Other mutations in this stock |
Total: 31 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Apob |
G |
T |
12: 8,042,979 (GRCm39) |
V787F |
probably benign |
Het |
Atg14 |
T |
C |
14: 47,786,451 (GRCm39) |
I268V |
probably benign |
Het |
Atg14 |
T |
A |
14: 47,783,081 (GRCm39) |
|
probably benign |
Het |
Atm |
A |
T |
9: 53,408,562 (GRCm39) |
|
probably benign |
Het |
Ccdc9 |
A |
G |
7: 16,018,434 (GRCm39) |
|
probably benign |
Het |
Cers6 |
T |
C |
2: 68,899,013 (GRCm39) |
F217S |
probably benign |
Het |
Crebbp |
A |
C |
16: 3,944,469 (GRCm39) |
|
probably null |
Het |
Csmd1 |
T |
A |
8: 16,049,869 (GRCm39) |
|
probably benign |
Het |
Dmac2l |
A |
T |
12: 69,787,819 (GRCm39) |
Y85F |
probably benign |
Het |
Eml1 |
T |
A |
12: 108,496,571 (GRCm39) |
V609E |
probably damaging |
Het |
Fryl |
A |
G |
5: 73,222,636 (GRCm39) |
S204P |
probably damaging |
Het |
Gpr152 |
A |
G |
19: 4,192,843 (GRCm39) |
D128G |
probably damaging |
Het |
Itgal |
T |
A |
7: 126,927,844 (GRCm39) |
V1013D |
possibly damaging |
Het |
Kctd18 |
A |
G |
1: 58,004,559 (GRCm39) |
Y112H |
probably damaging |
Het |
Kdm4d |
T |
A |
9: 14,375,850 (GRCm39) |
T3S |
probably benign |
Het |
Lrp1b |
C |
T |
2: 41,000,765 (GRCm39) |
|
probably null |
Het |
Mex3c |
T |
A |
18: 73,723,360 (GRCm39) |
D484E |
possibly damaging |
Het |
Nalf1 |
T |
A |
8: 9,257,930 (GRCm39) |
D406V |
probably benign |
Het |
Nat14 |
T |
C |
7: 4,927,050 (GRCm39) |
V74A |
possibly damaging |
Het |
Or2b6 |
A |
G |
13: 21,823,510 (GRCm39) |
F61S |
probably damaging |
Het |
Pabpc2 |
C |
T |
18: 39,908,193 (GRCm39) |
T486I |
probably benign |
Het |
Pgm2 |
A |
G |
5: 64,260,289 (GRCm39) |
|
probably benign |
Het |
Pkn3 |
T |
A |
2: 29,973,149 (GRCm39) |
I353N |
probably damaging |
Het |
Rbm44 |
T |
A |
1: 91,083,260 (GRCm39) |
S594R |
possibly damaging |
Het |
Rrbp1 |
C |
T |
2: 143,830,350 (GRCm39) |
A606T |
possibly damaging |
Het |
Tg |
A |
G |
15: 66,577,123 (GRCm39) |
E1482G |
probably benign |
Het |
Uba1 |
A |
G |
X: 20,541,885 (GRCm39) |
T546A |
probably benign |
Het |
Vmn2r37 |
T |
C |
7: 9,220,934 (GRCm39) |
K310E |
probably benign |
Het |
Zbtb38 |
A |
T |
9: 96,569,126 (GRCm39) |
W653R |
probably damaging |
Het |
Zdhhc19 |
A |
T |
16: 32,318,440 (GRCm39) |
I99F |
probably damaging |
Het |
Zfp236 |
T |
C |
18: 82,648,239 (GRCm39) |
Y974C |
probably damaging |
Het |
|
Other mutations in Tcof1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00468:Tcof1
|
APN |
18 |
60,947,640 (GRCm39) |
unclassified |
probably benign |
|
IGL01339:Tcof1
|
APN |
18 |
60,951,167 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL02072:Tcof1
|
APN |
18 |
60,964,637 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL02160:Tcof1
|
APN |
18 |
60,981,815 (GRCm39) |
unclassified |
probably benign |
|
IGL02823:Tcof1
|
APN |
18 |
60,949,120 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03161:Tcof1
|
APN |
18 |
60,966,560 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL03291:Tcof1
|
APN |
18 |
60,962,133 (GRCm39) |
missense |
possibly damaging |
0.71 |
FR4304:Tcof1
|
UTSW |
18 |
60,968,814 (GRCm39) |
unclassified |
probably benign |
|
FR4589:Tcof1
|
UTSW |
18 |
60,961,722 (GRCm39) |
critical splice donor site |
probably benign |
|
FR4737:Tcof1
|
UTSW |
18 |
60,961,722 (GRCm39) |
critical splice donor site |
probably benign |
|
PIT4802001:Tcof1
|
UTSW |
18 |
60,965,010 (GRCm39) |
missense |
unknown |
|
R0569:Tcof1
|
UTSW |
18 |
60,962,107 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0602:Tcof1
|
UTSW |
18 |
60,966,605 (GRCm39) |
missense |
probably damaging |
1.00 |
R0744:Tcof1
|
UTSW |
18 |
60,978,904 (GRCm39) |
missense |
probably damaging |
1.00 |
R0782:Tcof1
|
UTSW |
18 |
60,949,352 (GRCm39) |
missense |
probably damaging |
0.97 |
R0833:Tcof1
|
UTSW |
18 |
60,978,904 (GRCm39) |
missense |
probably damaging |
1.00 |
R0836:Tcof1
|
UTSW |
18 |
60,978,904 (GRCm39) |
missense |
probably damaging |
1.00 |
R0885:Tcof1
|
UTSW |
18 |
60,968,922 (GRCm39) |
missense |
possibly damaging |
0.84 |
R1465:Tcof1
|
UTSW |
18 |
60,952,026 (GRCm39) |
splice site |
probably benign |
|
R1528:Tcof1
|
UTSW |
18 |
60,948,071 (GRCm39) |
nonsense |
probably null |
|
R1643:Tcof1
|
UTSW |
18 |
60,949,300 (GRCm39) |
missense |
possibly damaging |
0.72 |
R1919:Tcof1
|
UTSW |
18 |
60,949,156 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1920:Tcof1
|
UTSW |
18 |
60,971,927 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1921:Tcof1
|
UTSW |
18 |
60,971,927 (GRCm39) |
missense |
possibly damaging |
0.87 |
R2023:Tcof1
|
UTSW |
18 |
60,966,605 (GRCm39) |
missense |
probably damaging |
1.00 |
R2108:Tcof1
|
UTSW |
18 |
60,968,845 (GRCm39) |
missense |
probably damaging |
0.97 |
R2114:Tcof1
|
UTSW |
18 |
60,965,857 (GRCm39) |
missense |
possibly damaging |
0.85 |
R2115:Tcof1
|
UTSW |
18 |
60,965,857 (GRCm39) |
missense |
possibly damaging |
0.85 |
R2116:Tcof1
|
UTSW |
18 |
60,965,857 (GRCm39) |
missense |
possibly damaging |
0.85 |
R2117:Tcof1
|
UTSW |
18 |
60,965,857 (GRCm39) |
missense |
possibly damaging |
0.85 |
R2156:Tcof1
|
UTSW |
18 |
60,964,901 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2221:Tcof1
|
UTSW |
18 |
60,970,973 (GRCm39) |
missense |
possibly damaging |
0.51 |
R2229:Tcof1
|
UTSW |
18 |
60,965,249 (GRCm39) |
intron |
probably benign |
|
R2913:Tcof1
|
UTSW |
18 |
60,949,156 (GRCm39) |
missense |
possibly damaging |
0.85 |
R2914:Tcof1
|
UTSW |
18 |
60,949,156 (GRCm39) |
missense |
possibly damaging |
0.85 |
R3944:Tcof1
|
UTSW |
18 |
60,955,909 (GRCm39) |
missense |
probably damaging |
0.98 |
R3979:Tcof1
|
UTSW |
18 |
60,964,605 (GRCm39) |
missense |
possibly damaging |
0.71 |
R4049:Tcof1
|
UTSW |
18 |
60,965,975 (GRCm39) |
missense |
possibly damaging |
0.84 |
R4125:Tcof1
|
UTSW |
18 |
60,952,673 (GRCm39) |
missense |
unknown |
|
R5047:Tcof1
|
UTSW |
18 |
60,964,986 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5433:Tcof1
|
UTSW |
18 |
60,951,105 (GRCm39) |
utr 3 prime |
probably benign |
|
R5546:Tcof1
|
UTSW |
18 |
60,964,628 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5832:Tcof1
|
UTSW |
18 |
60,952,611 (GRCm39) |
missense |
unknown |
|
R5965:Tcof1
|
UTSW |
18 |
60,966,490 (GRCm39) |
critical splice donor site |
probably null |
|
R6301:Tcof1
|
UTSW |
18 |
60,961,897 (GRCm39) |
missense |
probably damaging |
0.97 |
R6480:Tcof1
|
UTSW |
18 |
60,947,852 (GRCm39) |
splice site |
probably null |
|
R6910:Tcof1
|
UTSW |
18 |
60,962,123 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6911:Tcof1
|
UTSW |
18 |
60,962,123 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7105:Tcof1
|
UTSW |
18 |
60,976,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R7225:Tcof1
|
UTSW |
18 |
60,961,520 (GRCm39) |
missense |
unknown |
|
R7356:Tcof1
|
UTSW |
18 |
60,951,166 (GRCm39) |
missense |
unknown |
|
R7467:Tcof1
|
UTSW |
18 |
60,964,977 (GRCm39) |
missense |
unknown |
|
R7536:Tcof1
|
UTSW |
18 |
60,962,123 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7804:Tcof1
|
UTSW |
18 |
60,962,123 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7818:Tcof1
|
UTSW |
18 |
60,962,123 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7863:Tcof1
|
UTSW |
18 |
60,962,123 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8006:Tcof1
|
UTSW |
18 |
60,962,123 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8007:Tcof1
|
UTSW |
18 |
60,962,123 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8008:Tcof1
|
UTSW |
18 |
60,962,123 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8063:Tcof1
|
UTSW |
18 |
60,971,834 (GRCm39) |
missense |
probably damaging |
1.00 |
R8192:Tcof1
|
UTSW |
18 |
60,976,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R8200:Tcof1
|
UTSW |
18 |
60,962,123 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8203:Tcof1
|
UTSW |
18 |
60,962,123 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8204:Tcof1
|
UTSW |
18 |
60,962,123 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8207:Tcof1
|
UTSW |
18 |
60,962,123 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8217:Tcof1
|
UTSW |
18 |
60,962,123 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8300:Tcof1
|
UTSW |
18 |
60,962,123 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8517:Tcof1
|
UTSW |
18 |
60,962,123 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8518:Tcof1
|
UTSW |
18 |
60,962,123 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8553:Tcof1
|
UTSW |
18 |
60,964,643 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8729:Tcof1
|
UTSW |
18 |
60,962,145 (GRCm39) |
missense |
unknown |
|
R8732:Tcof1
|
UTSW |
18 |
60,962,123 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8749:Tcof1
|
UTSW |
18 |
60,962,123 (GRCm39) |
missense |
possibly damaging |
0.84 |
R9800:Tcof1
|
UTSW |
18 |
60,949,558 (GRCm39) |
missense |
unknown |
|
RF001:Tcof1
|
UTSW |
18 |
60,968,811 (GRCm39) |
unclassified |
probably benign |
|
RF007:Tcof1
|
UTSW |
18 |
60,966,640 (GRCm39) |
small insertion |
probably benign |
|
RF009:Tcof1
|
UTSW |
18 |
60,968,815 (GRCm39) |
unclassified |
probably benign |
|
RF010:Tcof1
|
UTSW |
18 |
60,968,816 (GRCm39) |
unclassified |
probably benign |
|
RF011:Tcof1
|
UTSW |
18 |
60,968,811 (GRCm39) |
unclassified |
probably benign |
|
RF013:Tcof1
|
UTSW |
18 |
60,968,815 (GRCm39) |
unclassified |
probably benign |
|
RF015:Tcof1
|
UTSW |
18 |
60,966,656 (GRCm39) |
small insertion |
probably benign |
|
RF016:Tcof1
|
UTSW |
18 |
60,966,647 (GRCm39) |
small insertion |
probably benign |
|
RF022:Tcof1
|
UTSW |
18 |
60,968,807 (GRCm39) |
unclassified |
probably benign |
|
RF024:Tcof1
|
UTSW |
18 |
60,968,810 (GRCm39) |
unclassified |
probably benign |
|
RF027:Tcof1
|
UTSW |
18 |
60,968,808 (GRCm39) |
unclassified |
probably benign |
|
RF029:Tcof1
|
UTSW |
18 |
60,968,807 (GRCm39) |
unclassified |
probably benign |
|
RF029:Tcof1
|
UTSW |
18 |
60,968,817 (GRCm39) |
unclassified |
probably benign |
|
RF030:Tcof1
|
UTSW |
18 |
60,968,795 (GRCm39) |
unclassified |
probably benign |
|
RF030:Tcof1
|
UTSW |
18 |
60,966,646 (GRCm39) |
small insertion |
probably benign |
|
RF030:Tcof1
|
UTSW |
18 |
60,966,640 (GRCm39) |
small insertion |
probably benign |
|
RF031:Tcof1
|
UTSW |
18 |
60,968,817 (GRCm39) |
unclassified |
probably benign |
|
RF031:Tcof1
|
UTSW |
18 |
60,966,637 (GRCm39) |
small insertion |
probably benign |
|
RF035:Tcof1
|
UTSW |
18 |
60,966,625 (GRCm39) |
small insertion |
probably benign |
|
RF036:Tcof1
|
UTSW |
18 |
60,968,808 (GRCm39) |
unclassified |
probably benign |
|
RF036:Tcof1
|
UTSW |
18 |
60,961,480 (GRCm39) |
small insertion |
probably benign |
|
RF038:Tcof1
|
UTSW |
18 |
60,966,638 (GRCm39) |
small insertion |
probably benign |
|
RF040:Tcof1
|
UTSW |
18 |
60,966,655 (GRCm39) |
small insertion |
probably benign |
|
RF040:Tcof1
|
UTSW |
18 |
60,961,480 (GRCm39) |
small insertion |
probably benign |
|
RF041:Tcof1
|
UTSW |
18 |
60,966,648 (GRCm39) |
small insertion |
probably benign |
|
RF041:Tcof1
|
UTSW |
18 |
60,966,644 (GRCm39) |
small insertion |
probably benign |
|
RF043:Tcof1
|
UTSW |
18 |
60,966,644 (GRCm39) |
small insertion |
probably benign |
|
RF050:Tcof1
|
UTSW |
18 |
60,966,651 (GRCm39) |
small insertion |
probably benign |
|
RF051:Tcof1
|
UTSW |
18 |
60,966,651 (GRCm39) |
small insertion |
probably benign |
|
RF053:Tcof1
|
UTSW |
18 |
60,968,819 (GRCm39) |
unclassified |
probably benign |
|
RF056:Tcof1
|
UTSW |
18 |
60,966,647 (GRCm39) |
small insertion |
probably benign |
|
RF057:Tcof1
|
UTSW |
18 |
60,966,638 (GRCm39) |
small insertion |
probably benign |
|
RF057:Tcof1
|
UTSW |
18 |
60,966,637 (GRCm39) |
small insertion |
probably benign |
|
RF057:Tcof1
|
UTSW |
18 |
60,966,636 (GRCm39) |
small insertion |
probably benign |
|
RF057:Tcof1
|
UTSW |
18 |
60,966,643 (GRCm39) |
small insertion |
probably benign |
|
RF060:Tcof1
|
UTSW |
18 |
60,968,816 (GRCm39) |
unclassified |
probably benign |
|
RF060:Tcof1
|
UTSW |
18 |
60,968,819 (GRCm39) |
unclassified |
probably benign |
|
RF063:Tcof1
|
UTSW |
18 |
60,966,645 (GRCm39) |
small insertion |
probably benign |
|
RF064:Tcof1
|
UTSW |
18 |
60,966,646 (GRCm39) |
small insertion |
probably benign |
|
RF064:Tcof1
|
UTSW |
18 |
60,966,643 (GRCm39) |
small insertion |
probably benign |
|
|