Other mutations in this stock |
Total: 84 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
6430550D23Rik |
T |
C |
2: 156,003,230 (GRCm38) |
H113R |
possibly damaging |
Het |
Adgrf3 |
A |
T |
5: 30,197,533 (GRCm38) |
M499K |
probably benign |
Het |
Adgrv1 |
G |
A |
13: 81,106,931 (GRCm38) |
T211I |
probably damaging |
Het |
Adss2 |
C |
T |
1: 177,776,829 (GRCm38) |
E153K |
probably benign |
Het |
Ago4 |
C |
A |
4: 126,511,487 (GRCm38) |
G431V |
possibly damaging |
Het |
Araf |
G |
T |
X: 20,860,100 (GRCm38) |
R601L |
probably damaging |
Homo |
Atp2b4 |
T |
A |
1: 133,726,561 (GRCm38) |
I769F |
probably damaging |
Het |
Atp9a |
T |
C |
2: 168,689,352 (GRCm38) |
|
probably null |
Het |
Bltp1 |
T |
C |
3: 36,956,999 (GRCm38) |
V1782A |
probably benign |
Het |
Brap |
C |
A |
5: 121,665,309 (GRCm38) |
D173E |
probably benign |
Het |
Brca2 |
G |
T |
5: 150,566,978 (GRCm38) |
R3035L |
probably benign |
Het |
Ccdc8 |
C |
A |
7: 16,996,251 (GRCm38) |
P555Q |
probably benign |
Het |
Ccser2 |
A |
G |
14: 36,940,718 (GRCm38) |
S170P |
probably benign |
Het |
Cenpc1 |
C |
A |
5: 86,046,385 (GRCm38) |
R174M |
probably damaging |
Het |
Cfap57 |
T |
G |
4: 118,579,410 (GRCm38) |
I930L |
probably damaging |
Het |
Cx3cr1 |
C |
T |
9: 120,051,694 (GRCm38) |
R214H |
probably damaging |
Het |
Cyp4f14 |
T |
A |
17: 32,906,317 (GRCm38) |
H429L |
probably benign |
Het |
D5Ertd579e |
A |
G |
5: 36,615,276 (GRCm38) |
F592L |
probably damaging |
Het |
Ddb1 |
A |
G |
19: 10,625,923 (GRCm38) |
E865G |
probably damaging |
Het |
Ddx50 |
A |
T |
10: 62,621,566 (GRCm38) |
|
probably null |
Het |
Dpp6 |
A |
G |
5: 27,049,628 (GRCm38) |
T14A |
probably damaging |
Het |
Echs1 |
C |
A |
7: 140,113,069 (GRCm38) |
Q51H |
possibly damaging |
Het |
Ecm2 |
A |
T |
13: 49,530,307 (GRCm38) |
D587V |
probably damaging |
Het |
Ect2l |
A |
T |
10: 18,140,397 (GRCm38) |
Y666N |
possibly damaging |
Het |
Epha2 |
G |
A |
4: 141,316,912 (GRCm38) |
G342S |
probably benign |
Het |
Fbxo33 |
C |
A |
12: 59,206,079 (GRCm38) |
K211N |
probably benign |
Het |
Fchsd2 |
A |
G |
7: 101,259,776 (GRCm38) |
|
probably null |
Het |
Fen1 |
A |
G |
19: 10,200,687 (GRCm38) |
V131A |
probably damaging |
Het |
Fetub |
C |
T |
16: 22,932,331 (GRCm38) |
R143C |
probably damaging |
Het |
Flnb |
A |
G |
14: 7,892,092 (GRCm38) |
E587G |
probably damaging |
Het |
Foxd3 |
A |
G |
4: 99,657,240 (GRCm38) |
T206A |
possibly damaging |
Het |
Fut1 |
A |
G |
7: 45,619,306 (GRCm38) |
E228G |
possibly damaging |
Het |
Galnt13 |
T |
C |
2: 54,933,548 (GRCm38) |
F379L |
probably damaging |
Het |
Gcnt2 |
A |
C |
13: 40,861,241 (GRCm38) |
E296A |
probably damaging |
Het |
Gm7145 |
T |
A |
1: 117,986,140 (GRCm38) |
C251S |
probably damaging |
Het |
Gpam |
G |
A |
19: 55,070,985 (GRCm38) |
P810L |
probably damaging |
Het |
Il1rl2 |
T |
A |
1: 40,327,566 (GRCm38) |
L87M |
possibly damaging |
Het |
Itgae |
A |
G |
11: 73,145,601 (GRCm38) |
S1122G |
probably damaging |
Het |
Kcnh7 |
T |
A |
2: 63,182,226 (GRCm38) |
D46V |
probably damaging |
Het |
Kcnn3 |
T |
G |
3: 89,645,523 (GRCm38) |
Y511* |
probably null |
Het |
Kdm3b |
T |
A |
18: 34,793,005 (GRCm38) |
I66N |
probably damaging |
Het |
Klk1b27 |
A |
T |
7: 44,054,550 (GRCm38) |
H39L |
probably benign |
Het |
Kmo |
C |
T |
1: 175,659,695 (GRCm38) |
T404I |
possibly damaging |
Het |
Krt222 |
C |
T |
11: 99,235,058 (GRCm38) |
|
probably null |
Het |
Magi3 |
G |
C |
3: 104,015,697 (GRCm38) |
H1235D |
probably benign |
Het |
Mapk8ip1 |
C |
A |
2: 92,389,244 (GRCm38) |
G81C |
probably damaging |
Het |
Med15 |
G |
A |
16: 17,652,745 (GRCm38) |
Q583* |
probably null |
Het |
Mroh2a |
T |
C |
1: 88,256,754 (GRCm38) |
V1453A |
probably benign |
Het |
Myh13 |
A |
G |
11: 67,362,501 (GRCm38) |
M1488V |
probably benign |
Het |
Naip2 |
A |
T |
13: 100,152,137 (GRCm38) |
F1193L |
probably damaging |
Het |
Nop58 |
T |
A |
1: 59,702,855 (GRCm38) |
M181K |
probably damaging |
Het |
Npepps |
A |
T |
11: 97,213,790 (GRCm38) |
V796D |
probably damaging |
Het |
Nr1d1 |
A |
G |
11: 98,770,537 (GRCm38) |
F301S |
probably damaging |
Het |
Nynrin |
G |
A |
14: 55,868,028 (GRCm38) |
V832I |
probably damaging |
Het |
Or13a28 |
C |
A |
7: 140,638,433 (GRCm38) |
S244Y |
probably damaging |
Het |
Or1j14 |
T |
A |
2: 36,528,341 (GRCm38) |
C310S |
probably benign |
Het |
Or2ak7 |
A |
T |
11: 58,684,004 (GRCm38) |
T44S |
possibly damaging |
Het |
Or4e1 |
T |
A |
14: 52,463,895 (GRCm38) |
Y38F |
probably damaging |
Het |
Or8k1 |
T |
A |
2: 86,217,222 (GRCm38) |
T163S |
possibly damaging |
Het |
Phrf1 |
T |
A |
7: 141,237,673 (GRCm38) |
C132S |
probably damaging |
Het |
Plekhn1 |
T |
C |
4: 156,230,558 (GRCm38) |
|
probably null |
Het |
Polr2a |
G |
A |
11: 69,744,226 (GRCm38) |
T569M |
probably damaging |
Het |
Prr29 |
A |
G |
11: 106,376,632 (GRCm38) |
|
probably null |
Het |
Rsf1 |
CG |
CGACGGCGGAG |
7: 97,579,908 (GRCm38) |
|
probably benign |
Homo |
Sc5d |
T |
C |
9: 42,255,421 (GRCm38) |
E274G |
probably benign |
Het |
Serpina1d |
A |
T |
12: 103,764,828 (GRCm38) |
|
probably null |
Het |
Serpinb11 |
T |
A |
1: 107,372,242 (GRCm38) |
I106N |
probably damaging |
Het |
Setd2 |
G |
A |
9: 110,548,665 (GRCm38) |
R516K |
probably damaging |
Het |
Sirt2 |
G |
T |
7: 28,787,797 (GRCm38) |
C291F |
probably damaging |
Het |
Stac3 |
T |
C |
10: 127,508,175 (GRCm38) |
V314A |
probably damaging |
Het |
Stat6 |
C |
T |
10: 127,657,712 (GRCm38) |
|
probably null |
Het |
Strn3 |
A |
G |
12: 51,610,107 (GRCm38) |
V712A |
probably damaging |
Het |
Tmc5 |
G |
T |
7: 118,634,214 (GRCm38) |
G84C |
possibly damaging |
Het |
Tnik |
C |
A |
3: 28,650,179 (GRCm38) |
L996I |
probably damaging |
Het |
Trim30d |
G |
T |
7: 104,487,610 (GRCm38) |
T129K |
probably damaging |
Het |
Triml1 |
G |
T |
8: 43,138,756 (GRCm38) |
Y188* |
probably null |
Het |
Trpc7 |
A |
G |
13: 56,773,892 (GRCm38) |
Y760H |
probably damaging |
Het |
Uaca |
G |
A |
9: 60,870,044 (GRCm38) |
R571Q |
probably damaging |
Het |
Ubash3a |
A |
T |
17: 31,239,272 (GRCm38) |
Q575L |
possibly damaging |
Het |
Usp49 |
T |
A |
17: 47,672,902 (GRCm38) |
C61* |
probably null |
Het |
Vmn2r18 |
A |
T |
5: 151,584,651 (GRCm38) |
V336E |
probably damaging |
Het |
Vwa8 |
T |
C |
14: 79,086,662 (GRCm38) |
V1135A |
probably benign |
Het |
Zcchc4 |
T |
C |
5: 52,783,161 (GRCm38) |
V24A |
probably benign |
Het |
Zfp354c |
A |
G |
11: 50,814,971 (GRCm38) |
Y426H |
probably benign |
Het |
|
Other mutations in Celsr2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00898:Celsr2
|
APN |
3 |
108,413,879 (GRCm38) |
missense |
possibly damaging |
0.49 |
IGL01020:Celsr2
|
APN |
3 |
108,403,270 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL01420:Celsr2
|
APN |
3 |
108,393,763 (GRCm38) |
missense |
probably benign |
0.13 |
IGL01448:Celsr2
|
APN |
3 |
108,393,239 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL01559:Celsr2
|
APN |
3 |
108,406,867 (GRCm38) |
missense |
possibly damaging |
0.75 |
IGL01674:Celsr2
|
APN |
3 |
108,414,843 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01863:Celsr2
|
APN |
3 |
108,394,022 (GRCm38) |
missense |
probably benign |
0.00 |
IGL02309:Celsr2
|
APN |
3 |
108,396,011 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02325:Celsr2
|
APN |
3 |
108,412,871 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02409:Celsr2
|
APN |
3 |
108,413,955 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02514:Celsr2
|
APN |
3 |
108,397,510 (GRCm38) |
missense |
probably benign |
0.01 |
IGL02812:Celsr2
|
APN |
3 |
108,414,113 (GRCm38) |
missense |
probably benign |
0.25 |
IGL02894:Celsr2
|
APN |
3 |
108,395,210 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03281:Celsr2
|
APN |
3 |
108,412,940 (GRCm38) |
missense |
probably damaging |
1.00 |
barrow
|
UTSW |
3 |
108,394,965 (GRCm38) |
missense |
possibly damaging |
0.92 |
goldeneye
|
UTSW |
3 |
108,394,919 (GRCm38) |
missense |
probably damaging |
1.00 |
1mM(1):Celsr2
|
UTSW |
3 |
108,400,838 (GRCm38) |
missense |
probably benign |
0.01 |
ANU74:Celsr2
|
UTSW |
3 |
108,412,499 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02799:Celsr2
|
UTSW |
3 |
108,414,062 (GRCm38) |
missense |
probably damaging |
1.00 |
R0011:Celsr2
|
UTSW |
3 |
108,413,402 (GRCm38) |
missense |
probably benign |
0.19 |
R0031:Celsr2
|
UTSW |
3 |
108,413,063 (GRCm38) |
missense |
probably damaging |
1.00 |
R0049:Celsr2
|
UTSW |
3 |
108,397,254 (GRCm38) |
missense |
probably benign |
0.12 |
R0049:Celsr2
|
UTSW |
3 |
108,397,254 (GRCm38) |
missense |
probably benign |
0.12 |
R0090:Celsr2
|
UTSW |
3 |
108,393,327 (GRCm38) |
splice site |
probably benign |
|
R0140:Celsr2
|
UTSW |
3 |
108,397,933 (GRCm38) |
missense |
probably benign |
0.00 |
R0524:Celsr2
|
UTSW |
3 |
108,401,587 (GRCm38) |
missense |
probably damaging |
1.00 |
R0607:Celsr2
|
UTSW |
3 |
108,403,895 (GRCm38) |
critical splice donor site |
probably null |
|
R0662:Celsr2
|
UTSW |
3 |
108,398,520 (GRCm38) |
missense |
probably damaging |
0.99 |
R0690:Celsr2
|
UTSW |
3 |
108,414,977 (GRCm38) |
missense |
probably damaging |
1.00 |
R0691:Celsr2
|
UTSW |
3 |
108,412,623 (GRCm38) |
missense |
probably damaging |
1.00 |
R0710:Celsr2
|
UTSW |
3 |
108,412,712 (GRCm38) |
missense |
probably benign |
0.42 |
R0730:Celsr2
|
UTSW |
3 |
108,398,606 (GRCm38) |
missense |
probably damaging |
1.00 |
R0815:Celsr2
|
UTSW |
3 |
108,401,301 (GRCm38) |
missense |
possibly damaging |
0.56 |
R0848:Celsr2
|
UTSW |
3 |
108,414,338 (GRCm38) |
missense |
probably benign |
|
R0989:Celsr2
|
UTSW |
3 |
108,403,272 (GRCm38) |
missense |
probably benign |
0.00 |
R1185:Celsr2
|
UTSW |
3 |
108,399,709 (GRCm38) |
missense |
possibly damaging |
0.95 |
R1185:Celsr2
|
UTSW |
3 |
108,399,709 (GRCm38) |
missense |
possibly damaging |
0.95 |
R1185:Celsr2
|
UTSW |
3 |
108,399,709 (GRCm38) |
missense |
possibly damaging |
0.95 |
R1469:Celsr2
|
UTSW |
3 |
108,414,108 (GRCm38) |
missense |
probably damaging |
1.00 |
R1469:Celsr2
|
UTSW |
3 |
108,414,108 (GRCm38) |
missense |
probably damaging |
1.00 |
R1474:Celsr2
|
UTSW |
3 |
108,393,739 (GRCm38) |
missense |
possibly damaging |
0.91 |
R1608:Celsr2
|
UTSW |
3 |
108,402,483 (GRCm38) |
missense |
probably damaging |
1.00 |
R1653:Celsr2
|
UTSW |
3 |
108,413,520 (GRCm38) |
missense |
possibly damaging |
0.52 |
R1659:Celsr2
|
UTSW |
3 |
108,414,095 (GRCm38) |
missense |
probably benign |
|
R1689:Celsr2
|
UTSW |
3 |
108,407,304 (GRCm38) |
missense |
possibly damaging |
0.63 |
R1848:Celsr2
|
UTSW |
3 |
108,401,310 (GRCm38) |
missense |
probably benign |
0.35 |
R1859:Celsr2
|
UTSW |
3 |
108,396,630 (GRCm38) |
missense |
probably damaging |
1.00 |
R1918:Celsr2
|
UTSW |
3 |
108,398,650 (GRCm38) |
missense |
probably benign |
0.05 |
R1974:Celsr2
|
UTSW |
3 |
108,414,214 (GRCm38) |
missense |
probably damaging |
1.00 |
R2042:Celsr2
|
UTSW |
3 |
108,402,495 (GRCm38) |
missense |
probably damaging |
0.98 |
R2167:Celsr2
|
UTSW |
3 |
108,413,193 (GRCm38) |
missense |
probably damaging |
0.96 |
R2333:Celsr2
|
UTSW |
3 |
108,398,605 (GRCm38) |
missense |
probably benign |
0.16 |
R2434:Celsr2
|
UTSW |
3 |
108,404,479 (GRCm38) |
missense |
probably damaging |
1.00 |
R2504:Celsr2
|
UTSW |
3 |
108,413,591 (GRCm38) |
missense |
probably benign |
0.11 |
R3420:Celsr2
|
UTSW |
3 |
108,414,416 (GRCm38) |
missense |
probably benign |
0.03 |
R3712:Celsr2
|
UTSW |
3 |
108,400,839 (GRCm38) |
missense |
probably benign |
|
R3723:Celsr2
|
UTSW |
3 |
108,397,415 (GRCm38) |
splice site |
probably benign |
|
R3809:Celsr2
|
UTSW |
3 |
108,403,239 (GRCm38) |
missense |
possibly damaging |
0.67 |
R4018:Celsr2
|
UTSW |
3 |
108,394,965 (GRCm38) |
missense |
possibly damaging |
0.92 |
R4126:Celsr2
|
UTSW |
3 |
108,402,097 (GRCm38) |
missense |
possibly damaging |
0.71 |
R4177:Celsr2
|
UTSW |
3 |
108,413,978 (GRCm38) |
missense |
probably damaging |
0.96 |
R4232:Celsr2
|
UTSW |
3 |
108,413,772 (GRCm38) |
missense |
probably benign |
0.02 |
R4293:Celsr2
|
UTSW |
3 |
108,393,677 (GRCm38) |
missense |
probably benign |
0.01 |
R4458:Celsr2
|
UTSW |
3 |
108,394,997 (GRCm38) |
missense |
probably damaging |
0.98 |
R4621:Celsr2
|
UTSW |
3 |
108,395,216 (GRCm38) |
missense |
possibly damaging |
0.86 |
R4645:Celsr2
|
UTSW |
3 |
108,395,969 (GRCm38) |
missense |
probably damaging |
1.00 |
R4700:Celsr2
|
UTSW |
3 |
108,397,231 (GRCm38) |
missense |
probably benign |
0.24 |
R4732:Celsr2
|
UTSW |
3 |
108,398,952 (GRCm38) |
missense |
probably damaging |
0.99 |
R4733:Celsr2
|
UTSW |
3 |
108,398,952 (GRCm38) |
missense |
probably damaging |
0.99 |
R4901:Celsr2
|
UTSW |
3 |
108,406,987 (GRCm38) |
missense |
possibly damaging |
0.81 |
R4932:Celsr2
|
UTSW |
3 |
108,402,758 (GRCm38) |
missense |
probably damaging |
1.00 |
R4989:Celsr2
|
UTSW |
3 |
108,412,629 (GRCm38) |
missense |
possibly damaging |
0.62 |
R5052:Celsr2
|
UTSW |
3 |
108,412,358 (GRCm38) |
missense |
probably damaging |
1.00 |
R5093:Celsr2
|
UTSW |
3 |
108,413,373 (GRCm38) |
missense |
possibly damaging |
0.66 |
R5114:Celsr2
|
UTSW |
3 |
108,393,996 (GRCm38) |
missense |
probably benign |
0.05 |
R5120:Celsr2
|
UTSW |
3 |
108,393,120 (GRCm38) |
missense |
probably benign |
0.02 |
R5135:Celsr2
|
UTSW |
3 |
108,398,659 (GRCm38) |
missense |
probably damaging |
1.00 |
R5247:Celsr2
|
UTSW |
3 |
108,397,630 (GRCm38) |
missense |
probably benign |
0.34 |
R5381:Celsr2
|
UTSW |
3 |
108,402,757 (GRCm38) |
missense |
probably damaging |
1.00 |
R5412:Celsr2
|
UTSW |
3 |
108,399,995 (GRCm38) |
missense |
probably damaging |
1.00 |
R5445:Celsr2
|
UTSW |
3 |
108,392,658 (GRCm38) |
missense |
probably benign |
0.01 |
R5528:Celsr2
|
UTSW |
3 |
108,413,294 (GRCm38) |
missense |
probably damaging |
1.00 |
R5598:Celsr2
|
UTSW |
3 |
108,402,803 (GRCm38) |
missense |
possibly damaging |
0.82 |
R5652:Celsr2
|
UTSW |
3 |
108,396,735 (GRCm38) |
missense |
probably null |
0.49 |
R5697:Celsr2
|
UTSW |
3 |
108,403,921 (GRCm38) |
nonsense |
probably null |
|
R5718:Celsr2
|
UTSW |
3 |
108,393,358 (GRCm38) |
missense |
probably benign |
|
R5869:Celsr2
|
UTSW |
3 |
108,413,909 (GRCm38) |
missense |
probably damaging |
1.00 |
R5876:Celsr2
|
UTSW |
3 |
108,413,943 (GRCm38) |
missense |
probably damaging |
0.96 |
R6021:Celsr2
|
UTSW |
3 |
108,401,245 (GRCm38) |
missense |
probably benign |
|
R6054:Celsr2
|
UTSW |
3 |
108,406,963 (GRCm38) |
missense |
possibly damaging |
0.95 |
R6313:Celsr2
|
UTSW |
3 |
108,401,214 (GRCm38) |
missense |
probably damaging |
0.99 |
R6322:Celsr2
|
UTSW |
3 |
108,412,574 (GRCm38) |
missense |
probably damaging |
1.00 |
R6555:Celsr2
|
UTSW |
3 |
108,394,919 (GRCm38) |
missense |
probably damaging |
1.00 |
R6682:Celsr2
|
UTSW |
3 |
108,400,501 (GRCm38) |
critical splice donor site |
probably null |
|
R7062:Celsr2
|
UTSW |
3 |
108,402,510 (GRCm38) |
missense |
possibly damaging |
0.95 |
R7110:Celsr2
|
UTSW |
3 |
108,397,865 (GRCm38) |
missense |
probably damaging |
1.00 |
R7139:Celsr2
|
UTSW |
3 |
108,415,359 (GRCm38) |
missense |
unknown |
|
R7326:Celsr2
|
UTSW |
3 |
108,394,995 (GRCm38) |
missense |
possibly damaging |
0.85 |
R7425:Celsr2
|
UTSW |
3 |
108,402,457 (GRCm38) |
missense |
probably damaging |
1.00 |
R7452:Celsr2
|
UTSW |
3 |
108,413,090 (GRCm38) |
missense |
possibly damaging |
0.95 |
R7461:Celsr2
|
UTSW |
3 |
108,395,640 (GRCm38) |
missense |
probably damaging |
1.00 |
R7502:Celsr2
|
UTSW |
3 |
108,398,902 (GRCm38) |
missense |
probably benign |
0.00 |
R7613:Celsr2
|
UTSW |
3 |
108,395,640 (GRCm38) |
missense |
probably damaging |
1.00 |
R7644:Celsr2
|
UTSW |
3 |
108,413,490 (GRCm38) |
missense |
probably damaging |
0.99 |
R7666:Celsr2
|
UTSW |
3 |
108,398,588 (GRCm38) |
missense |
probably benign |
|
R7687:Celsr2
|
UTSW |
3 |
108,397,769 (GRCm38) |
missense |
probably benign |
0.27 |
R7695:Celsr2
|
UTSW |
3 |
108,402,753 (GRCm38) |
missense |
probably damaging |
1.00 |
R8002:Celsr2
|
UTSW |
3 |
108,403,969 (GRCm38) |
missense |
probably damaging |
1.00 |
R8052:Celsr2
|
UTSW |
3 |
108,412,655 (GRCm38) |
missense |
probably damaging |
1.00 |
R8283:Celsr2
|
UTSW |
3 |
108,396,455 (GRCm38) |
missense |
probably damaging |
1.00 |
R8356:Celsr2
|
UTSW |
3 |
108,413,531 (GRCm38) |
missense |
possibly damaging |
0.90 |
R8381:Celsr2
|
UTSW |
3 |
108,395,636 (GRCm38) |
missense |
probably damaging |
1.00 |
R8427:Celsr2
|
UTSW |
3 |
108,392,633 (GRCm38) |
makesense |
probably null |
|
R8435:Celsr2
|
UTSW |
3 |
108,414,399 (GRCm38) |
missense |
probably benign |
|
R8438:Celsr2
|
UTSW |
3 |
108,393,823 (GRCm38) |
missense |
probably damaging |
1.00 |
R8458:Celsr2
|
UTSW |
3 |
108,398,902 (GRCm38) |
missense |
probably benign |
0.00 |
R8460:Celsr2
|
UTSW |
3 |
108,396,777 (GRCm38) |
missense |
possibly damaging |
0.84 |
R8462:Celsr2
|
UTSW |
3 |
108,412,851 (GRCm38) |
nonsense |
probably null |
|
R8479:Celsr2
|
UTSW |
3 |
108,398,902 (GRCm38) |
missense |
probably benign |
0.00 |
R8480:Celsr2
|
UTSW |
3 |
108,398,902 (GRCm38) |
missense |
probably benign |
0.00 |
R8512:Celsr2
|
UTSW |
3 |
108,413,838 (GRCm38) |
missense |
probably damaging |
1.00 |
R8694:Celsr2
|
UTSW |
3 |
108,406,860 (GRCm38) |
missense |
probably damaging |
1.00 |
R8772:Celsr2
|
UTSW |
3 |
108,397,073 (GRCm38) |
missense |
possibly damaging |
0.84 |
R8843:Celsr2
|
UTSW |
3 |
108,396,127 (GRCm38) |
splice site |
probably benign |
|
R8888:Celsr2
|
UTSW |
3 |
108,413,564 (GRCm38) |
missense |
possibly damaging |
0.95 |
R8895:Celsr2
|
UTSW |
3 |
108,413,564 (GRCm38) |
missense |
possibly damaging |
0.95 |
R8917:Celsr2
|
UTSW |
3 |
108,396,566 (GRCm38) |
missense |
probably benign |
0.00 |
R9119:Celsr2
|
UTSW |
3 |
108,401,972 (GRCm38) |
missense |
possibly damaging |
0.90 |
R9169:Celsr2
|
UTSW |
3 |
108,402,546 (GRCm38) |
missense |
probably benign |
0.04 |
R9209:Celsr2
|
UTSW |
3 |
108,414,033 (GRCm38) |
missense |
probably benign |
0.02 |
R9342:Celsr2
|
UTSW |
3 |
108,413,126 (GRCm38) |
missense |
probably damaging |
1.00 |
R9416:Celsr2
|
UTSW |
3 |
108,414,768 (GRCm38) |
missense |
probably damaging |
0.96 |
R9493:Celsr2
|
UTSW |
3 |
108,393,758 (GRCm38) |
missense |
probably damaging |
1.00 |
R9564:Celsr2
|
UTSW |
3 |
108,414,518 (GRCm38) |
missense |
probably damaging |
1.00 |
R9598:Celsr2
|
UTSW |
3 |
108,415,262 (GRCm38) |
missense |
possibly damaging |
0.72 |
R9629:Celsr2
|
UTSW |
3 |
108,401,599 (GRCm38) |
missense |
probably damaging |
1.00 |
R9691:Celsr2
|
UTSW |
3 |
108,394,235 (GRCm38) |
missense |
probably damaging |
1.00 |
X0020:Celsr2
|
UTSW |
3 |
108,396,110 (GRCm38) |
missense |
probably damaging |
1.00 |
X0050:Celsr2
|
UTSW |
3 |
108,401,272 (GRCm38) |
missense |
probably benign |
0.09 |
Z1088:Celsr2
|
UTSW |
3 |
108,414,117 (GRCm38) |
missense |
probably damaging |
1.00 |
Z1176:Celsr2
|
UTSW |
3 |
108,412,341 (GRCm38) |
missense |
probably benign |
0.07 |
Z1176:Celsr2
|
UTSW |
3 |
108,393,131 (GRCm38) |
missense |
probably benign |
0.10 |
Z1177:Celsr2
|
UTSW |
3 |
108,413,571 (GRCm38) |
missense |
probably benign |
0.32 |
Z1177:Celsr2
|
UTSW |
3 |
108,412,220 (GRCm38) |
missense |
probably damaging |
1.00 |
Z1191:Celsr2
|
UTSW |
3 |
108,414,549 (GRCm38) |
missense |
possibly damaging |
0.68 |
|