| geneid | 10071 |
|---|---|
| ensemblid | ENSG00000205277.10 |
| hgncid | 7510 |
| symbol | MUC12 |
| name | mucin 12, cell surface associated |
| refseq_nuc | NM_001164462.2 |
| refseq_prot | NP_001157934.1 |
| ensembl_nuc | ENST00000536621.6 |
| ensembl_prot | ENSP00000441929.1 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 100969565 |
| end | 101018936 |
| strand | + |
| ver | v1.2 |
| region | chr7:100969565-101018936 |
| region5000 | chr7:100964565-101023936 |
| regionname0 | MUC12_chr7_100969565_101018936 |
| regionname5000 | MUC12_chr7_100964565_101023936 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 10044 | 9 | 0 | 0 | 8 | 0 | 1 | 8 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0002 | 0/0 | 7917 | 8 | 0 | 4 | 4 | 0 | 0 | 2 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0003 | 0/0 | 7917 | 7 | 0 | 0 | 7 | 0 | 0 | 6 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0004 | 0/0 | 4668 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0005 | 0/0 | 10083 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0006 | 0/0 | 7917 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0007 | 0/0 | 4668 | 3 | 0 | 0 | 0 | 0 | 3 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0008 | 0/0 | 8961 | 3 | 0 | 0 | 3 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0009 | 0/0 | 11127 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0010 | 0/0 | 11166 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0011 | 0/0 | 10441 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0012 | 0/0 | 8961 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0013 | 0/0 | 6834 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0014 | 0/0 | 7917 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0015 | 0/0 | 9000 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0016 | 0/0 | 9000 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0017 | 0/0 | 7917 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0018 | 0/0 | 7917 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0019 | 0/0 | 9358 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0020 | 0/0 | 11813 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0021 | 0/0 | 11813 | 2 | 0 | 0 | 1 | 1 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0022 | 0/0 | 9647 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0023 | 0/0 | 11813 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0024 | 0/0 | 8961 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0025 | 0/0 | 14376 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0026 | 0/0 | 10044 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0027 | 0/0 | 8961 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0028 | 0/0 | 8961 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0029 | 0/0 | 12210 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0030 | 0/0 | 10044 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0031 | 0/0 | 11127 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0032 | 0/0 | 11127 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0033 | 0/0 | 13332 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0034 | 0/0 | 12249 | 2 | 0 | 0 | 0 | 1 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0035 | 0/0 | 9000 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0036 | 0/0 | 4668 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0037 | 0/0 | 6996 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0038 | 0/0 | 11166 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0039 | 0/0 | 11166 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0040 | 0/0 | 10083 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0041 | 0/0 | 10083 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0042 | 0/0 | 10083 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0043 | 0/0 | 8961 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0044 | 0/0 | 11524 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0045 | 0/0 | 9358 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0046 | 0/0 | 7595 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0047 | 0/0 | 10441 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0048 | 0/0 | 10083 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0049 | 0/0 | 9000 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0050 | 0/0 | 10044 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0051 | 0/0 | 11813 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0052 | 0/0 | 11127 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0053 | 0/0 | 11127 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0054 | 0/0 | 7917 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0055 | 0/0 | 5751 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0056 | 0/0 | 7917 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0057 | 0/0 | 7917 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0058 | 0/0 | 7917 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0059 | 0/0 | 11166 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0060 | 0/0 | 7917 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0061 | 0/0 | 6815 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0062 | 0/0 | 7917 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0063 | 0/0 | 7666 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0064 | 0/0 | 7917 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0065 | 0/0 | 6834 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0066 | 0/0 | 6834 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0067 | 0/0 | 7917 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0068 | 0/0 | 7917 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0069 | 0/0 | 3778 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0070 | 0/0 | 6834 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0071 | 0/0 | 7917 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0072 | 0/0 | 6834 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0073 | 0/0 | 7917 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0074 | 0/0 | 7917 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0075 | 0/0 | 7917 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0076 | 0/0 | 9000 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0077 | 0/0 | 9000 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0078 | 0/0 | 9000 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0079 | 0/0 | 7917 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0080 | 0/0 | 7917 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0081 | 0/0 | 9000 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0082 | 0/0 | 9000 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0083 | 0/0 | 13690 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0084 | 0/0 | 11813 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0085 | 0/0 | 11813 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0086 | 0/0 | 15351 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0087 | 0/0 | 9647 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0088 | 0/0 | 10044 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0089 | 0/0 | 8961 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0090 | 0/0 | 5332 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0091 | 0/0 | 14773 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0092 | 0/0 | 10441 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0093 | 0/0 | 8961 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0094 | 0/0 | 12607 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0095 | 0/0 | 10441 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0096 | 0/0 | 15748 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0097 | 0/0 | 10044 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0098 | 0/0 | 11127 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0099 | 0/0 | 13582 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0100 | 0/0 | 11813 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0101 | 0/0 | 11813 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0102 | 0/0 | 11813 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0103 | 0/0 | 10730 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0104 | 0/0 | 11813 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0105 | 0/0 | 11813 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0106 | 0/0 | 11813 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0107 | 0/0 | 13582 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0108 | 0/0 | 11813 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0109 | 0/0 | 11813 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0110 | 0/0 | 11813 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0111 | 0/0 | 11813 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0112 | 0/0 | 11813 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0113 | 0/0 | 11813 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0114 | 0/0 | 13582 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0115 | 0/0 | 11127 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0116 | 0/0 | 11813 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0117 | 0/0 | 11813 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0118 | 0/0 | 15748 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0119 | 0/0 | 16939 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0120 | 0/0 | 14376 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0121 | 0/0 | 17625 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0122 | 0/0 | 13293 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0123 | 0/0 | 13293 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0124 | 0/0 | 14376 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0125 | 0/0 | 13293 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0126 | 0/0 | 15459 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0127 | 0/0 | 17228 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0128 | 0/0 | 7192 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0129 | 0/0 | 5026 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0130 | 0/0 | 10441 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0131 | 0/0 | 11524 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0132 | 0/0 | 8275 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0133 | 0/0 | 9358 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0134 | 0/0 | 8961 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0135 | 0/0 | 10044 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0136 | 0/0 | 10044 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0137 | 0/0 | 12210 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0138 | 0/0 | 11127 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0139 | 0/0 | 11813 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0140 | 0/0 | 11127 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0141 | 0/0 | 10044 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0142 | 0/0 | 8961 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0143 | 0/0 | 8961 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0144 | 0/0 | 10044 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0145 | 0/0 | 11127 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0146 | 0/0 | 10044 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0147 | 0/0 | 10044 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0148 | 0/0 | 10044 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0149 | 0/0 | 8961 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0150 | 0/0 | 8961 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0151 | 0/0 | 10044 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0152 | 0/0 | 10044 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0153 | 0/0 | 10044 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0154 | 0/0 | 10044 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0155 | 0/0 | 10044 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0156 | 0/0 | 11127 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0157 | 0/0 | 11127 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0158 | 0/0 | 10044 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0159 | 0/0 | 10044 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0160 | 0/0 | 11127 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0161 | 0/0 | 10044 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0162 | 0/0 | 10044 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0163 | 0/0 | 10044 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0164 | 0/0 | 10044 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0165 | 0/0 | 10044 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0166 | 0/0 | 10044 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0167 | 0/0 | 9212 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0168 | 0/0 | 7878 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0169 | 0/0 | 11127 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0170 | 0/0 | 8961 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0171 | 0/0 | 8961 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0172 | 0/0 | 12538 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0173 | 0/0 | 11813 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0174 | 0/0 | 2548 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0175 | 0/0 | 6834 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0176 | 0/0 | 12249 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0177 | 0/0 | 14415 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0178 | 0/0 | 10083 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0179 | 0/0 | 12249 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0180 | 0/0 | 12249 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0181 | 0/0 | 10083 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0182 | 0/0 | 11166 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0183 | 0/0 | 11166 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0184 | 0/0 | 10083 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0185 | 0/0 | 10083 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0186 | 0/0 | 12249 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0187 | 0/0 | 13332 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0188 | 0/0 | 14415 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0189 | 0/0 | 12249 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0190 | 0/0 | 12249 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0191 | 0/0 | 11166 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0192 | 0/0 | 11914 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0193 | 0/0 | 13332 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0194 | 0/0 | 12249 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0195 | 0/0 | 10083 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0196 | 0/0 | 13332 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0197 | 0/0 | 13332 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0198 | 0/0 | 11166 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0199 | 0/0 | 13332 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0200 | 0/0 | 6834 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0201 | 0/0 | 12249 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0202 | 0/0 | 11166 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0203 | 0/0 | 7917 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0204 | 0/0 | 11166 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0205 | 0/0 | 11166 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0206 | 0/0 | 4668 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0207 | 0/0 | 4668 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0208 | 0/0 | 10083 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0209 | 0/0 | 10083 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0210 | 0/0 | 10083 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0211 | 0/0 | 9000 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0212 | 1/0 | 5335 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0213 | 0/0 | 11166 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0214 | 0/0 | 12249 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0215 | 0/0 | 11166 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0216 | 0/0 | 10083 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0217 | 0/0 | 11166 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0218 | 0/0 | 11166 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0219 | 0/0 | 10245 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0220 | 0/0 | 9162 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0221 | 0/0 | 13332 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0222 | 0/0 | 11166 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0223 | 0/0 | 11166 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0224 | 0/0 | 12249 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0225 | 0/0 | 11166 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0226 | 0/0 | 8079 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0227 | 0/0 | 11166 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0228 | 0/0 | 10083 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0229 | 0/0 | 7917 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0230 | 0/0 | 10083 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0231 | 0/0 | 10083 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0232 | 0/0 | 10083 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0233 | 0/0 | 9000 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0234 | 0/0 | 4988 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0235 | 0/0 | 10083 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0236 | 0/0 | 10083 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0237 | 0/0 | 10083 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0238 | 0/0 | 10083 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0239 | 0/0 | 10083 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0240 | 0/0 | 11891 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0241 | 0/0 | 10083 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0242 | 0/0 | 10083 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0243 | 0/0 | 11166 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0244 | 0/0 | 7582 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0245 | 0/0 | 7917 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0246 | 0/0 | 9000 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0247 | 0/0 | 10083 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0248 | 0/0 | 2986 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0249 | 0/0 | 9000 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0250 | 0/0 | 10083 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0251 | 0/0 | 9000 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0252 | 0/1 | 8079 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0253 | 0/0 | 8079 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0254 | 0/0 | 8079 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0255 | 0/0 | 8079 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0256 | 0/0 | 10083 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0257 | 0/0 | 10044 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0258 | 0/0 | 10083 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0259 | 0/0 | 11166 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0260 | 0/0 | 11166 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0261 | 0/0 | 13332 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0262 | 0/0 | 14415 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0263 | 0/0 | 13332 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0264 | 0/0 | 13332 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0265 | 0/0 | 14415 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0266 | 0/0 | 13332 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0267 | 0/0 | 11166 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0268 | 0/0 | 12249 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0269 | 0/0 | 11166 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0270 | 0/0 | 11166 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0271 | 0/0 | 14415 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0272 | 0/0 | 12249 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 30135 | 7 | 0 | 0 | 7 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0002 | 0/0 | 23754 | 5 | 0 | 0 | 5 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0003 | 0/0 | 30252 | 4 | 0 | 0 | 4 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0004 | 0/0 | 23754 | 4 | 0 | 0 | 4 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0005 | 0/0 | 33501 | 3 | 0 | 3 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0006 | 0/0 | 33384 | 3 | 0 | 3 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0007 | 0/0 | 23754 | 3 | 0 | 3 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0008 | 0/0 | 14007 | 3 | 0 | 0 | 0 | 0 | 3 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0009 | 0/0 | 31326 | 2 | 0 | 2 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0010 | 0/0 | 36750 | 2 | 0 | 0 | 0 | 1 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0011 | 0/0 | 39999 | 2 | 2 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0012 | 0/0 | 14007 | 2 | 2 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0013 | 0/0 | 14007 | 2 | 2 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0014 | 0/0 | 14007 | 2 | 2 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0015 | 0/0 | 33501 | 2 | 0 | 1 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0016 | 0/0 | 33501 | 2 | 0 | 2 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0017 | 0/0 | 30252 | 2 | 0 | 2 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0018 | 0/0 | 30252 | 2 | 0 | 0 | 0 | 0 | 2 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0019 | 0/0 | 30252 | 2 | 0 | 0 | 2 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0020 | 0/0 | 27003 | 2 | 0 | 0 | 2 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0021 | 0/0 | 26886 | 2 | 2 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0022 | 0/0 | 35442 | 2 | 0 | 0 | 1 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0023 | 0/0 | 35442 | 2 | 0 | 0 | 2 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0024 | 0/0 | 35442 | 2 | 0 | 0 | 0 | 0 | 2 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0025 | 0/0 | 28944 | 2 | 0 | 2 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0026 | 0/0 | 33384 | 2 | 0 | 2 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0027 | 0/0 | 30135 | 2 | 1 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0028 | 0/0 | 26886 | 2 | 0 | 0 | 2 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0029 | 0/0 | 36633 | 2 | 0 | 0 | 0 | 0 | 2 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0030 | 0/0 | 26886 | 2 | 2 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0031 | 0/0 | 26886 | 2 | 2 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0032 | 0/0 | 43131 | 2 | 2 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0033 | 0/0 | 28077 | 2 | 0 | 0 | 2 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0034 | 0/0 | 23754 | 2 | 0 | 2 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0035 | 0/0 | 27003 | 2 | 0 | 2 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0036 | 0/0 | 23754 | 2 | 2 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0037 | 0/0 | 20505 | 2 | 0 | 0 | 2 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0038 | 0/0 | 23754 | 2 | 0 | 0 | 2 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0039 | 0/0 | 23754 | 2 | 0 | 0 | 2 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0040 | 0/0 | 26886 | 2 | 0 | 0 | 2 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0041 | 0/0 | 36750 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0042 | 0/0 | 34575 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0043 | 0/0 | 31326 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0044 | 0/0 | 28077 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0045 | 0/0 | 31326 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0046 | 0/0 | 30252 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0047 | 0/0 | 27003 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0048 | 0/0 | 30135 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0049 | 0/0 | 20505 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0050 | 0/0 | 36750 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0051 | 0/0 | 39998 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0052 | 0/0 | 33501 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0053 | 0/0 | 39999 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0054 | 0/0 | 36750 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0055 | 0/0 | 33501 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0056 | 0/0 | 39999 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0057 | 0/0 | 30252 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0058 | 0/0 | 36750 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0059 | 0/0 | 39999 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0060 | 0/0 | 39999 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0061 | 0/0 | 30252 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0062 | 0/0 | 33501 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0063 | 0/0 | 33501 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0064 | 0/0 | 30252 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0065 | 0/0 | 36750 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0066 | 0/0 | 30252 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0067 | 0/0 | 36750 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0068 | 0/0 | 30252 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0069 | 0/0 | 43248 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0070 | 0/0 | 39999 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0071 | 0/0 | 36750 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0072 | 0/0 | 43248 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0073 | 0/0 | 36750 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0074 | 0/0 | 36750 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0075 | 0/0 | 30252 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0076 | 0/0 | 30252 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0077 | 0/0 | 14007 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0078 | 0/0 | 14007 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0079 | 0/0 | 14007 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0080 | 0/0 | 27003 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0081 | 0/0 | 30252 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0082 | 0/0 | 30252 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0083 | 0/0 | 30252 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0084 | 0/0 | 30252 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0085 | 0/0 | 33501 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0086 | 0/0 | 33501 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0087 | 0/0 | 36750 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0088 | 0/0 | 39999 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0089 | 0/0 | 33501 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0090 | 0/0 | 39999 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0091 | 0/0 | 33501 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0092 | 0/0 | 36750 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0093 | 0/0 | 33501 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0094 | 0/0 | 33501 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0095 | 0/0 | 33501 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0096 | 0/0 | 33501 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0097 | 0/0 | 33501 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0098 | 0/0 | 36750 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0099 | 1/0 | 16008 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0100 | 0/0 | 30252 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0101 | 0/0 | 23754 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0102 | 0/0 | 30252 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0103 | 0/0 | 30252 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0104 | 0/0 | 30252 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0105 | 0/0 | 30252 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0106 | 0/0 | 30252 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0107 | 0/0 | 30252 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0108 | 0/0 | 35676 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0109 | 0/0 | 33501 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0110 | 0/0 | 30252 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0111 | 0/0 | 30252 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0112 | 0/0 | 23754 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0113 | 0/0 | 27003 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0114 | 0/0 | 30252 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0115 | 0/0 | 30252 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0116 | 0/0 | 30252 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0117 | 0/0 | 30252 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0118 | 0/0 | 30252 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0119 | 0/0 | 27003 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0120 | 0/0 | 30252 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0121 | 0/0 | 36751 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0122 | 0/0 | 27003 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0123 | 0/0 | 27003 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0124 | 0/0 | 33501 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0125 | 0/0 | 33501 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0126 | 0/0 | 33501 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0127 | 0/1 | 33501 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0128 | 0/0 | 33501 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0129 | 0/0 | 33501 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0130 | 0/0 | 30252 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0131 | 0/0 | 23754 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0132 | 0/0 | 33501 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0133 | 0/0 | 20505 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0134 | 0/0 | 35442 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0135 | 0/0 | 37617 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0136 | 0/0 | 26886 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0137 | 0/0 | 26886 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0138 | 0/0 | 28944 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0139 | 0/0 | 23637 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0140 | 0/0 | 44322 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0141 | 0/0 | 31326 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0142 | 0/0 | 26886 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0143 | 0/0 | 47247 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0144 | 0/0 | 30135 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0145 | 0/0 | 35442 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0146 | 0/0 | 35442 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0147 | 0/0 | 33384 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0148 | 0/0 | 40749 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0149 | 0/0 | 35442 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0150 | 0/0 | 32193 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0151 | 0/0 | 40749 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0152 | 0/0 | 35442 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0153 | 0/0 | 35442 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0154 | 0/0 | 35442 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0155 | 0/0 | 35442 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0156 | 0/0 | 35442 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0157 | 0/0 | 35442 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0158 | 0/0 | 35442 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0159 | 0/0 | 35442 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0160 | 0/0 | 35442 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0161 | 0/0 | 40749 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0162 | 0/0 | 33384 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0163 | 0/0 | 35442 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0164 | 0/0 | 35442 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0165 | 0/0 | 33384 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0166 | 0/0 | 30135 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0167 | 0/0 | 35442 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0168 | 0/0 | 30135 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0169 | 0/0 | 33384 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0170 | 0/0 | 33384 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0171 | 0/0 | 33384 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0172 | 0/0 | 30135 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0173 | 0/0 | 30135 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0174 | 0/0 | 30135 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0175 | 0/0 | 30135 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0176 | 0/0 | 30135 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0177 | 0/0 | 30135 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0178 | 0/0 | 30135 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0179 | 0/0 | 30135 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0180 | 0/0 | 33384 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0181 | 0/0 | 30135 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0182 | 0/0 | 30135 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0183 | 0/0 | 30135 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0184 | 0/0 | 33384 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0185 | 0/0 | 26886 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0186 | 0/0 | 30135 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0187 | 0/0 | 30135 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0188 | 0/0 | 30135 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0189 | 0/0 | 33384 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0190 | 0/0 | 33384 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0191 | 0/0 | 30135 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0192 | 0/0 | 30135 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0193 | 0/0 | 30135 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0194 | 0/0 | 26886 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0195 | 0/0 | 26886 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0196 | 0/0 | 26886 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0197 | 0/0 | 30135 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0198 | 0/0 | 33384 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0199 | 0/0 | 36633 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0200 | 0/0 | 30135 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0201 | 0/0 | 26886 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0202 | 0/0 | 30135 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0203 | 0/0 | 28077 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0204 | 0/0 | 24828 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0205 | 0/0 | 26886 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0206 | 0/0 | 34575 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0207 | 0/0 | 31326 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0208 | 0/0 | 21579 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0209 | 0/0 | 15081 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0210 | 0/0 | 43131 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0211 | 0/0 | 51687 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0212 | 0/0 | 46380 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0213 | 0/0 | 39882 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0214 | 0/0 | 43131 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0215 | 0/0 | 39882 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0216 | 0/0 | 39882 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0217 | 0/0 | 52878 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0218 | 0/0 | 50820 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0219 | 0/0 | 27639 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0220 | 0/0 | 47247 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0221 | 0/0 | 31326 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0222 | 0/0 | 37824 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0223 | 0/0 | 30135 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0224 | 0/0 | 26886 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0225 | 0/0 | 30135 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0226 | 0/0 | 30135 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0227 | 0/0 | 35442 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0228 | 0/0 | 46056 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0229 | 0/0 | 35442 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0230 | 0/0 | 41073 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0231 | 0/0 | 30135 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0232 | 0/0 | 23754 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0233 | 0/0 | 27003 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0234 | 0/0 | 23754 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0235 | 0/0 | 27003 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0236 | 0/0 | 23754 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0237 | 0/0 | 23754 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0238 | 0/0 | 27003 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0239 | 0/0 | 27003 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0240 | 0/0 | 27003 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0241 | 0/0 | 23754 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0242 | 0/0 | 27003 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0243 | 0/0 | 23754 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0244 | 0/0 | 23754 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0245 | 0/0 | 23754 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0246 | 0/0 | 23754 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0247 | 0/0 | 20505 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0248 | 0/0 | 20505 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0249 | 0/0 | 23754 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0250 | 0/0 | 20505 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0251 | 0/0 | 20505 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0252 | 0/0 | 23754 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0253 | 0/0 | 23001 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0254 | 0/0 | 23754 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0255 | 0/0 | 23752 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0256 | 0/0 | 23754 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0257 | 0/0 | 23754 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0258 | 0/0 | 33501 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0259 | 0/0 | 23754 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0260 | 0/0 | 23754 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0261 | 0/0 | 23754 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0262 | 0/0 | 23754 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0263 | 0/0 | 27003 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0264 | 0/0 | 17256 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0265 | 0/0 | 23754 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0266 | 0/0 | 23754 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0267 | 0/0 | 33384 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0268 | 0/0 | 30134 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0269 | 0/0 | 33384 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0270 | 0/0 | 35442 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0271 | 0/0 | 30135 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0272 | 0/0 | 33501 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0273 | 0/0 | 33501 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0274 | 0/0 | 43248 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0275 | 0/0 | 39999 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0276 | 0/0 | 39999 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0277 | 0/0 | 39999 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0278 | 0/0 | 43248 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0279 | 0/0 | 30252 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0280 | 0/0 | 39999 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0281 | 0/0 | 43248 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0282 | 0/0 | 33501 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0283 | 0/0 | 36750 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0284 | 0/0 | 33501 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0285 | 0/0 | 33501 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| c0286 | 0/0 | 26886 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 359 | 339 | 90 | 74 | 117 | 14 | 43 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| t0002 | 0/0 | 359 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| t0003 | 0/0 | 359 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| t0004 | 1/0 | 359 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 15 | 0 | 7 | 8 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0002 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0009 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0011 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0012 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0021 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0089 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 30135 | 7 | 0 | 0 | 7 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0001c0168 | 0/0 | 30135 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0001c0181 | 0/0 | 30135 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0002c0004 | 0/0 | 23754 | 4 | 0 | 0 | 4 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0002c0007 | 0/0 | 23754 | 3 | 0 | 3 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0002c0245 | 0/0 | 23754 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0003c0002 | 0/0 | 23754 | 5 | 0 | 0 | 5 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0003c0254 | 0/0 | 23754 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0003c0261 | 0/0 | 23754 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0004c0012 | 0/0 | 14007 | 2 | 2 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0004c0013 | 0/0 | 14007 | 2 | 2 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0004c0079 | 0/0 | 14007 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0005c0003 | 0/0 | 30252 | 4 | 0 | 0 | 4 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0006c0038 | 0/0 | 23754 | 2 | 0 | 0 | 2 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0006c0256 | 0/0 | 23754 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0007c0008 | 0/0 | 14007 | 3 | 0 | 0 | 0 | 0 | 3 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0008c0028 | 0/0 | 26886 | 2 | 0 | 0 | 2 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0008c0205 | 0/0 | 26886 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0009c0006 | 0/0 | 33384 | 3 | 0 | 3 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0010c0005 | 0/0 | 33501 | 3 | 0 | 3 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0011c0009 | 0/0 | 31326 | 2 | 0 | 2 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0012c0040 | 0/0 | 26886 | 2 | 0 | 0 | 2 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0013c0037 | 0/0 | 20505 | 2 | 0 | 0 | 2 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0014c0036 | 0/0 | 23754 | 2 | 2 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0015c0240 | 0/0 | 27003 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0015c0242 | 0/0 | 27003 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0016c0035 | 0/0 | 27003 | 2 | 0 | 2 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0017c0034 | 0/0 | 23754 | 2 | 0 | 2 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0018c0039 | 0/0 | 23754 | 2 | 0 | 0 | 2 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0019c0033 | 0/0 | 28077 | 2 | 0 | 0 | 2 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0020c0023 | 0/0 | 35442 | 2 | 0 | 0 | 2 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0021c0022 | 0/0 | 35442 | 2 | 0 | 0 | 1 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0022c0025 | 0/0 | 28944 | 2 | 0 | 2 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0023c0024 | 0/0 | 35442 | 2 | 0 | 0 | 0 | 0 | 2 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0024c0021 | 0/0 | 26886 | 2 | 2 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0025c0032 | 0/0 | 43131 | 2 | 2 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0026c0202 | 0/0 | 30135 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0026c0231 | 0/0 | 30135 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0027c0031 | 0/0 | 26886 | 2 | 2 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0028c0030 | 0/0 | 26886 | 2 | 2 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0029c0029 | 0/0 | 36633 | 2 | 0 | 0 | 0 | 0 | 2 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0030c0027 | 0/0 | 30135 | 2 | 1 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0031c0026 | 0/0 | 33384 | 2 | 0 | 2 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0032c0170 | 0/0 | 33384 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0032c0171 | 0/0 | 33384 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0033c0011 | 0/0 | 39999 | 2 | 2 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0034c0010 | 0/0 | 36750 | 2 | 0 | 0 | 0 | 1 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0035c0020 | 0/0 | 27003 | 2 | 0 | 0 | 2 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0036c0014 | 0/0 | 14007 | 2 | 2 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0037c0017 | 0/0 | 30252 | 2 | 0 | 2 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0038c0016 | 0/0 | 33501 | 2 | 0 | 2 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0039c0015 | 0/0 | 33501 | 2 | 0 | 1 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0040c0018 | 0/0 | 30252 | 2 | 0 | 0 | 0 | 0 | 2 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0041c0019 | 0/0 | 30252 | 2 | 0 | 0 | 2 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0042c0117 | 0/0 | 30252 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0042c0118 | 0/0 | 30252 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0043c0286 | 0/0 | 26886 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0044c0042 | 0/0 | 34575 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0045c0044 | 0/0 | 28077 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0046c0045 | 0/0 | 31326 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0047c0043 | 0/0 | 31326 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0048c0046 | 0/0 | 30252 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0049c0047 | 0/0 | 27003 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0050c0271 | 0/0 | 30135 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0051c0270 | 0/0 | 35442 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0052c0269 | 0/0 | 33384 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0053c0267 | 0/0 | 33384 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0054c0266 | 0/0 | 23754 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0055c0264 | 0/0 | 17256 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0056c0262 | 0/0 | 23754 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0057c0232 | 0/0 | 23754 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0058c0259 | 0/0 | 23754 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0059c0258 | 0/0 | 33501 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0060c0257 | 0/0 | 23754 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0061c0255 | 0/0 | 23752 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0062c0260 | 0/0 | 23754 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0063c0253 | 0/0 | 23001 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0064c0234 | 0/0 | 23754 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0065c0248 | 0/0 | 20505 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0066c0247 | 0/0 | 20505 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0067c0249 | 0/0 | 23754 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0068c0244 | 0/0 | 23754 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0069c0243 | 0/0 | 23754 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0070c0250 | 0/0 | 20505 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0071c0241 | 0/0 | 23754 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0072c0251 | 0/0 | 20505 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0073c0246 | 0/0 | 23754 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0074c0252 | 0/0 | 23754 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0075c0265 | 0/0 | 23754 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0076c0239 | 0/0 | 27003 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0077c0238 | 0/0 | 27003 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0078c0235 | 0/0 | 27003 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0079c0237 | 0/0 | 23754 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0080c0236 | 0/0 | 23754 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0081c0263 | 0/0 | 27003 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0082c0233 | 0/0 | 27003 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0083c0230 | 0/0 | 41073 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0084c0227 | 0/0 | 35442 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0085c0229 | 0/0 | 35442 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0086c0228 | 0/0 | 46056 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0087c0138 | 0/0 | 28944 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0088c0225 | 0/0 | 30135 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0089c0224 | 0/0 | 26886 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0090c0223 | 0/0 | 30135 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0091c0140 | 0/0 | 44322 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0092c0141 | 0/0 | 31326 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0093c0142 | 0/0 | 26886 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0094c0222 | 0/0 | 37824 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0095c0221 | 0/0 | 31326 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0096c0220 | 0/0 | 47247 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0097c0144 | 0/0 | 30135 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0098c0147 | 0/0 | 33384 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0099c0148 | 0/0 | 40749 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0100c0157 | 0/0 | 35442 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0101c0156 | 0/0 | 35442 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0102c0155 | 0/0 | 35442 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0103c0150 | 0/0 | 32193 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0104c0154 | 0/0 | 35442 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0105c0153 | 0/0 | 35442 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0106c0152 | 0/0 | 35442 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0107c0151 | 0/0 | 40749 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0108c0149 | 0/0 | 35442 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0109c0164 | 0/0 | 35442 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0110c0163 | 0/0 | 35442 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0111c0160 | 0/0 | 35442 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0112c0159 | 0/0 | 35442 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0113c0158 | 0/0 | 35442 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0114c0161 | 0/0 | 40749 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0115c0162 | 0/0 | 33384 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0116c0145 | 0/0 | 35442 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0117c0146 | 0/0 | 35442 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0118c0143 | 0/0 | 47247 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0119c0218 | 0/0 | 50820 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0120c0210 | 0/0 | 43131 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0121c0217 | 0/0 | 52878 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0122c0216 | 0/0 | 39882 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0123c0215 | 0/0 | 39882 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0124c0214 | 0/0 | 43131 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0125c0213 | 0/0 | 39882 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0126c0212 | 0/0 | 46380 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0127c0211 | 0/0 | 51687 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0128c0208 | 0/0 | 21579 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0129c0209 | 0/0 | 15081 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0130c0207 | 0/0 | 31326 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0131c0206 | 0/0 | 34575 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0132c0204 | 0/0 | 24828 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0133c0203 | 0/0 | 28077 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0134c0201 | 0/0 | 26886 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0135c0200 | 0/0 | 30135 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0136c0166 | 0/0 | 30135 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0137c0199 | 0/0 | 36633 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0138c0198 | 0/0 | 33384 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0139c0167 | 0/0 | 35442 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0140c0169 | 0/0 | 33384 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0141c0197 | 0/0 | 30135 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0142c0194 | 0/0 | 26886 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0143c0195 | 0/0 | 26886 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0144c0191 | 0/0 | 30135 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0145c0189 | 0/0 | 33384 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0146c0188 | 0/0 | 30135 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0147c0187 | 0/0 | 30135 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0148c0226 | 0/0 | 30135 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0149c0185 | 0/0 | 26886 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0150c0196 | 0/0 | 26886 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0151c0186 | 0/0 | 30135 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0152c0176 | 0/0 | 30135 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0153c0183 | 0/0 | 30135 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0154c0173 | 0/0 | 30135 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0155c0182 | 0/0 | 30135 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0156c0184 | 0/0 | 33384 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0157c0180 | 0/0 | 33384 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0158c0179 | 0/0 | 30135 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0159c0178 | 0/0 | 30135 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0160c0190 | 0/0 | 33384 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0161c0177 | 0/0 | 30135 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0162c0174 | 0/0 | 30135 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0163c0175 | 0/0 | 30135 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0164c0192 | 0/0 | 30135 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0165c0193 | 0/0 | 30135 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0166c0172 | 0/0 | 30135 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0167c0219 | 0/0 | 27639 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0168c0139 | 0/0 | 23637 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0169c0165 | 0/0 | 33384 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0170c0137 | 0/0 | 26886 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0171c0136 | 0/0 | 26886 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0172c0135 | 0/0 | 37617 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0173c0134 | 0/0 | 35442 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0174c0268 | 0/0 | 30134 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0175c0133 | 0/0 | 20505 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0176c0073 | 0/0 | 36750 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0177c0072 | 0/0 | 43248 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0178c0068 | 0/0 | 30252 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0179c0071 | 0/0 | 36750 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0180c0067 | 0/0 | 36750 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0181c0066 | 0/0 | 30252 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0182c0063 | 0/0 | 33501 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0183c0062 | 0/0 | 33501 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0184c0064 | 0/0 | 30252 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0185c0061 | 0/0 | 30252 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0186c0065 | 0/0 | 36750 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0187c0060 | 0/0 | 39999 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0188c0069 | 0/0 | 43248 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0189c0058 | 0/0 | 36750 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0190c0050 | 0/0 | 36750 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0191c0052 | 0/0 | 33501 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0192c0051 | 0/0 | 39998 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0193c0053 | 0/0 | 39999 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0194c0054 | 0/0 | 36750 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0195c0057 | 0/0 | 30252 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0196c0056 | 0/0 | 39999 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0197c0059 | 0/0 | 39999 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0198c0055 | 0/0 | 33501 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0199c0070 | 0/0 | 39999 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0200c0049 | 0/0 | 20505 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0201c0074 | 0/0 | 36750 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0202c0132 | 0/0 | 33501 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0203c0131 | 0/0 | 23754 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0204c0128 | 0/0 | 33501 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0205c0129 | 0/0 | 33501 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0206c0077 | 0/0 | 14007 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0207c0078 | 0/0 | 14007 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0208c0083 | 0/0 | 30252 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0209c0082 | 0/0 | 30252 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0210c0081 | 0/0 | 30252 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0211c0080 | 0/0 | 27003 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0212c0099 | 1/0 | 16008 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0213c0097 | 0/0 | 33501 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0214c0098 | 0/0 | 36750 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0215c0096 | 0/0 | 33501 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0216c0084 | 0/0 | 30252 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0217c0085 | 0/0 | 33501 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0218c0086 | 0/0 | 33501 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0219c0088 | 0/0 | 39999 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0220c0087 | 0/0 | 36750 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0221c0090 | 0/0 | 39999 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0222c0094 | 0/0 | 33501 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0223c0091 | 0/0 | 33501 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0224c0092 | 0/0 | 36750 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0225c0093 | 0/0 | 33501 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0226c0089 | 0/0 | 33501 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0227c0095 | 0/0 | 33501 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0228c0100 | 0/0 | 30252 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0229c0101 | 0/0 | 23754 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0230c0102 | 0/0 | 30252 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0231c0120 | 0/0 | 30252 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0232c0075 | 0/0 | 30252 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0233c0119 | 0/0 | 27003 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0234c0107 | 0/0 | 30252 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0235c0105 | 0/0 | 30252 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0236c0106 | 0/0 | 30252 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0237c0104 | 0/0 | 30252 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0238c0103 | 0/0 | 30252 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0239c0115 | 0/0 | 30252 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0240c0108 | 0/0 | 35676 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0241c0111 | 0/0 | 30252 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0242c0110 | 0/0 | 30252 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0243c0109 | 0/0 | 33501 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0244c0116 | 0/0 | 30252 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0245c0112 | 0/0 | 23754 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0246c0113 | 0/0 | 27003 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0247c0114 | 0/0 | 30252 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0248c0121 | 0/0 | 36751 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0249c0123 | 0/0 | 27003 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0250c0130 | 0/0 | 30252 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0251c0122 | 0/0 | 27003 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0252c0127 | 0/1 | 33501 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0253c0126 | 0/0 | 33501 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0254c0125 | 0/0 | 33501 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0255c0124 | 0/0 | 33501 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0256c0076 | 0/0 | 30252 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0257c0048 | 0/0 | 30135 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0258c0279 | 0/0 | 30252 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0259c0272 | 0/0 | 33501 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0260c0273 | 0/0 | 33501 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0261c0280 | 0/0 | 39999 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0262c0274 | 0/0 | 43248 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0263c0275 | 0/0 | 39999 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0264c0276 | 0/0 | 39999 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0265c0278 | 0/0 | 43248 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0266c0277 | 0/0 | 39999 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0267c0285 | 0/0 | 33501 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0268c0283 | 0/0 | 36750 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0269c0284 | 0/0 | 33501 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0270c0282 | 0/0 | 33501 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0271c0281 | 0/0 | 43248 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0272c0041 | 0/0 | 36750 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 30493 | 7 | 0 | 0 | 7 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0001c0168t0001 | 0/0 | 30493 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0001c0181t0001 | 0/0 | 30493 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0002c0004t0001 | 0/0 | 24112 | 4 | 0 | 0 | 4 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0002c0007t0001 | 0/0 | 24112 | 3 | 0 | 3 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0002c0245t0001 | 0/0 | 24112 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0003c0002t0001 | 0/0 | 24112 | 5 | 0 | 0 | 5 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0003c0254t0001 | 0/0 | 24112 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0003c0261t0001 | 0/0 | 24112 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0004c0012t0001 | 0/0 | 14365 | 2 | 2 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0004c0013t0001 | 0/0 | 14365 | 2 | 2 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0004c0079t0001 | 0/0 | 14365 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0005c0003t0001 | 0/0 | 30610 | 4 | 0 | 0 | 4 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0006c0038t0001 | 0/0 | 24112 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0006c0038t0003 | 0/0 | 24112 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0006c0256t0001 | 0/0 | 24112 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0007c0008t0001 | 0/0 | 14365 | 3 | 0 | 0 | 0 | 0 | 3 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0008c0028t0001 | 0/0 | 27244 | 2 | 0 | 0 | 2 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0008c0205t0001 | 0/0 | 27244 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0009c0006t0001 | 0/0 | 33742 | 3 | 0 | 3 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0010c0005t0001 | 0/0 | 33859 | 3 | 0 | 3 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0011c0009t0001 | 0/0 | 31684 | 2 | 0 | 2 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0012c0040t0001 | 0/0 | 27244 | 2 | 0 | 0 | 2 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0013c0037t0001 | 0/0 | 20863 | 2 | 0 | 0 | 2 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0014c0036t0001 | 0/0 | 24112 | 2 | 2 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0015c0240t0001 | 0/0 | 27361 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0015c0242t0001 | 0/0 | 27361 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0016c0035t0001 | 0/0 | 27361 | 2 | 0 | 2 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0017c0034t0001 | 0/0 | 24112 | 2 | 0 | 2 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0018c0039t0001 | 0/0 | 24112 | 2 | 0 | 0 | 2 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0019c0033t0001 | 0/0 | 28435 | 2 | 0 | 0 | 2 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0020c0023t0001 | 0/0 | 35800 | 2 | 0 | 0 | 2 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0021c0022t0001 | 0/0 | 35800 | 2 | 0 | 0 | 1 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0022c0025t0001 | 0/0 | 29302 | 2 | 0 | 2 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0023c0024t0001 | 0/0 | 35800 | 2 | 0 | 0 | 0 | 0 | 2 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0024c0021t0001 | 0/0 | 27244 | 2 | 2 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0025c0032t0001 | 0/0 | 43489 | 2 | 2 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0026c0202t0001 | 0/0 | 30493 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0026c0231t0001 | 0/0 | 30493 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0027c0031t0001 | 0/0 | 27244 | 2 | 2 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0028c0030t0001 | 0/0 | 27244 | 2 | 2 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0029c0029t0001 | 0/0 | 36991 | 2 | 0 | 0 | 0 | 0 | 2 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0030c0027t0001 | 0/0 | 30493 | 2 | 1 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0031c0026t0001 | 0/0 | 33742 | 2 | 0 | 2 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0032c0170t0001 | 0/0 | 33742 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0032c0171t0001 | 0/0 | 33742 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0033c0011t0001 | 0/0 | 40357 | 2 | 2 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0034c0010t0001 | 0/0 | 37108 | 2 | 0 | 0 | 0 | 1 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0035c0020t0001 | 0/0 | 27361 | 2 | 0 | 0 | 2 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0036c0014t0001 | 0/0 | 14365 | 2 | 2 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0037c0017t0001 | 0/0 | 30610 | 2 | 0 | 2 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0038c0016t0001 | 0/0 | 33859 | 2 | 0 | 2 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0039c0015t0001 | 0/0 | 33859 | 2 | 0 | 1 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0040c0018t0001 | 0/0 | 30610 | 2 | 0 | 0 | 0 | 0 | 2 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0041c0019t0001 | 0/0 | 30610 | 2 | 0 | 0 | 2 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0042c0117t0001 | 0/0 | 30610 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0042c0118t0001 | 0/0 | 30610 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0043c0286t0001 | 0/0 | 27244 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0044c0042t0001 | 0/0 | 34933 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0045c0044t0001 | 0/0 | 28435 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0046c0045t0001 | 0/0 | 31684 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0047c0043t0001 | 0/0 | 31684 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0048c0046t0001 | 0/0 | 30610 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0049c0047t0001 | 0/0 | 27361 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0050c0271t0001 | 0/0 | 30493 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0051c0270t0001 | 0/0 | 35800 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0052c0269t0001 | 0/0 | 33742 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0053c0267t0001 | 0/0 | 33742 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0054c0266t0001 | 0/0 | 24112 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0055c0264t0001 | 0/0 | 17614 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0056c0262t0001 | 0/0 | 24112 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0057c0232t0001 | 0/0 | 24112 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0058c0259t0001 | 0/0 | 24112 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0059c0258t0001 | 0/0 | 33859 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0060c0257t0001 | 0/0 | 24112 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0061c0255t0001 | 0/0 | 24110 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0062c0260t0001 | 0/0 | 24112 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0063c0253t0001 | 0/0 | 23359 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0064c0234t0001 | 0/0 | 24112 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0065c0248t0001 | 0/0 | 20863 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0066c0247t0001 | 0/0 | 20863 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0067c0249t0001 | 0/0 | 24112 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0068c0244t0001 | 0/0 | 24112 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0069c0243t0001 | 0/0 | 24112 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0070c0250t0001 | 0/0 | 20863 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0071c0241t0001 | 0/0 | 24112 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0072c0251t0001 | 0/0 | 20863 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0073c0246t0001 | 0/0 | 24112 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0074c0252t0001 | 0/0 | 24112 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0075c0265t0001 | 0/0 | 24112 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0076c0239t0001 | 0/0 | 27361 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0077c0238t0001 | 0/0 | 27361 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0078c0235t0001 | 0/0 | 27361 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0079c0237t0001 | 0/0 | 24112 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0080c0236t0001 | 0/0 | 24112 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0081c0263t0001 | 0/0 | 27361 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0082c0233t0001 | 0/0 | 27361 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0083c0230t0001 | 0/0 | 41431 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0084c0227t0001 | 0/0 | 35800 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0085c0229t0001 | 0/0 | 35800 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0086c0228t0001 | 0/0 | 46414 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0087c0138t0001 | 0/0 | 29302 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0088c0225t0001 | 0/0 | 30493 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0089c0224t0001 | 0/0 | 27244 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0090c0223t0001 | 0/0 | 30493 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0091c0140t0001 | 0/0 | 44680 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0092c0141t0001 | 0/0 | 31684 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0093c0142t0001 | 0/0 | 27244 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0094c0222t0001 | 0/0 | 38182 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0095c0221t0001 | 0/0 | 31684 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0096c0220t0001 | 0/0 | 47605 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0097c0144t0001 | 0/0 | 30493 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0098c0147t0001 | 0/0 | 33742 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0099c0148t0001 | 0/0 | 41107 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0100c0157t0001 | 0/0 | 35800 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0101c0156t0001 | 0/0 | 35800 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0102c0155t0001 | 0/0 | 35800 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0103c0150t0001 | 0/0 | 32551 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0104c0154t0001 | 0/0 | 35800 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0105c0153t0001 | 0/0 | 35800 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0106c0152t0001 | 0/0 | 35800 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0107c0151t0001 | 0/0 | 41107 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0108c0149t0001 | 0/0 | 35800 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0109c0164t0001 | 0/0 | 35800 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0110c0163t0001 | 0/0 | 35800 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0111c0160t0001 | 0/0 | 35800 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0112c0159t0001 | 0/0 | 35800 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0113c0158t0001 | 0/0 | 35800 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0114c0161t0001 | 0/0 | 41107 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0115c0162t0001 | 0/0 | 33742 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0116c0145t0001 | 0/0 | 35800 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0117c0146t0001 | 0/0 | 35800 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0118c0143t0001 | 0/0 | 47605 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0119c0218t0001 | 0/0 | 51178 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0120c0210t0001 | 0/0 | 43489 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0121c0217t0001 | 0/0 | 53236 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0122c0216t0001 | 0/0 | 40240 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0123c0215t0001 | 0/0 | 40240 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0124c0214t0001 | 0/0 | 43489 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0125c0213t0001 | 0/0 | 40240 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0126c0212t0001 | 0/0 | 46738 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0127c0211t0001 | 0/0 | 52045 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0128c0208t0001 | 0/0 | 21937 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0129c0209t0001 | 0/0 | 15439 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0130c0207t0001 | 0/0 | 31684 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0131c0206t0001 | 0/0 | 34933 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0132c0204t0001 | 0/0 | 25186 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0133c0203t0001 | 0/0 | 28435 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0134c0201t0001 | 0/0 | 27244 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0135c0200t0001 | 0/0 | 30493 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0136c0166t0001 | 0/0 | 30493 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0137c0199t0001 | 0/0 | 36991 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0138c0198t0001 | 0/0 | 33742 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0139c0167t0002 | 0/0 | 35800 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0140c0169t0001 | 0/0 | 33742 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0141c0197t0001 | 0/0 | 30493 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0142c0194t0001 | 0/0 | 27244 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0143c0195t0001 | 0/0 | 27244 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0144c0191t0001 | 0/0 | 30493 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0145c0189t0001 | 0/0 | 33742 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0146c0188t0001 | 0/0 | 30493 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0147c0187t0001 | 0/0 | 30493 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0148c0226t0001 | 0/0 | 30493 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0149c0185t0001 | 0/0 | 27244 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0150c0196t0001 | 0/0 | 27244 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0151c0186t0001 | 0/0 | 30493 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0152c0176t0001 | 0/0 | 30493 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0153c0183t0001 | 0/0 | 30493 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0154c0173t0001 | 0/0 | 30493 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0155c0182t0001 | 0/0 | 30493 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0156c0184t0001 | 0/0 | 33742 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0157c0180t0001 | 0/0 | 33742 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0158c0179t0001 | 0/0 | 30493 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0159c0178t0001 | 0/0 | 30493 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0160c0190t0001 | 0/0 | 33742 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0161c0177t0001 | 0/0 | 30493 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0162c0174t0001 | 0/0 | 30493 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0163c0175t0001 | 0/0 | 30493 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0164c0192t0001 | 0/0 | 30493 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0165c0193t0001 | 0/0 | 30493 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0166c0172t0001 | 0/0 | 30493 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0167c0219t0001 | 0/0 | 27997 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0168c0139t0001 | 0/0 | 23995 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0169c0165t0001 | 0/0 | 33742 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0170c0137t0001 | 0/0 | 27244 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0171c0136t0001 | 0/0 | 27244 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0172c0135t0001 | 0/0 | 37975 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0173c0134t0001 | 0/0 | 35800 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0174c0268t0001 | 0/0 | 30492 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0175c0133t0001 | 0/0 | 20863 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0176c0073t0001 | 0/0 | 37108 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0177c0072t0001 | 0/0 | 43606 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0178c0068t0001 | 0/0 | 30610 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0179c0071t0001 | 0/0 | 37108 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0180c0067t0001 | 0/0 | 37108 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0181c0066t0001 | 0/0 | 30610 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0182c0063t0001 | 0/0 | 33859 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0183c0062t0001 | 0/0 | 33859 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0184c0064t0001 | 0/0 | 30610 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0185c0061t0001 | 0/0 | 30610 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0186c0065t0001 | 0/0 | 37108 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0187c0060t0001 | 0/0 | 40357 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0188c0069t0001 | 0/0 | 43606 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0189c0058t0001 | 0/0 | 37108 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0190c0050t0001 | 0/0 | 37108 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0191c0052t0001 | 0/0 | 33859 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0192c0051t0001 | 0/0 | 40356 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0193c0053t0001 | 0/0 | 40357 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0194c0054t0001 | 0/0 | 37108 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0195c0057t0001 | 0/0 | 30610 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0196c0056t0001 | 0/0 | 40357 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0197c0059t0001 | 0/0 | 40357 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0198c0055t0001 | 0/0 | 33859 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0199c0070t0001 | 0/0 | 40357 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0200c0049t0001 | 0/0 | 20863 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0201c0074t0001 | 0/0 | 37108 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0202c0132t0001 | 0/0 | 33859 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0203c0131t0001 | 0/0 | 24112 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0204c0128t0001 | 0/0 | 33859 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0205c0129t0001 | 0/0 | 33859 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0206c0077t0001 | 0/0 | 14365 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0207c0078t0001 | 0/0 | 14365 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0208c0083t0001 | 0/0 | 30610 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0209c0082t0001 | 0/0 | 30610 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0210c0081t0001 | 0/0 | 30610 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0211c0080t0001 | 0/0 | 27361 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0212c0099t0004 | 1/0 | 16366 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0213c0097t0001 | 0/0 | 33859 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0214c0098t0001 | 0/0 | 37108 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0215c0096t0001 | 0/0 | 33859 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0216c0084t0001 | 0/0 | 30610 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0217c0085t0001 | 0/0 | 33859 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0218c0086t0001 | 0/0 | 33859 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0219c0088t0001 | 0/0 | 40357 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0220c0087t0001 | 0/0 | 37108 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0221c0090t0001 | 0/0 | 40357 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0222c0094t0001 | 0/0 | 33859 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0223c0091t0001 | 0/0 | 33859 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0224c0092t0001 | 0/0 | 37108 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0225c0093t0001 | 0/0 | 33859 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0226c0089t0001 | 0/0 | 33859 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0227c0095t0001 | 0/0 | 33859 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0228c0100t0001 | 0/0 | 30610 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0229c0101t0001 | 0/0 | 24112 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0230c0102t0001 | 0/0 | 30610 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0231c0120t0001 | 0/0 | 30610 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0232c0075t0001 | 0/0 | 30610 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0233c0119t0001 | 0/0 | 27361 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0234c0107t0001 | 0/0 | 30610 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0235c0105t0001 | 0/0 | 30610 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0236c0106t0001 | 0/0 | 30610 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0237c0104t0001 | 0/0 | 30610 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0238c0103t0001 | 0/0 | 30610 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0239c0115t0001 | 0/0 | 30610 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0240c0108t0001 | 0/0 | 36034 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0241c0111t0001 | 0/0 | 30610 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0242c0110t0001 | 0/0 | 30610 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0243c0109t0001 | 0/0 | 33859 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0244c0116t0001 | 0/0 | 30610 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0245c0112t0001 | 0/0 | 24112 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0246c0113t0001 | 0/0 | 27361 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0247c0114t0001 | 0/0 | 30610 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0248c0121t0001 | 0/0 | 37109 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0249c0123t0001 | 0/0 | 27361 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0250c0130t0001 | 0/0 | 30610 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0251c0122t0001 | 0/0 | 27361 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0252c0127t0001 | 0/1 | 33859 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0253c0126t0001 | 0/0 | 33859 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0254c0125t0001 | 0/0 | 33859 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0255c0124t0001 | 0/0 | 33859 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0256c0076t0001 | 0/0 | 30610 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0257c0048t0001 | 0/0 | 30493 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0258c0279t0001 | 0/0 | 30610 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0259c0272t0001 | 0/0 | 33859 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0260c0273t0001 | 0/0 | 33859 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0261c0280t0001 | 0/0 | 40357 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0262c0274t0001 | 0/0 | 43606 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0263c0275t0001 | 0/0 | 40357 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0264c0276t0001 | 0/0 | 40357 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0265c0278t0001 | 0/0 | 43606 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0266c0277t0001 | 0/0 | 40357 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0267c0285t0001 | 0/0 | 33859 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0268c0283t0001 | 0/0 | 37108 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0269c0284t0001 | 0/0 | 33859 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0270c0282t0001 | 0/0 | 33859 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0271c0281t0001 | 0/0 | 43606 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| a0272c0041t0001 | 0/0 | 37108 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | copy fasta | chr7 | 100964565 | 101023936 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0001c0168t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0001c0181t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0002c0004t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0002c0004t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0002c0004t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0002c0007t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0002c0007t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0002c0245t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0003c0002t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0003c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0003c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0003c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0003c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0003c0254t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0003c0261t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0004c0012t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0004c0012t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0004c0013t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0004c0013t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0004c0079t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0005c0003t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0005c0003t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0006c0038t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0006c0038t0003g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0006c0256t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0007c0008t0001g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0007c0008t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0008c0028t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0008c0028t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0008c0205t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0009c0006t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0009c0006t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0010c0005t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0010c0005t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0011c0009t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0011c0009t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0012c0040t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0013c0037t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0013c0037t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0014c0036t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0014c0036t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0015c0240t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0015c0242t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0016c0035t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0016c0035t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0017c0034t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0017c0034t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0018c0039t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0018c0039t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0019c0033t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0019c0033t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0020c0023t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0020c0023t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0021c0022t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0021c0022t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0022c0025t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0022c0025t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0023c0024t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0023c0024t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0024c0021t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0025c0032t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0025c0032t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0026c0202t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0026c0231t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0027c0031t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0027c0031t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0028c0030t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0028c0030t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0029c0029t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0029c0029t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0030c0027t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0030c0027t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0031c0026t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0032c0170t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0032c0171t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0033c0011t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0033c0011t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0034c0010t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0034c0010t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0035c0020t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0035c0020t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0036c0014t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0036c0014t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0037c0017t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0037c0017t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0038c0016t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0038c0016t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0039c0015t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0039c0015t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0040c0018t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0040c0018t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0041c0019t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0041c0019t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0042c0117t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0042c0118t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0043c0286t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0044c0042t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0045c0044t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0046c0045t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0047c0043t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0048c0046t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0049c0047t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0050c0271t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0051c0270t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0052c0269t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0053c0267t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0054c0266t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0055c0264t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0056c0262t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0057c0232t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0058c0259t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0059c0258t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0060c0257t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0061c0255t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0062c0260t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0063c0253t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0064c0234t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0065c0248t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0066c0247t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0067c0249t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0068c0244t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0069c0243t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0070c0250t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0071c0241t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0072c0251t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0073c0246t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0074c0252t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0075c0265t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0076c0239t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0077c0238t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0078c0235t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0079c0237t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0080c0236t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0081c0263t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0082c0233t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0083c0230t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0084c0227t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0085c0229t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0086c0228t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0087c0138t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0088c0225t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0089c0224t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0090c0223t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0091c0140t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0092c0141t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0093c0142t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0094c0222t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0095c0221t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0096c0220t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0097c0144t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0098c0147t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0099c0148t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0100c0157t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0101c0156t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0102c0155t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0103c0150t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0104c0154t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0105c0153t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0106c0152t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0107c0151t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0108c0149t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0109c0164t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0110c0163t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0111c0160t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0112c0159t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0113c0158t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0114c0161t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0115c0162t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0116c0145t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0117c0146t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0118c0143t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0119c0218t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0120c0210t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0121c0217t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0122c0216t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0123c0215t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0124c0214t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0125c0213t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0126c0212t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0127c0211t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0128c0208t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0129c0209t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0130c0207t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0131c0206t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0132c0204t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0133c0203t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0134c0201t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0135c0200t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0136c0166t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0137c0199t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0138c0198t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0139c0167t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0140c0169t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0141c0197t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0142c0194t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0143c0195t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0144c0191t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0145c0189t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0146c0188t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0147c0187t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0148c0226t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0149c0185t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0150c0196t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0151c0186t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0152c0176t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0153c0183t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0154c0173t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0155c0182t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0156c0184t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0157c0180t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0158c0179t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0159c0178t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0160c0190t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0161c0177t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0162c0174t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0163c0175t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0164c0192t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0165c0193t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0166c0172t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0167c0219t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0168c0139t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0169c0165t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0170c0137t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0171c0136t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0172c0135t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0173c0134t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0174c0268t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0175c0133t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0176c0073t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0177c0072t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0178c0068t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0179c0071t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0180c0067t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0181c0066t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0182c0063t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0183c0062t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0184c0064t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0185c0061t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0186c0065t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0187c0060t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0188c0069t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0189c0058t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0190c0050t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0191c0052t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0192c0051t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0193c0053t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0194c0054t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0195c0057t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0196c0056t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0197c0059t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0198c0055t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0199c0070t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0200c0049t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0201c0074t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0202c0132t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0203c0131t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0204c0128t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0205c0129t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0206c0077t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0207c0078t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0208c0083t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0209c0082t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0210c0081t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0211c0080t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0212c0099t0004g0089 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0213c0097t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0214c0098t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0215c0096t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0216c0084t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0217c0085t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0218c0086t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0219c0088t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0220c0087t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0221c0090t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0222c0094t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0223c0091t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0224c0092t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0225c0093t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0226c0089t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0227c0095t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0228c0100t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0229c0101t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0230c0102t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0231c0120t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0232c0075t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0233c0119t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0234c0107t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0235c0105t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0236c0106t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0237c0104t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0238c0103t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0239c0115t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0240c0108t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0241c0111t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0242c0110t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0243c0109t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0244c0116t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0245c0112t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0246c0113t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0247c0114t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0248c0121t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0249c0123t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0250c0130t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0251c0122t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0252c0127t0001g0011 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0253c0126t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0254c0125t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0255c0124t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0256c0076t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0257c0048t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0258c0279t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0259c0272t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0260c0273t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0261c0280t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0262c0274t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0263c0275t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0264c0276t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0265c0278t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0266c0277t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0267c0285t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0268c0283t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0269c0284t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0270c0282t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0271c0281t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| a0272c0041t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0103 | c0150 | t0001 | g0165 | EUR | GBR | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG00099 | hp2 | a0082 | c0233 | t0001 | g0226 | EUR | GBR | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG00140 | hp1 | a0106 | c0152 | t0001 | g0210 | EUR | GBR | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG00140 | hp2 | a0164 | c0192 | t0001 | g0201 | EUR | GBR | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG00323 | hp1 | a0045 | c0044 | t0001 | g0140 | EUR | FIN | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG00323 | hp2 | a0021 | c0022 | t0001 | g0283 | EUR | FIN | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG00408 | hp1 | a0090 | c0223 | t0001 | g0070 | EAS | CHS | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG00408 | hp2 | a0108 | c0149 | t0001 | g0216 | EAS | CHS | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG00423 | hp1 | a0104 | c0154 | t0001 | g0208 | EAS | CHS | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG00423 | hp2 | a0256 | c0076 | t0001 | g0113 | EAS | CHS | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG00558 | hp1 | a0155 | c0182 | t0001 | g0132 | EAS | CHS | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG00558 | hp2 | a0002 | c0004 | t0001 | g0001 | EAS | CHS | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG00621 | hp1 | a0042 | c0118 | t0001 | g0109 | EAS | CHS | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG00621 | hp2 | a0020 | c0023 | t0001 | g0188 | EAS | CHS | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG00639 | hp1 | a0254 | c0125 | t0001 | g0090 | AMR | PUR | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG00639 | hp2 | a0011 | c0009 | t0001 | g0139 | AMR | PUR | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG00642 | hp1 | a0169 | c0165 | t0001 | g0136 | AMR | PUR | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG00642 | hp2 | a0195 | c0057 | t0001 | g0279 | AMR | PUR | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG00673 | hp1 | a0191 | c0052 | t0001 | g0133 | EAS | CHS | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG00673 | hp2 | a0150 | c0196 | t0001 | g0171 | EAS | CHS | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG00735 | hp1 | a0118 | c0143 | t0001 | g0206 | AMR | PUR | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG00735 | hp2 | a0084 | c0227 | t0001 | g0009 | AMR | PUR | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG00738 | hp1 | a0157 | c0180 | t0001 | g0021 | AMR | PUR | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG00738 | hp2 | a0099 | c0148 | t0001 | g0242 | AMR | PUR | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG00741 | hp1 | a0098 | c0147 | t0001 | g0087 | AMR | PUR | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG00741 | hp2 | a0050 | c0271 | t0001 | g0073 | AMR | PUR | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01069 | hp1 | a0115 | c0162 | t0001 | g0170 | AMR | PUR | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01069 | hp2 | a0037 | c0017 | t0001 | g0231 | AMR | PUR | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01070 | hp1 | a0037 | c0017 | t0001 | g0232 | AMR | PUR | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01070 | hp2 | a0117 | c0146 | t0001 | g0228 | AMR | PUR | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01074 | hp1 | a0140 | c0169 | t0001 | g0202 | AMR | PUR | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01074 | hp2 | a0011 | c0009 | t0001 | g0137 | AMR | PUR | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01081 | hp1 | a0218 | c0086 | t0001 | g0166 | AMR | PUR | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01081 | hp2 | a0031 | c0026 | t0001 | g0018 | AMR | PUR | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01099 | hp1 | a0080 | c0236 | t0001 | g0001 | AMR | PUR | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01099 | hp2 | a0030 | c0027 | t0001 | g0141 | AMR | PUR | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01106 | hp1 | a0189 | c0058 | t0001 | g0269 | AMR | PUR | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01106 | hp2 | a0219 | c0088 | t0001 | g0081 | AMR | PUR | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01109 | hp1 | a0201 | c0074 | t0001 | g0012 | AMR | PUR | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01109 | hp2 | a0186 | c0065 | t0001 | g0219 | AMR | PUR | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01168 | hp1 | a0016 | c0035 | t0001 | g0259 | AMR | PUR | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01168 | hp2 | a0044 | c0042 | t0001 | g0138 | AMR | PUR | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01169 | hp1 | a0031 | c0026 | t0001 | g0018 | AMR | PUR | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01169 | hp2 | a0016 | c0035 | t0001 | g0258 | AMR | PUR | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01175 | hp1 | a0132 | c0204 | t0001 | g0156 | AMR | PUR | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01175 | hp2 | a0105 | c0153 | t0001 | g0189 | AMR | PUR | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01192 | hp1 | a0079 | c0237 | t0001 | g0041 | AMR | PUR | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01192 | hp2 | a0217 | c0085 | t0001 | g0153 | AMR | PUR | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01243 | hp1 | a0081 | c0263 | t0001 | g0144 | AMR | PUR | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01243 | hp2 | a0120 | c0210 | t0001 | g0026 | AMR | PUR | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01255 | hp1 | a0039 | c0015 | t0001 | g0251 | AMR | CLM | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01255 | hp2 | a0227 | c0095 | t0001 | g0016 | AMR | CLM | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01256 | hp1 | a0046 | c0045 | t0001 | g0142 | AMR | CLM | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01256 | hp2 | a0010 | c0005 | t0001 | g0147 | AMR | CLM | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01257 | hp1 | a0093 | c0142 | t0001 | g0094 | AMR | CLM | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01257 | hp2 | a0022 | c0025 | t0001 | g0224 | AMR | CLM | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01258 | hp1 | a0010 | c0005 | t0001 | g0015 | AMR | CLM | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01258 | hp2 | a0022 | c0025 | t0001 | g0223 | AMR | CLM | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01261 | hp1 | a0038 | c0016 | t0001 | g0016 | AMR | CLM | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01261 | hp2 | a0056 | c0262 | t0001 | g0056 | AMR | CLM | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01346 | hp1 | a0002 | c0007 | t0001 | g0001 | AMR | CLM | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01346 | hp2 | a0038 | c0016 | t0001 | g0154 | AMR | CLM | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01358 | hp1 | a0071 | c0241 | t0001 | g0001 | AMR | CLM | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01358 | hp2 | a0226 | c0089 | t0001 | g0071 | AMR | CLM | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01361 | hp1 | a0213 | c0097 | t0001 | g0152 | AMR | CLM | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01361 | hp2 | a0192 | c0051 | t0001 | g0262 | AMR | CLM | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01433 | hp1 | a0064 | c0234 | t0001 | g0001 | AMR | CLM | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01433 | hp2 | a0253 | c0126 | t0001 | g0011 | AMR | CLM | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01496 | hp1 | a0009 | c0006 | t0001 | g0020 | AMR | CLM | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01496 | hp2 | a0010 | c0005 | t0001 | g0015 | AMR | CLM | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01515 | hp1 | a0220 | c0087 | t0001 | g0091 | EUR | IBS | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01515 | hp2 | a0034 | c0010 | t0001 | g0268 | EUR | IBS | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01516 | hp1 | a0039 | c0015 | t0001 | g0155 | EUR | IBS | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01516 | hp2 | a0053 | c0267 | t0001 | g0143 | EUR | IBS | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01884 | hp1 | a0014 | c0036 | t0001 | g0006 | AFR | ACB | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01884 | hp2 | a0270 | c0282 | t0001 | g0098 | AFR | ACB | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01928 | hp1 | a0202 | c0132 | t0001 | g0040 | AMR | PEL | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01928 | hp2 | a0017 | c0034 | t0001 | g0049 | AMR | PEL | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01934 | hp1 | a0112 | c0159 | t0001 | g0167 | AMR | PEL | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01934 | hp2 | a0222 | c0094 | t0001 | g0217 | AMR | PEL | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01943 | hp1 | a0002 | c0245 | t0001 | g0050 | AMR | PEL | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01943 | hp2 | a0009 | c0006 | t0001 | g0203 | AMR | PEL | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01952 | hp1 | a0054 | c0266 | t0001 | g0001 | AMR | PEL | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01952 | hp2 | a0058 | c0259 | t0001 | g0064 | AMR | PEL | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01978 | hp1 | a0073 | c0246 | t0001 | g0059 | AMR | PEL | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01978 | hp2 | a0193 | c0053 | t0001 | g0263 | AMR | PEL | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01981 | hp1 | a0009 | c0006 | t0001 | g0020 | AMR | PEL | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01981 | hp2 | a0017 | c0034 | t0001 | g0002 | AMR | PEL | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01993 | hp1 | a0002 | c0007 | t0001 | g0042 | AMR | PEL | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01993 | hp2 | a0101 | c0156 | t0001 | g0250 | AMR | PEL | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02015 | hp1 | a0149 | c0185 | t0001 | g0175 | EAS | KHV | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02015 | hp2 | a0002 | c0004 | t0001 | g0046 | EAS | KHV | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02027 | hp1 | a0231 | c0120 | t0001 | g0103 | EAS | KHV | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02027 | hp2 | a0257 | c0048 | t0001 | g0008 | EAS | KHV | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02040 | hp1 | a0015 | c0240 | t0001 | g0048 | EAS | KHV | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02040 | hp2 | a0100 | c0157 | t0001 | g0179 | EAS | KHV | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02055 | hp1 | a0122 | c0216 | t0001 | g0296 | AFR | ACB | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02055 | hp2 | a0138 | c0198 | t0001 | g0086 | AFR | ACB | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02056 | hp1 | a0018 | c0039 | t0001 | g0002 | EAS | KHV | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02056 | hp2 | a0008 | c0205 | t0001 | g0234 | EAS | KHV | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02071 | hp1 | a0013 | c0037 | t0001 | g0062 | EAS | KHV | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02071 | hp2 | a0248 | c0121 | t0001 | g0278 | EAS | KHV | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02074 | hp1 | a0068 | c0244 | t0001 | g0044 | EAS | KHV | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02074 | hp2 | a0249 | c0123 | t0001 | g0013 | EAS | KHV | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02080 | hp1 | a0102 | c0155 | t0001 | g0215 | EAS | KHV | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02080 | hp2 | a0135 | c0200 | t0001 | g0248 | EAS | KHV | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02083 | hp1 | a0008 | c0028 | t0001 | g0169 | EAS | KHV | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02083 | hp2 | a0019 | c0033 | t0001 | g0238 | EAS | KHV | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02132 | hp1 | a0141 | c0197 | t0001 | g0195 | EAS | KHV | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02132 | hp2 | a0239 | c0115 | t0001 | g0135 | EAS | KHV | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02135 | hp1 | a0006 | c0038 | t0001 | g0047 | EAS | KHV | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02135 | hp2 | a0173 | c0134 | t0001 | g0209 | EAS | KHV | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02145 | hp1 | a0214 | c0098 | t0001 | g0146 | AFR | ACB | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02145 | hp2 | a0167 | c0219 | t0001 | g0227 | AFR | ACB | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02148 | hp1 | a0109 | c0164 | t0001 | g0229 | AMR | PEL | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02148 | hp2 | a0069 | c0243 | t0001 | g0057 | AMR | PEL | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02155 | hp1 | a0162 | c0174 | t0001 | g0181 | EAS | CDX | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02155 | hp2 | a0245 | c0112 | t0001 | g0111 | EAS | CDX | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02165 | hp1 | a0043 | c0286 | t0001 | g0182 | EAS | CDX | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02165 | hp2 | a0238 | c0103 | t0001 | g0211 | EAS | CDX | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02257 | hp1 | a0124 | c0214 | t0001 | g0005 | AFR | ACB | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02257 | hp2 | a0269 | c0284 | t0001 | g0101 | AFR | ACB | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02258 | hp1 | a0262 | c0274 | t0001 | g0294 | AFR | ACB | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02258 | hp2 | a0272 | c0041 | t0001 | g0213 | AFR | ACB | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02280 | hp1 | a0176 | c0073 | t0001 | g0148 | AFR | ACB | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02280 | hp2 | a0030 | c0027 | t0001 | g0239 | AFR | ACB | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02293 | hp1 | a0051 | c0270 | t0001 | g0220 | AMR | PEL | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02293 | hp2 | a0002 | c0007 | t0001 | g0001 | AMR | PEL | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02451 | hp1 | a0143 | c0195 | t0001 | g0255 | AFR | ACB | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02451 | hp2 | a0261 | c0280 | t0001 | g0254 | AFR | ACB | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02523 | hp1 | a0020 | c0023 | t0001 | g0200 | EAS | KHV | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02523 | hp2 | a0003 | c0254 | t0001 | g0051 | EAS | KHV | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02572 | hp1 | a0200 | c0049 | t0001 | g0106 | AFR | GWD | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02572 | hp2 | a0210 | c0081 | t0001 | g0093 | AFR | GWD | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02602 | hp1 | a0007 | c0008 | t0001 | g0010 | SAS | PJL | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02602 | hp2 | a0139 | c0167 | t0002 | g0222 | SAS | PJL | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02615 | hp1 | a0074 | c0252 | t0001 | g0024 | AFR | GWD | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02615 | hp2 | a0209 | c0082 | t0001 | g0145 | AFR | GWD | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02622 | hp1 | a0260 | c0273 | t0001 | g0007 | AFR | GWD | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02622 | hp2 | a0131 | c0206 | t0001 | g0023 | AFR | GWD | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02630 | hp1 | a0036 | c0014 | t0001 | g0291 | AFR | GWD | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02630 | hp2 | a0197 | c0059 | t0001 | g0265 | AFR | GWD | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02647 | hp1 | a0179 | c0071 | t0001 | g0160 | AFR | GWD | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02647 | hp2 | a0065 | c0248 | t0001 | g0030 | AFR | GWD | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02683 | hp1 | a0001 | c0181 | t0001 | g0069 | SAS | PJL | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02683 | hp2 | a0096 | c0220 | t0001 | g0230 | SAS | PJL | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02698 | hp1 | a0116 | c0145 | t0001 | g0072 | SAS | PJL | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02698 | hp2 | a0034 | c0010 | t0001 | g0267 | SAS | PJL | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02717 | hp1 | a0207 | c0078 | t0001 | g0292 | AFR | GWD | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02717 | hp2 | a0184 | c0064 | t0001 | g0159 | AFR | GWD | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02723 | hp1 | a0178 | c0068 | t0001 | g0158 | AFR | GWD | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02723 | hp2 | a0266 | c0277 | t0001 | g0107 | AFR | GWD | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02735 | hp1 | a0199 | c0070 | t0001 | g0270 | SAS | PJL | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02735 | hp2 | a0113 | c0158 | t0001 | g0241 | SAS | PJL | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02809 | hp1 | a0066 | c0247 | t0001 | g0024 | AFR | GWD | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02809 | hp2 | a0224 | c0092 | t0001 | g0038 | AFR | GWD | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02886 | hp1 | a0142 | c0194 | t0001 | g0256 | AFR | GWD | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02886 | hp2 | a0004 | c0013 | t0001 | g0084 | AFR | GWD | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02895 | hp1 | a0175 | c0133 | t0001 | g0006 | AFR | GWD | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02895 | hp2 | a0004 | c0012 | t0001 | g0287 | AFR | GWD | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02896 | hp1 | a0024 | c0021 | t0001 | g0022 | AFR | GWD | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02896 | hp2 | a0083 | c0230 | t0001 | g0077 | AFR | GWD | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02897 | hp1 | a0024 | c0021 | t0001 | g0022 | AFR | GWD | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02897 | hp2 | a0004 | c0012 | t0001 | g0288 | AFR | GWD | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02922 | hp1 | a0130 | c0207 | t0001 | g0023 | AFR | ESN | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02922 | hp2 | a0047 | c0043 | t0001 | g0285 | AFR | ESN | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02970 | hp1 | a0027 | c0031 | t0001 | g0192 | AFR | ESN | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02970 | hp2 | a0225 | c0093 | t0001 | g0037 | AFR | ESN | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02976 | hp1 | a0014 | c0036 | t0001 | g0027 | AFR | ESN | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02976 | hp2 | a0180 | c0067 | t0001 | g0080 | AFR | ESN | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG03017 | hp1 | a0007 | c0008 | t0001 | g0010 | SAS | PJL | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG03017 | hp2 | a0232 | c0075 | t0001 | g0014 | SAS | PJL | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG03041 | hp1 | a0033 | c0011 | t0001 | g0149 | AFR | GWD | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG03041 | hp2 | a0128 | c0208 | t0001 | g0174 | AFR | GWD | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG03098 | hp1 | a0127 | c0211 | t0001 | g0286 | AFR | MSL | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG03098 | hp2 | a0265 | c0278 | t0001 | g0097 | AFR | MSL | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG03130 | hp1 | a0196 | c0056 | t0001 | g0264 | AFR | ESN | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG03130 | hp2 | a0258 | c0279 | t0001 | g0173 | AFR | ESN | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG03139 | hp1 | a0125 | c0213 | t0001 | g0005 | AFR | ESN | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG03139 | hp2 | a0223 | c0091 | t0001 | g0039 | AFR | ESN | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG03195 | hp1 | a0126 | c0212 | t0001 | g0297 | AFR | ESN | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG03195 | hp2 | a0259 | c0272 | t0001 | g0007 | AFR | ESN | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG03209 | hp1 | a0119 | c0218 | t0001 | g0025 | AFR | MSL | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG03209 | hp2 | a0211 | c0080 | t0001 | g0092 | AFR | MSL | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG03225 | hp1 | a0004 | c0013 | t0001 | g0082 | AFR | MSL | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG03225 | hp2 | a0170 | c0137 | t0001 | g0035 | AFR | MSL | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG03239 | hp1 | a0023 | c0024 | t0001 | g0205 | SAS | PJL | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG03239 | hp2 | a0190 | c0050 | t0001 | g0266 | SAS | PJL | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG03453 | hp1 | a0215 | c0096 | t0001 | g0036 | AFR | MSL | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG03453 | hp2 | a0025 | c0032 | t0001 | g0026 | AFR | MSL | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG03486 | hp1 | a0267 | c0285 | t0001 | g0289 | AFR | MSL | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG03486 | hp2 | a0025 | c0032 | t0001 | g0295 | AFR | MSL | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG03492 | hp1 | a0241 | c0111 | t0001 | g0102 | SAS | PJL | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG03492 | hp2 | a0166 | c0172 | t0001 | g0280 | SAS | PJL | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG03516 | hp1 | a0049 | c0047 | t0001 | g0034 | AFR | ESN | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG03516 | hp2 | a0168 | c0139 | t0001 | g0131 | AFR | ESN | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG03540 | hp1 | a0183 | c0062 | t0001 | g0163 | AFR | GWD | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG03540 | hp2 | a0177 | c0072 | t0001 | g0281 | AFR | GWD | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG03579 | hp1 | a0268 | c0283 | t0001 | g0100 | AFR | MSL | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG03579 | hp2 | a0036 | c0014 | t0001 | g0290 | AFR | MSL | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG03654 | hp1 | a0145 | c0189 | t0001 | g0276 | SAS | PJL | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG03654 | hp2 | a0086 | c0228 | t0001 | g0075 | SAS | PJL | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG03669 | hp1 | a0070 | c0250 | t0001 | g0088 | SAS | PJL | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG03669 | hp2 | a0255 | c0124 | t0001 | g0012 | SAS | PJL | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG03688 | hp1 | a0221 | c0090 | t0001 | g0128 | SAS | STU | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG03688 | hp2 | a0144 | c0191 | t0001 | g0104 | SAS | STU | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG03704 | hp1 | a0242 | c0110 | t0001 | g0115 | SAS | PJL | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG03704 | hp2 | a0097 | c0144 | t0001 | g0212 | SAS | PJL | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG03710 | hp1 | a0023 | c0024 | t0001 | g0204 | SAS | PJL | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG03710 | hp2 | a0233 | c0119 | t0001 | g0116 | SAS | PJL | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG03831 | hp1 | a0032 | c0171 | t0001 | g0273 | SAS | BEB | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG03831 | hp2 | a0085 | c0229 | t0001 | g0076 | SAS | BEB | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG03834 | hp1 | a0040 | c0018 | t0001 | g0014 | SAS | BEB | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG03834 | hp2 | a0216 | c0084 | t0001 | g0079 | SAS | BEB | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG03927 | hp1 | a0247 | c0114 | t0001 | g0261 | SAS | BEB | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG03927 | hp2 | a0110 | c0163 | t0001 | g0225 | SAS | BEB | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG03942 | hp1 | a0243 | c0109 | t0001 | g0125 | SAS | BEB | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG03942 | hp2 | a0007 | c0008 | t0001 | g0078 | SAS | BEB | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG04115 | hp1 | a0029 | c0029 | t0001 | g0274 | SAS | STU | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG04115 | hp2 | a0229 | c0101 | t0001 | g0118 | SAS | STU | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG04184 | hp1 | a0077 | c0238 | t0001 | g0176 | SAS | BEB | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG04184 | hp2 | a0032 | c0170 | t0001 | g0272 | SAS | BEB | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG04199 | hp1 | a0240 | c0108 | t0001 | g0032 | SAS | STU | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG04199 | hp2 | a0181 | c0066 | t0001 | g0162 | SAS | STU | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG04204 | hp1 | a0040 | c0018 | t0001 | g0126 | SAS | STU | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG04204 | hp2 | a0055 | c0264 | t0001 | g0002 | SAS | STU | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG04228 | hp1 | a0114 | c0161 | t0001 | g0243 | SAS | STU | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG04228 | hp2 | a0091 | c0140 | t0001 | g0275 | SAS | STU | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA18522 | hp1 | a0188 | c0069 | t0001 | g0150 | AFR | YRI | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA18522 | hp2 | a0123 | c0215 | t0001 | g0005 | AFR | YRI | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA18747 | hp1 | a0013 | c0037 | t0001 | g0001 | EAS | CHB | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA18747 | hp2 | a0228 | c0100 | t0001 | g0043 | EAS | CHB | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA18941 | hp1 | a0234 | c0107 | t0001 | g0112 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA18941 | hp2 | a0129 | c0209 | t0001 | g0127 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA18942 | hp1 | a0136 | c0166 | t0001 | g0253 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA18942 | hp2 | a0005 | c0003 | t0001 | g0003 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA18946 | hp1 | a0244 | c0116 | t0001 | g0120 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA18946 | hp2 | a0019 | c0033 | t0001 | g0237 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA18947 | hp1 | a0041 | c0019 | t0001 | g0129 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA18947 | hp2 | a0153 | c0183 | t0001 | g0246 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA18948 | hp2 | a0089 | c0224 | t0001 | g0068 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA18950 | hp1 | a0018 | c0039 | t0001 | g0055 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA18950 | hp2 | a0107 | c0151 | t0001 | g0221 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA18952 | hp1 | a0002 | c0004 | t0001 | g0001 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA18952 | hp2 | a0021 | c0022 | t0001 | g0284 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA18954 | hp1 | a0148 | c0226 | t0001 | g0244 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA18954 | hp2 | a0003 | c0002 | t0001 | g0058 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA18959 | hp1 | a0251 | c0122 | t0001 | g0240 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA18959 | hp2 | a0003 | c0002 | t0001 | g0066 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA18964 | hp1 | a0042 | c0117 | t0001 | g0095 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA18967 | hp1 | a0111 | c0160 | t0001 | g0177 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA18967 | hp2 | a0203 | c0131 | t0001 | g0214 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA18970 | hp1 | a0205 | c0129 | t0001 | g0187 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA18970 | hp2 | a0006 | c0038 | t0003 | g0001 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA18971 | hp1 | a0087 | c0138 | t0001 | g0282 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA18971 | hp2 | a0005 | c0003 | t0001 | g0003 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA18977 | hp1 | a0003 | c0002 | t0001 | g0001 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA18977 | hp2 | a0005 | c0003 | t0001 | g0003 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA18978 | hp2 | a0092 | c0141 | t0001 | g0249 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA18980 | hp1 | a0194 | c0054 | t0001 | g0178 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA18980 | hp2 | a0062 | c0260 | t0001 | g0052 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA18982 | hp1 | a0133 | c0203 | t0001 | g0235 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA18982 | hp2 | a0237 | c0104 | t0001 | g0119 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA18983 | hp2 | a0063 | c0253 | t0001 | g0001 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA18984 | hp1 | a0012 | c0040 | t0001 | g0017 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA18984 | hp2 | a0236 | c0106 | t0001 | g0117 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA18985 | hp1 | a0165 | c0193 | t0001 | g0194 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA18985 | hp2 | a0008 | c0028 | t0001 | g0184 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA18989 | hp1 | a0171 | c0136 | t0001 | g0183 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA18989 | hp2 | a0061 | c0255 | t0001 | g0045 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA18990 | hp2 | a0250 | c0130 | t0001 | g0013 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA18994 | hp1 | a0001 | c0168 | t0001 | g0247 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA18994 | hp2 | a0060 | c0257 | t0001 | g0060 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA18995 | hp2 | a0078 | c0235 | t0001 | g0001 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA18999 | hp1 | a0094 | c0222 | t0001 | g0185 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA18999 | hp2 | a0015 | c0242 | t0001 | g0053 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA19000 | hp1 | a0095 | c0221 | t0001 | g0236 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA19000 | hp2 | a0059 | c0258 | t0001 | g0061 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA19004 | hp1 | a0005 | c0003 | t0001 | g0124 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA19004 | hp2 | a0012 | c0040 | t0001 | g0017 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA19005 | hp1 | a0204 | c0128 | t0001 | g0108 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA19005 | hp2 | a0146 | c0188 | t0001 | g0245 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA19007 | hp1 | a0088 | c0225 | t0001 | g0008 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA19007 | hp2 | a0041 | c0019 | t0001 | g0130 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA19010 | hp1 | a0026 | c0202 | t0001 | g0196 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA19010 | hp2 | a0035 | c0020 | t0001 | g0121 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA19011 | hp1 | a0006 | c0256 | t0001 | g0063 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA19011 | hp2 | a0161 | c0177 | t0001 | g0172 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA19030 | hp1 | a0028 | c0030 | t0001 | g0257 | AFR | LWK | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA19030 | hp2 | a0048 | c0046 | t0001 | g0299 | AFR | LWK | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA19043 | hp1 | a0075 | c0265 | t0001 | g0031 | AFR | LWK | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA19043 | hp2 | a0182 | c0063 | t0001 | g0161 | AFR | LWK | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA19057 | hp1 | a0163 | c0175 | t0001 | g0180 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA19057 | hp2 | a0208 | c0083 | t0001 | g0134 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA19060 | hp1 | a0230 | c0102 | t0001 | g0298 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA19060 | hp2 | a0003 | c0002 | t0001 | g0065 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA19066 | hp1 | a0206 | c0077 | t0001 | g0123 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA19068 | hp1 | a0002 | c0004 | t0001 | g0054 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA19068 | hp2 | a0156 | c0184 | t0001 | g0021 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA19081 | hp1 | a0174 | c0268 | t0001 | g0207 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA19081 | hp2 | a0003 | c0261 | t0001 | g0001 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA19084 | hp1 | a0003 | c0002 | t0001 | g0067 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA19084 | hp2 | a0159 | c0178 | t0001 | g0004 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA19088 | hp1 | a0035 | c0020 | t0001 | g0122 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA19088 | hp2 | a0147 | c0187 | t0001 | g0218 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA19090 | hp1 | a0026 | c0231 | t0001 | g0193 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA19090 | hp2 | a0235 | c0105 | t0001 | g0110 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA19240 | hp1 | a0134 | c0201 | t0001 | g0191 | AFR | YRI | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA19240 | hp2 | a0187 | c0060 | t0001 | g0033 | AFR | YRI | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA20129 | hp1 | a0263 | c0275 | t0001 | g0293 | AFR | ASW | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA20129 | hp2 | a0264 | c0276 | t0001 | g0096 | AFR | ASW | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA20752 | hp1 | a0076 | c0239 | t0001 | g0186 | EUR | TSI | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA20752 | hp2 | a0172 | c0135 | t0001 | g0009 | EUR | TSI | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA20805 | hp1 | a0160 | c0190 | t0001 | g0164 | EUR | TSI | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA20805 | hp2 | a0158 | c0179 | t0001 | g0074 | EUR | TSI | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA20905 | hp1 | a0029 | c0029 | t0001 | g0277 | SAS | GIH | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA20905 | hp2 | a0052 | c0269 | t0001 | g0105 | SAS | GIH | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01123 | hp1 | a0152 | c0176 | t0001 | g0233 | AMR | CLM | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG01123 | hp2 | a0057 | c0232 | t0001 | g0001 | AMR | CLM | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02109 | hp1 | a0004 | c0079 | t0001 | g0083 | AFR | ACB | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02109 | hp2 | a0121 | c0217 | t0001 | g0025 | AFR | ACB | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02486 | hp1 | a0028 | c0030 | t0001 | g0157 | AFR | ACB | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02486 | hp2 | a0137 | c0199 | t0001 | g0085 | AFR | ACB | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02559 | hp1 | a0033 | c0011 | t0001 | g0151 | AFR | ACB | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG02559 | hp2 | a0072 | c0251 | t0001 | g0029 | AFR | ACB | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG03471 | hp1 | a0271 | c0281 | t0001 | g0099 | AFR | MSL | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG03471 | hp2 | a0185 | c0061 | t0001 | g0168 | AFR | MSL | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG06807 | hp1 | a0027 | c0031 | t0001 | g0190 | AFR | USA | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| HG06807 | hp2 | a0198 | c0055 | t0001 | g0271 | AFR | USA | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA18955 | hp1 | a0151 | c0186 | t0001 | g0260 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA18955 | hp2 | a0154 | c0173 | t0001 | g0199 | EAS | JPT | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA20300 | hp1 | a0067 | c0249 | t0001 | g0028 | AFR | USA | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| NA20300 | hp2 | a0246 | c0113 | t0001 | g0114 | AFR | USA | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| homoSapiens_chm13v2 | hp1 | a0252 | c0127 | t0001 | g0011 | REF | REF | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| homoSapiens_grch38 | hp1 | a0212 | c0099 | t0004 | g0089 | REF | REF | MUC12_chr7_100964565_101023936 | MUC12 | chr7 | 100964565 | 101023936 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:100990657
|
G | A | 1 | a0272 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.94G>A | p.Gly32Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 152/16366 | 94/16008 | 32/5335 | chr7 | 100990657 | ||
| chr7:100990907
|
C | T | 1 | a0043 | 1 | HG02165.hp1 | missense_variant | MODERATE | c.344C>T | p.Thr115Ile | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 402/16366 | 344/16008 | 115/5335 | chr7 | 100990907 | ||
| chr7:100991075
|
G | A | 5 | a0011a0044a0045others(2): Show | 6 | HG00323.hp1 HG00639.hp2 HG01074.hp2 others(3): Show |
missense_variant | MODERATE | c.512G>A | p.Arg171Gln | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 570/16366 | 512/16008 | 171/5335 | chr7 | 100991075 | ||
| chr7:100991077
|
C | T | 15 | a0258a0259a0260others(12): Show | 15 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(12): Show |
missense_variant | MODERATE | c.514C>T | p.Pro172Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 572/16366 | 514/16008 | 172/5335 | chr7 | 100991077 | ||
| chr7:100991128
|
G | A | 2 | a0048a0049 | 2 | HG03516.hp1 NA19030.hp2 |
missense_variant | MODERATE | c.565G>A | p.Val189Ile | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 623/16366 | 565/16008 | 189/5335 | chr7 | 100991128 | ||
| chr7:100991150
|
C | T | 1 | a0050 | 1 | HG00741.hp2 | missense_variant | MODERATE | c.587C>T | p.Ser196Phe | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 645/16366 | 587/16008 | 196/5335 | chr7 | 100991150 | ||
| chr7:100991159
|
T | G | 1 | a0257 | 1 | HG02027.hp2 | missense_variant | MODERATE | c.596T>G | p.Ile199Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 654/16366 | 596/16008 | 199/5335 | chr7 | 100991159 | ||
| chr7:100991195
|
C | G | 161 | a0001a0002a0003others(158): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
missense_variant | MODERATE | c.632C>G | p.Thr211Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 690/16366 | 632/16008 | 211/5335 | chr7 | 100991195 | ||
| chr7:100991203
|
C | G | 2 | a0012a0051 | 3 | HG02293.hp1 NA18984.hp1 NA19004.hp2 |
missense_variant | MODERATE | c.640C>G | p.Pro214Ala | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 698/16366 | 640/16008 | 214/5335 | chr7 | 100991203 | ||
| chr7:100991287
|
A | G | 1 | a0052 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.724A>G | p.Thr242Ala | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 782/16366 | 724/16008 | 242/5335 | chr7 | 100991287 | ||
| chr7:100991359
|
T | G | 205 | a0001a0002a0003others(202): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
missense_variant | MODERATE | c.796T>G | p.Ser266Ala | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 854/16366 | 796/16008 | 266/5335 | chr7 | 100991359 | ||
| chr7:100991360
|
C | G | 5 | a0267a0268a0269others(2): Show | 5 | HG01884.hp2 HG02257.hp2 HG03471.hp1 others(2): Show |
missense_variant | MODERATE | c.797C>G | p.Ser266Cys | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 855/16366 | 797/16008 | 266/5335 | chr7 | 100991360 | ||
| chr7:100991362
|
A | G | 1 | a0052 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.799A>G | p.Ser267Gly | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 857/16366 | 799/16008 | 267/5335 | chr7 | 100991362 | ||
| chr7:100991375
|
A | G | 1 | a0052 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.812A>G | p.His271Arg | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 870/16366 | 812/16008 | 271/5335 | chr7 | 100991375 | ||
| chr7:100991377
|
G | C | 1 | a0052 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.814G>C | p.Glu272Gln | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 872/16366 | 814/16008 | 272/5335 | chr7 | 100991377 | ||
| chr7:100991386
|
C | T | 1 | a0052 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.823C>T | p.Pro275Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 881/16366 | 823/16008 | 275/5335 | chr7 | 100991386 | ||
| chr7:100991411
|
G | A | 1 | a0052 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.848G>A | p.Ser283Asn | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 906/16366 | 848/16008 | 283/5335 | chr7 | 100991411 | ||
| chr7:100991425
|
T | A | 1 | a0052 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.862T>A | p.Ser288Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 920/16366 | 862/16008 | 288/5335 | chr7 | 100991425 | ||
| chr7:100991437
|
T | C | 1 | a0052 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.874T>C | p.Ser292Pro | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 932/16366 | 874/16008 | 292/5335 | chr7 | 100991437 | ||
| chr7:100991440
|
G | A | 2 | a0052a0175 | 2 | HG02895.hp1 NA20905.hp2 |
missense_variant | MODERATE | c.877G>A | p.Gly293Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 935/16366 | 877/16008 | 293/5335 | chr7 | 100991440 | ||
| chr7:100991441
|
G | C | 1 | a0052 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.878G>C | p.Gly293Ala | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 936/16366 | 878/16008 | 293/5335 | chr7 | 100991441 | ||
| chr7:100991461
|
A | G | 1 | a0052 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.898A>G | p.Lys300Glu | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 956/16366 | 898/16008 | 300/5335 | chr7 | 100991461 | ||
| chr7:100991477
|
A | C | 1 | a0052 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.914A>C | p.Tyr305Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 972/16366 | 914/16008 | 305/5335 | chr7 | 100991477 | ||
| chr7:100991482
|
A | G | 1 | a0052 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.919A>G | p.Ser307Gly | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 977/16366 | 919/16008 | 307/5335 | chr7 | 100991482 | ||
| chr7:100991500
|
C | G | 2 | a0176a0177 | 2 | HG02280.hp1 HG03540.hp2 |
missense_variant | MODERATE | c.937C>G | p.Pro313Ala | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 995/16366 | 937/16008 | 313/5335 | chr7 | 100991500 | ||
| chr7:100991533
|
T | A | 1 | a0200 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.970T>A | p.Leu324Met | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 1028/16366 | 970/16008 | 324/5335 | chr7 | 100991533 | ||
| chr7:100991540
|
A | G | 2 | a0052a0174 | 2 | NA19081.hp1 NA20905.hp2 |
missense_variant | MODERATE | c.977A>G | p.His326Arg | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 1035/16366 | 977/16008 | 326/5335 | chr7 | 100991540 | ||
| chr7:100991552
|
C | T | 1 | a0053 | 1 | HG01516.hp2 | missense_variant | MODERATE | c.989C>T | p.Ser330Leu | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 1047/16366 | 989/16008 | 330/5335 | chr7 | 100991552 | ||
| chr7:100991557
|
C | A | 3 | a0052a0173a0174 | 3 | HG02135.hp2 NA19081.hp1 NA20905.hp2 |
missense_variant | MODERATE | c.994C>A | p.Pro332Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 1052/16366 | 994/16008 | 332/5335 | chr7 | 100991557 | ||
| chr7:100991596
|
C | T | 2 | a0052a0174 | 2 | NA19081.hp1 NA20905.hp2 |
missense_variant | MODERATE | c.1033C>T | p.Pro345Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 1091/16366 | 1033/16008 | 345/5335 | chr7 | 100991596 | ||
| chr7:100991606
|
G | A | 1 | a0201 | 1 | HG01109.hp1 | missense_variant | MODERATE | c.1043G>A | p.Arg348His | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 1101/16366 | 1043/16008 | 348/5335 | chr7 | 100991606 | ||
| chr7:100991611
|
G | A | 2 | a0052a0174 | 2 | NA19081.hp1 NA20905.hp2 |
missense_variant | MODERATE | c.1048G>A | p.Ala350Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 1106/16366 | 1048/16008 | 350/5335 | chr7 | 100991611 | ||
| chr7:100991624
|
A | T | 2 | a0052a0174 | 2 | NA19081.hp1 NA20905.hp2 |
missense_variant | MODERATE | c.1061A>T | p.His354Leu | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 1119/16366 | 1061/16008 | 354/5335 | chr7 | 100991624 | ||
| chr7:100991641
|
G | A | 2 | a0052a0174 | 2 | NA19081.hp1 NA20905.hp2 |
missense_variant | MODERATE | c.1078G>A | p.Ala360Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 1136/16366 | 1078/16008 | 360/5335 | chr7 | 100991641 | ||
| chr7:100991652
|
G | C | 2 | a0052a0174 | 2 | NA19081.hp1 NA20905.hp2 |
missense_variant | MODERATE | c.1089G>C | p.Arg363Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 1147/16366 | 1089/16008 | 363/5335 | chr7 | 100991652 | ||
| chr7:100991683
|
C | A | 120 | a0001a0008a0009others(117): Show | 148 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(145): Show |
missense_variant | MODERATE | c.1120C>A | p.Pro374Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 1178/16366 | 1120/16008 | 374/5335 | chr7 | 100991683 | ||
| chr7:100991683
|
C | CCTGAAAG others(3242): Show |
1 | a0052 | 1 | NA20905.hp2 | conservative_inframe_insertion | MODERATE | c.1128_1129insAACACA others(3243): Show |
p.Ser376_Ser377insAs others(3247): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 1187/16366 | 1129/16008 | 377/5335 | INFO_REALIGN_3_PRIME | chr7 | 100991683 | |
| chr7:100991924
|
C | T | 40 | a0002a0003a0006others(37): Show | 63 | HG00099.hp2 HG00558.hp2 HG01099.hp1 others(60): Show |
missense_variant | MODERATE | c.1361C>T | p.Ala454Val | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 1419/16366 | 1361/16008 | 454/5335 | chr7 | 100991924 | ||
| chr7:100991929
|
T | C | 1 | a0044 | 1 | HG01168.hp2 | missense_variant | MODERATE | c.1366T>C | p.Ser456Pro | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 1424/16366 | 1366/16008 | 456/5335 | chr7 | 100991929 | ||
| chr7:100992007
|
G | A | 1 | a0052 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.1444G>A | p.Gly482Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 1502/16366 | 1444/16008 | 482/5335 | chr7 | 100992007 | ||
| chr7:100992094
|
A | C | 136 | a0001a0008a0009others(133): Show | 164 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(161): Show |
missense_variant | MODERATE | c.1531A>C | p.Ser511Arg | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 1589/16366 | 1531/16008 | 511/5335 | chr7 | 100992094 | ||
| chr7:100992096
|
C | G | 1 | a0054 | 1 | HG01952.hp1 | missense_variant | MODERATE | c.1533C>G | p.Ser511Arg | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 1591/16366 | 1533/16008 | 511/5335 | chr7 | 100992096 | ||
| chr7:100992239
|
C | T | 1 | a0202 | 1 | HG01928.hp1 | missense_variant | MODERATE | c.1676C>T | p.Thr559Ile | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 1734/16366 | 1676/16008 | 559/5335 | chr7 | 100992239 | ||
| chr7:100992254
|
C | T | 26 | a0033a0034a0176others(23): Show | 28 | HG00642.hp2 HG00673.hp1 HG01106.hp1 others(25): Show |
missense_variant | MODERATE | c.1691C>T | p.Ser564Phe | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 1749/16366 | 1691/16008 | 564/5335 | chr7 | 100992254 | ||
| chr7:100992293
|
A | C | 2 | a0005a0203 | 5 | NA18942.hp2 NA18967.hp2 NA18971.hp2 others(2): Show |
missense_variant | MODERATE | c.1730A>C | p.Tyr577Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 1788/16366 | 1730/16008 | 577/5335 | chr7 | 100992293 | ||
| chr7:100992310
|
C | A | 136 | a0001a0008a0009others(133): Show | 164 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(161): Show |
missense_variant | MODERATE | c.1747C>A | p.Arg583Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 1805/16366 | 1747/16008 | 583/5335 | chr7 | 100992310 | ||
| chr7:100992310
|
C | G | 2 | a0005a0203 | 5 | NA18942.hp2 NA18967.hp2 NA18971.hp2 others(2): Show |
missense_variant | MODERATE | c.1747C>G | p.Arg583Gly | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 1805/16366 | 1747/16008 | 583/5335 | chr7 | 100992310 | ||
| chr7:100992364
|
C | A | 1 | a0200 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.1801C>A | p.Leu601Ile | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 1859/16366 | 1801/16008 | 601/5335 | chr7 | 100992364 | ||
| chr7:100992380
|
T | C | 205 | a0001a0002a0003others(202): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
missense_variant | MODERATE | c.1817T>C | p.Met606Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 1875/16366 | 1817/16008 | 606/5335 | chr7 | 100992380 | ||
| chr7:100992398
|
C | G | 121 | a0001a0008a0009others(118): Show | 149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
missense_variant | MODERATE | c.1835C>G | p.Thr612Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 1893/16366 | 1835/16008 | 612/5335 | chr7 | 100992398 | ||
| chr7:100992486
|
G | C | 26 | a0033a0034a0176others(23): Show | 28 | HG00642.hp2 HG00673.hp1 HG01106.hp1 others(25): Show |
missense_variant | MODERATE | c.1923G>C | p.Lys641Asn | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 1981/16366 | 1923/16008 | 641/5335 | chr7 | 100992486 | ||
| chr7:100992563
|
C | T | 1 | a0083 | 1 | HG02896.hp2 | missense_variant | MODERATE | c.2000C>T | p.Ser667Leu | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 2058/16366 | 2000/16008 | 667/5335 | chr7 | 100992563 | ||
| chr7:100992676
|
G | A | 2 | a0172a0256 | 2 | HG00423.hp2 NA20752.hp2 |
missense_variant | MODERATE | c.2113G>A | p.Asp705Asn | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 2171/16366 | 2113/16008 | 705/5335 | chr7 | 100992676 | ||
| chr7:100992761
|
C | G | 1 | a0200 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.2198C>G | p.Ser733Cys | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 2256/16366 | 2198/16008 | 733/5335 | chr7 | 100992761 | ||
| chr7:100992802
|
G | A | 5 | a0267a0268a0269others(2): Show | 5 | HG01884.hp2 HG02257.hp2 HG03471.hp1 others(2): Show |
missense_variant | MODERATE | c.2239G>A | p.Gly747Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 2297/16366 | 2239/16008 | 747/5335 | chr7 | 100992802 | ||
| chr7:100992866
|
C | T | 26 | a0033a0034a0176others(23): Show | 28 | HG00642.hp2 HG00673.hp1 HG01106.hp1 others(25): Show |
missense_variant | MODERATE | c.2303C>T | p.Thr768Ile | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 2361/16366 | 2303/16008 | 768/5335 | chr7 | 100992866 | ||
| chr7:100992888
|
C | A | 1 | a0172 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.2325C>A | p.Asp775Glu | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 2383/16366 | 2325/16008 | 775/5335 | chr7 | 100992888 | ||
| chr7:100992889
|
G | A | 1 | a0172 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.2326G>A | p.Ala776Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 2384/16366 | 2326/16008 | 776/5335 | chr7 | 100992889 | ||
| chr7:100992893
|
C | T | 1 | a0055 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.2330C>T | p.Thr777Met | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 2388/16366 | 2330/16008 | 777/5335 | chr7 | 100992893 | ||
| chr7:100992926
|
C | A | 25 | a0033a0034a0176others(22): Show | 27 | HG00642.hp2 HG00673.hp1 HG01106.hp1 others(24): Show |
missense_variant | MODERATE | c.2363C>A | p.Thr788Asn | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 2421/16366 | 2363/16008 | 788/5335 | chr7 | 100992926 | ||
| chr7:100992926
|
C | T | 1 | a0172 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.2363C>T | p.Thr788Ile | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 2421/16366 | 2363/16008 | 788/5335 | chr7 | 100992926 | ||
| chr7:100992983
|
C | T | 3 | a0035a0204a0205 | 4 | NA18970.hp1 NA19005.hp1 NA19010.hp2 others(1): Show |
missense_variant | MODERATE | c.2420C>T | p.Thr807Met | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 2478/16366 | 2420/16008 | 807/5335 | chr7 | 100992983 | ||
| chr7:100993004
|
C | T | 3 | a0084a0085a0086 | 3 | HG00735.hp2 HG03654.hp2 HG03831.hp2 |
missense_variant | MODERATE | c.2441C>T | p.Thr814Ile | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 2499/16366 | 2441/16008 | 814/5335 | chr7 | 100993004 | ||
| chr7:100993010
|
C | T | 1 | a0272 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.2447C>T | p.Thr816Met | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 2505/16366 | 2447/16008 | 816/5335 | chr7 | 100993010 | ||
| chr7:100993028
|
G | A | 3 | a0172a0206a0256 | 3 | HG00423.hp2 NA19066.hp1 NA20752.hp2 |
missense_variant | MODERATE | c.2465G>A | p.Arg822Lys | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 2523/16366 | 2465/16008 | 822/5335 | chr7 | 100993028 | ||
| chr7:100993044
|
T | TAGTAGCC others(1067): Show |
1 | a0052 | 1 | NA20905.hp2 | conservative_inframe_insertion | MODERATE | c.2538_2539insATCAGT others(1068): Show |
p.Gly846_Val847insIl others(1072): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 2597/16366 | 2539/16008 | 847/5335 | INFO_REALIGN_3_PRIME | chr7 | 100993044 | |
| chr7:100993044
|
T | TAGTAGCC others(1067): Show |
1 | a0174 | 1 | NA19081.hp1 | conservative_inframe_insertion | MODERATE | c.2538_2539insATCAGT others(1068): Show |
p.Gly846_Val847insIl others(1072): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 2597/16366 | 2539/16008 | 847/5335 | INFO_REALIGN_3_PRIME | chr7 | 100993044 | |
| chr7:100993044
|
T | TAGTAGCC others(1067): Show |
1 | a0171 | 1 | NA18989.hp1 | disruptive_inframe_insertion | MODERATE | c.2563_2564insACAGCC others(1068): Show |
p.Ser854_Arg855insHi others(1072): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 2622/16366 | 2564/16008 | 855/5335 | INFO_REALIGN_3_PRIME | chr7 | 100993044 | |
| chr7:100993044
|
T | TAGTAGCC others(1067): Show |
1 | a0170 | 1 | HG03225.hp2 | disruptive_inframe_insertion | MODERATE | c.2563_2564insACAGCC others(1068): Show |
p.Ser854_Arg855insHi others(1072): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 2622/16366 | 2564/16008 | 855/5335 | INFO_REALIGN_3_PRIME | chr7 | 100993044 | |
| chr7:100993044
|
T | TAGTAGCC others(1067): Show |
1 | a0087 | 1 | NA18971.hp1 | disruptive_inframe_insertion | MODERATE | c.2563_2564insACAGCC others(1068): Show |
p.Ser854_Arg855insHi others(1072): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 2622/16366 | 2564/16008 | 855/5335 | INFO_REALIGN_3_PRIME | chr7 | 100993044 | |
| chr7:100993044
|
T | TAGTAGCC others(1067): Show |
1 | a0168 | 1 | HG03516.hp2 | disruptive_inframe_insertion | MODERATE | c.2563_2564insACAGCC others(1068): Show |
p.Ser854_Arg855insHi others(1072): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 2622/16366 | 2564/16008 | 855/5335 | INFO_REALIGN_3_PRIME | chr7 | 100993044 | |
| chr7:100993044
|
T | TAGTAGCC others(1067): Show |
1 | a0091 | 1 | HG04228.hp2 | disruptive_inframe_insertion | MODERATE | c.2563_2564insACAGCC others(1068): Show |
p.Ser854_Arg855insHi others(1072): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 2622/16366 | 2564/16008 | 855/5335 | INFO_REALIGN_3_PRIME | chr7 | 100993044 | |
| chr7:100993044
|
T | TAGTAGCC others(1067): Show |
1 | a0092 | 1 | NA18978.hp2 | disruptive_inframe_insertion | MODERATE | c.2563_2564insACAGCC others(1068): Show |
p.Ser854_Arg855insHi others(1072): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 2622/16366 | 2564/16008 | 855/5335 | INFO_REALIGN_3_PRIME | chr7 | 100993044 | |
| chr7:100993044
|
T | TAGTAGCC others(1067): Show |
1 | a0093 | 1 | HG01257.hp1 | disruptive_inframe_insertion | MODERATE | c.2563_2564insACAGCC others(1068): Show |
p.Ser854_Arg855insHi others(1072): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 2622/16366 | 2564/16008 | 855/5335 | INFO_REALIGN_3_PRIME | chr7 | 100993044 | |
| chr7:100993044
|
T | TAGTAGCC others(1067): Show |
102 | a0001a0008a0009others(99): Show | 129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
disruptive_inframe_insertion | MODERATE | c.2563_2564insACAGCC others(1068): Show |
p.Ser854_Arg855insHi others(1072): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 2622/16366 | 2564/16008 | 855/5335 | INFO_REALIGN_3_PRIME | chr7 | 100993044 | |
| chr7:100993044
|
T | TAGTAGCC others(1067): Show |
4 | a0088a0089a0090others(1): Show | 4 | HG00408.hp1 HG02027.hp2 NA18948.hp2 others(1): Show |
disruptive_inframe_insertion | MODERATE | c.2563_2564insACAGCC others(1068): Show |
p.Ser854_Arg855insHi others(1072): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 2622/16366 | 2564/16008 | 855/5335 | INFO_REALIGN_3_PRIME | chr7 | 100993044 | |
| chr7:100993044
|
T | TAGTAGCC others(1067): Show |
1 | a0148 | 1 | NA18954.hp1 | disruptive_inframe_insertion | MODERATE | c.2563_2564insACAGCC others(1068): Show |
p.Ser854_Arg855insHi others(1072): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 2622/16366 | 2564/16008 | 855/5335 | INFO_REALIGN_3_PRIME | chr7 | 100993044 | |
| chr7:100993044
|
T | TAGTAGCC others(1067): Show |
3 | a0011a0045a0046 | 4 | HG00323.hp1 HG00639.hp2 HG01074.hp2 others(1): Show |
disruptive_inframe_insertion | MODERATE | c.2563_2564insACAGCC others(1068): Show |
p.Ser854_Arg855insHi others(1072): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 2622/16366 | 2564/16008 | 855/5335 | INFO_REALIGN_3_PRIME | chr7 | 100993044 | |
| chr7:100993044
|
T | TAGTAGCC others(1067): Show |
1 | a0044 | 1 | HG01168.hp2 | disruptive_inframe_insertion | MODERATE | c.2563_2564insACAGCC others(1068): Show |
p.Ser854_Arg855insHi others(1072): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 2622/16366 | 2564/16008 | 855/5335 | INFO_REALIGN_3_PRIME | chr7 | 100993044 | |
| chr7:100993102
|
G | A | 2 | a0201a0256 | 2 | HG00423.hp2 HG01109.hp1 |
missense_variant | MODERATE | c.2539G>A | p.Val847Ile | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 2597/16366 | 2539/16008 | 847/5335 | chr7 | 100993102 | ||
| chr7:100993127
|
G | A | 210 | a0001a0002a0003others(207): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
missense_variant | MODERATE | c.2564G>A | p.Arg855His | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 2622/16366 | 2564/16008 | 855/5335 | chr7 | 100993127 | ||
| chr7:100993178
|
C | G | 5 | a0019a0083a0092others(2): Show | 6 | HG02083.hp2 HG02896.hp2 NA18946.hp2 others(3): Show |
missense_variant | MODERATE | c.2615C>G | p.Thr872Arg | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 2673/16366 | 2615/16008 | 872/5335 | chr7 | 100993178 | ||
| chr7:100993180
|
C | A | 14 | a0034a0176a0177others(11): Show | 15 | HG00642.hp2 HG00673.hp1 HG01106.hp1 others(12): Show |
missense_variant | MODERATE | c.2617C>A | p.Pro873Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 2675/16366 | 2617/16008 | 873/5335 | chr7 | 100993180 | ||
| chr7:100993193
|
G | A | 1 | a0200 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.2630G>A | p.Arg877Gln | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 2688/16366 | 2630/16008 | 877/5335 | chr7 | 100993193 | ||
| chr7:100993270
|
C | T | 6 | a0049a0252a0253others(3): Show | 6 | HG00423.hp2 HG00639.hp1 HG01433.hp2 others(3): Show |
missense_variant | MODERATE | c.2707C>T | p.Pro903Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 2765/16366 | 2707/16008 | 903/5335 | chr7 | 100993270 | ||
| chr7:100993271
|
C | T | 1 | a0096 | 1 | HG02683.hp2 | missense_variant | MODERATE | c.2708C>T | p.Pro903Leu | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 2766/16366 | 2708/16008 | 903/5335 | chr7 | 100993271 | ||
| chr7:100993303
|
T | C | 209 | a0001a0002a0003others(206): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
missense_variant | MODERATE | c.2740T>C | p.Ser914Pro | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 2798/16366 | 2740/16008 | 914/5335 | chr7 | 100993303 | ||
| chr7:100993351
|
T | A | 5 | a0262a0263a0264others(2): Show | 5 | HG02258.hp1 HG02723.hp2 HG03098.hp2 others(2): Show |
missense_variant | MODERATE | c.2788T>A | p.Ser930Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 2846/16366 | 2788/16008 | 930/5335 | chr7 | 100993351 | ||
| chr7:100993385
|
A | G | 142 | a0001a0008a0009others(139): Show | 170 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(167): Show |
missense_variant | MODERATE | c.2822A>G | p.Asn941Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 2880/16366 | 2822/16008 | 941/5335 | chr7 | 100993385 | ||
| chr7:100993424
|
C | T | 15 | a0258a0259a0260others(12): Show | 15 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(12): Show |
missense_variant | MODERATE | c.2861C>T | p.Thr954Ile | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 2919/16366 | 2861/16008 | 954/5335 | chr7 | 100993424 | ||
| chr7:100993441
|
G | C | 26 | a0033a0034a0176others(23): Show | 28 | HG00642.hp2 HG00673.hp1 HG01106.hp1 others(25): Show |
missense_variant | MODERATE | c.2878G>C | p.Val960Leu | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 2936/16366 | 2878/16008 | 960/5335 | chr7 | 100993441 | ||
| chr7:100993442
|
T | C | 1 | a0170 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.2879T>C | p.Val960Ala | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 2937/16366 | 2879/16008 | 960/5335 | chr7 | 100993442 | ||
| chr7:100993591
|
A | C | 1 | a0083 | 1 | HG02896.hp2 | missense_variant | MODERATE | c.3028A>C | p.Thr1010Pro | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 3086/16366 | 3028/16008 | 1010/5335 | chr7 | 100993591 | ||
| chr7:100993685
|
G | A | 2 | a0258a0272 | 2 | HG02258.hp2 HG03130.hp2 |
missense_variant | MODERATE | c.3122G>A | p.Gly1041Asp | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 3180/16366 | 3122/16008 | 1041/5335 | chr7 | 100993685 | ||
| chr7:100993727
|
C | A | 42 | a0002a0003a0006others(39): Show | 65 | HG00099.hp2 HG00558.hp2 HG01099.hp1 others(62): Show |
missense_variant | MODERATE | c.3164C>A | p.Ala1055Glu | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 3222/16366 | 3164/16008 | 1055/5335 | chr7 | 100993727 | ||
| chr7:100993754
|
A | C | 42 | a0002a0003a0006others(39): Show | 65 | HG00099.hp2 HG00558.hp2 HG01099.hp1 others(62): Show |
missense_variant | MODERATE | c.3191A>C | p.His1064Pro | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 3249/16366 | 3191/16008 | 1064/5335 | chr7 | 100993754 | ||
| chr7:100993760
|
C | A | 42 | a0002a0003a0006others(39): Show | 65 | HG00099.hp2 HG00558.hp2 HG01099.hp1 others(62): Show |
missense_variant | MODERATE | c.3197C>A | p.Thr1066Lys | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 3255/16366 | 3197/16008 | 1066/5335 | chr7 | 100993760 | ||
| chr7:100993760
|
C | T | 1 | a0200 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.3197C>T | p.Thr1066Ile | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 3255/16366 | 3197/16008 | 1066/5335 | chr7 | 100993760 | ||
| chr7:100993792
|
C | T | 1 | a0189 | 1 | HG01106.hp1 | missense_variant | MODERATE | c.3229C>T | p.Arg1077Cys | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 3287/16366 | 3229/16008 | 1077/5335 | chr7 | 100993792 | ||
| chr7:100993793
|
G | A | 40 | a0020a0021a0022others(37): Show | 45 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(42): Show |
missense_variant | MODERATE | c.3230G>A | p.Arg1077His | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 3288/16366 | 3230/16008 | 1077/5335 | chr7 | 100993793 | ||
| chr7:100993873
|
T | C | 1 | a0271 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.3310T>C | p.Phe1104Leu | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 3368/16366 | 3310/16008 | 1104/5335 | chr7 | 100993873 | ||
| chr7:100993912
|
C | A | 79 | a0002a0003a0006others(76): Show | 104 | HG00099.hp2 HG00558.hp2 HG00642.hp2 others(101): Show |
missense_variant | MODERATE | c.3349C>A | p.Pro1117Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 3407/16366 | 3349/16008 | 1117/5335 | chr7 | 100993912 | ||
| chr7:100994057
|
G | C | 218 | a0001a0002a0003others(215): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
missense_variant | MODERATE | c.3494G>C | p.Arg1165Pro | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 3552/16366 | 3494/16008 | 1165/5335 | chr7 | 100994057 | ||
| chr7:100994087
|
A | G | 134 | a0001a0004a0008others(131): Show | 167 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(164): Show |
missense_variant | MODERATE | c.3524A>G | p.His1175Arg | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 3582/16366 | 3524/16008 | 1175/5335 | chr7 | 100994087 | ||
| chr7:100994108
|
A | G | 140 | a0001a0004a0008others(137): Show | 173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
missense_variant | MODERATE | c.3545A>G | p.His1182Arg | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 3603/16366 | 3545/16008 | 1182/5335 | chr7 | 100994108 | ||
| chr7:100994116
|
G | A | 2 | a0258a0261 | 2 | HG02451.hp2 HG03130.hp2 |
missense_variant | MODERATE | c.3553G>A | p.Glu1185Lys | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 3611/16366 | 3553/16008 | 1185/5335 | chr7 | 100994116 | ||
| chr7:100994138
|
G | A | 1 | a0271 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.3575G>A | p.Arg1192Gln | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 3633/16366 | 3575/16008 | 1192/5335 | chr7 | 100994138 | ||
| chr7:100994200
|
G | A | 1 | a0261 | 1 | HG02451.hp2 | missense_variant | MODERATE | c.3637G>A | p.Glu1213Lys | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 3695/16366 | 3637/16008 | 1213/5335 | chr7 | 100994200 | ||
| chr7:100994266
|
G | A | 43 | a0002a0003a0006others(40): Show | 66 | HG00099.hp2 HG00558.hp2 HG00642.hp1 others(63): Show |
missense_variant | MODERATE | c.3703G>A | p.Ala1235Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 3761/16366 | 3703/16008 | 1235/5335 | chr7 | 100994266 | ||
| chr7:100994275
|
G | A | 3 | a0258a0261a0272 | 3 | HG02258.hp2 HG02451.hp2 HG03130.hp2 |
missense_variant | MODERATE | c.3712G>A | p.Gly1238Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 3770/16366 | 3712/16008 | 1238/5335 | chr7 | 100994275 | ||
| chr7:100994318
|
G | C | 2 | a0262a0263 | 2 | HG02258.hp1 NA20129.hp1 |
missense_variant | MODERATE | c.3755G>C | p.Gly1252Ala | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 3813/16366 | 3755/16008 | 1252/5335 | chr7 | 100994318 | ||
| chr7:100994324
|
A | C | 251 | a0001a0002a0003others(248): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
missense_variant | MODERATE | c.3761A>C | p.Lys1254Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 3819/16366 | 3761/16008 | 1254/5335 | chr7 | 100994324 | ||
| chr7:100994359
|
G | A | 1 | a0190 | 1 | HG03239.hp2 | missense_variant | MODERATE | c.3796G>A | p.Val1266Ile | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 3854/16366 | 3796/16008 | 1266/5335 | chr7 | 100994359 | ||
| chr7:100994380
|
C | T | 1 | a0088 | 1 | NA19007.hp1 | missense_variant | MODERATE | c.3817C>T | p.Arg1273Cys | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 3875/16366 | 3817/16008 | 1273/5335 | chr7 | 100994380 | ||
| chr7:100994467
|
A | G | 1 | a0056 | 1 | HG01261.hp2 | missense_variant | MODERATE | c.3904A>G | p.Thr1302Ala | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 3962/16366 | 3904/16008 | 1302/5335 | chr7 | 100994467 | ||
| chr7:100994483
|
C | A | 3 | a0258a0261a0272 | 3 | HG02258.hp2 HG02451.hp2 HG03130.hp2 |
missense_variant | MODERATE | c.3920C>A | p.Pro1307Gln | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 3978/16366 | 3920/16008 | 1307/5335 | chr7 | 100994483 | ||
| chr7:100994530
|
G | A | 1 | a0118 | 1 | HG00735.hp1 | missense_variant | MODERATE | c.3967G>A | p.Glu1323Lys | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 4025/16366 | 3967/16008 | 1323/5335 | chr7 | 100994530 | ||
| chr7:100994558
|
C | G | 38 | a0033a0034a0176others(35): Show | 40 | HG00642.hp2 HG01106.hp1 HG01109.hp2 others(37): Show |
missense_variant | MODERATE | c.3995C>G | p.Pro1332Arg | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 4053/16366 | 3995/16008 | 1332/5335 | chr7 | 100994558 | ||
| chr7:100994606
|
A | G | 220 | a0001a0002a0003others(217): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
missense_variant | MODERATE | c.4043A>G | p.Asp1348Gly | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 4101/16366 | 4043/16008 | 1348/5335 | chr7 | 100994606 | ||
| chr7:100994624
|
C | A | 1 | a0191 | 1 | HG00673.hp1 | missense_variant | MODERATE | c.4061C>A | p.Thr1354Lys | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 4119/16366 | 4061/16008 | 1354/5335 | chr7 | 100994624 | ||
| chr7:100994626
|
A | G | 16 | a0004a0036a0200others(13): Show | 21 | HG00423.hp2 HG00639.hp1 HG01433.hp2 others(18): Show |
missense_variant | MODERATE | c.4063A>G | p.Thr1355Ala | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 4121/16366 | 4063/16008 | 1355/5335 | chr7 | 100994626 | ||
| chr7:100994668
|
C | A | 1 | a0190 | 1 | HG03239.hp2 | missense_variant | MODERATE | c.4105C>A | p.Pro1369Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 4163/16366 | 4105/16008 | 1369/5335 | chr7 | 100994668 | ||
| chr7:100994711
|
C | A | 1 | a0261 | 1 | HG02451.hp2 | missense_variant | MODERATE | c.4148C>A | p.Thr1383Asn | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 4206/16366 | 4148/16008 | 1383/5335 | chr7 | 100994711 | ||
| chr7:100994854
|
G | A | 80 | a0005a0033a0034others(77): Show | 92 | HG00621.hp1 HG00642.hp2 HG01069.hp2 others(89): Show |
missense_variant | MODERATE | c.4291G>A | p.Ala1431Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 4349/16366 | 4291/16008 | 1431/5335 | chr7 | 100994854 | ||
| chr7:100994854
|
G | T | 1 | a0272 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.4291G>T | p.Ala1431Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 4349/16366 | 4291/16008 | 1431/5335 | chr7 | 100994854 | ||
| chr7:100994926
|
G | A | 127 | a0002a0003a0005others(124): Show | 164 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(161): Show |
missense_variant | MODERATE | c.4363G>A | p.Gly1455Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 4421/16366 | 4363/16008 | 1455/5335 | chr7 | 100994926 | ||
| chr7:100994939
|
C | T | 131 | a0002a0003a0005others(128): Show | 168 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(165): Show |
missense_variant | MODERATE | c.4376C>T | p.Ala1459Val | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 4434/16366 | 4376/16008 | 1459/5335 | chr7 | 100994939 | ||
| chr7:100994975
|
C | T | 10 | a0025a0119a0120others(7): Show | 11 | HG01243.hp2 HG02055.hp1 HG02109.hp2 others(8): Show |
missense_variant | MODERATE | c.4412C>T | p.Pro1471Leu | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 4470/16366 | 4412/16008 | 1471/5335 | chr7 | 100994975 | ||
| chr7:100994998
|
T | C | 29 | a0011a0033a0034others(26): Show | 32 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(29): Show |
missense_variant | MODERATE | c.4435T>C | p.Phe1479Leu | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 4493/16366 | 4435/16008 | 1479/5335 | chr7 | 100994998 | ||
| chr7:100995034
|
G | A | 1 | a0191 | 1 | HG00673.hp1 | missense_variant | MODERATE | c.4471G>A | p.Glu1491Lys | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 4529/16366 | 4471/16008 | 1491/5335 | chr7 | 100995034 | ||
| chr7:100995103
|
T | A | 1 | a0082 | 1 | HG00099.hp2 | missense_variant | MODERATE | c.4540T>A | p.Ser1514Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 4598/16366 | 4540/16008 | 1514/5335 | chr7 | 100995103 | ||
| chr7:100995121
|
C | A | 1 | a0057 | 1 | HG01123.hp2 | missense_variant | MODERATE | c.4558C>A | p.Pro1520Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 4616/16366 | 4558/16008 | 1520/5335 | chr7 | 100995121 | ||
| chr7:100995136
|
A | G | 1 | a0191 | 1 | HG00673.hp1 | missense_variant | MODERATE | c.4573A>G | p.Ile1525Val | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 4631/16366 | 4573/16008 | 1525/5335 | chr7 | 100995136 | ||
| chr7:100995152
|
C | T | 2 | a0044a0178 | 2 | HG01168.hp2 HG02723.hp1 |
missense_variant | MODERATE | c.4589C>T | p.Thr1530Met | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 4647/16366 | 4589/16008 | 1530/5335 | chr7 | 100995152 | ||
| chr7:100995163
|
G | A | 25 | a0033a0034a0176others(22): Show | 27 | HG00642.hp2 HG01106.hp1 HG01109.hp2 others(24): Show |
missense_variant | MODERATE | c.4600G>A | p.Ala1534Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 4658/16366 | 4600/16008 | 1534/5335 | chr7 | 100995163 | ||
| chr7:100995181
|
A | G | 1 | a0261 | 1 | HG02451.hp2 | missense_variant | MODERATE | c.4618A>G | p.Thr1540Ala | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 4676/16366 | 4618/16008 | 1540/5335 | chr7 | 100995181 | ||
| chr7:100995239
|
A | ACACAACA others(2051): Show |
2 | a0109a0171 | 2 | HG02148.hp1 NA18989.hp1 |
conservative_inframe_insertion | MODERATE | c.4851_4852insCTGTCC others(2052): Show |
p.Leu1618_Ser1619ins others(2058): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 4910/16366 | 4852/16008 | 1618/5335 | INFO_REALIGN_3_PRIME | chr7 | 100995239 | |
| chr7:100995308
|
G | A | 1 | a0097 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.4745G>A | p.Arg1582Gln | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 4803/16366 | 4745/16008 | 1582/5335 | chr7 | 100995308 | ||
| chr7:100995320
|
C | T | 93 | a0002a0003a0005others(90): Show | 128 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(125): Show |
missense_variant | MODERATE | c.4757C>T | p.Thr1586Met | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 4815/16366 | 4757/16008 | 1586/5335 | chr7 | 100995320 | ||
| chr7:100995340
|
G | A | 128 | a0002a0003a0005others(125): Show | 165 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(162): Show |
missense_variant | MODERATE | c.4777G>A | p.Gly1593Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 4835/16366 | 4777/16008 | 1593/5335 | chr7 | 100995340 | ||
| chr7:100995340
|
G | GGCAGTAC others(2051): Show |
1 | a0170 | 1 | HG03225.hp2 | conservative_inframe_insertion | MODERATE | c.4851_4852insCTGTCC others(2052): Show |
p.Leu1618_Ser1619ins others(2058): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 4910/16366 | 4852/16008 | 1618/5335 | INFO_REALIGN_3_PRIME | chr7 | 100995340 | |
| chr7:100995340
|
G | GGCAGTAC others(2051): Show |
1 | a0116 | 1 | HG02698.hp1 | conservative_inframe_insertion | MODERATE | c.4851_4852insCTGTCC others(2052): Show |
p.Leu1618_Ser1619ins others(2058): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 4910/16366 | 4852/16008 | 1618/5335 | INFO_REALIGN_3_PRIME | chr7 | 100995340 | |
| chr7:100995340
|
G | GGCAGTAC others(2051): Show |
1 | a0117 | 1 | HG01070.hp2 | conservative_inframe_insertion | MODERATE | c.4851_4852insCTGTCC others(2052): Show |
p.Leu1618_Ser1619ins others(2058): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 4910/16366 | 4852/16008 | 1618/5335 | INFO_REALIGN_3_PRIME | chr7 | 100995340 | |
| chr7:100995340
|
G | GGCAGTAC others(2051): Show |
1 | a0098 | 1 | HG00741.hp1 | conservative_inframe_insertion | MODERATE | c.4851_4852insCTGTCC others(2052): Show |
p.Leu1618_Ser1619ins others(2058): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 4910/16366 | 4852/16008 | 1618/5335 | INFO_REALIGN_3_PRIME | chr7 | 100995340 | |
| chr7:100995340
|
G | GGCAGTAC others(2051): Show |
14 | a0020a0021a0087others(11): Show | 16 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(13): Show |
conservative_inframe_insertion | MODERATE | c.4851_4852insCTGTCC others(2052): Show |
p.Leu1618_Ser1619ins others(2058): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 4910/16366 | 4852/16008 | 1618/5335 | INFO_REALIGN_3_PRIME | chr7 | 100995340 | |
| chr7:100995340
|
G | GGCAGTAC others(2051): Show |
67 | a0001a0008a0009others(64): Show | 86 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(83): Show |
conservative_inframe_insertion | MODERATE | c.4851_4852insCTGTCC others(2052): Show |
p.Leu1618_Ser1619ins others(2058): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 4910/16366 | 4852/16008 | 1618/5335 | INFO_REALIGN_3_PRIME | chr7 | 100995340 | |
| chr7:100995340
|
G | GGCAGTAC others(2051): Show |
1 | a0027 | 2 | HG02970.hp1 HG06807.hp1 |
conservative_inframe_insertion | MODERATE | c.4851_4852insCTGTCC others(2052): Show |
p.Leu1618_Ser1619ins others(2058): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 4910/16366 | 4852/16008 | 1618/5335 | INFO_REALIGN_3_PRIME | chr7 | 100995340 | |
| chr7:100995340
|
G | GGCAGTAC others(2051): Show |
8 | a0025a0121a0122others(5): Show | 9 | HG02055.hp1 HG02109.hp2 HG02257.hp1 others(6): Show |
conservative_inframe_insertion | MODERATE | c.4851_4852insCTGTCC others(2052): Show |
p.Leu1618_Ser1619ins others(2058): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 4910/16366 | 4852/16008 | 1618/5335 | INFO_REALIGN_3_PRIME | chr7 | 100995340 | |
| chr7:100995340
|
G | GGCAGTAC others(2050): Show |
1 | a0174 | 1 | NA19081.hp1 | frameshift_variant&stop_gained | HIGH | c.4851_4852insCTGTCC others(2051): Show |
p.Ser1638fs | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 4910/16366 | 4852/16008 | 1618/5335 | INFO_REALIGN_3_PRIME | chr7 | 100995340 | |
| chr7:100995340
|
G | GGCAGTAC others(2051): Show |
1 | a0026 | 2 | NA19010.hp1 NA19090.hp1 |
conservative_inframe_insertion | MODERATE | c.4851_4852insCTGTCC others(2052): Show |
p.Leu1618_Ser1619ins others(2058): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 4910/16366 | 4852/16008 | 1618/5335 | INFO_REALIGN_3_PRIME | chr7 | 100995340 | |
| chr7:100995340
|
G | GGCAGTAC others(2051): Show |
1 | a0168 | 1 | HG03516.hp2 | conservative_inframe_insertion | MODERATE | c.4851_4852insCTGTCC others(2052): Show |
p.Leu1618_Ser1619ins others(2058): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 4910/16366 | 4852/16008 | 1618/5335 | INFO_REALIGN_3_PRIME | chr7 | 100995340 | |
| chr7:100995340
|
G | GGCAGTAC others(2051): Show |
1 | a0008 | 1 | HG02056.hp2 | conservative_inframe_insertion | MODERATE | c.4851_4852insCTGTCC others(2052): Show |
p.Leu1618_Ser1619ins others(2058): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 4910/16366 | 4852/16008 | 1618/5335 | INFO_REALIGN_3_PRIME | chr7 | 100995340 | |
| chr7:100995475
|
A | G | 46 | a0004a0011a0019others(43): Show | 54 | HG00323.hp1 HG00423.hp2 HG00639.hp1 others(51): Show |
missense_variant | MODERATE | c.4912A>G | p.Ser1638Gly | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 4970/16366 | 4912/16008 | 1638/5335 | chr7 | 100995475 | ||
| chr7:100995478
|
C | T | 2 | a0085a0086 | 2 | HG03654.hp2 HG03831.hp2 |
missense_variant | MODERATE | c.4915C>T | p.Pro1639Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 4973/16366 | 4915/16008 | 1639/5335 | chr7 | 100995478 | ||
| chr7:100995607
|
C | T | 1 | a0110 | 1 | HG03927.hp2 | missense_variant | MODERATE | c.5044C>T | p.Arg1682Cys | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 5102/16366 | 5044/16008 | 1682/5335 | chr7 | 100995607 | ||
| chr7:100995608
|
G | A | 1 | a0228 | 1 | NA18747.hp2 | missense_variant | MODERATE | c.5045G>A | p.Arg1682His | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 5103/16366 | 5045/16008 | 1682/5335 | chr7 | 100995608 | ||
| chr7:100995623
|
C | T | 25 | a0033a0034a0176others(22): Show | 27 | HG00642.hp2 HG01106.hp1 HG01109.hp2 others(24): Show |
missense_variant | MODERATE | c.5060C>T | p.Thr1687Ile | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 5118/16366 | 5060/16008 | 1687/5335 | chr7 | 100995623 | ||
| chr7:100995644
|
G | A | 271 | a0001a0002a0003others(268): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
missense_variant | MODERATE | c.5081G>A | p.Ser1694Asn | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 5139/16366 | 5081/16008 | 1694/5335 | chr7 | 100995644 | ||
| chr7:100995645
|
C | G | 7 | a0259a0260a0262others(4): Show | 7 | HG02258.hp1 HG02622.hp1 HG02723.hp2 others(4): Show |
missense_variant | MODERATE | c.5082C>G | p.Ser1694Arg | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 5140/16366 | 5082/16008 | 1694/5335 | chr7 | 100995645 | ||
| chr7:100995659
|
T | C | 271 | a0001a0002a0003others(268): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
missense_variant | MODERATE | c.5096T>C | p.Met1699Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 5154/16366 | 5096/16008 | 1699/5335 | chr7 | 100995659 | ||
| chr7:100995660
|
G | C | 271 | a0001a0002a0003others(268): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
missense_variant | MODERATE | c.5097G>C | p.Met1699Ile | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 5155/16366 | 5097/16008 | 1699/5335 | chr7 | 100995660 | ||
| chr7:100995686
|
C | G | 5 | a0267a0268a0269others(2): Show | 5 | HG01884.hp2 HG02257.hp2 HG03471.hp1 others(2): Show |
missense_variant | MODERATE | c.5123C>G | p.Ala1708Gly | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 5181/16366 | 5123/16008 | 1708/5335 | chr7 | 100995686 | ||
| chr7:100995839
|
G | A | 2 | a0054a0204 | 2 | HG01952.hp1 NA19005.hp1 |
missense_variant | MODERATE | c.5276G>A | p.Arg1759His | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 5334/16366 | 5276/16008 | 1759/5335 | chr7 | 100995839 | ||
| chr7:100995872
|
C | T | 40 | a0002a0003a0006others(37): Show | 63 | HG00099.hp2 HG00558.hp2 HG01099.hp1 others(60): Show |
missense_variant | MODERATE | c.5309C>T | p.Thr1770Met | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 5367/16366 | 5309/16008 | 1770/5335 | chr7 | 100995872 | ||
| chr7:100995874
|
G | A | 271 | a0001a0002a0003others(268): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
missense_variant | MODERATE | c.5311G>A | p.Ala1771Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 5369/16366 | 5311/16008 | 1771/5335 | chr7 | 100995874 | ||
| chr7:100995880
|
C | G | 1 | a0128 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.5317C>G | p.His1773Asp | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 5375/16366 | 5317/16008 | 1773/5335 | chr7 | 100995880 | ||
| chr7:100995916
|
C | A | 4 | a0024a0120a0134others(1): Show | 5 | HG01243.hp2 HG02145.hp2 HG02896.hp1 others(2): Show |
missense_variant | MODERATE | c.5353C>A | p.Pro1785Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 5411/16366 | 5353/16008 | 1785/5335 | chr7 | 100995916 | ||
| chr7:100995925
|
T | A | 151 | a0001a0005a0008others(148): Show | 188 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(185): Show |
missense_variant | MODERATE | c.5362T>A | p.Ser1788Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 5420/16366 | 5362/16008 | 1788/5335 | chr7 | 100995925 | ||
| chr7:100995925
|
T | G | 116 | a0002a0003a0004others(113): Show | 148 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(145): Show |
missense_variant | MODERATE | c.5362T>G | p.Ser1788Ala | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 5420/16366 | 5362/16008 | 1788/5335 | chr7 | 100995925 | ||
| chr7:100995926
|
C | A | 267 | a0001a0002a0003others(264): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
missense_variant | MODERATE | c.5363C>A | p.Ser1788Tyr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 5421/16366 | 5363/16008 | 1788/5335 | chr7 | 100995926 | ||
| chr7:100995926
|
C | CCACAACT others(2804): Show |
1 | a0167 | 1 | HG02145.hp2 | conservative_inframe_insertion | MODERATE | c.5367_5368insACTTCA others(2805): Show |
p.Thr1789_Ala1790ins others(2811): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 5426/16366 | 5368/16008 | 1790/5335 | INFO_REALIGN_3_PRIME | chr7 | 100995926 | |
| chr7:100995926
|
C | CCACAACT others(2051): Show |
1 | a0024 | 2 | HG02896.hp1 HG02897.hp1 |
conservative_inframe_insertion | MODERATE | c.5367_5368insACTTCA others(2052): Show |
p.Thr1789_Ala1790ins others(2058): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 5426/16366 | 5368/16008 | 1790/5335 | INFO_REALIGN_3_PRIME | chr7 | 100995926 | |
| chr7:100995926
|
C | CCACAACT others(2051): Show |
1 | a0134 | 1 | NA19240.hp1 | conservative_inframe_insertion | MODERATE | c.5367_5368insACTTCA others(2052): Show |
p.Thr1789_Ala1790ins others(2058): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 5426/16366 | 5368/16008 | 1790/5335 | INFO_REALIGN_3_PRIME | chr7 | 100995926 | |
| chr7:100995926
|
C | CCACAACT others(2051): Show |
1 | a0120 | 1 | HG01243.hp2 | conservative_inframe_insertion | MODERATE | c.5367_5368insACTTCA others(2052): Show |
p.Thr1789_Ala1790ins others(2058): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 5426/16366 | 5368/16008 | 1790/5335 | INFO_REALIGN_3_PRIME | chr7 | 100995926 | |
| chr7:100995931
|
G | A | 271 | a0001a0002a0003others(268): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
missense_variant | MODERATE | c.5368G>A | p.Ala1790Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 5426/16366 | 5368/16008 | 1790/5335 | chr7 | 100995931 | ||
| chr7:100995941
|
G | A | 1 | a0200 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.5378G>A | p.Arg1793His | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 5436/16366 | 5378/16008 | 1793/5335 | chr7 | 100995941 | ||
| chr7:100995943
|
A | G | 271 | a0001a0002a0003others(268): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
missense_variant | MODERATE | c.5380A>G | p.Ser1794Gly | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 5438/16366 | 5380/16008 | 1794/5335 | chr7 | 100995943 | ||
| chr7:100995956
|
G | C | 271 | a0001a0002a0003others(268): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
missense_variant | MODERATE | c.5393G>C | p.Arg1798Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 5451/16366 | 5393/16008 | 1798/5335 | chr7 | 100995956 | ||
| chr7:100995994
|
C | G | 271 | a0001a0002a0003others(268): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
missense_variant | MODERATE | c.5431C>G | p.Pro1811Ala | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 5489/16366 | 5431/16008 | 1811/5335 | chr7 | 100995994 | ||
| chr7:100996051
|
G | A | 1 | a0270 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.5488G>A | p.Gly1830Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 5546/16366 | 5488/16008 | 1830/5335 | chr7 | 100996051 | ||
| chr7:100996075
|
C | A | 1 | a0191 | 1 | HG00673.hp1 | missense_variant | MODERATE | c.5512C>A | p.Pro1838Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 5570/16366 | 5512/16008 | 1838/5335 | chr7 | 100996075 | ||
| chr7:100996107
|
G | C | 2 | a0206a0229 | 2 | HG04115.hp2 NA19066.hp1 |
missense_variant | MODERATE | c.5544G>C | p.Glu1848Asp | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 5602/16366 | 5544/16008 | 1848/5335 | chr7 | 100996107 | ||
| chr7:100996130
|
G | A | 1 | a0129 | 1 | NA18941.hp2 | missense_variant | MODERATE | c.5567G>A | p.Ser1856Asn | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 5625/16366 | 5567/16008 | 1856/5335 | chr7 | 100996130 | ||
| chr7:100996137
|
C | A | 107 | a0001a0008a0009others(104): Show | 133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
missense_variant | MODERATE | c.5574C>A | p.Asp1858Glu | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 5632/16366 | 5574/16008 | 1858/5335 | chr7 | 100996137 | ||
| chr7:100996138
|
G | A | 110 | a0001a0008a0009others(107): Show | 136 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(133): Show |
missense_variant | MODERATE | c.5575G>A | p.Ala1859Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 5633/16366 | 5575/16008 | 1859/5335 | chr7 | 100996138 | ||
| chr7:100996175
|
C | T | 94 | a0001a0008a0009others(91): Show | 119 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(116): Show |
missense_variant | MODERATE | c.5612C>T | p.Thr1871Ile | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 5670/16366 | 5612/16008 | 1871/5335 | chr7 | 100996175 | ||
| chr7:100996225
|
A | G | 1 | a0018 | 2 | HG02056.hp1 NA18950.hp1 |
missense_variant | MODERATE | c.5662A>G | p.Met1888Val | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 5720/16366 | 5662/16008 | 1888/5335 | chr7 | 100996225 | ||
| chr7:100996232
|
C | T | 10 | a0025a0119a0120others(7): Show | 11 | HG01243.hp2 HG02055.hp1 HG02109.hp2 others(8): Show |
missense_variant | MODERATE | c.5669C>T | p.Thr1890Met | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 5727/16366 | 5669/16008 | 1890/5335 | chr7 | 100996232 | ||
| chr7:100996246
|
G | T | 8 | a0011a0044a0045others(5): Show | 9 | HG00323.hp1 HG00639.hp2 HG01074.hp2 others(6): Show |
missense_variant | MODERATE | c.5683G>T | p.Gly1895Cys | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 5741/16366 | 5683/16008 | 1895/5335 | chr7 | 100996246 | ||
| chr7:100996256
|
C | T | 2 | a0036a0207 | 3 | HG02630.hp1 HG02717.hp1 HG03579.hp2 |
missense_variant | MODERATE | c.5693C>T | p.Thr1898Ile | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 5751/16366 | 5693/16008 | 1898/5335 | chr7 | 100996256 | ||
| chr7:100996351
|
G | A | 51 | a0005a0010a0035others(48): Show | 63 | HG00621.hp1 HG01069.hp2 HG01070.hp1 others(60): Show |
missense_variant | MODERATE | c.5788G>A | p.Val1930Ile | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 5846/16366 | 5788/16008 | 1930/5335 | chr7 | 100996351 | ||
| chr7:100996382
|
GACCAGGC others(1415): Show |
G | 1 | a0206 | 1 | NA19066.hp1 | disruptive_inframe_deletion | MODERATE | c.6093_7514del | p.Leu2032_Thr2505del | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 6151/16366 | 6093/16008 | 2031/5335 | INFO_REALIGN_3_PRIME | chr7 | 100996382 | |
| chr7:100996394
|
C | T | 1 | a0047 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.5831C>T | p.Thr1944Met | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 5889/16366 | 5831/16008 | 1944/5335 | chr7 | 100996394 | ||
| chr7:100996432
|
G | C | 1 | a0187 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.5869G>C | p.Gly1957Arg | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 5927/16366 | 5869/16008 | 1957/5335 | chr7 | 100996432 | ||
| chr7:100996478
|
C | T | 1 | a0058 | 1 | HG01952.hp2 | missense_variant | MODERATE | c.5915C>T | p.Thr1972Met | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 5973/16366 | 5915/16008 | 1972/5335 | chr7 | 100996478 | ||
| chr7:100996505
|
C | G | 1 | a0215 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.5942C>G | p.Thr1981Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 6000/16366 | 5942/16008 | 1981/5335 | chr7 | 100996505 | ||
| chr7:100996519
|
C | T | 104 | a0002a0003a0005others(101): Show | 139 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(136): Show |
missense_variant | MODERATE | c.5956C>T | p.Pro1986Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 6014/16366 | 5956/16008 | 1986/5335 | chr7 | 100996519 | ||
| chr7:100996552
|
C | T | 105 | a0002a0003a0005others(102): Show | 140 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(137): Show |
missense_variant | MODERATE | c.5989C>T | p.Pro1997Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 6047/16366 | 5989/16008 | 1997/5335 | chr7 | 100996552 | ||
| chr7:100996595
|
C | A | 1 | a0251 | 1 | NA18959.hp1 | missense_variant | MODERATE | c.6032C>A | p.Ala2011Asp | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 6090/16366 | 6032/16008 | 2011/5335 | chr7 | 100996595 | ||
| chr7:100996673
|
C | T | 9 | a0259a0260a0261others(6): Show | 9 | HG02258.hp1 HG02258.hp2 HG02451.hp2 others(6): Show |
missense_variant | MODERATE | c.6110C>T | p.Thr2037Ile | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 6168/16366 | 6110/16008 | 2037/5335 | chr7 | 100996673 | ||
| chr7:100996706
|
G | A | 1 | a0117 | 1 | HG01070.hp2 | missense_variant | MODERATE | c.6143G>A | p.Arg2048His | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 6201/16366 | 6143/16008 | 2048/5335 | chr7 | 100996706 | ||
| chr7:100996708
|
G | A | 2 | a0136a0230 | 2 | NA18942.hp1 NA19060.hp1 |
missense_variant | MODERATE | c.6145G>A | p.Val2049Ile | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 6203/16366 | 6145/16008 | 2049/5335 | chr7 | 100996708 | ||
| chr7:100996732
|
C | T | 3 | a0049a0059a0060 | 3 | HG03516.hp1 NA18994.hp2 NA19000.hp2 |
missense_variant | MODERATE | c.6169C>T | p.Arg2057Cys | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 6227/16366 | 6169/16008 | 2057/5335 | chr7 | 100996732 | ||
| chr7:100996789
|
GCCTTCCA others(1415): Show |
G | 5 | a0004a0007a0036others(2): Show | 12 | HG02109.hp1 HG02602.hp1 HG02630.hp1 others(9): Show |
disruptive_inframe_deletion | MODERATE | c.6776_8197del | p.Thr2259_Arg2732del | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 6834/16366 | 6776/16008 | 2259/5335 | INFO_REALIGN_3_PRIME | chr7 | 100996789 | |
| chr7:100996823
|
C | T | 1 | a0188 | 1 | NA18522.hp1 | missense_variant | MODERATE | c.6260C>T | p.Thr2087Met | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 6318/16366 | 6260/16008 | 2087/5335 | chr7 | 100996823 | ||
| chr7:100996841
|
C | T | 6 | a0003a0006a0013others(3): Show | 15 | HG02071.hp1 HG02135.hp1 HG02523.hp2 others(12): Show |
missense_variant | MODERATE | c.6278C>T | p.Thr2093Ile | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 6336/16366 | 6278/16008 | 2093/5335 | chr7 | 100996841 | ||
| chr7:100996916
|
C | T | 2 | a0011a0046 | 3 | HG00639.hp2 HG01074.hp2 HG01256.hp1 |
missense_variant | MODERATE | c.6353C>T | p.Ala2118Val | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 6411/16366 | 6353/16008 | 2118/5335 | chr7 | 100996916 | ||
| chr7:100996922
|
C | T | 12 | a0011a0019a0044others(9): Show | 14 | HG00323.hp1 HG00639.hp2 HG01074.hp2 others(11): Show |
missense_variant | MODERATE | c.6359C>T | p.Ser2120Phe | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 6417/16366 | 6359/16008 | 2120/5335 | chr7 | 100996922 | ||
| chr7:100996928
|
C | T | 2 | a0137a0138 | 2 | HG02055.hp2 HG02486.hp2 |
missense_variant | MODERATE | c.6365C>T | p.Thr2122Ile | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 6423/16366 | 6365/16008 | 2122/5335 | chr7 | 100996928 | ||
| chr7:100996972
|
G | C | 1 | a0272 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.6409G>C | p.Asp2137His | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 6467/16366 | 6409/16008 | 2137/5335 | chr7 | 100996972 | ||
| chr7:100996988
|
C | T | 1 | a0272 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.6425C>T | p.Thr2142Ile | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 6483/16366 | 6425/16008 | 2142/5335 | chr7 | 100996988 | ||
| chr7:100997042
|
G | A | 30 | a0020a0021a0022others(27): Show | 34 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(31): Show |
missense_variant | MODERATE | c.6479G>A | p.Arg2160His | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 6537/16366 | 6479/16008 | 2160/5335 | chr7 | 100997042 | ||
| chr7:100997210
|
G | A | 2 | a0128a0133 | 2 | HG03041.hp2 NA18982.hp1 |
missense_variant | MODERATE | c.6647G>A | p.Arg2216His | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 6705/16366 | 6647/16008 | 2216/5335 | chr7 | 100997210 | ||
| chr7:100997222
|
G | T | 1 | a0272 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.6659G>T | p.Gly2220Val | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 6717/16366 | 6659/16008 | 2220/5335 | chr7 | 100997222 | ||
| chr7:100997339
|
C | G | 261 | a0001a0002a0003others(258): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
missense_variant | MODERATE | c.6776C>G | p.Thr2259Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 6834/16366 | 6776/16008 | 2259/5335 | chr7 | 100997339 | ||
| chr7:100997341
|
C | A | 261 | a0001a0002a0003others(258): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
missense_variant | MODERATE | c.6778C>A | p.Pro2260Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 6836/16366 | 6778/16008 | 2260/5335 | chr7 | 100997341 | ||
| chr7:100997375
|
C | G | 1 | a0200 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.6812C>G | p.Thr2271Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 6870/16366 | 6812/16008 | 2271/5335 | chr7 | 100997375 | ||
| chr7:100997506
|
C | T | 1 | a0272 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.6943C>T | p.Leu2315Phe | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7001/16366 | 6943/16008 | 2315/5335 | chr7 | 100997506 | ||
| chr7:100997567
|
G | C | 2 | a0262a0263 | 2 | HG02258.hp1 NA20129.hp1 |
missense_variant | MODERATE | c.7004G>C | p.Gly2335Ala | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7062/16366 | 7004/16008 | 2335/5335 | chr7 | 100997567 | ||
| chr7:100997587
|
C | T | 1 | a0231 | 1 | HG02027.hp1 | missense_variant | MODERATE | c.7024C>T | p.Arg2342Cys | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7082/16366 | 7024/16008 | 2342/5335 | chr7 | 100997587 | ||
| chr7:100997608
|
G | A | 1 | a0064 | 1 | HG01433.hp1 | missense_variant | MODERATE | c.7045G>A | p.Val2349Ile | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7103/16366 | 7045/16008 | 2349/5335 | chr7 | 100997608 | ||
| chr7:100997617
|
T | A | 12 | a0011a0019a0044others(9): Show | 14 | HG00323.hp1 HG00639.hp2 HG01074.hp2 others(11): Show |
missense_variant | MODERATE | c.7054T>A | p.Ser2352Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7112/16366 | 7054/16008 | 2352/5335 | chr7 | 100997617 | ||
| chr7:100997752
|
G | A | 10 | a0209a0210a0211others(7): Show | 10 | HG00423.hp2 HG00639.hp1 HG01433.hp2 others(7): Show |
missense_variant | MODERATE | c.7189G>A | p.Ala2397Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7247/16366 | 7189/16008 | 2397/5335 | chr7 | 100997752 | ||
| chr7:100997773
|
G | A | 3 | a0040a0140a0232 | 4 | HG01074.hp1 HG03017.hp2 HG03834.hp1 others(1): Show |
missense_variant | MODERATE | c.7210G>A | p.Val2404Ile | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7268/16366 | 7210/16008 | 2404/5335 | chr7 | 100997773 | ||
| chr7:100997779
|
G | A | 2 | a0032a0166 | 3 | HG03492.hp2 HG03831.hp1 HG04184.hp2 |
missense_variant | MODERATE | c.7216G>A | p.Glu2406Lys | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7274/16366 | 7216/16008 | 2406/5335 | chr7 | 100997779 | ||
| chr7:100997802
|
T | TCAACCAG others(1820): Show |
1 | a0272 | 1 | HG02258.hp2 | disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(1821): Show |
p.Ala2422_Phe2423ins others(1827): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997802 | |
| chr7:100997804
|
A | AACCAGGC others(3878): Show |
1 | a0113 | 1 | HG02735.hp2 | disruptive_inframe_insertion | MODERATE | c.7286_7287insCTCAGG others(3879): Show |
p.Thr2429_Pro2430ins others(3885): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7345/16366 | 7287/16008 | 2429/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(1820): Show |
1 | a0078 | 1 | NA18995.hp2 | disruptive_inframe_insertion | MODERATE | c.7286_7287insCTCAGG others(1821): Show |
p.Thr2429_Pro2430ins others(1827): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7345/16366 | 7287/16008 | 2429/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(1820): Show |
5 | a0017a0054a0064others(2): Show | 6 | HG01099.hp1 HG01192.hp1 HG01433.hp1 others(3): Show |
disruptive_inframe_insertion | MODERATE | c.7286_7287insCTCAGG others(1821): Show |
p.Thr2429_Pro2430ins others(1827): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7345/16366 | 7287/16008 | 2429/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(1820): Show |
3 | a0076a0077a0082 | 3 | HG00099.hp2 HG04184.hp1 NA20752.hp1 |
disruptive_inframe_insertion | MODERATE | c.7286_7287insCTCAGG others(1821): Show |
p.Thr2429_Pro2430ins others(1827): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7345/16366 | 7287/16008 | 2429/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(1820): Show |
1 | a0063 | 1 | NA18983.hp2 | disruptive_inframe_insertion | MODERATE | c.7286_7287insCTCAGG others(1821): Show |
p.Thr2429_Pro2430ins others(1827): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7345/16366 | 7287/16008 | 2429/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(1820): Show |
18 | a0002a0003a0006others(15): Show | 37 | HG00558.hp2 HG01123.hp2 HG01168.hp1 others(34): Show |
disruptive_inframe_insertion | MODERATE | c.7286_7287insCTCAGG others(1821): Show |
p.Thr2429_Pro2430ins others(1827): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7345/16366 | 7287/16008 | 2429/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(1820): Show |
8 | a0033a0182a0183others(5): Show | 9 | HG01109.hp2 HG02559.hp1 HG02717.hp2 others(6): Show |
disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(1821): Show |
p.Ala2422_Phe2423ins others(1827): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(1820): Show |
1 | a0181 | 1 | HG04199.hp2 | disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(1821): Show |
p.Ala2422_Phe2423ins others(1827): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(1820): Show |
1 | a0180 | 1 | HG02976.hp2 | disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(1821): Show |
p.Ala2422_Phe2423ins others(1827): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(1820): Show |
3 | a0176a0179a0190 | 3 | HG02280.hp1 HG02647.hp1 HG03239.hp2 |
disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(1821): Show |
p.Ala2422_Phe2423ins others(1827): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(1820): Show |
1 | a0191 | 1 | HG00673.hp1 | disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(1821): Show |
p.Ala2422_Phe2423ins others(1827): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(1820): Show |
8 | a0034a0177a0189others(5): Show | 9 | HG01106.hp1 HG01515.hp2 HG01978.hp2 others(6): Show |
disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(1821): Show |
p.Ala2422_Phe2423ins others(1827): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(1820): Show |
1 | a0195 | 1 | HG00642.hp2 | disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(1821): Show |
p.Ala2422_Phe2423ins others(1827): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(1820): Show |
1 | a0192 | 1 | HG01361.hp2 | disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(1821): Show |
p.Ala2422_Phe2423ins others(1827): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(1820): Show |
1 | a0194 | 1 | NA18980.hp1 | disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(1821): Show |
p.Ala2422_Phe2423ins others(1827): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(1820): Show |
1 | a0128 | 1 | HG03041.hp2 | disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(1821): Show |
p.Ala2422_Phe2423ins others(1827): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(1820): Show |
1 | a0258 | 1 | HG03130.hp2 | disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(1821): Show |
p.Ala2422_Phe2423ins others(1827): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(1820): Show |
1 | a0154 | 1 | NA18955.hp2 | disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(1821): Show |
p.Ala2422_Phe2423ins others(1827): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(3878): Show |
1 | a0099 | 1 | HG00738.hp2 | disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(3879): Show |
p.Ala2422_Phe2423ins others(3885): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(3878): Show |
1 | a0114 | 1 | HG04228.hp1 | disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(3879): Show |
p.Ala2422_Phe2423ins others(3885): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(1820): Show |
1 | a0024 | 2 | HG02896.hp1 HG02897.hp1 |
disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(1821): Show |
p.Ala2422_Phe2423ins others(1827): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(3878): Show |
1 | a0108 | 1 | HG00408.hp2 | disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(3879): Show |
p.Ala2422_Phe2423ins others(3885): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(3878): Show |
1 | a0103 | 1 | HG00099.hp1 | disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(3879): Show |
p.Ala2422_Phe2423ins others(3885): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(3878): Show |
1 | a0139 | 1 | HG02602.hp2 | disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(3879): Show |
p.Ala2422_Phe2423ins others(3885): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(3878): Show |
1 | a0173 | 1 | HG02135.hp2 | disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(3879): Show |
p.Ala2422_Phe2423ins others(3885): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(3878): Show |
19 | a0021a0022a0023others(16): Show | 22 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(19): Show |
disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(3879): Show |
p.Ala2422_Phe2423ins others(3885): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(3878): Show |
1 | a0110 | 1 | HG03927.hp2 | disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(3879): Show |
p.Ala2422_Phe2423ins others(3885): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(3878): Show |
1 | a0101 | 1 | HG01993.hp2 | disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(3879): Show |
p.Ala2422_Phe2423ins others(3885): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(3878): Show |
1 | a0127 | 1 | HG03098.hp1 | disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(3879): Show |
p.Ala2422_Phe2423ins others(3885): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(3878): Show |
2 | a0020a0100 | 3 | HG00621.hp2 HG02040.hp2 HG02523.hp1 |
disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(3879): Show |
p.Ala2422_Phe2423ins others(3885): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(1820): Show |
3 | a0264a0265a0266 | 3 | HG02723.hp2 HG03098.hp2 NA20129.hp2 |
disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(1821): Show |
p.Ala2422_Phe2423ins others(1827): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(1820): Show |
1 | a0261 | 1 | HG02451.hp2 | disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(1821): Show |
p.Ala2422_Phe2423ins others(1827): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(1820): Show |
2 | a0027a0134 | 3 | HG02970.hp1 HG06807.hp1 NA19240.hp1 |
disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(1821): Show |
p.Ala2422_Phe2423ins others(1827): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(1820): Show |
51 | a0001a0008a0009others(48): Show | 70 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(67): Show |
disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(1821): Show |
p.Ala2422_Phe2423ins others(1827): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(1820): Show |
1 | a0165 | 1 | NA18985.hp1 | disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(1821): Show |
p.Ala2422_Phe2423ins others(1827): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(1820): Show |
1 | a0170 | 1 | HG03225.hp2 | disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(1821): Show |
p.Ala2422_Phe2423ins others(1827): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(1820): Show |
1 | a0043 | 1 | HG02165.hp1 | disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(1821): Show |
p.Ala2422_Phe2423ins others(1827): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(3878): Show |
1 | a0051 | 1 | HG02293.hp1 | disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(3879): Show |
p.Ala2422_Phe2423ins others(3885): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(1820): Show |
13 | a0011a0019a0045others(10): Show | 15 | HG00323.hp1 HG00639.hp2 HG00741.hp1 others(12): Show |
disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(1821): Show |
p.Ala2422_Phe2423ins others(1827): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(1820): Show |
1 | a0044 | 1 | HG01168.hp2 | disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(1821): Show |
p.Ala2422_Phe2423ins others(1827): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(1820): Show |
8 | a0028a0089a0093others(5): Show | 9 | HG01175.hp1 HG01257.hp1 HG02055.hp1 others(6): Show |
disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(1821): Show |
p.Ala2422_Phe2423ins others(1827): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(3878): Show |
1 | a0111 | 1 | NA18967.hp1 | disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(3879): Show |
p.Ala2422_Phe2423ins others(3885): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(1820): Show |
1 | a0150 | 1 | HG00673.hp2 | disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(1821): Show |
p.Ala2422_Phe2423ins others(1827): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(1820): Show |
1 | a0168 | 1 | HG03516.hp2 | disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(1821): Show |
p.Ala2422_Phe2423ins others(1827): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(1820): Show |
1 | a0169 | 1 | HG00642.hp1 | disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(1821): Show |
p.Ala2422_Phe2423ins others(1827): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(1820): Show |
2 | a0119a0121 | 2 | HG02109.hp2 HG03209.hp1 |
disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(1821): Show |
p.Ala2422_Phe2423ins others(1827): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(1820): Show |
1 | a0141 | 1 | HG02132.hp1 | disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(1821): Show |
p.Ala2422_Phe2423ins others(1827): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(1820): Show |
2 | a0262a0263 | 2 | HG02258.hp1 NA20129.hp1 |
disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(1821): Show |
p.Ala2422_Phe2423ins others(1827): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(1820): Show |
2 | a0259a0260 | 2 | HG02622.hp1 HG03195.hp2 |
disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(1821): Show |
p.Ala2422_Phe2423ins others(1827): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(1820): Show |
1 | a0268 | 1 | HG03579.hp1 | disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(1821): Show |
p.Ala2422_Phe2423ins others(1827): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(1820): Show |
3 | a0269a0270a0271 | 3 | HG01884.hp2 HG02257.hp2 HG03471.hp1 |
disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(1821): Show |
p.Ala2422_Phe2423ins others(1827): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(1820): Show |
1 | a0267 | 1 | HG03486.hp1 | disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(1821): Show |
p.Ala2422_Phe2423ins others(1827): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(1820): Show |
1 | a0216 | 1 | HG03834.hp2 | disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(1821): Show |
p.Ala2422_Phe2423ins others(1827): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(1820): Show |
3 | a0211a0249a0251 | 3 | HG02074.hp2 HG03209.hp2 NA18959.hp1 |
disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(1821): Show |
p.Ala2422_Phe2423ins others(1827): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(1820): Show |
1 | a0048 | 1 | NA19030.hp2 | disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(1821): Show |
p.Ala2422_Phe2423ins others(1827): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(1821): Show |
1 | a0248 | 1 | HG02071.hp2 | frameshift_variant&stop_gained | HIGH | c.7265_7266insGTTCCC others(1822): Show |
p.Pro2430fs | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(1820): Show |
63 | a0005a0010a0014others(60): Show | 76 | HG00423.hp2 HG00621.hp1 HG00639.hp1 others(73): Show |
disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(1821): Show |
p.Ala2422_Phe2423ins others(1827): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(1820): Show |
1 | a0222 | 1 | HG01934.hp2 | disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(1821): Show |
p.Ala2422_Phe2423ins others(1827): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(1820): Show |
1 | a0200 | 1 | HG02572.hp1 | disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(1821): Show |
p.Ala2422_Phe2423ins others(1827): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(1820): Show |
1 | a0227 | 1 | HG01255.hp2 | disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(1821): Show |
p.Ala2422_Phe2423ins others(1827): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(1820): Show |
1 | a0074 | 1 | HG02615.hp1 | disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(1821): Show |
p.Ala2422_Phe2423ins others(1827): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(1820): Show |
1 | a0075 | 1 | NA19043.hp1 | disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(1821): Show |
p.Ala2422_Phe2423ins others(1827): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(1820): Show |
1 | a0049 | 1 | HG03516.hp1 | disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(1821): Show |
p.Ala2422_Phe2423ins others(1827): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997804
|
A | AACCAGGC others(1820): Show |
1 | a0202 | 1 | HG01928.hp1 | disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(1821): Show |
p.Ala2422_Phe2423ins others(1827): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997804 | |
| chr7:100997816
|
C | CGCACACA others(1820): Show |
1 | a0178 | 1 | HG02723.hp1 | disruptive_inframe_insertion | MODERATE | c.7265_7266insGTTCCC others(1821): Show |
p.Ala2422_Phe2423ins others(1827): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7324/16366 | 7266/16008 | 2422/5335 | INFO_REALIGN_3_PRIME | chr7 | 100997816 | |
| chr7:100997864
|
G | A | 3 | a0055a0065a0066 | 3 | HG02647.hp2 HG02809.hp1 HG04204.hp2 |
missense_variant | MODERATE | c.7301G>A | p.Arg2434Gln | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7359/16366 | 7301/16008 | 2434/5335 | chr7 | 100997864 | ||
| chr7:100997941
|
C | T | 83 | a0002a0003a0005others(80): Show | 115 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(112): Show |
missense_variant | MODERATE | c.7378C>T | p.Pro2460Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7436/16366 | 7378/16008 | 2460/5335 | chr7 | 100997941 | ||
| chr7:100997974
|
C | T | 85 | a0002a0003a0005others(82): Show | 117 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(114): Show |
missense_variant | MODERATE | c.7411C>T | p.Pro2471Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7469/16366 | 7411/16008 | 2471/5335 | chr7 | 100997974 | ||
| chr7:100997978
|
G | T | 1 | a0073 | 1 | HG01978.hp1 | missense_variant | MODERATE | c.7415G>T | p.Gly2472Val | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7473/16366 | 7415/16008 | 2472/5335 | chr7 | 100997978 | ||
| chr7:100998095
|
C | T | 1 | a0258 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.7532C>T | p.Thr2511Ile | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7590/16366 | 7532/16008 | 2511/5335 | chr7 | 100998095 | ||
| chr7:100998127
|
C | T | 1 | a0110 | 1 | HG03927.hp2 | missense_variant | MODERATE | c.7564C>T | p.Arg2522Cys | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7622/16366 | 7564/16008 | 2522/5335 | chr7 | 100998127 | ||
| chr7:100998211
|
A | G | 258 | a0001a0002a0003others(255): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
missense_variant | MODERATE | c.7648A>G | p.Thr2550Ala | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7706/16366 | 7648/16008 | 2550/5335 | chr7 | 100998211 | ||
| chr7:100998245
|
C | T | 3 | a0176a0179a0190 | 3 | HG02280.hp1 HG02647.hp1 HG03239.hp2 |
missense_variant | MODERATE | c.7682C>T | p.Thr2561Met | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7740/16366 | 7682/16008 | 2561/5335 | chr7 | 100998245 | ||
| chr7:100998262
|
A | C | 12 | a0011a0019a0044others(9): Show | 14 | HG00323.hp1 HG00639.hp2 HG01074.hp2 others(11): Show |
missense_variant | MODERATE | c.7699A>C | p.Thr2567Pro | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7757/16366 | 7699/16008 | 2567/5335 | chr7 | 100998262 | ||
| chr7:100998350
|
C | T | 1 | a0129 | 1 | NA18941.hp2 | missense_variant | MODERATE | c.7787C>T | p.Thr2596Ile | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7845/16366 | 7787/16008 | 2596/5335 | chr7 | 100998350 | ||
| chr7:100998463
|
C | T | 3 | a0093a0132a0167 | 3 | HG01175.hp1 HG01257.hp1 HG02145.hp2 |
missense_variant | MODERATE | c.7900C>T | p.Arg2634Cys | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7958/16366 | 7900/16008 | 2634/5335 | chr7 | 100998463 | ||
| chr7:100998464
|
G | A | 4 | a0096a0099a0114others(1): Show | 4 | HG00735.hp1 HG00738.hp2 HG02683.hp2 others(1): Show |
missense_variant | MODERATE | c.7901G>A | p.Arg2634His | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7959/16366 | 7901/16008 | 2634/5335 | chr7 | 100998464 | ||
| chr7:100998517
|
C | G | 1 | a0055 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.7954C>G | p.Pro2652Ala | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 8012/16366 | 7954/16008 | 2652/5335 | chr7 | 100998517 | ||
| chr7:100998554
|
G | T | 1 | a0177 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.7991G>T | p.Ser2664Ile | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 8049/16366 | 7991/16008 | 2664/5335 | chr7 | 100998554 | ||
| chr7:100998607
|
G | A | 2 | a0219a0220 | 2 | HG01106.hp2 HG01515.hp1 |
missense_variant | MODERATE | c.8044G>A | p.Val2682Ile | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 8102/16366 | 8044/16008 | 2682/5335 | chr7 | 100998607 | ||
| chr7:100998632
|
G | A | 10 | a0027a0028a0089others(7): Show | 12 | HG01175.hp1 HG01257.hp1 HG02055.hp1 others(9): Show |
missense_variant | MODERATE | c.8069G>A | p.Arg2690His | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 8127/16366 | 8069/16008 | 2690/5335 | chr7 | 100998632 | ||
| chr7:100998641
|
C | G | 1 | a0089 | 1 | NA18948.hp2 | missense_variant | MODERATE | c.8078C>G | p.Pro2693Arg | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 8136/16366 | 8078/16008 | 2693/5335 | chr7 | 100998641 | ||
| chr7:100998652
|
C | T | 1 | a0186 | 1 | HG01109.hp2 | missense_variant | MODERATE | c.8089C>T | p.His2697Tyr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 8147/16366 | 8089/16008 | 2697/5335 | chr7 | 100998652 | ||
| chr7:100998677
|
C | A | 1 | a0272 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.8114C>A | p.Thr2705Asn | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 8172/16366 | 8114/16008 | 2705/5335 | chr7 | 100998677 | ||
| chr7:100998712
|
G | A | 1 | a0170 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.8149G>A | p.Val2717Ile | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 8207/16366 | 8149/16008 | 2717/5335 | chr7 | 100998712 | ||
| chr7:100998761
|
G | C | 4 | a0226a0252a0254others(1): Show | 4 | HG00639.hp1 HG01358.hp2 HG03669.hp2 others(1): Show |
missense_variant | MODERATE | c.8198G>C | p.Ser2733Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 8256/16366 | 8198/16008 | 2733/5335 | chr7 | 100998761 | ||
| chr7:100998763
|
A | C | 4 | a0226a0252a0254others(1): Show | 4 | HG00639.hp1 HG01358.hp2 HG03669.hp2 others(1): Show |
missense_variant | MODERATE | c.8200A>C | p.Thr2734Pro | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 8258/16366 | 8200/16008 | 2734/5335 | chr7 | 100998763 | ||
| chr7:100998770
|
C | T | 1 | a0272 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.8207C>T | p.Thr2736Ile | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 8265/16366 | 8207/16008 | 2736/5335 | chr7 | 100998770 | ||
| chr7:100998797
|
C | G | 1 | a0200 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.8234C>G | p.Thr2745Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 8292/16366 | 8234/16008 | 2745/5335 | chr7 | 100998797 | ||
| chr7:100998809
|
G | A | 2 | a0142a0272 | 2 | HG02258.hp2 HG02886.hp1 |
missense_variant | MODERATE | c.8246G>A | p.Arg2749Gln | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 8304/16366 | 8246/16008 | 2749/5335 | chr7 | 100998809 | ||
| chr7:100998937
|
G | A | 8 | a0025a0119a0120others(5): Show | 9 | HG01243.hp2 HG02109.hp2 HG02257.hp1 others(6): Show |
missense_variant | MODERATE | c.8374G>A | p.Ala2792Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 8432/16366 | 8374/16008 | 2792/5335 | chr7 | 100998937 | ||
| chr7:100999174
|
G | A | 43 | a0005a0010a0035others(40): Show | 54 | HG00423.hp2 HG00621.hp1 HG01081.hp1 others(51): Show |
missense_variant | MODERATE | c.8611G>A | p.Ala2871Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 8669/16366 | 8611/16008 | 2871/5335 | chr7 | 100999174 | ||
| chr7:100999229
|
C | G | 4 | a0176a0179a0190others(1): Show | 4 | HG00673.hp1 HG02280.hp1 HG02647.hp1 others(1): Show |
missense_variant | MODERATE | c.8666C>G | p.Pro2889Arg | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 8724/16366 | 8666/16008 | 2889/5335 | chr7 | 100999229 | ||
| chr7:100999295
|
C | A | 15 | a0177a0178a0181others(12): Show | 15 | HG00642.hp2 HG01109.hp2 HG01361.hp2 others(12): Show |
missense_variant | MODERATE | c.8732C>A | p.Thr2911Lys | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 8790/16366 | 8732/16008 | 2911/5335 | chr7 | 100999295 | ||
| chr7:100999297
|
G | A | 167 | a0001a0008a0009others(164): Show | 197 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(194): Show |
missense_variant | MODERATE | c.8734G>A | p.Ala2912Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 8792/16366 | 8734/16008 | 2912/5335 | chr7 | 100999297 | ||
| chr7:100999376
|
C | A | 1 | a0090 | 1 | HG00408.hp1 | missense_variant | MODERATE | c.8813C>A | p.Ser2938Tyr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 8871/16366 | 8813/16008 | 2938/5335 | chr7 | 100999376 | ||
| chr7:100999508
|
C | T | 1 | a0102 | 1 | HG02080.hp1 | missense_variant | MODERATE | c.8945C>T | p.Pro2982Leu | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 9003/16366 | 8945/16008 | 2982/5335 | chr7 | 100999508 | ||
| chr7:100999525
|
G | A | 12 | a0034a0176a0178others(9): Show | 13 | HG00673.hp1 HG01106.hp1 HG01515.hp2 others(10): Show |
missense_variant | MODERATE | c.8962G>A | p.Ala2988Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 9020/16366 | 8962/16008 | 2988/5335 | chr7 | 100999525 | ||
| chr7:100999574
|
G | C | 1 | a0271 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.9011G>C | p.Ser3004Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 9069/16366 | 9011/16008 | 3004/5335 | chr7 | 100999574 | ||
| chr7:100999597
|
G | A | 12 | a0034a0176a0178others(9): Show | 13 | HG00673.hp1 HG01106.hp1 HG01515.hp2 others(10): Show |
missense_variant | MODERATE | c.9034G>A | p.Gly3012Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 9092/16366 | 9034/16008 | 3012/5335 | chr7 | 100999597 | ||
| chr7:100999610
|
C | T | 13 | a0034a0176a0178others(10): Show | 14 | HG00673.hp1 HG01106.hp1 HG01515.hp2 others(11): Show |
missense_variant | MODERATE | c.9047C>T | p.Ala3016Val | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 9105/16366 | 9047/16008 | 3016/5335 | chr7 | 100999610 | ||
| chr7:100999646
|
C | T | 1 | a0122 | 1 | HG02055.hp1 | missense_variant | MODERATE | c.9083C>T | p.Pro3028Leu | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 9141/16366 | 9083/16008 | 3028/5335 | chr7 | 100999646 | ||
| chr7:100999669
|
T | C | 21 | a0027a0028a0034others(18): Show | 24 | HG00673.hp1 HG01106.hp1 HG01175.hp1 others(21): Show |
missense_variant | MODERATE | c.9106T>C | p.Phe3036Leu | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 9164/16366 | 9106/16008 | 3036/5335 | chr7 | 100999669 | ||
| chr7:100999705
|
G | A | 14 | a0033a0177a0180others(11): Show | 15 | HG01109.hp2 HG01361.hp2 HG01978.hp2 others(12): Show |
missense_variant | MODERATE | c.9142G>A | p.Glu3048Lys | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 9200/16366 | 9142/16008 | 3048/5335 | chr7 | 100999705 | ||
| chr7:100999792
|
C | A | 2 | a0065a0066 | 2 | HG02647.hp2 HG02809.hp1 |
missense_variant | MODERATE | c.9229C>A | p.Pro3077Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 9287/16366 | 9229/16008 | 3077/5335 | chr7 | 100999792 | ||
| chr7:100999823
|
C | T | 1 | a0055 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.9260C>T | p.Thr3087Met | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 9318/16366 | 9260/16008 | 3087/5335 | chr7 | 100999823 | ||
| chr7:100999834
|
G | A | 12 | a0034a0176a0178others(9): Show | 13 | HG00673.hp1 HG01106.hp1 HG01515.hp2 others(10): Show |
missense_variant | MODERATE | c.9271G>A | p.Ala3091Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 9329/16366 | 9271/16008 | 3091/5335 | chr7 | 100999834 | ||
| chr7:100999835
|
C | T | 1 | a0164 | 1 | HG00140.hp2 | missense_variant | MODERATE | c.9272C>T | p.Ala3091Val | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 9330/16366 | 9272/16008 | 3091/5335 | chr7 | 100999835 | ||
| chr7:100999874
|
A | T | 10 | a0027a0028a0089others(7): Show | 12 | HG01175.hp1 HG01257.hp1 HG02145.hp2 others(9): Show |
missense_variant | MODERATE | c.9311A>T | p.Lys3104Ile | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 9369/16366 | 9311/16008 | 3104/5335 | chr7 | 100999874 | ||
| chr7:100999907
|
C | T | 1 | a0271 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.9344C>T | p.Pro3115Leu | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 9402/16366 | 9344/16008 | 3115/5335 | chr7 | 100999907 | ||
| chr7:100999991
|
C | T | 4 | a0055a0065a0066others(1): Show | 4 | HG02074.hp1 HG02647.hp2 HG02809.hp1 others(1): Show |
missense_variant | MODERATE | c.9428C>T | p.Thr3143Met | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 9486/16366 | 9428/16008 | 3143/5335 | chr7 | 100999991 | ||
| chr7:101000011
|
G | A | 17 | a0034a0055a0065others(14): Show | 18 | HG00673.hp1 HG01106.hp1 HG01515.hp2 others(15): Show |
missense_variant | MODERATE | c.9448G>A | p.Gly3150Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 9506/16366 | 9448/16008 | 3150/5335 | chr7 | 101000011 | ||
| chr7:101000072
|
C | G | 1 | a0069 | 1 | HG02148.hp2 | missense_variant | MODERATE | c.9509C>G | p.Ser3170Cys | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 9567/16366 | 9509/16008 | 3170/5335 | chr7 | 101000072 | ||
| chr7:101000146
|
G | A | 13 | a0034a0176a0177others(10): Show | 14 | HG00673.hp1 HG01106.hp1 HG01515.hp2 others(11): Show |
missense_variant | MODERATE | c.9583G>A | p.Gly3195Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 9641/16366 | 9583/16008 | 3195/5335 | chr7 | 101000146 | ||
| chr7:101000146
|
G | GGCCCAGG others(2051): Show |
3 | a0099a0107a0114 | 3 | HG00738.hp2 HG04228.hp1 NA18950.hp2 |
disruptive_inframe_insertion | MODERATE | c.9749_9750insAAACTC others(2052): Show |
p.Pro3250_Asn3251ins others(2058): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 9808/16366 | 9750/16008 | 3250/5335 | INFO_REALIGN_3_PRIME | chr7 | 101000146 | |
| chr7:101000149
|
C | CCAGGCTC others(2051): Show |
1 | a0086 | 1 | HG03654.hp2 | disruptive_inframe_insertion | MODERATE | c.9749_9750insAAACTC others(2052): Show |
p.Pro3250_Asn3251ins others(2058): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 9808/16366 | 9750/16008 | 3250/5335 | INFO_REALIGN_3_PRIME | chr7 | 101000149 | |
| chr7:101000204
|
T | C | 1 | a0167 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.9641T>C | p.Leu3214Pro | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 9699/16366 | 9641/16008 | 3214/5335 | chr7 | 101000204 | ||
| chr7:101000209
|
G | T | 13 | a0010a0038a0039others(10): Show | 17 | HG01081.hp1 HG01192.hp2 HG01255.hp1 others(14): Show |
missense_variant | MODERATE | c.9646G>T | p.Ala3216Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 9704/16366 | 9646/16008 | 3216/5335 | chr7 | 101000209 | ||
| chr7:101000240
|
C | T | 1 | a0022 | 2 | HG01257.hp2 HG01258.hp2 |
missense_variant | MODERATE | c.9677C>T | p.Ser3226Leu | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 9735/16366 | 9677/16008 | 3226/5335 | chr7 | 101000240 | ||
| chr7:101000266
|
G | A | 1 | a0141 | 1 | HG02132.hp1 | missense_variant | MODERATE | c.9703G>A | p.Gly3235Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 9761/16366 | 9703/16008 | 3235/5335 | chr7 | 101000266 | ||
| chr7:101000278
|
C | T | 1 | a0144 | 1 | HG03688.hp2 | missense_variant | MODERATE | c.9715C>T | p.Arg3239Cys | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 9773/16366 | 9715/16008 | 3239/5335 | chr7 | 101000278 | ||
| chr7:101000294
|
C | T | 13 | a0034a0176a0177others(10): Show | 14 | HG00673.hp1 HG01106.hp1 HG01515.hp2 others(11): Show |
missense_variant | MODERATE | c.9731C>T | p.Thr3244Ile | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 9789/16366 | 9731/16008 | 3244/5335 | chr7 | 101000294 | ||
| chr7:101000378
|
C | A | 1 | a0268 | 1 | HG03579.hp1 | missense_variant | MODERATE | c.9815C>A | p.Thr3272Asn | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 9873/16366 | 9815/16008 | 3272/5335 | chr7 | 101000378 | ||
| chr7:101000408
|
C | G | 3 | a0048a0065a0066 | 3 | HG02647.hp2 HG02809.hp1 NA19030.hp2 |
missense_variant | MODERATE | c.9845C>G | p.Thr3282Arg | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 9903/16366 | 9845/16008 | 3282/5335 | chr7 | 101000408 | ||
| chr7:101000422
|
G | C | 10 | a0033a0180a0187others(7): Show | 11 | HG01361.hp2 HG01978.hp2 HG02559.hp1 others(8): Show |
missense_variant | MODERATE | c.9859G>C | p.Ala3287Pro | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 9917/16366 | 9859/16008 | 3287/5335 | chr7 | 101000422 | ||
| chr7:101000444
|
G | A | 5 | a0234a0235a0236others(2): Show | 5 | HG02165.hp2 NA18941.hp1 NA18982.hp2 others(2): Show |
missense_variant | MODERATE | c.9881G>A | p.Arg3294His | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 9939/16366 | 9881/16008 | 3294/5335 | chr7 | 101000444 | ||
| chr7:101000510
|
G | A | 2 | a0055a0068 | 2 | HG02074.hp1 HG04204.hp2 |
missense_variant | MODERATE | c.9947G>A | p.Arg3316His | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 10005/16366 | 9947/16008 | 3316/5335 | chr7 | 101000510 | ||
| chr7:101000536
|
G | C | 1 | a0031 | 2 | HG01081.hp2 HG01169.hp1 |
missense_variant | MODERATE | c.9973G>C | p.Glu3325Gln | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 10031/16366 | 9973/16008 | 3325/5335 | chr7 | 101000536 | ||
| chr7:101000551
|
C | G | 64 | a0001a0008a0009others(61): Show | 85 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(82): Show |
missense_variant | MODERATE | c.9988C>G | p.His3330Asp | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 10046/16366 | 9988/16008 | 3330/5335 | chr7 | 101000551 | ||
| chr7:101000575
|
A | G | 4 | a0258a0261a0268others(1): Show | 4 | HG02451.hp2 HG03130.hp2 HG03471.hp1 others(1): Show |
missense_variant | MODERATE | c.10012A>G | p.Thr3338Ala | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 10070/16366 | 10012/16008 | 3338/5335 | chr7 | 101000575 | ||
| chr7:101000596
|
G | A | 5 | a0086a0099a0107others(2): Show | 5 | HG00738.hp2 HG02735.hp2 HG03654.hp2 others(2): Show |
missense_variant | MODERATE | c.10033G>A | p.Asp3345Asn | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 10091/16366 | 10033/16008 | 3345/5335 | chr7 | 101000596 | ||
| chr7:101000746
|
C | A | 1 | a0195 | 1 | HG00642.hp2 | missense_variant | MODERATE | c.10183C>A | p.Pro3395Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 10241/16366 | 10183/16008 | 3395/5335 | chr7 | 101000746 | ||
| chr7:101000746
|
C | T | 1 | a0037 | 2 | HG01069.hp2 HG01070.hp1 |
missense_variant | MODERATE | c.10183C>T | p.Pro3395Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 10241/16366 | 10183/16008 | 3395/5335 | chr7 | 101000746 | ||
| chr7:101000778
|
G | C | 5 | a0004a0036a0203others(2): Show | 10 | HG01515.hp1 HG02109.hp1 HG02630.hp1 others(7): Show |
missense_variant | MODERATE | c.10215G>C | p.Glu3405Asp | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 10273/16366 | 10215/16008 | 3405/5335 | chr7 | 101000778 | ||
| chr7:101000801
|
G | A | 3 | a0088a0128a0168 | 3 | HG03041.hp2 HG03516.hp2 NA19007.hp1 |
missense_variant | MODERATE | c.10238G>A | p.Ser3413Asn | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 10296/16366 | 10238/16008 | 3413/5335 | chr7 | 101000801 | ||
| chr7:101000808
|
C | A | 31 | a0020a0021a0023others(28): Show | 34 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(31): Show |
missense_variant | MODERATE | c.10245C>A | p.Asp3415Glu | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 10303/16366 | 10245/16008 | 3415/5335 | chr7 | 101000808 | ||
| chr7:101000809
|
G | A | 31 | a0020a0021a0023others(28): Show | 34 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(31): Show |
missense_variant | MODERATE | c.10246G>A | p.Ala3416Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 10304/16366 | 10246/16008 | 3416/5335 | chr7 | 101000809 | ||
| chr7:101000846
|
C | T | 5 | a0086a0099a0107others(2): Show | 5 | HG00738.hp2 HG02735.hp2 HG03654.hp2 others(2): Show |
missense_variant | MODERATE | c.10283C>T | p.Thr3428Ile | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 10341/16366 | 10283/16008 | 3428/5335 | chr7 | 101000846 | ||
| chr7:101000870
|
C | T | 3 | a0123a0124a0125 | 3 | HG02257.hp1 HG03139.hp1 NA18522.hp2 |
missense_variant | MODERATE | c.10307C>T | p.Thr3436Met | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 10365/16366 | 10307/16008 | 3436/5335 | chr7 | 101000870 | ||
| chr7:101000917
|
G | T | 12 | a0011a0019a0044others(9): Show | 14 | HG00323.hp1 HG00639.hp2 HG01074.hp2 others(11): Show |
missense_variant | MODERATE | c.10354G>T | p.Gly3452Cys | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 10412/16366 | 10354/16008 | 3452/5335 | chr7 | 101000917 | ||
| chr7:101000927
|
C | T | 1 | a0036 | 2 | HG02630.hp1 HG03579.hp2 |
missense_variant | MODERATE | c.10364C>T | p.Thr3455Ile | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 10422/16366 | 10364/16008 | 3455/5335 | chr7 | 101000927 | ||
| chr7:101000930
|
C | T | 15 | a0007a0033a0055others(12): Show | 18 | HG00642.hp2 HG01361.hp2 HG01978.hp2 others(15): Show |
missense_variant | MODERATE | c.10367C>T | p.Thr3456Met | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 10425/16366 | 10367/16008 | 3456/5335 | chr7 | 101000930 | ||
| chr7:101000948
|
A | G | 1 | a0247 | 1 | HG03927.hp1 | missense_variant | MODERATE | c.10385A>G | p.Lys3462Arg | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 10443/16366 | 10385/16008 | 3462/5335 | chr7 | 101000948 | ||
| chr7:101000962
|
C | T | 1 | a0135 | 1 | HG02080.hp2 | missense_variant | MODERATE | c.10399C>T | p.His3467Tyr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 10457/16366 | 10399/16008 | 3467/5335 | chr7 | 101000962 | ||
| chr7:101001022
|
G | A | 1 | a0049 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.10459G>A | p.Val3487Ile | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 10517/16366 | 10459/16008 | 3487/5335 | chr7 | 101001022 | ||
| chr7:101001047
|
A | G | 1 | a0247 | 1 | HG03927.hp1 | missense_variant | MODERATE | c.10484A>G | p.His3495Arg | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 10542/16366 | 10484/16008 | 3495/5335 | chr7 | 101001047 | ||
| chr7:101001113
|
G | A | 25 | a0002a0003a0006others(22): Show | 43 | HG00423.hp2 HG00558.hp2 HG01099.hp1 others(40): Show |
missense_variant | MODERATE | c.10550G>A | p.Arg3517Gln | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 10608/16366 | 10550/16008 | 3517/5335 | chr7 | 101001113 | ||
| chr7:101001190
|
T | C | 253 | a0001a0002a0003others(250): Show | 315 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(312): Show |
missense_variant | MODERATE | c.10627T>C | p.Ser3543Pro | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 10685/16366 | 10627/16008 | 3543/5335 | chr7 | 101001190 | ||
| chr7:101001223
|
T | C | 252 | a0001a0002a0003others(249): Show | 314 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(311): Show |
missense_variant | MODERATE | c.10660T>C | p.Ser3554Pro | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 10718/16366 | 10660/16008 | 3554/5335 | chr7 | 101001223 | ||
| chr7:101001227
|
G | T | 4 | a0011a0044a0045others(1): Show | 5 | HG00323.hp1 HG00639.hp2 HG01074.hp2 others(2): Show |
missense_variant | MODERATE | c.10664G>T | p.Gly3555Val | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 10722/16366 | 10664/16008 | 3555/5335 | chr7 | 101001227 | ||
| chr7:101001260
|
C | A | 1 | a0047 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.10697C>A | p.Thr3566Asn | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 10755/16366 | 10697/16008 | 3566/5335 | chr7 | 101001260 | ||
| chr7:101001344
|
C | T | 1 | a0110 | 1 | HG03927.hp2 | missense_variant | MODERATE | c.10781C>T | p.Thr3594Ile | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 10839/16366 | 10781/16008 | 3594/5335 | chr7 | 101001344 | ||
| chr7:101001460
|
G | A | 32 | a0002a0003a0006others(29): Show | 52 | HG00558.hp2 HG01099.hp1 HG01123.hp2 others(49): Show |
missense_variant | MODERATE | c.10897G>A | p.Ala3633Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 10955/16366 | 10897/16008 | 3633/5335 | chr7 | 101001460 | ||
| chr7:101001491
|
C | T | 1 | a0206 | 1 | NA19066.hp1 | missense_variant | MODERATE | c.10928C>T | p.Thr3643Met | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 10986/16366 | 10928/16008 | 3643/5335 | chr7 | 101001491 | ||
| chr7:101001494
|
C | T | 13 | a0033a0180a0181others(10): Show | 14 | HG00642.hp2 HG01109.hp2 HG01361.hp2 others(11): Show |
missense_variant | MODERATE | c.10931C>T | p.Thr3644Met | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 10989/16366 | 10931/16008 | 3644/5335 | chr7 | 101001494 | ||
| chr7:101001511
|
A | C | 12 | a0011a0019a0044others(9): Show | 14 | HG00323.hp1 HG00639.hp2 HG01074.hp2 others(11): Show |
missense_variant | MODERATE | c.10948A>C | p.Thr3650Pro | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 11006/16366 | 10948/16008 | 3650/5335 | chr7 | 101001511 | ||
| chr7:101001599
|
C | T | 4 | a0123a0128a0129others(1): Show | 4 | HG03041.hp2 HG03516.hp2 NA18522.hp2 others(1): Show |
missense_variant | MODERATE | c.11036C>T | p.Thr3679Ile | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 11094/16366 | 11036/16008 | 3679/5335 | chr7 | 101001599 | ||
| chr7:101001602
|
C | A | 1 | a0090 | 1 | HG00408.hp1 | stop_gained | HIGH | c.11039C>A | p.Ser3680* | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 11097/16366 | 11039/16008 | 3680/5335 | chr7 | 101001602 | ||
| chr7:101001712
|
C | T | 38 | a0001a0008a0009others(35): Show | 55 | HG00558.hp1 HG00642.hp1 HG00673.hp2 others(52): Show |
missense_variant | MODERATE | c.11149C>T | p.Arg3717Cys | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 11207/16366 | 11149/16008 | 3717/5335 | chr7 | 101001712 | ||
| chr7:101001713
|
G | A | 1 | a0086 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.11150G>A | p.Arg3717His | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 11208/16366 | 11150/16008 | 3717/5335 | chr7 | 101001713 | ||
| chr7:101001719
|
G | A | 1 | a0262 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.11156G>A | p.Ser3719Asn | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 11214/16366 | 11156/16008 | 3719/5335 | chr7 | 101001719 | ||
| chr7:101001766
|
C | G | 19 | a0002a0006a0017others(16): Show | 30 | HG00558.hp2 HG01099.hp1 HG01123.hp2 others(27): Show |
missense_variant | MODERATE | c.11203C>G | p.Pro3735Ala | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 11261/16366 | 11203/16008 | 3735/5335 | chr7 | 101001766 | ||
| chr7:101001796
|
T | C | 4 | a0267a0269a0270others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG03471.hp1 others(1): Show |
missense_variant | MODERATE | c.11233T>C | p.Tyr3745His | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 11291/16366 | 11233/16008 | 3745/5335 | chr7 | 101001796 | ||
| chr7:101001881
|
G | A | 55 | a0001a0008a0009others(52): Show | 74 | HG00099.hp1 HG00408.hp1 HG00558.hp1 others(71): Show |
missense_variant | MODERATE | c.11318G>A | p.Arg3773His | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 11376/16366 | 11318/16008 | 3773/5335 | chr7 | 101001881 | ||
| chr7:101001890
|
C | G | 12 | a0022a0024a0052others(9): Show | 14 | HG00099.hp1 HG00408.hp1 HG00735.hp1 others(11): Show |
missense_variant | MODERATE | c.11327C>G | p.Pro3776Arg | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 11385/16366 | 11327/16008 | 3776/5335 | chr7 | 101001890 | ||
| chr7:101002010
|
G | C | 1 | a0226 | 1 | HG01358.hp2 | missense_variant | MODERATE | c.11447G>C | p.Ser3816Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 11505/16366 | 11447/16008 | 3816/5335 | chr7 | 101002010 | ||
| chr7:101002012
|
A | C | 1 | a0226 | 1 | HG01358.hp2 | missense_variant | MODERATE | c.11449A>C | p.Thr3817Pro | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 11507/16366 | 11449/16008 | 3817/5335 | chr7 | 101002012 | ||
| chr7:101002030
|
C | G | 270 | a0001a0002a0003others(267): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
missense_variant | MODERATE | c.11467C>G | p.Arg3823Gly | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 11525/16366 | 11467/16008 | 3823/5335 | chr7 | 101002030 | ||
| chr7:101002046
|
C | G | 1 | a0200 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.11483C>G | p.Thr3828Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 11541/16366 | 11483/16008 | 3828/5335 | chr7 | 101002046 | ||
| chr7:101002168
|
C | A | 1 | a0058 | 1 | HG01952.hp2 | missense_variant | MODERATE | c.11605C>A | p.Pro3869Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 11663/16366 | 11605/16008 | 3869/5335 | chr7 | 101002168 | ||
| chr7:101002186
|
G | A | 1 | a0127 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.11623G>A | p.Ala3875Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 11681/16366 | 11623/16008 | 3875/5335 | chr7 | 101002186 | ||
| chr7:101002244
|
A | C | 271 | a0001a0002a0003others(268): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
missense_variant | MODERATE | c.11681A>C | p.Lys3894Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 11739/16366 | 11681/16008 | 3894/5335 | chr7 | 101002244 | ||
| chr7:101002423
|
G | A | 4 | a0035a0204a0205others(1): Show | 5 | HG02071.hp2 NA18970.hp1 NA19005.hp1 others(2): Show |
missense_variant | MODERATE | c.11860G>A | p.Ala3954Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 11918/16366 | 11860/16008 | 3954/5335 | chr7 | 101002423 | ||
| chr7:101002450
|
G | A | 2 | a0129a0174 | 2 | NA18941.hp2 NA19081.hp1 |
missense_variant | MODERATE | c.11887G>A | p.Glu3963Lys | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 11945/16366 | 11887/16008 | 3963/5335 | chr7 | 101002450 | ||
| chr7:101002463
|
C | T | 1 | a0195 | 1 | HG00642.hp2 | missense_variant | MODERATE | c.11900C>T | p.Thr3967Ile | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 11958/16366 | 11900/16008 | 3967/5335 | chr7 | 101002463 | ||
| chr7:101002478
|
C | G | 10 | a0033a0180a0187others(7): Show | 11 | HG01361.hp2 HG01978.hp2 HG02559.hp1 others(8): Show |
missense_variant | MODERATE | c.11915C>G | p.Pro3972Arg | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 11973/16366 | 11915/16008 | 3972/5335 | chr7 | 101002478 | ||
| chr7:101002487
|
C | T | 1 | a0022 | 2 | HG01257.hp2 HG01258.hp2 |
missense_variant | MODERATE | c.11924C>T | p.Thr3975Met | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 11982/16366 | 11924/16008 | 3975/5335 | chr7 | 101002487 | ||
| chr7:101002544
|
C | A | 16 | a0034a0176a0177others(13): Show | 17 | HG00642.hp2 HG00673.hp1 HG01106.hp1 others(14): Show |
missense_variant | MODERATE | c.11981C>A | p.Thr3994Lys | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 12039/16366 | 11981/16008 | 3994/5335 | chr7 | 101002544 | ||
| chr7:101002546
|
A | G | 73 | a0005a0010a0014others(70): Show | 88 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(85): Show |
missense_variant | MODERATE | c.11983A>G | p.Thr3995Ala | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 12041/16366 | 11983/16008 | 3995/5335 | chr7 | 101002546 | ||
| chr7:101002565
|
G | C | 4 | a0267a0269a0270others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG03471.hp1 others(1): Show |
missense_variant | MODERATE | c.12002G>C | p.Gly4001Ala | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 12060/16366 | 12002/16008 | 4001/5335 | chr7 | 101002565 | ||
| chr7:101002610
|
C | A | 1 | a0159 | 1 | NA19084.hp2 | missense_variant | MODERATE | c.12047C>A | p.Ser4016Tyr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 12105/16366 | 12047/16008 | 4016/5335 | chr7 | 101002610 | ||
| chr7:101002651
|
G | A | 1 | a0055 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.12088G>A | p.Asp4030Asn | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 12146/16366 | 12088/16008 | 4030/5335 | chr7 | 101002651 | ||
| chr7:101002774
|
A | G | 263 | a0001a0002a0003others(260): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
missense_variant | MODERATE | c.12211A>G | p.Thr4071Ala | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 12269/16366 | 12211/16008 | 4071/5335 | chr7 | 101002774 | ||
| chr7:101002796
|
C | T | 2 | a0007a0055 | 4 | HG02602.hp1 HG03017.hp1 HG03942.hp2 others(1): Show |
missense_variant | MODERATE | c.12233C>T | p.Thr4078Ile | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 12291/16366 | 12233/16008 | 4078/5335 | chr7 | 101002796 | ||
| chr7:101002810
|
T | G | 4 | a0267a0269a0270others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG03471.hp1 others(1): Show |
missense_variant | MODERATE | c.12247T>G | p.Trp4083Gly | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 12305/16366 | 12247/16008 | 4083/5335 | chr7 | 101002810 | ||
| chr7:101002846
|
A | G | 263 | a0001a0002a0003others(260): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
missense_variant | MODERATE | c.12283A>G | p.Ser4095Gly | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 12341/16366 | 12283/16008 | 4095/5335 | chr7 | 101002846 | ||
| chr7:101002859
|
T | C | 263 | a0001a0002a0003others(260): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
missense_variant | MODERATE | c.12296T>C | p.Val4099Ala | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 12354/16366 | 12296/16008 | 4099/5335 | chr7 | 101002859 | ||
| chr7:101002891
|
C | T | 4 | a0262a0264a0265others(1): Show | 4 | HG02258.hp1 HG02723.hp2 HG03098.hp2 others(1): Show |
missense_variant | MODERATE | c.12328C>T | p.Arg4110Cys | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 12386/16366 | 12328/16008 | 4110/5335 | chr7 | 101002891 | ||
| chr7:101002895
|
C | T | 9 | a0025a0119a0120others(6): Show | 10 | HG01243.hp2 HG02055.hp1 HG02109.hp2 others(7): Show |
missense_variant | MODERATE | c.12332C>T | p.Pro4111Leu | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 12390/16366 | 12332/16008 | 4111/5335 | chr7 | 101002895 | ||
| chr7:101002918
|
T | C | 63 | a0001a0008a0009others(60): Show | 80 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(77): Show |
missense_variant | MODERATE | c.12355T>C | p.Phe4119Leu | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 12413/16366 | 12355/16008 | 4119/5335 | chr7 | 101002918 | ||
| chr7:101002954
|
G | A | 22 | a0033a0034a0176others(19): Show | 24 | HG00642.hp2 HG00673.hp1 HG01106.hp1 others(21): Show |
missense_variant | MODERATE | c.12391G>A | p.Glu4131Lys | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 12449/16366 | 12391/16008 | 4131/5335 | chr7 | 101002954 | ||
| chr7:101002961
|
C | A | 1 | a0049 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.12398C>A | p.Thr4133Lys | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 12456/16366 | 12398/16008 | 4133/5335 | chr7 | 101002961 | ||
| chr7:101003041
|
C | A | 24 | a0002a0003a0006others(21): Show | 41 | HG00558.hp2 HG01099.hp1 HG01123.hp2 others(38): Show |
missense_variant | MODERATE | c.12478C>A | p.Pro4160Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 12536/16366 | 12478/16008 | 4160/5335 | chr7 | 101003041 | ||
| chr7:101003056
|
A | G | 3 | a0181a0186a0195 | 3 | HG00642.hp2 HG01109.hp2 HG04199.hp2 |
missense_variant | MODERATE | c.12493A>G | p.Ile4165Val | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 12551/16366 | 12493/16008 | 4165/5335 | chr7 | 101003056 | ||
| chr7:101003072
|
C | T | 1 | a0170 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.12509C>T | p.Thr4170Met | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 12567/16366 | 12509/16008 | 4170/5335 | chr7 | 101003072 | ||
| chr7:101003083
|
G | A | 8 | a0180a0187a0192others(5): Show | 8 | HG01361.hp2 HG01978.hp2 HG02630.hp2 others(5): Show |
missense_variant | MODERATE | c.12520G>A | p.Ala4174Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 12578/16366 | 12520/16008 | 4174/5335 | chr7 | 101003083 | ||
| chr7:101003084
|
C | T | 1 | a0246 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.12521C>T | p.Ala4174Val | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 12579/16366 | 12521/16008 | 4174/5335 | chr7 | 101003084 | ||
| chr7:101003123
|
A | T | 56 | a0001a0008a0009others(53): Show | 73 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(70): Show |
missense_variant | MODERATE | c.12560A>T | p.Lys4187Ile | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 12618/16366 | 12560/16008 | 4187/5335 | chr7 | 101003123 | ||
| chr7:101003158
|
G | A | 1 | a0158 | 1 | NA20805.hp2 | missense_variant | MODERATE | c.12595G>A | p.Asp4199Asn | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 12653/16366 | 12595/16008 | 4199/5335 | chr7 | 101003158 | ||
| chr7:101003167
|
C | T | 1 | a0049 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.12604C>T | p.Leu4202Phe | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 12662/16366 | 12604/16008 | 4202/5335 | chr7 | 101003167 | ||
| chr7:101003240
|
T | C | 241 | a0001a0004a0005others(238): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
missense_variant | MODERATE | c.12677T>C | p.Met4226Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 12735/16366 | 12677/16008 | 4226/5335 | chr7 | 101003240 | ||
| chr7:101003260
|
A | G | 232 | a0001a0004a0005others(229): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
missense_variant | MODERATE | c.12697A>G | p.Ser4233Gly | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 12755/16366 | 12697/16008 | 4233/5335 | chr7 | 101003260 | ||
| chr7:101003267
|
C | T | 1 | a0160 | 1 | NA20805.hp1 | missense_variant | MODERATE | c.12704C>T | p.Thr4235Ile | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 12762/16366 | 12704/16008 | 4235/5335 | chr7 | 101003267 | ||
| chr7:101003281
|
G | A | 1 | a0239 | 1 | HG02132.hp2 | missense_variant | MODERATE | c.12718G>A | p.Val4240Ile | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 12776/16366 | 12718/16008 | 4240/5335 | chr7 | 101003281 | ||
| chr7:101003395
|
A | G | 255 | a0001a0002a0003others(252): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
missense_variant | MODERATE | c.12832A>G | p.Ser4278Gly | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 12890/16366 | 12832/16008 | 4278/5335 | chr7 | 101003395 | ||
| chr7:101003467
|
C | T | 2 | a0007a0055 | 4 | HG02602.hp1 HG03017.hp1 HG03942.hp2 others(1): Show |
missense_variant | MODERATE | c.12904C>T | p.Pro4302Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 12962/16366 | 12904/16008 | 4302/5335 | chr7 | 101003467 | ||
| chr7:101003470
|
G | A | 1 | a0162 | 1 | HG02155.hp1 | missense_variant | MODERATE | c.12907G>A | p.Val4303Ile | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 12965/16366 | 12907/16008 | 4303/5335 | chr7 | 101003470 | ||
| chr7:101003495
|
A | G | 3 | a0007a0055a0129 | 5 | HG02602.hp1 HG03017.hp1 HG03942.hp2 others(2): Show |
missense_variant | MODERATE | c.12932A>G | p.His4311Arg | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 12990/16366 | 12932/16008 | 4311/5335 | chr7 | 101003495 | ||
| chr7:101003543
|
C | T | 9 | a0179a0180a0187others(6): Show | 9 | HG01361.hp2 HG01978.hp2 HG02630.hp2 others(6): Show |
missense_variant | MODERATE | c.12980C>T | p.Thr4327Ile | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13038/16366 | 12980/16008 | 4327/5335 | chr7 | 101003543 | ||
| chr7:101003564
|
A | G | 7 | a0004a0007a0036others(4): Show | 14 | HG02109.hp1 HG02602.hp1 HG02630.hp1 others(11): Show |
missense_variant | MODERATE | c.13001A>G | p.Asn4334Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13059/16366 | 13001/16008 | 4334/5335 | chr7 | 101003564 | ||
| chr7:101003579
|
C | T | 7 | a0004a0007a0036others(4): Show | 14 | HG02109.hp1 HG02602.hp1 HG02630.hp1 others(11): Show |
missense_variant | MODERATE | c.13016C>T | p.Thr4339Ile | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13074/16366 | 13016/16008 | 4339/5335 | chr7 | 101003579 | ||
| chr7:101003606
|
C | G | 6 | a0259a0260a0263others(3): Show | 6 | HG02622.hp1 HG02723.hp2 HG03098.hp2 others(3): Show |
missense_variant | MODERATE | c.13043C>G | p.Ala4348Gly | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13101/16366 | 13043/16008 | 4348/5335 | chr7 | 101003606 | ||
| chr7:101003637
|
CAGCCCGA others(572): Show |
C | 6 | a0004a0007a0036others(3): Show | 13 | HG02109.hp1 HG02602.hp1 HG02630.hp1 others(10): Show |
disruptive_inframe_deletion | MODERATE | c.13122_13700del | p.Leu4375_Thr4567del | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13180/16366 | 13122/16008 | 4374/5335 | INFO_REALIGN_3_PRIME | chr7 | 101003637 | |
| chr7:101003651
|
C | T | 1 | a0129 | 1 | NA18941.hp2 | missense_variant | MODERATE | c.13088C>T | p.Thr4363Ile | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13146/16366 | 13088/16008 | 4363/5335 | chr7 | 101003651 | ||
| chr7:101003657
|
C | G | 22 | a0002a0003a0006others(19): Show | 39 | HG00558.hp2 HG01123.hp2 HG01192.hp1 others(36): Show |
missense_variant | MODERATE | c.13094C>G | p.Thr4365Arg | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13152/16366 | 13094/16008 | 4365/5335 | chr7 | 101003657 | ||
| chr7:101003671
|
G | C | 4 | a0033a0177a0188others(1): Show | 5 | HG00673.hp1 HG02559.hp1 HG03041.hp1 others(2): Show |
missense_variant | MODERATE | c.13108G>C | p.Ala4370Pro | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13166/16366 | 13108/16008 | 4370/5335 | chr7 | 101003671 | ||
| chr7:101003685
|
ATTGGGCC others(572): Show |
A | 1 | a0129 | 1 | NA18941.hp2 | conservative_inframe_deletion | MODERATE | c.13231_13809del | p.Thr4411_Thr4603del | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13289/16366 | 13231/16008 | 4411/5335 | INFO_REALIGN_3_PRIME | chr7 | 101003685 | |
| chr7:101003693
|
G | A | 4 | a0267a0269a0270others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG03471.hp1 others(1): Show |
missense_variant | MODERATE | c.13130G>A | p.Arg4377His | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13188/16366 | 13130/16008 | 4377/5335 | chr7 | 101003693 | ||
| chr7:101003701
|
G | T | 1 | a0234 | 1 | NA18941.hp1 | stop_gained | HIGH | c.13138G>T | p.Glu4380* | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13196/16366 | 13138/16008 | 4380/5335 | chr7 | 101003701 | ||
| chr7:101003747
|
C | T | 1 | a0222 | 1 | HG01934.hp2 | missense_variant | MODERATE | c.13184C>T | p.Pro4395Leu | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13242/16366 | 13184/16008 | 4395/5335 | chr7 | 101003747 | ||
| chr7:101003752
|
C | CCTGCCCG others(977): Show |
1 | a0086 | 1 | HG03654.hp2 | conservative_inframe_insertion | MODERATE | c.13272_13273insACTG others(980): Show |
p.Phe4424_Pro4425ins others(984): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13331/16366 | 13273/16008 | 4425/5335 | INFO_REALIGN_3_PRIME | chr7 | 101003752 | |
| chr7:101003759
|
G | A | 7 | a0013a0048a0065others(4): Show | 8 | HG02071.hp1 HG02559.hp2 HG02647.hp2 others(5): Show |
missense_variant | MODERATE | c.13196G>A | p.Arg4399His | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13254/16366 | 13196/16008 | 4399/5335 | chr7 | 101003759 | ||
| chr7:101003792
|
C | T | 4 | a0267a0269a0270others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG03471.hp1 others(1): Show |
missense_variant | MODERATE | c.13229C>T | p.Thr4410Met | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13287/16366 | 13229/16008 | 4410/5335 | chr7 | 101003792 | ||
| chr7:101003800
|
C | G | 37 | a0011a0019a0020others(34): Show | 44 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(41): Show |
missense_variant | MODERATE | c.13237C>G | p.His4413Asp | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13295/16366 | 13237/16008 | 4413/5335 | chr7 | 101003800 | ||
| chr7:101003810
|
C | T | 3 | a0020a0100a0111 | 4 | HG00621.hp2 HG02040.hp2 HG02523.hp1 others(1): Show |
missense_variant | MODERATE | c.13247C>T | p.Pro4416Leu | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13305/16366 | 13247/16008 | 4416/5335 | chr7 | 101003810 | ||
| chr7:101003845
|
A | G | 264 | a0001a0002a0003others(261): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
missense_variant | MODERATE | c.13282A>G | p.Asn4428Asp | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13340/16366 | 13282/16008 | 4428/5335 | chr7 | 101003845 | ||
| chr7:101003969
|
C | T | 1 | a0054 | 1 | HG01952.hp1 | missense_variant | MODERATE | c.13406C>T | p.Pro4469Leu | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13464/16366 | 13406/16008 | 4469/5335 | chr7 | 101003969 | ||
| chr7:101003995
|
C | A | 8 | a0034a0181a0186others(5): Show | 9 | HG00642.hp2 HG01106.hp1 HG01109.hp2 others(6): Show |
missense_variant | MODERATE | c.13432C>A | p.Pro4478Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13490/16366 | 13432/16008 | 4478/5335 | chr7 | 101003995 | ||
| chr7:101004020
|
G | A | 2 | a0059a0060 | 2 | NA18994.hp2 NA19000.hp2 |
missense_variant | MODERATE | c.13457G>A | p.Arg4486His | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13515/16366 | 13457/16008 | 4486/5335 | chr7 | 101004020 | ||
| chr7:101004027
|
G | C | 5 | a0219a0229a0246others(2): Show | 5 | HG01106.hp2 HG02074.hp2 HG04115.hp2 others(2): Show |
missense_variant | MODERATE | c.13464G>C | p.Glu4488Asp | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13522/16366 | 13464/16008 | 4488/5335 | chr7 | 101004027 | ||
| chr7:101004050
|
G | A | 9 | a0022a0027a0028others(6): Show | 12 | HG01257.hp2 HG01258.hp2 HG02486.hp1 others(9): Show |
missense_variant | MODERATE | c.13487G>A | p.Ser4496Asn | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13545/16366 | 13487/16008 | 4496/5335 | chr7 | 101004050 | ||
| chr7:101004057
|
C | A | 6 | a0099a0106a0107others(3): Show | 6 | HG00140.hp1 HG00738.hp2 HG02735.hp2 others(3): Show |
missense_variant | MODERATE | c.13494C>A | p.Asp4498Glu | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13552/16366 | 13494/16008 | 4498/5335 | chr7 | 101004057 | ||
| chr7:101004058
|
G | A | 6 | a0099a0106a0107others(3): Show | 6 | HG00140.hp1 HG00738.hp2 HG02735.hp2 others(3): Show |
missense_variant | MODERATE | c.13495G>A | p.Ala4499Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13553/16366 | 13495/16008 | 4499/5335 | chr7 | 101004058 | ||
| chr7:101004073
|
G | C | 4 | a0031a0053a0140others(1): Show | 5 | HG01074.hp1 HG01081.hp2 HG01169.hp1 others(2): Show |
missense_variant | MODERATE | c.13510G>C | p.Val4504Leu | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13568/16366 | 13510/16008 | 4504/5335 | chr7 | 101004073 | ||
| chr7:101004095
|
C | T | 1 | a0146 | 1 | NA19005.hp2 | missense_variant | MODERATE | c.13532C>T | p.Thr4511Ile | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13590/16366 | 13532/16008 | 4511/5335 | chr7 | 101004095 | ||
| chr7:101004166
|
G | A | 1 | a0211 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.13603G>A | p.Gly4535Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13661/16366 | 13603/16008 | 4535/5335 | chr7 | 101004166 | ||
| chr7:101004179
|
C | T | 43 | a0002a0003a0006others(40): Show | 63 | HG00558.hp2 HG00642.hp2 HG00673.hp1 others(60): Show |
missense_variant | MODERATE | c.13616C>T | p.Thr4539Met | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13674/16366 | 13616/16008 | 4539/5335 | chr7 | 101004179 | ||
| chr7:101004197
|
A | G | 7 | a0086a0259a0260others(4): Show | 7 | HG02622.hp1 HG02723.hp2 HG03098.hp2 others(4): Show |
missense_variant | MODERATE | c.13634A>G | p.Lys4545Arg | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13692/16366 | 13634/16008 | 4545/5335 | chr7 | 101004197 | ||
| chr7:101004216
|
T | TAGCCCCA others(488): Show |
1 | a0086 | 1 | HG03654.hp2 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(491): Show |
p.Pro4553_Ser4554ins others(495): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
1 | a0187 | 1 | NA19240.hp2 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
2 | a0015a0078 | 3 | HG02040.hp1 NA18995.hp2 NA18999.hp2 |
disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
1 | a0272 | 1 | HG02258.hp2 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
1 | a0259 | 1 | HG03195.hp2 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
11 | a0002a0003a0006others(8): Show | 23 | HG00558.hp2 HG01884.hp1 HG01952.hp2 others(20): Show |
disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
1 | a0067 | 1 | NA20300.hp1 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
1 | a0073 | 1 | HG01978.hp1 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
1 | a0048 | 1 | NA19030.hp2 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
3 | a0065a0066a0072 | 3 | HG02559.hp2 HG02647.hp2 HG02809.hp1 |
disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
11 | a0002a0017a0018others(8): Show | 16 | HG01099.hp1 HG01123.hp2 HG01192.hp1 others(13): Show |
disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(5912): Show |
1 | a0056 | 1 | HG01261.hp2 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(5915): Show |
p.Pro4553_Ser4554ins others(5919): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
2 | a0013a0070 | 3 | HG02071.hp1 HG03669.hp1 NA18747.hp1 |
disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
1 | a0059 | 1 | NA19000.hp2 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(9161): Show |
1 | a0249 | 1 | HG02074.hp2 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(9164): Show |
p.Pro4553_Ser4554ins others(9168): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(9161): Show |
1 | a0246 | 1 | NA20300.hp2 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(9164): Show |
p.Pro4553_Ser4554ins others(9168): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(9161): Show |
1 | a0251 | 1 | NA18959.hp1 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(9164): Show |
p.Pro4553_Ser4554ins others(9168): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(18908): Show |
1 | a0220 | 1 | HG01515.hp1 | stop_gained&disruptive_inframe_insertion | HIGH | c.13658_13659insCAGA others(18911): Show |
p.Pro4553_Ser4554ins others(18915): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
4 | a0016a0077a0081others(1): Show | 5 | HG00099.hp2 HG01168.hp1 HG01169.hp2 others(2): Show |
disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
1 | a0076 | 1 | NA20752.hp1 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
1 | a0148 | 1 | NA18954.hp1 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
1 | a0268 | 1 | HG03579.hp1 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
10 | a0011a0019a0045others(7): Show | 12 | HG00323.hp1 HG00639.hp2 HG01074.hp2 others(9): Show |
disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
3 | a0050a0158a0163 | 3 | HG00741.hp2 NA19057.hp1 NA20805.hp2 |
disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
1 | a0030 | 2 | HG01099.hp2 HG02280.hp2 |
disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
1 | a0087 | 1 | NA18971.hp1 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
1 | a0189 | 1 | HG01106.hp1 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
4 | a0267a0269a0270others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG03471.hp1 others(1): Show |
disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
1 | a0258 | 1 | HG03130.hp2 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
1 | a0001 | 1 | NA18994.hp1 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
26 | a0001a0009a0026others(23): Show | 37 | HG00558.hp1 HG00642.hp1 HG00738.hp1 others(34): Show |
disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
1 | a0185 | 1 | HG03471.hp2 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
3 | a0181a0186a0195 | 3 | HG00642.hp2 HG01109.hp2 HG04199.hp2 |
disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
1 | a0174 | 1 | NA19081.hp1 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
4 | a0263a0264a0265others(1): Show | 4 | HG02723.hp2 HG03098.hp2 NA20129.hp1 others(1): Show |
disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
10 | a0099a0106a0107others(7): Show | 10 | HG00140.hp1 HG00738.hp2 HG02055.hp1 others(7): Show |
disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
9 | a0024a0088a0090others(6): Show | 10 | HG00099.hp1 HG00408.hp1 HG01069.hp1 others(7): Show |
disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
1 | a0052 | 1 | NA20905.hp2 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
5 | a0025a0119a0120others(2): Show | 6 | HG01243.hp2 HG02109.hp2 HG03195.hp1 others(3): Show |
disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
1 | a0127 | 1 | HG03098.hp1 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
1 | a0191 | 1 | HG00673.hp1 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
1 | a0261 | 1 | HG02451.hp2 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
1 | a0098 | 1 | HG00741.hp1 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
11 | a0008a0012a0043others(8): Show | 14 | HG00140.hp2 HG00673.hp2 HG01175.hp1 others(11): Show |
disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
1 | a0151 | 1 | NA18955.hp1 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
1 | a0168 | 1 | HG03516.hp2 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
3 | a0089a0128a0142 | 3 | HG02886.hp1 HG03041.hp2 NA18948.hp2 |
disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
2 | a0027a0134 | 3 | HG02970.hp1 HG06807.hp1 NA19240.hp1 |
disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
1 | a0022 | 2 | HG01257.hp2 HG01258.hp2 |
disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
1 | a0047 | 1 | HG02922.hp2 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
7 | a0034a0176a0182others(4): Show | 8 | HG01515.hp2 HG02280.hp1 HG02698.hp2 others(5): Show |
disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
2 | a0033a0177 | 3 | HG02559.hp1 HG03041.hp1 HG03540.hp2 |
disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
1 | a0188 | 1 | NA18522.hp1 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
2 | a0102a0108 | 2 | HG00408.hp2 HG02080.hp1 |
disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
13 | a0020a0021a0084others(10): Show | 15 | HG00323.hp2 HG00621.hp2 HG00735.hp2 others(12): Show |
disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(20966): Show |
1 | a0096 | 1 | HG02683.hp2 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(20969): Show |
p.Pro4553_Ser4554ins others(20973): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(20966): Show |
1 | a0118 | 1 | HG00735.hp1 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(20969): Show |
p.Pro4553_Ser4554ins others(20973): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
1 | a0104 | 1 | HG00423.hp1 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
1 | a0023 | 2 | HG03239.hp1 HG03710.hp1 |
disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
5 | a0029a0032a0051others(2): Show | 7 | HG02293.hp1 HG03654.hp1 HG03831.hp1 others(4): Show |
disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
1 | a0101 | 1 | HG01993.hp2 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
1 | a0147 | 1 | NA19088.hp2 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(12410): Show |
1 | a0210 | 1 | HG02572.hp2 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(12413): Show |
p.Pro4553_Ser4554ins others(12417): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(12410): Show |
1 | a0209 | 1 | HG02615.hp2 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(12413): Show |
p.Pro4553_Ser4554ins others(12417): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(17834): Show |
1 | a0240 | 1 | HG04199.hp1 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(17837): Show |
p.Pro4553_Ser4554ins others(17841): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(18908): Show |
1 | a0214 | 1 | HG02145.hp1 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(18911): Show |
p.Pro4553_Ser4554ins others(18915): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(9161): Show |
1 | a0035 | 2 | NA19010.hp2 NA19088.hp1 |
disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(9164): Show |
p.Pro4553_Ser4554ins others(9168): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(15659): Show |
1 | a0205 | 1 | NA18970.hp1 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(15662): Show |
p.Pro4553_Ser4554ins others(15666): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(15659): Show |
1 | a0204 | 1 | NA19005.hp1 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(15662): Show |
p.Pro4553_Ser4554ins others(15666): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(18908): Show |
1 | a0248 | 1 | HG02071.hp2 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(18911): Show |
p.Pro4553_Ser4554ins others(18915): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(9161): Show |
1 | a0211 | 1 | HG03209.hp2 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(9164): Show |
p.Pro4553_Ser4554ins others(9168): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(5912): Show |
1 | a0229 | 1 | HG04115.hp2 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(5915): Show |
p.Pro4553_Ser4554ins others(5919): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(5912): Show |
1 | a0203 | 1 | NA18967.hp2 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(5915): Show |
p.Pro4553_Ser4554ins others(5919): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(12410): Show |
1 | a0238 | 1 | HG02165.hp2 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(12413): Show |
p.Pro4553_Ser4554ins others(12417): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(12410): Show |
1 | a0247 | 1 | HG03927.hp1 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(12413): Show |
p.Pro4553_Ser4554ins others(12417): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(12410): Show |
1 | a0232 | 1 | HG03017.hp2 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(12413): Show |
p.Pro4553_Ser4554ins others(12417): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(12410): Show |
1 | a0250 | 1 | NA18990.hp2 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(12413): Show |
p.Pro4553_Ser4554ins others(12417): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(12410): Show |
1 | a0239 | 1 | HG02132.hp2 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(12413): Show |
p.Pro4553_Ser4554ins others(12417): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(12410): Show |
1 | a0244 | 1 | NA18946.hp1 | stop_gained&disruptive_inframe_insertion | HIGH | c.13658_13659insCAGA others(12413): Show |
p.Pro4553_Ser4554ins others(12417): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(22157): Show |
1 | a0221 | 1 | HG03688.hp1 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(22160): Show |
p.Pro4553_Ser4554ins others(22164): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(15659): Show |
2 | a0215a0225 | 2 | HG02970.hp2 HG03453.hp1 |
disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(15662): Show |
p.Pro4553_Ser4554ins others(15666): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(12410): Show |
1 | a0234 | 1 | NA18941.hp1 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(12413): Show |
p.Pro4553_Ser4554ins others(12417): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(12410): Show |
1 | a0216 | 1 | HG03834.hp2 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(12413): Show |
p.Pro4553_Ser4554ins others(12417): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(15659): Show |
1 | a0243 | 1 | HG03942.hp1 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(15662): Show |
p.Pro4553_Ser4554ins others(15666): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(12410): Show |
1 | a0237 | 1 | NA18982.hp2 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(12413): Show |
p.Pro4553_Ser4554ins others(12417): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(12410): Show |
2 | a0230a0256 | 2 | HG00423.hp2 NA19060.hp1 |
disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(12413): Show |
p.Pro4553_Ser4554ins others(12417): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(12410): Show |
1 | a0005 | 4 | NA18942.hp2 NA18971.hp2 NA18977.hp2 others(1): Show |
disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(12413): Show |
p.Pro4553_Ser4554ins others(12417): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(12410): Show |
2 | a0042a0228 | 2 | NA18747.hp2 NA18964.hp1 |
disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(12413): Show |
p.Pro4553_Ser4554ins others(12417): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(12410): Show |
1 | a0041 | 2 | NA18947.hp1 NA19007.hp2 |
disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(12413): Show |
p.Pro4553_Ser4554ins others(12417): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(12410): Show |
1 | a0242 | 1 | HG03704.hp1 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(12413): Show |
p.Pro4553_Ser4554ins others(12417): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(15659): Show |
1 | a0226 | 1 | HG01358.hp2 | stop_gained&disruptive_inframe_insertion | HIGH | c.13658_13659insCAGA others(15662): Show |
p.Pro4553_Ser4554ins others(15666): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(15659): Show |
2 | a0252a0255 | 2 | HG03669.hp2 homoSapiens_chm13v2.hp1 |
stop_gained&disruptive_inframe_insertion | HIGH | c.13658_13659insCAGA others(15662): Show |
p.Pro4553_Ser4554ins others(15666): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(22157): Show |
1 | a0219 | 1 | HG01106.hp2 | stop_gained&disruptive_inframe_insertion | HIGH | c.13658_13659insCAGA others(22160): Show |
p.Pro4553_Ser4554ins others(22164): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(15659): Show |
1 | a0254 | 1 | HG00639.hp1 | stop_gained&disruptive_inframe_insertion | HIGH | c.13658_13659insCAGA others(15662): Show |
p.Pro4553_Ser4554ins others(15666): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(12410): Show |
1 | a0208 | 1 | NA19057.hp2 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(12413): Show |
p.Pro4553_Ser4554ins others(12417): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(18908): Show |
1 | a0224 | 1 | HG02809.hp2 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(18911): Show |
p.Pro4553_Ser4554ins others(18915): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(12410): Show |
1 | a0037 | 2 | HG01069.hp2 HG01070.hp1 |
stop_gained&disruptive_inframe_insertion | HIGH | c.13658_13659insCAGA others(12413): Show |
p.Pro4553_Ser4554ins others(12417): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(12410): Show |
1 | a0042 | 1 | HG00621.hp1 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(12413): Show |
p.Pro4553_Ser4554ins others(12417): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(12410): Show |
1 | a0241 | 1 | HG03492.hp1 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(12413): Show |
p.Pro4553_Ser4554ins others(12417): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(12410): Show |
1 | a0235 | 1 | NA19090.hp2 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(12413): Show |
p.Pro4553_Ser4554ins others(12417): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(9161): Show |
1 | a0233 | 1 | HG03710.hp2 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(9164): Show |
p.Pro4553_Ser4554ins others(9168): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(12410): Show |
1 | a0236 | 1 | NA18984.hp2 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(12413): Show |
p.Pro4553_Ser4554ins others(12417): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(12410): Show |
1 | a0040 | 2 | HG03834.hp1 HG04204.hp1 |
disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(12413): Show |
p.Pro4553_Ser4554ins others(12417): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(15659): Show |
1 | a0222 | 1 | HG01934.hp2 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(15662): Show |
p.Pro4553_Ser4554ins others(15666): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(15659): Show |
3 | a0038a0217a0227 | 4 | HG01192.hp2 HG01255.hp2 HG01261.hp1 others(1): Show |
disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(15662): Show |
p.Pro4553_Ser4554ins others(15666): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(15659): Show |
1 | a0213 | 1 | HG01361.hp1 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(15662): Show |
p.Pro4553_Ser4554ins others(15666): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(15659): Show |
1 | a0010 | 3 | HG01256.hp2 HG01258.hp1 HG01496.hp2 |
disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(15662): Show |
p.Pro4553_Ser4554ins others(15666): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(18908): Show |
1 | a0201 | 1 | HG01109.hp1 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(18911): Show |
p.Pro4553_Ser4554ins others(18915): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(5912): Show |
1 | a0245 | 1 | HG02155.hp2 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(5915): Show |
p.Pro4553_Ser4554ins others(5919): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(15659): Show |
1 | a0039 | 2 | HG01255.hp1 HG01516.hp1 |
disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(15662): Show |
p.Pro4553_Ser4554ins others(15666): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(15659): Show |
1 | a0218 | 1 | HG01081.hp1 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(15662): Show |
p.Pro4553_Ser4554ins others(15666): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(15659): Show |
1 | a0223 | 1 | HG03139.hp2 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(15662): Show |
p.Pro4553_Ser4554ins others(15666): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
1 | a0028 | 2 | HG02486.hp1 NA19030.hp1 |
disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
1 | a0260 | 1 | HG02622.hp1 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
1 | a0044 | 1 | HG01168.hp2 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
1 | a0175 | 1 | HG02895.hp1 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
1 | a0200 | 1 | HG02572.hp1 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
1 | a0116 | 1 | HG02698.hp1 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(12410): Show |
1 | a0231 | 1 | HG02027.hp1 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(12413): Show |
p.Pro4553_Ser4554ins others(12417): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(15659): Show |
1 | a0253 | 1 | HG01433.hp2 | stop_gained&disruptive_inframe_insertion | HIGH | c.13658_13659insCAGA others(15662): Show |
p.Pro4553_Ser4554ins others(15666): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(15659): Show |
1 | a0202 | 1 | HG01928.hp1 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(15662): Show |
p.Pro4553_Ser4554ins others(15666): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
1 | a0049 | 1 | HG03516.hp1 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
1 | a0199 | 1 | HG02735.hp1 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
1 | a0178 | 1 | HG02723.hp1 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
1 | a0180 | 1 | HG02976.hp2 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
5 | a0179a0192a0194others(2): Show | 5 | HG01361.hp2 HG02630.hp2 HG02647.hp1 others(2): Show |
disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
1 | a0193 | 1 | HG01978.hp2 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004216
|
T | TAGCCCCA others(2663): Show |
1 | a0262 | 1 | HG02258.hp1 | disruptive_inframe_insertion | MODERATE | c.13658_13659insCAGA others(2666): Show |
p.Pro4553_Ser4554ins others(2670): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13717/16366 | 13659/16008 | 4553/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004216 | |
| chr7:101004230
|
C | T | 11 | a0007a0013a0055others(8): Show | 14 | HG01261.hp2 HG02071.hp1 HG02559.hp2 others(11): Show |
missense_variant | MODERATE | c.13667C>T | p.Thr4556Ile | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13725/16366 | 13667/16008 | 4556/5335 | chr7 | 101004230 | ||
| chr7:101004236
|
C | G | 8 | a0015a0016a0048others(5): Show | 10 | HG00099.hp2 HG01168.hp1 HG01169.hp2 others(7): Show |
missense_variant | MODERATE | c.13673C>G | p.Thr4558Arg | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13731/16366 | 13673/16008 | 4558/5335 | chr7 | 101004236 | ||
| chr7:101004250
|
G | C | 2 | a0179a0188 | 2 | HG02647.hp1 NA18522.hp1 |
missense_variant | MODERATE | c.13687G>C | p.Ala4563Pro | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13745/16366 | 13687/16008 | 4563/5335 | chr7 | 101004250 | ||
| chr7:101004267
|
G | C | 13 | a0007a0013a0055others(10): Show | 16 | HG01261.hp2 HG02071.hp1 HG02559.hp2 others(13): Show |
missense_variant | MODERATE | c.13704G>C | p.Leu4568Phe | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13762/16366 | 13704/16008 | 4568/5335 | chr7 | 101004267 | ||
| chr7:101004272
|
G | A | 4 | a0128a0129a0168others(1): Show | 4 | HG03041.hp2 HG03516.hp2 HG03579.hp1 others(1): Show |
missense_variant | MODERATE | c.13709G>A | p.Arg4570His | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13767/16366 | 13709/16008 | 4570/5335 | chr7 | 101004272 | ||
| chr7:101004284
|
C | T | 13 | a0007a0013a0055others(10): Show | 16 | HG01261.hp2 HG02071.hp1 HG02559.hp2 others(13): Show |
missense_variant | MODERATE | c.13721C>T | p.Ser4574Leu | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13779/16366 | 13721/16008 | 4574/5335 | chr7 | 101004284 | ||
| chr7:101004313
|
A | C | 13 | a0007a0013a0055others(10): Show | 16 | HG01261.hp2 HG02071.hp1 HG02559.hp2 others(13): Show |
missense_variant | MODERATE | c.13750A>C | p.Thr4584Pro | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13808/16366 | 13750/16008 | 4584/5335 | chr7 | 101004313 | ||
| chr7:101004330
|
G | GCCTGCCC others(3240): Show |
1 | a0061 | 1 | NA18989.hp2 | frameshift_variant&stop_gained | HIGH | c.13774_13775insACTC others(3243): Show |
p.Arg4592fs | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13833/16366 | 13775/16008 | 4592/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004330 | |
| chr7:101004330
|
G | GCCTGCCC others(3242): Show |
5 | a0014a0058a0067others(2): Show | 6 | HG01884.hp1 HG01952.hp2 HG02615.hp1 others(3): Show |
disruptive_inframe_insertion | MODERATE | c.13774_13775insACTC others(3245): Show |
p.Ala4591_Arg4592ins others(3249): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13833/16366 | 13775/16008 | 4592/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004330 | |
| chr7:101004330
|
G | GCCTGCCC others(3242): Show |
1 | a0079 | 1 | HG01192.hp1 | disruptive_inframe_insertion | MODERATE | c.13774_13775insACTC others(3245): Show |
p.Ala4591_Arg4592ins others(3249): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13833/16366 | 13775/16008 | 4592/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004330 | |
| chr7:101004330
|
G | GCCTGCCC others(3242): Show |
14 | a0002a0003a0006others(11): Show | 30 | HG00558.hp2 HG01099.hp1 HG01123.hp2 others(27): Show |
disruptive_inframe_insertion | MODERATE | c.13774_13775insACTC others(3245): Show |
p.Ala4591_Arg4592ins others(3249): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13833/16366 | 13775/16008 | 4592/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004330 | |
| chr7:101004330
|
G | GCCTGCCC others(2489): Show |
1 | a0063 | 1 | NA18983.hp2 | disruptive_inframe_insertion | MODERATE | c.13774_13775insACTC others(2492): Show |
p.Ala4591_Arg4592ins others(2496): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13833/16366 | 13775/16008 | 4592/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004330 | |
| chr7:101004330
|
G | GCCTGCCC others(3242): Show |
1 | a0003 | 1 | NA19081.hp2 | disruptive_inframe_insertion | MODERATE | c.13774_13775insACTC others(3245): Show |
p.Ala4591_Arg4592ins others(3249): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13833/16366 | 13775/16008 | 4592/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004330 | |
| chr7:101004330
|
G | GCCTGCCC others(3242): Show |
1 | a0054 | 1 | HG01952.hp1 | disruptive_inframe_insertion | MODERATE | c.13774_13775insACTC others(3245): Show |
p.Ala4591_Arg4592ins others(3249): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13833/16366 | 13775/16008 | 4592/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004330 | |
| chr7:101004357
|
C | CGTTGAAG others(12989): Show |
1 | a0198 | 1 | HG06807.hp2 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(12992): Show |
p.Thr4603_Ala4604ins others(12996): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004357 | |
| chr7:101004357
|
C | CGTTGAAG others(9740): Show |
1 | a0181 | 1 | HG04199.hp2 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(9743): Show |
p.Thr4603_Ala4604ins others(9747): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004357 | |
| chr7:101004357
|
C | CGTTGAAG others(16238): Show |
1 | a0186 | 1 | HG01109.hp2 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(16241): Show |
p.Thr4603_Ala4604ins others(16245): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004357 | |
| chr7:101004357
|
C | CGTTGAAG others(16238): Show |
1 | a0176 | 1 | HG02280.hp1 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(16241): Show |
p.Thr4603_Ala4604ins others(16245): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004357 | |
| chr7:101004357
|
C | CGTTGAAG others(9740): Show |
1 | a0195 | 1 | HG00642.hp2 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(9743): Show |
p.Thr4603_Ala4604ins others(9747): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004357 | |
| chr7:101004357
|
C | CGTTGAAG others(9740): Show |
1 | a0185 | 1 | HG03471.hp2 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(9743): Show |
p.Thr4603_Ala4604ins others(9747): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004357 | |
| chr7:101004357
|
C | CGTTGAAG others(12989): Show |
1 | a0183 | 1 | HG03540.hp1 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(12992): Show |
p.Thr4603_Ala4604ins others(12996): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004357 | |
| chr7:101004357
|
C | CGTTGAAG others(12989): Show |
1 | a0182 | 1 | NA19043.hp2 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(12992): Show |
p.Thr4603_Ala4604ins others(12996): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004357 | |
| chr7:101004357
|
C | CGTTGAAG others(16238): Show |
1 | a0034 | 2 | HG01515.hp2 HG02698.hp2 |
conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(16241): Show |
p.Thr4603_Ala4604ins others(16245): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004357 | |
| chr7:101004357
|
C | CGTTGAAG others(16238): Show |
1 | a0190 | 1 | HG03239.hp2 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(16241): Show |
p.Thr4603_Ala4604ins others(16245): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004357 | |
| chr7:101004357
|
C | CGTTGAAG others(16238): Show |
1 | a0189 | 1 | HG01106.hp1 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(16241): Show |
p.Thr4603_Ala4604ins others(16245): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004357 | |
| chr7:101004357
|
C | CGTTGAAG others(16238): Show |
1 | a0194 | 1 | NA18980.hp1 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(16241): Show |
p.Thr4603_Ala4604ins others(16245): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004357 | |
| chr7:101004357
|
C | CGTTGAAG others(19486): Show |
1 | a0192 | 1 | HG01361.hp2 | frameshift_variant&stop_gained | HIGH | c.13809_13810insACCT others(19489): Show |
p.Ala4604fs | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004357 | |
| chr7:101004357
|
C | CGTTGAAG others(19487): Show |
1 | a0193 | 1 | HG01978.hp2 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(19490): Show |
p.Thr4603_Ala4604ins others(19494): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004357 | |
| chr7:101004357
|
C | CGTTGAAG others(19487): Show |
1 | a0199 | 1 | HG02735.hp1 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(19490): Show |
p.Thr4603_Ala4604ins others(19494): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004357 | |
| chr7:101004357
|
C | CGTTGAAG others(22736): Show |
1 | a0271 | 1 | HG03471.hp1 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(22739): Show |
p.Thr4603_Ala4604ins others(22743): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004357 | |
| chr7:101004357
|
C | CGTTGAAG others(12989): Show |
1 | a0270 | 1 | HG01884.hp2 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(12992): Show |
p.Thr4603_Ala4604ins others(12996): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004357 | |
| chr7:101004357
|
C | CGTTGAAG others(12989): Show |
1 | a0269 | 1 | HG02257.hp2 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(12992): Show |
p.Thr4603_Ala4604ins others(12996): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004357 | |
| chr7:101004357
|
C | CGTTGAAG others(16238): Show |
1 | a0180 | 1 | HG02976.hp2 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(16241): Show |
p.Thr4603_Ala4604ins others(16245): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004357 | |
| chr7:101004357
|
C | CGTTGAAG others(19487): Show |
1 | a0187 | 1 | NA19240.hp2 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(19490): Show |
p.Thr4603_Ala4604ins others(19494): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004357 | |
| chr7:101004357
|
C | CGTTGAAG others(12989): Show |
1 | a0267 | 1 | HG03486.hp1 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(12992): Show |
p.Thr4603_Ala4604ins others(12996): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004357 | |
| chr7:101004357
|
C | CGTTGAAG others(9740): Show |
1 | a0178 | 1 | HG02723.hp1 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(9743): Show |
p.Thr4603_Ala4604ins others(9747): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004357 | |
| chr7:101004357
|
C | CGTTGAAG others(19487): Show |
1 | a0033 | 2 | HG02559.hp1 HG03041.hp1 |
conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(19490): Show |
p.Thr4603_Ala4604ins others(19494): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004357 | |
| chr7:101004357
|
C | CGTTGAAG others(12989): Show |
1 | a0191 | 1 | HG00673.hp1 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(12992): Show |
p.Thr4603_Ala4604ins others(12996): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004357 | |
| chr7:101004357
|
C | CGTTGAAG others(22736): Show |
1 | a0177 | 1 | HG03540.hp2 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(22739): Show |
p.Thr4603_Ala4604ins others(22743): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004357 | |
| chr7:101004357
|
C | CGTTGAAG others(19487): Show |
1 | a0196 | 1 | HG03130.hp1 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(19490): Show |
p.Thr4603_Ala4604ins others(19494): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004357 | |
| chr7:101004357
|
C | CGTTGAAG others(19487): Show |
1 | a0197 | 1 | HG02630.hp2 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(19490): Show |
p.Thr4603_Ala4604ins others(19494): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004357 | |
| chr7:101004357
|
C | CGTTGAAG others(22736): Show |
1 | a0188 | 1 | NA18522.hp1 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(22739): Show |
p.Thr4603_Ala4604ins others(22743): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004357 | |
| chr7:101004357
|
C | CGTTGAAG others(16238): Show |
1 | a0179 | 1 | HG02647.hp1 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(16241): Show |
p.Thr4603_Ala4604ins others(16245): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004357 | |
| chr7:101004357
|
C | CGTTGAAG others(9740): Show |
1 | a0184 | 1 | HG02717.hp2 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(9743): Show |
p.Thr4603_Ala4604ins others(9747): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004357 | |
| chr7:101004357
|
C | CGTTGAAG others(9740): Show |
1 | a0258 | 1 | HG03130.hp2 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(9743): Show |
p.Thr4603_Ala4604ins others(9747): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004357 | |
| chr7:101004357
|
C | CGTTGAAG others(12989): Show |
1 | a0259 | 1 | HG03195.hp2 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(12992): Show |
p.Thr4603_Ala4604ins others(12996): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004357 | |
| chr7:101004357
|
C | CGTTGAAG others(12989): Show |
1 | a0260 | 1 | HG02622.hp1 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(12992): Show |
p.Thr4603_Ala4604ins others(12996): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004357 | |
| chr7:101004357
|
C | CGTTGAAG others(16238): Show |
1 | a0272 | 1 | HG02258.hp2 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(16241): Show |
p.Thr4603_Ala4604ins others(16245): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004357 | |
| chr7:101004357
|
C | CGTTGAAG others(19487): Show |
1 | a0261 | 1 | HG02451.hp2 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(19490): Show |
p.Thr4603_Ala4604ins others(19494): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004357 | |
| chr7:101004357
|
C | CGTTGAAG others(19487): Show |
1 | a0266 | 1 | HG02723.hp2 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(19490): Show |
p.Thr4603_Ala4604ins others(19494): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004357 | |
| chr7:101004357
|
C | CGTTGAAG others(22736): Show |
1 | a0265 | 1 | HG03098.hp2 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(22739): Show |
p.Thr4603_Ala4604ins others(22743): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004357 | |
| chr7:101004357
|
C | CGTTGAAG others(19487): Show |
1 | a0263 | 1 | NA20129.hp1 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(19490): Show |
p.Thr4603_Ala4604ins others(19494): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004357 | |
| chr7:101004357
|
C | CGTTGAAG others(19487): Show |
1 | a0264 | 1 | NA20129.hp2 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(19490): Show |
p.Thr4603_Ala4604ins others(19494): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004357 | |
| chr7:101004357
|
C | CGTTGAAG others(16238): Show |
1 | a0268 | 1 | HG03579.hp1 | disruptive_inframe_insertion | MODERATE | c.13807_13808insTGAC others(16241): Show |
p.Ser4602_Thr4603ins others(16245): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13866/16366 | 13808/16008 | 4603/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004357 | |
| chr7:101004365
|
A | G | 3 | a0128a0129a0168 | 3 | HG03041.hp2 HG03516.hp2 NA18941.hp2 |
missense_variant | MODERATE | c.13802A>G | p.Glu4601Gly | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13860/16366 | 13802/16008 | 4601/5335 | chr7 | 101004365 | ||
| chr7:101004371
|
C | CGACCTAC others(16238): Show |
1 | a0122 | 1 | HG02055.hp1 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(16241): Show |
p.Thr4603_Ala4604ins others(16245): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(16238): Show |
2 | a0123a0125 | 2 | HG03139.hp1 NA18522.hp2 |
conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(16241): Show |
p.Thr4603_Ala4604ins others(16245): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(19487): Show |
1 | a0124 | 1 | HG02257.hp1 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(19490): Show |
p.Thr4603_Ala4604ins others(19494): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(19487): Show |
1 | a0086 | 1 | HG03654.hp2 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(19490): Show |
p.Thr4603_Ala4604ins others(19494): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(6491): Show |
1 | a0162 | 1 | HG02155.hp1 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(6494): Show |
p.Thr4603_Ala4604ins others(6498): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(3242): Show |
7 | a0008a0012a0043others(4): Show | 10 | HG00673.hp2 HG01175.hp1 HG02056.hp2 others(7): Show |
conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(3245): Show |
p.Thr4603_Ala4604ins others(3249): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(3242): Show |
1 | a0170 | 1 | HG03225.hp2 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(3245): Show |
p.Thr4603_Ala4604ins others(3249): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(3242): Show |
3 | a0028a0142a0143 | 4 | HG02451.hp1 HG02486.hp1 HG02886.hp1 others(1): Show |
conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(3245): Show |
p.Thr4603_Ala4604ins others(3249): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(6491): Show |
2 | a0030a0164 | 3 | HG00140.hp2 HG01099.hp2 HG02280.hp2 |
conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(6494): Show |
p.Thr4603_Ala4604ins others(6498): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(9740): Show |
1 | a0138 | 1 | HG02055.hp2 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(9743): Show |
p.Thr4603_Ala4604ins others(9747): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(9740): Show |
1 | a0115 | 1 | HG01069.hp1 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(9743): Show |
p.Thr4603_Ala4604ins others(9747): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(9740): Show |
1 | a0098 | 1 | HG00741.hp1 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(9743): Show |
p.Thr4603_Ala4604ins others(9747): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(6491): Show |
3 | a0052a0097a0174 | 3 | HG03704.hp2 NA19081.hp1 NA20905.hp2 |
conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(6494): Show |
p.Thr4603_Ala4604ins others(6498): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(6491): Show |
1 | a0090 | 1 | HG00408.hp1 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(6494): Show |
p.Thr4603_Ala4604ins others(6498): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(3242): Show |
2 | a0027a0134 | 3 | HG02970.hp1 HG06807.hp1 NA19240.hp1 |
conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(3245): Show |
p.Thr4603_Ala4604ins others(3249): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(6491): Show |
1 | a0088 | 1 | NA19007.hp1 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(6494): Show |
p.Thr4603_Ala4604ins others(6498): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(3242): Show |
1 | a0149 | 1 | HG02015.hp1 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(3245): Show |
p.Thr4603_Ala4604ins others(3249): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(6491): Show |
1 | a0257 | 1 | HG02027.hp2 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(6494): Show |
p.Thr4603_Ala4604ins others(6498): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(3242): Show |
1 | a0024 | 2 | HG02896.hp1 HG02897.hp1 |
conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(3245): Show |
p.Thr4603_Ala4604ins others(3249): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(3242): Show |
3 | a0022a0087a0089 | 4 | HG01257.hp2 HG01258.hp2 NA18948.hp2 others(1): Show |
conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(3245): Show |
p.Thr4603_Ala4604ins others(3249): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(3242): Show |
2 | a0096a0118 | 2 | HG00735.hp1 HG02683.hp2 |
conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(3245): Show |
p.Thr4603_Ala4604ins others(3249): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(9740): Show |
1 | a0009 | 3 | HG01496.hp1 HG01943.hp2 HG01981.hp1 |
conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(9743): Show |
p.Thr4603_Ala4604ins others(9747): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(6491): Show |
1 | a0163 | 1 | NA19057.hp1 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(6494): Show |
p.Thr4603_Ala4604ins others(6498): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(9740): Show |
1 | a0157 | 1 | HG00738.hp1 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(9743): Show |
p.Thr4603_Ala4604ins others(9747): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(9740): Show |
1 | a0032 | 1 | HG04184.hp2 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(9743): Show |
p.Thr4603_Ala4604ins others(9747): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(9740): Show |
1 | a0032 | 1 | HG03831.hp1 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(9743): Show |
p.Thr4603_Ala4604ins others(9747): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(12989): Show |
1 | a0029 | 2 | HG04115.hp1 NA20905.hp1 |
conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(12992): Show |
p.Thr4603_Ala4604ins others(12996): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(9740): Show |
1 | a0145 | 1 | HG03654.hp1 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(9743): Show |
p.Thr4603_Ala4604ins others(9747): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(9740): Show |
1 | a0020 | 2 | HG00621.hp2 HG02523.hp1 |
conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(9743): Show |
p.Thr4603_Ala4604ins others(9747): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(9740): Show |
2 | a0100a0111 | 2 | HG02040.hp2 NA18967.hp1 |
conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(9743): Show |
p.Thr4603_Ala4604ins others(9747): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(9740): Show |
1 | a0085 | 1 | HG03831.hp2 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(9743): Show |
p.Thr4603_Ala4604ins others(9747): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(6491): Show |
1 | a0026 | 1 | NA19010.hp1 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(6494): Show |
p.Thr4603_Ala4604ins others(6498): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(6491): Show |
1 | a0001 | 1 | HG02683.hp1 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(6494): Show |
p.Thr4603_Ala4604ins others(6498): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(12989): Show |
1 | a0137 | 1 | HG02486.hp2 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(12992): Show |
p.Thr4603_Ala4604ins others(12996): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(6491): Show |
1 | a0155 | 1 | HG00558.hp1 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(6494): Show |
p.Thr4603_Ala4604ins others(6498): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(6491): Show |
1 | a0166 | 1 | HG03492.hp2 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(6494): Show |
p.Thr4603_Ala4604ins others(6498): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(6491): Show |
12 | a0001a0050a0133others(9): Show | 19 | HG00741.hp2 HG02080.hp2 HG03688.hp2 others(16): Show |
conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(6494): Show |
p.Thr4603_Ala4604ins others(6498): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(6491): Show |
1 | a0159 | 1 | NA19084.hp2 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(6494): Show |
p.Thr4603_Ala4604ins others(6498): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(9740): Show |
1 | a0169 | 1 | HG00642.hp1 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(9743): Show |
p.Thr4603_Ala4604ins others(9747): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(6491): Show |
1 | a0153 | 1 | NA18947.hp2 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(6494): Show |
p.Thr4603_Ala4604ins others(6498): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(9740): Show |
1 | a0156 | 1 | NA19068.hp2 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(9743): Show |
p.Thr4603_Ala4604ins others(9747): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(6491): Show |
1 | a0152 | 1 | HG01123.hp1 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(6494): Show |
p.Thr4603_Ala4604ins others(6498): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(6491): Show |
1 | a0158 | 1 | NA20805.hp2 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(6494): Show |
p.Thr4603_Ala4604ins others(6498): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(22736): Show |
1 | a0091 | 1 | HG04228.hp2 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(22739): Show |
p.Thr4603_Ala4604ins others(22743): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(6491): Show |
2 | a0026a0151 | 2 | NA18955.hp1 NA19090.hp1 |
conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(6494): Show |
p.Thr4603_Ala4604ins others(6498): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(9740): Show |
1 | a0047 | 1 | HG02922.hp2 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(9743): Show |
p.Thr4603_Ala4604ins others(9747): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(12989): Show |
1 | a0131 | 1 | HG02622.hp2 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(12992): Show |
p.Thr4603_Ala4604ins others(12996): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(6491): Show |
1 | a0045 | 1 | HG00323.hp1 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(6494): Show |
p.Thr4603_Ala4604ins others(6498): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(6491): Show |
1 | a0019 | 2 | HG02083.hp2 NA18946.hp2 |
conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(6494): Show |
p.Thr4603_Ala4604ins others(6498): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(19487): Show |
1 | a0083 | 1 | HG02896.hp2 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(19490): Show |
p.Thr4603_Ala4604ins others(19494): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(9740): Show |
1 | a0011 | 2 | HG00639.hp2 HG01074.hp2 |
conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(9743): Show |
p.Thr4603_Ala4604ins others(9747): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(9740): Show |
3 | a0092a0095a0130 | 3 | HG02922.hp1 NA18978.hp2 NA19000.hp1 |
conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(9743): Show |
p.Thr4603_Ala4604ins others(9747): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(16238): Show |
1 | a0094 | 1 | NA18999.hp1 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(16241): Show |
p.Thr4603_Ala4604ins others(16245): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(9740): Show |
1 | a0046 | 1 | HG01256.hp1 | stop_gained&conservative_inframe_insertion | HIGH | c.13809_13810insACCT others(9743): Show |
p.Thr4603_Ala4604ins others(9747): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(9740): Show |
1 | a0031 | 2 | HG01081.hp2 HG01169.hp1 |
conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(9743): Show |
p.Thr4603_Ala4604ins others(9747): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(9740): Show |
1 | a0160 | 1 | NA20805.hp1 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(9743): Show |
p.Thr4603_Ala4604ins others(9747): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(9740): Show |
1 | a0053 | 1 | HG01516.hp2 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(9743): Show |
p.Thr4603_Ala4604ins others(9747): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(9740): Show |
1 | a0140 | 1 | HG01074.hp1 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(9743): Show |
p.Thr4603_Ala4604ins others(9747): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(6491): Show |
1 | a0141 | 1 | HG02132.hp1 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(6494): Show |
p.Thr4603_Ala4604ins others(6498): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(3242): Show |
1 | a0093 | 1 | HG01257.hp1 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(3245): Show |
p.Thr4603_Ala4604ins others(3249): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(19487): Show |
2 | a0025a0120 | 3 | HG01243.hp2 HG03453.hp2 HG03486.hp2 |
conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(19490): Show |
p.Thr4603_Ala4604ins others(19494): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(22736): Show |
1 | a0126 | 1 | HG03195.hp1 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(22739): Show |
p.Thr4603_Ala4604ins others(22743): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(29234): Show |
1 | a0119 | 1 | HG03209.hp1 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(29237): Show |
p.Thr4603_Ala4604ins others(29241): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(29234): Show |
1 | a0121 | 1 | HG02109.hp2 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(29237): Show |
p.Thr4603_Ala4604ins others(29241): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(12989): Show |
1 | a0044 | 1 | HG01168.hp2 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(12992): Show |
p.Thr4603_Ala4604ins others(12996): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(12989): Show |
1 | a0114 | 1 | HG04228.hp1 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(12992): Show |
p.Thr4603_Ala4604ins others(12996): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(12989): Show |
1 | a0107 | 1 | NA18950.hp2 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(12992): Show |
p.Thr4603_Ala4604ins others(12996): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(12989): Show |
1 | a0099 | 1 | HG00738.hp2 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(12992): Show |
p.Thr4603_Ala4604ins others(12996): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(12989): Show |
1 | a0172 | 1 | NA20752.hp2 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(12992): Show |
p.Thr4603_Ala4604ins others(12996): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | CGACCTAC others(9740): Show |
1 | a0113 | 1 | HG02735.hp2 | conservative_inframe_insertion | MODERATE | c.13809_13810insACCT others(9743): Show |
p.Thr4603_Ala4604ins others(9747): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004371 | |
| chr7:101004371
|
C | T | 3 | a0128a0129a0168 | 3 | HG03041.hp2 HG03516.hp2 NA18941.hp2 |
missense_variant | MODERATE | c.13808C>T | p.Thr4603Met | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13866/16366 | 13808/16008 | 4603/5335 | chr7 | 101004371 | ||
| chr7:101004373
|
G | A | 30 | a0015a0016a0021others(27): Show | 34 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(31): Show |
missense_variant | MODERATE | c.13810G>A | p.Ala4604Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13868/16366 | 13810/16008 | 4604/5335 | chr7 | 101004373 | ||
| chr7:101004375
|
G | CTACCACA others(22736): Show |
1 | a0262 | 1 | HG02258.hp1 | disruptive_inframe_insertion | MODERATE | c.13811_13812insCTAC others(22739): Show |
p.Ala4604_Tyr4605ins others(22743): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13870/16366 | 13812/16008 | 4604/5335 | chr7 | 101004375 | ||
| chr7:101004375
|
G | CTACCACA others(6491): Show |
1 | a0016 | 2 | HG01168.hp1 HG01169.hp2 |
disruptive_inframe_insertion | MODERATE | c.13811_13812insCTAC others(6494): Show |
p.Ala4604_Tyr4605ins others(6498): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13870/16366 | 13812/16008 | 4604/5335 | chr7 | 101004375 | ||
| chr7:101004375
|
G | CTACCACA others(9740): Show |
1 | a0048 | 1 | NA19030.hp2 | disruptive_inframe_insertion | MODERATE | c.13811_13812insCTAC others(9743): Show |
p.Ala4604_Tyr4605ins others(9747): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13870/16366 | 13812/16008 | 4604/5335 | chr7 | 101004375 | ||
| chr7:101004375
|
G | CTACCACA others(12989): Show |
1 | a0059 | 1 | NA19000.hp2 | disruptive_inframe_insertion | MODERATE | c.13811_13812insCTAC others(12992): Show |
p.Ala4604_Tyr4605ins others(12996): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13870/16366 | 13812/16008 | 4604/5335 | chr7 | 101004375 | ||
| chr7:101004375
|
G | CTACCACA others(6491): Show |
1 | a0077 | 1 | HG04184.hp1 | disruptive_inframe_insertion | MODERATE | c.13811_13812insCTAC others(6494): Show |
p.Ala4604_Tyr4605ins others(6498): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13870/16366 | 13812/16008 | 4604/5335 | chr7 | 101004375 | ||
| chr7:101004375
|
G | CTACCACA others(6491): Show |
1 | a0015 | 2 | HG02040.hp1 NA18999.hp2 |
disruptive_inframe_insertion | MODERATE | c.13811_13812insCTAC others(6494): Show |
p.Ala4604_Tyr4605ins others(6498): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13870/16366 | 13812/16008 | 4604/5335 | chr7 | 101004375 | ||
| chr7:101004375
|
G | CTACCACA others(6491): Show |
3 | a0076a0081a0082 | 3 | HG00099.hp2 HG01243.hp1 NA20752.hp1 |
disruptive_inframe_insertion | MODERATE | c.13811_13812insCTAC others(6494): Show |
p.Ala4604_Tyr4605ins others(6498): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13870/16366 | 13812/16008 | 4604/5335 | chr7 | 101004375 | ||
| chr7:101004375
|
G | CTACCACA others(6491): Show |
1 | a0049 | 1 | HG03516.hp1 | disruptive_inframe_insertion | MODERATE | c.13811_13812insCTAC others(6494): Show |
p.Ala4604_Tyr4605ins others(6498): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13870/16366 | 13812/16008 | 4604/5335 | chr7 | 101004375 | ||
| chr7:101004375
|
G | CTACCACA others(6491): Show |
1 | a0078 | 1 | NA18995.hp2 | disruptive_inframe_insertion | MODERATE | c.13811_13812insCTAC others(6494): Show |
p.Ala4604_Tyr4605ins others(6498): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13870/16366 | 13812/16008 | 4604/5335 | chr7 | 101004375 | ||
| chr7:101004395
|
C | CAACTCAA others(6491): Show |
1 | a0103 | 1 | HG00099.hp1 | conservative_inframe_insertion | MODERATE | c.13860_13861insGACA others(6494): Show |
p.Ser4620_Ser4621ins others(6498): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13919/16366 | 13861/16008 | 4621/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004395 | |
| chr7:101004395
|
C | CAACTCAA others(9740): Show |
1 | a0023 | 2 | HG03239.hp1 HG03710.hp1 |
conservative_inframe_insertion | MODERATE | c.13860_13861insGACA others(9743): Show |
p.Ser4620_Ser4621ins others(9747): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13919/16366 | 13861/16008 | 4621/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004395 | |
| chr7:101004395
|
C | CAACTCAA others(9740): Show |
1 | a0051 | 1 | HG02293.hp1 | conservative_inframe_insertion | MODERATE | c.13860_13861insGACA others(9743): Show |
p.Ser4620_Ser4621ins others(9747): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13919/16366 | 13861/16008 | 4621/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004395 | |
| chr7:101004395
|
C | CAACTCAA others(9740): Show |
1 | a0021 | 2 | HG00323.hp2 NA18952.hp2 |
conservative_inframe_insertion | MODERATE | c.13860_13861insGACA others(9743): Show |
p.Ser4620_Ser4621ins others(9747): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13919/16366 | 13861/16008 | 4621/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004395 | |
| chr7:101004395
|
C | CAACTCAA others(9740): Show |
1 | a0112 | 1 | HG01934.hp1 | conservative_inframe_insertion | MODERATE | c.13860_13861insGACA others(9743): Show |
p.Ser4620_Ser4621ins others(9747): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13919/16366 | 13861/16008 | 4621/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004395 | |
| chr7:101004395
|
C | CAACTCAA others(9740): Show |
1 | a0101 | 1 | HG01993.hp2 | conservative_inframe_insertion | MODERATE | c.13860_13861insGACA others(9743): Show |
p.Ser4620_Ser4621ins others(9747): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13919/16366 | 13861/16008 | 4621/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004395 | |
| chr7:101004395
|
C | CAACTCAA others(9740): Show |
4 | a0102a0104a0108others(1): Show | 4 | HG00408.hp2 HG00423.hp1 HG02080.hp1 others(1): Show |
conservative_inframe_insertion | MODERATE | c.13860_13861insGACA others(9743): Show |
p.Ser4620_Ser4621ins others(9747): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13919/16366 | 13861/16008 | 4621/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004395 | |
| chr7:101004395
|
C | CAACTCAA others(9740): Show |
1 | a0106 | 1 | HG00140.hp1 | conservative_inframe_insertion | MODERATE | c.13860_13861insGACA others(9743): Show |
p.Ser4620_Ser4621ins others(9747): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13919/16366 | 13861/16008 | 4621/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004395 | |
| chr7:101004395
|
C | CAACTCAA others(9740): Show |
2 | a0109a0117 | 2 | HG01070.hp2 HG02148.hp1 |
conservative_inframe_insertion | MODERATE | c.13860_13861insGACA others(9743): Show |
p.Ser4620_Ser4621ins others(9747): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13919/16366 | 13861/16008 | 4621/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004395 | |
| chr7:101004395
|
C | CAACTCAA others(9740): Show |
1 | a0173 | 1 | HG02135.hp2 | conservative_inframe_insertion | MODERATE | c.13860_13861insGACA others(9743): Show |
p.Ser4620_Ser4621ins others(9747): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13919/16366 | 13861/16008 | 4621/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004395 | |
| chr7:101004395
|
C | CAACTCAA others(9740): Show |
1 | a0105 | 1 | HG01175.hp2 | conservative_inframe_insertion | MODERATE | c.13860_13861insGACA others(9743): Show |
p.Ser4620_Ser4621ins others(9747): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13919/16366 | 13861/16008 | 4621/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004395 | |
| chr7:101004395
|
C | CAACTCAA others(9740): Show |
1 | a0116 | 1 | HG02698.hp1 | conservative_inframe_insertion | MODERATE | c.13860_13861insGACA others(9743): Show |
p.Ser4620_Ser4621ins others(9747): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13919/16366 | 13861/16008 | 4621/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004395 | |
| chr7:101004395
|
C | CAACTCAA others(25985): Show |
1 | a0127 | 1 | HG03098.hp1 | conservative_inframe_insertion | MODERATE | c.13860_13861insGACA others(25988): Show |
p.Ser4620_Ser4621ins others(25992): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13919/16366 | 13861/16008 | 4621/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004395 | |
| chr7:101004395
|
C | CAACTCAA others(9740): Show |
1 | a0139 | 1 | HG02602.hp2 | conservative_inframe_insertion | MODERATE | c.13860_13861insGACA others(9743): Show |
p.Ser4620_Ser4621ins others(9747): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13919/16366 | 13861/16008 | 4621/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004395 | |
| chr7:101004395
|
C | CAACTCAA others(9740): Show |
1 | a0084 | 1 | HG00735.hp2 | conservative_inframe_insertion | MODERATE | c.13860_13861insGACA others(9743): Show |
p.Ser4620_Ser4621ins others(9747): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13919/16366 | 13861/16008 | 4621/5335 | INFO_REALIGN_3_PRIME | chr7 | 101004395 | |
| chr7:101004395
|
C | T | 102 | a0001a0008a0009others(99): Show | 128 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(125): Show |
missense_variant | MODERATE | c.13832C>T | p.Ser4611Leu | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13890/16366 | 13832/16008 | 4611/5335 | chr7 | 101004395 | ||
| chr7:101004421
|
A | C | 36 | a0005a0035a0040others(33): Show | 43 | HG00423.hp2 HG00621.hp1 HG01928.hp1 others(40): Show |
missense_variant | MODERATE | c.13858A>C | p.Ser4620Arg | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13916/16366 | 13858/16008 | 4620/5335 | chr7 | 101004421 | ||
| chr7:101004439
|
C | T | 1 | a0238 | 1 | HG02165.hp2 | missense_variant | MODERATE | c.13876C>T | p.Arg4626Cys | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13934/16366 | 13876/16008 | 4626/5335 | chr7 | 101004439 | ||
| chr7:101004538
|
C | T | 98 | a0001a0008a0009others(95): Show | 123 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(120): Show |
missense_variant | MODERATE | c.13975C>T | p.His4659Tyr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 14033/16366 | 13975/16008 | 4659/5335 | chr7 | 101004538 | ||
| chr7:101004623
|
A | C | 1 | a0265 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.14060A>C | p.His4687Pro | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 14118/16366 | 14060/16008 | 4687/5335 | chr7 | 101004623 | ||
| chr7:101004748
|
G | A | 205 | a0001a0002a0003others(202): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
missense_variant | MODERATE | c.14185G>A | p.Ala4729Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 14243/16366 | 14185/16008 | 4729/5335 | chr7 | 101004748 | ||
| chr7:101004763
|
C | G | 3 | a0258a0261a0272 | 3 | HG02258.hp2 HG02451.hp2 HG03130.hp2 |
missense_variant | MODERATE | c.14200C>G | p.Leu4734Val | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 14258/16366 | 14200/16008 | 4734/5335 | chr7 | 101004763 | ||
| chr7:101004836
|
C | G | 122 | a0001a0008a0009others(119): Show | 150 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(147): Show |
missense_variant | MODERATE | c.14273C>G | p.Thr4758Arg | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 14331/16366 | 14273/16008 | 4758/5335 | chr7 | 101004836 | ||
| chr7:101005058
|
C | T | 1 | a0200 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.14495C>T | p.Ala4832Val | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 14553/16366 | 14495/16008 | 4832/5335 | chr7 | 101005058 | ||
| chr7:101005195
|
T | C | 10 | a0025a0119a0120others(7): Show | 11 | HG01243.hp2 HG02055.hp1 HG02109.hp2 others(8): Show |
missense_variant | MODERATE | c.14632T>C | p.Ser4878Pro | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 14690/16366 | 14632/16008 | 4878/5335 | chr7 | 101005195 | ||
| chr7:101005313
|
C | G | 1 | a0139 | 1 | HG02602.hp2 | missense_variant | MODERATE | c.14750C>G | p.Thr4917Arg | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 14808/16366 | 14750/16008 | 4917/5335 | chr7 | 101005313 | ||
| chr7:101005323
|
A | T | 2 | a0196a0197 | 2 | HG02630.hp2 HG03130.hp1 |
missense_variant | MODERATE | c.14760A>T | p.Leu4920Phe | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 14818/16366 | 14760/16008 | 4920/5335 | chr7 | 101005323 | ||
| chr7:101005432
|
C | T | 1 | a0065 | 1 | HG02647.hp2 | missense_variant | MODERATE | c.14869C>T | p.Leu4957Phe | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 14927/16366 | 14869/16008 | 4957/5335 | chr7 | 101005432 | ||
| chr7:101006570
|
T | C | 1 | a0053 | 1 | HG01516.hp2 | missense_variant&splice_region_variant | MODERATE | c.15056T>C | p.Val5019Ala | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 3/12 | 15114/16366 | 15056/16008 | 5019/5335 | chr7 | 101006570 | ||
| chr7:101012432
|
C | T | 1 | a0150 | 1 | HG00673.hp2 | missense_variant | MODERATE | c.15388C>T | p.Pro5130Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 6/12 | 15446/16366 | 15388/16008 | 5130/5335 | chr7 | 101012432 | ||
| chr7:101017628
|
C | T | 1 | a0154 | 1 | NA18955.hp2 | missense_variant | MODERATE | c.15931C>T | p.Arg5311Trp | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/12 | 15989/16366 | 15931/16008 | 5311/5335 | chr7 | 101017628 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:100991163
|
C | A | 1 | a0257c0048 | 1 | HG02027.hp2 | synonymous_variant | LOW | c.600C>A | p.Pro200Pro | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 658/16366 | 600/16008 | 200/5335 | chr7 | 100991163 | ||
| chr7:100991415
|
A | G | 1 | a0052c0269 | 1 | NA20905.hp2 | synonymous_variant | LOW | c.852A>G | p.Ser284Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 910/16366 | 852/16008 | 284/5335 | chr7 | 100991415 | ||
| chr7:100991427
|
G | C | 1 | a0052c0269 | 1 | NA20905.hp2 | synonymous_variant | LOW | c.864G>C | p.Ser288Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 922/16366 | 864/16008 | 288/5335 | chr7 | 100991427 | ||
| chr7:100991463
|
A | G | 1 | a0052c0269 | 1 | NA20905.hp2 | synonymous_variant | LOW | c.900A>G | p.Lys300Lys | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 958/16366 | 900/16008 | 300/5335 | chr7 | 100991463 | ||
| chr7:100991475
|
T | C | 1 | a0052c0269 | 1 | NA20905.hp2 | synonymous_variant | LOW | c.912T>C | p.Thr304Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 970/16366 | 912/16008 | 304/5335 | chr7 | 100991475 | ||
| chr7:100991478
|
T | C | 1 | a0052c0269 | 1 | NA20905.hp2 | synonymous_variant | LOW | c.915T>C | p.Tyr305Tyr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 973/16366 | 915/16008 | 305/5335 | chr7 | 100991478 | ||
| chr7:100991502
|
A | C | 26 | a0033c0011a0034c0010a0176c0073others(23): Show | 28 | HG00642.hp2 HG00673.hp1 HG01106.hp1 others(25): Show |
synonymous_variant | LOW | c.939A>C | p.Pro313Pro | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 997/16366 | 939/16008 | 313/5335 | chr7 | 100991502 | ||
| chr7:100991598
|
A | G | 2 | a0052c0269a0174c0268 | 2 | NA19081.hp1 NA20905.hp2 |
synonymous_variant | LOW | c.1035A>G | p.Pro345Pro | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 1093/16366 | 1035/16008 | 345/5335 | chr7 | 100991598 | ||
| chr7:100991613
|
G | A | 2 | a0052c0269a0174c0268 | 2 | NA19081.hp1 NA20905.hp2 |
synonymous_variant | LOW | c.1050G>A | p.Ala350Ala | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 1108/16366 | 1050/16008 | 350/5335 | chr7 | 100991613 | ||
| chr7:100991625
|
T | C | 2 | a0052c0269a0174c0268 | 2 | NA19081.hp1 NA20905.hp2 |
synonymous_variant | LOW | c.1062T>C | p.His354His | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 1120/16366 | 1062/16008 | 354/5335 | chr7 | 100991625 | ||
| chr7:100991640
|
A | G | 2 | a0052c0269a0174c0268 | 2 | NA19081.hp1 NA20905.hp2 |
synonymous_variant | LOW | c.1077A>G | p.Thr359Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 1135/16366 | 1077/16008 | 359/5335 | chr7 | 100991640 | ||
| chr7:100991862
|
T | C | 26 | a0033c0011a0034c0010a0176c0073others(23): Show | 28 | HG00642.hp2 HG00673.hp1 HG01106.hp1 others(25): Show |
synonymous_variant | LOW | c.1299T>C | p.Arg433Arg | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 1357/16366 | 1299/16008 | 433/5335 | chr7 | 100991862 | ||
| chr7:100991925
|
C | T | 1 | a0179c0071 | 1 | HG02647.hp1 | synonymous_variant | LOW | c.1362C>T | p.Ala454Ala | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 1420/16366 | 1362/16008 | 454/5335 | chr7 | 100991925 | ||
| chr7:100992111
|
C | T | 1 | a0026c0231 | 1 | NA19090.hp1 | synonymous_variant | LOW | c.1548C>T | p.Gly516Gly | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 1606/16366 | 1548/16008 | 516/5335 | chr7 | 100992111 | ||
| chr7:100992114
|
C | T | 1 | a0075c0265 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.1551C>T | p.Val517Val | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 1609/16366 | 1551/16008 | 517/5335 | chr7 | 100992114 | ||
| chr7:100992294
|
T | C | 1 | a0232c0075 | 1 | HG03017.hp2 | synonymous_variant | LOW | c.1731T>C | p.Tyr577Tyr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 1789/16366 | 1731/16008 | 577/5335 | chr7 | 100992294 | ||
| chr7:100992363
|
A | C | 1 | a0200c0049 | 1 | HG02572.hp1 | synonymous_variant | LOW | c.1800A>C | p.Gly600Gly | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 1858/16366 | 1800/16008 | 600/5335 | chr7 | 100992363 | ||
| chr7:100992468
|
T | C | 1 | a0175c0133 | 1 | HG02895.hp1 | synonymous_variant | LOW | c.1905T>C | p.His635His | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 1963/16366 | 1905/16008 | 635/5335 | chr7 | 100992468 | ||
| chr7:100992609
|
C | T | 26 | a0033c0011a0034c0010a0176c0073others(23): Show | 28 | HG00642.hp2 HG00673.hp1 HG01106.hp1 others(25): Show |
synonymous_variant | LOW | c.2046C>T | p.Leu682Leu | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 2104/16366 | 2046/16008 | 682/5335 | chr7 | 100992609 | ||
| chr7:100992831
|
C | T | 1 | a0250c0130 | 1 | NA18990.hp2 | synonymous_variant | LOW | c.2268C>T | p.Asp756Asp | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 2326/16366 | 2268/16008 | 756/5335 | chr7 | 100992831 | ||
| chr7:100992873
|
G | C | 3 | a0172c0135a0206c0077a0256c0076 | 3 | HG00423.hp2 NA19066.hp1 NA20752.hp2 |
synonymous_variant | LOW | c.2310G>C | p.Ser770Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 2368/16366 | 2310/16008 | 770/5335 | chr7 | 100992873 | ||
| chr7:100992894
|
G | A | 2 | a0259c0272a0260c0273 | 2 | HG02622.hp1 HG03195.hp2 |
synonymous_variant | LOW | c.2331G>A | p.Thr777Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 2389/16366 | 2331/16008 | 777/5335 | chr7 | 100992894 | ||
| chr7:100993044
|
T | C | 18 | a0172c0135a0206c0077a0256c0076others(15): Show | 18 | HG00423.hp2 HG01884.hp2 HG02257.hp2 others(15): Show |
synonymous_variant | LOW | c.2481T>C | p.His827His | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 2539/16366 | 2481/16008 | 827/5335 | chr7 | 100993044 | ||
| chr7:100993101
|
C | T | 1 | a0081c0263 | 1 | HG01243.hp1 | synonymous_variant | LOW | c.2538C>T | p.Gly846Gly | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 2596/16366 | 2538/16008 | 846/5335 | chr7 | 100993101 | ||
| chr7:100993146
|
G | A | 1 | a0207c0078 | 1 | HG02717.hp1 | synonymous_variant | LOW | c.2583G>A | p.Thr861Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 2641/16366 | 2583/16008 | 861/5335 | chr7 | 100993146 | ||
| chr7:100993407
|
A | G | 1 | a0206c0077 | 1 | NA19066.hp1 | synonymous_variant | LOW | c.2844A>G | p.Thr948Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 2902/16366 | 2844/16008 | 948/5335 | chr7 | 100993407 | ||
| chr7:100993434
|
A | C | 1 | a0197c0059 | 1 | HG02630.hp2 | synonymous_variant | LOW | c.2871A>C | p.Ser957Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 2929/16366 | 2871/16008 | 957/5335 | chr7 | 100993434 | ||
| chr7:100993455
|
A | C | 1 | a0206c0077 | 1 | NA19066.hp1 | synonymous_variant | LOW | c.2892A>C | p.Thr964Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 2950/16366 | 2892/16008 | 964/5335 | chr7 | 100993455 | ||
| chr7:100993539
|
T | C | 150 | a0001c0001a0001c0168a0001c0181others(147): Show | 173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
synonymous_variant | LOW | c.2976T>C | p.Thr992Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 3034/16366 | 2976/16008 | 992/5335 | chr7 | 100993539 | ||
| chr7:100993572
|
A | G | 181 | a0001c0001a0001c0168a0001c0181others(178): Show | 209 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(206): Show |
synonymous_variant | LOW | c.3009A>G | p.Thr1003Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 3067/16366 | 3009/16008 | 1003/5335 | chr7 | 100993572 | ||
| chr7:100993920
|
C | T | 14 | a0004c0012a0004c0013a0004c0079others(11): Show | 17 | HG00423.hp2 HG00639.hp1 HG01433.hp2 others(14): Show |
synonymous_variant | LOW | c.3357C>T | p.Ser1119Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 3415/16366 | 3357/16008 | 1119/5335 | chr7 | 100993920 | ||
| chr7:100993932
|
G | A | 145 | a0001c0001a0001c0168a0001c0181others(142): Show | 171 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(168): Show |
synonymous_variant | LOW | c.3369G>A | p.Leu1123Leu | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 3427/16366 | 3369/16008 | 1123/5335 | chr7 | 100993932 | ||
| chr7:100994184
|
C | T | 48 | a0002c0004a0002c0007a0002c0245others(45): Show | 65 | HG00099.hp2 HG00558.hp2 HG01099.hp1 others(62): Show |
synonymous_variant | LOW | c.3621C>T | p.Thr1207Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 3679/16366 | 3621/16008 | 1207/5335 | chr7 | 100994184 | ||
| chr7:100994358
|
C | T | 48 | a0002c0004a0002c0007a0002c0245others(45): Show | 65 | HG00099.hp2 HG00558.hp2 HG01099.hp1 others(62): Show |
synonymous_variant | LOW | c.3795C>T | p.Leu1265Leu | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 3853/16366 | 3795/16008 | 1265/5335 | chr7 | 100994358 | ||
| chr7:100994418
|
T | C | 217 | a0001c0001a0001c0168a0001c0181others(214): Show | 251 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(248): Show |
synonymous_variant | LOW | c.3855T>C | p.Pro1285Pro | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 3913/16366 | 3855/16008 | 1285/5335 | chr7 | 100994418 | ||
| chr7:100994466
|
C | T | 1 | a0167c0219 | 1 | HG02145.hp2 | synonymous_variant | LOW | c.3903C>T | p.Tyr1301Tyr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 3961/16366 | 3903/16008 | 1301/5335 | chr7 | 100994466 | ||
| chr7:100994529
|
C | T | 18 | a0004c0012a0004c0013a0004c0079others(15): Show | 21 | HG00423.hp2 HG00639.hp1 HG01433.hp2 others(18): Show |
synonymous_variant | LOW | c.3966C>T | p.Ser1322Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 4024/16366 | 3966/16008 | 1322/5335 | chr7 | 100994529 | ||
| chr7:100994580
|
A | G | 146 | a0001c0001a0001c0168a0001c0181others(143): Show | 172 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(169): Show |
synonymous_variant | LOW | c.4017A>G | p.Ala1339Ala | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 4075/16366 | 4017/16008 | 1339/5335 | chr7 | 100994580 | ||
| chr7:100994817
|
G | A | 1 | a0057c0232 | 1 | HG01123.hp2 | synonymous_variant | LOW | c.4254G>A | p.Ser1418Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 4312/16366 | 4254/16008 | 1418/5335 | chr7 | 100994817 | ||
| chr7:100994877
|
C | T | 1 | a0191c0052 | 1 | HG00673.hp1 | synonymous_variant | LOW | c.4314C>T | p.Thr1438Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 4372/16366 | 4314/16008 | 1438/5335 | chr7 | 100994877 | ||
| chr7:100994919
|
A | G | 1 | a0057c0232 | 1 | HG01123.hp2 | synonymous_variant | LOW | c.4356A>G | p.Ser1452Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 4414/16366 | 4356/16008 | 1452/5335 | chr7 | 100994919 | ||
| chr7:100995165
|
G | A | 1 | a0092c0141 | 1 | NA18978.hp2 | synonymous_variant | LOW | c.4602G>A | p.Ala1534Ala | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 4660/16366 | 4602/16008 | 1534/5335 | chr7 | 100995165 | ||
| chr7:100995237
|
G | A | 4 | a0024c0021a0213c0097a0258c0279others(1): Show | 5 | HG01361.hp1 HG02451.hp2 HG02896.hp1 others(2): Show |
synonymous_variant | LOW | c.4674G>A | p.Pro1558Pro | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 4732/16366 | 4674/16008 | 1558/5335 | chr7 | 100995237 | ||
| chr7:100995249
|
C | T | 51 | a0005c0003a0010c0005a0035c0020others(48): Show | 62 | HG00621.hp1 HG01069.hp2 HG01070.hp1 others(59): Show |
synonymous_variant | LOW | c.4686C>T | p.Leu1562Leu | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 4744/16366 | 4686/16008 | 1562/5335 | chr7 | 100995249 | ||
| chr7:100995285
|
A | G | 1 | a0206c0077 | 1 | NA19066.hp1 | synonymous_variant | LOW | c.4722A>G | p.Glu1574Glu | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 4780/16366 | 4722/16008 | 1574/5335 | chr7 | 100995285 | ||
| chr7:100995415
|
T | C | 285 | a0001c0001a0001c0168a0001c0181others(282): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
synonymous_variant | LOW | c.4852T>C | p.Leu1618Leu | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 4910/16366 | 4852/16008 | 1618/5335 | chr7 | 100995415 | ||
| chr7:100995465
|
T | C | 285 | a0001c0001a0001c0168a0001c0181others(282): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
synonymous_variant | LOW | c.4902T>C | p.Thr1634Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 4960/16366 | 4902/16008 | 1634/5335 | chr7 | 100995465 | ||
| chr7:100995525
|
A | C | 1 | a0129c0209 | 1 | NA18941.hp2 | synonymous_variant | LOW | c.4962A>C | p.Ser1654Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 5020/16366 | 4962/16008 | 1654/5335 | chr7 | 100995525 | ||
| chr7:100995546
|
G | A | 52 | a0005c0003a0010c0005a0035c0020others(49): Show | 63 | HG00621.hp1 HG01069.hp2 HG01070.hp1 others(60): Show |
synonymous_variant | LOW | c.4983G>A | p.Thr1661Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 5041/16366 | 4983/16008 | 1661/5335 | chr7 | 100995546 | ||
| chr7:100995606
|
A | C | 285 | a0001c0001a0001c0168a0001c0181others(282): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
synonymous_variant | LOW | c.5043A>C | p.Thr1681Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 5101/16366 | 5043/16008 | 1681/5335 | chr7 | 100995606 | ||
| chr7:100995642
|
A | T | 40 | a0004c0012a0004c0013a0004c0079others(37): Show | 45 | HG00323.hp1 HG00423.hp2 HG00639.hp1 others(42): Show |
synonymous_variant | LOW | c.5079A>T | p.Pro1693Pro | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 5137/16366 | 5079/16008 | 1693/5335 | chr7 | 100995642 | ||
| chr7:100995648
|
A | G | 285 | a0001c0001a0001c0168a0001c0181others(282): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
synonymous_variant | LOW | c.5085A>G | p.Ser1695Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 5143/16366 | 5085/16008 | 1695/5335 | chr7 | 100995648 | ||
| chr7:100995765
|
C | A | 105 | a0002c0004a0002c0007a0002c0245others(102): Show | 129 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(126): Show |
synonymous_variant | LOW | c.5202C>A | p.Thr1734Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 5260/16366 | 5202/16008 | 1734/5335 | chr7 | 100995765 | ||
| chr7:100995876
|
G | C | 285 | a0001c0001a0001c0168a0001c0181others(282): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
synonymous_variant | LOW | c.5313G>C | p.Ala1771Ala | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 5371/16366 | 5313/16008 | 1771/5335 | chr7 | 100995876 | ||
| chr7:100995891
|
G | A | 2 | a0091c0140a0132c0204 | 2 | HG01175.hp1 HG04228.hp2 |
synonymous_variant | LOW | c.5328G>A | p.Pro1776Pro | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 5386/16366 | 5328/16008 | 1776/5335 | chr7 | 100995891 | ||
| chr7:100995924
|
C | T | 1 | a0128c0208 | 1 | HG03041.hp2 | synonymous_variant | LOW | c.5361C>T | p.Ser1787Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 5419/16366 | 5361/16008 | 1787/5335 | chr7 | 100995924 | ||
| chr7:100995939
|
T | C | 285 | a0001c0001a0001c0168a0001c0181others(282): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
synonymous_variant | LOW | c.5376T>C | p.Gly1792Gly | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 5434/16366 | 5376/16008 | 1792/5335 | chr7 | 100995939 | ||
| chr7:100995960
|
T | A | 1 | a0026c0202 | 1 | NA19010.hp1 | synonymous_variant | LOW | c.5397T>A | p.Thr1799Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 5455/16366 | 5397/16008 | 1799/5335 | chr7 | 100995960 | ||
| chr7:100996479
|
G | A | 1 | a0031c0026 | 2 | HG01081.hp2 HG01169.hp1 |
synonymous_variant | LOW | c.5916G>A | p.Thr1972Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 5974/16366 | 5916/16008 | 1972/5335 | chr7 | 100996479 | ||
| chr7:100996518
|
C | T | 25 | a0033c0011a0034c0010a0176c0073others(22): Show | 27 | HG00642.hp2 HG01106.hp1 HG01109.hp2 others(24): Show |
synonymous_variant | LOW | c.5955C>T | p.Gly1985Gly | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 6013/16366 | 5955/16008 | 1985/5335 | chr7 | 100996518 | ||
| chr7:100996656
|
G | A | 279 | a0001c0001a0001c0168a0001c0181others(276): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
synonymous_variant | LOW | c.6093G>A | p.Thr2031Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 6151/16366 | 6093/16008 | 2031/5335 | chr7 | 100996656 | ||
| chr7:100996704
|
A | C | 1 | a0248c0121 | 1 | HG02071.hp2 | synonymous_variant | LOW | c.6141A>C | p.Thr2047Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 6199/16366 | 6141/16008 | 2047/5335 | chr7 | 100996704 | ||
| chr7:100996740
|
A | G | 1 | a0128c0208 | 1 | HG03041.hp2 | synonymous_variant | LOW | c.6177A>G | p.Thr2059Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 6235/16366 | 6177/16008 | 2059/5335 | chr7 | 100996740 | ||
| chr7:100996752
|
C | A | 1 | a0258c0279 | 1 | HG03130.hp2 | synonymous_variant | LOW | c.6189C>A | p.Ala2063Ala | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 6247/16366 | 6189/16008 | 2063/5335 | chr7 | 100996752 | ||
| chr7:100997169
|
T | C | 166 | a0001c0001a0001c0168a0001c0181others(163): Show | 191 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(188): Show |
synonymous_variant | LOW | c.6606T>C | p.Ser2202Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 6664/16366 | 6606/16008 | 2202/5335 | chr7 | 100997169 | ||
| chr7:100997526
|
T | G | 1 | a0001c0168 | 1 | NA18994.hp1 | synonymous_variant | LOW | c.6963T>G | p.Gly2321Gly | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7021/16366 | 6963/16008 | 2321/5335 | chr7 | 100997526 | ||
| chr7:100997772
|
C | T | 2 | a0176c0073a0190c0050 | 2 | HG02280.hp1 HG03239.hp2 |
synonymous_variant | LOW | c.7209C>T | p.Gly2403Gly | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7267/16366 | 7209/16008 | 2403/5335 | chr7 | 100997772 | ||
| chr7:100997778
|
T | C | 166 | a0001c0001a0001c0168a0001c0181others(163): Show | 191 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(188): Show |
synonymous_variant | LOW | c.7215T>C | p.Ser2405Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7273/16366 | 7215/16008 | 2405/5335 | chr7 | 100997778 | ||
| chr7:100997940
|
C | T | 22 | a0033c0011a0034c0010a0177c0072others(19): Show | 24 | HG00673.hp1 HG01106.hp1 HG01109.hp2 others(21): Show |
synonymous_variant | LOW | c.7377C>T | p.Gly2459Gly | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7435/16366 | 7377/16008 | 2459/5335 | chr7 | 100997940 | ||
| chr7:100998078
|
A | G | 17 | a0037c0017a0201c0074a0209c0082others(14): Show | 18 | HG00639.hp1 HG01069.hp2 HG01070.hp1 others(15): Show |
synonymous_variant | LOW | c.7515A>G | p.Thr2505Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7573/16366 | 7515/16008 | 2505/5335 | chr7 | 100998078 | ||
| chr7:100998162
|
A | G | 9 | a0027c0031a0028c0030a0089c0224others(6): Show | 11 | HG01175.hp1 HG02145.hp2 HG02451.hp1 others(8): Show |
synonymous_variant | LOW | c.7599A>G | p.Thr2533Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7657/16366 | 7599/16008 | 2533/5335 | chr7 | 100998162 | ||
| chr7:100998192
|
A | G | 1 | a0002c0245 | 1 | HG01943.hp1 | synonymous_variant | LOW | c.7629A>G | p.Gly2543Gly | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 7687/16366 | 7629/16008 | 2543/5335 | chr7 | 100998192 | ||
| chr7:100998591
|
T | C | 167 | a0001c0001a0001c0168a0001c0181others(164): Show | 192 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(189): Show |
synonymous_variant | LOW | c.8028T>C | p.Ser2676Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 8086/16366 | 8028/16008 | 2676/5335 | chr7 | 100998591 | ||
| chr7:100998948
|
T | G | 1 | a0168c0139 | 1 | HG03516.hp2 | synonymous_variant | LOW | c.8385T>G | p.Gly2795Gly | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 8443/16366 | 8385/16008 | 2795/5335 | chr7 | 100998948 | ||
| chr7:100999089
|
C | T | 1 | a0200c0049 | 1 | HG02572.hp1 | synonymous_variant | LOW | c.8526C>T | p.Pro2842Pro | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 8584/16366 | 8526/16008 | 2842/5335 | chr7 | 100999089 | ||
| chr7:100999194
|
C | T | 5 | a0192c0051a0193c0053a0196c0056others(2): Show | 5 | HG01361.hp2 HG01978.hp2 HG02630.hp2 others(2): Show |
synonymous_variant | LOW | c.8631C>T | p.Gly2877Gly | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 8689/16366 | 8631/16008 | 2877/5335 | chr7 | 100999194 | ||
| chr7:100999200
|
T | C | 171 | a0001c0001a0001c0168a0001c0181others(168): Show | 196 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(193): Show |
synonymous_variant | LOW | c.8637T>C | p.Ser2879Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 8695/16366 | 8637/16008 | 2879/5335 | chr7 | 100999200 | ||
| chr7:100999239
|
G | A | 1 | a0096c0220 | 1 | HG02683.hp2 | synonymous_variant | LOW | c.8676G>A | p.Thr2892Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 8734/16366 | 8676/16008 | 2892/5335 | chr7 | 100999239 | ||
| chr7:100999251
|
G | A | 13 | a0004c0079a0015c0240a0016c0035others(10): Show | 14 | HG00099.hp2 HG00673.hp1 HG01168.hp1 others(11): Show |
synonymous_variant | LOW | c.8688G>A | p.Ala2896Ala | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 8746/16366 | 8688/16008 | 2896/5335 | chr7 | 100999251 | ||
| chr7:100999269
|
C | T | 1 | a0170c0137 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.8706C>T | p.Thr2902Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 8764/16366 | 8706/16008 | 2902/5335 | chr7 | 100999269 | ||
| chr7:100999305
|
C | T | 1 | a0268c0283 | 1 | HG03579.hp1 | synonymous_variant | LOW | c.8742C>T | p.His2914His | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 8800/16366 | 8742/16008 | 2914/5335 | chr7 | 100999305 | ||
| chr7:100999428
|
C | T | 1 | a0177c0072 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.8865C>T | p.Asp2955Asp | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 8923/16366 | 8865/16008 | 2955/5335 | chr7 | 100999428 | ||
| chr7:100999488
|
G | A | 5 | a0055c0264a0065c0248a0066c0247others(2): Show | 5 | HG02647.hp2 HG02723.hp2 HG02809.hp1 others(2): Show |
synonymous_variant | LOW | c.8925G>A | p.Ser2975Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 8983/16366 | 8925/16008 | 2975/5335 | chr7 | 100999488 | ||
| chr7:100999548
|
C | T | 15 | a0033c0011a0177c0072a0180c0067others(12): Show | 16 | HG00642.hp2 HG01109.hp2 HG01361.hp2 others(13): Show |
synonymous_variant | LOW | c.8985C>T | p.Thr2995Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 9043/16366 | 8985/16008 | 2995/5335 | chr7 | 100999548 | ||
| chr7:100999590
|
A | G | 2 | a0065c0248a0066c0247 | 2 | HG02647.hp2 HG02809.hp1 |
synonymous_variant | LOW | c.9027A>G | p.Ser3009Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 9085/16366 | 9027/16008 | 3009/5335 | chr7 | 100999590 | ||
| chr7:100999956
|
A | G | 1 | a0206c0077 | 1 | NA19066.hp1 | synonymous_variant | LOW | c.9393A>G | p.Glu3131Glu | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 9451/16366 | 9393/16008 | 3131/5335 | chr7 | 100999956 | ||
| chr7:101000073
|
C | A | 1 | a0069c0243 | 1 | HG02148.hp2 | synonymous_variant | LOW | c.9510C>A | p.Ser3170Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 9568/16366 | 9510/16008 | 3170/5335 | chr7 | 101000073 | ||
| chr7:101000086
|
C | T | 9 | a0027c0031a0028c0030a0089c0224others(6): Show | 11 | HG01175.hp1 HG01257.hp1 HG02145.hp2 others(8): Show |
synonymous_variant | LOW | c.9523C>T | p.Leu3175Leu | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 9581/16366 | 9523/16008 | 3175/5335 | chr7 | 101000086 | ||
| chr7:101000091
|
C | T | 3 | a0028c0030a0142c0194a0143c0195 | 4 | HG02451.hp1 HG02486.hp1 HG02886.hp1 others(1): Show |
synonymous_variant | LOW | c.9528C>T | p.Ser3176Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 9586/16366 | 9528/16008 | 3176/5335 | chr7 | 101000091 | ||
| chr7:101000118
|
T | C | 1 | a0127c0211 | 1 | HG03098.hp1 | synonymous_variant | LOW | c.9555T>C | p.Leu3185Leu | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 9613/16366 | 9555/16008 | 3185/5335 | chr7 | 101000118 | ||
| chr7:101000196
|
A | C | 4 | a0128c0208a0129c0209a0139c0167others(1): Show | 4 | HG02602.hp2 HG03041.hp2 HG03516.hp2 others(1): Show |
synonymous_variant | LOW | c.9633A>C | p.Ser3211Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 9691/16366 | 9633/16008 | 3211/5335 | chr7 | 101000196 | ||
| chr7:101000220
|
C | T | 1 | a0143c0195 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.9657C>T | p.Pro3219Pro | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 9715/16366 | 9657/16008 | 3219/5335 | chr7 | 101000220 | ||
| chr7:101000313
|
T | A | 62 | a0011c0009a0019c0033a0033c0011others(59): Show | 66 | HG00323.hp1 HG00639.hp2 HG00642.hp2 others(63): Show |
synonymous_variant | LOW | c.9750T>A | p.Pro3250Pro | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 9808/16366 | 9750/16008 | 3250/5335 | chr7 | 101000313 | ||
| chr7:101000388
|
C | G | 1 | a0088c0225 | 1 | NA19007.hp1 | synonymous_variant | LOW | c.9825C>G | p.Gly3275Gly | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 9883/16366 | 9825/16008 | 3275/5335 | chr7 | 101000388 | ||
| chr7:101000394
|
G | A | 27 | a0010c0005a0038c0016a0039c0015others(24): Show | 32 | HG01081.hp1 HG01192.hp2 HG01255.hp1 others(29): Show |
synonymous_variant | LOW | c.9831G>A | p.Pro3277Pro | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 9889/16366 | 9831/16008 | 3277/5335 | chr7 | 101000394 | ||
| chr7:101000412
|
C | G | 1 | a0272c0041 | 1 | HG02258.hp2 | synonymous_variant | LOW | c.9849C>G | p.Thr3283Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 9907/16366 | 9849/16008 | 3283/5335 | chr7 | 101000412 | ||
| chr7:101000457
|
G | A | 1 | a0128c0208 | 1 | HG03041.hp2 | synonymous_variant | LOW | c.9894G>A | p.Ser3298Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 9952/16366 | 9894/16008 | 3298/5335 | chr7 | 101000457 | ||
| chr7:101000544
|
G | A | 1 | a0129c0209 | 1 | NA18941.hp2 | synonymous_variant | LOW | c.9981G>A | p.Thr3327Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 10039/16366 | 9981/16008 | 3327/5335 | chr7 | 101000544 | ||
| chr7:101000562
|
G | A | 37 | a0011c0009a0019c0033a0020c0023others(34): Show | 42 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(39): Show |
synonymous_variant | LOW | c.9999G>A | p.Pro3333Pro | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 10057/16366 | 9999/16008 | 3333/5335 | chr7 | 101000562 | ||
| chr7:101000595
|
C | T | 68 | a0001c0001a0001c0168a0001c0181others(65): Show | 84 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(81): Show |
synonymous_variant | LOW | c.10032C>T | p.Ser3344Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 10090/16366 | 10032/16008 | 3344/5335 | chr7 | 101000595 | ||
| chr7:101000793
|
C | G | 2 | a0170c0137a0247c0114 | 2 | HG03225.hp2 HG03927.hp1 |
synonymous_variant | LOW | c.10230C>G | p.Ser3410Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 10288/16366 | 10230/16008 | 3410/5335 | chr7 | 101000793 | ||
| chr7:101000964
|
C | T | 1 | a0247c0114 | 1 | HG03927.hp1 | synonymous_variant | LOW | c.10401C>T | p.His3467His | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 10459/16366 | 10401/16008 | 3467/5335 | chr7 | 101000964 | ||
| chr7:101001021
|
C | T | 1 | a0263c0275 | 1 | NA20129.hp1 | synonymous_variant | LOW | c.10458C>T | p.Gly3486Gly | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 10516/16366 | 10458/16008 | 3486/5335 | chr7 | 101001021 | ||
| chr7:101001189
|
C | T | 13 | a0034c0010a0176c0073a0177c0072others(10): Show | 14 | HG00673.hp1 HG01106.hp1 HG01515.hp2 others(11): Show |
synonymous_variant | LOW | c.10626C>T | p.Gly3542Gly | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 10684/16366 | 10626/16008 | 3542/5335 | chr7 | 101001189 | ||
| chr7:101001327
|
A | G | 58 | a0005c0003a0010c0005a0036c0014others(55): Show | 69 | HG00423.hp2 HG00621.hp1 HG00639.hp1 others(66): Show |
synonymous_variant | LOW | c.10764A>G | p.Thr3588Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 10822/16366 | 10764/16008 | 3588/5335 | chr7 | 101001327 | ||
| chr7:101001411
|
A | G | 58 | a0001c0001a0001c0168a0001c0181others(55): Show | 72 | HG00099.hp1 HG00408.hp1 HG00558.hp1 others(69): Show |
synonymous_variant | LOW | c.10848A>G | p.Thr3616Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 10906/16366 | 10848/16008 | 3616/5335 | chr7 | 101001411 | ||
| chr7:101001513
|
C | T | 1 | a0206c0077 | 1 | NA19066.hp1 | synonymous_variant | LOW | c.10950C>T | p.Thr3650Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 11008/16366 | 10950/16008 | 3650/5335 | chr7 | 101001513 | ||
| chr7:101001780
|
G | A | 10 | a0011c0009a0019c0033a0044c0042others(7): Show | 12 | HG00639.hp2 HG01074.hp2 HG01168.hp2 others(9): Show |
synonymous_variant | LOW | c.11217G>A | p.Glu3739Glu | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 11275/16366 | 11217/16008 | 3739/5335 | chr7 | 101001780 | ||
| chr7:101001840
|
T | C | 167 | a0001c0001a0001c0168a0001c0181others(164): Show | 192 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(189): Show |
synonymous_variant | LOW | c.11277T>C | p.Ser3759Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 11335/16366 | 11277/16008 | 3759/5335 | chr7 | 101001840 | ||
| chr7:101001960
|
C | T | 1 | a0075c0265 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.11397C>T | p.Thr3799Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 11455/16366 | 11397/16008 | 3799/5335 | chr7 | 101001960 | ||
| chr7:101002197
|
T | G | 1 | a0132c0204 | 1 | HG01175.hp1 | synonymous_variant | LOW | c.11634T>G | p.Gly3878Gly | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 11692/16366 | 11634/16008 | 3878/5335 | chr7 | 101002197 | ||
| chr7:101002320
|
C | T | 1 | a0266c0277 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.11757C>T | p.Thr3919Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 11815/16366 | 11757/16008 | 3919/5335 | chr7 | 101002320 | ||
| chr7:101002338
|
C | T | 1 | a0200c0049 | 1 | HG02572.hp1 | synonymous_variant | LOW | c.11775C>T | p.Pro3925Pro | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 11833/16366 | 11775/16008 | 3925/5335 | chr7 | 101002338 | ||
| chr7:101002443
|
C | T | 1 | a0177c0072 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.11880C>T | p.Gly3960Gly | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 11938/16366 | 11880/16008 | 3960/5335 | chr7 | 101002443 | ||
| chr7:101002449
|
C | T | 74 | a0005c0003a0010c0005a0014c0036others(71): Show | 87 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(84): Show |
synonymous_variant | LOW | c.11886C>T | p.Ser3962Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 11944/16366 | 11886/16008 | 3962/5335 | chr7 | 101002449 | ||
| chr7:101002500
|
G | A | 10 | a0033c0011a0180c0067a0187c0060others(7): Show | 11 | HG01361.hp2 HG01978.hp2 HG02559.hp1 others(8): Show |
synonymous_variant | LOW | c.11937G>A | p.Ala3979Ala | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 11995/16366 | 11937/16008 | 3979/5335 | chr7 | 101002500 | ||
| chr7:101002572
|
A | G | 4 | a0267c0285a0269c0284a0270c0282others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG03471.hp1 others(1): Show |
synonymous_variant | LOW | c.12009A>G | p.Thr4003Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 12067/16366 | 12009/16008 | 4003/5335 | chr7 | 101002572 | ||
| chr7:101002650
|
C | T | 1 | a0006c0256 | 1 | NA19011.hp1 | synonymous_variant | LOW | c.12087C>T | p.Gly4029Gly | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 12145/16366 | 12087/16008 | 4029/5335 | chr7 | 101002650 | ||
| chr7:101002737
|
G | A | 36 | a0002c0004a0002c0007a0002c0245others(33): Show | 49 | HG00558.hp2 HG01099.hp1 HG01106.hp2 others(46): Show |
synonymous_variant | LOW | c.12174G>A | p.Ser4058Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 12232/16366 | 12174/16008 | 4058/5335 | chr7 | 101002737 | ||
| chr7:101002797
|
C | T | 18 | a0033c0011a0034c0010a0176c0073others(15): Show | 20 | HG00642.hp2 HG00673.hp1 HG01106.hp1 others(17): Show |
synonymous_variant | LOW | c.12234C>T | p.Thr4078Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 12292/16366 | 12234/16008 | 4078/5335 | chr7 | 101002797 | ||
| chr7:101002839
|
A | G | 29 | a0002c0004a0002c0007a0002c0245others(26): Show | 41 | HG00558.hp2 HG01099.hp1 HG01123.hp2 others(38): Show |
synonymous_variant | LOW | c.12276A>G | p.Ser4092Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 12334/16366 | 12276/16008 | 4092/5335 | chr7 | 101002839 | ||
| chr7:101003169
|
T | C | 285 | a0001c0001a0001c0168a0001c0181others(282): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
synonymous_variant | LOW | c.12606T>C | p.Leu4202Leu | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 12664/16366 | 12606/16008 | 4202/5335 | chr7 | 101003169 | ||
| chr7:101003205
|
A | G | 5 | a0220c0087a0224c0092a0229c0101others(2): Show | 5 | HG01515.hp1 HG02074.hp2 HG02809.hp2 others(2): Show |
synonymous_variant | LOW | c.12642A>G | p.Glu4214Glu | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 12700/16366 | 12642/16008 | 4214/5335 | chr7 | 101003205 | ||
| chr7:101003250
|
A | G | 1 | a0176c0073 | 1 | HG02280.hp1 | synonymous_variant | LOW | c.12687A>G | p.Thr4229Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 12745/16366 | 12687/16008 | 4229/5335 | chr7 | 101003250 | ||
| chr7:101003335
|
C | T | 77 | a0001c0001a0001c0168a0001c0181others(74): Show | 96 | HG00140.hp2 HG00408.hp1 HG00558.hp1 others(93): Show |
synonymous_variant | LOW | c.12772C>T | p.Leu4258Leu | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 12830/16366 | 12772/16008 | 4258/5335 | chr7 | 101003335 | ||
| chr7:101003385
|
C | T | 9 | a0004c0012a0004c0013a0004c0079others(6): Show | 14 | HG02109.hp1 HG02602.hp1 HG02630.hp1 others(11): Show |
synonymous_variant | LOW | c.12822C>T | p.Thr4274Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 12880/16366 | 12822/16008 | 4274/5335 | chr7 | 101003385 | ||
| chr7:101003445
|
A | C | 12 | a0022c0025a0027c0031a0028c0030others(9): Show | 15 | HG00099.hp1 HG01257.hp2 HG01258.hp2 others(12): Show |
synonymous_variant | LOW | c.12882A>C | p.Ser4294Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 12940/16366 | 12882/16008 | 4294/5335 | chr7 | 101003445 | ||
| chr7:101003466
|
A | G | 285 | a0001c0001a0001c0168a0001c0181others(282): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
synonymous_variant | LOW | c.12903A>G | p.Thr4301Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 12961/16366 | 12903/16008 | 4301/5335 | chr7 | 101003466 | ||
| chr7:101003526
|
C | A | 8 | a0004c0012a0004c0013a0004c0079others(5): Show | 13 | HG02109.hp1 HG02602.hp1 HG02630.hp1 others(10): Show |
synonymous_variant | LOW | c.12963C>A | p.Thr4321Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13021/16366 | 12963/16008 | 4321/5335 | chr7 | 101003526 | ||
| chr7:101003562
|
A | T | 205 | a0001c0001a0001c0168a0001c0181others(202): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
synonymous_variant | LOW | c.12999A>T | p.Pro4333Pro | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13057/16366 | 12999/16008 | 4333/5335 | chr7 | 101003562 | ||
| chr7:101003568
|
G | A | 9 | a0004c0012a0004c0013a0004c0079others(6): Show | 14 | HG02109.hp1 HG02602.hp1 HG02630.hp1 others(11): Show |
synonymous_variant | LOW | c.13005G>A | p.Ser4335Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13063/16366 | 13005/16008 | 4335/5335 | chr7 | 101003568 | ||
| chr7:101003580
|
C | G | 9 | a0004c0012a0004c0013a0004c0079others(6): Show | 14 | HG02109.hp1 HG02602.hp1 HG02630.hp1 others(11): Show |
synonymous_variant | LOW | c.13017C>G | p.Thr4339Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13075/16366 | 13017/16008 | 4339/5335 | chr7 | 101003580 | ||
| chr7:101003643
|
G | A | 1 | a0248c0121 | 1 | HG02071.hp2 | synonymous_variant | LOW | c.13080G>A | p.Pro4360Pro | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13138/16366 | 13080/16008 | 4360/5335 | chr7 | 101003643 | ||
| chr7:101003679
|
C | T | 1 | a0129c0209 | 1 | NA18941.hp2 | synonymous_variant | LOW | c.13116C>T | p.Ser4372Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13174/16366 | 13116/16008 | 4372/5335 | chr7 | 101003679 | ||
| chr7:101003685
|
A | C | 276 | a0001c0001a0001c0168a0001c0181others(273): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
synonymous_variant | LOW | c.13122A>C | p.Thr4374Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13180/16366 | 13122/16008 | 4374/5335 | chr7 | 101003685 | ||
| chr7:101003751
|
G | C | 8 | a0003c0002a0003c0254a0003c0261others(5): Show | 13 | HG02135.hp1 HG02523.hp2 NA18954.hp2 others(10): Show |
synonymous_variant | LOW | c.13188G>C | p.Ser4396Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13246/16366 | 13188/16008 | 4396/5335 | chr7 | 101003751 | ||
| chr7:101003811
|
G | A | 5 | a0099c0148a0107c0151a0113c0158others(2): Show | 5 | HG00738.hp2 HG02735.hp2 HG04228.hp1 others(2): Show |
synonymous_variant | LOW | c.13248G>A | p.Pro4416Pro | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13306/16366 | 13248/16008 | 4416/5335 | chr7 | 101003811 | ||
| chr7:101003844
|
C | T | 39 | a0011c0009a0019c0033a0020c0023others(36): Show | 45 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(42): Show |
synonymous_variant | LOW | c.13281C>T | p.Ser4427Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13339/16366 | 13281/16008 | 4427/5335 | chr7 | 101003844 | ||
| chr7:101003877
|
A | C | 2 | a0258c0279a0261c0280 | 2 | HG02451.hp2 HG03130.hp2 |
synonymous_variant | LOW | c.13314A>C | p.Thr4438Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13372/16366 | 13314/16008 | 4438/5335 | chr7 | 101003877 | ||
| chr7:101003973
|
C | T | 2 | a0038c0016a0227c0095 | 3 | HG01255.hp2 HG01261.hp1 HG01346.hp2 |
synonymous_variant | LOW | c.13410C>T | p.Gly4470Gly | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13468/16366 | 13410/16008 | 4470/5335 | chr7 | 101003973 | ||
| chr7:101004042
|
C | G | 1 | a0086c0228 | 1 | HG03654.hp2 | synonymous_variant | LOW | c.13479C>G | p.Ser4493Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13537/16366 | 13479/16008 | 4493/5335 | chr7 | 101004042 | ||
| chr7:101004063
|
G | A | 1 | a0258c0279 | 1 | HG03130.hp2 | synonymous_variant | LOW | c.13500G>A | p.Thr4500Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13558/16366 | 13500/16008 | 4500/5335 | chr7 | 101004063 | ||
| chr7:101004159
|
G | A | 1 | a0258c0279 | 1 | HG03130.hp2 | synonymous_variant | LOW | c.13596G>A | p.Ala4532Ala | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13654/16366 | 13596/16008 | 4532/5335 | chr7 | 101004159 | ||
| chr7:101004165
|
C | T | 1 | a0263c0275 | 1 | NA20129.hp1 | synonymous_variant | LOW | c.13602C>T | p.Pro4534Pro | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13660/16366 | 13602/16008 | 4534/5335 | chr7 | 101004165 | ||
| chr7:101004213
|
C | T | 1 | a0086c0228 | 1 | HG03654.hp2 | synonymous_variant | LOW | c.13650C>T | p.His4550His | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13708/16366 | 13650/16008 | 4550/5335 | chr7 | 101004213 | ||
| chr7:101004258
|
C | T | 11 | a0007c0008a0013c0037a0055c0264others(8): Show | 14 | HG01261.hp2 HG02071.hp1 HG02559.hp2 others(11): Show |
synonymous_variant | LOW | c.13695C>T | p.Ser4565Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13753/16366 | 13695/16008 | 4565/5335 | chr7 | 101004258 | ||
| chr7:101004270
|
C | T | 1 | a0216c0084 | 1 | HG03834.hp2 | synonymous_variant | LOW | c.13707C>T | p.Gly4569Gly | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13765/16366 | 13707/16008 | 4569/5335 | chr7 | 101004270 | ||
| chr7:101004330
|
G | C | 13 | a0007c0008a0013c0037a0055c0264others(10): Show | 16 | HG01261.hp2 HG02071.hp1 HG02559.hp2 others(13): Show |
synonymous_variant | LOW | c.13767G>C | p.Ser4589Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13825/16366 | 13767/16008 | 4589/5335 | chr7 | 101004330 | ||
| chr7:101004357
|
C | T | 41 | a0002c0004a0002c0007a0002c0245others(38): Show | 57 | HG00558.hp2 HG01099.hp1 HG01123.hp2 others(54): Show |
synonymous_variant | LOW | c.13794C>T | p.Leu4598Leu | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13852/16366 | 13794/16008 | 4598/5335 | chr7 | 101004357 | ||
| chr7:101004375
|
G | C | 19 | a0021c0022a0023c0024a0051c0270others(16): Show | 21 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(18): Show |
synonymous_variant | LOW | c.13812G>C | p.Ala4604Ala | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13870/16366 | 13812/16008 | 4604/5335 | chr7 | 101004375 | ||
| chr7:101004378
|
C | T | 25 | a0020c0023a0022c0025a0024c0021others(22): Show | 28 | HG00408.hp1 HG00621.hp2 HG00735.hp1 others(25): Show |
synonymous_variant | LOW | c.13815C>T | p.Tyr4605Tyr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13873/16366 | 13815/16008 | 4605/5335 | chr7 | 101004378 | ||
| chr7:101004390
|
G | A | 2 | a0102c0155a0108c0149 | 2 | HG00408.hp2 HG02080.hp1 |
synonymous_variant | LOW | c.13827G>A | p.Pro4609Pro | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13885/16366 | 13827/16008 | 4609/5335 | chr7 | 101004390 | ||
| chr7:101004477
|
A | G | 1 | a0037c0017 | 2 | HG01069.hp2 HG01070.hp1 |
synonymous_variant | LOW | c.13914A>G | p.Thr4638Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 13972/16366 | 13914/16008 | 4638/5335 | chr7 | 101004477 | ||
| chr7:101004594
|
C | A | 168 | a0001c0001a0001c0168a0001c0181others(165): Show | 193 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(190): Show |
synonymous_variant | LOW | c.14031C>A | p.Ser4677Ser | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 14089/16366 | 14031/16008 | 4677/5335 | chr7 | 101004594 | ||
| chr7:101004639
|
A | C | 127 | a0001c0001a0001c0168a0001c0181others(124): Show | 150 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(147): Show |
synonymous_variant | LOW | c.14076A>C | p.Thr4692Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 14134/16366 | 14076/16008 | 4692/5335 | chr7 | 101004639 | ||
| chr7:101004675
|
C | G | 1 | a0206c0077 | 1 | NA19066.hp1 | synonymous_variant | LOW | c.14112C>G | p.Thr4704Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 14170/16366 | 14112/16008 | 4704/5335 | chr7 | 101004675 | ||
| chr7:101005302
|
C | T | 1 | a0170c0137 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.14739C>T | p.Asp4913Asp | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/12 | 14797/16366 | 14739/16008 | 4913/5335 | chr7 | 101005302 | ||
| chr7:101013005
|
A | G | 1 | a0207c0078 | 1 | HG02717.hp1 | synonymous_variant | LOW | c.15501A>G | p.Glu5167Glu | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 8/12 | 15559/16366 | 15501/16008 | 5167/5335 | chr7 | 101013005 | ||
| chr7:101013080
|
G | A | 7 | a0259c0272a0260c0273a0262c0274others(4): Show | 7 | HG02258.hp1 HG02622.hp1 HG02723.hp2 others(4): Show |
synonymous_variant | LOW | c.15576G>A | p.Thr5192Thr | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 8/12 | 15634/16366 | 15576/16008 | 5192/5335 | chr7 | 101013080 | ||
| chr7:101017639
|
G | A | 3 | a0004c0012a0036c0014a0207c0078 | 5 | HG02630.hp1 HG02717.hp1 HG02895.hp2 others(2): Show |
synonymous_variant | LOW | c.15942G>A | p.Leu5314Leu | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/12 | 16000/16366 | 15942/16008 | 5314/5335 | chr7 | 101017639 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:100969584
|
T | C | 286 | a0001c0001t0001a0001c0168t0001a0001c0181t0001others(283): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
5_prime_UTR_variant | MODIFIER | c.-39T>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/12 | 39 | chr7 | 100969584 | |||||
| chr7:100969588
|
A | G | 286 | a0001c0001t0001a0001c0168t0001a0001c0181t0001others(283): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
5_prime_UTR_variant | MODIFIER | c.-35A>G | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/12 | 35 | chr7 | 100969588 | |||||
| chr7:100969594
|
T | C | 286 | a0001c0001t0001a0001c0168t0001a0001c0181t0001others(283): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
5_prime_UTR_variant | MODIFIER | c.-29T>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/12 | 29 | chr7 | 100969594 | |||||
| chr7:100969617
|
C | T | 286 | a0001c0001t0001a0001c0168t0001a0001c0181t0001others(283): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-6C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/12 | chr7 | 100969617 | ||||||
| chr7:101018742
|
C | A | 1 | a0139c0167t0002 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*106C>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 12/12 | 106 | chr7 | 101018742 | |||||
| chr7:101018863
|
G | A | 1 | a0006c0038t0003 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*227G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 12/12 | 227 | chr7 | 101018863 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:100969974
|
G | A | 7 | a0014c0036t0001g0006a0014c0036t0001g0027a0065c0248t0001g0030others(4): Show | 7 | HG01884.hp1 HG02559.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.67+285G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100969974 | ||||||
| chr7:100970058
|
C | G | 1 | a0048c0046t0001g0299 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.67+369C>G | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100970058 | ||||||
| chr7:100970163
|
C | G | 1 | a0230c0102t0001g0298 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.67+474C>G | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100970163 | ||||||
| chr7:100970355
|
C | T | 21 | a0004c0012t0001g0287a0004c0012t0001g0288a0025c0032t0001g0026others(18): Show | 21 | HG01243.hp2 HG02055.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.67+666C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100970355 | ||||||
| chr7:100970392
|
C | T | 34 | a0016c0035t0001g0258a0016c0035t0001g0259a0021c0022t0001g0283others(31): Show | 34 | HG00323.hp2 HG00642.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.67+703C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100970392 | ||||||
| chr7:100970434
|
G | A | 1 | a0240c0108t0001g0032 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.67+745G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100970434 | ||||||
| chr7:100970485
|
C | CA | 10 | a0049c0047t0001g0034a0127c0211t0001g0286a0170c0137t0001g0035others(7): Show | 10 | HG02622.hp1 HG02809.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.67+807dupA | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 100970485 | |||||
| chr7:100970493
|
AAAAGAGA others(9): Show |
A | 1 | a0261c0280t0001g0254 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.67+814_67+829delGA others(14): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 100970493 | |||||
| chr7:100970590
|
T | C | 3 | a0187c0060t0001g0033a0259c0272t0001g0007a0260c0273t0001g0007 | 3 | HG02622.hp1 HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.67+901T>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100970590 | ||||||
| chr7:100970639
|
C | T | 2 | a0001c0001t0001g0252a0136c0166t0001g0253 | 2 | NA18942.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.67+950C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100970639 | ||||||
| chr7:100970773
|
G | A | 3 | a0028c0030t0001g0257a0142c0194t0001g0256a0143c0195t0001g0255 | 3 | HG02451.hp1 HG02886.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.67+1084G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100970773 | ||||||
| chr7:100970920
|
C | A | 1 | a0202c0132t0001g0040 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.67+1231C>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100970920 | ||||||
| chr7:100970934
|
C | T | 1 | a0039c0015t0001g0251 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.67+1245C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100970934 | ||||||
| chr7:100970945
|
C | T | 127 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0197others(124): Show | 133 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.67+1256C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100970945 | ||||||
| chr7:100970952
|
G | A | 1 | a0079c0237t0001g0041 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.67+1263G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100970952 | ||||||
| chr7:100970994
|
C | CAA | 56 | a0001c0181t0001g0069a0002c0004t0001g0001a0002c0004t0001g0046others(53): Show | 58 | HG00408.hp1 HG00558.hp2 HG01099.hp1 others(55): Show |
intron_variant | MODIFIER | c.67+1316_67+1317dup others(2): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 100970994 | |||||
| chr7:100971028
|
C | T | 1 | a0261c0280t0001g0254 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.67+1339C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100971028 | ||||||
| chr7:100971105
|
G | A | 103 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0197others(100): Show | 109 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.67+1416G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100971105 | ||||||
| chr7:100971141
|
C | T | 1 | a0218c0086t0001g0166 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.67+1452C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100971141 | ||||||
| chr7:100971152
|
C | CA | 17 | a0002c0007t0001g0042a0004c0012t0001g0287a0004c0012t0001g0288others(14): Show | 17 | HG01069.hp1 HG01934.hp1 HG01993.hp1 others(14): Show |
intron_variant | MODIFIER | c.67+1472dupA | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 100971152 | |||||
| chr7:100971181
|
C | CAA | 19 | a0029c0029t0001g0274a0029c0029t0001g0277a0032c0170t0001g0272others(16): Show | 19 | HG01106.hp1 HG01361.hp2 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.67+1501_67+1502dup others(2): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 100971181 | |||||
| chr7:100971181
|
C | CAAA | 91 | a0001c0001t0001g0019a0001c0001t0001g0197a0001c0001t0001g0198others(88): Show | 95 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(92): Show |
intron_variant | MODIFIER | c.67+1500_67+1502dup others(3): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 100971181 | |||||
| chr7:100971182
|
A | AAAC | 25 | a0001c0001t0001g0004a0001c0168t0001g0247a0011c0009t0001g0137others(22): Show | 26 | HG00323.hp1 HG00323.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.67+1495_67+1496ins others(3): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 100971182 | |||||
| chr7:100971184
|
A | AC | 57 | a0004c0012t0001g0287a0004c0012t0001g0288a0010c0005t0001g0015others(54): Show | 58 | HG00099.hp1 HG01081.hp1 HG01175.hp1 others(55): Show |
intron_variant | MODIFIER | c.67+1495_67+1496ins others(1): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100971184 | ||||||
| chr7:100971214
|
A | G | 1 | a0103c0150t0001g0165 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.67+1525A>G | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100971214 | ||||||
| chr7:100971218
|
G | A | 1 | a0103c0150t0001g0165 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.67+1529G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100971218 | ||||||
| chr7:100971232
|
A | G | 198 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0197others(195): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.67+1543A>G | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100971232 | ||||||
| chr7:100971235
|
G | T | 2 | a0103c0150t0001g0165a0160c0190t0001g0164 | 2 | HG00099.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.67+1546G>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100971235 | ||||||
| chr7:100971275
|
A | C | 11 | a0024c0021t0001g0022a0029c0029t0001g0274a0029c0029t0001g0277others(8): Show | 12 | HG00099.hp1 HG02896.hp1 HG02897.hp1 others(9): Show |
intron_variant | MODIFIER | c.67+1586A>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100971275 | ||||||
| chr7:100971285
|
G | A | 56 | a0004c0012t0001g0287a0004c0012t0001g0288a0010c0005t0001g0015others(53): Show | 57 | HG01081.hp1 HG01175.hp1 HG01192.hp2 others(54): Show |
intron_variant | MODIFIER | c.67+1596G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100971285 | ||||||
| chr7:100971395
|
A | C | 1 | a0198c0055t0001g0271 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.67+1706A>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100971395 | ||||||
| chr7:100971402
|
G | A | 1 | a0261c0280t0001g0254 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.67+1713G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100971402 | ||||||
| chr7:100971431
|
G | T | 136 | a0001c0181t0001g0069a0002c0004t0001g0001a0002c0004t0001g0046others(133): Show | 140 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(137): Show |
intron_variant | MODIFIER | c.67+1742G>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100971431 | ||||||
| chr7:100971435
|
CT | C | 17 | a0007c0008t0001g0010a0007c0008t0001g0078a0008c0028t0001g0169others(14): Show | 18 | HG01257.hp1 HG02056.hp2 HG02083.hp1 others(15): Show |
intron_variant | MODIFIER | c.67+1747delT | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100971435 | ||||||
| chr7:100971459
|
C | T | 17 | a0007c0008t0001g0010a0007c0008t0001g0078a0037c0017t0001g0231others(14): Show | 18 | HG00099.hp2 HG00642.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.67+1770C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100971459 | ||||||
| chr7:100971531
|
C | A | 102 | a0001c0181t0001g0069a0002c0004t0001g0001a0002c0004t0001g0046others(99): Show | 105 | HG00323.hp1 HG00408.hp1 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.67+1842C>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100971531 | ||||||
| chr7:100971532
|
G | A | 2 | a0135c0200t0001g0248a0149c0185t0001g0175 | 2 | HG02015.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.67+1843G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100971532 | ||||||
| chr7:100971547
|
A | T | 1 | a0152c0176t0001g0233 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.67+1858A>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100971547 | ||||||
| chr7:100971561
|
AC | A | 95 | a0001c0181t0001g0069a0002c0004t0001g0001a0002c0004t0001g0046others(92): Show | 98 | HG00408.hp1 HG00558.hp2 HG00673.hp2 others(95): Show |
intron_variant | MODIFIER | c.67+1877delC | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 100971561 | |||||
| chr7:100971570
|
C | T | 89 | a0001c0181t0001g0069a0002c0004t0001g0001a0002c0004t0001g0046others(86): Show | 92 | HG00408.hp1 HG00558.hp2 HG00673.hp2 others(89): Show |
intron_variant | MODIFIER | c.67+1881C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100971570 | ||||||
| chr7:100971582
|
G | A | 1 | a0241c0111t0001g0102 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.67+1893G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100971582 | ||||||
| chr7:100971596
|
C | T | 20 | a0001c0168t0001g0247a0011c0009t0001g0139a0030c0027t0001g0141others(17): Show | 20 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.67+1907C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100971596 | ||||||
| chr7:100971597
|
A | G | 141 | a0001c0001t0001g0004a0001c0001t0001g0252a0001c0168t0001g0247others(138): Show | 146 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.67+1908A>G | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100971597 | ||||||
| chr7:100971703
|
C | G | 1 | a0203c0131t0001g0214 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.67+2014C>G | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100971703 | ||||||
| chr7:100971709
|
A | G | 1 | a0203c0131t0001g0214 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.67+2020A>G | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100971709 | ||||||
| chr7:100971779
|
T | C | 3 | a0144c0191t0001g0104a0150c0196t0001g0171a0231c0120t0001g0103 | 3 | HG00673.hp2 HG02027.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.67+2090T>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100971779 | ||||||
| chr7:100971834
|
C | T | 1 | a0090c0223t0001g0070 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.67+2145C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100971834 | ||||||
| chr7:100971841
|
G | A | 3 | a0008c0028t0001g0184a0012c0040t0001g0017a0171c0136t0001g0183 | 4 | NA18984.hp1 NA18985.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+2152G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100971841 | ||||||
| chr7:100971847
|
C | T | 1 | a0189c0058t0001g0269 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.67+2158C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100971847 | ||||||
| chr7:100971860
|
AGGTGGCA others(20): Show |
A | 1 | a0208c0083t0001g0134 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.67+2173_67+2199del others(27): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 100971860 | |||||
| chr7:100971901
|
G | A | 28 | a0011c0009t0001g0137a0011c0009t0001g0139a0019c0033t0001g0237others(25): Show | 28 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(25): Show |
intron_variant | MODIFIER | c.67+2212G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100971901 | ||||||
| chr7:100971926
|
G | A | 3 | a0052c0269t0001g0105a0103c0150t0001g0165a0116c0145t0001g0072 | 3 | HG00099.hp1 HG02698.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.67+2237G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100971926 | ||||||
| chr7:100971928
|
T | C | 1 | a0258c0279t0001g0173 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.67+2239T>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100971928 | ||||||
| chr7:100972045
|
G | A | 1 | a0053c0267t0001g0143 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.67+2356G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100972045 | ||||||
| chr7:100972299
|
T | C | 66 | a0002c0004t0001g0001a0002c0004t0001g0046a0002c0004t0001g0054others(63): Show | 69 | HG00099.hp2 HG00558.hp2 HG01099.hp1 others(66): Show |
intron_variant | MODIFIER | c.67+2610T>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100972299 | ||||||
| chr7:100972464
|
G | T | 1 | a0258c0279t0001g0173 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.67+2775G>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100972464 | ||||||
| chr7:100972651
|
C | T | 1 | a0138c0198t0001g0086 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.67+2962C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100972651 | ||||||
| chr7:100972662
|
T | A | 1 | a0099c0148t0001g0242 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.67+2973T>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100972662 | ||||||
| chr7:100972676
|
T | C | 1 | a0180c0067t0001g0080 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.67+2987T>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100972676 | ||||||
| chr7:100972784
|
G | T | 1 | a0208c0083t0001g0134 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.67+3095G>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100972784 | ||||||
| chr7:100972786
|
G | A | 5 | a0187c0060t0001g0033a0259c0272t0001g0007a0260c0273t0001g0007others(2): Show | 5 | HG02258.hp1 HG02622.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+3097G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100972786 | ||||||
| chr7:100972939
|
T | A | 1 | a0266c0277t0001g0107 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.67+3250T>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100972939 | ||||||
| chr7:100973127
|
G | A | 38 | a0005c0003t0001g0003a0005c0003t0001g0124a0035c0020t0001g0121others(35): Show | 40 | HG00423.hp2 HG00621.hp1 HG01928.hp1 others(37): Show |
intron_variant | MODIFIER | c.67+3438G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100973127 | ||||||
| chr7:100973143
|
G | A | 1 | a0239c0115t0001g0135 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.67+3454G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100973143 | ||||||
| chr7:100973269
|
C | T | 3 | a0007c0008t0001g0010a0007c0008t0001g0078a0216c0084t0001g0079 | 4 | HG02602.hp1 HG03017.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+3580C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100973269 | ||||||
| chr7:100973291
|
G | A | 5 | a0088c0225t0001g0008a0089c0224t0001g0068a0090c0223t0001g0070others(2): Show | 5 | HG00408.hp1 HG02027.hp2 NA18941.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+3602G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100973291 | ||||||
| chr7:100973477
|
C | T | 2 | a0037c0017t0001g0231a0037c0017t0001g0232 | 2 | HG01069.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.67+3788C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100973477 | ||||||
| chr7:100973551
|
A | T | 1 | a0181c0066t0001g0162 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.67+3862A>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100973551 | ||||||
| chr7:100973611
|
G | A | 1 | a0128c0208t0001g0174 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.67+3922G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100973611 | ||||||
| chr7:100973737
|
A | G | 1 | a0208c0083t0001g0134 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.67+4048A>G | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100973737 | ||||||
| chr7:100973755
|
C | A | 1 | a0208c0083t0001g0134 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.67+4066C>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100973755 | ||||||
| chr7:100973951
|
G | A | 63 | a0002c0004t0001g0001a0002c0004t0001g0046a0002c0004t0001g0054others(60): Show | 65 | HG00099.hp2 HG00558.hp2 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.67+4262G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100973951 | ||||||
| chr7:100973976
|
G | C | 5 | a0187c0060t0001g0033a0259c0272t0001g0007a0260c0273t0001g0007others(2): Show | 5 | HG02258.hp1 HG02622.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+4287G>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100973976 | ||||||
| chr7:100974052
|
G | C | 4 | a0020c0023t0001g0188a0100c0157t0001g0179a0111c0160t0001g0177others(1): Show | 4 | HG00621.hp2 HG02040.hp2 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+4363G>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100974052 | ||||||
| chr7:100974103
|
T | G | 1 | a0211c0080t0001g0092 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.67+4414T>G | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100974103 | ||||||
| chr7:100974413
|
C | T | 323 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0197others(320): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.67+4724C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100974413 | ||||||
| chr7:100974427
|
A | G | 1 | a0046c0045t0001g0142 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.67+4738A>G | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100974427 | ||||||
| chr7:100974491
|
CT | C | 63 | a0002c0004t0001g0001a0002c0004t0001g0046a0002c0004t0001g0054others(60): Show | 65 | HG00099.hp2 HG00558.hp2 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.67+4803delT | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100974491 | ||||||
| chr7:100974698
|
G | A | 1 | a0215c0096t0001g0036 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.67+5009G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100974698 | ||||||
| chr7:100974757
|
C | T | 1 | a0228c0100t0001g0043 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.67+5068C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100974757 | ||||||
| chr7:100974763
|
T | C | 63 | a0002c0004t0001g0001a0002c0004t0001g0046a0002c0004t0001g0054others(60): Show | 65 | HG00099.hp2 HG00558.hp2 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.67+5074T>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100974763 | ||||||
| chr7:100974825
|
A | AAATAAT | 189 | a0001c0001t0001g0019a0001c0001t0001g0197a0001c0001t0001g0198others(186): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.67+5151_67+5156dup others(6): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 100974825 | |||||
| chr7:100974825
|
A | AAATAATA others(2): Show |
32 | a0001c0001t0001g0004a0001c0001t0001g0252a0033c0011t0001g0149others(29): Show | 33 | HG00642.hp2 HG00673.hp1 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.67+5148_67+5156dup others(9): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 100974825 | |||||
| chr7:100974847
|
T | A | 1 | a0016c0035t0001g0258 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.67+5158T>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100974847 | ||||||
| chr7:100974850
|
A | T | 1 | a0016c0035t0001g0258 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.67+5161A>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100974850 | ||||||
| chr7:100974920
|
C | A | 3 | a0007c0008t0001g0010a0007c0008t0001g0078a0216c0084t0001g0079 | 4 | HG02602.hp1 HG03017.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+5231C>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100974920 | ||||||
| chr7:100974936
|
G | A | 2 | a0119c0218t0001g0025a0121c0217t0001g0025 | 2 | HG02109.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.67+5247G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100974936 | ||||||
| chr7:100975142
|
C | A | 1 | a0049c0047t0001g0034 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.67+5453C>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100975142 | ||||||
| chr7:100975155
|
A | G | 1 | a0182c0063t0001g0161 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.67+5466A>G | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100975155 | ||||||
| chr7:100975332
|
G | A | 1 | a0014c0036t0001g0027 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.67+5643G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100975332 | ||||||
| chr7:100975420
|
G | T | 67 | a0002c0004t0001g0001a0002c0004t0001g0046a0002c0004t0001g0054others(64): Show | 70 | HG00099.hp2 HG00558.hp2 HG01099.hp1 others(67): Show |
intron_variant | MODIFIER | c.67+5731G>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100975420 | ||||||
| chr7:100975595
|
G | C | 1 | a0105c0153t0001g0189 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.67+5906G>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100975595 | ||||||
| chr7:100975712
|
A | G | 317 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0197others(314): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.67+6023A>G | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100975712 | ||||||
| chr7:100975738
|
G | T | 222 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0197others(219): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.67+6049G>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100975738 | ||||||
| chr7:100975857
|
C | T | 4 | a0040c0018t0001g0014a0040c0018t0001g0126a0232c0075t0001g0014others(1): Show | 4 | HG03017.hp2 HG03834.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+6168C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100975857 | ||||||
| chr7:100975871
|
C | G | 5 | a0187c0060t0001g0033a0259c0272t0001g0007a0260c0273t0001g0007others(2): Show | 5 | HG02258.hp1 HG02622.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+6182C>G | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100975871 | ||||||
| chr7:100975962
|
A | C | 4 | a0065c0248t0001g0030a0066c0247t0001g0024a0074c0252t0001g0024others(1): Show | 4 | HG02615.hp1 HG02647.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+6273A>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100975962 | ||||||
| chr7:100976042
|
AG | A | 63 | a0002c0004t0001g0001a0002c0004t0001g0046a0002c0004t0001g0054others(60): Show | 65 | HG00099.hp2 HG00558.hp2 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.67+6354delG | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100976042 | ||||||
| chr7:100976239
|
C | T | 2 | a0022c0025t0001g0223a0022c0025t0001g0224 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.67+6550C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100976239 | ||||||
| chr7:100976291
|
A | T | 16 | a0011c0009t0001g0137a0011c0009t0001g0139a0019c0033t0001g0237others(13): Show | 16 | HG00323.hp1 HG00639.hp2 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.67+6602A>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100976291 | ||||||
| chr7:100976343
|
T | C | 222 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0197others(219): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.67+6654T>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100976343 | ||||||
| chr7:100976401
|
C | T | 159 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0197others(156): Show | 165 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.67+6712C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100976401 | ||||||
| chr7:100976448
|
A | AC | 222 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0197others(219): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.67+6759_67+6760ins others(1): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100976448 | ||||||
| chr7:100976461
|
G | A | 5 | a0187c0060t0001g0033a0259c0272t0001g0007a0260c0273t0001g0007others(2): Show | 5 | HG02258.hp1 HG02622.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+6772G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100976461 | ||||||
| chr7:100976567
|
G | A | 1 | a0127c0211t0001g0286 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.67+6878G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100976567 | ||||||
| chr7:100976580
|
G | A | 63 | a0002c0004t0001g0001a0002c0004t0001g0046a0002c0004t0001g0054others(60): Show | 65 | HG00099.hp2 HG00558.hp2 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.67+6891G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100976580 | ||||||
| chr7:100976597
|
CT | C | 3 | a0027c0031t0001g0190a0027c0031t0001g0192a0134c0201t0001g0191 | 3 | HG02970.hp1 HG06807.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.67+6911delT | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 100976597 | |||||
| chr7:100976602
|
TA | T | 230 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0197others(227): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.67+6926delA | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 100976602 | |||||
| chr7:100976657
|
T | C | 118 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0197others(115): Show | 124 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.67+6968T>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100976657 | ||||||
| chr7:100976777
|
G | A | 1 | a0200c0049t0001g0106 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.67+7088G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100976777 | ||||||
| chr7:100976900
|
A | G | 1 | a0269c0284t0001g0101 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.67+7211A>G | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100976900 | ||||||
| chr7:100976945
|
G | A | 1 | a0239c0115t0001g0135 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.67+7256G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100976945 | ||||||
| chr7:100976994
|
T | C | 63 | a0002c0004t0001g0001a0002c0004t0001g0046a0002c0004t0001g0054others(60): Show | 65 | HG00099.hp2 HG00558.hp2 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.67+7305T>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100976994 | ||||||
| chr7:100977050
|
C | CA | 23 | a0036c0014t0001g0290a0036c0014t0001g0291a0042c0118t0001g0109others(20): Show | 23 | HG00621.hp1 HG01106.hp2 HG01361.hp1 others(20): Show |
intron_variant | MODIFIER | c.67+7393dupA | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 100977050 | |||||
| chr7:100977050
|
CA | C | 17 | a0005c0003t0001g0124a0007c0008t0001g0010a0011c0009t0001g0137others(14): Show | 18 | HG00323.hp1 HG00639.hp2 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.67+7393delA | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 100977050 | |||||
| chr7:100977050
|
CAAAAAAA others(2): Show |
C | 148 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0197others(145): Show | 154 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.67+7385_67+7393del others(9): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 100977050 | |||||
| chr7:100977050
|
CAAAAAAA others(3): Show |
C | 8 | a0022c0025t0001g0224a0053c0267t0001g0143a0061c0255t0001g0045others(5): Show | 8 | HG01257.hp2 HG01516.hp2 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+7384_67+7393del others(10): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 100977050 | |||||
| chr7:100977050
|
CAAAAAAA others(4): Show |
C | 55 | a0002c0004t0001g0001a0002c0004t0001g0046a0002c0004t0001g0054others(52): Show | 57 | HG00099.hp2 HG00558.hp2 HG01099.hp1 others(54): Show |
intron_variant | MODIFIER | c.67+7383_67+7393del others(11): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 100977050 | |||||
| chr7:100977050
|
CAAAAAAA others(5): Show |
C | 7 | a0003c0002t0001g0065a0003c0002t0001g0066a0003c0002t0001g0067others(4): Show | 7 | HG01884.hp2 HG02257.hp2 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.67+7382_67+7393del others(12): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 100977050 | |||||
| chr7:100977050
|
CAAAAAAA others(11): Show |
C | 1 | a0200c0049t0001g0106 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.67+7376_67+7393del others(18): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 100977050 | |||||
| chr7:100977096
|
A | G | 222 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0197others(219): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.67+7407A>G | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100977096 | ||||||
| chr7:100977175
|
C | T | 1 | a0223c0091t0001g0039 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.67+7486C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100977175 | ||||||
| chr7:100977285
|
C | T | 1 | a0058c0259t0001g0064 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.67+7596C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100977285 | ||||||
| chr7:100977330
|
T | G | 1 | a0165c0193t0001g0194 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.67+7641T>G | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100977330 | ||||||
| chr7:100977370
|
CT | C | 221 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0197others(218): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.67+7695delT | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 100977370 | |||||
| chr7:100977387
|
G | A | 1 | a0270c0282t0001g0098 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.67+7698G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100977387 | ||||||
| chr7:100977390
|
G | A | 63 | a0002c0004t0001g0001a0002c0004t0001g0046a0002c0004t0001g0054others(60): Show | 65 | HG00099.hp2 HG00558.hp2 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.67+7701G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100977390 | ||||||
| chr7:100977430
|
G | A | 1 | a0031c0026t0001g0018 | 2 | HG01081.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.67+7741G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100977430 | ||||||
| chr7:100977514
|
C | T | 1 | a0036c0014t0001g0291 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.67+7825C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100977514 | ||||||
| chr7:100977554
|
C | T | 159 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0197others(156): Show | 165 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.67+7865C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100977554 | ||||||
| chr7:100977600
|
G | A | 1 | a0200c0049t0001g0106 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.67+7911G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100977600 | ||||||
| chr7:100977706
|
G | C | 6 | a0001c0001t0001g0004a0001c0001t0001g0252a0136c0166t0001g0253others(3): Show | 7 | NA18942.hp1 NA18947.hp2 NA18964.hp2 others(4): Show |
intron_variant | MODIFIER | c.67+8017G>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100977706 | ||||||
| chr7:100977855
|
A | C | 63 | a0002c0004t0001g0001a0002c0004t0001g0046a0002c0004t0001g0054others(60): Show | 65 | HG00099.hp2 HG00558.hp2 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.67+8166A>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100977855 | ||||||
| chr7:100977891
|
G | A | 1 | a0129c0209t0001g0127 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.67+8202G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100977891 | ||||||
| chr7:100977979
|
C | T | 5 | a0187c0060t0001g0033a0259c0272t0001g0007a0260c0273t0001g0007others(2): Show | 5 | HG02258.hp1 HG02622.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+8290C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100977979 | ||||||
| chr7:100977995
|
A | G | 3 | a0034c0010t0001g0267a0034c0010t0001g0268a0189c0058t0001g0269 | 3 | HG01106.hp1 HG01515.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.67+8306A>G | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100977995 | ||||||
| chr7:100978329
|
G | T | 5 | a0187c0060t0001g0033a0259c0272t0001g0007a0260c0273t0001g0007others(2): Show | 5 | HG02258.hp1 HG02622.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+8640G>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100978329 | ||||||
| chr7:100978345
|
C | A | 1 | a0095c0221t0001g0236 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.67+8656C>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100978345 | ||||||
| chr7:100978680
|
G | T | 1 | a0013c0037t0001g0062 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.67+8991G>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100978680 | ||||||
| chr7:100978686
|
G | A | 16 | a0011c0009t0001g0137a0011c0009t0001g0139a0019c0033t0001g0237others(13): Show | 16 | HG00323.hp1 HG00639.hp2 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.67+8997G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100978686 | ||||||
| chr7:100979171
|
T | A | 1 | a0200c0049t0001g0106 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.67+9482T>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100979171 | ||||||
| chr7:100979462
|
C | CAAAAT | 17 | a0004c0012t0001g0287a0004c0012t0001g0288a0004c0013t0001g0082others(14): Show | 17 | HG00639.hp2 HG01074.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.67+9799_67+9803dup others(5): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 100979462 | |||||
| chr7:100979574
|
G | A | 1 | a0049c0047t0001g0034 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.67+9885G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100979574 | ||||||
| chr7:100979577
|
C | T | 4 | a0231c0120t0001g0103a0245c0112t0001g0111a0249c0123t0001g0013others(1): Show | 4 | HG02027.hp1 HG02074.hp2 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+9888C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100979577 | ||||||
| chr7:100979599
|
G | T | 2 | a0059c0258t0001g0061a0060c0257t0001g0060 | 2 | NA18994.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.67+9910G>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100979599 | ||||||
| chr7:100979706
|
A | T | 131 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0197others(128): Show | 137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.67+10017A>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100979706 | ||||||
| chr7:100979709
|
G | A | 3 | a0007c0008t0001g0010a0007c0008t0001g0078a0216c0084t0001g0079 | 4 | HG02602.hp1 HG03017.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+10020G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100979709 | ||||||
| chr7:100979732
|
C | T | 1 | a0160c0190t0001g0164 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.67+10043C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100979732 | ||||||
| chr7:100979805
|
G | GTA | 157 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0197others(154): Show | 163 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.67+10127_67+10128d others(4): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 100979805 | |||||
| chr7:100979887
|
C | T | 7 | a0008c0028t0001g0184a0012c0040t0001g0017a0073c0246t0001g0059others(4): Show | 8 | HG01978.hp1 HG02015.hp1 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.67+10198C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100979887 | ||||||
| chr7:100980042
|
C | T | 1 | a0162c0174t0001g0181 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.67+10353C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100980042 | ||||||
| chr7:100980299
|
C | G | 5 | a0187c0060t0001g0033a0259c0272t0001g0007a0260c0273t0001g0007others(2): Show | 5 | HG02258.hp1 HG02622.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-10332C>G | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100980299 | ||||||
| chr7:100980322
|
G | A | 3 | a0007c0008t0001g0010a0007c0008t0001g0078a0216c0084t0001g0079 | 4 | HG02602.hp1 HG03017.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-10309G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100980322 | ||||||
| chr7:100980568
|
A | C | 132 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0197others(129): Show | 138 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.68-10063A>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100980568 | ||||||
| chr7:100980624
|
C | T | 1 | a0195c0057t0001g0279 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.68-10007C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100980624 | ||||||
| chr7:100981028
|
C | T | 24 | a0033c0011t0001g0149a0033c0011t0001g0151a0034c0010t0001g0267others(21): Show | 24 | HG00642.hp2 HG00673.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.68-9603C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100981028 | ||||||
| chr7:100981149
|
C | T | 1 | a0049c0047t0001g0034 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.68-9482C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100981149 | ||||||
| chr7:100981322
|
G | A | 1 | a0032c0171t0001g0273 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.68-9309G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100981322 | ||||||
| chr7:100981362
|
T | G | 50 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0197others(47): Show | 53 | HG00558.hp1 HG00673.hp2 HG00738.hp1 others(50): Show |
intron_variant | MODIFIER | c.68-9269T>G | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100981362 | ||||||
| chr7:100981437
|
G | C | 239 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0197others(236): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.68-9194G>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100981437 | ||||||
| chr7:100981528
|
G | C | 2 | a0004c0012t0001g0287a0004c0012t0001g0288 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.68-9103G>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100981528 | ||||||
| chr7:100981866
|
C | CT | 123 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0197others(120): Show | 130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.68-8747dupT | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 100981866 | |||||
| chr7:100982027
|
C | T | 3 | a0005c0003t0001g0003a0005c0003t0001g0124a0244c0116t0001g0120 | 5 | NA18942.hp2 NA18946.hp1 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-8604C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100982027 | ||||||
| chr7:100982046
|
T | C | 2 | a0059c0258t0001g0061a0060c0257t0001g0060 | 2 | NA18994.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.68-8585T>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100982046 | ||||||
| chr7:100982048
|
G | C | 1 | a0200c0049t0001g0106 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.68-8583G>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100982048 | ||||||
| chr7:100982440
|
C | CT | 44 | a0020c0023t0001g0188a0020c0023t0001g0200a0021c0022t0001g0283others(41): Show | 45 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.68-8178dupT | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 100982440 | |||||
| chr7:100982440
|
C | G | 61 | a0002c0004t0001g0001a0002c0004t0001g0046a0002c0004t0001g0054others(58): Show | 63 | HG00099.hp2 HG00558.hp2 HG01099.hp1 others(60): Show |
intron_variant | MODIFIER | c.68-8191C>G | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100982440 | ||||||
| chr7:100982445
|
T | C | 3 | a0027c0031t0001g0190a0027c0031t0001g0192a0134c0201t0001g0191 | 3 | HG02970.hp1 HG06807.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.68-8186T>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100982445 | ||||||
| chr7:100982593
|
C | T | 1 | a0269c0284t0001g0101 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.68-8038C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100982593 | ||||||
| chr7:100982751
|
A | G | 27 | a0033c0011t0001g0149a0033c0011t0001g0151a0034c0010t0001g0267others(24): Show | 27 | HG00642.hp2 HG00673.hp1 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.68-7880A>G | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100982751 | ||||||
| chr7:100982806
|
T | C | 2 | a0192c0051t0001g0262a0193c0053t0001g0263 | 2 | HG01361.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.68-7825T>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100982806 | ||||||
| chr7:100982909
|
T | G | 1 | a0103c0150t0001g0165 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.68-7722T>G | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100982909 | ||||||
| chr7:100982916
|
G | C | 1 | a0122c0216t0001g0296 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.68-7715G>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100982916 | ||||||
| chr7:100983113
|
G | C | 3 | a0023c0024t0001g0204a0023c0024t0001g0205a0113c0158t0001g0241 | 3 | HG02735.hp2 HG03239.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.68-7518G>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100983113 | ||||||
| chr7:100983211
|
G | A | 5 | a0011c0009t0001g0137a0011c0009t0001g0139a0044c0042t0001g0138others(2): Show | 5 | HG00323.hp1 HG00639.hp2 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-7420G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100983211 | ||||||
| chr7:100983291
|
G | T | 61 | a0002c0004t0001g0001a0002c0004t0001g0046a0002c0004t0001g0054others(58): Show | 63 | HG00099.hp2 HG00558.hp2 HG01099.hp1 others(60): Show |
intron_variant | MODIFIER | c.68-7340G>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100983291 | ||||||
| chr7:100983417
|
TA | T | 6 | a0003c0002t0001g0058a0010c0005t0001g0147a0023c0024t0001g0205others(3): Show | 6 | HG01256.hp2 HG02155.hp1 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-7198delA | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 100983417 | |||||
| chr7:100983440
|
G | A | 1 | a0027c0031t0001g0190 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.68-7191G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100983440 | ||||||
| chr7:100983466
|
T | C | 145 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0197others(142): Show | 151 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.68-7165T>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100983466 | ||||||
| chr7:100983585
|
C | T | 3 | a0209c0082t0001g0145a0210c0081t0001g0093a0211c0080t0001g0092 | 3 | HG02572.hp2 HG02615.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.68-7046C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100983585 | ||||||
| chr7:100983674
|
G | A | 257 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0197others(254): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.68-6957G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100983674 | ||||||
| chr7:100983770
|
T | A | 61 | a0002c0004t0001g0001a0002c0004t0001g0046a0002c0004t0001g0054others(58): Show | 63 | HG00099.hp2 HG00558.hp2 HG01099.hp1 others(60): Show |
intron_variant | MODIFIER | c.68-6861T>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100983770 | ||||||
| chr7:100984041
|
G | A | 1 | a0093c0142t0001g0094 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.68-6590G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100984041 | ||||||
| chr7:100984259
|
C | CT | 7 | a0001c0168t0001g0247a0056c0262t0001g0056a0059c0258t0001g0061others(4): Show | 7 | HG01261.hp2 HG02148.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.68-6355dupT | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 100984259 | |||||
| chr7:100984259
|
CT | C | 33 | a0005c0003t0001g0124a0008c0028t0001g0169a0008c0205t0001g0234others(30): Show | 33 | HG00642.hp2 HG00673.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.68-6355delT | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 100984259 | |||||
| chr7:100984310
|
A | G | 257 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0197others(254): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.68-6321A>G | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100984310 | ||||||
| chr7:100984378
|
G | A | 2 | a0258c0279t0001g0173a0261c0280t0001g0254 | 2 | HG02451.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.68-6253G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100984378 | ||||||
| chr7:100984401
|
C | T | 1 | a0051c0270t0001g0220 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.68-6230C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100984401 | ||||||
| chr7:100984402
|
G | A | 1 | a0151c0186t0001g0260 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.68-6229G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100984402 | ||||||
| chr7:100984611
|
G | A | 1 | a0200c0049t0001g0106 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.68-6020G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100984611 | ||||||
| chr7:100984657
|
T | C | 61 | a0002c0004t0001g0001a0002c0004t0001g0046a0002c0004t0001g0054others(58): Show | 63 | HG00099.hp2 HG00558.hp2 HG01099.hp1 others(60): Show |
intron_variant | MODIFIER | c.68-5974T>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100984657 | ||||||
| chr7:100984826
|
C | T | 181 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0197others(178): Show | 188 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.68-5805C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100984826 | ||||||
| chr7:100984860
|
T | C | 3 | a0007c0008t0001g0010a0007c0008t0001g0078a0216c0084t0001g0079 | 4 | HG02602.hp1 HG03017.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-5771T>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100984860 | ||||||
| chr7:100985043
|
T | C | 1 | a0002c0004t0001g0046 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.68-5588T>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100985043 | ||||||
| chr7:100985133
|
T | C | 1 | a0094c0222t0001g0185 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.68-5498T>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100985133 | ||||||
| chr7:100985380
|
A | G | 145 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0197others(142): Show | 151 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.68-5251A>G | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100985380 | ||||||
| chr7:100985570
|
C | T | 1 | a0155c0182t0001g0132 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.68-5061C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100985570 | ||||||
| chr7:100985680
|
G | T | 1 | a0220c0087t0001g0091 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.68-4951G>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100985680 | ||||||
| chr7:100986060
|
C | A | 146 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0197others(143): Show | 152 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.68-4571C>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100986060 | ||||||
| chr7:100986088
|
T | G | 13 | a0009c0006t0001g0020a0009c0006t0001g0203a0030c0027t0001g0141others(10): Show | 15 | HG00140.hp2 HG00642.hp1 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.68-4543T>G | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100986088 | ||||||
| chr7:100986174
|
A | T | 1 | a0001c0168t0001g0247 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.68-4457A>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100986174 | ||||||
| chr7:100986178
|
A | G | 5 | a0011c0009t0001g0137a0011c0009t0001g0139a0044c0042t0001g0138others(2): Show | 5 | HG00323.hp1 HG00639.hp2 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-4453A>G | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100986178 | ||||||
| chr7:100986190
|
T | A | 1 | a0048c0046t0001g0299 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.68-4441T>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100986190 | ||||||
| chr7:100986280
|
G | A | 1 | a0263c0275t0001g0293 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.68-4351G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100986280 | ||||||
| chr7:100986417
|
C | CA | 165 | a0001c0001t0001g0198a0002c0004t0001g0001a0002c0004t0001g0046others(162): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.68-4202dupA | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 100986417 | |||||
| chr7:100986417
|
C | CAA | 49 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0197others(46): Show | 52 | HG00558.hp1 HG00673.hp2 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.68-4203_68-4202dup others(2): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 100986417 | |||||
| chr7:100986430
|
G | A | 1 | a0046c0045t0001g0142 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.68-4201G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100986430 | ||||||
| chr7:100986522
|
A | C | 10 | a0049c0047t0001g0034a0259c0272t0001g0007a0260c0273t0001g0007others(7): Show | 10 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.68-4109A>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100986522 | ||||||
| chr7:100986601
|
G | T | 1 | a0009c0006t0001g0203 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.68-4030G>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100986601 | ||||||
| chr7:100986759
|
A | G | 2 | a0007c0008t0001g0010a0007c0008t0001g0078 | 3 | HG02602.hp1 HG03017.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.68-3872A>G | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100986759 | ||||||
| chr7:100986984
|
C | A | 1 | a0082c0233t0001g0226 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.68-3647C>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100986984 | ||||||
| chr7:100987006
|
C | G | 9 | a0259c0272t0001g0007a0260c0273t0001g0007a0262c0274t0001g0294others(6): Show | 9 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.68-3625C>G | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100987006 | ||||||
| chr7:100987060
|
G | GT | 62 | a0002c0004t0001g0001a0002c0004t0001g0046a0002c0007t0001g0001others(59): Show | 64 | HG00099.hp2 HG00558.hp2 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.68-3547dupT | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 100987060 | |||||
| chr7:100987060
|
G | GTT | 30 | a0002c0004t0001g0054a0003c0002t0001g0066a0003c0002t0001g0067others(27): Show | 30 | HG01106.hp1 HG01109.hp2 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.68-3548_68-3547dup others(2): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 100987060 | |||||
| chr7:100987060
|
GT | G | 44 | a0005c0003t0001g0003a0005c0003t0001g0124a0010c0005t0001g0015others(41): Show | 47 | HG00423.hp2 HG00621.hp1 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.68-3547delT | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 100987060 | |||||
| chr7:100987060
|
GTTTT | G | 25 | a0001c0001t0001g0197a0001c0168t0001g0247a0008c0028t0001g0184others(22): Show | 25 | HG00642.hp1 HG00738.hp2 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.68-3550_68-3547del others(4): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 100987060 | |||||
| chr7:100987060
|
GTTTTT | G | 107 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0198others(104): Show | 113 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.68-3551_68-3547del others(5): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 100987060 | |||||
| chr7:100987060
|
GTTTTTT | G | 13 | a0025c0032t0001g0026a0029c0029t0001g0274a0044c0042t0001g0138others(10): Show | 13 | HG01168.hp2 HG01243.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.68-3552_68-3547del others(6): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 100987060 | |||||
| chr7:100987097
|
C | T | 144 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0197others(141): Show | 150 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.68-3534C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100987097 | ||||||
| chr7:100987169
|
C | T | 62 | a0002c0004t0001g0001a0002c0004t0001g0046a0002c0004t0001g0054others(59): Show | 64 | HG00099.hp2 HG00558.hp2 HG01099.hp1 others(61): Show |
intron_variant | MODIFIER | c.68-3462C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100987169 | ||||||
| chr7:100987211
|
C | T | 1 | a0049c0047t0001g0034 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.68-3420C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100987211 | ||||||
| chr7:100987239
|
G | T | 2 | a0258c0279t0001g0173a0261c0280t0001g0254 | 2 | HG02451.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.68-3392G>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100987239 | ||||||
| chr7:100987252
|
G | A | 184 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0197others(181): Show | 191 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.68-3379G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100987252 | ||||||
| chr7:100987264
|
A | G | 247 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0197others(244): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.68-3367A>G | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100987264 | ||||||
| chr7:100987399
|
T | C | 1 | a0241c0111t0001g0102 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.68-3232T>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100987399 | ||||||
| chr7:100987709
|
G | A | 175 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0197others(172): Show | 182 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.68-2922G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100987709 | ||||||
| chr7:100987748
|
A | G | 2 | a0137c0199t0001g0085a0138c0198t0001g0086 | 2 | HG02055.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.68-2883A>G | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100987748 | ||||||
| chr7:100987862
|
T | A | 1 | a0091c0140t0001g0275 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.68-2769T>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100987862 | ||||||
| chr7:100987862
|
T | C | 28 | a0033c0011t0001g0149a0033c0011t0001g0151a0034c0010t0001g0267others(25): Show | 28 | HG00642.hp2 HG00673.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.68-2769T>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100987862 | ||||||
| chr7:100987895
|
G | A | 2 | a0007c0008t0001g0010a0007c0008t0001g0078 | 3 | HG02602.hp1 HG03017.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.68-2736G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100987895 | ||||||
| chr7:100987927
|
C | T | 1 | a0099c0148t0001g0242 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.68-2704C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100987927 | ||||||
| chr7:100987952
|
C | T | 1 | a0132c0204t0001g0156 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.68-2679C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100987952 | ||||||
| chr7:100987966
|
C | T | 145 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0197others(142): Show | 151 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.68-2665C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100987966 | ||||||
| chr7:100987970
|
T | TA | 28 | a0033c0011t0001g0149a0033c0011t0001g0151a0034c0010t0001g0267others(25): Show | 28 | HG00642.hp2 HG00673.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.68-2648dupA | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 100987970 | |||||
| chr7:100988018
|
G | T | 1 | a0158c0179t0001g0074 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.68-2613G>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100988018 | ||||||
| chr7:100988075
|
A | C | 1 | a0261c0280t0001g0254 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.68-2556A>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100988075 | ||||||
| chr7:100988289
|
G | GA | 62 | a0002c0004t0001g0001a0002c0004t0001g0046a0002c0004t0001g0054others(59): Show | 64 | HG00558.hp2 HG01099.hp1 HG01123.hp2 others(61): Show |
intron_variant | MODIFIER | c.68-2320dupA | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 100988289 | |||||
| chr7:100988289
|
GA | G | 29 | a0001c0001t0001g0198a0004c0012t0001g0288a0033c0011t0001g0151others(26): Show | 29 | HG00642.hp2 HG00673.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.68-2320delA | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 100988289 | |||||
| chr7:100988289
|
GAAAAAAA others(3): Show |
G | 1 | a0171c0136t0001g0183 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.68-2329_68-2320del others(10): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 100988289 | |||||
| chr7:100988291
|
A | AC | 3 | a0007c0008t0001g0010a0007c0008t0001g0078a0094c0222t0001g0185 | 4 | HG02602.hp1 HG03017.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-2340_68-2339ins others(1): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100988291 | ||||||
| chr7:100988292
|
A | C | 13 | a0011c0009t0001g0137a0011c0009t0001g0139a0019c0033t0001g0237others(10): Show | 13 | HG00323.hp1 HG00639.hp2 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.68-2339A>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100988292 | ||||||
| chr7:100988308
|
A | G | 16 | a0007c0008t0001g0010a0007c0008t0001g0078a0011c0009t0001g0137others(13): Show | 17 | HG00323.hp1 HG00639.hp2 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.68-2323A>G | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100988308 | ||||||
| chr7:100988582
|
T | C | 5 | a0019c0033t0001g0237a0019c0033t0001g0238a0092c0141t0001g0249others(2): Show | 5 | HG02083.hp2 NA18946.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-2049T>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100988582 | ||||||
| chr7:100988640
|
T | G | 2 | a0223c0091t0001g0039a0224c0092t0001g0038 | 2 | HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.68-1991T>G | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100988640 | ||||||
| chr7:100988693
|
G | A | 1 | a0272c0041t0001g0213 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.68-1938G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100988693 | ||||||
| chr7:100988841
|
T | C | 3 | a0005c0003t0001g0003a0005c0003t0001g0124a0244c0116t0001g0120 | 5 | NA18942.hp2 NA18946.hp1 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-1790T>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100988841 | ||||||
| chr7:100989010
|
G | A | 1 | a0261c0280t0001g0254 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.68-1621G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100989010 | ||||||
| chr7:100989096
|
C | CT | 9 | a0001c0168t0001g0247a0008c0028t0001g0184a0008c0205t0001g0234others(6): Show | 9 | HG00140.hp1 HG00741.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.68-1533dupT | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 100989096 | |||||
| chr7:100989096
|
CTTCTTTT others(6): Show |
C | 2 | a0022c0025t0001g0223a0022c0025t0001g0224 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.68-1532_68-1520del others(13): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 100989096 | |||||
| chr7:100989098
|
TC | T | 3 | a0143c0195t0001g0255a0170c0137t0001g0035a0272c0041t0001g0213 | 3 | HG02258.hp2 HG02451.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.68-1532delC | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100989098 | ||||||
| chr7:100989099
|
C | CT | 20 | a0004c0012t0001g0287a0004c0012t0001g0288a0004c0013t0001g0082others(17): Show | 20 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.68-1513dupT | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 100989099 | |||||
| chr7:100989099
|
C | T | 125 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0197others(122): Show | 131 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.68-1532C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100989099 | ||||||
| chr7:100989099
|
CTT | C | 26 | a0033c0011t0001g0151a0034c0010t0001g0267a0034c0010t0001g0268others(23): Show | 26 | HG00642.hp2 HG00673.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.68-1514_68-1513del others(2): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 100989099 | |||||
| chr7:100989101
|
T | TC | 6 | a0007c0008t0001g0010a0007c0008t0001g0078a0259c0272t0001g0007others(3): Show | 7 | HG02258.hp1 HG02602.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.68-1530_68-1529ins others(1): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100989101 | ||||||
| chr7:100989113
|
T | G | 3 | a0038c0016t0001g0016a0038c0016t0001g0154a0227c0095t0001g0016 | 3 | HG01255.hp2 HG01261.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.68-1518T>G | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100989113 | ||||||
| chr7:100989131
|
C | T | 1 | a0117c0146t0001g0228 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.68-1500C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100989131 | ||||||
| chr7:100989308
|
A | G | 1 | a0224c0092t0001g0038 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.68-1323A>G | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100989308 | ||||||
| chr7:100989328
|
G | A | 1 | a0272c0041t0001g0213 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.68-1303G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100989328 | ||||||
| chr7:100989446
|
A | G | 1 | a0003c0254t0001g0051 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.68-1185A>G | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100989446 | ||||||
| chr7:100989463
|
C | A | 8 | a0004c0012t0001g0287a0004c0012t0001g0288a0004c0013t0001g0082others(5): Show | 8 | HG02109.hp1 HG02630.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.68-1168C>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100989463 | ||||||
| chr7:100989509
|
C | T | 317 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0197others(314): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.68-1122C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100989509 | ||||||
| chr7:100989510
|
G | T | 5 | a0267c0285t0001g0289a0268c0283t0001g0100a0269c0284t0001g0101others(2): Show | 5 | HG01884.hp2 HG02257.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-1121G>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100989510 | ||||||
| chr7:100989516
|
G | T | 1 | a0258c0279t0001g0173 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.68-1115G>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100989516 | ||||||
| chr7:100989698
|
AT | A | 133 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0197others(130): Show | 141 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.68-921delT | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 100989698 | |||||
| chr7:100989707
|
T | G | 1 | a0202c0132t0001g0040 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.68-924T>G | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100989707 | ||||||
| chr7:100989934
|
C | T | 8 | a0010c0005t0001g0015a0010c0005t0001g0147a0039c0015t0001g0155others(5): Show | 9 | HG01081.hp1 HG01192.hp2 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.68-697C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100989934 | ||||||
| chr7:100990112
|
A | G | 1 | a0049c0047t0001g0034 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.68-519A>G | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100990112 | ||||||
| chr7:100990140
|
C | T | 2 | a0090c0223t0001g0070a0167c0219t0001g0227 | 2 | HG00408.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.68-491C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100990140 | ||||||
| chr7:100990311
|
C | T | 6 | a0001c0001t0001g0004a0001c0001t0001g0252a0136c0166t0001g0253others(3): Show | 7 | NA18942.hp1 NA18947.hp2 NA18964.hp2 others(4): Show |
intron_variant | MODIFIER | c.68-320C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100990311 | ||||||
| chr7:100990546
|
C | A | 13 | a0033c0011t0001g0149a0033c0011t0001g0151a0178c0068t0001g0158others(10): Show | 13 | HG01109.hp2 HG02559.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.68-85C>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100990546 | ||||||
| chr7:100990563
|
G | A | 8 | a0004c0012t0001g0287a0004c0012t0001g0288a0004c0013t0001g0082others(5): Show | 8 | HG02109.hp1 HG02630.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.68-68G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100990563 | ||||||
| chr7:100990563
|
G | C | 1 | a0149c0185t0001g0175 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.68-68G>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100990563 | ||||||
| chr7:100990572
|
C | A | 2 | a0258c0279t0001g0173a0261c0280t0001g0254 | 2 | HG02451.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.68-59C>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 1/11 | chr7 | 100990572 | ||||||
| chr7:101005586
|
C | T | 3 | a0034c0010t0001g0267a0034c0010t0001g0268a0189c0058t0001g0269 | 3 | HG01106.hp1 HG01515.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.14956+67C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/11 | chr7 | 101005586 | ||||||
| chr7:101005594
|
A | T | 43 | a0033c0011t0001g0149a0033c0011t0001g0151a0034c0010t0001g0267others(40): Show | 43 | HG00642.hp2 HG00673.hp1 HG01106.hp1 others(40): Show |
intron_variant | MODIFIER | c.14956+75A>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/11 | chr7 | 101005594 | ||||||
| chr7:101005800
|
AT | A | 31 | a0002c0004t0001g0054a0004c0012t0001g0287a0004c0012t0001g0288others(28): Show | 31 | HG01884.hp2 HG02071.hp2 HG02109.hp1 others(28): Show |
intron_variant | MODIFIER | c.14956+296delT | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 101005800 | |||||
| chr7:101005800
|
ATT | A | 91 | a0002c0004t0001g0001a0002c0004t0001g0046a0002c0007t0001g0001others(88): Show | 94 | HG00099.hp2 HG00558.hp2 HG00642.hp2 others(91): Show |
intron_variant | MODIFIER | c.14956+295_14956+29 others(6): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 101005800 | |||||
| chr7:101005800
|
ATTT | A | 144 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0197others(141): Show | 150 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.14956+294_14956+29 others(7): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 101005800 | |||||
| chr7:101005851
|
G | C | 72 | a0002c0004t0001g0001a0002c0004t0001g0046a0002c0004t0001g0054others(69): Show | 75 | HG00099.hp2 HG00558.hp2 HG01099.hp1 others(72): Show |
intron_variant | MODIFIER | c.14956+332G>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/11 | chr7 | 101005851 | ||||||
| chr7:101006083
|
C | T | 64 | a0002c0004t0001g0001a0002c0004t0001g0046a0002c0004t0001g0054others(61): Show | 67 | HG00099.hp2 HG00558.hp2 HG01099.hp1 others(64): Show |
intron_variant | MODIFIER | c.14957-388C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/11 | chr7 | 101006083 | ||||||
| chr7:101006088
|
G | A | 28 | a0033c0011t0001g0149a0033c0011t0001g0151a0034c0010t0001g0267others(25): Show | 28 | HG00642.hp2 HG00673.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.14957-383G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/11 | chr7 | 101006088 | ||||||
| chr7:101006090
|
G | T | 64 | a0002c0004t0001g0001a0002c0004t0001g0046a0002c0004t0001g0054others(61): Show | 67 | HG00099.hp2 HG00558.hp2 HG01099.hp1 others(64): Show |
intron_variant | MODIFIER | c.14957-381G>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/11 | chr7 | 101006090 | ||||||
| chr7:101006107
|
C | G | 5 | a0267c0285t0001g0289a0268c0283t0001g0100a0269c0284t0001g0101others(2): Show | 5 | HG01884.hp2 HG02257.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.14957-364C>G | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/11 | chr7 | 101006107 | ||||||
| chr7:101006158
|
C | G | 1 | a0173c0134t0001g0209 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.14957-313C>G | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/11 | chr7 | 101006158 | ||||||
| chr7:101006396
|
G | T | 3 | a0123c0215t0001g0005a0124c0214t0001g0005a0125c0213t0001g0005 | 3 | HG02257.hp1 HG03139.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.14957-75G>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 2/11 | chr7 | 101006396 | ||||||
| chr7:101006790
|
T | A | 1 | a0244c0116t0001g0120 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.15058+218T>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 3/11 | chr7 | 101006790 | ||||||
| chr7:101006792
|
A | T | 1 | a0244c0116t0001g0120 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.15058+220A>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 3/11 | chr7 | 101006792 | ||||||
| chr7:101007099
|
G | C | 247 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0197others(244): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.15058+527G>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 3/11 | chr7 | 101007099 | ||||||
| chr7:101007105
|
T | C | 1 | a0006c0038t0001g0047 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.15058+533T>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 3/11 | chr7 | 101007105 | ||||||
| chr7:101007248
|
C | T | 1 | a0254c0125t0001g0090 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.15058+676C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 3/11 | chr7 | 101007248 | ||||||
| chr7:101007438
|
C | T | 8 | a0258c0279t0001g0173a0259c0272t0001g0007a0260c0273t0001g0007others(5): Show | 8 | HG02258.hp1 HG02622.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.15058+866C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 3/11 | chr7 | 101007438 | ||||||
| chr7:101007660
|
C | T | 2 | a0267c0285t0001g0289a0268c0283t0001g0100 | 2 | HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.15059-974C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 3/11 | chr7 | 101007660 | ||||||
| chr7:101007707
|
T | C | 1 | a0004c0013t0001g0082 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.15059-927T>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 3/11 | chr7 | 101007707 | ||||||
| chr7:101007727
|
C | T | 3 | a0004c0013t0001g0082a0004c0013t0001g0084a0004c0079t0001g0083 | 3 | HG02109.hp1 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.15059-907C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 3/11 | chr7 | 101007727 | ||||||
| chr7:101007815
|
A | T | 254 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0197others(251): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.15059-819A>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 3/11 | chr7 | 101007815 | ||||||
| chr7:101007948
|
T | C | 252 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0197others(249): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.15059-686T>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 3/11 | chr7 | 101007948 | ||||||
| chr7:101007963
|
A | AT | 83 | a0002c0004t0001g0001a0002c0004t0001g0046a0002c0007t0001g0001others(80): Show | 86 | HG00099.hp2 HG00558.hp2 HG00642.hp2 others(83): Show |
intron_variant | MODIFIER | c.15059-657dupT | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 101007963 | |||||
| chr7:101008005
|
C | T | 5 | a0267c0285t0001g0289a0268c0283t0001g0100a0269c0284t0001g0101others(2): Show | 5 | HG01884.hp2 HG02257.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.15059-629C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 3/11 | chr7 | 101008005 | ||||||
| chr7:101008094
|
G | A | 2 | a0206c0077t0001g0123a0248c0121t0001g0278 | 2 | HG02071.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.15059-540G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 3/11 | chr7 | 101008094 | ||||||
| chr7:101008113
|
A | G | 1 | a0034c0010t0001g0268 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.15059-521A>G | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 3/11 | chr7 | 101008113 | ||||||
| chr7:101008191
|
A | C | 145 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0197others(142): Show | 151 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.15059-443A>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 3/11 | chr7 | 101008191 | ||||||
| chr7:101008211
|
C | G | 7 | a0259c0272t0001g0007a0260c0273t0001g0007a0262c0274t0001g0294others(4): Show | 7 | HG02258.hp1 HG02622.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.15059-423C>G | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 3/11 | chr7 | 101008211 | ||||||
| chr7:101008523
|
C | T | 1 | a0082c0233t0001g0226 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.15059-111C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 3/11 | chr7 | 101008523 | ||||||
| chr7:101008546
|
A | C | 1 | a0261c0280t0001g0254 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.15059-88A>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 3/11 | chr7 | 101008546 | ||||||
| chr7:101008548
|
G | T | 1 | a0200c0049t0001g0106 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.15059-86G>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 3/11 | chr7 | 101008548 | ||||||
| chr7:101008574
|
A | G | 146 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0197others(143): Show | 152 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.15059-60A>G | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 3/11 | chr7 | 101008574 | ||||||
| chr7:101008826
|
C | T | 7 | a0259c0272t0001g0007a0260c0273t0001g0007a0262c0274t0001g0294others(4): Show | 7 | HG02258.hp1 HG02622.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.15186+65C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 4/11 | chr7 | 101008826 | ||||||
| chr7:101008900
|
G | A | 156 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0197others(153): Show | 162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.15186+139G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 4/11 | chr7 | 101008900 | ||||||
| chr7:101009036
|
T | G | 157 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0197others(154): Show | 163 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.15187-59T>G | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 4/11 | chr7 | 101009036 | ||||||
| chr7:101009362
|
C | T | 1 | a0197c0059t0001g0265 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.15251+203C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 5/11 | chr7 | 101009362 | ||||||
| chr7:101009374
|
G | A | 1 | a0004c0079t0001g0083 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.15251+215G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 5/11 | chr7 | 101009374 | ||||||
| chr7:101009746
|
G | A | 14 | a0004c0013t0001g0082a0004c0013t0001g0084a0004c0079t0001g0083others(11): Show | 14 | HG01243.hp2 HG02055.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.15251+587G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 5/11 | chr7 | 101009746 | ||||||
| chr7:101009829
|
C | T | 1 | a0258c0279t0001g0173 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.15251+670C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 5/11 | chr7 | 101009829 | ||||||
| chr7:101010170
|
C | T | 14 | a0011c0009t0001g0137a0011c0009t0001g0139a0019c0033t0001g0237others(11): Show | 14 | HG00323.hp1 HG00639.hp2 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.15251+1011C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 5/11 | chr7 | 101010170 | ||||||
| chr7:101010224
|
A | G | 11 | a0014c0036t0001g0006a0014c0036t0001g0027a0048c0046t0001g0299others(8): Show | 11 | HG01884.hp1 HG01952.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.15251+1065A>G | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 5/11 | chr7 | 101010224 | ||||||
| chr7:101010227
|
G | C | 5 | a0011c0009t0001g0137a0011c0009t0001g0139a0044c0042t0001g0138others(2): Show | 5 | HG00323.hp1 HG00639.hp2 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.15251+1068G>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 5/11 | chr7 | 101010227 | ||||||
| chr7:101010319
|
G | A | 1 | a0216c0084t0001g0079 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.15251+1160G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 5/11 | chr7 | 101010319 | ||||||
| chr7:101010485
|
C | T | 11 | a0014c0036t0001g0006a0014c0036t0001g0027a0048c0046t0001g0299others(8): Show | 11 | HG01884.hp1 HG01952.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.15251+1326C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 5/11 | chr7 | 101010485 | ||||||
| chr7:101010584
|
C | T | 1 | a0049c0047t0001g0034 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.15251+1425C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 5/11 | chr7 | 101010584 | ||||||
| chr7:101010930
|
G | A | 5 | a0004c0012t0001g0287a0004c0012t0001g0288a0036c0014t0001g0290others(2): Show | 5 | HG02630.hp1 HG02717.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.15252-1366G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 5/11 | chr7 | 101010930 | ||||||
| chr7:101011173
|
C | G | 1 | a0001c0181t0001g0069 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.15252-1123C>G | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 5/11 | chr7 | 101011173 | ||||||
| chr7:101011362
|
C | T | 1 | a0173c0134t0001g0209 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.15252-934C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 5/11 | chr7 | 101011362 | ||||||
| chr7:101011409
|
A | G | 2 | a0104c0154t0001g0208a0174c0268t0001g0207 | 2 | HG00423.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.15252-887A>G | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 5/11 | chr7 | 101011409 | ||||||
| chr7:101011638
|
T | C | 1 | a0261c0280t0001g0254 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.15252-658T>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 5/11 | chr7 | 101011638 | ||||||
| chr7:101011682
|
A | C | 3 | a0190c0050t0001g0266a0192c0051t0001g0262a0193c0053t0001g0263 | 3 | HG01361.hp2 HG01978.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.15252-614A>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 5/11 | chr7 | 101011682 | ||||||
| chr7:101011709
|
A | C | 10 | a0258c0279t0001g0173a0259c0272t0001g0007a0260c0273t0001g0007others(7): Show | 10 | HG02258.hp1 HG02258.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.15252-587A>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 5/11 | chr7 | 101011709 | ||||||
| chr7:101011712
|
G | A | 1 | a0049c0047t0001g0034 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.15252-584G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 5/11 | chr7 | 101011712 | ||||||
| chr7:101011772
|
T | A | 1 | a0092c0141t0001g0249 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.15252-524T>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 5/11 | chr7 | 101011772 | ||||||
| chr7:101011798
|
CCCTTGGT others(3): Show |
C | 5 | a0008c0028t0001g0184a0012c0040t0001g0017a0062c0260t0001g0052others(2): Show | 6 | HG02015.hp1 NA18980.hp2 NA18984.hp1 others(3): Show |
intron_variant | MODIFIER | c.15252-496_15252-48 others(14): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr7 | 101011798 | |||||
| chr7:101011826
|
T | C | 1 | a0193c0053t0001g0263 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.15252-470T>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 5/11 | chr7 | 101011826 | ||||||
| chr7:101011998
|
C | T | 2 | a0259c0272t0001g0007a0260c0273t0001g0007 | 2 | HG02622.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.15252-298C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 5/11 | chr7 | 101011998 | ||||||
| chr7:101012083
|
G | A | 6 | a0011c0009t0001g0137a0011c0009t0001g0139a0044c0042t0001g0138others(3): Show | 6 | HG00323.hp1 HG00639.hp2 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.15252-213G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 5/11 | chr7 | 101012083 | ||||||
| chr7:101012136
|
C | G | 1 | a0002c0245t0001g0050 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.15252-160C>G | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 5/11 | chr7 | 101012136 | ||||||
| chr7:101012156
|
G | A | 1 | a0049c0047t0001g0034 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.15252-140G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 5/11 | chr7 | 101012156 | ||||||
| chr7:101012722
|
G | C | 149 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0197others(146): Show | 155 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.15404-97G>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 6/11 | chr7 | 101012722 | ||||||
| chr7:101012897
|
G | A | 2 | a0219c0088t0001g0081a0220c0087t0001g0091 | 2 | HG01106.hp2 HG01515.hp1 |
splice_region_variant&intron_variant | LOW | c.15475+7G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 7/11 | chr7 | 101012897 | ||||||
| chr7:101013427
|
G | GTATCTC | 3 | a0049c0047t0001g0034a0258c0279t0001g0173a0261c0280t0001g0254 | 3 | HG02451.hp2 HG03130.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.15638+303_15638+30 others(10): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr7 | 101013427 | |||||
| chr7:101014201
|
T | C | 2 | a0130c0207t0001g0023a0131c0206t0001g0023 | 2 | HG02622.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.15800+127T>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 9/11 | chr7 | 101014201 | ||||||
| chr7:101014290
|
G | A | 4 | a0030c0027t0001g0141a0030c0027t0001g0239a0164c0192t0001g0201others(1): Show | 4 | HG00140.hp2 HG00642.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.15800+216G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 9/11 | chr7 | 101014290 | ||||||
| chr7:101014777
|
C | CTTAAA | 26 | a0004c0012t0001g0287a0004c0012t0001g0288a0014c0036t0001g0006others(23): Show | 26 | HG01884.hp1 HG01934.hp2 HG01952.hp2 others(23): Show |
intron_variant | MODIFIER | c.15800+745_15800+74 others(9): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr7 | 101014777 | |||||
| chr7:101014777
|
C | CTTAAATT others(3): Show |
8 | a0200c0049t0001g0106a0223c0091t0001g0039a0240c0108t0001g0032others(5): Show | 8 | HG02258.hp1 HG02572.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.15800+740_15800+74 others(14): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr7 | 101014777 | |||||
| chr7:101014777
|
CTTAAA | C | 180 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0197others(177): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.15800+745_15800+74 others(9): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr7 | 101014777 | |||||
| chr7:101014777
|
CTTAAATT others(3): Show |
C | 1 | a0008c0028t0001g0169 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.15800+740_15800+74 others(14): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr7 | 101014777 | |||||
| chr7:101014777
|
CTTAAATT others(8): Show |
C | 3 | a0106c0152t0001g0210a0177c0072t0001g0281a0213c0097t0001g0152 | 3 | HG00140.hp1 HG01361.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.15800+735_15800+74 others(19): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr7 | 101014777 | |||||
| chr7:101014858
|
G | A | 1 | a0174c0268t0001g0207 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.15801-757G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 9/11 | chr7 | 101014858 | ||||||
| chr7:101015026
|
C | T | 6 | a0258c0279t0001g0173a0267c0285t0001g0289a0268c0283t0001g0100others(3): Show | 6 | HG01884.hp2 HG02257.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.15801-589C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 9/11 | chr7 | 101015026 | ||||||
| chr7:101015211
|
G | C | 1 | a0049c0047t0001g0034 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.15801-404G>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 9/11 | chr7 | 101015211 | ||||||
| chr7:101015214
|
C | T | 1 | a0015c0242t0001g0053 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.15801-401C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 9/11 | chr7 | 101015214 | ||||||
| chr7:101015330
|
C | G | 1 | a0058c0259t0001g0064 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.15801-285C>G | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 9/11 | chr7 | 101015330 | ||||||
| chr7:101015361
|
C | T | 7 | a0027c0031t0001g0190a0027c0031t0001g0192a0028c0030t0001g0157others(4): Show | 7 | HG02451.hp1 HG02486.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.15801-254C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 9/11 | chr7 | 101015361 | ||||||
| chr7:101015436
|
T | C | 165 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0197others(162): Show | 171 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.15801-179T>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 9/11 | chr7 | 101015436 | ||||||
| chr7:101015540
|
A | C | 2 | a0176c0073t0001g0148a0177c0072t0001g0281 | 2 | HG02280.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.15801-75A>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 9/11 | chr7 | 101015540 | ||||||
| chr7:101015732
|
G | A | 2 | a0209c0082t0001g0145a0210c0081t0001g0093 | 2 | HG02572.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.15877+41G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 10/11 | chr7 | 101015732 | ||||||
| chr7:101015749
|
C | T | 1 | a0200c0049t0001g0106 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.15877+58C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 10/11 | chr7 | 101015749 | ||||||
| chr7:101015765
|
G | A | 1 | a0122c0216t0001g0296 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.15877+74G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 10/11 | chr7 | 101015765 | ||||||
| chr7:101015823
|
T | C | 164 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0197others(161): Show | 170 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.15877+132T>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 10/11 | chr7 | 101015823 | ||||||
| chr7:101015830
|
C | T | 1 | a0272c0041t0001g0213 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.15877+139C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 10/11 | chr7 | 101015830 | ||||||
| chr7:101015841
|
C | T | 14 | a0258c0279t0001g0173a0259c0272t0001g0007a0260c0273t0001g0007others(11): Show | 14 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.15877+150C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 10/11 | chr7 | 101015841 | ||||||
| chr7:101015914
|
C | G | 2 | a0215c0096t0001g0036a0225c0093t0001g0037 | 2 | HG02970.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.15877+223C>G | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 10/11 | chr7 | 101015914 | ||||||
| chr7:101016438
|
G | A | 1 | a0100c0157t0001g0179 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.15877+747G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 10/11 | chr7 | 101016438 | ||||||
| chr7:101016540
|
C | G | 1 | a0219c0088t0001g0081 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.15877+849C>G | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 10/11 | chr7 | 101016540 | ||||||
| chr7:101016611
|
G | A | 1 | a0026c0202t0001g0196 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.15877+920G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 10/11 | chr7 | 101016611 | ||||||
| chr7:101016701
|
G | T | 1 | a0229c0101t0001g0118 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.15878-874G>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 10/11 | chr7 | 101016701 | ||||||
| chr7:101016702
|
G | T | 80 | a0002c0004t0001g0001a0002c0004t0001g0046a0002c0004t0001g0054others(77): Show | 83 | HG00099.hp2 HG00558.hp2 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.15878-873G>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 10/11 | chr7 | 101016702 | ||||||
| chr7:101016720
|
C | T | 2 | a0022c0025t0001g0223a0022c0025t0001g0224 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.15878-855C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 10/11 | chr7 | 101016720 | ||||||
| chr7:101016832
|
G | C | 2 | a0093c0142t0001g0094a0152c0176t0001g0233 | 2 | HG01123.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.15878-743G>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 10/11 | chr7 | 101016832 | ||||||
| chr7:101017008
|
C | A | 1 | a0270c0282t0001g0098 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.15878-567C>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 10/11 | chr7 | 101017008 | ||||||
| chr7:101017009
|
C | G | 1 | a0153c0183t0001g0246 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.15878-566C>G | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 10/11 | chr7 | 101017009 | ||||||
| chr7:101017032
|
A | G | 12 | a0184c0064t0001g0159a0258c0279t0001g0173a0262c0274t0001g0294others(9): Show | 12 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.15878-543A>G | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 10/11 | chr7 | 101017032 | ||||||
| chr7:101017175
|
A | G | 1 | a0089c0224t0001g0068 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.15878-400A>G | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 10/11 | chr7 | 101017175 | ||||||
| chr7:101017358
|
C | G | 15 | a0015c0240t0001g0048a0034c0010t0001g0267a0034c0010t0001g0268others(12): Show | 15 | HG00673.hp1 HG00738.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.15878-217C>G | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 10/11 | chr7 | 101017358 | ||||||
| chr7:101017382
|
G | A | 2 | a0196c0056t0001g0264a0197c0059t0001g0265 | 2 | HG02630.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.15878-193G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 10/11 | chr7 | 101017382 | ||||||
| chr7:101017430
|
G | T | 2 | a0142c0194t0001g0256a0143c0195t0001g0255 | 2 | HG02451.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.15878-145G>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 10/11 | chr7 | 101017430 | ||||||
| chr7:101017732
|
C | CGGGACTC others(12): Show |
6 | a0016c0035t0001g0258a0016c0035t0001g0259a0076c0239t0001g0186others(3): Show | 6 | HG00099.hp2 HG01168.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.15966+99_15966+117 others(22): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr7 | 101017732 | |||||
| chr7:101017732
|
CGGGACTC others(12): Show |
C | 58 | a0004c0012t0001g0287a0004c0012t0001g0288a0005c0003t0001g0003others(55): Show | 60 | HG00423.hp2 HG00621.hp1 HG01928.hp1 others(57): Show |
intron_variant | MODIFIER | c.15966+99_15966+117 others(22): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr7 | 101017732 | |||||
| chr7:101017769
|
C | T | 1 | a0129c0209t0001g0127 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.15966+106C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | chr7 | 101017769 | ||||||
| chr7:101017817
|
C | A | 1 | a0160c0190t0001g0164 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.15966+154C>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | chr7 | 101017817 | ||||||
| chr7:101017844
|
C | A | 1 | a0200c0049t0001g0106 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.15966+181C>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | chr7 | 101017844 | ||||||
| chr7:101017851
|
T | TTTCCCCC others(73): Show |
1 | a0165c0193t0001g0194 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.15966+215_15966+21 others(84): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr7 | 101017851 | |||||
| chr7:101017852
|
TTCCCCCT others(13): Show |
T | 10 | a0008c0205t0001g0234a0014c0036t0001g0006a0014c0036t0001g0027others(7): Show | 10 | HG01884.hp1 HG01952.hp2 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.15966+202_15966+22 others(24): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr7 | 101017852 | |||||
| chr7:101017878
|
CT | C | 143 | a0002c0004t0001g0001a0002c0004t0001g0046a0002c0004t0001g0054others(140): Show | 148 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(145): Show |
intron_variant | MODIFIER | c.15966+216delT | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | chr7 | 101017878 | ||||||
| chr7:101017892
|
C | T | 10 | a0008c0205t0001g0234a0014c0036t0001g0006a0014c0036t0001g0027others(7): Show | 10 | HG01884.hp1 HG01952.hp2 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.15966+229C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | chr7 | 101017892 | ||||||
| chr7:101017905
|
C | T | 1 | a0164c0192t0001g0201 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.15966+242C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | chr7 | 101017905 | ||||||
| chr7:101017919
|
CT | C | 152 | a0002c0004t0001g0001a0002c0004t0001g0046a0002c0004t0001g0054others(149): Show | 157 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(154): Show |
intron_variant | MODIFIER | c.15966+257delT | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | chr7 | 101017919 | ||||||
| chr7:101017946
|
T | C | 155 | a0002c0004t0001g0001a0002c0004t0001g0046a0002c0004t0001g0054others(152): Show | 160 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.15966+283T>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | chr7 | 101017946 | ||||||
| chr7:101017960
|
CT | C | 10 | a0008c0205t0001g0234a0014c0036t0001g0006a0014c0036t0001g0027others(7): Show | 10 | HG01884.hp1 HG01952.hp2 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.15966+298delT | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | chr7 | 101017960 | ||||||
| chr7:101017961
|
T | TGGGACCC others(33): Show |
1 | a0164c0192t0001g0201 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.15966+299_15966+33 others(44): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr7 | 101017961 | |||||
| chr7:101017961
|
T | TGGGACCC others(318): Show |
1 | a0160c0190t0001g0164 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.15966+358_15966+35 others(329): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr7 | 101017961 | |||||
| chr7:101017961
|
T | TGGGACCC others(73): Show |
1 | a0171c0136t0001g0183 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.15966+299_15966+37 others(84): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr7 | 101017961 | |||||
| chr7:101017961
|
T | TGGGACCC others(74): Show |
160 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0197others(157): Show | 166 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.15966+299_15966+37 others(85): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr7 | 101017961 | |||||
| chr7:101017965
|
A | ACCCCTTC others(75): Show |
1 | a0028c0030t0001g0257 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.15966+379_15966+38 others(86): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr7 | 101017965 | |||||
| chr7:101017987
|
C | T | 1 | a0204c0128t0001g0108 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.15966+324C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | chr7 | 101017987 | ||||||
| chr7:101017992
|
TCCCTCCC others(158): Show |
T | 1 | a0229c0101t0001g0118 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.15966+401_15967-36 others(4): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr7 | 101017992 | |||||
| chr7:101018018
|
C | CCCCCTGG others(74): Show |
1 | a0020c0023t0001g0188 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.15966+379_15966+38 others(85): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr7 | 101018018 | |||||
| chr7:101018028
|
C | T | 42 | a0005c0003t0001g0003a0005c0003t0001g0124a0035c0020t0001g0121others(39): Show | 44 | HG00423.hp2 HG00621.hp1 HG01928.hp1 others(41): Show |
intron_variant | MODIFIER | c.15966+365C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | chr7 | 101018028 | ||||||
| chr7:101018033
|
TCCCTCCC others(117): Show |
T | 1 | a0204c0128t0001g0108 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.15966+431_15967-37 others(4): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr7 | 101018033 | |||||
| chr7:101018042
|
CT | C | 10 | a0001c0181t0001g0069a0010c0005t0001g0015a0010c0005t0001g0147others(7): Show | 11 | HG01081.hp1 HG01192.hp2 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.15966+380delT | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | chr7 | 101018042 | ||||||
| chr7:101018065
|
GGGACTCC others(33): Show |
G | 85 | a0002c0004t0001g0001a0002c0004t0001g0046a0002c0004t0001g0054others(82): Show | 88 | HG00558.hp2 HG00673.hp1 HG01099.hp1 others(85): Show |
intron_variant | MODIFIER | c.15966+406_15966+44 others(44): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr7 | 101018065 | |||||
| chr7:101018069
|
C | T | 11 | a0004c0012t0001g0287a0004c0012t0001g0288a0016c0035t0001g0258others(8): Show | 11 | HG00099.hp2 HG01168.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.15966+406C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | chr7 | 101018069 | ||||||
| chr7:101018074
|
TCCCTCCC others(76): Show |
T | 40 | a0005c0003t0001g0003a0005c0003t0001g0124a0035c0020t0001g0121others(37): Show | 42 | HG00423.hp2 HG00621.hp1 HG01928.hp1 others(39): Show |
intron_variant | MODIFIER | c.15966+431_15967-41 others(87): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr7 | 101018074 | |||||
| chr7:101018092
|
C | CT | 197 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0197others(194): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.15966+430dupT | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr7 | 101018092 | |||||
| chr7:101018092
|
C | CTTCCCTT others(77): Show |
1 | a0095c0221t0001g0236 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.15966+430_15966+43 others(88): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr7 | 101018092 | |||||
| chr7:101018092
|
CTCCCTTC others(34): Show |
C | 4 | a0035c0020t0001g0122a0264c0276t0001g0096a0265c0278t0001g0097others(1): Show | 4 | HG02723.hp2 HG03098.hp2 NA19088.hp1 others(1): Show |
intron_variant | MODIFIER | c.15966+434_15967-45 others(45): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr7 | 101018092 | |||||
| chr7:101018104
|
C | T | 198 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0197others(195): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.15966+441C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | chr7 | 101018104 | ||||||
| chr7:101018105
|
T | G | 198 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0197others(195): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.15966+442T>G | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | chr7 | 101018105 | ||||||
| chr7:101018109
|
T | C | 23 | a0001c0181t0001g0069a0004c0012t0001g0287a0004c0012t0001g0288others(20): Show | 24 | HG00099.hp2 HG01081.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.15966+446T>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | chr7 | 101018109 | ||||||
| chr7:101018134
|
TC | T | 282 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0197others(279): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.15967-457delC | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr7 | 101018134 | |||||
| chr7:101018135
|
C | T | 4 | a0035c0020t0001g0122a0264c0276t0001g0096a0265c0278t0001g0097others(1): Show | 4 | HG02723.hp2 HG03098.hp2 NA19088.hp1 others(1): Show |
intron_variant | MODIFIER | c.15967-460C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | chr7 | 101018135 | ||||||
| chr7:101018141
|
C | T | 1 | a0206c0077t0001g0123 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.15967-454C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | chr7 | 101018141 | ||||||
| chr7:101018146
|
T | A | 1 | a0206c0077t0001g0123 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.15967-449T>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | chr7 | 101018146 | ||||||
| chr7:101018155
|
CTCCCCTC others(55): Show |
C | 1 | a0206c0077t0001g0123 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.15967-435_15967-37 others(66): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr7 | 101018155 | |||||
| chr7:101018156
|
TC | T | 286 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0197others(283): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.15967-435delC | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr7 | 101018156 | |||||
| chr7:101018182
|
TC | T | 11 | a0004c0012t0001g0287a0004c0012t0001g0288a0016c0035t0001g0258others(8): Show | 11 | HG00099.hp2 HG01168.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.15967-408delC | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr7 | 101018182 | |||||
| chr7:101018188
|
T | A | 11 | a0004c0012t0001g0287a0004c0012t0001g0288a0016c0035t0001g0258others(8): Show | 11 | HG00099.hp2 HG01168.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.15967-407T>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | chr7 | 101018188 | ||||||
| chr7:101018193
|
C | T | 1 | a0001c0181t0001g0069 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.15967-402C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | chr7 | 101018193 | ||||||
| chr7:101018197
|
CTCCCTCC others(13): Show |
C | 11 | a0004c0012t0001g0287a0004c0012t0001g0288a0016c0035t0001g0258others(8): Show | 11 | HG00099.hp2 HG01168.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.15967-392_15967-37 others(24): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr7 | 101018197 | |||||
| chr7:101018214
|
C | CCCCTTCC others(14): Show |
1 | a0217c0085t0001g0153 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.15967-379_15967-37 others(25): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr7 | 101018214 | |||||
| chr7:101018217
|
T | C | 1 | a0217c0085t0001g0153 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.15967-378T>C | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | chr7 | 101018217 | ||||||
| chr7:101018217
|
T | TTCCCTTC others(13): Show |
292 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0197others(289): Show | 304 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(301): Show |
intron_variant | MODIFIER | c.15967-368_15967-36 others(24): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr7 | 101018217 | |||||
| chr7:101018217
|
T | TTCCCTTC others(54): Show |
1 | a0144c0191t0001g0104 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.15967-367_15967-36 others(65): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr7 | 101018217 | |||||
| chr7:101018217
|
T | TTCCCTTC others(95): Show |
1 | a0001c0181t0001g0069 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.15967-367_15967-36 others(106): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr7 | 101018217 | |||||
| chr7:101018228
|
C | A | 10 | a0103c0150t0001g0165a0229c0101t0001g0118a0233c0119t0001g0116others(7): Show | 10 | HG00099.hp1 HG02165.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.15967-367C>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | chr7 | 101018228 | ||||||
| chr7:101018249
|
G | A | 5 | a0004c0012t0001g0287a0004c0012t0001g0288a0036c0014t0001g0290others(2): Show | 5 | HG02630.hp1 HG02717.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.15967-346G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | chr7 | 101018249 | ||||||
| chr7:101018249
|
G | GGGACTCC others(11): Show |
5 | a0234c0107t0001g0112a0235c0105t0001g0110a0236c0106t0001g0117others(2): Show | 5 | HG02165.hp2 NA18941.hp1 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.15967-332_15967-31 others(22): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr7 | 101018249 | |||||
| chr7:101018249
|
GGGACTCC others(11): Show |
G | 1 | a0272c0041t0001g0213 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.15967-332_15967-31 others(22): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr7 | 101018249 | |||||
| chr7:101018278
|
C | T | 1 | a0194c0054t0001g0178 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.15967-317C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | chr7 | 101018278 | ||||||
| chr7:101018311
|
A | ACTCTCCC others(13): Show |
4 | a0011c0009t0001g0137a0011c0009t0001g0139a0045c0044t0001g0140others(1): Show | 4 | HG00323.hp1 HG00639.hp2 HG01074.hp2 others(1): Show |
intron_variant | MODIFIER | c.15967-282_15967-26 others(24): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr7 | 101018311 | |||||
| chr7:101018379
|
C | T | 1 | a0233c0119t0001g0116 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.15967-216C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | chr7 | 101018379 | ||||||
| chr7:101018410
|
C | A | 2 | a0137c0199t0001g0085a0138c0198t0001g0086 | 2 | HG02055.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.15967-185C>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | chr7 | 101018410 | ||||||
| chr7:101018430
|
C | A | 1 | a0261c0280t0001g0254 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.15967-165C>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | chr7 | 101018430 | ||||||
| chr7:101018434
|
CCCCGCCA others(11): Show |
C | 3 | a0011c0009t0001g0137a0011c0009t0001g0139a0046c0045t0001g0142 | 3 | HG00639.hp2 HG01074.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.15967-157_15967-14 others(22): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr7 | 101018434 | |||||
| chr7:101018455
|
C | T | 1 | a0138c0198t0001g0086 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.15967-140C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | chr7 | 101018455 | ||||||
| chr7:101018457
|
AGGACTCC others(13): Show |
A | 17 | a0014c0036t0001g0006a0014c0036t0001g0027a0029c0029t0001g0274others(14): Show | 17 | HG01884.hp1 HG02258.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.15967-115_15967-96 others(23): Show |
MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr7 | 101018457 | |||||
| chr7:101018492
|
C | T | 1 | a0085c0229t0001g0076 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.15967-103C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | chr7 | 101018492 | ||||||
| chr7:101018507
|
C | T | 1 | a0093c0142t0001g0094 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.15967-88C>T | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | chr7 | 101018507 | ||||||
| chr7:101018586
|
G | A | 2 | a0037c0017t0001g0231a0037c0017t0001g0232 | 2 | HG01069.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.15967-9G>A | MUC12 | ENSG00000205277.10 | transcript | ENST00000536621.6 | protein_coding | 11/11 | chr7 | 101018586 |