Other mutations in this stock |
Total: 95 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930522L14Rik |
A |
G |
5: 109,884,655 (GRCm39) |
V401A |
probably benign |
Het |
Abca7 |
G |
T |
10: 79,844,784 (GRCm39) |
W1502L |
probably damaging |
Het |
Adcy7 |
A |
G |
8: 89,035,468 (GRCm39) |
E124G |
probably benign |
Het |
Aif1l |
G |
A |
2: 31,855,118 (GRCm39) |
E66K |
probably benign |
Het |
Aldh8a1 |
A |
T |
10: 21,271,392 (GRCm39) |
M373L |
probably benign |
Het |
Alg6 |
T |
C |
4: 99,629,815 (GRCm39) |
Y131H |
probably benign |
Het |
Arhgef6 |
T |
C |
X: 56,383,922 (GRCm39) |
M5V |
probably benign |
Het |
Arrdc4 |
A |
T |
7: 68,391,622 (GRCm39) |
I215K |
probably damaging |
Het |
Asb4 |
A |
G |
6: 5,390,798 (GRCm39) |
|
probably null |
Het |
Astn1 |
T |
C |
1: 158,331,821 (GRCm39) |
I305T |
probably benign |
Het |
Atp5f1b |
T |
A |
10: 127,919,949 (GRCm39) |
|
probably benign |
Het |
Atp8a1 |
C |
A |
5: 67,788,910 (GRCm39) |
M1044I |
probably benign |
Het |
Atp9b |
C |
T |
18: 80,952,806 (GRCm39) |
|
probably null |
Het |
Brd10 |
T |
A |
19: 29,696,560 (GRCm39) |
T978S |
possibly damaging |
Het |
Btaf1 |
A |
G |
19: 36,928,518 (GRCm39) |
H113R |
probably benign |
Het |
C87436 |
G |
T |
6: 86,430,594 (GRCm39) |
C338F |
possibly damaging |
Het |
Casz1 |
T |
C |
4: 149,027,357 (GRCm39) |
|
probably benign |
Het |
Cbr3 |
T |
A |
16: 93,487,370 (GRCm39) |
H184Q |
probably damaging |
Het |
Cct8l1 |
T |
C |
5: 25,722,097 (GRCm39) |
S271P |
possibly damaging |
Het |
Cdc34 |
A |
G |
10: 79,521,174 (GRCm39) |
K77R |
probably benign |
Het |
Cdc34 |
G |
T |
10: 79,521,172 (GRCm39) |
|
probably null |
Het |
Cdh20 |
A |
G |
1: 104,862,070 (GRCm39) |
|
probably benign |
Het |
Cers1 |
T |
G |
8: 70,774,141 (GRCm39) |
|
probably null |
Het |
Cntn5 |
T |
C |
9: 9,673,988 (GRCm39) |
I705V |
probably benign |
Het |
Dennd4c |
T |
A |
4: 86,721,247 (GRCm39) |
D636E |
probably damaging |
Het |
Dnah11 |
T |
C |
12: 118,154,560 (GRCm39) |
E240G |
probably benign |
Het |
Dnah2 |
T |
C |
11: 69,314,369 (GRCm39) |
Y4100C |
probably damaging |
Het |
Dpysl3 |
T |
C |
18: 43,496,583 (GRCm39) |
E151G |
probably damaging |
Het |
Efcab9 |
T |
G |
11: 32,474,457 (GRCm39) |
T9P |
possibly damaging |
Het |
Eif4g2 |
A |
T |
7: 110,673,694 (GRCm39) |
F725Y |
probably damaging |
Het |
Epha6 |
T |
A |
16: 59,596,091 (GRCm39) |
I867F |
probably null |
Het |
Erbin |
T |
C |
13: 103,979,959 (GRCm39) |
|
probably benign |
Het |
Evi5l |
A |
G |
8: 4,253,560 (GRCm39) |
E468G |
probably damaging |
Het |
Filip1l |
C |
T |
16: 57,390,401 (GRCm39) |
R330W |
probably damaging |
Het |
Fmo3 |
C |
T |
1: 162,786,142 (GRCm39) |
V283M |
possibly damaging |
Het |
Gabarapl1 |
A |
T |
6: 129,510,481 (GRCm39) |
K24N |
possibly damaging |
Het |
Gigyf1 |
C |
T |
5: 137,520,770 (GRCm39) |
|
probably benign |
Het |
Gm5581 |
T |
A |
6: 131,158,362 (GRCm39) |
|
noncoding transcript |
Het |
Gon4l |
G |
T |
3: 88,799,906 (GRCm39) |
K850N |
probably damaging |
Het |
Igf2bp3 |
C |
T |
6: 49,085,980 (GRCm39) |
R233H |
probably damaging |
Het |
Iqcf4 |
G |
A |
9: 106,445,893 (GRCm39) |
R85C |
probably benign |
Het |
Kalrn |
C |
T |
16: 34,033,243 (GRCm39) |
R473Q |
probably damaging |
Het |
Lmod2 |
T |
A |
6: 24,603,376 (GRCm39) |
V117E |
probably damaging |
Het |
Mapk11 |
A |
G |
15: 89,028,594 (GRCm39) |
|
probably null |
Het |
Mcm3 |
G |
A |
1: 20,876,103 (GRCm39) |
R664C |
probably damaging |
Het |
Mex3d |
A |
G |
10: 80,222,770 (GRCm39) |
M162T |
probably benign |
Het |
Mrgprb3 |
A |
G |
7: 48,292,771 (GRCm39) |
I260T |
probably benign |
Het |
Ncor2 |
G |
T |
5: 125,105,679 (GRCm39) |
A1637D |
possibly damaging |
Het |
Nedd4 |
T |
A |
9: 72,638,189 (GRCm39) |
D441E |
probably damaging |
Het |
Nek5 |
A |
T |
8: 22,599,928 (GRCm39) |
C194S |
probably damaging |
Het |
Nos1ap |
T |
C |
1: 170,146,447 (GRCm39) |
D369G |
possibly damaging |
Het |
Ntrk1 |
G |
T |
3: 87,687,391 (GRCm39) |
T681K |
probably damaging |
Het |
Or13a24 |
T |
C |
7: 140,154,383 (GRCm39) |
W106R |
probably damaging |
Het |
Or4f14 |
A |
G |
2: 111,742,526 (GRCm39) |
F250L |
possibly damaging |
Het |
Otogl |
C |
T |
10: 107,735,322 (GRCm39) |
W154* |
probably null |
Het |
Pcdh20 |
T |
C |
14: 88,706,620 (GRCm39) |
T227A |
possibly damaging |
Het |
Pcdhb17 |
T |
C |
18: 37,620,324 (GRCm39) |
S705P |
probably damaging |
Het |
Piezo2 |
T |
C |
18: 63,257,713 (GRCm39) |
H335R |
possibly damaging |
Het |
Pkn2 |
T |
C |
3: 142,499,615 (GRCm39) |
Q954R |
probably damaging |
Het |
Pramel23 |
C |
A |
4: 143,424,840 (GRCm39) |
C201F |
probably benign |
Het |
Prkcq |
G |
A |
2: 11,237,442 (GRCm39) |
V74M |
probably damaging |
Het |
Prkrip1 |
A |
T |
5: 136,218,489 (GRCm39) |
|
probably null |
Het |
Pttg1ip2 |
A |
T |
5: 5,528,943 (GRCm39) |
I24N |
possibly damaging |
Het |
Rb1cc1 |
A |
G |
1: 6,284,904 (GRCm39) |
|
probably benign |
Het |
Rbm5 |
A |
T |
9: 107,644,763 (GRCm39) |
Y11* |
probably null |
Het |
Rsf1 |
CG |
CGACGGCGGTG |
7: 97,229,115 (GRCm39) |
|
probably benign |
Het |
Ryr3 |
C |
A |
2: 112,690,805 (GRCm39) |
V1082L |
probably damaging |
Het |
Scart2 |
A |
G |
7: 139,877,178 (GRCm39) |
E831G |
probably benign |
Het |
Sel1l3 |
C |
A |
5: 53,327,789 (GRCm39) |
E497* |
probably null |
Het |
Serpina6 |
A |
T |
12: 103,620,182 (GRCm39) |
I189N |
probably damaging |
Het |
Serpinb11 |
A |
T |
1: 107,304,532 (GRCm39) |
T166S |
probably benign |
Het |
Skint7 |
T |
C |
4: 111,839,270 (GRCm39) |
L188S |
probably benign |
Het |
Slc25a45 |
C |
T |
19: 5,934,958 (GRCm39) |
A269V |
probably damaging |
Het |
Sltm |
A |
G |
9: 70,469,082 (GRCm39) |
T114A |
probably benign |
Het |
Sned1 |
G |
A |
1: 93,209,376 (GRCm39) |
V830M |
possibly damaging |
Het |
Spen |
C |
A |
4: 141,200,261 (GRCm39) |
V2766L |
probably damaging |
Het |
Srgap2 |
T |
A |
1: 131,247,275 (GRCm39) |
I445F |
possibly damaging |
Het |
Stox2 |
A |
T |
8: 47,647,051 (GRCm39) |
Y200* |
probably null |
Het |
Strada |
C |
A |
11: 106,055,010 (GRCm39) |
R384L |
probably damaging |
Het |
Tctn2 |
G |
A |
5: 124,757,094 (GRCm39) |
|
noncoding transcript |
Het |
Tgfbr3l |
G |
T |
8: 4,299,282 (GRCm39) |
R461L |
probably benign |
Het |
Tmem65 |
A |
G |
15: 58,661,998 (GRCm39) |
|
probably benign |
Het |
Tpst1 |
G |
T |
5: 130,143,343 (GRCm39) |
V294F |
possibly damaging |
Het |
Trim23 |
A |
G |
13: 104,335,126 (GRCm39) |
Y384C |
probably damaging |
Het |
Ube3b |
C |
G |
5: 114,542,678 (GRCm39) |
L512V |
possibly damaging |
Het |
Ubxn4 |
T |
A |
1: 128,183,916 (GRCm39) |
V92E |
probably damaging |
Het |
Vmn2r57 |
A |
T |
7: 41,050,067 (GRCm39) |
C561S |
probably damaging |
Het |
Vwa8 |
A |
G |
14: 79,145,635 (GRCm39) |
D104G |
probably damaging |
Het |
Wdr25 |
T |
A |
12: 108,992,364 (GRCm39) |
L73* |
probably null |
Het |
Wnt9a |
G |
A |
11: 59,221,728 (GRCm39) |
A209T |
probably benign |
Het |
Zcchc17 |
A |
C |
4: 130,223,388 (GRCm39) |
C133G |
probably damaging |
Het |
Zdhhc18 |
T |
A |
4: 133,335,987 (GRCm39) |
M375L |
probably benign |
Het |
Zfhx3 |
T |
C |
8: 109,678,276 (GRCm39) |
F3109L |
probably benign |
Het |
Zfp202 |
T |
A |
9: 40,121,762 (GRCm39) |
D286E |
probably benign |
Het |
Zzef1 |
T |
C |
11: 72,784,158 (GRCm39) |
L2021P |
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 |
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 |
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 |
|