Other mutations in this stock |
Total: 90 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca16 |
A |
G |
7: 120,533,657 (GRCm38) |
K1270E |
possibly damaging |
Het |
Adgrb2 |
T |
C |
4: 130,010,084 (GRCm38) |
S668P |
probably damaging |
Het |
Ahdc1 |
T |
G |
4: 133,064,277 (GRCm38) |
L943R |
possibly damaging |
Het |
Ank2 |
T |
C |
3: 126,945,476 (GRCm38) |
K2253R |
unknown |
Het |
Arhgap23 |
T |
C |
11: 97,463,561 (GRCm38) |
S767P |
probably damaging |
Het |
Arhgef12 |
A |
G |
9: 42,989,989 (GRCm38) |
I839T |
possibly damaging |
Het |
Begain |
CGCCGC |
CGCCGCGGCCGC |
12: 109,033,424 (GRCm38) |
|
probably benign |
Het |
Btbd19 |
A |
T |
4: 117,122,275 (GRCm38) |
C116S |
probably damaging |
Het |
Cbr1 |
C |
T |
16: 93,610,179 (GRCm38) |
A261V |
probably benign |
Het |
Ccdc137 |
A |
G |
11: 120,458,196 (GRCm38) |
R18G |
probably benign |
Het |
Cdsn |
AG |
AGACAGGAAGTAGTAGCTCTCAG |
17: 35,554,979 (GRCm38) |
|
probably benign |
Het |
Cep350 |
A |
T |
1: 155,915,478 (GRCm38) |
V1300E |
probably benign |
Het |
Cluh |
G |
GCCAGAT |
11: 74,669,538 (GRCm38) |
|
probably benign |
Het |
Cmya5 |
G |
T |
13: 93,069,291 (GRCm38) |
Q3357K |
possibly damaging |
Het |
Col6a2 |
T |
G |
10: 76,606,209 (GRCm38) |
|
probably null |
Het |
Cyp2j9 |
T |
A |
4: 96,577,652 (GRCm38) |
T315S |
probably damaging |
Het |
Cyp3a13 |
CATTATT |
CATT |
5: 137,894,263 (GRCm38) |
|
probably null |
Het |
Dnah6 |
T |
A |
6: 73,118,057 (GRCm38) |
Y2181F |
probably benign |
Het |
Dnah7b |
A |
G |
1: 46,373,261 (GRCm38) |
D4010G |
possibly damaging |
Het |
E4f1 |
CCG |
CCGACG |
17: 24,455,195 (GRCm38) |
|
probably benign |
Het |
Ep300 |
A |
T |
15: 81,586,571 (GRCm38) |
|
probably benign |
Het |
Fam234a |
A |
G |
17: 26,218,751 (GRCm38) |
V90A |
probably benign |
Het |
Fam71e1 |
GGA |
GGAAGGGTGGATCCTGGATACCTGGGTCTGAGGGAAGA |
7: 44,500,535 (GRCm38) |
|
probably null |
Het |
Gab3 |
TCT |
TCTGCT |
X: 75,000,017 (GRCm38) |
|
probably benign |
Het |
Gal3st1 |
A |
G |
11: 3,998,153 (GRCm38) |
Y120C |
possibly damaging |
Het |
Gm5475 |
GTGGAAGGAAAGGT |
G |
15: 100,427,149 (GRCm38) |
|
probably null |
Het |
Gm6665 |
T |
TC |
18: 31,820,377 (GRCm38) |
|
probably null |
Het |
Hdlbp |
T |
C |
1: 93,440,734 (GRCm38) |
T8A |
probably benign |
Het |
Hnrnpa2b1 |
T |
A |
6: 51,466,694 (GRCm38) |
K92N |
probably damaging |
Het |
Hsdl2 |
GGAGCAGCCACAGCTGCAGGAGAAGCCACAGCTGCAGGAGCAGCCACAGC |
GGAGCAGCCACAGCTGCAGGAGCAGCCACAGCTGCAGGAGAAGCCACAGCTGCAGGAGCAGCCACAGC |
4: 59,610,640 (GRCm38) |
|
probably benign |
Het |
Klhl10 |
C |
G |
11: 100,442,070 (GRCm38) |
Q14E |
probably benign |
Het |
Klra2 |
GAAAGAAATCCA |
GAAAGAAATCCAAAGAAATCCA |
6: 131,221,838 (GRCm38) |
|
probably null |
Het |
Kmt2b |
CC |
CCTCCTGC |
7: 30,586,382 (GRCm38) |
|
probably benign |
Het |
Krt2 |
A |
G |
15: 101,817,968 (GRCm38) |
I45T |
unknown |
Het |
Ksr2 |
T |
C |
5: 117,555,218 (GRCm38) |
S244P |
probably benign |
Het |
Lama5 |
A |
T |
2: 180,196,178 (GRCm38) |
M915K |
probably benign |
Het |
Lrp1b |
A |
C |
2: 41,770,846 (GRCm38) |
H197Q |
|
Het |
Lrrc1 |
T |
C |
9: 77,452,631 (GRCm38) |
E293G |
probably damaging |
Het |
Med12l |
AACA |
AACAACA |
3: 59,275,958 (GRCm38) |
|
probably benign |
Het |
Mgam |
T |
A |
6: 40,685,309 (GRCm38) |
Y1179N |
probably damaging |
Het |
Mgat4c |
A |
G |
10: 102,389,067 (GRCm38) |
I381V |
probably benign |
Het |
Mrgprx1 |
A |
AGAC |
7: 48,021,511 (GRCm38) |
|
probably benign |
Het |
Myc |
A |
T |
15: 61,985,823 (GRCm38) |
|
probably benign |
Het |
Nipbl |
A |
G |
15: 8,358,934 (GRCm38) |
S401P |
probably damaging |
Het |
Nlrp9c |
A |
T |
7: 26,385,224 (GRCm38) |
I310N |
probably benign |
Het |
Nwd2 |
C |
A |
5: 63,805,723 (GRCm38) |
Y883* |
probably null |
Het |
Oas1e |
T |
A |
5: 120,794,318 (GRCm38) |
T87S |
possibly damaging |
Het |
Olfr586 |
A |
T |
7: 103,121,891 (GRCm38) |
C294S |
probably benign |
Het |
Olfr653 |
A |
G |
7: 104,580,290 (GRCm38) |
M215V |
probably benign |
Het |
Olfr885 |
G |
A |
9: 38,061,324 (GRCm38) |
M1I |
probably null |
Het |
Olfr964-ps1 |
GA |
GATACA |
9: 39,686,753 (GRCm38) |
|
probably null |
Het |
Pappa |
T |
G |
4: 65,205,045 (GRCm38) |
S872R |
possibly damaging |
Het |
Parp4 |
T |
C |
14: 56,647,349 (GRCm38) |
L1295P |
unknown |
Het |
Pcdh15 |
A |
T |
10: 74,185,410 (GRCm38) |
Y152F |
probably damaging |
Het |
Pdk1 |
A |
T |
2: 71,883,896 (GRCm38) |
I217L |
possibly damaging |
Het |
Phldb1 |
A |
C |
9: 44,697,946 (GRCm38) |
C450W |
probably damaging |
Het |
Pnmal1 |
C |
CCATGATGCACCTGCTTCAACATCA |
7: 16,961,451 (GRCm38) |
|
probably benign |
Het |
Prl2c5 |
G |
A |
13: 13,185,912 (GRCm38) |
G55S |
probably benign |
Het |
Psme2b |
A |
T |
11: 48,945,570 (GRCm38) |
H183Q |
probably damaging |
Het |
Ptms |
CCTCCTC |
CCTCCTCCTC |
6: 124,914,449 (GRCm38) |
|
probably benign |
Het |
Rln3 |
T |
C |
8: 84,043,302 (GRCm38) |
T73A |
probably benign |
Het |
Rprd1a |
T |
A |
18: 24,530,005 (GRCm38) |
Q21L |
probably damaging |
Het |
Sept3 |
A |
T |
15: 82,284,461 (GRCm38) |
D155V |
probably damaging |
Het |
Sh3rf3 |
T |
A |
10: 58,813,768 (GRCm38) |
V65E |
probably damaging |
Het |
Shank3 |
A |
G |
15: 89,500,390 (GRCm38) |
N155S |
probably benign |
Het |
Shox2 |
G |
T |
3: 66,973,813 (GRCm38) |
P278Q |
probably damaging |
Het |
Slc1a1 |
T |
C |
19: 28,879,155 (GRCm38) |
|
probably null |
Het |
Slc39a10 |
A |
T |
1: 46,810,015 (GRCm38) |
F814I |
probably damaging |
Het |
Slc5a1 |
T |
C |
5: 33,133,429 (GRCm38) |
I119T |
probably damaging |
Het |
Slc6a13 |
T |
C |
6: 121,324,351 (GRCm38) |
|
probably null |
Het |
Spta1 |
A |
G |
1: 174,213,444 (GRCm38) |
D1270G |
probably benign |
Het |
Spta1 |
T |
A |
1: 174,217,903 (GRCm38) |
F1542L |
probably damaging |
Het |
Tacc3 |
T |
A |
5: 33,661,224 (GRCm38) |
M1K |
probably null |
Het |
Tax1bp1 |
T |
C |
6: 52,721,354 (GRCm38) |
V17A |
probably damaging |
Het |
Thegl |
CAGCGATCCTCCCCAGTCCCGCAAGGC |
CAGCGATCCTCCCCAGTCCCGCAAGGCGAGCGATCCTCCCCAGTCCCGCAAGGC |
5: 77,016,400 (GRCm38) |
|
probably benign |
Het |
Tmem156 |
T |
A |
5: 65,091,547 (GRCm38) |
E3D |
probably benign |
Het |
Tmem209 |
T |
A |
6: 30,487,418 (GRCm38) |
M530L |
probably benign |
Het |
Trpc2 |
A |
G |
7: 102,096,226 (GRCm38) |
D883G |
unknown |
Het |
Tsen34 |
GGAGCCAAAAT |
G |
7: 3,695,796 (GRCm38) |
|
probably null |
Het |
Uhrf2 |
T |
C |
19: 30,086,391 (GRCm38) |
Y585H |
probably damaging |
Het |
Vmn1r26 |
T |
A |
6: 58,008,720 (GRCm38) |
K161N |
probably benign |
Het |
Vmn1r29 |
A |
G |
6: 58,307,543 (GRCm38) |
S83G |
probably benign |
Het |
Vps13b |
G |
T |
15: 35,925,406 (GRCm38) |
W3829L |
probably null |
Het |
Vwce |
G |
A |
19: 10,653,085 (GRCm38) |
G503R |
probably damaging |
Het |
Zc3h11a |
T |
C |
1: 133,626,997 (GRCm38) |
E415G |
possibly damaging |
Het |
Zc3h14 |
T |
A |
12: 98,780,282 (GRCm38) |
|
probably null |
Het |
Zfp119b |
A |
T |
17: 55,939,499 (GRCm38) |
M229K |
probably benign |
Het |
Zfp384 |
GGCCCAGGC |
GGCCCAGGCCCACGCCCAGGC |
6: 125,036,488 (GRCm38) |
|
probably benign |
Het |
Zfp384 |
CCAAGCTCAAGC |
CCAAGC |
6: 125,036,455 (GRCm38) |
|
probably benign |
Het |
Zyx |
T |
A |
6: 42,357,396 (GRCm38) |
L518Q |
probably damaging |
Het |
|
Other mutations in Celsr3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00233:Celsr3
|
APN |
9 |
108,848,925 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL00536:Celsr3
|
APN |
9 |
108,829,192 (GRCm38) |
missense |
probably benign |
0.33 |
IGL00552:Celsr3
|
APN |
9 |
108,841,263 (GRCm38) |
missense |
possibly damaging |
0.88 |
IGL00801:Celsr3
|
APN |
9 |
108,842,576 (GRCm38) |
missense |
probably benign |
|
IGL01420:Celsr3
|
APN |
9 |
108,841,190 (GRCm38) |
critical splice acceptor site |
probably null |
|
IGL01541:Celsr3
|
APN |
9 |
108,831,708 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01619:Celsr3
|
APN |
9 |
108,834,557 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01619:Celsr3
|
APN |
9 |
108,837,404 (GRCm38) |
missense |
probably benign |
0.00 |
IGL01631:Celsr3
|
APN |
9 |
108,837,404 (GRCm38) |
missense |
probably benign |
0.00 |
IGL01777:Celsr3
|
APN |
9 |
108,835,942 (GRCm38) |
missense |
probably benign |
0.08 |
IGL01938:Celsr3
|
APN |
9 |
108,828,415 (GRCm38) |
missense |
probably benign |
0.34 |
IGL02135:Celsr3
|
APN |
9 |
108,827,556 (GRCm38) |
missense |
probably benign |
0.11 |
IGL02231:Celsr3
|
APN |
9 |
108,842,510 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02234:Celsr3
|
APN |
9 |
108,829,960 (GRCm38) |
missense |
probably benign |
|
IGL02392:Celsr3
|
APN |
9 |
108,834,721 (GRCm38) |
splice site |
probably benign |
|
IGL02416:Celsr3
|
APN |
9 |
108,832,119 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02421:Celsr3
|
APN |
9 |
108,840,463 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02455:Celsr3
|
APN |
9 |
108,842,893 (GRCm38) |
missense |
probably benign |
0.15 |
IGL02798:Celsr3
|
APN |
9 |
108,843,575 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02939:Celsr3
|
APN |
9 |
108,849,453 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02947:Celsr3
|
APN |
9 |
108,845,935 (GRCm38) |
missense |
probably benign |
0.12 |
IGL02986:Celsr3
|
APN |
9 |
108,841,255 (GRCm38) |
splice site |
probably null |
|
IGL03089:Celsr3
|
APN |
9 |
108,826,607 (GRCm38) |
missense |
probably benign |
0.04 |
IGL03162:Celsr3
|
APN |
9 |
108,842,558 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03267:Celsr3
|
APN |
9 |
108,836,525 (GRCm38) |
splice site |
probably benign |
|
Diminishment
|
UTSW |
9 |
108,842,708 (GRCm38) |
intron |
probably benign |
|
little_d
|
UTSW |
9 |
108,827,692 (GRCm38) |
missense |
probably damaging |
0.98 |
nogal
|
UTSW |
9 |
108,835,838 (GRCm38) |
missense |
probably benign |
|
F6893:Celsr3
|
UTSW |
9 |
108,835,067 (GRCm38) |
missense |
probably benign |
0.00 |
PIT4243001:Celsr3
|
UTSW |
9 |
108,832,308 (GRCm38) |
missense |
probably benign |
0.13 |
PIT4810001:Celsr3
|
UTSW |
9 |
108,845,733 (GRCm38) |
missense |
probably damaging |
1.00 |
R0110:Celsr3
|
UTSW |
9 |
108,827,005 (GRCm38) |
missense |
possibly damaging |
0.62 |
R0243:Celsr3
|
UTSW |
9 |
108,843,724 (GRCm38) |
splice site |
probably benign |
|
R0382:Celsr3
|
UTSW |
9 |
108,829,218 (GRCm38) |
missense |
probably damaging |
1.00 |
R0482:Celsr3
|
UTSW |
9 |
108,829,073 (GRCm38) |
nonsense |
probably null |
|
R0510:Celsr3
|
UTSW |
9 |
108,827,005 (GRCm38) |
missense |
possibly damaging |
0.62 |
R0630:Celsr3
|
UTSW |
9 |
108,827,692 (GRCm38) |
missense |
probably damaging |
0.98 |
R0656:Celsr3
|
UTSW |
9 |
108,834,655 (GRCm38) |
missense |
possibly damaging |
0.89 |
R0764:Celsr3
|
UTSW |
9 |
108,827,818 (GRCm38) |
missense |
probably damaging |
1.00 |
R0883:Celsr3
|
UTSW |
9 |
108,842,633 (GRCm38) |
missense |
probably damaging |
1.00 |
R0924:Celsr3
|
UTSW |
9 |
108,846,025 (GRCm38) |
missense |
possibly damaging |
0.78 |
R1015:Celsr3
|
UTSW |
9 |
108,833,176 (GRCm38) |
missense |
probably benign |
0.17 |
R1321:Celsr3
|
UTSW |
9 |
108,835,870 (GRCm38) |
missense |
probably damaging |
1.00 |
R1423:Celsr3
|
UTSW |
9 |
108,826,905 (GRCm38) |
missense |
probably benign |
0.00 |
R1497:Celsr3
|
UTSW |
9 |
108,848,865 (GRCm38) |
missense |
probably benign |
0.14 |
R1520:Celsr3
|
UTSW |
9 |
108,848,658 (GRCm38) |
missense |
probably damaging |
1.00 |
R1534:Celsr3
|
UTSW |
9 |
108,848,884 (GRCm38) |
missense |
probably damaging |
0.99 |
R1569:Celsr3
|
UTSW |
9 |
108,829,068 (GRCm38) |
missense |
probably damaging |
1.00 |
R1657:Celsr3
|
UTSW |
9 |
108,842,952 (GRCm38) |
nonsense |
probably null |
|
R1753:Celsr3
|
UTSW |
9 |
108,831,857 (GRCm38) |
missense |
probably damaging |
0.99 |
R1764:Celsr3
|
UTSW |
9 |
108,828,958 (GRCm38) |
missense |
probably damaging |
1.00 |
R1801:Celsr3
|
UTSW |
9 |
108,834,626 (GRCm38) |
missense |
possibly damaging |
0.88 |
R1838:Celsr3
|
UTSW |
9 |
108,829,906 (GRCm38) |
missense |
probably benign |
|
R1839:Celsr3
|
UTSW |
9 |
108,829,906 (GRCm38) |
missense |
probably benign |
|
R1874:Celsr3
|
UTSW |
9 |
108,835,838 (GRCm38) |
missense |
probably benign |
|
R1875:Celsr3
|
UTSW |
9 |
108,835,838 (GRCm38) |
missense |
probably benign |
|
R1953:Celsr3
|
UTSW |
9 |
108,843,182 (GRCm38) |
missense |
probably benign |
0.19 |
R1960:Celsr3
|
UTSW |
9 |
108,845,817 (GRCm38) |
missense |
probably benign |
|
R2113:Celsr3
|
UTSW |
9 |
108,838,470 (GRCm38) |
missense |
probably damaging |
1.00 |
R2290:Celsr3
|
UTSW |
9 |
108,843,224 (GRCm38) |
missense |
probably damaging |
1.00 |
R2369:Celsr3
|
UTSW |
9 |
108,842,552 (GRCm38) |
missense |
probably benign |
|
R2373:Celsr3
|
UTSW |
9 |
108,842,552 (GRCm38) |
missense |
probably benign |
|
R2374:Celsr3
|
UTSW |
9 |
108,842,552 (GRCm38) |
missense |
probably benign |
|
R2375:Celsr3
|
UTSW |
9 |
108,842,552 (GRCm38) |
missense |
probably benign |
|
R2844:Celsr3
|
UTSW |
9 |
108,829,308 (GRCm38) |
missense |
probably damaging |
1.00 |
R2968:Celsr3
|
UTSW |
9 |
108,832,191 (GRCm38) |
missense |
probably damaging |
1.00 |
R3103:Celsr3
|
UTSW |
9 |
108,837,139 (GRCm38) |
missense |
probably benign |
0.31 |
R3159:Celsr3
|
UTSW |
9 |
108,827,710 (GRCm38) |
missense |
possibly damaging |
0.94 |
R3791:Celsr3
|
UTSW |
9 |
108,842,552 (GRCm38) |
missense |
probably benign |
|
R4194:Celsr3
|
UTSW |
9 |
108,843,302 (GRCm38) |
critical splice donor site |
probably null |
|
R4329:Celsr3
|
UTSW |
9 |
108,846,049 (GRCm38) |
missense |
probably benign |
0.00 |
R4365:Celsr3
|
UTSW |
9 |
108,829,847 (GRCm38) |
missense |
possibly damaging |
0.47 |
R4419:Celsr3
|
UTSW |
9 |
108,843,244 (GRCm38) |
missense |
possibly damaging |
0.84 |
R4484:Celsr3
|
UTSW |
9 |
108,846,063 (GRCm38) |
critical splice donor site |
probably null |
|
R4582:Celsr3
|
UTSW |
9 |
108,845,723 (GRCm38) |
missense |
probably damaging |
1.00 |
R4681:Celsr3
|
UTSW |
9 |
108,827,754 (GRCm38) |
missense |
possibly damaging |
0.58 |
R4729:Celsr3
|
UTSW |
9 |
108,847,652 (GRCm38) |
missense |
probably benign |
0.05 |
R4881:Celsr3
|
UTSW |
9 |
108,843,941 (GRCm38) |
missense |
probably damaging |
1.00 |
R4893:Celsr3
|
UTSW |
9 |
108,849,421 (GRCm38) |
missense |
probably damaging |
1.00 |
R5183:Celsr3
|
UTSW |
9 |
108,837,560 (GRCm38) |
missense |
probably damaging |
0.99 |
R5207:Celsr3
|
UTSW |
9 |
108,832,759 (GRCm38) |
missense |
probably benign |
0.01 |
R5290:Celsr3
|
UTSW |
9 |
108,843,158 (GRCm38) |
missense |
probably benign |
0.01 |
R5327:Celsr3
|
UTSW |
9 |
108,842,708 (GRCm38) |
intron |
probably benign |
|
R5345:Celsr3
|
UTSW |
9 |
108,832,124 (GRCm38) |
missense |
probably damaging |
1.00 |
R5358:Celsr3
|
UTSW |
9 |
108,832,025 (GRCm38) |
missense |
possibly damaging |
0.96 |
R5396:Celsr3
|
UTSW |
9 |
108,828,582 (GRCm38) |
missense |
probably damaging |
1.00 |
R5414:Celsr3
|
UTSW |
9 |
108,840,042 (GRCm38) |
missense |
possibly damaging |
0.88 |
R5452:Celsr3
|
UTSW |
9 |
108,844,034 (GRCm38) |
missense |
possibly damaging |
0.68 |
R5467:Celsr3
|
UTSW |
9 |
108,828,637 (GRCm38) |
missense |
probably damaging |
1.00 |
R5479:Celsr3
|
UTSW |
9 |
108,844,544 (GRCm38) |
critical splice donor site |
probably null |
|
R5629:Celsr3
|
UTSW |
9 |
108,849,067 (GRCm38) |
missense |
probably benign |
0.41 |
R5637:Celsr3
|
UTSW |
9 |
108,837,133 (GRCm38) |
missense |
probably damaging |
1.00 |
R5652:Celsr3
|
UTSW |
9 |
108,838,472 (GRCm38) |
missense |
probably benign |
0.03 |
R5739:Celsr3
|
UTSW |
9 |
108,827,158 (GRCm38) |
missense |
probably benign |
|
R5785:Celsr3
|
UTSW |
9 |
108,827,797 (GRCm38) |
missense |
probably damaging |
1.00 |
R5877:Celsr3
|
UTSW |
9 |
108,845,727 (GRCm38) |
missense |
probably damaging |
0.98 |
R5961:Celsr3
|
UTSW |
9 |
108,831,794 (GRCm38) |
missense |
probably damaging |
1.00 |
R6046:Celsr3
|
UTSW |
9 |
108,837,151 (GRCm38) |
missense |
probably benign |
0.01 |
R6176:Celsr3
|
UTSW |
9 |
108,828,355 (GRCm38) |
missense |
probably damaging |
1.00 |
R6291:Celsr3
|
UTSW |
9 |
108,828,842 (GRCm38) |
missense |
probably damaging |
1.00 |
R6468:Celsr3
|
UTSW |
9 |
108,835,790 (GRCm38) |
missense |
probably benign |
0.08 |
R6481:Celsr3
|
UTSW |
9 |
108,837,084 (GRCm38) |
missense |
possibly damaging |
0.92 |
R6547:Celsr3
|
UTSW |
9 |
108,829,128 (GRCm38) |
missense |
probably damaging |
1.00 |
R6763:Celsr3
|
UTSW |
9 |
108,827,350 (GRCm38) |
missense |
probably damaging |
1.00 |
R6870:Celsr3
|
UTSW |
9 |
108,829,191 (GRCm38) |
missense |
probably benign |
0.02 |
R6977:Celsr3
|
UTSW |
9 |
108,827,715 (GRCm38) |
missense |
probably benign |
|
R7061:Celsr3
|
UTSW |
9 |
108,847,594 (GRCm38) |
nonsense |
probably null |
|
R7122:Celsr3
|
UTSW |
9 |
108,828,567 (GRCm38) |
missense |
possibly damaging |
0.90 |
R7156:Celsr3
|
UTSW |
9 |
108,838,004 (GRCm38) |
missense |
possibly damaging |
0.95 |
R7166:Celsr3
|
UTSW |
9 |
108,842,951 (GRCm38) |
missense |
probably damaging |
1.00 |
R7176:Celsr3
|
UTSW |
9 |
108,845,762 (GRCm38) |
missense |
probably benign |
|
R7213:Celsr3
|
UTSW |
9 |
108,849,040 (GRCm38) |
missense |
probably damaging |
0.98 |
R7314:Celsr3
|
UTSW |
9 |
108,829,144 (GRCm38) |
missense |
probably damaging |
1.00 |
R7478:Celsr3
|
UTSW |
9 |
108,843,578 (GRCm38) |
missense |
probably benign |
0.37 |
R7508:Celsr3
|
UTSW |
9 |
108,836,622 (GRCm38) |
missense |
probably benign |
|
R7554:Celsr3
|
UTSW |
9 |
108,841,209 (GRCm38) |
missense |
probably benign |
|
R7615:Celsr3
|
UTSW |
9 |
108,837,652 (GRCm38) |
missense |
possibly damaging |
0.75 |
R7653:Celsr3
|
UTSW |
9 |
108,835,070 (GRCm38) |
nonsense |
probably null |
|
R7747:Celsr3
|
UTSW |
9 |
108,829,978 (GRCm38) |
missense |
possibly damaging |
0.61 |
R7881:Celsr3
|
UTSW |
9 |
108,828,072 (GRCm38) |
missense |
probably benign |
0.28 |
R7935:Celsr3
|
UTSW |
9 |
108,829,641 (GRCm38) |
missense |
probably benign |
0.01 |
R7995:Celsr3
|
UTSW |
9 |
108,845,083 (GRCm38) |
missense |
probably damaging |
0.99 |
R8006:Celsr3
|
UTSW |
9 |
108,829,107 (GRCm38) |
missense |
probably damaging |
1.00 |
R8077:Celsr3
|
UTSW |
9 |
108,828,331 (GRCm38) |
missense |
probably benign |
0.15 |
R8284:Celsr3
|
UTSW |
9 |
108,846,413 (GRCm38) |
missense |
probably damaging |
0.99 |
R8291:Celsr3
|
UTSW |
9 |
108,837,970 (GRCm38) |
missense |
probably damaging |
1.00 |
R8322:Celsr3
|
UTSW |
9 |
108,848,794 (GRCm38) |
missense |
probably damaging |
1.00 |
R8334:Celsr3
|
UTSW |
9 |
108,841,272 (GRCm38) |
frame shift |
probably null |
|
R8337:Celsr3
|
UTSW |
9 |
108,841,272 (GRCm38) |
frame shift |
probably null |
|
R8338:Celsr3
|
UTSW |
9 |
108,827,340 (GRCm38) |
nonsense |
probably null |
|
R8353:Celsr3
|
UTSW |
9 |
108,826,535 (GRCm38) |
missense |
probably benign |
0.00 |
R8407:Celsr3
|
UTSW |
9 |
108,829,057 (GRCm38) |
missense |
probably damaging |
1.00 |
R8408:Celsr3
|
UTSW |
9 |
108,831,789 (GRCm38) |
missense |
probably damaging |
1.00 |
R8459:Celsr3
|
UTSW |
9 |
108,829,630 (GRCm38) |
missense |
probably damaging |
1.00 |
R8510:Celsr3
|
UTSW |
9 |
108,838,120 (GRCm38) |
missense |
possibly damaging |
0.93 |
R8713:Celsr3
|
UTSW |
9 |
108,829,863 (GRCm38) |
missense |
probably benign |
|
R8728:Celsr3
|
UTSW |
9 |
108,846,741 (GRCm38) |
missense |
probably benign |
0.24 |
R8829:Celsr3
|
UTSW |
9 |
108,840,383 (GRCm38) |
missense |
probably benign |
|
R8877:Celsr3
|
UTSW |
9 |
108,829,678 (GRCm38) |
missense |
probably damaging |
1.00 |
R8905:Celsr3
|
UTSW |
9 |
108,841,302 (GRCm38) |
missense |
probably damaging |
1.00 |
R9008:Celsr3
|
UTSW |
9 |
108,828,952 (GRCm38) |
missense |
possibly damaging |
0.94 |
R9072:Celsr3
|
UTSW |
9 |
108,827,094 (GRCm38) |
missense |
probably benign |
|
R9157:Celsr3
|
UTSW |
9 |
108,829,986 (GRCm38) |
missense |
probably damaging |
1.00 |
R9183:Celsr3
|
UTSW |
9 |
108,829,396 (GRCm38) |
missense |
probably damaging |
1.00 |
R9275:Celsr3
|
UTSW |
9 |
108,838,490 (GRCm38) |
missense |
probably benign |
0.27 |
R9361:Celsr3
|
UTSW |
9 |
108,849,322 (GRCm38) |
missense |
probably damaging |
1.00 |
R9382:Celsr3
|
UTSW |
9 |
108,829,762 (GRCm38) |
missense |
possibly damaging |
0.60 |
R9407:Celsr3
|
UTSW |
9 |
108,846,397 (GRCm38) |
missense |
probably damaging |
1.00 |
R9432:Celsr3
|
UTSW |
9 |
108,848,833 (GRCm38) |
missense |
probably benign |
0.00 |
R9607:Celsr3
|
UTSW |
9 |
108,840,502 (GRCm38) |
critical splice donor site |
probably null |
|
R9626:Celsr3
|
UTSW |
9 |
108,849,322 (GRCm38) |
missense |
probably damaging |
1.00 |
R9628:Celsr3
|
UTSW |
9 |
108,826,360 (GRCm38) |
nonsense |
probably null |
|
R9630:Celsr3
|
UTSW |
9 |
108,827,097 (GRCm38) |
missense |
probably benign |
|
R9645:Celsr3
|
UTSW |
9 |
108,827,492 (GRCm38) |
nonsense |
probably null |
|
R9683:Celsr3
|
UTSW |
9 |
108,827,323 (GRCm38) |
missense |
probably damaging |
1.00 |
R9794:Celsr3
|
UTSW |
9 |
108,851,303 (GRCm38) |
missense |
probably benign |
0.00 |
R9798:Celsr3
|
UTSW |
9 |
108,828,595 (GRCm38) |
missense |
probably damaging |
1.00 |
X0018:Celsr3
|
UTSW |
9 |
108,840,412 (GRCm38) |
missense |
probably benign |
0.01 |
X0018:Celsr3
|
UTSW |
9 |
108,827,778 (GRCm38) |
missense |
possibly damaging |
0.65 |
X0026:Celsr3
|
UTSW |
9 |
108,828,930 (GRCm38) |
missense |
probably damaging |
0.99 |
Z1177:Celsr3
|
UTSW |
9 |
108,826,477 (GRCm38) |
missense |
probably benign |
0.34 |
|