Other mutations in this stock |
Total: 104 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
AA986860 |
A |
G |
1: 130,670,428 (GRCm39) |
S217G |
probably benign |
Het |
Adrb3 |
C |
A |
8: 27,717,591 (GRCm39) |
R286L |
probably damaging |
Het |
Akap11 |
T |
A |
14: 78,749,306 (GRCm39) |
D1027V |
probably benign |
Het |
Ank3 |
A |
T |
10: 69,733,913 (GRCm39) |
I726F |
probably damaging |
Het |
Ankmy2 |
T |
A |
12: 36,215,930 (GRCm39) |
D43E |
possibly damaging |
Het |
Ankrd34b |
A |
G |
13: 92,576,064 (GRCm39) |
D432G |
probably damaging |
Het |
Ano3 |
A |
C |
2: 110,715,217 (GRCm39) |
S74A |
probably benign |
Het |
B4galnt4 |
T |
A |
7: 140,650,439 (GRCm39) |
S769T |
probably damaging |
Het |
Bicral |
T |
A |
17: 47,136,104 (GRCm39) |
T369S |
probably benign |
Het |
Blm |
A |
G |
7: 80,147,166 (GRCm39) |
L738P |
probably damaging |
Het |
Bpifb3 |
A |
G |
2: 153,767,760 (GRCm39) |
T278A |
probably benign |
Het |
Bpifb5 |
A |
G |
2: 154,069,122 (GRCm39) |
|
probably benign |
Het |
Brd8 |
G |
C |
18: 34,743,527 (GRCm39) |
P266R |
probably damaging |
Het |
Btaf1 |
A |
T |
19: 36,957,983 (GRCm39) |
M587L |
probably benign |
Het |
Casz1 |
C |
G |
4: 149,027,668 (GRCm39) |
T1015S |
probably damaging |
Het |
Cdh23 |
A |
G |
10: 60,272,597 (GRCm39) |
I524T |
possibly damaging |
Het |
Cenpf |
A |
G |
1: 189,416,013 (GRCm39) |
L104P |
probably damaging |
Het |
Clasp1 |
G |
T |
1: 118,528,315 (GRCm39) |
|
probably null |
Het |
Coprs |
A |
G |
8: 13,935,112 (GRCm39) |
W148R |
probably damaging |
Het |
Cpne1 |
A |
G |
2: 155,920,302 (GRCm39) |
S168P |
probably damaging |
Het |
Cpxm2 |
T |
C |
7: 131,661,563 (GRCm39) |
Y408C |
probably damaging |
Het |
Ctnna3 |
A |
G |
10: 63,339,886 (GRCm39) |
E24G |
possibly damaging |
Het |
Cubn |
T |
A |
2: 13,327,813 (GRCm39) |
S2671C |
probably damaging |
Het |
Cyp4f39 |
T |
A |
17: 32,702,298 (GRCm39) |
F265Y |
probably damaging |
Het |
Dgkq |
C |
A |
5: 108,808,461 (GRCm39) |
R34L |
probably benign |
Het |
Dnajc7 |
C |
T |
11: 100,490,139 (GRCm39) |
|
probably benign |
Het |
Eml6 |
T |
G |
11: 29,781,136 (GRCm39) |
D632A |
probably damaging |
Het |
Fbxl18 |
G |
A |
5: 142,871,978 (GRCm39) |
A419V |
probably damaging |
Het |
Fbxw22 |
A |
T |
9: 109,214,179 (GRCm39) |
C212* |
probably null |
Het |
Ffar2 |
A |
G |
7: 30,518,839 (GRCm39) |
|
probably null |
Het |
Fga |
A |
T |
3: 82,940,028 (GRCm39) |
T561S |
probably damaging |
Het |
Fry |
A |
G |
5: 150,269,386 (GRCm39) |
Y159C |
probably damaging |
Het |
Gal3st1 |
A |
G |
11: 3,948,231 (GRCm39) |
Y146C |
probably damaging |
Het |
Gapvd1 |
A |
T |
2: 34,596,033 (GRCm39) |
H788Q |
probably damaging |
Het |
Gimap7 |
G |
A |
6: 48,700,449 (GRCm39) |
V12I |
possibly damaging |
Het |
Gli2 |
C |
A |
1: 118,929,779 (GRCm39) |
A43S |
possibly damaging |
Het |
Gm15446 |
T |
C |
5: 110,090,419 (GRCm39) |
F224L |
probably damaging |
Het |
Gm21738 |
C |
T |
14: 19,418,824 (GRCm38) |
V35I |
possibly damaging |
Het |
Grhl1 |
T |
C |
12: 24,636,155 (GRCm39) |
|
probably benign |
Het |
Grk6 |
T |
C |
13: 55,598,086 (GRCm39) |
Y53H |
probably damaging |
Het |
Hcar1 |
C |
T |
5: 124,017,328 (GRCm39) |
R121K |
probably damaging |
Het |
Hmcn1 |
A |
C |
1: 150,596,446 (GRCm39) |
S1797A |
probably damaging |
Het |
Hsd17b7 |
A |
T |
1: 169,783,562 (GRCm39) |
L282Q |
possibly damaging |
Het |
Irs1 |
TTCTCTGAGTGGCCACAGCGTCT |
TTCT |
1: 82,267,574 (GRCm39) |
|
probably null |
Het |
Kif1b |
C |
T |
4: 149,272,089 (GRCm39) |
V1571I |
probably benign |
Het |
Lpl |
T |
A |
8: 69,349,271 (GRCm39) |
C266S |
probably damaging |
Het |
Mag |
G |
A |
7: 30,608,476 (GRCm39) |
H213Y |
probably benign |
Het |
Mansc4 |
T |
G |
6: 146,976,688 (GRCm39) |
R309S |
probably benign |
Het |
Mlh3 |
A |
G |
12: 85,284,287 (GRCm39) |
|
probably null |
Het |
Mndal |
G |
A |
1: 173,687,933 (GRCm39) |
|
probably benign |
Het |
Mrgpra2b |
T |
A |
7: 47,113,742 (GRCm39) |
E330V |
probably damaging |
Het |
Myh3 |
A |
G |
11: 66,984,005 (GRCm39) |
I990V |
probably benign |
Het |
Myoz2 |
A |
T |
3: 122,819,765 (GRCm39) |
S65T |
probably damaging |
Het |
Naa16 |
T |
C |
14: 79,593,183 (GRCm39) |
E463G |
possibly damaging |
Het |
Nadsyn1 |
A |
G |
7: 143,351,581 (GRCm39) |
F684S |
probably damaging |
Het |
Notch1 |
T |
C |
2: 26,371,591 (GRCm39) |
E286G |
possibly damaging |
Het |
Nynrin |
A |
T |
14: 56,100,950 (GRCm39) |
I247L |
probably benign |
Het |
Oprm1 |
A |
G |
10: 6,739,035 (GRCm39) |
H54R |
probably benign |
Het |
Or10g6 |
T |
A |
9: 39,934,151 (GRCm39) |
I154N |
possibly damaging |
Het |
Or2n1d |
C |
T |
17: 38,646,860 (GRCm39) |
P271S |
probably damaging |
Het |
Or51a43 |
T |
C |
7: 103,717,336 (GRCm39) |
I301V |
probably null |
Het |
P4hb |
C |
T |
11: 120,452,992 (GRCm39) |
D483N |
probably benign |
Het |
Pak1 |
T |
C |
7: 97,520,787 (GRCm39) |
S149P |
probably benign |
Het |
Pars2 |
T |
C |
4: 106,510,913 (GRCm39) |
F232L |
possibly damaging |
Het |
Pih1d2 |
A |
G |
9: 50,532,245 (GRCm39) |
M88V |
possibly damaging |
Het |
Pms1 |
A |
T |
1: 53,246,392 (GRCm39) |
N382K |
probably benign |
Het |
Pnliprp2 |
G |
T |
19: 58,751,821 (GRCm39) |
V189L |
probably benign |
Het |
Pole |
G |
A |
5: 110,471,530 (GRCm39) |
V1425M |
possibly damaging |
Het |
Pot1b |
T |
A |
17: 55,961,805 (GRCm39) |
Q591L |
probably benign |
Het |
Ppp1r9a |
C |
T |
6: 4,906,348 (GRCm39) |
T301M |
possibly damaging |
Het |
Psg21 |
T |
C |
7: 18,384,741 (GRCm39) |
E335G |
probably benign |
Het |
Ptpru |
T |
A |
4: 131,497,066 (GRCm39) |
M1416L |
probably benign |
Het |
Pxn |
T |
C |
5: 115,683,049 (GRCm39) |
V117A |
probably damaging |
Het |
Qsox1 |
C |
T |
1: 155,688,385 (GRCm39) |
R54H |
possibly damaging |
Het |
Rad1 |
A |
G |
15: 10,488,092 (GRCm39) |
E42G |
probably damaging |
Het |
Rpp14 |
A |
G |
14: 8,090,145 (GRCm38) |
Y23C |
probably benign |
Het |
Sdk2 |
C |
T |
11: 113,725,782 (GRCm39) |
V1156I |
probably benign |
Het |
Serpina3j |
G |
T |
12: 104,285,958 (GRCm39) |
R371L |
probably benign |
Het |
Serpinb9d |
T |
A |
13: 33,381,946 (GRCm39) |
|
probably null |
Het |
Sirt5 |
C |
T |
13: 43,524,267 (GRCm39) |
S13F |
possibly damaging |
Het |
Slc6a7 |
T |
A |
18: 61,134,470 (GRCm39) |
|
probably benign |
Het |
Slx4 |
A |
G |
16: 3,804,712 (GRCm39) |
S701P |
probably benign |
Het |
Snx29 |
A |
G |
16: 11,185,545 (GRCm39) |
T43A |
probably benign |
Het |
Speg |
T |
C |
1: 75,400,550 (GRCm39) |
V2570A |
probably benign |
Het |
Srrm4 |
T |
A |
5: 116,591,565 (GRCm39) |
|
probably benign |
Het |
Stk32a |
A |
G |
18: 43,394,381 (GRCm39) |
Y110C |
probably damaging |
Het |
Tbc1d31 |
G |
A |
15: 57,779,506 (GRCm39) |
G73E |
probably benign |
Het |
Thsd7a |
A |
T |
6: 12,555,434 (GRCm39) |
I150N |
possibly damaging |
Het |
Tjp1 |
A |
T |
7: 64,969,001 (GRCm39) |
D699E |
probably damaging |
Het |
Tmem143 |
A |
G |
7: 45,565,988 (GRCm39) |
D437G |
possibly damaging |
Het |
Tmem45a2 |
A |
G |
16: 56,867,447 (GRCm39) |
Y85H |
possibly damaging |
Het |
Tmem45b |
T |
A |
9: 31,340,383 (GRCm39) |
T7S |
probably damaging |
Het |
Tut4 |
T |
A |
4: 108,407,922 (GRCm39) |
V1397D |
probably damaging |
Het |
Ube4b |
A |
G |
4: 149,432,428 (GRCm39) |
L832P |
probably damaging |
Het |
Ugp2 |
G |
T |
11: 21,279,048 (GRCm39) |
F379L |
probably damaging |
Het |
Ugt3a1 |
A |
T |
15: 9,365,437 (GRCm39) |
D350V |
probably damaging |
Het |
Vmn2r8 |
T |
A |
5: 108,950,284 (GRCm39) |
T188S |
possibly damaging |
Het |
Vwa7 |
C |
G |
17: 35,236,088 (GRCm39) |
P14R |
probably benign |
Het |
Vwc2 |
C |
A |
11: 11,211,495 (GRCm39) |
T317K |
probably damaging |
Het |
Vwf |
A |
T |
6: 125,605,335 (GRCm39) |
Q906L |
probably benign |
Het |
Wdr49 |
A |
G |
3: 75,336,654 (GRCm39) |
V351A |
probably damaging |
Het |
Wdr7 |
A |
G |
18: 63,861,575 (GRCm39) |
S196G |
probably benign |
Het |
Xkr6 |
C |
A |
14: 64,035,745 (GRCm39) |
A26E |
unknown |
Het |
Zfp955b |
T |
C |
17: 33,524,427 (GRCm39) |
I47V |
probably benign |
Het |
|
Other mutations in Celsr3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00233:Celsr3
|
APN |
9 |
108,726,124 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00536:Celsr3
|
APN |
9 |
108,706,391 (GRCm39) |
missense |
probably benign |
0.33 |
IGL00552:Celsr3
|
APN |
9 |
108,718,462 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL00801:Celsr3
|
APN |
9 |
108,719,775 (GRCm39) |
missense |
probably benign |
|
IGL01420:Celsr3
|
APN |
9 |
108,718,389 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL01541:Celsr3
|
APN |
9 |
108,708,907 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01619:Celsr3
|
APN |
9 |
108,711,756 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01619:Celsr3
|
APN |
9 |
108,714,603 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01631:Celsr3
|
APN |
9 |
108,714,603 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01777:Celsr3
|
APN |
9 |
108,713,141 (GRCm39) |
missense |
probably benign |
0.08 |
IGL01938:Celsr3
|
APN |
9 |
108,705,614 (GRCm39) |
missense |
probably benign |
0.34 |
IGL02135:Celsr3
|
APN |
9 |
108,704,755 (GRCm39) |
missense |
probably benign |
0.11 |
IGL02231:Celsr3
|
APN |
9 |
108,719,709 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02234:Celsr3
|
APN |
9 |
108,707,159 (GRCm39) |
missense |
probably benign |
|
IGL02392:Celsr3
|
APN |
9 |
108,711,920 (GRCm39) |
splice site |
probably benign |
|
IGL02416:Celsr3
|
APN |
9 |
108,709,318 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02421:Celsr3
|
APN |
9 |
108,717,662 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02455:Celsr3
|
APN |
9 |
108,720,092 (GRCm39) |
missense |
probably benign |
0.15 |
IGL02798:Celsr3
|
APN |
9 |
108,720,774 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02939:Celsr3
|
APN |
9 |
108,726,652 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02947:Celsr3
|
APN |
9 |
108,723,134 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02986:Celsr3
|
APN |
9 |
108,718,454 (GRCm39) |
splice site |
probably null |
|
IGL03089:Celsr3
|
APN |
9 |
108,703,806 (GRCm39) |
missense |
probably benign |
0.04 |
IGL03162:Celsr3
|
APN |
9 |
108,719,757 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03267:Celsr3
|
APN |
9 |
108,713,724 (GRCm39) |
splice site |
probably benign |
|
Diminishment
|
UTSW |
9 |
108,719,907 (GRCm39) |
intron |
probably benign |
|
little_d
|
UTSW |
9 |
108,704,891 (GRCm39) |
missense |
probably damaging |
0.98 |
nogal
|
UTSW |
9 |
108,713,037 (GRCm39) |
missense |
probably benign |
|
F6893:Celsr3
|
UTSW |
9 |
108,712,266 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4243001:Celsr3
|
UTSW |
9 |
108,709,507 (GRCm39) |
missense |
probably benign |
0.13 |
PIT4810001:Celsr3
|
UTSW |
9 |
108,722,932 (GRCm39) |
missense |
probably damaging |
1.00 |
R0110:Celsr3
|
UTSW |
9 |
108,704,204 (GRCm39) |
missense |
possibly damaging |
0.62 |
R0243:Celsr3
|
UTSW |
9 |
108,720,923 (GRCm39) |
splice site |
probably benign |
|
R0382:Celsr3
|
UTSW |
9 |
108,706,417 (GRCm39) |
missense |
probably damaging |
1.00 |
R0482:Celsr3
|
UTSW |
9 |
108,706,272 (GRCm39) |
nonsense |
probably null |
|
R0510:Celsr3
|
UTSW |
9 |
108,704,204 (GRCm39) |
missense |
possibly damaging |
0.62 |
R0630:Celsr3
|
UTSW |
9 |
108,704,891 (GRCm39) |
missense |
probably damaging |
0.98 |
R0656:Celsr3
|
UTSW |
9 |
108,711,854 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0764:Celsr3
|
UTSW |
9 |
108,705,017 (GRCm39) |
missense |
probably damaging |
1.00 |
R0883:Celsr3
|
UTSW |
9 |
108,719,832 (GRCm39) |
missense |
probably damaging |
1.00 |
R0924:Celsr3
|
UTSW |
9 |
108,723,224 (GRCm39) |
missense |
possibly damaging |
0.78 |
R1015:Celsr3
|
UTSW |
9 |
108,710,375 (GRCm39) |
missense |
probably benign |
0.17 |
R1321:Celsr3
|
UTSW |
9 |
108,713,069 (GRCm39) |
missense |
probably damaging |
1.00 |
R1423:Celsr3
|
UTSW |
9 |
108,704,104 (GRCm39) |
missense |
probably benign |
0.00 |
R1497:Celsr3
|
UTSW |
9 |
108,726,064 (GRCm39) |
missense |
probably benign |
0.14 |
R1520:Celsr3
|
UTSW |
9 |
108,725,857 (GRCm39) |
missense |
probably damaging |
1.00 |
R1534:Celsr3
|
UTSW |
9 |
108,726,083 (GRCm39) |
missense |
probably damaging |
0.99 |
R1569:Celsr3
|
UTSW |
9 |
108,706,267 (GRCm39) |
missense |
probably damaging |
1.00 |
R1657:Celsr3
|
UTSW |
9 |
108,720,151 (GRCm39) |
nonsense |
probably null |
|
R1753:Celsr3
|
UTSW |
9 |
108,709,056 (GRCm39) |
missense |
probably damaging |
0.99 |
R1764:Celsr3
|
UTSW |
9 |
108,706,157 (GRCm39) |
missense |
probably damaging |
1.00 |
R1801:Celsr3
|
UTSW |
9 |
108,711,825 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1838:Celsr3
|
UTSW |
9 |
108,707,105 (GRCm39) |
missense |
probably benign |
|
R1839:Celsr3
|
UTSW |
9 |
108,707,105 (GRCm39) |
missense |
probably benign |
|
R1875:Celsr3
|
UTSW |
9 |
108,713,037 (GRCm39) |
missense |
probably benign |
|
R1953:Celsr3
|
UTSW |
9 |
108,720,381 (GRCm39) |
missense |
probably benign |
0.19 |
R1960:Celsr3
|
UTSW |
9 |
108,723,016 (GRCm39) |
missense |
probably benign |
|
R2113:Celsr3
|
UTSW |
9 |
108,715,669 (GRCm39) |
missense |
probably damaging |
1.00 |
R2290:Celsr3
|
UTSW |
9 |
108,720,423 (GRCm39) |
missense |
probably damaging |
1.00 |
R2369:Celsr3
|
UTSW |
9 |
108,719,751 (GRCm39) |
missense |
probably benign |
|
R2373:Celsr3
|
UTSW |
9 |
108,719,751 (GRCm39) |
missense |
probably benign |
|
R2374:Celsr3
|
UTSW |
9 |
108,719,751 (GRCm39) |
missense |
probably benign |
|
R2375:Celsr3
|
UTSW |
9 |
108,719,751 (GRCm39) |
missense |
probably benign |
|
R2844:Celsr3
|
UTSW |
9 |
108,706,507 (GRCm39) |
missense |
probably damaging |
1.00 |
R2968:Celsr3
|
UTSW |
9 |
108,709,390 (GRCm39) |
missense |
probably damaging |
1.00 |
R3103:Celsr3
|
UTSW |
9 |
108,714,338 (GRCm39) |
missense |
probably benign |
0.31 |
R3159:Celsr3
|
UTSW |
9 |
108,704,909 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3791:Celsr3
|
UTSW |
9 |
108,719,751 (GRCm39) |
missense |
probably benign |
|
R4194:Celsr3
|
UTSW |
9 |
108,720,501 (GRCm39) |
critical splice donor site |
probably null |
|
R4329:Celsr3
|
UTSW |
9 |
108,723,248 (GRCm39) |
missense |
probably benign |
0.00 |
R4365:Celsr3
|
UTSW |
9 |
108,707,046 (GRCm39) |
missense |
possibly damaging |
0.47 |
R4419:Celsr3
|
UTSW |
9 |
108,720,443 (GRCm39) |
missense |
possibly damaging |
0.84 |
R4484:Celsr3
|
UTSW |
9 |
108,723,262 (GRCm39) |
critical splice donor site |
probably null |
|
R4582:Celsr3
|
UTSW |
9 |
108,722,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R4681:Celsr3
|
UTSW |
9 |
108,704,953 (GRCm39) |
missense |
possibly damaging |
0.58 |
R4729:Celsr3
|
UTSW |
9 |
108,724,851 (GRCm39) |
missense |
probably benign |
0.05 |
R4881:Celsr3
|
UTSW |
9 |
108,721,140 (GRCm39) |
missense |
probably damaging |
1.00 |
R4893:Celsr3
|
UTSW |
9 |
108,726,620 (GRCm39) |
missense |
probably damaging |
1.00 |
R5183:Celsr3
|
UTSW |
9 |
108,714,759 (GRCm39) |
missense |
probably damaging |
0.99 |
R5207:Celsr3
|
UTSW |
9 |
108,709,958 (GRCm39) |
missense |
probably benign |
0.01 |
R5290:Celsr3
|
UTSW |
9 |
108,720,357 (GRCm39) |
missense |
probably benign |
0.01 |
R5327:Celsr3
|
UTSW |
9 |
108,719,907 (GRCm39) |
intron |
probably benign |
|
R5345:Celsr3
|
UTSW |
9 |
108,709,323 (GRCm39) |
missense |
probably damaging |
1.00 |
R5358:Celsr3
|
UTSW |
9 |
108,709,224 (GRCm39) |
missense |
possibly damaging |
0.96 |
R5396:Celsr3
|
UTSW |
9 |
108,705,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R5414:Celsr3
|
UTSW |
9 |
108,717,241 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5452:Celsr3
|
UTSW |
9 |
108,721,233 (GRCm39) |
missense |
possibly damaging |
0.68 |
R5467:Celsr3
|
UTSW |
9 |
108,705,836 (GRCm39) |
missense |
probably damaging |
1.00 |
R5479:Celsr3
|
UTSW |
9 |
108,721,743 (GRCm39) |
critical splice donor site |
probably null |
|
R5629:Celsr3
|
UTSW |
9 |
108,726,266 (GRCm39) |
missense |
probably benign |
0.41 |
R5637:Celsr3
|
UTSW |
9 |
108,714,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R5652:Celsr3
|
UTSW |
9 |
108,715,671 (GRCm39) |
missense |
probably benign |
0.03 |
R5739:Celsr3
|
UTSW |
9 |
108,704,357 (GRCm39) |
missense |
probably benign |
|
R5785:Celsr3
|
UTSW |
9 |
108,704,996 (GRCm39) |
missense |
probably damaging |
1.00 |
R5877:Celsr3
|
UTSW |
9 |
108,722,926 (GRCm39) |
missense |
probably damaging |
0.98 |
R5961:Celsr3
|
UTSW |
9 |
108,708,993 (GRCm39) |
missense |
probably damaging |
1.00 |
R6046:Celsr3
|
UTSW |
9 |
108,714,350 (GRCm39) |
missense |
probably benign |
0.01 |
R6176:Celsr3
|
UTSW |
9 |
108,705,554 (GRCm39) |
missense |
probably damaging |
1.00 |
R6291:Celsr3
|
UTSW |
9 |
108,706,041 (GRCm39) |
missense |
probably damaging |
1.00 |
R6468:Celsr3
|
UTSW |
9 |
108,712,989 (GRCm39) |
missense |
probably benign |
0.08 |
R6481:Celsr3
|
UTSW |
9 |
108,714,283 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6547:Celsr3
|
UTSW |
9 |
108,706,327 (GRCm39) |
missense |
probably damaging |
1.00 |
R6763:Celsr3
|
UTSW |
9 |
108,704,549 (GRCm39) |
missense |
probably damaging |
1.00 |
R6870:Celsr3
|
UTSW |
9 |
108,706,390 (GRCm39) |
missense |
probably benign |
0.02 |
R6977:Celsr3
|
UTSW |
9 |
108,704,914 (GRCm39) |
missense |
probably benign |
|
R7061:Celsr3
|
UTSW |
9 |
108,724,793 (GRCm39) |
nonsense |
probably null |
|
R7122:Celsr3
|
UTSW |
9 |
108,705,766 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7156:Celsr3
|
UTSW |
9 |
108,715,203 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7166:Celsr3
|
UTSW |
9 |
108,720,150 (GRCm39) |
missense |
probably damaging |
1.00 |
R7176:Celsr3
|
UTSW |
9 |
108,722,961 (GRCm39) |
missense |
probably benign |
|
R7213:Celsr3
|
UTSW |
9 |
108,726,239 (GRCm39) |
missense |
probably damaging |
0.98 |
R7314:Celsr3
|
UTSW |
9 |
108,706,343 (GRCm39) |
missense |
probably damaging |
1.00 |
R7478:Celsr3
|
UTSW |
9 |
108,720,777 (GRCm39) |
missense |
probably benign |
0.37 |
R7508:Celsr3
|
UTSW |
9 |
108,713,821 (GRCm39) |
missense |
probably benign |
|
R7554:Celsr3
|
UTSW |
9 |
108,718,408 (GRCm39) |
missense |
probably benign |
|
R7615:Celsr3
|
UTSW |
9 |
108,714,851 (GRCm39) |
missense |
possibly damaging |
0.75 |
R7653:Celsr3
|
UTSW |
9 |
108,712,269 (GRCm39) |
nonsense |
probably null |
|
R7747:Celsr3
|
UTSW |
9 |
108,707,177 (GRCm39) |
missense |
possibly damaging |
0.61 |
R7881:Celsr3
|
UTSW |
9 |
108,705,271 (GRCm39) |
missense |
probably benign |
0.28 |
R7935:Celsr3
|
UTSW |
9 |
108,706,840 (GRCm39) |
missense |
probably benign |
0.01 |
R7995:Celsr3
|
UTSW |
9 |
108,722,282 (GRCm39) |
missense |
probably damaging |
0.99 |
R8006:Celsr3
|
UTSW |
9 |
108,706,306 (GRCm39) |
missense |
probably damaging |
1.00 |
R8077:Celsr3
|
UTSW |
9 |
108,705,530 (GRCm39) |
missense |
probably benign |
0.15 |
R8284:Celsr3
|
UTSW |
9 |
108,723,612 (GRCm39) |
missense |
probably damaging |
0.99 |
R8291:Celsr3
|
UTSW |
9 |
108,715,169 (GRCm39) |
missense |
probably damaging |
1.00 |
R8322:Celsr3
|
UTSW |
9 |
108,725,993 (GRCm39) |
missense |
probably damaging |
1.00 |
R8334:Celsr3
|
UTSW |
9 |
108,718,471 (GRCm39) |
frame shift |
probably null |
|
R8337:Celsr3
|
UTSW |
9 |
108,718,471 (GRCm39) |
frame shift |
probably null |
|
R8338:Celsr3
|
UTSW |
9 |
108,704,539 (GRCm39) |
nonsense |
probably null |
|
R8353:Celsr3
|
UTSW |
9 |
108,703,734 (GRCm39) |
missense |
probably benign |
0.00 |
R8407:Celsr3
|
UTSW |
9 |
108,706,256 (GRCm39) |
missense |
probably damaging |
1.00 |
R8408:Celsr3
|
UTSW |
9 |
108,708,988 (GRCm39) |
missense |
probably damaging |
1.00 |
R8459:Celsr3
|
UTSW |
9 |
108,706,829 (GRCm39) |
missense |
probably damaging |
1.00 |
R8510:Celsr3
|
UTSW |
9 |
108,715,319 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8713:Celsr3
|
UTSW |
9 |
108,707,062 (GRCm39) |
missense |
probably benign |
|
R8728:Celsr3
|
UTSW |
9 |
108,723,940 (GRCm39) |
missense |
probably benign |
0.24 |
R8829:Celsr3
|
UTSW |
9 |
108,717,582 (GRCm39) |
missense |
probably benign |
|
R8877:Celsr3
|
UTSW |
9 |
108,706,877 (GRCm39) |
missense |
probably damaging |
1.00 |
R8905:Celsr3
|
UTSW |
9 |
108,718,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R9008:Celsr3
|
UTSW |
9 |
108,706,151 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9072:Celsr3
|
UTSW |
9 |
108,704,293 (GRCm39) |
missense |
probably benign |
|
R9157:Celsr3
|
UTSW |
9 |
108,707,185 (GRCm39) |
missense |
probably damaging |
1.00 |
R9183:Celsr3
|
UTSW |
9 |
108,706,595 (GRCm39) |
missense |
probably damaging |
1.00 |
R9275:Celsr3
|
UTSW |
9 |
108,715,689 (GRCm39) |
missense |
probably benign |
0.27 |
R9361:Celsr3
|
UTSW |
9 |
108,726,521 (GRCm39) |
missense |
probably damaging |
1.00 |
R9382:Celsr3
|
UTSW |
9 |
108,706,961 (GRCm39) |
missense |
possibly damaging |
0.60 |
R9407:Celsr3
|
UTSW |
9 |
108,723,596 (GRCm39) |
missense |
probably damaging |
1.00 |
R9432:Celsr3
|
UTSW |
9 |
108,726,032 (GRCm39) |
missense |
probably benign |
0.00 |
R9607:Celsr3
|
UTSW |
9 |
108,717,701 (GRCm39) |
critical splice donor site |
probably null |
|
R9626:Celsr3
|
UTSW |
9 |
108,726,521 (GRCm39) |
missense |
probably damaging |
1.00 |
R9628:Celsr3
|
UTSW |
9 |
108,703,559 (GRCm39) |
nonsense |
probably null |
|
R9630:Celsr3
|
UTSW |
9 |
108,704,296 (GRCm39) |
missense |
probably benign |
|
R9645:Celsr3
|
UTSW |
9 |
108,704,691 (GRCm39) |
nonsense |
probably null |
|
R9683:Celsr3
|
UTSW |
9 |
108,704,522 (GRCm39) |
missense |
probably damaging |
1.00 |
R9794:Celsr3
|
UTSW |
9 |
108,728,502 (GRCm39) |
missense |
probably benign |
0.00 |
R9798:Celsr3
|
UTSW |
9 |
108,705,794 (GRCm39) |
missense |
probably damaging |
1.00 |
RF020:Celsr3
|
UTSW |
9 |
108,726,256 (GRCm39) |
missense |
probably benign |
|
X0018:Celsr3
|
UTSW |
9 |
108,717,611 (GRCm39) |
missense |
probably benign |
0.01 |
X0018:Celsr3
|
UTSW |
9 |
108,704,977 (GRCm39) |
missense |
possibly damaging |
0.65 |
X0026:Celsr3
|
UTSW |
9 |
108,706,129 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Celsr3
|
UTSW |
9 |
108,703,676 (GRCm39) |
missense |
probably benign |
0.34 |
|