Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A330087D11Rik |
A |
T |
7: 29,273,303 (GRCm39) |
|
noncoding transcript |
Het |
Amfr |
A |
T |
8: 94,731,842 (GRCm39) |
N11K |
probably damaging |
Het |
Bpifa6 |
G |
A |
2: 153,831,194 (GRCm39) |
M253I |
probably benign |
Het |
C330018D20Rik |
A |
G |
18: 57,095,531 (GRCm39) |
L18P |
probably benign |
Het |
Cd109 |
CATTTATTTATTTATTTATTTATTTATTTATTTAT |
CATTTATTTATTTATTTATTTATTTATTTATTTATTTAT |
9: 78,619,782 (GRCm39) |
|
probably benign |
Het |
Cdh23 |
C |
T |
10: 60,218,432 (GRCm39) |
|
probably null |
Het |
Ceacam1 |
T |
A |
7: 25,173,442 (GRCm39) |
I249F |
probably damaging |
Het |
Cfap54 |
C |
T |
10: 92,881,144 (GRCm39) |
R348Q |
probably damaging |
Het |
Cfap91 |
A |
C |
16: 38,123,075 (GRCm39) |
L651R |
probably damaging |
Het |
Crygs |
C |
T |
16: 22,624,301 (GRCm39) |
G102D |
possibly damaging |
Het |
Cuzd1 |
C |
T |
7: 130,917,863 (GRCm39) |
V246M |
probably damaging |
Het |
Ehd2 |
A |
T |
7: 15,698,054 (GRCm39) |
V61E |
probably damaging |
Het |
Erich5 |
C |
T |
15: 34,471,560 (GRCm39) |
T263I |
probably damaging |
Het |
Fbxo36 |
A |
G |
1: 84,874,316 (GRCm39) |
K104R |
probably benign |
Het |
Fibin |
C |
T |
2: 110,192,542 (GRCm39) |
R200H |
probably damaging |
Het |
Gad2 |
A |
C |
2: 22,563,987 (GRCm39) |
M397L |
probably benign |
Het |
Garin3 |
T |
C |
11: 46,296,039 (GRCm39) |
I137T |
probably damaging |
Het |
Iqgap3 |
C |
A |
3: 88,014,903 (GRCm39) |
S873* |
probably null |
Het |
Mau2 |
T |
C |
8: 70,472,474 (GRCm39) |
M570V |
probably benign |
Het |
Mrgprb4 |
T |
A |
7: 47,848,084 (GRCm39) |
R281S |
possibly damaging |
Het |
Mthfd1 |
T |
C |
12: 76,335,699 (GRCm39) |
Y258H |
probably damaging |
Het |
Nexn |
C |
T |
3: 151,953,680 (GRCm39) |
E247K |
probably damaging |
Het |
Or11g27 |
T |
A |
14: 50,770,897 (GRCm39) |
N9K |
probably benign |
Het |
Or3a10 |
C |
T |
11: 73,935,653 (GRCm39) |
G149D |
possibly damaging |
Het |
Or9e1 |
T |
A |
11: 58,732,708 (GRCm39) |
V256E |
probably benign |
Het |
Phrf1 |
T |
A |
7: 140,839,593 (GRCm39) |
|
probably benign |
Het |
Prc1 |
A |
G |
7: 79,961,969 (GRCm39) |
N52S |
probably damaging |
Het |
Psd |
G |
C |
19: 46,312,859 (GRCm39) |
S170R |
probably benign |
Het |
Riok1 |
T |
C |
13: 38,233,053 (GRCm39) |
F229L |
probably damaging |
Het |
Slco1a7 |
A |
G |
6: 141,690,264 (GRCm39) |
V163A |
probably benign |
Het |
Stat2 |
A |
G |
10: 128,112,770 (GRCm39) |
|
probably null |
Het |
Sycp3 |
A |
G |
10: 88,303,234 (GRCm39) |
E166G |
probably damaging |
Het |
Szt2 |
G |
A |
4: 118,226,599 (GRCm39) |
T510I |
probably damaging |
Het |
Trank1 |
A |
T |
9: 111,196,001 (GRCm39) |
T1342S |
probably benign |
Het |
Trav3-1 |
C |
A |
14: 52,818,515 (GRCm39) |
A63E |
probably benign |
Het |
Trim34b |
A |
T |
7: 103,985,439 (GRCm39) |
N358I |
probably benign |
Het |
Trmt11 |
G |
C |
10: 30,423,744 (GRCm39) |
P387R |
probably damaging |
Het |
Vmn2r82 |
T |
A |
10: 79,217,090 (GRCm39) |
I474N |
probably damaging |
Het |
Vrk2 |
C |
A |
11: 26,433,324 (GRCm39) |
S286I |
possibly damaging |
Het |
Wdfy3 |
A |
T |
5: 102,023,796 (GRCm39) |
I2451N |
probably benign |
Het |
Zfp326 |
G |
A |
5: 106,036,395 (GRCm39) |
R102H |
probably benign |
Het |
|
Other mutations in Kcnh8 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01313:Kcnh8
|
APN |
17 |
53,141,708 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01901:Kcnh8
|
APN |
17 |
53,201,148 (GRCm39) |
splice site |
probably benign |
|
IGL01959:Kcnh8
|
APN |
17 |
53,141,635 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02214:Kcnh8
|
APN |
17 |
53,184,939 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02528:Kcnh8
|
APN |
17 |
53,110,556 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02620:Kcnh8
|
APN |
17 |
53,205,525 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02688:Kcnh8
|
APN |
17 |
53,266,471 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02931:Kcnh8
|
APN |
17 |
53,263,650 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02950:Kcnh8
|
APN |
17 |
53,263,795 (GRCm39) |
missense |
probably benign |
0.22 |
Incompetent
|
UTSW |
17 |
53,201,129 (GRCm39) |
missense |
probably damaging |
1.00 |
leak
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R0282:Kcnh8
|
UTSW |
17 |
53,032,879 (GRCm39) |
missense |
probably damaging |
1.00 |
R0448:Kcnh8
|
UTSW |
17 |
53,284,648 (GRCm39) |
splice site |
probably null |
|
R0496:Kcnh8
|
UTSW |
17 |
53,032,886 (GRCm39) |
missense |
probably benign |
0.19 |
R0601:Kcnh8
|
UTSW |
17 |
53,201,033 (GRCm39) |
missense |
probably damaging |
1.00 |
R0671:Kcnh8
|
UTSW |
17 |
53,285,141 (GRCm39) |
nonsense |
probably null |
|
R0891:Kcnh8
|
UTSW |
17 |
53,212,242 (GRCm39) |
missense |
probably damaging |
1.00 |
R0971:Kcnh8
|
UTSW |
17 |
53,032,927 (GRCm39) |
missense |
probably benign |
0.00 |
R1054:Kcnh8
|
UTSW |
17 |
53,110,512 (GRCm39) |
missense |
probably damaging |
1.00 |
R1237:Kcnh8
|
UTSW |
17 |
53,200,989 (GRCm39) |
missense |
probably damaging |
1.00 |
R1237:Kcnh8
|
UTSW |
17 |
53,200,988 (GRCm39) |
missense |
probably damaging |
1.00 |
R1565:Kcnh8
|
UTSW |
17 |
53,263,909 (GRCm39) |
missense |
probably benign |
|
R1657:Kcnh8
|
UTSW |
17 |
53,146,153 (GRCm39) |
missense |
probably damaging |
1.00 |
R1669:Kcnh8
|
UTSW |
17 |
53,200,996 (GRCm39) |
missense |
probably damaging |
1.00 |
R1786:Kcnh8
|
UTSW |
17 |
53,200,961 (GRCm39) |
missense |
probably damaging |
1.00 |
R1803:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R1804:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R1929:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R1980:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R1981:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R1982:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R2016:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R2017:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R2132:Kcnh8
|
UTSW |
17 |
53,200,961 (GRCm39) |
missense |
probably damaging |
1.00 |
R2133:Kcnh8
|
UTSW |
17 |
53,200,961 (GRCm39) |
missense |
probably damaging |
1.00 |
R2208:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R2265:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R2266:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R2267:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R2303:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R2309:Kcnh8
|
UTSW |
17 |
53,285,067 (GRCm39) |
missense |
probably damaging |
1.00 |
R2760:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R2764:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R2898:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R2987:Kcnh8
|
UTSW |
17 |
53,263,763 (GRCm39) |
missense |
probably benign |
0.05 |
R3031:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R3157:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R3158:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R4080:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R4081:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R4082:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R4087:Kcnh8
|
UTSW |
17 |
53,110,428 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4132:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R4158:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R4213:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R4301:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R4302:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R4383:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R4385:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R4400:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R4490:Kcnh8
|
UTSW |
17 |
53,268,905 (GRCm39) |
critical splice donor site |
probably null |
|
R4493:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R4494:Kcnh8
|
UTSW |
17 |
53,032,934 (GRCm39) |
small deletion |
probably benign |
|
R4611:Kcnh8
|
UTSW |
17 |
52,909,864 (GRCm39) |
missense |
probably benign |
0.22 |
R4728:Kcnh8
|
UTSW |
17 |
53,032,898 (GRCm39) |
missense |
probably damaging |
1.00 |
R4810:Kcnh8
|
UTSW |
17 |
53,212,248 (GRCm39) |
splice site |
probably null |
|
R4927:Kcnh8
|
UTSW |
17 |
53,185,009 (GRCm39) |
missense |
probably damaging |
1.00 |
R4984:Kcnh8
|
UTSW |
17 |
53,184,995 (GRCm39) |
missense |
probably damaging |
1.00 |
R5017:Kcnh8
|
UTSW |
17 |
53,200,958 (GRCm39) |
missense |
probably damaging |
1.00 |
R5214:Kcnh8
|
UTSW |
17 |
53,205,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R5272:Kcnh8
|
UTSW |
17 |
53,212,043 (GRCm39) |
missense |
probably damaging |
0.97 |
R5386:Kcnh8
|
UTSW |
17 |
53,033,023 (GRCm39) |
missense |
probably benign |
0.10 |
R5472:Kcnh8
|
UTSW |
17 |
53,284,844 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5500:Kcnh8
|
UTSW |
17 |
53,033,008 (GRCm39) |
missense |
probably benign |
0.00 |
R5714:Kcnh8
|
UTSW |
17 |
53,285,150 (GRCm39) |
missense |
probably benign |
0.31 |
R5866:Kcnh8
|
UTSW |
17 |
53,263,804 (GRCm39) |
missense |
probably benign |
0.05 |
R5903:Kcnh8
|
UTSW |
17 |
53,110,364 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6969:Kcnh8
|
UTSW |
17 |
53,184,971 (GRCm39) |
nonsense |
probably null |
|
R6994:Kcnh8
|
UTSW |
17 |
53,284,723 (GRCm39) |
missense |
probably benign |
0.02 |
R7101:Kcnh8
|
UTSW |
17 |
53,212,038 (GRCm39) |
missense |
probably damaging |
1.00 |
R7189:Kcnh8
|
UTSW |
17 |
53,201,145 (GRCm39) |
splice site |
probably null |
|
R7228:Kcnh8
|
UTSW |
17 |
53,263,744 (GRCm39) |
missense |
probably benign |
0.01 |
R7372:Kcnh8
|
UTSW |
17 |
53,201,129 (GRCm39) |
missense |
probably damaging |
1.00 |
R7751:Kcnh8
|
UTSW |
17 |
53,268,871 (GRCm39) |
missense |
probably damaging |
1.00 |
R7819:Kcnh8
|
UTSW |
17 |
53,263,743 (GRCm39) |
missense |
probably benign |
|
R7952:Kcnh8
|
UTSW |
17 |
53,266,493 (GRCm39) |
missense |
probably benign |
0.02 |
R8176:Kcnh8
|
UTSW |
17 |
53,285,122 (GRCm39) |
missense |
probably damaging |
1.00 |
R8190:Kcnh8
|
UTSW |
17 |
53,263,936 (GRCm39) |
missense |
probably damaging |
1.00 |
R8407:Kcnh8
|
UTSW |
17 |
53,212,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R8473:Kcnh8
|
UTSW |
17 |
53,285,320 (GRCm39) |
missense |
probably benign |
|
R8716:Kcnh8
|
UTSW |
17 |
53,284,780 (GRCm39) |
missense |
probably benign |
0.02 |
R8943:Kcnh8
|
UTSW |
17 |
53,104,486 (GRCm39) |
missense |
probably benign |
0.00 |
R9051:Kcnh8
|
UTSW |
17 |
53,141,642 (GRCm39) |
missense |
probably damaging |
1.00 |
R9211:Kcnh8
|
UTSW |
17 |
53,146,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R9233:Kcnh8
|
UTSW |
17 |
53,285,168 (GRCm39) |
missense |
probably damaging |
1.00 |
R9243:Kcnh8
|
UTSW |
17 |
53,205,542 (GRCm39) |
missense |
probably damaging |
1.00 |
R9327:Kcnh8
|
UTSW |
17 |
53,146,084 (GRCm39) |
missense |
probably damaging |
0.99 |
R9640:Kcnh8
|
UTSW |
17 |
53,185,089 (GRCm39) |
missense |
probably damaging |
1.00 |
R9646:Kcnh8
|
UTSW |
17 |
53,104,573 (GRCm39) |
missense |
probably benign |
0.25 |
RF009:Kcnh8
|
UTSW |
17 |
53,285,267 (GRCm39) |
missense |
probably benign |
0.00 |
RF010:Kcnh8
|
UTSW |
17 |
53,285,267 (GRCm39) |
missense |
probably benign |
0.00 |
RF011:Kcnh8
|
UTSW |
17 |
53,285,267 (GRCm39) |
missense |
probably benign |
0.00 |
RF021:Kcnh8
|
UTSW |
17 |
53,285,267 (GRCm39) |
missense |
probably benign |
0.00 |
RF022:Kcnh8
|
UTSW |
17 |
53,285,267 (GRCm39) |
missense |
probably benign |
0.00 |
Z1088:Kcnh8
|
UTSW |
17 |
53,285,320 (GRCm39) |
missense |
probably benign |
|
Z1088:Kcnh8
|
UTSW |
17 |
53,032,918 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Kcnh8
|
UTSW |
17 |
53,201,089 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1177:Kcnh8
|
UTSW |
17 |
53,285,121 (GRCm39) |
missense |
possibly damaging |
0.91 |
Z1177:Kcnh8
|
UTSW |
17 |
53,110,499 (GRCm39) |
missense |
probably damaging |
1.00 |
|