Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts7 |
T |
C |
9: 90,074,489 (GRCm39) |
S884P |
probably benign |
Het |
Akap13 |
C |
A |
7: 75,236,028 (GRCm39) |
A201E |
probably benign |
Het |
Ces1f |
T |
G |
8: 93,983,124 (GRCm39) |
E540A |
probably benign |
Het |
Chid1 |
T |
A |
7: 141,108,415 (GRCm39) |
M137L |
probably benign |
Het |
Chsy3 |
A |
G |
18: 59,312,414 (GRCm39) |
T296A |
probably benign |
Het |
Clec4f |
A |
G |
6: 83,622,284 (GRCm39) |
V519A |
probably benign |
Het |
Clk4 |
T |
A |
11: 51,159,009 (GRCm39) |
F41I |
possibly damaging |
Het |
Ctsl |
T |
C |
13: 64,515,786 (GRCm39) |
Y95C |
probably damaging |
Het |
Cyp2c54 |
T |
C |
19: 40,036,005 (GRCm39) |
M302V |
probably benign |
Het |
Cyp2c65 |
C |
G |
19: 39,049,606 (GRCm39) |
L45V |
probably benign |
Het |
Cyp2j6 |
G |
C |
4: 96,424,323 (GRCm39) |
L145V |
probably damaging |
Het |
Daam1 |
C |
T |
12: 72,006,661 (GRCm39) |
Q693* |
probably null |
Het |
Dgcr8 |
A |
T |
16: 18,098,172 (GRCm39) |
D406E |
probably benign |
Het |
Dock2 |
G |
T |
11: 34,179,476 (GRCm39) |
P1760Q |
probably damaging |
Het |
Epb41l2 |
G |
A |
10: 25,383,715 (GRCm39) |
R940H |
probably damaging |
Het |
Erc2 |
A |
C |
14: 28,039,210 (GRCm39) |
D951A |
probably damaging |
Het |
Fbxw7 |
T |
C |
3: 84,723,078 (GRCm39) |
|
probably null |
Het |
Frem2 |
T |
A |
3: 53,555,390 (GRCm39) |
I1716F |
probably damaging |
Het |
Fus |
A |
G |
7: 127,576,465 (GRCm39) |
D295G |
probably damaging |
Het |
Gm5093 |
A |
G |
17: 46,750,568 (GRCm39) |
I153T |
probably benign |
Het |
Gnptab |
T |
C |
10: 88,265,342 (GRCm39) |
V318A |
possibly damaging |
Het |
Gpc2 |
T |
C |
5: 138,276,676 (GRCm39) |
D150G |
probably benign |
Het |
Gsc2 |
A |
G |
16: 17,731,483 (GRCm39) |
*215R |
probably null |
Het |
Hectd3 |
T |
C |
4: 116,857,476 (GRCm39) |
S552P |
probably damaging |
Het |
Katnal1 |
C |
A |
5: 148,841,407 (GRCm39) |
K152N |
possibly damaging |
Het |
Kcnh1 |
A |
T |
1: 191,873,361 (GRCm39) |
T16S |
probably damaging |
Het |
Lrrc71 |
T |
C |
3: 87,653,101 (GRCm39) |
D105G |
probably benign |
Het |
Mon2 |
T |
C |
10: 122,874,564 (GRCm39) |
|
probably null |
Het |
Mroh9 |
G |
A |
1: 162,893,612 (GRCm39) |
Q188* |
probably null |
Het |
Mtmr14 |
A |
G |
6: 113,246,469 (GRCm39) |
S81G |
possibly damaging |
Het |
Nrap |
T |
A |
19: 56,350,130 (GRCm39) |
M628L |
probably benign |
Het |
Odad3 |
A |
G |
9: 21,901,698 (GRCm39) |
F553S |
probably damaging |
Het |
Or1o1 |
T |
A |
17: 37,716,883 (GRCm39) |
I148K |
possibly damaging |
Het |
Or5k1 |
A |
G |
16: 58,617,655 (GRCm39) |
Y185H |
probably damaging |
Het |
Pals2 |
A |
G |
6: 50,175,206 (GRCm39) |
I506V |
probably benign |
Het |
Pate4 |
A |
T |
9: 35,519,586 (GRCm39) |
S35T |
possibly damaging |
Het |
Pkd1l1 |
T |
C |
11: 8,815,555 (GRCm39) |
E1452G |
probably benign |
Het |
Pld5 |
T |
C |
1: 175,872,420 (GRCm39) |
D239G |
probably benign |
Het |
Ppef2 |
C |
T |
5: 92,374,925 (GRCm39) |
V728M |
probably damaging |
Het |
Rasip1 |
TGCCGCCGCCGCCGCCGCCGCCGC |
TGCCGCCGCCGCCGCCGCCGC |
7: 45,277,879 (GRCm39) |
|
probably benign |
Het |
Rsf1 |
G |
A |
7: 97,229,117 (GRCm39) |
|
probably benign |
Het |
Serpina3c |
C |
A |
12: 104,115,690 (GRCm39) |
V285L |
probably benign |
Het |
Serpinb9f |
T |
C |
13: 33,518,405 (GRCm39) |
S302P |
probably damaging |
Het |
Sis |
C |
T |
3: 72,811,626 (GRCm39) |
V1642I |
probably benign |
Het |
Slc12a4 |
G |
A |
8: 106,674,531 (GRCm39) |
L601F |
probably damaging |
Het |
Slc39a6 |
G |
T |
18: 24,734,013 (GRCm39) |
N225K |
probably benign |
Het |
Snrnp70 |
G |
A |
7: 45,026,497 (GRCm39) |
R291* |
probably null |
Het |
Spin1 |
C |
T |
13: 51,298,374 (GRCm39) |
T131I |
probably benign |
Het |
St18 |
T |
G |
1: 6,914,342 (GRCm39) |
|
probably null |
Het |
Stox1 |
A |
G |
10: 62,500,721 (GRCm39) |
L613P |
probably damaging |
Het |
Tgm3 |
T |
G |
2: 129,867,221 (GRCm39) |
Y155* |
probably null |
Het |
Tmem67 |
T |
C |
4: 12,051,402 (GRCm39) |
I809V |
probably benign |
Het |
Tnc |
T |
A |
4: 63,927,033 (GRCm39) |
D831V |
probably damaging |
Het |
Ttll13 |
A |
T |
7: 79,909,981 (GRCm39) |
E762D |
probably benign |
Het |
Unc5b |
A |
T |
10: 60,601,015 (GRCm39) |
V937E |
probably damaging |
Het |
Vmn1r34 |
A |
G |
6: 66,614,312 (GRCm39) |
I142T |
probably damaging |
Het |
Vmn2r104 |
A |
G |
17: 20,250,507 (GRCm39) |
M588T |
probably benign |
Het |
Vmn2r77 |
T |
C |
7: 86,460,957 (GRCm39) |
V761A |
probably damaging |
Het |
Wdr48 |
G |
T |
9: 119,753,832 (GRCm39) |
G665W |
probably damaging |
Het |
Xpot |
T |
A |
10: 121,442,163 (GRCm39) |
R550S |
probably damaging |
Het |
Ydjc |
A |
G |
16: 16,964,943 (GRCm39) |
T33A |
probably benign |
Het |
Zfc3h1 |
A |
G |
10: 115,226,764 (GRCm39) |
T274A |
probably benign |
Het |
Zfp202 |
G |
A |
9: 40,118,638 (GRCm39) |
G17E |
probably damaging |
Het |
Zfp788 |
T |
A |
7: 41,299,940 (GRCm39) |
C859S |
probably damaging |
Het |
Zscan4c |
T |
C |
7: 10,740,709 (GRCm39) |
M76T |
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 |
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 |
R8451: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 |
|