Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
AI837181 |
GCG |
GCGCCG |
19: 5,475,246 (GRCm39) |
|
probably benign |
Het |
Blm |
CTCCTCCTCCTCCTCCTCCTCCTC |
CTCCTCCTCCTCTTCCTCCTCCTCCTCCTCCTCCTC |
7: 80,162,654 (GRCm39) |
|
probably benign |
Het |
Blm |
CCTCCTCCTCC |
CCTCCTCCTCCTGCTCCTCCTCC |
7: 80,162,671 (GRCm39) |
|
probably benign |
Het |
Cyb5r4 |
GGGA |
GGGATGTGACAGACACACTGCCCATGGA |
9: 86,922,498 (GRCm39) |
|
probably benign |
Het |
Dcdc2b |
GCTGC |
GCTGCCAGGACTGC |
4: 129,503,444 (GRCm39) |
|
probably benign |
Het |
Dclre1a |
CTTTGCT |
C |
19: 56,532,564 (GRCm39) |
|
probably benign |
Het |
Dctn6 |
AAATCATGGCTTGCGATCT |
A |
8: 34,572,236 (GRCm39) |
|
probably null |
Het |
Elovl5 |
G |
T |
9: 77,888,755 (GRCm39) |
|
probably null |
Het |
Ermn |
AACT |
AACTACT |
2: 57,938,078 (GRCm39) |
|
probably benign |
Het |
Fbrsl1 |
G |
GCGTGTGCTGGTC |
5: 110,526,017 (GRCm39) |
|
probably benign |
Het |
Fgd6 |
ATT |
A |
10: 93,880,187 (GRCm39) |
|
probably null |
Het |
Flywch1 |
TCACTCACCCACTCCTGGTGT |
TCACTCACCCACTCCTGGTGTGGGGAGGCTACGCACTCACCCACTCCTGGTGT |
17: 23,981,132 (GRCm39) |
|
probably null |
Het |
Gab3 |
TCT |
TCTGCT |
X: 74,043,602 (GRCm39) |
|
probably benign |
Het |
Gab3 |
TTC |
TTCATC |
X: 74,043,607 (GRCm39) |
|
probably benign |
Het |
Gab3 |
CTT |
CTTATT |
X: 74,043,603 (GRCm39) |
|
probably null |
Het |
Gm11060 |
CTGTGTG |
CTG |
2: 104,922,385 (GRCm39) |
|
probably null |
Het |
Gm5475 |
GGTGGAAGGAAAG |
GG |
15: 100,325,029 (GRCm39) |
|
probably null |
Het |
Heatr3 |
TAT |
TATTAAT |
8: 88,883,085 (GRCm39) |
|
probably benign |
Het |
Iqcf4 |
TTTCCTTTT |
TTTCCTTTTCCTTTTCCTTTTCCTTTTCCTTTTCCTCTTCCTTTT |
9: 106,447,814 (GRCm39) |
|
probably benign |
Het |
Ivl |
GCTGCTGCTGCTGC |
G |
3: 92,479,625 (GRCm39) |
|
probably null |
Het |
Kif12 |
GGC |
GGCCTCCACCCGGCGTGC |
4: 63,089,662 (GRCm39) |
|
probably benign |
Het |
L1td1 |
AGGAGGAGGAGGAGGAGGAGGAGGGGGAGGAGGAG |
AGGAGGAGGAG |
4: 98,625,026 (GRCm39) |
|
probably benign |
Het |
Lca5l |
CCCTGGCCCCGGCC |
CCC |
16: 95,960,504 (GRCm39) |
|
probably null |
Het |
Loricrin |
ATAGCCG |
A |
3: 91,989,183 (GRCm39) |
|
probably benign |
Het |
Mapk7 |
GGGGCA |
GGGGCACGGGCA |
11: 61,381,060 (GRCm39) |
|
probably benign |
Het |
Nf2 |
AAAAG |
A |
11: 4,779,936 (GRCm39) |
|
probably null |
Het |
Nlrp3 |
GGGTA |
G |
11: 59,449,378 (GRCm39) |
|
probably null |
Het |
Nolc1 |
CAGCAGC |
CAGCAGCAGGAGCAGC |
19: 46,069,810 (GRCm39) |
|
probably benign |
Het |
Pdik1l |
TTTT |
TTTTGTTTTTGATTT |
4: 134,006,685 (GRCm39) |
|
probably null |
Het |
Phldb3 |
CGCCCCCG |
C |
7: 24,325,918 (GRCm39) |
|
probably null |
Het |
Setd1a |
GGTGGTAGT |
GGTGGTAGTAGTGGTAGT |
7: 127,384,483 (GRCm39) |
|
probably benign |
Het |
Spmap2l |
CCCCAGTCCCGCAAGGCCAG |
CCCCAGTCCCGCAAGGCCAGCGATCCTACCCAGTCCCGCAAGGCCAG |
5: 77,164,257 (GRCm39) |
|
probably benign |
Het |
Strn |
CTTACCCCAGTC |
CTTACCCCAGTCCGTGCTCCCTTACCCCAGTCCGTGATCCATTACCCCAGTC |
17: 78,984,706 (GRCm39) |
|
probably null |
Het |
Tedc2 |
AGGAACCCT |
AGGAACCCTGGAACCCT |
17: 24,435,213 (GRCm39) |
|
probably benign |
Het |
Tmem59 |
T |
TGTTTGTTG |
4: 107,047,729 (GRCm39) |
|
probably benign |
Het |
Zfhx3 |
C |
CCGCAGCAAA |
8: 109,682,730 (GRCm39) |
|
probably benign |
Het |
Zfp335 |
TCGTCGTC |
TCGTCGTCGTC |
2: 164,749,383 (GRCm39) |
|
probably benign |
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 |
|
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 |
60,968,817 (GRCm39) |
unclassified |
probably benign |
|
RF029:Tcof1
|
UTSW |
18 |
60,968,807 (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 |
|
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 |
|
|