Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ahctf1 |
A |
T |
1: 179,621,159 (GRCm39) |
|
probably benign |
Het |
Alg6 |
C |
T |
4: 99,607,431 (GRCm39) |
L15F |
possibly damaging |
Het |
Allc |
T |
A |
12: 28,605,325 (GRCm39) |
M325L |
probably benign |
Het |
Ap3b2 |
T |
C |
7: 81,126,517 (GRCm39) |
N361S |
possibly damaging |
Het |
Bmp8b |
A |
G |
4: 123,009,714 (GRCm39) |
|
probably benign |
Het |
Borcs6 |
A |
T |
11: 68,951,674 (GRCm39) |
T351S |
probably damaging |
Het |
Ccar1 |
T |
C |
10: 62,589,060 (GRCm39) |
R808G |
unknown |
Het |
Chdh |
C |
T |
14: 29,753,318 (GRCm39) |
P76S |
probably damaging |
Het |
Chmp7 |
T |
C |
14: 69,969,755 (GRCm39) |
S62G |
probably benign |
Het |
Cldn23 |
A |
T |
8: 36,293,182 (GRCm39) |
V102E |
probably damaging |
Het |
Csn2 |
G |
A |
5: 87,842,821 (GRCm39) |
Q69* |
probably null |
Het |
Ctrc |
A |
C |
4: 141,567,695 (GRCm39) |
I136S |
probably damaging |
Het |
Cysltr2 |
A |
C |
14: 73,266,951 (GRCm39) |
L253R |
probably damaging |
Het |
Ddr2 |
G |
A |
1: 169,812,530 (GRCm39) |
T654M |
probably damaging |
Het |
Derl2 |
G |
T |
11: 70,910,073 (GRCm39) |
|
probably null |
Het |
Dnai7 |
A |
T |
6: 145,124,794 (GRCm39) |
D510E |
probably damaging |
Het |
Dock5 |
T |
C |
14: 68,013,733 (GRCm39) |
S1330G |
probably benign |
Het |
Emp3 |
T |
C |
7: 45,569,373 (GRCm39) |
N56S |
probably benign |
Het |
Fam161a |
A |
T |
11: 22,970,583 (GRCm39) |
K195* |
probably null |
Het |
Ficd |
T |
A |
5: 113,875,072 (GRCm39) |
V47E |
probably benign |
Het |
Garin3 |
T |
C |
11: 46,295,990 (GRCm39) |
S121P |
probably benign |
Het |
Gbp10 |
T |
C |
5: 105,372,575 (GRCm39) |
T123A |
probably benign |
Het |
Gdf7 |
C |
T |
12: 8,348,371 (GRCm39) |
A309T |
unknown |
Het |
Gm14486 |
G |
T |
2: 30,548,572 (GRCm39) |
|
noncoding transcript |
Het |
Herc1 |
T |
A |
9: 66,307,151 (GRCm39) |
C990* |
probably null |
Het |
Itgb4 |
T |
C |
11: 115,897,365 (GRCm39) |
V1530A |
probably damaging |
Het |
Itpka |
G |
A |
2: 119,580,974 (GRCm39) |
R374H |
probably damaging |
Het |
Lacc1 |
T |
A |
14: 77,271,594 (GRCm39) |
|
probably null |
Het |
Med23 |
A |
T |
10: 24,771,734 (GRCm39) |
K225* |
probably null |
Het |
Mrgpra3 |
T |
A |
7: 47,239,909 (GRCm39) |
T6S |
probably benign |
Het |
Mroh7 |
T |
A |
4: 106,578,583 (GRCm39) |
N32Y |
probably damaging |
Het |
Mrps2 |
A |
G |
2: 28,359,763 (GRCm39) |
R207G |
probably damaging |
Het |
Mup20 |
A |
C |
4: 61,969,823 (GRCm39) |
|
probably null |
Het |
Nagpa |
A |
G |
16: 5,017,478 (GRCm39) |
|
probably null |
Het |
Nek3 |
A |
T |
8: 22,622,243 (GRCm39) |
|
probably benign |
Het |
Nes |
G |
A |
3: 87,885,935 (GRCm39) |
G1398E |
probably damaging |
Het |
Nf1 |
G |
T |
11: 79,345,015 (GRCm39) |
V1323L |
probably damaging |
Het |
Or5b96 |
T |
A |
19: 12,867,801 (GRCm39) |
I47F |
probably benign |
Het |
Or6b2 |
A |
T |
1: 92,407,594 (GRCm39) |
F250I |
probably benign |
Het |
Or6c2 |
T |
C |
10: 129,362,773 (GRCm39) |
F226L |
probably benign |
Het |
Paqr8 |
G |
T |
1: 21,005,482 (GRCm39) |
C212F |
probably benign |
Het |
Pcdhb1 |
T |
C |
18: 37,399,515 (GRCm39) |
Y489H |
probably damaging |
Het |
Piwil2 |
T |
C |
14: 70,629,966 (GRCm39) |
K683E |
probably damaging |
Het |
Pjvk |
A |
C |
2: 76,480,734 (GRCm39) |
|
probably null |
Het |
Pkd1l3 |
A |
T |
8: 110,359,823 (GRCm39) |
S893C |
probably damaging |
Het |
Plxna2 |
A |
G |
1: 194,471,207 (GRCm39) |
T993A |
probably benign |
Het |
Ppp2r2b |
A |
T |
18: 42,821,417 (GRCm39) |
I247N |
probably damaging |
Het |
Rac2 |
T |
C |
15: 78,449,654 (GRCm39) |
N92S |
probably damaging |
Het |
Senp2 |
A |
T |
16: 21,860,130 (GRCm39) |
H501L |
possibly damaging |
Het |
Snx29 |
A |
T |
16: 11,556,227 (GRCm39) |
I753F |
probably damaging |
Het |
Tcf20 |
T |
A |
15: 82,740,386 (GRCm39) |
H355L |
probably damaging |
Het |
Tex2 |
T |
C |
11: 106,437,666 (GRCm39) |
D668G |
unknown |
Het |
Tlr12 |
G |
A |
4: 128,510,502 (GRCm39) |
Q583* |
probably null |
Het |
Tmem119 |
T |
C |
5: 113,933,289 (GRCm39) |
I171V |
probably damaging |
Het |
Ube2m |
C |
T |
7: 12,770,249 (GRCm39) |
|
probably null |
Het |
Vmn2r25 |
A |
T |
6: 123,817,062 (GRCm39) |
I173N |
probably damaging |
Het |
Whrn |
A |
T |
4: 63,350,951 (GRCm39) |
V15E |
probably damaging |
Het |
Zfp558 |
A |
C |
9: 18,368,296 (GRCm39) |
V164G |
possibly damaging |
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 |
|
R1874:Celsr3
|
UTSW |
9 |
108,713,037 (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 |
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 |
|