C |
2: 11,630,460 (GRCm39) |
|
probably benign |
Het |
Gtf2ird2 |
T |
A |
5: 134,237,785 (GRCm39) |
|
probably null |
Het |
H2-Q1 |
A |
G |
17: 35,540,373 (GRCm39) |
T153A |
possibly damaging |
Het |
Ina |
A |
C |
19: 47,011,938 (GRCm39) |
E452A |
probably benign |
Het |
Kars1 |
A |
G |
8: 112,721,494 (GRCm39) |
|
probably null |
Het |
Kif1c |
A |
G |
11: 70,595,291 (GRCm39) |
E124G |
probably damaging |
Het |
Lpin3 |
T |
C |
2: 160,745,944 (GRCm39) |
|
probably benign |
Het |
Lrp1 |
A |
T |
10: 127,390,878 (GRCm39) |
C3006* |
probably null |
Het |
Lyst |
T |
C |
13: 13,883,971 (GRCm39) |
L2953P |
probably benign |
Het |
Mb21d2 |
G |
A |
16: 28,748,324 (GRCm39) |
A31V |
probably benign |
Het |
Melk |
T |
C |
4: 44,308,906 (GRCm39) |
Y88H |
probably damaging |
Het |
Myrf |
A |
G |
19: 10,189,161 (GRCm39) |
S857P |
probably damaging |
Het |
Nos2 |
A |
G |
11: 78,826,187 (GRCm39) |
I153M |
possibly damaging |
Het |
Or4n4 |
T |
G |
14: 50,519,370 (GRCm39) |
L113F |
probably benign |
Het |
Otof |
A |
G |
5: 30,529,225 (GRCm39) |
|
probably benign |
Het |
Patl2 |
A |
G |
2: 121,955,789 (GRCm39) |
V249A |
probably damaging |
Het |
Pcgf5 |
A |
G |
19: 36,389,580 (GRCm39) |
Y19C |
probably benign |
Het |
Pcnt |
A |
T |
10: 76,247,941 (GRCm39) |
V951E |
probably damaging |
Het |
Pcolce2 |
T |
C |
9: 95,520,710 (GRCm39) |
V29A |
probably benign |
Het |
Pdgfrb |
A |
T |
18: 61,210,775 (GRCm39) |
M761L |
probably benign |
Het |
Pi16 |
A |
T |
17: 29,538,189 (GRCm39) |
M1L |
possibly damaging |
Het |
Pkd2 |
T |
A |
5: 104,603,471 (GRCm39) |
|
probably benign |
Het |
Plcb2 |
A |
G |
2: 118,547,806 (GRCm39) |
W474R |
probably benign |
Het |
Psapl1 |
A |
G |
5: 36,361,624 (GRCm39) |
D72G |
possibly damaging |
Het |
Ptpn5 |
T |
A |
7: 46,728,681 (GRCm39) |
|
probably benign |
Het |
Ptprg |
A |
G |
14: 12,215,896 (GRCm38) |
E1115G |
probably damaging |
Het |
Rassf1 |
C |
T |
9: 107,435,165 (GRCm39) |
T224I |
probably damaging |
Het |
Rbpms2 |
T |
A |
9: 65,566,476 (GRCm39) |
C168* |
probably null |
Het |
Rhag |
A |
G |
17: 41,139,804 (GRCm39) |
|
probably benign |
Het |
Rhebl1 |
C |
T |
15: 98,779,034 (GRCm39) |
V17I |
probably benign |
Het |
Rnf130 |
A |
T |
11: 49,986,703 (GRCm39) |
D349V |
possibly damaging |
Het |
Rprd1a |
A |
G |
18: 24,642,952 (GRCm39) |
L60P |
probably damaging |
Het |
Rspry1 |
T |
C |
8: 95,356,420 (GRCm39) |
I25T |
probably damaging |
Het |
Ruvbl2 |
C |
T |
7: 45,071,621 (GRCm39) |
V421M |
probably damaging |
Het |
Sap30 |
T |
C |
8: 57,936,000 (GRCm39) |
N209D |
possibly damaging |
Het |
Sfswap |
T |
C |
5: 129,581,042 (GRCm39) |
|
probably benign |
Het |
Slc1a2 |
G |
A |
2: 102,586,352 (GRCm39) |
V319M |
probably damaging |
Het |
Smad2 |
T |
C |
18: 76,422,250 (GRCm39) |
|
probably benign |
Het |
Spdya |
T |
C |
17: 71,869,585 (GRCm39) |
|
probably null |
Het |
Stk39 |
G |
A |
2: 68,240,392 (GRCm39) |
T113M |
probably damaging |
Het |
Tanc1 |
A |
G |
2: 59,626,382 (GRCm39) |
|
probably benign |
Het |
Tas2r122 |
T |
C |
6: 132,688,774 (GRCm39) |
K40E |
probably damaging |
Het |
Tph2 |
G |
T |
10: 115,010,039 (GRCm39) |
|
probably benign |
Het |
Trip12 |
G |
A |
1: 84,729,269 (GRCm39) |
S1083F |
probably damaging |
Het |
Tsc2 |
A |
T |
17: 24,845,701 (GRCm39) |
C206S |
probably damaging |
Het |
Tsc22d4 |
A |
G |
5: 137,760,681 (GRCm39) |
Q34R |
possibly damaging |
Het |
Uroc1 |
G |
T |
6: 90,315,546 (GRCm39) |
M142I |
possibly damaging |
Het |
Uso1 |
T |
C |
5: 92,347,682 (GRCm39) |
S766P |
probably benign |
Het |
Usp21 |
G |
A |
1: 171,111,319 (GRCm39) |
|
probably benign |
Het |
Usp48 |
T |
A |
4: 137,360,437 (GRCm39) |
I658K |
possibly damaging |
Het |
Vmn1r206 |
T |
C |
13: 22,804,583 (GRCm39) |
H208R |
probably damaging |
Het |
Vmn2r109 |
C |
T |
17: 20,760,937 (GRCm39) |
A807T |
probably damaging |
Het |
Zfp329 |
A |
T |
7: 12,544,379 (GRCm39) |
C382S |
probably damaging |
Het |
Zfp341 |
A |
G |
2: 154,487,988 (GRCm39) |
E817G |
probably benign |
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 |
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 |
|
R8924:Celsr1
|
UTSW |
15 |
85,916,671 (GRCm39) |
missense |
possibly damaging |
0.94 |
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 |
|