Other mutations in this stock |
Total: 31 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2300003K06Rik |
A |
G |
11: 99,728,079 (GRCm39) |
S255P |
unknown |
Het |
Adamtsl2 |
T |
A |
2: 26,974,071 (GRCm39) |
Y125N |
probably damaging |
Het |
Ankrd9 |
T |
C |
12: 110,943,293 (GRCm39) |
E214G |
probably benign |
Het |
Bhmt2 |
T |
A |
13: 93,803,161 (GRCm39) |
D124V |
possibly damaging |
Het |
Ccdc150 |
A |
G |
1: 54,317,874 (GRCm39) |
H271R |
possibly damaging |
Het |
Clcn1 |
T |
G |
6: 42,276,925 (GRCm39) |
|
probably null |
Het |
Col6a3 |
T |
A |
1: 90,755,588 (GRCm39) |
I234F |
probably benign |
Het |
Cpa5 |
T |
A |
6: 30,630,436 (GRCm39) |
M330K |
probably damaging |
Het |
Csmd2 |
G |
A |
4: 128,278,062 (GRCm39) |
C995Y |
probably damaging |
Het |
D630003M21Rik |
T |
C |
2: 158,059,144 (GRCm39) |
E252G |
probably damaging |
Het |
Dhrs1 |
A |
T |
14: 55,978,748 (GRCm39) |
Y133* |
probably null |
Het |
Dnaaf10 |
G |
A |
11: 17,179,845 (GRCm39) |
G282E |
probably damaging |
Het |
Dock10 |
T |
C |
1: 80,518,075 (GRCm39) |
I1300V |
probably benign |
Het |
Efcab12 |
T |
C |
6: 115,787,952 (GRCm39) |
Y670C |
probably damaging |
Het |
Frg1 |
T |
G |
8: 41,864,321 (GRCm39) |
K66N |
probably benign |
Het |
Gbp2b |
C |
A |
3: 142,312,642 (GRCm39) |
H342N |
probably benign |
Het |
Gria4 |
T |
A |
9: 4,464,295 (GRCm39) |
I556F |
possibly damaging |
Het |
Map1b |
A |
G |
13: 99,578,203 (GRCm39) |
L150P |
probably damaging |
Het |
Map3k4 |
C |
T |
17: 12,457,045 (GRCm39) |
R1299Q |
probably benign |
Het |
Mapk10 |
T |
C |
5: 103,073,971 (GRCm39) |
N407D |
probably damaging |
Het |
Mcemp1 |
T |
A |
8: 3,717,390 (GRCm39) |
|
probably null |
Het |
Nav1 |
A |
C |
1: 135,397,762 (GRCm39) |
N802K |
possibly damaging |
Het |
Pcdhb2 |
T |
A |
18: 37,429,831 (GRCm39) |
N601K |
probably damaging |
Het |
Pi4ka |
T |
A |
16: 17,172,053 (GRCm39) |
H564L |
probably damaging |
Het |
Pnp |
T |
A |
14: 51,188,185 (GRCm39) |
|
probably benign |
Het |
Ppp2r2a |
G |
T |
14: 67,259,744 (GRCm39) |
N317K |
probably benign |
Het |
Pramel47 |
A |
G |
5: 95,489,177 (GRCm39) |
T207A |
possibly damaging |
Het |
Rars2 |
A |
T |
4: 34,650,243 (GRCm39) |
I343F |
possibly damaging |
Het |
Rnf213 |
T |
C |
11: 119,355,833 (GRCm39) |
F4092S |
probably damaging |
Het |
Tcp11 |
A |
G |
17: 28,289,444 (GRCm39) |
V209A |
possibly damaging |
Het |
Tet2 |
T |
C |
3: 133,187,124 (GRCm39) |
S1102G |
probably benign |
Het |
|
Other mutations in Kcnh1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00424:Kcnh1
|
APN |
1 |
192,101,190 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01675:Kcnh1
|
APN |
1 |
192,019,901 (GRCm39) |
missense |
probably benign |
0.09 |
IGL01726:Kcnh1
|
APN |
1 |
192,188,164 (GRCm39) |
missense |
possibly damaging |
0.47 |
IGL02006:Kcnh1
|
APN |
1 |
191,873,323 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL02428:Kcnh1
|
APN |
1 |
192,019,851 (GRCm39) |
nonsense |
probably null |
|
IGL02447:Kcnh1
|
APN |
1 |
191,907,224 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL02512:Kcnh1
|
APN |
1 |
192,187,689 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL02748:Kcnh1
|
APN |
1 |
191,903,728 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02879:Kcnh1
|
APN |
1 |
191,959,223 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02926:Kcnh1
|
APN |
1 |
191,959,208 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03058:Kcnh1
|
APN |
1 |
192,117,199 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03078:Kcnh1
|
APN |
1 |
192,117,108 (GRCm39) |
missense |
probably damaging |
1.00 |
3-1:Kcnh1
|
UTSW |
1 |
192,019,995 (GRCm39) |
nonsense |
probably null |
|
PIT4449001:Kcnh1
|
UTSW |
1 |
192,100,992 (GRCm39) |
missense |
probably damaging |
1.00 |
R0226:Kcnh1
|
UTSW |
1 |
191,959,113 (GRCm39) |
missense |
probably damaging |
1.00 |
R0226:Kcnh1
|
UTSW |
1 |
191,959,112 (GRCm39) |
nonsense |
probably null |
|
R0240:Kcnh1
|
UTSW |
1 |
192,187,648 (GRCm39) |
missense |
probably benign |
|
R0240:Kcnh1
|
UTSW |
1 |
192,187,648 (GRCm39) |
missense |
probably benign |
|
R0422:Kcnh1
|
UTSW |
1 |
192,019,888 (GRCm39) |
missense |
probably benign |
|
R0510:Kcnh1
|
UTSW |
1 |
192,101,249 (GRCm39) |
splice site |
probably benign |
|
R0612:Kcnh1
|
UTSW |
1 |
191,959,361 (GRCm39) |
missense |
probably damaging |
1.00 |
R0667:Kcnh1
|
UTSW |
1 |
192,188,346 (GRCm39) |
missense |
probably benign |
0.00 |
R0838:Kcnh1
|
UTSW |
1 |
192,095,514 (GRCm39) |
missense |
probably damaging |
0.99 |
R1303:Kcnh1
|
UTSW |
1 |
191,959,010 (GRCm39) |
missense |
probably damaging |
1.00 |
R1389:Kcnh1
|
UTSW |
1 |
192,188,071 (GRCm39) |
missense |
probably benign |
0.00 |
R1826:Kcnh1
|
UTSW |
1 |
192,095,376 (GRCm39) |
missense |
possibly damaging |
0.64 |
R1997:Kcnh1
|
UTSW |
1 |
191,959,243 (GRCm39) |
missense |
probably damaging |
0.99 |
R2254:Kcnh1
|
UTSW |
1 |
192,187,722 (GRCm39) |
splice site |
probably null |
|
R2274:Kcnh1
|
UTSW |
1 |
192,019,829 (GRCm39) |
missense |
probably damaging |
1.00 |
R2275:Kcnh1
|
UTSW |
1 |
192,019,829 (GRCm39) |
missense |
probably damaging |
1.00 |
R3029:Kcnh1
|
UTSW |
1 |
192,188,368 (GRCm39) |
missense |
probably benign |
0.00 |
R3427:Kcnh1
|
UTSW |
1 |
191,924,238 (GRCm39) |
missense |
probably benign |
0.06 |
R3552:Kcnh1
|
UTSW |
1 |
191,921,074 (GRCm39) |
missense |
probably damaging |
1.00 |
R3718:Kcnh1
|
UTSW |
1 |
191,921,107 (GRCm39) |
missense |
probably damaging |
1.00 |
R3760:Kcnh1
|
UTSW |
1 |
192,188,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R4009:Kcnh1
|
UTSW |
1 |
191,959,448 (GRCm39) |
missense |
probably benign |
|
R4027:Kcnh1
|
UTSW |
1 |
191,959,007 (GRCm39) |
missense |
probably benign |
0.05 |
R4453:Kcnh1
|
UTSW |
1 |
192,187,825 (GRCm39) |
missense |
probably damaging |
0.97 |
R4717:Kcnh1
|
UTSW |
1 |
191,959,025 (GRCm39) |
missense |
probably damaging |
0.99 |
R5014:Kcnh1
|
UTSW |
1 |
191,959,388 (GRCm39) |
missense |
probably damaging |
0.99 |
R5040:Kcnh1
|
UTSW |
1 |
192,187,783 (GRCm39) |
missense |
probably benign |
0.00 |
R5110:Kcnh1
|
UTSW |
1 |
192,020,055 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5190:Kcnh1
|
UTSW |
1 |
192,187,836 (GRCm39) |
missense |
probably benign |
0.00 |
R5244:Kcnh1
|
UTSW |
1 |
191,907,184 (GRCm39) |
missense |
probably benign |
0.23 |
R5383:Kcnh1
|
UTSW |
1 |
192,187,999 (GRCm39) |
missense |
probably benign |
0.03 |
R5926:Kcnh1
|
UTSW |
1 |
192,095,385 (GRCm39) |
missense |
probably benign |
0.01 |
R6182:Kcnh1
|
UTSW |
1 |
191,873,361 (GRCm39) |
missense |
probably damaging |
0.97 |
R6516:Kcnh1
|
UTSW |
1 |
192,101,089 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6567:Kcnh1
|
UTSW |
1 |
191,959,412 (GRCm39) |
missense |
probably benign |
|
R6655:Kcnh1
|
UTSW |
1 |
192,095,391 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6715:Kcnh1
|
UTSW |
1 |
192,019,949 (GRCm39) |
missense |
probably benign |
0.00 |
R6823:Kcnh1
|
UTSW |
1 |
192,187,597 (GRCm39) |
makesense |
probably null |
|
R6972:Kcnh1
|
UTSW |
1 |
191,959,144 (GRCm39) |
missense |
probably damaging |
1.00 |
R7199:Kcnh1
|
UTSW |
1 |
192,019,913 (GRCm39) |
missense |
probably benign |
0.01 |
R7219:Kcnh1
|
UTSW |
1 |
192,187,945 (GRCm39) |
missense |
probably benign |
|
R7749:Kcnh1
|
UTSW |
1 |
191,959,447 (GRCm39) |
missense |
probably benign |
|
R7799:Kcnh1
|
UTSW |
1 |
192,117,183 (GRCm39) |
missense |
probably damaging |
0.96 |
R7862:Kcnh1
|
UTSW |
1 |
191,873,167 (GRCm39) |
start gained |
probably benign |
|
R8068:Kcnh1
|
UTSW |
1 |
191,924,250 (GRCm39) |
missense |
probably benign |
0.00 |
R8375:Kcnh1
|
UTSW |
1 |
192,117,124 (GRCm39) |
missense |
probably damaging |
1.00 |
R8694:Kcnh1
|
UTSW |
1 |
191,921,031 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R8734:Kcnh1
|
UTSW |
1 |
192,188,320 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8809:Kcnh1
|
UTSW |
1 |
191,903,722 (GRCm39) |
missense |
probably damaging |
1.00 |
R9007:Kcnh1
|
UTSW |
1 |
192,188,055 (GRCm39) |
missense |
probably benign |
0.01 |
R9218:Kcnh1
|
UTSW |
1 |
192,135,938 (GRCm39) |
missense |
unknown |
|
R9431:Kcnh1
|
UTSW |
1 |
192,101,123 (GRCm39) |
missense |
probably benign |
0.23 |
R9465:Kcnh1
|
UTSW |
1 |
191,924,233 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1176:Kcnh1
|
UTSW |
1 |
192,101,045 (GRCm39) |
missense |
probably damaging |
1.00 |
|