Other mutations in this stock |
Total: 30 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acad12 |
T |
C |
5: 121,736,962 (GRCm39) |
T526A |
probably benign |
Het |
Acad12 |
T |
C |
5: 121,736,964 (GRCm39) |
Q525R |
probably benign |
Het |
Cnot3 |
T |
C |
7: 3,661,073 (GRCm39) |
V558A |
probably benign |
Het |
Col22a1 |
T |
C |
15: 71,878,998 (GRCm39) |
D53G |
probably damaging |
Het |
Cspp1 |
T |
A |
1: 10,137,072 (GRCm39) |
|
probably benign |
Het |
Cyp2d10 |
T |
A |
15: 82,289,462 (GRCm39) |
T217S |
probably benign |
Het |
Dcaf6 |
T |
C |
1: 165,239,036 (GRCm39) |
T229A |
probably damaging |
Het |
E4f1 |
A |
T |
17: 24,664,961 (GRCm39) |
S408T |
possibly damaging |
Het |
Eif1ad19 |
G |
A |
12: 87,740,314 (GRCm39) |
Q82* |
probably null |
Het |
Gpr149 |
A |
G |
3: 62,510,099 (GRCm39) |
F339L |
probably benign |
Het |
Hmbox1 |
A |
T |
14: 65,062,938 (GRCm39) |
C413S |
probably benign |
Het |
Kmo |
T |
C |
1: 175,487,273 (GRCm39) |
|
probably null |
Het |
Lin54 |
G |
A |
5: 100,594,419 (GRCm39) |
T582I |
possibly damaging |
Het |
Lrpprc |
T |
C |
17: 85,020,215 (GRCm39) |
I1157V |
probably benign |
Het |
Obscn |
A |
G |
11: 58,898,700 (GRCm39) |
|
probably benign |
Het |
Or14c40 |
T |
A |
7: 86,313,479 (GRCm39) |
L203H |
probably benign |
Het |
Or8k23 |
A |
T |
2: 86,186,318 (GRCm39) |
M136K |
probably damaging |
Het |
Pclo |
A |
G |
5: 14,825,422 (GRCm39) |
D4657G |
unknown |
Het |
Pgd |
T |
C |
4: 149,241,234 (GRCm39) |
K225R |
probably benign |
Het |
Poli |
A |
T |
18: 70,650,548 (GRCm39) |
H297Q |
probably benign |
Het |
Rufy4 |
T |
C |
1: 74,186,822 (GRCm39) |
C537R |
probably damaging |
Het |
Slc24a2 |
T |
C |
4: 86,909,715 (GRCm39) |
I668V |
possibly damaging |
Het |
Tdrd6 |
A |
G |
17: 43,939,645 (GRCm39) |
S468P |
probably damaging |
Het |
Trav6-4 |
A |
G |
14: 53,691,790 (GRCm39) |
T3A |
probably benign |
Het |
Trpc2 |
G |
T |
7: 101,745,205 (GRCm39) |
R807L |
probably damaging |
Het |
Ttc3 |
T |
A |
16: 94,267,736 (GRCm39) |
|
probably benign |
Het |
Tubgcp3 |
G |
T |
8: 12,713,932 (GRCm39) |
L62I |
probably damaging |
Het |
Ubqlnl |
C |
T |
7: 103,798,925 (GRCm39) |
V191M |
probably benign |
Het |
Vwce |
A |
C |
19: 10,641,710 (GRCm39) |
E812A |
probably benign |
Het |
Zmynd12 |
T |
C |
4: 119,280,194 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Cntnap4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00847:Cntnap4
|
APN |
8 |
113,494,251 (GRCm39) |
splice site |
probably benign |
|
IGL01898:Cntnap4
|
APN |
8 |
113,582,939 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL01918:Cntnap4
|
APN |
8 |
113,478,866 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL02257:Cntnap4
|
APN |
8 |
113,343,126 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02302:Cntnap4
|
APN |
8 |
113,512,535 (GRCm39) |
splice site |
probably benign |
|
IGL02621:Cntnap4
|
APN |
8 |
113,537,355 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03008:Cntnap4
|
APN |
8 |
113,500,222 (GRCm39) |
missense |
probably benign |
0.06 |
IGL03327:Cntnap4
|
APN |
8 |
113,500,208 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03346:Cntnap4
|
APN |
8 |
113,500,208 (GRCm39) |
missense |
probably benign |
0.00 |
R0025:Cntnap4
|
UTSW |
8 |
113,529,796 (GRCm39) |
missense |
probably damaging |
1.00 |
R0025:Cntnap4
|
UTSW |
8 |
113,529,796 (GRCm39) |
missense |
probably damaging |
1.00 |
R0058:Cntnap4
|
UTSW |
8 |
113,512,416 (GRCm39) |
missense |
probably damaging |
0.98 |
R0310:Cntnap4
|
UTSW |
8 |
113,569,148 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0363:Cntnap4
|
UTSW |
8 |
113,583,143 (GRCm39) |
nonsense |
probably null |
|
R0497:Cntnap4
|
UTSW |
8 |
113,296,783 (GRCm39) |
missense |
probably benign |
0.00 |
R1495:Cntnap4
|
UTSW |
8 |
113,608,395 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1579:Cntnap4
|
UTSW |
8 |
113,608,462 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1704:Cntnap4
|
UTSW |
8 |
113,484,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R1943:Cntnap4
|
UTSW |
8 |
113,542,128 (GRCm39) |
missense |
probably benign |
0.10 |
R2160:Cntnap4
|
UTSW |
8 |
113,484,203 (GRCm39) |
missense |
probably damaging |
1.00 |
R2226:Cntnap4
|
UTSW |
8 |
113,542,120 (GRCm39) |
missense |
probably damaging |
0.98 |
R3148:Cntnap4
|
UTSW |
8 |
113,484,071 (GRCm39) |
missense |
probably damaging |
1.00 |
R3916:Cntnap4
|
UTSW |
8 |
113,602,165 (GRCm39) |
missense |
probably benign |
0.02 |
R3917:Cntnap4
|
UTSW |
8 |
113,602,165 (GRCm39) |
missense |
probably benign |
0.02 |
R4097:Cntnap4
|
UTSW |
8 |
113,478,939 (GRCm39) |
missense |
probably benign |
0.03 |
R4348:Cntnap4
|
UTSW |
8 |
113,480,554 (GRCm39) |
missense |
probably damaging |
1.00 |
R4469:Cntnap4
|
UTSW |
8 |
113,391,898 (GRCm39) |
missense |
probably damaging |
1.00 |
R4530:Cntnap4
|
UTSW |
8 |
113,584,842 (GRCm39) |
missense |
probably benign |
0.32 |
R4586:Cntnap4
|
UTSW |
8 |
113,537,342 (GRCm39) |
missense |
probably benign |
|
R4611:Cntnap4
|
UTSW |
8 |
113,500,371 (GRCm39) |
critical splice donor site |
probably null |
|
R4675:Cntnap4
|
UTSW |
8 |
113,512,468 (GRCm39) |
missense |
probably damaging |
1.00 |
R4801:Cntnap4
|
UTSW |
8 |
113,500,222 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4802:Cntnap4
|
UTSW |
8 |
113,500,222 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5273:Cntnap4
|
UTSW |
8 |
113,460,070 (GRCm39) |
missense |
probably damaging |
1.00 |
R6114:Cntnap4
|
UTSW |
8 |
113,568,385 (GRCm39) |
missense |
probably damaging |
1.00 |
R6194:Cntnap4
|
UTSW |
8 |
113,602,061 (GRCm39) |
missense |
probably damaging |
1.00 |
R6222:Cntnap4
|
UTSW |
8 |
113,569,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R6262:Cntnap4
|
UTSW |
8 |
113,529,843 (GRCm39) |
missense |
probably damaging |
0.99 |
R6276:Cntnap4
|
UTSW |
8 |
113,478,921 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6483:Cntnap4
|
UTSW |
8 |
113,484,105 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6819:Cntnap4
|
UTSW |
8 |
113,529,858 (GRCm39) |
missense |
probably benign |
0.03 |
R7031:Cntnap4
|
UTSW |
8 |
113,584,874 (GRCm39) |
missense |
probably benign |
0.01 |
R7107:Cntnap4
|
UTSW |
8 |
113,542,120 (GRCm39) |
missense |
probably damaging |
0.98 |
R7146:Cntnap4
|
UTSW |
8 |
113,537,268 (GRCm39) |
missense |
probably damaging |
1.00 |
R7192:Cntnap4
|
UTSW |
8 |
113,608,432 (GRCm39) |
missense |
probably benign |
0.05 |
R7232:Cntnap4
|
UTSW |
8 |
113,391,731 (GRCm39) |
splice site |
probably null |
|
R7348:Cntnap4
|
UTSW |
8 |
113,391,909 (GRCm39) |
missense |
probably damaging |
1.00 |
R7482:Cntnap4
|
UTSW |
8 |
113,460,194 (GRCm39) |
critical splice donor site |
probably null |
|
R7832:Cntnap4
|
UTSW |
8 |
113,484,113 (GRCm39) |
missense |
probably benign |
|
R7895:Cntnap4
|
UTSW |
8 |
113,478,829 (GRCm39) |
missense |
probably damaging |
0.99 |
R8014:Cntnap4
|
UTSW |
8 |
113,480,577 (GRCm39) |
missense |
probably damaging |
0.99 |
R8185:Cntnap4
|
UTSW |
8 |
113,391,897 (GRCm39) |
missense |
probably damaging |
1.00 |
R8197:Cntnap4
|
UTSW |
8 |
113,296,857 (GRCm39) |
missense |
probably benign |
0.00 |
R8287:Cntnap4
|
UTSW |
8 |
113,585,775 (GRCm39) |
missense |
probably damaging |
1.00 |
R8299:Cntnap4
|
UTSW |
8 |
113,500,324 (GRCm39) |
missense |
probably damaging |
1.00 |
R8498:Cntnap4
|
UTSW |
8 |
113,602,211 (GRCm39) |
missense |
possibly damaging |
0.52 |
R8699:Cntnap4
|
UTSW |
8 |
113,484,228 (GRCm39) |
missense |
probably damaging |
1.00 |
R8774:Cntnap4
|
UTSW |
8 |
113,529,820 (GRCm39) |
missense |
probably benign |
0.01 |
R8774-TAIL:Cntnap4
|
UTSW |
8 |
113,529,820 (GRCm39) |
missense |
probably benign |
0.01 |
R8872:Cntnap4
|
UTSW |
8 |
113,585,759 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8895:Cntnap4
|
UTSW |
8 |
113,479,598 (GRCm39) |
missense |
probably benign |
0.40 |
R8965:Cntnap4
|
UTSW |
8 |
113,479,646 (GRCm39) |
missense |
probably damaging |
1.00 |
R9189:Cntnap4
|
UTSW |
8 |
113,602,600 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9260:Cntnap4
|
UTSW |
8 |
113,500,276 (GRCm39) |
missense |
probably benign |
0.08 |
R9474:Cntnap4
|
UTSW |
8 |
113,460,103 (GRCm39) |
missense |
probably damaging |
0.99 |
R9565:Cntnap4
|
UTSW |
8 |
113,582,982 (GRCm39) |
missense |
probably benign |
0.43 |
R9625:Cntnap4
|
UTSW |
8 |
113,602,181 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9629:Cntnap4
|
UTSW |
8 |
113,568,349 (GRCm39) |
missense |
probably damaging |
1.00 |
R9745:Cntnap4
|
UTSW |
8 |
113,391,808 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9765:Cntnap4
|
UTSW |
8 |
113,568,496 (GRCm39) |
missense |
probably damaging |
0.97 |
R9765:Cntnap4
|
UTSW |
8 |
113,484,110 (GRCm39) |
missense |
probably benign |
0.00 |
R9793:Cntnap4
|
UTSW |
8 |
113,608,357 (GRCm39) |
missense |
probably benign |
0.00 |
R9795:Cntnap4
|
UTSW |
8 |
113,608,357 (GRCm39) |
missense |
probably benign |
0.00 |
X0025:Cntnap4
|
UTSW |
8 |
113,585,775 (GRCm39) |
missense |
probably damaging |
1.00 |
X0063:Cntnap4
|
UTSW |
8 |
113,602,211 (GRCm39) |
missense |
probably benign |
0.05 |
Z1088:Cntnap4
|
UTSW |
8 |
113,542,152 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Cntnap4
|
UTSW |
8 |
113,584,821 (GRCm39) |
missense |
possibly damaging |
0.70 |
Z1186:Cntnap4
|
UTSW |
8 |
113,479,002 (GRCm39) |
missense |
probably damaging |
0.99 |
|