Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700123K08Rik |
G |
A |
5: 138,561,188 (GRCm39) |
T158M |
probably benign |
Het |
Acss3 |
T |
C |
10: 106,885,265 (GRCm39) |
H242R |
probably damaging |
Het |
Ago2 |
G |
T |
15: 73,002,739 (GRCm39) |
D164E |
probably damaging |
Het |
Arl2bp |
G |
A |
8: 95,393,507 (GRCm39) |
E6K |
unknown |
Het |
Bola1 |
G |
A |
3: 96,104,573 (GRCm39) |
A7V |
probably benign |
Het |
Ccdc18 |
A |
G |
5: 108,303,663 (GRCm39) |
E249G |
probably damaging |
Het |
Cep162 |
G |
A |
9: 87,074,903 (GRCm39) |
Q1360* |
probably null |
Het |
Cep350 |
T |
C |
1: 155,747,780 (GRCm39) |
I2047V |
probably damaging |
Het |
Eif4a3l1 |
T |
A |
6: 136,305,542 (GRCm39) |
M1K |
probably null |
Het |
Fmo6 |
C |
T |
1: 162,748,174 (GRCm39) |
V297M |
probably damaging |
Het |
Furin |
C |
T |
7: 80,048,470 (GRCm39) |
V17M |
probably benign |
Het |
Hs6st1 |
A |
G |
1: 36,108,141 (GRCm39) |
T135A |
probably damaging |
Het |
Idh2 |
TCCCAGG |
T |
7: 79,748,079 (GRCm39) |
|
probably benign |
Het |
Klk1 |
A |
G |
7: 43,878,410 (GRCm39) |
E190G |
probably benign |
Het |
Map3k21 |
T |
C |
8: 126,671,472 (GRCm39) |
L920P |
probably benign |
Het |
Mecom |
T |
A |
3: 30,039,519 (GRCm39) |
H180L |
probably benign |
Het |
Mras |
T |
C |
9: 99,293,548 (GRCm39) |
I31V |
probably damaging |
Het |
Nrxn3 |
A |
G |
12: 89,477,413 (GRCm39) |
D532G |
probably damaging |
Het |
Nufip2 |
A |
G |
11: 77,583,181 (GRCm39) |
N365S |
probably damaging |
Het |
Or12j2 |
T |
C |
7: 139,916,518 (GRCm39) |
Y248H |
probably damaging |
Het |
Or4f47 |
A |
T |
2: 111,972,406 (GRCm39) |
M39L |
probably benign |
Het |
Or6b2 |
T |
C |
1: 92,407,660 (GRCm39) |
I228V |
probably benign |
Het |
Pgbd1 |
A |
T |
13: 21,607,550 (GRCm39) |
S215T |
probably benign |
Het |
Ptcd3 |
A |
G |
6: 71,885,625 (GRCm39) |
C34R |
probably benign |
Het |
S100a7l2 |
A |
T |
3: 90,995,671 (GRCm39) |
M77K |
probably benign |
Het |
Samd4 |
A |
G |
14: 47,338,888 (GRCm39) |
D703G |
probably damaging |
Het |
Scaper |
A |
T |
9: 55,724,088 (GRCm39) |
N623K |
possibly damaging |
Het |
Slc12a9 |
C |
A |
5: 137,313,737 (GRCm39) |
V741L |
probably benign |
Het |
Slc12a9 |
T |
C |
5: 137,326,710 (GRCm39) |
D249G |
probably benign |
Het |
Slc3a1 |
A |
G |
17: 85,335,924 (GRCm39) |
N22S |
possibly damaging |
Het |
Sugct |
A |
G |
13: 17,427,143 (GRCm39) |
L339P |
probably damaging |
Het |
Tenm3 |
T |
C |
8: 48,740,907 (GRCm39) |
D1192G |
probably damaging |
Het |
Tinagl1 |
T |
A |
4: 130,061,376 (GRCm39) |
D289V |
probably damaging |
Het |
Tnrc6b |
C |
A |
15: 80,807,691 (GRCm39) |
P1548T |
probably damaging |
Het |
Trmt1l |
A |
G |
1: 151,324,039 (GRCm39) |
K152E |
unknown |
Het |
Vmn1r173 |
T |
A |
7: 23,401,957 (GRCm39) |
L64* |
probably null |
Het |
Zcchc2 |
T |
A |
1: 105,958,662 (GRCm39) |
N1044K |
probably damaging |
Het |
Zfp750 |
T |
C |
11: 121,404,135 (GRCm39) |
I247V |
probably benign |
Het |
|
Other mutations in Cntnap5c |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00495:Cntnap5c
|
APN |
17 |
58,469,272 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00543:Cntnap5c
|
APN |
17 |
58,601,345 (GRCm39) |
missense |
probably benign |
|
IGL00679:Cntnap5c
|
APN |
17 |
58,362,673 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL00942:Cntnap5c
|
APN |
17 |
58,076,593 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01352:Cntnap5c
|
APN |
17 |
58,600,896 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01822:Cntnap5c
|
APN |
17 |
58,362,700 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01864:Cntnap5c
|
APN |
17 |
58,717,237 (GRCm39) |
missense |
probably benign |
|
IGL01922:Cntnap5c
|
APN |
17 |
58,637,114 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02111:Cntnap5c
|
APN |
17 |
58,409,103 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02112:Cntnap5c
|
APN |
17 |
58,620,853 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02259:Cntnap5c
|
APN |
17 |
58,341,857 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02270:Cntnap5c
|
APN |
17 |
58,341,848 (GRCm39) |
missense |
probably benign |
0.08 |
IGL02312:Cntnap5c
|
APN |
17 |
58,445,694 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02456:Cntnap5c
|
APN |
17 |
58,714,739 (GRCm39) |
splice site |
probably benign |
|
IGL02755:Cntnap5c
|
APN |
17 |
58,671,189 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02955:Cntnap5c
|
APN |
17 |
58,199,097 (GRCm39) |
splice site |
probably benign |
|
IGL03001:Cntnap5c
|
APN |
17 |
58,362,634 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03012:Cntnap5c
|
APN |
17 |
58,666,229 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03243:Cntnap5c
|
APN |
17 |
58,409,171 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03375:Cntnap5c
|
APN |
17 |
58,469,200 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02802:Cntnap5c
|
UTSW |
17 |
58,612,679 (GRCm39) |
missense |
probably benign |
0.04 |
LCD18:Cntnap5c
|
UTSW |
17 |
58,469,155 (GRCm39) |
intron |
probably benign |
|
R0003:Cntnap5c
|
UTSW |
17 |
58,506,012 (GRCm39) |
missense |
probably benign |
|
R0041:Cntnap5c
|
UTSW |
17 |
58,183,464 (GRCm39) |
missense |
probably benign |
0.00 |
R0041:Cntnap5c
|
UTSW |
17 |
58,183,464 (GRCm39) |
missense |
probably benign |
0.00 |
R0046:Cntnap5c
|
UTSW |
17 |
58,666,295 (GRCm39) |
missense |
probably benign |
|
R0046:Cntnap5c
|
UTSW |
17 |
58,666,295 (GRCm39) |
missense |
probably benign |
|
R0179:Cntnap5c
|
UTSW |
17 |
58,076,620 (GRCm39) |
missense |
probably benign |
0.19 |
R0244:Cntnap5c
|
UTSW |
17 |
58,409,163 (GRCm39) |
missense |
probably damaging |
1.00 |
R0445:Cntnap5c
|
UTSW |
17 |
58,411,738 (GRCm39) |
missense |
probably benign |
0.01 |
R0626:Cntnap5c
|
UTSW |
17 |
58,349,422 (GRCm39) |
missense |
probably benign |
0.29 |
R0675:Cntnap5c
|
UTSW |
17 |
58,341,990 (GRCm39) |
missense |
probably damaging |
1.00 |
R0681:Cntnap5c
|
UTSW |
17 |
58,612,550 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0699:Cntnap5c
|
UTSW |
17 |
58,349,493 (GRCm39) |
missense |
probably damaging |
1.00 |
R0927:Cntnap5c
|
UTSW |
17 |
58,349,553 (GRCm39) |
missense |
possibly damaging |
0.78 |
R1081:Cntnap5c
|
UTSW |
17 |
58,612,520 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1132:Cntnap5c
|
UTSW |
17 |
58,601,351 (GRCm39) |
missense |
probably damaging |
1.00 |
R1175:Cntnap5c
|
UTSW |
17 |
58,671,241 (GRCm39) |
missense |
possibly damaging |
0.51 |
R1640:Cntnap5c
|
UTSW |
17 |
58,702,289 (GRCm39) |
missense |
probably benign |
0.01 |
R1664:Cntnap5c
|
UTSW |
17 |
58,600,985 (GRCm39) |
missense |
probably benign |
0.00 |
R1758:Cntnap5c
|
UTSW |
17 |
58,349,545 (GRCm39) |
missense |
probably damaging |
1.00 |
R1785:Cntnap5c
|
UTSW |
17 |
58,469,286 (GRCm39) |
missense |
probably benign |
0.00 |
R1789:Cntnap5c
|
UTSW |
17 |
58,320,916 (GRCm39) |
missense |
probably damaging |
1.00 |
R1968:Cntnap5c
|
UTSW |
17 |
58,666,291 (GRCm39) |
missense |
probably damaging |
1.00 |
R2041:Cntnap5c
|
UTSW |
17 |
58,505,984 (GRCm39) |
missense |
probably benign |
0.02 |
R2041:Cntnap5c
|
UTSW |
17 |
58,411,765 (GRCm39) |
critical splice donor site |
probably null |
|
R2073:Cntnap5c
|
UTSW |
17 |
58,612,547 (GRCm39) |
missense |
possibly damaging |
0.58 |
R2093:Cntnap5c
|
UTSW |
17 |
58,505,995 (GRCm39) |
missense |
probably benign |
0.00 |
R2134:Cntnap5c
|
UTSW |
17 |
58,714,717 (GRCm39) |
missense |
probably damaging |
1.00 |
R2153:Cntnap5c
|
UTSW |
17 |
58,362,666 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2176:Cntnap5c
|
UTSW |
17 |
58,320,941 (GRCm39) |
missense |
probably benign |
0.04 |
R2256:Cntnap5c
|
UTSW |
17 |
58,637,310 (GRCm39) |
missense |
probably benign |
0.00 |
R2847:Cntnap5c
|
UTSW |
17 |
58,183,387 (GRCm39) |
missense |
probably damaging |
0.99 |
R2848:Cntnap5c
|
UTSW |
17 |
58,183,387 (GRCm39) |
missense |
probably damaging |
0.99 |
R2850:Cntnap5c
|
UTSW |
17 |
58,717,343 (GRCm39) |
utr 3 prime |
probably benign |
|
R3008:Cntnap5c
|
UTSW |
17 |
58,666,204 (GRCm39) |
missense |
probably damaging |
1.00 |
R3714:Cntnap5c
|
UTSW |
17 |
58,199,062 (GRCm39) |
nonsense |
probably null |
|
R3720:Cntnap5c
|
UTSW |
17 |
58,637,197 (GRCm39) |
missense |
probably benign |
|
R3755:Cntnap5c
|
UTSW |
17 |
58,411,594 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4001:Cntnap5c
|
UTSW |
17 |
58,714,735 (GRCm39) |
critical splice donor site |
probably null |
|
R4619:Cntnap5c
|
UTSW |
17 |
58,717,263 (GRCm39) |
missense |
probably benign |
|
R5146:Cntnap5c
|
UTSW |
17 |
58,320,842 (GRCm39) |
missense |
probably damaging |
0.96 |
R5309:Cntnap5c
|
UTSW |
17 |
58,666,249 (GRCm39) |
missense |
probably benign |
0.05 |
R5312:Cntnap5c
|
UTSW |
17 |
58,666,249 (GRCm39) |
missense |
probably benign |
0.05 |
R5722:Cntnap5c
|
UTSW |
17 |
58,620,852 (GRCm39) |
missense |
probably benign |
0.01 |
R5974:Cntnap5c
|
UTSW |
17 |
58,183,480 (GRCm39) |
missense |
probably benign |
0.00 |
R6017:Cntnap5c
|
UTSW |
17 |
58,411,693 (GRCm39) |
missense |
probably benign |
0.41 |
R6059:Cntnap5c
|
UTSW |
17 |
58,620,707 (GRCm39) |
missense |
probably damaging |
0.99 |
R6152:Cntnap5c
|
UTSW |
17 |
58,593,881 (GRCm39) |
missense |
possibly damaging |
0.65 |
R6182:Cntnap5c
|
UTSW |
17 |
58,183,390 (GRCm39) |
missense |
probably benign |
0.00 |
R6298:Cntnap5c
|
UTSW |
17 |
58,411,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R6301:Cntnap5c
|
UTSW |
17 |
58,199,032 (GRCm39) |
missense |
probably benign |
0.01 |
R6514:Cntnap5c
|
UTSW |
17 |
58,637,165 (GRCm39) |
missense |
probably damaging |
0.96 |
R6583:Cntnap5c
|
UTSW |
17 |
58,637,272 (GRCm39) |
missense |
probably damaging |
1.00 |
R6688:Cntnap5c
|
UTSW |
17 |
58,600,899 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6781:Cntnap5c
|
UTSW |
17 |
58,445,648 (GRCm39) |
nonsense |
probably null |
|
R6866:Cntnap5c
|
UTSW |
17 |
58,399,289 (GRCm39) |
missense |
probably benign |
|
R6906:Cntnap5c
|
UTSW |
17 |
58,702,302 (GRCm39) |
missense |
probably benign |
0.18 |
R6911:Cntnap5c
|
UTSW |
17 |
58,199,009 (GRCm39) |
missense |
probably damaging |
1.00 |
R6919:Cntnap5c
|
UTSW |
17 |
58,600,948 (GRCm39) |
missense |
probably benign |
0.02 |
R6923:Cntnap5c
|
UTSW |
17 |
58,399,345 (GRCm39) |
missense |
possibly damaging |
0.96 |
R6925:Cntnap5c
|
UTSW |
17 |
58,702,261 (GRCm39) |
missense |
probably benign |
0.39 |
R6982:Cntnap5c
|
UTSW |
17 |
58,399,247 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7144:Cntnap5c
|
UTSW |
17 |
58,593,883 (GRCm39) |
missense |
probably benign |
|
R7422:Cntnap5c
|
UTSW |
17 |
58,717,226 (GRCm39) |
nonsense |
probably null |
|
R7797:Cntnap5c
|
UTSW |
17 |
58,666,270 (GRCm39) |
missense |
probably benign |
0.11 |
R7830:Cntnap5c
|
UTSW |
17 |
58,469,245 (GRCm39) |
missense |
probably damaging |
1.00 |
R8169:Cntnap5c
|
UTSW |
17 |
58,411,765 (GRCm39) |
critical splice donor site |
probably null |
|
R8351:Cntnap5c
|
UTSW |
17 |
58,362,687 (GRCm39) |
missense |
probably damaging |
1.00 |
R8352:Cntnap5c
|
UTSW |
17 |
58,362,687 (GRCm39) |
missense |
probably damaging |
1.00 |
R8452:Cntnap5c
|
UTSW |
17 |
58,362,687 (GRCm39) |
missense |
probably damaging |
1.00 |
R8696:Cntnap5c
|
UTSW |
17 |
58,601,294 (GRCm39) |
missense |
probably damaging |
1.00 |
R8725:Cntnap5c
|
UTSW |
17 |
58,362,663 (GRCm39) |
missense |
probably damaging |
1.00 |
R8838:Cntnap5c
|
UTSW |
17 |
58,198,964 (GRCm39) |
missense |
|
|
R8901:Cntnap5c
|
UTSW |
17 |
58,637,156 (GRCm39) |
missense |
probably benign |
0.03 |
R8911:Cntnap5c
|
UTSW |
17 |
58,506,043 (GRCm39) |
missense |
probably damaging |
0.98 |
R9010:Cntnap5c
|
UTSW |
17 |
58,671,159 (GRCm39) |
missense |
probably benign |
0.00 |
R9065:Cntnap5c
|
UTSW |
17 |
58,445,642 (GRCm39) |
missense |
probably damaging |
1.00 |
R9082:Cntnap5c
|
UTSW |
17 |
58,637,335 (GRCm39) |
missense |
probably damaging |
0.98 |
R9122:Cntnap5c
|
UTSW |
17 |
58,411,601 (GRCm39) |
missense |
probably benign |
0.01 |
R9137:Cntnap5c
|
UTSW |
17 |
58,601,203 (GRCm39) |
splice site |
probably benign |
|
R9176:Cntnap5c
|
UTSW |
17 |
58,620,730 (GRCm39) |
missense |
probably damaging |
1.00 |
R9179:Cntnap5c
|
UTSW |
17 |
58,600,912 (GRCm39) |
missense |
probably benign |
0.14 |
R9352:Cntnap5c
|
UTSW |
17 |
58,399,463 (GRCm39) |
missense |
probably benign |
0.01 |
R9485:Cntnap5c
|
UTSW |
17 |
58,409,103 (GRCm39) |
missense |
probably damaging |
1.00 |
R9558:Cntnap5c
|
UTSW |
17 |
58,671,157 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9792:Cntnap5c
|
UTSW |
17 |
58,409,192 (GRCm39) |
missense |
probably benign |
0.03 |
R9793:Cntnap5c
|
UTSW |
17 |
58,409,192 (GRCm39) |
missense |
probably benign |
0.03 |
R9795:Cntnap5c
|
UTSW |
17 |
58,409,192 (GRCm39) |
missense |
probably benign |
0.03 |
RF010:Cntnap5c
|
UTSW |
17 |
58,593,790 (GRCm39) |
missense |
probably damaging |
1.00 |
|