Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A030005L19Rik |
T |
TTTGGCTGCC |
1: 82,891,310 (GRCm39) |
|
probably benign |
Het |
Acap3 |
TGCATCCTGGGCTGC |
TGCATCCTGGGCTGCCGCATCCTGGGCTGC |
4: 155,989,548 (GRCm39) |
|
probably benign |
Het |
AI837181 |
G |
GGCT |
19: 5,475,266 (GRCm39) |
|
probably benign |
Het |
Amfr |
GCC |
GCCGGCGCGAGCTCC |
8: 94,738,920 (GRCm39) |
|
probably benign |
Het |
Amot |
GGAGCAGCAA |
G |
X: 144,233,984 (GRCm39) |
|
probably benign |
Het |
Bltp1 |
TAT |
TATTATTATTATTATGAT |
3: 37,104,907 (GRCm39) |
|
probably benign |
Het |
Cacna1f |
GAG |
GAGTAG |
X: 7,486,293 (GRCm39) |
|
probably null |
Het |
Calhm1 |
CTGTGGCTGTGGCTGTGGCTGTGG |
CTGTGGCTGTGGTTGTGGCTGTGGCTGTGGCTGTGG |
19: 47,129,692 (GRCm39) |
|
probably benign |
Het |
Chga |
G |
GCAT |
12: 102,527,686 (GRCm39) |
|
probably benign |
Het |
E4f1 |
CGC |
CGCTGC |
17: 24,674,164 (GRCm39) |
|
probably benign |
Het |
E4f1 |
CCG |
CCGGCG |
17: 24,674,169 (GRCm39) |
|
probably benign |
Het |
Eps8 |
C |
CTCAG |
6: 137,494,068 (GRCm39) |
|
probably null |
Het |
Exd2 |
GCAGCCACAGCAGCCGCAGCAGCCGCAGCCACAGCCACAGCCACAGCCACAGCCACAGC |
GCAGCCACAGC |
12: 80,522,674 (GRCm39) |
|
probably benign |
Het |
Exd2 |
CAGCCAGAGC |
CAGC |
12: 80,522,729 (GRCm39) |
|
probably benign |
Het |
Gm10447 |
AAAAAAAAAGAAAAA |
AAAAAA |
11: 53,347,165 (GRCm39) |
|
probably benign |
Het |
Gm10521 |
CTCTCTCTCT |
CTCTCTCTCTCTCT |
1: 171,723,860 (GRCm39) |
|
probably null |
Het |
Gm8369 |
TGTG |
TGTGCGAGTG |
19: 11,489,137 (GRCm39) |
|
probably benign |
Het |
Gucy1b2 |
CACACACACACACACACTTAC |
CAC |
14: 62,646,090 (GRCm39) |
|
probably benign |
Het |
Ier5l |
TTGCTGCTGCTGCTGCTG |
TTGCTGCTGCTGCTG |
2: 30,363,832 (GRCm39) |
|
probably benign |
Het |
Kmt2b |
TTCTCCT |
TTCTCCTTCTCCT |
7: 30,285,782 (GRCm39) |
|
probably benign |
Het |
Krtap28-10 |
CAG |
CAGCCAAAG |
1: 83,019,867 (GRCm39) |
|
probably benign |
Het |
Krtap28-10 |
CCACCACAGC |
CCACCACAGCCACAGTCACCACAGC |
1: 83,020,002 (GRCm39) |
|
probably benign |
Het |
Lmx1b |
TCCATCTTGATGCCGTCCAACATCTTGATGCCGTCCA |
TACATCTTGATGCCGTCCA |
2: 33,530,501 (GRCm39) |
|
probably null |
Het |
Mamld1 |
GCAACA |
GCAACAACA |
X: 70,162,418 (GRCm39) |
|
probably benign |
Het |
Mamld1 |
AGC |
AGCGGC |
X: 70,162,456 (GRCm39) |
|
probably benign |
Het |
Mamld1 |
AGC |
AGCCGC |
X: 70,162,444 (GRCm39) |
|
probably benign |
Het |
Manbal |
CGATAGAAT |
C |
2: 157,237,932 (GRCm39) |
|
probably null |
Het |
Map1a |
GCTCCAGCTCCAGCTCCA |
GCTCCAGCTCCAGCTCCAGCTCCAGCTCCATCTCCAGCTCCAGCTCCA |
2: 121,136,782 (GRCm39) |
|
probably benign |
Het |
Mcph1 |
CTCT |
CTCTTCT |
8: 18,702,541 (GRCm39) |
|
probably benign |
Het |
Nefh |
CCTCACCTGGGGACTTGG |
CCTCACCTGGGGACTTGGGCTCACCTGGGGACTTGG |
11: 4,891,039 (GRCm39) |
|
probably benign |
Het |
Nusap1 |
GATACACGTTAGCAGTGAGGAGCAAGCTGA |
GATACACGTTAGCAGTGAGGAGCAAGCTGATATACACGTTAGCAGTGAGGAGCAAGCTGA |
2: 119,458,060 (GRCm39) |
|
probably benign |
Het |
Or2t49 |
TGGAGGTGGATTGG |
TG |
11: 58,393,208 (GRCm39) |
|
probably benign |
Het |
P4ha2 |
CCAGGTG |
C |
11: 54,001,061 (GRCm39) |
|
probably benign |
Het |
Pdik1l |
CCACCA |
CCACCAACACCA |
4: 134,006,821 (GRCm39) |
|
probably benign |
Het |
Polr1has |
CACCAC |
CACCACCCCCACCACCACCACAACCAC |
17: 37,275,958 (GRCm39) |
|
probably benign |
Het |
Rassf6 |
GCCTCACTCATGGTCCTGTAGAGCAATGGGGATTC |
GCCTCACTCATGGTCCTGTAGAGCAATGGGGATTCTTCCTCACTCATGGTCCTGTAGAGCAATGGGGATTC |
5: 90,756,767 (GRCm39) |
|
probably benign |
Het |
Rfx4 |
TCTCTCTCTCTCTCT |
TCTCTCTCTCTCTCTCGCTCTCTCTCTCTCT |
10: 84,694,344 (GRCm39) |
|
probably benign |
Het |
Rgs22 |
GCTAAAAAAAAAAAAAAAAA |
G |
15: 36,010,981 (GRCm39) |
|
probably benign |
Het |
Rpgrip1 |
AGG |
AGGGGG |
14: 52,386,850 (GRCm39) |
|
probably benign |
Het |
Slc39a4 |
TGTGGTC |
TGTGGTCATCATGATCACCATGGTCACCATGAGCACGGTGGTC |
15: 76,499,066 (GRCm39) |
|
probably benign |
Het |
Srpk2 |
ATCCT |
AT |
5: 23,730,573 (GRCm39) |
|
probably benign |
Het |
Strn |
AGTC |
AGTCCGTGCTCCCTTACCCCAGTCCGTGCTCCCTTACCCCTGTC |
17: 78,984,714 (GRCm39) |
|
probably null |
Het |
Tfeb |
AGC |
AGCCGC |
17: 48,097,036 (GRCm39) |
|
probably benign |
Het |
Tmem59 |
T |
TGTTTGTTG |
4: 107,047,729 (GRCm39) |
|
probably benign |
Het |
Trav6d-5 |
ATTTTT |
ATTTTTTTTTT |
14: 53,032,791 (GRCm39) |
|
probably benign |
Het |
Triobp |
CAGGACTCCCTGTGCCCAACGG |
CAGGACTCCCTGTGCCCAACGGAACAACCCAAGGACTCCCTGTGCCCAACGG |
15: 78,851,239 (GRCm39) |
|
probably benign |
Het |
Tsen2 |
GGA |
GGATGA |
6: 115,537,028 (GRCm39) |
|
probably benign |
Het |
Ttf2 |
TTCT |
TTCTTCT |
3: 100,870,473 (GRCm39) |
|
probably benign |
Het |
Vat1l |
C |
T |
8: 115,016,069 (GRCm39) |
L320F |
probably damaging |
Het |
Xirp2 |
TT |
TTTAT |
2: 67,355,888 (GRCm39) |
|
probably benign |
Het |
Yipf3 |
AGAGGA |
AGA |
17: 46,559,898 (GRCm39) |
|
probably benign |
Het |
Zfp933 |
TT |
TTTGCGT |
4: 147,910,188 (GRCm39) |
|
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 |
|
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 |
|
RF031:Tcof1
|
UTSW |
18 |
60,966,637 (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 |
|
|