Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930503E14Rik |
A |
T |
14: 44,406,698 (GRCm39) |
M117K |
possibly damaging |
Het |
Adamts13 |
G |
A |
2: 26,886,922 (GRCm39) |
A1020T |
probably damaging |
Het |
Armh4 |
G |
T |
14: 50,007,895 (GRCm39) |
A526D |
probably damaging |
Het |
Atg3 |
C |
A |
16: 44,998,595 (GRCm39) |
D132E |
probably benign |
Het |
Blzf1 |
A |
G |
1: 164,134,037 (GRCm39) |
M4T |
possibly damaging |
Het |
Cdon |
G |
A |
9: 35,389,935 (GRCm39) |
R863Q |
probably damaging |
Het |
Cyp2d40 |
C |
T |
15: 82,644,460 (GRCm39) |
R255H |
unknown |
Het |
Evi5 |
T |
C |
5: 107,969,740 (GRCm39) |
K57R |
probably damaging |
Het |
Fam186b |
T |
C |
15: 99,178,567 (GRCm39) |
E253G |
probably damaging |
Het |
Fcgr1 |
A |
T |
3: 96,193,200 (GRCm39) |
F266I |
probably benign |
Het |
Fchsd1 |
C |
T |
18: 38,092,926 (GRCm39) |
|
probably benign |
Het |
Gm10142 |
G |
T |
10: 77,551,996 (GRCm39) |
C119F |
probably damaging |
Het |
Gpr63 |
A |
G |
4: 25,008,202 (GRCm39) |
S309G |
probably benign |
Het |
Herc3 |
C |
T |
6: 58,832,745 (GRCm39) |
Q137* |
probably null |
Het |
Jmy |
T |
A |
13: 93,578,080 (GRCm39) |
H696L |
possibly damaging |
Het |
Kif13a |
T |
C |
13: 46,941,561 (GRCm39) |
H972R |
probably benign |
Het |
Lama1 |
C |
T |
17: 68,050,276 (GRCm39) |
Q296* |
probably null |
Het |
Lmf1 |
C |
T |
17: 25,850,812 (GRCm39) |
|
probably benign |
Het |
Lpp |
T |
C |
16: 24,790,596 (GRCm39) |
C352R |
probably damaging |
Het |
Ltbp1 |
T |
C |
17: 75,599,881 (GRCm39) |
|
probably benign |
Het |
Maml3 |
G |
T |
3: 51,598,262 (GRCm39) |
D807E |
possibly damaging |
Het |
Mdc1 |
T |
A |
17: 36,158,736 (GRCm39) |
V372D |
probably benign |
Het |
Mst1 |
C |
A |
9: 107,961,508 (GRCm39) |
H579Q |
probably benign |
Het |
Or11g24 |
T |
C |
14: 50,662,696 (GRCm39) |
F240S |
probably damaging |
Het |
Or1r1 |
T |
C |
11: 73,875,204 (GRCm39) |
T77A |
probably damaging |
Het |
Or4a39 |
A |
G |
2: 89,237,057 (GRCm39) |
V122A |
probably damaging |
Het |
Or8d1 |
G |
A |
9: 38,766,585 (GRCm39) |
V76I |
probably benign |
Het |
Pcdhb22 |
G |
T |
18: 37,652,179 (GRCm39) |
G216C |
probably damaging |
Het |
Phlpp2 |
A |
T |
8: 110,640,251 (GRCm39) |
H472L |
probably benign |
Het |
Plscr3 |
A |
G |
11: 69,740,917 (GRCm39) |
|
probably null |
Het |
Rab7 |
A |
T |
6: 87,982,205 (GRCm39) |
|
probably null |
Het |
Rad50 |
A |
G |
11: 53,565,523 (GRCm39) |
|
probably null |
Het |
Scgb1b20 |
A |
G |
7: 33,072,737 (GRCm39) |
|
probably null |
Het |
Scn9a |
A |
C |
2: 66,392,824 (GRCm39) |
L256R |
probably damaging |
Het |
Spag1 |
G |
T |
15: 36,195,588 (GRCm39) |
Q260H |
probably damaging |
Het |
Tatdn3 |
T |
A |
1: 190,778,475 (GRCm39) |
I239F |
probably damaging |
Het |
Top3b |
A |
G |
16: 16,709,282 (GRCm39) |
T657A |
probably benign |
Het |
Tstd3 |
A |
G |
4: 21,759,621 (GRCm39) |
|
probably null |
Het |
Ttc4 |
A |
T |
4: 106,525,435 (GRCm39) |
L233H |
probably damaging |
Het |
Vmn2r130 |
T |
A |
17: 23,282,794 (GRCm39) |
M158K |
probably benign |
Het |
Yeats2 |
A |
T |
16: 20,027,215 (GRCm39) |
Q822L |
probably damaging |
Het |
Zfp976 |
A |
T |
7: 42,262,843 (GRCm39) |
C331* |
probably null |
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 |
|
IGL02513:Tcof1
|
APN |
18 |
60,964,850 (GRCm39) |
missense |
possibly damaging |
0.51 |
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 |
|
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 |
|
|