Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 160418 |
| ensemblid | ENSG00000139324.12 |
| hgncid | 26899 |
| symbol | TMTC3 |
| name | transmembrane O-mannosyltransferase targeting cadherins 3 |
| refseq_nuc | NM_181783.4 |
| refseq_prot | NP_861448.2 |
| ensembl_nuc | ENST00000266712.11 |
| ensembl_prot | ENSP00000266712.6 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 88142307 |
| end | 88199887 |
| strand | + |
| ver | v1.2 |
| region | chr12:88142307-88199887 |
| region5000 | chr12:88137307-88204887 |
| regionname0 | TMTC3_chr12_88142307_88199887 |
| regionname5000 | TMTC3_chr12_88137307_88204887 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 914 | 217 | 75 | 38 | 72 | 8 | 22 | 54 | TMTC3_chr12_88137307_88204887 | TMTC3 | MANIN others(909): Show |
chr12 | 88137307 | 88204887 |
| a0002 | 0/0 | 914 | 17 | 8 | 0 | 9 | 0 | 0 | 7 | TMTC3_chr12_88137307_88204887 | TMTC3 | MANIN others(909): Show |
chr12 | 88137307 | 88204887 |
| a0003 | 0/0 | 914 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | MANIN others(909): Show |
chr12 | 88137307 | 88204887 |
| a0004 | 0/0 | 914 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | MANIN others(909): Show |
chr12 | 88137307 | 88204887 |
| a0005 | 0/0 | 914 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TMTC3_chr12_88137307_88204887 | TMTC3 | MANIN others(909): Show |
chr12 | 88137307 | 88204887 |
| a0006 | 0/0 | 914 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | MANIN others(909): Show |
chr12 | 88137307 | 88204887 |
| a0007 | 0/0 | 914 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TMTC3_chr12_88137307_88204887 | TMTC3 | MANIN others(909): Show |
chr12 | 88137307 | 88204887 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2742 | 216 | 75 | 38 | 72 | 8 | 21 | TMTC3_chr12_88137307_88204887 | TMTC3 | ATGGC others(2737): Show |
chr12 | 88137307 | 88204887 | ||
| a0001c0006 | 0/0 | 2742 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC3_chr12_88137307_88204887 | TMTC3 | ATGGC others(2737): Show |
chr12 | 88137307 | 88204887 | ||
| a0002c0002 | 0/0 | 2742 | 17 | 8 | 0 | 9 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | ATGGC others(2737): Show |
chr12 | 88137307 | 88204887 | ||
| a0003c0004 | 0/0 | 2742 | 2 | 2 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | ATGGC others(2737): Show |
chr12 | 88137307 | 88204887 | ||
| a0004c0003 | 0/0 | 2742 | 2 | 2 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | ATGGC others(2737): Show |
chr12 | 88137307 | 88204887 | ||
| a0005c0005 | 0/0 | 2742 | 2 | 0 | 0 | 2 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | ATGGC others(2737): Show |
chr12 | 88137307 | 88204887 | ||
| a0006c0007 | 0/0 | 2742 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | ATGGC others(2737): Show |
chr12 | 88137307 | 88204887 | ||
| a0007c0008 | 0/0 | 2742 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | ATGGC others(2737): Show |
chr12 | 88137307 | 88204887 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 7196 | 78 | 17 | 16 | 31 | 4 | 9 | TMTC3_chr12_88137307_88204887 | TMTC3 | AAGAC others(7191): Show |
chr12 | 88137307 | 88204887 |
| a0001c0001t0002 | 0/0 | 7195 | 39 | 1 | 7 | 27 | 0 | 4 | TMTC3_chr12_88137307_88204887 | TMTC3 | AAGAC others(7190): Show |
chr12 | 88137307 | 88204887 |
| a0001c0001t0003 | 0/0 | 7199 | 11 | 9 | 2 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | AAGAC others(7194): Show |
chr12 | 88137307 | 88204887 |
| a0001c0001t0004 | 0/0 | 7189 | 14 | 14 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | AAGAC others(7184): Show |
chr12 | 88137307 | 88204887 |
| a0001c0001t0005 | 0/0 | 7190 | 12 | 8 | 2 | 1 | 0 | 1 | TMTC3_chr12_88137307_88204887 | TMTC3 | AAGAC others(7185): Show |
chr12 | 88137307 | 88204887 |
| a0001c0001t0006 | 0/0 | 7196 | 11 | 0 | 5 | 2 | 2 | 2 | TMTC3_chr12_88137307_88204887 | TMTC3 | AAGAC others(7191): Show |
chr12 | 88137307 | 88204887 |
| a0001c0001t0007 | 0/0 | 7197 | 10 | 4 | 1 | 4 | 0 | 1 | TMTC3_chr12_88137307_88204887 | TMTC3 | AAGAC others(7192): Show |
chr12 | 88137307 | 88204887 |
| a0001c0001t0009 | 0/0 | 7196 | 4 | 4 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | AAGAC others(7191): Show |
chr12 | 88137307 | 88204887 |
| a0001c0001t0010 | 0/0 | 7200 | 4 | 3 | 1 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | AAGAC others(7195): Show |
chr12 | 88137307 | 88204887 |
| a0001c0001t0011 | 0/0 | 7197 | 4 | 0 | 2 | 0 | 0 | 2 | TMTC3_chr12_88137307_88204887 | TMTC3 | AAGAC others(7192): Show |
chr12 | 88137307 | 88204887 |
| a0001c0001t0013 | 0/0 | 7191 | 3 | 3 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | AAGAC others(7186): Show |
chr12 | 88137307 | 88204887 |
| a0001c0001t0014 | 0/0 | 7195 | 2 | 0 | 0 | 2 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | AAGAC others(7190): Show |
chr12 | 88137307 | 88204887 |
| a0001c0001t0015 | 0/0 | 7192 | 2 | 2 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | AAGAC others(7187): Show |
chr12 | 88137307 | 88204887 |
| a0001c0001t0016 | 0/0 | 7195 | 2 | 0 | 0 | 2 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | AAGAC others(7190): Show |
chr12 | 88137307 | 88204887 |
| a0001c0001t0017 | 0/0 | 7196 | 2 | 1 | 1 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | AAGAC others(7191): Show |
chr12 | 88137307 | 88204887 |
| a0001c0001t0018 | 0/0 | 7189 | 2 | 2 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | AAGAC others(7184): Show |
chr12 | 88137307 | 88204887 |
| a0001c0001t0019 | 0/0 | 7196 | 1 | 0 | 0 | 0 | 1 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | AAGAC others(7191): Show |
chr12 | 88137307 | 88204887 |
| a0001c0001t0021 | 0/0 | 7196 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC3_chr12_88137307_88204887 | TMTC3 | AAGAC others(7191): Show |
chr12 | 88137307 | 88204887 |
| a0001c0001t0022 | 0/0 | 7193 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | AAGAC others(7188): Show |
chr12 | 88137307 | 88204887 |
| a0001c0001t0023 | 0/0 | 7199 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | AAGAC others(7194): Show |
chr12 | 88137307 | 88204887 |
| a0001c0001t0025 | 0/0 | 7196 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | AAGAC others(7191): Show |
chr12 | 88137307 | 88204887 |
| a0001c0001t0026 | 1/0 | 7192 | 1 | 0 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | AAGAC others(7187): Show |
chr12 | 88137307 | 88204887 |
| a0001c0001t0028 | 0/0 | 7196 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | AAGAC others(7191): Show |
chr12 | 88137307 | 88204887 |
| a0001c0001t0029 | 0/0 | 7195 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | AAGAC others(7190): Show |
chr12 | 88137307 | 88204887 |
| a0001c0001t0030 | 0/0 | 7196 | 1 | 0 | 0 | 0 | 1 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | AAGAC others(7191): Show |
chr12 | 88137307 | 88204887 |
| a0001c0001t0033 | 0/0 | 7195 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | AAGAC others(7190): Show |
chr12 | 88137307 | 88204887 |
| a0001c0001t0034 | 0/0 | 7189 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | AAGAC others(7184): Show |
chr12 | 88137307 | 88204887 |
| a0001c0001t0035 | 0/0 | 7190 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | AAGAC others(7185): Show |
chr12 | 88137307 | 88204887 |
| a0001c0001t0036 | 0/0 | 7190 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC3_chr12_88137307_88204887 | TMTC3 | AAGAC others(7185): Show |
chr12 | 88137307 | 88204887 |
| a0001c0001t0037 | 0/0 | 7189 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | AAGAC others(7184): Show |
chr12 | 88137307 | 88204887 |
| a0001c0001t0038 | 0/0 | 7191 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | AAGAC others(7186): Show |
chr12 | 88137307 | 88204887 |
| a0001c0001t0039 | 0/0 | 7189 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | AAGAC others(7184): Show |
chr12 | 88137307 | 88204887 |
| a0001c0006t0024 | 0/0 | 7196 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC3_chr12_88137307_88204887 | TMTC3 | AAGAC others(7191): Show |
chr12 | 88137307 | 88204887 |
| a0002c0002t0008 | 0/0 | 7193 | 10 | 1 | 0 | 9 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | AAGAC others(7188): Show |
chr12 | 88137307 | 88204887 |
| a0002c0002t0012 | 0/0 | 7197 | 3 | 3 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | AAGAC others(7192): Show |
chr12 | 88137307 | 88204887 |
| a0002c0002t0020 | 0/0 | 7197 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | AAGAC others(7192): Show |
chr12 | 88137307 | 88204887 |
| a0002c0002t0027 | 0/0 | 7196 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | AAGAC others(7191): Show |
chr12 | 88137307 | 88204887 |
| a0002c0002t0031 | 0/0 | 7198 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | AAGAC others(7193): Show |
chr12 | 88137307 | 88204887 |
| a0002c0002t0032 | 0/0 | 7198 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | AAGAC others(7193): Show |
chr12 | 88137307 | 88204887 |
| a0003c0004t0003 | 0/0 | 7199 | 2 | 2 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | AAGAC others(7194): Show |
chr12 | 88137307 | 88204887 |
| a0004c0003t0001 | 0/0 | 7196 | 2 | 2 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | AAGAC others(7191): Show |
chr12 | 88137307 | 88204887 |
| a0005c0005t0001 | 0/0 | 7196 | 2 | 0 | 0 | 2 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | AAGAC others(7191): Show |
chr12 | 88137307 | 88204887 |
| a0006c0007t0003 | 0/0 | 7199 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | AAGAC others(7194): Show |
chr12 | 88137307 | 88204887 |
| a0007c0008t0002 | 0/0 | 7195 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | AAGAC others(7190): Show |
chr12 | 88137307 | 88204887 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 9 | 0 | 2 | 6 | 0 | 1 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0117 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0002g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0002g0004 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0002g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0003g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0003g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0004g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0004g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0004g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0004g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0004g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0005g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0005g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0005g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0005g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0005g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0005g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0005g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0005g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0005g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0005g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0005g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0005g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0006g0003 | 0/0 | 5 | 0 | 2 | 2 | 0 | 1 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0006g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0006g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0006g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0006g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0006g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0006g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0007g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0007g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0007g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0007g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0007g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0007g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0007g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0007g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0007g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0007g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0009g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0009g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0009g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0009g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0010g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0010g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0010g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0011g0003 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0011g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0011g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0013g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0013g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0013g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0014g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0014g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0015g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0015g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0016g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0017g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0017g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0018g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0019g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0021g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0022g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0023g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0025g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0026g0162 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0028g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0029g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0030g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0033g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0034g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0035g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0036g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0037g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0038g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0001t0039g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0001c0006t0024g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0002c0002t0008g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0002c0002t0008g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0002c0002t0008g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0002c0002t0008g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0002c0002t0008g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0002c0002t0008g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0002c0002t0008g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0002c0002t0012g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0002c0002t0012g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0002c0002t0012g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0002c0002t0020g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0002c0002t0027g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0002c0002t0031g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0002c0002t0032g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0003c0004t0003g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0003c0004t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0004c0003t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0004c0003t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0005c0005t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0005c0005t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0006c0007t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| a0007c0008t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0030 | g0003 | EUR | GBR | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG00099 | hp2 | a0001 | c0001 | t0006 | g0011 | EUR | GBR | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | CHS | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG00639 | hp2 | a0001 | c0001 | t0017 | g0076 | AMR | PUR | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG00642 | hp2 | a0001 | c0001 | t0006 | g0078 | AMR | PUR | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG00735 | hp2 | a0001 | c0001 | t0006 | g0003 | AMR | PUR | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG01071 | hp1 | a0001 | c0001 | t0006 | g0003 | AMR | PUR | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG01071 | hp2 | a0001 | c0001 | t0005 | g0167 | AMR | PUR | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0123 | AMR | PUR | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | PUR | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG01081 | hp1 | a0001 | c0001 | t0006 | g0140 | AMR | PUR | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | PUR | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG01109 | hp2 | a0001 | c0001 | t0010 | g0009 | AMR | PUR | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0034 | AMR | PUR | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0033 | AMR | PUR | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG01496 | hp1 | a0001 | c0001 | t0033 | g0080 | AMR | CLM | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0128 | EUR | IBS | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0107 | EUR | IBS | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0029 | AFR | ACB | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG01884 | hp2 | a0001 | c0001 | t0022 | g0043 | AFR | ACB | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0021 | AFR | ACB | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG01934 | hp2 | a0001 | c0001 | t0006 | g0182 | AMR | PEL | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | PEL | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG01978 | hp1 | a0001 | c0001 | t0011 | g0003 | AMR | PEL | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG01978 | hp2 | a0001 | c0001 | t0007 | g0007 | AMR | PEL | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG01981 | hp2 | a0001 | c0001 | t0011 | g0085 | AMR | PEL | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02040 | hp1 | a0001 | c0001 | t0028 | g0088 | EAS | KHV | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02055 | hp1 | a0001 | c0001 | t0010 | g0032 | AFR | ACB | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02055 | hp2 | a0001 | c0001 | t0005 | g0159 | AFR | ACB | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02056 | hp1 | a0001 | c0001 | t0029 | g0131 | EAS | KHV | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02071 | hp1 | a0001 | c0001 | t0007 | g0126 | EAS | KHV | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | KHV | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0172 | AFR | ACB | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02145 | hp2 | a0001 | c0001 | t0007 | g0181 | AFR | ACB | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02155 | hp1 | a0002 | c0002 | t0008 | g0049 | EAS | CDX | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02257 | hp1 | a0001 | c0001 | t0035 | g0021 | AFR | ACB | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02257 | hp2 | a0001 | c0001 | t0009 | g0044 | AFR | ACB | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0022 | AFR | ACB | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02258 | hp2 | a0001 | c0001 | t0010 | g0009 | AFR | ACB | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0174 | AFR | ACB | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0176 | AMR | PEL | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02293 | hp2 | a0001 | c0001 | t0005 | g0165 | AMR | PEL | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02451 | hp2 | a0003 | c0004 | t0003 | g0036 | AFR | ACB | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0158 | AFR | GWD | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0149 | AFR | GWD | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0173 | AFR | GWD | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02622 | hp2 | a0004 | c0003 | t0001 | g0100 | AFR | GWD | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | GWD | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02630 | hp2 | a0006 | c0007 | t0003 | g0030 | AFR | GWD | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | GWD | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02647 | hp2 | a0001 | c0001 | t0015 | g0041 | AFR | GWD | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0171 | SAS | PJL | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02698 | hp2 | a0001 | c0006 | t0024 | g0105 | SAS | PJL | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0151 | AFR | GWD | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | GWD | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02735 | hp2 | a0001 | c0001 | t0006 | g0003 | SAS | PJL | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02809 | hp1 | a0004 | c0003 | t0001 | g0119 | AFR | GWD | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02809 | hp2 | a0001 | c0001 | t0013 | g0168 | AFR | GWD | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02818 | hp1 | a0001 | c0001 | t0013 | g0022 | AFR | GWD | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02886 | hp2 | a0002 | c0002 | t0031 | g0056 | AFR | GWD | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0156 | AFR | GWD | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02895 | hp2 | a0001 | c0001 | t0015 | g0042 | AFR | GWD | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02896 | hp1 | a0001 | c0001 | t0039 | g0153 | AFR | GWD | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02896 | hp2 | a0001 | c0001 | t0010 | g0037 | AFR | GWD | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02922 | hp1 | a0003 | c0004 | t0003 | g0008 | AFR | ESN | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02922 | hp2 | a0001 | c0001 | t0013 | g0166 | AFR | ESN | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | ESN | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0035 | AFR | ESN | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0157 | AFR | ESN | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ESN | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG03041 | hp1 | a0001 | c0001 | t0009 | g0047 | AFR | GWD | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0170 | AFR | GWD | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0038 | AFR | MSL | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG03098 | hp2 | a0002 | c0002 | t0012 | g0146 | AFR | MSL | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | ESN | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0154 | AFR | ESN | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | ESN | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG03209 | hp1 | a0001 | c0001 | t0018 | g0019 | AFR | MSL | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG03209 | hp2 | a0002 | c0002 | t0012 | g0053 | AFR | MSL | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0175 | AFR | MSL | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG03225 | hp2 | a0001 | c0001 | t0009 | g0046 | AFR | MSL | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG03453 | hp1 | a0002 | c0002 | t0012 | g0147 | AFR | MSL | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | MSL | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG03516 | hp1 | a0001 | c0001 | t0007 | g0089 | AFR | ESN | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG03516 | hp2 | a0002 | c0002 | t0032 | g0055 | AFR | ESN | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG03540 | hp1 | a0001 | c0001 | t0018 | g0019 | AFR | GWD | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG03540 | hp2 | a0001 | c0001 | t0009 | g0045 | AFR | GWD | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0092 | SAS | PJL | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG03834 | hp1 | a0001 | c0001 | t0021 | g0111 | SAS | BEB | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG03834 | hp2 | a0001 | c0001 | t0006 | g0079 | SAS | BEB | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | STU | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG04115 | hp2 | a0001 | c0001 | t0011 | g0003 | SAS | STU | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG04199 | hp1 | a0001 | c0001 | t0007 | g0110 | SAS | STU | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG04199 | hp2 | a0001 | c0001 | t0011 | g0071 | SAS | STU | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0010 | SAS | STU | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | STU | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG04228 | hp1 | a0001 | c0001 | t0005 | g0020 | SAS | STU | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | STU | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA18522 | hp1 | a0001 | c0001 | t0034 | g0005 | AFR | YRI | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0027 | AFR | YRI | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA18612 | hp1 | a0002 | c0002 | t0008 | g0052 | EAS | CHB | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | CHB | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | CHB | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | CHB | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0150 | AFR | YRI | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0160 | AFR | YRI | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA18944 | hp1 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA18947 | hp1 | a0001 | c0001 | t0005 | g0164 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA18948 | hp1 | a0001 | c0001 | t0014 | g0096 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA18949 | hp1 | a0002 | c0002 | t0008 | g0006 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA18951 | hp2 | a0001 | c0001 | t0014 | g0001 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA18960 | hp2 | a0005 | c0005 | t0001 | g0144 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA18964 | hp1 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA18966 | hp1 | a0001 | c0001 | t0007 | g0018 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA18969 | hp1 | a0005 | c0005 | t0001 | g0143 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA18969 | hp2 | a0001 | c0001 | t0016 | g0014 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA19004 | hp2 | a0002 | c0002 | t0008 | g0006 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA19030 | hp1 | a0001 | c0001 | t0038 | g0169 | AFR | LWK | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA19030 | hp2 | a0001 | c0001 | t0007 | g0090 | AFR | LWK | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0152 | AFR | LWK | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | LWK | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA19058 | hp1 | a0001 | c0001 | t0007 | g0136 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA19058 | hp2 | a0002 | c0002 | t0008 | g0006 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA19068 | hp1 | a0001 | c0001 | t0025 | g0102 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA19075 | hp2 | a0002 | c0002 | t0008 | g0048 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA19077 | hp1 | a0001 | c0001 | t0007 | g0135 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA19079 | hp1 | a0001 | c0001 | t0016 | g0014 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA19083 | hp2 | a0002 | c0002 | t0008 | g0006 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA19086 | hp2 | a0007 | c0008 | t0002 | g0127 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA19091 | hp2 | a0002 | c0002 | t0008 | g0183 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0031 | AFR | ASW | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0161 | AFR | ASW | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0086 | EUR | TSI | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0098 | EUR | TSI | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA20805 | hp1 | a0001 | c0001 | t0006 | g0077 | EUR | TSI | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA20805 | hp2 | a0001 | c0001 | t0019 | g0015 | EUR | TSI | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | GIH | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA20905 | hp2 | a0001 | c0001 | t0036 | g0020 | SAS | GIH | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02109 | hp1 | a0001 | c0001 | t0007 | g0075 | AFR | ACB | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02109 | hp2 | a0001 | c0001 | t0023 | g0039 | AFR | ACB | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02486 | hp2 | a0002 | c0002 | t0027 | g0054 | AFR | ACB | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02559 | hp1 | a0002 | c0002 | t0020 | g0148 | AFR | ACB | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG03471 | hp1 | a0001 | c0001 | t0017 | g0087 | AFR | MSL | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG03471 | hp2 | a0001 | c0001 | t0037 | g0155 | AFR | MSL | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | USA | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| HG06807 | hp2 | a0002 | c0002 | t0008 | g0050 | AFR | USA | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA18955 | hp1 | a0002 | c0002 | t0008 | g0051 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | USA | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | USA | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA21309 | hp1 | a0001 | c0001 | t0005 | g0163 | AFR | LWK | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0028 | AFR | LWK | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0117 | REF | REF | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0026 | g0162 | REF | REF | TMTC3_chr12_88137307_88204887 | TMTC3 | chr12 | 88137307 | 88204887 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:88153436 | A | G | 1 | a0005 | 2 | NA18960.hp2 NA18969.hp1 |
missense_variant | MODERATE | c.335A>G | p.Lys112Arg | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 3/14 | 544/7192 | 335/2745 | 112/914 | chr12 | 88153436 | |||
| chr12:88153438 | C | G | 1 | a0007 | 1 | NA19086.hp2 | missense_variant | MODERATE | c.337C>G | p.Leu113Val | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 3/14 | 546/7192 | 337/2745 | 113/914 | chr12 | 88153438 | |||
| chr12:88188925 | G | A | 1 | a0004 | 2 | HG02622.hp2 HG02809.hp1 |
missense_variant | MODERATE | c.1515G>A | p.Met505Ile | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 11/14 | 1724/7192 | 1515/2745 | 505/914 | chr12 | 88188925 | |||
| chr12:88190580 | C | T | 1 | a0003 | 2 | HG02451.hp2 HG02922.hp1 |
missense_variant | MODERATE | c.1664C>T | p.Ala555Val | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 12/14 | 1873/7192 | 1664/2745 | 555/914 | chr12 | 88190580 | |||
| chr12:88195456 | G | A | 1 | a0006 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.2552G>A | p.Gly851Asp | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 14/14 | 2761/7192 | 2552/2745 | 851/914 | chr12 | 88195456 | |||
| chr12:88195479 | G | A | 1 | a0002 | 17 | HG02155.hp1 HG02486.hp2 HG02559.hp1 others(14): Show |
missense_variant | MODERATE | c.2575G>A | p.Val859Ile | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 14/14 | 2784/7192 | 2575/2745 | 859/914 | chr12 | 88195479 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:88154356 | T | C | 1 | a0001c0006 | 1 | HG02698.hp2 | synonymous_variant | LOW | c.477T>C | p.Tyr159Tyr | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 4/14 | 686/7192 | 477/2745 | 159/914 | chr12 | 88154356 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:88142322 | C | G | 1 | a0001c0001t0039 | 1 | HG02896.hp1 | 5_prime_UTR_variant | MODIFIER | c.-194C>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/14 | 5994 | chr12 | 88142322 | ||||||
| chr12:88142431 | G | A | 1 | a0001c0001t0014 | 2 | NA18948.hp1 NA18951.hp2 |
5_prime_UTR_variant | MODIFIER | c.-85G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/14 | 5885 | chr12 | 88142431 | ||||||
| chr12:88195908 | AAAG | A | 10 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0013 others(7): Show |
37 | HG01071.hp2 HG01891.hp2 HG02055.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*263_*265delAAG | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 14/14 | 263 | INFO_REALIGN_3_PRIME | chr12 | 88195908 | |||||
| chr12:88195944 | C | T | 1 | a0001c0001t0018 | 2 | HG03209.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*295C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 14/14 | 295 | chr12 | 88195944 | ||||||
| chr12:88195965 | G | A | 1 | a0001c0001t0019 | 1 | NA20805.hp2 | 3_prime_UTR_variant | MODIFIER | c.*316G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 14/14 | 316 | chr12 | 88195965 | ||||||
| chr12:88195982 | C | T | 1 | a0001c0001t0038 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*333C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 14/14 | 333 | chr12 | 88195982 | ||||||
| chr12:88196199 | A | G | 1 | a0001c0001t0017 | 2 | HG00639.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*550A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 14/14 | 550 | chr12 | 88196199 | ||||||
| chr12:88196237 | A | G | 3 | a0001c0001t0006 a0001c0001t0011 a0001c0001t0033 |
16 | HG00099.hp2 HG00642.hp2 HG00735.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*588A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 14/14 | 588 | chr12 | 88196237 | ||||||
| chr12:88196331 | T | C | 1 | a0002c0002t0020 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*682T>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 14/14 | 682 | chr12 | 88196331 | ||||||
| chr12:88196464 | T | C | 1 | a0001c0001t0021 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*815T>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 14/14 | 815 | chr12 | 88196464 | ||||||
| chr12:88196662 | AACTT | A | 1 | a0002c0002t0008 | 10 | HG02155.hp1 HG06807.hp2 NA18612.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1014_*1017delACTT | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 14/14 | 1014 | chr12 | 88196662 | ||||||
| chr12:88196816 | A | T | 1 | a0001c0001t0037 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1167A>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 14/14 | 1167 | chr12 | 88196816 | ||||||
| chr12:88197259 | A | AT | 8 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0011 others(5): Show |
42 | HG01071.hp2 HG01891.hp2 HG01978.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*1635dupT | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 14/14 | 1636 | INFO_REALIGN_3_PRIME | chr12 | 88197259 | |||||
| chr12:88197259 | A | ATT | 4 | a0001c0001t0013 a0001c0001t0038 a0002c0002t0031 others(1): Show |
6 | HG02809.hp2 HG02818.hp1 HG02886.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1634_*1635dupTT | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 14/14 | 1636 | INFO_REALIGN_3_PRIME | chr12 | 88197259 | |||||
| chr12:88197259 | AT | A | 9 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0014 others(6): Show |
60 | HG00609.hp2 HG01074.hp1 HG01074.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*1635delT | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 14/14 | 1635 | INFO_REALIGN_3_PRIME | chr12 | 88197259 | |||||
| chr12:88197284 | T | A | 2 | a0001c0001t0015 a0001c0001t0022 |
3 | HG01884.hp2 HG02647.hp2 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1635T>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 14/14 | 1635 | chr12 | 88197284 | ||||||
| chr12:88197785 | A | T | 5 | a0001c0001t0003 a0001c0001t0010 a0001c0001t0023 others(2): Show |
19 | HG01109.hp2 HG01192.hp1 HG01243.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2136A>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 14/14 | 2136 | chr12 | 88197785 | ||||||
| chr12:88198321 | A | T | 1 | a0001c0001t0030 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2672A>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 14/14 | 2672 | chr12 | 88198321 | ||||||
| chr12:88198375 | C | G | 1 | a0001c0001t0029 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2726C>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 14/14 | 2726 | chr12 | 88198375 | ||||||
| chr12:88198583 | C | T | 1 | a0001c0001t0036 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2934C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 14/14 | 2934 | chr12 | 88198583 | ||||||
| chr12:88198777 | C | T | 1 | a0001c0001t0028 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3128C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 14/14 | 3128 | chr12 | 88198777 | ||||||
| chr12:88198885 | A | G | 2 | a0002c0002t0027 a0002c0002t0032 |
2 | HG02486.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3236A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 14/14 | 3236 | chr12 | 88198885 | ||||||
| chr12:88198989 | T | C | 1 | a0001c0006t0024 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3340T>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 14/14 | 3340 | chr12 | 88198989 | ||||||
| chr12:88199053 | T | TA | 33 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(30): Show |
203 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(200): Show |
3_prime_UTR_variant | MODIFIER | c.*3411dupA | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 14/14 | 3412 | INFO_REALIGN_3_PRIME | chr12 | 88199053 | |||||
| chr12:88199081 | T | TTTC | 31 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(28): Show |
200 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(197): Show |
3_prime_UTR_variant | MODIFIER | c.*3435_*3437dupCTT | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 14/14 | 3438 | INFO_REALIGN_3_PRIME | chr12 | 88199081 | |||||
| chr12:88199175 | G | A | 20 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(17): Show |
164 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(161): Show |
3_prime_UTR_variant | MODIFIER | c.*3526G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 14/14 | 3526 | chr12 | 88199175 | ||||||
| chr12:88199388 | A | ATATT | 5 | a0001c0001t0003 a0001c0001t0010 a0001c0001t0023 others(2): Show |
19 | HG01109.hp2 HG01192.hp1 HG01243.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*3740_*3743dupTATT | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 14/14 | 3744 | INFO_REALIGN_3_PRIME | chr12 | 88199388 | |||||
| chr12:88199413 | A | C | 1 | a0001c0001t0023 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3764A>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 14/14 | 3764 | chr12 | 88199413 | ||||||
| chr12:88199447 | T | C | 1 | a0001c0001t0015 | 2 | HG02647.hp2 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3798T>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 14/14 | 3798 | chr12 | 88199447 | ||||||
| chr12:88199600 | G | A | 1 | a0001c0001t0038 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3951G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 14/14 | 3951 | chr12 | 88199600 | ||||||
| chr12:88199613 | C | T | 1 | a0001c0001t0035 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3964C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 14/14 | 3964 | chr12 | 88199613 | ||||||
| chr12:88199649 | A | G | 1 | a0001c0001t0009 | 4 | HG02257.hp2 HG03041.hp1 HG03225.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4000A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 14/14 | 4000 | chr12 | 88199649 | ||||||
| chr12:88199755 | T | C | 1 | a0001c0001t0034 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4106T>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 14/14 | 4106 | chr12 | 88199755 | ||||||
| chr12:88199766 | T | A | 1 | a0001c0001t0025 | 1 | NA19068.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4117T>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 14/14 | 4117 | chr12 | 88199766 | ||||||
| chr12:88199878 | CA | C | 2 | a0001c0001t0016 a0001c0001t0029 |
3 | HG02056.hp1 NA18969.hp2 NA19079.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4235delA | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 14/14 | 4235 | INFO_REALIGN_3_PRIME | chr12 | 88199878 |
| view | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:88142599 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-29+112G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | chr12 | 88142599 | |||||||
| chr12:88142624 | G | A | 1 | a0001c0001t0001g0026 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-29+137G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | chr12 | 88142624 | |||||||
| chr12:88142633 | C | T | 1 | a0002c0002t0008g0183 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-29+146C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | chr12 | 88142633 | |||||||
| chr12:88142745 | C | T | 1 | a0001c0001t0006g0182 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-29+258C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | chr12 | 88142745 | |||||||
| chr12:88142773 | G | C | 17 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0027 others(14): Show |
19 | HG01109.hp2 HG01192.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.-29+286G>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | chr12 | 88142773 | |||||||
| chr12:88142910 | C | T | 5 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(2): Show |
5 | HG02145.hp2 HG02615.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-29+423C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | chr12 | 88142910 | |||||||
| chr12:88143107 | T | C | 1 | a0001c0001t0001g0040 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-29+620T>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | chr12 | 88143107 | |||||||
| chr12:88143238 | A | C | 4 | a0001c0001t0001g0023 a0001c0001t0002g0023 a0001c0001t0002g0024 others(1): Show |
5 | HG01074.hp2 HG01081.hp2 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.-29+751A>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | chr12 | 88143238 | |||||||
| chr12:88143680 | C | T | 3 | a0001c0001t0004g0173 a0001c0001t0004g0174 a0001c0001t0004g0175 |
3 | HG02280.hp1 HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-29+1193C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | chr12 | 88143680 | |||||||
| chr12:88143706 | A | T | 1 | a0001c0001t0002g0172 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-29+1219A>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | chr12 | 88143706 | |||||||
| chr12:88144076 | T | C | 3 | a0001c0001t0015g0041 a0001c0001t0015g0042 a0001c0001t0022g0043 |
3 | HG01884.hp2 HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-29+1589T>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | chr12 | 88144076 | |||||||
| chr12:88144381 | T | C | 20 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0027 others(17): Show |
22 | HG01109.hp2 HG01192.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.-29+1894T>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | chr12 | 88144381 | |||||||
| chr12:88144408 | GT | G | 15 | a0001c0001t0009g0044 a0001c0001t0009g0045 a0001c0001t0009g0046 others(12): Show |
18 | HG02155.hp1 HG02257.hp2 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.-29+1931delT | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 88144408 | ||||||
| chr12:88144423 | C | T | 1 | a0001c0001t0023g0039 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-29+1936C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | chr12 | 88144423 | |||||||
| chr12:88144429 | A | G | 1 | a0001c0001t0022g0043 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-29+1942A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | chr12 | 88144429 | |||||||
| chr12:88144449 | C | G | 1 | a0001c0001t0022g0043 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-29+1962C>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | chr12 | 88144449 | |||||||
| chr12:88144506 | G | A | 4 | a0001c0001t0009g0044 a0001c0001t0009g0045 a0001c0001t0009g0046 others(1): Show |
4 | HG02257.hp2 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-29+2019G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | chr12 | 88144506 | |||||||
| chr12:88144507 | C | T | 4 | a0001c0001t0009g0044 a0001c0001t0009g0045 a0001c0001t0009g0046 others(1): Show |
4 | HG02257.hp2 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-29+2020C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | chr12 | 88144507 | |||||||
| chr12:88144517 | T | G | 3 | a0001c0001t0015g0041 a0001c0001t0015g0042 a0001c0001t0022g0043 |
3 | HG01884.hp2 HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-29+2030T>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | chr12 | 88144517 | |||||||
| chr12:88144640 | AT | A | 7 | a0002c0002t0008g0006 a0002c0002t0008g0048 a0002c0002t0008g0049 others(4): Show |
10 | HG02155.hp1 HG06807.hp2 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.-29+2155delT | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 88144640 | ||||||
| chr12:88144685 | C | T | 1 | a0001c0001t0002g0171 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-29+2198C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | chr12 | 88144685 | |||||||
| chr12:88144793 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-29+2306G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | chr12 | 88144793 | |||||||
| chr12:88144858 | T | C | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(125): Show |
160 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(157): Show |
intron_variant | MODIFIER | c.-29+2371T>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | chr12 | 88144858 | |||||||
| chr12:88145155 | T | C | 14 | a0002c0002t0008g0006 a0002c0002t0008g0048 a0002c0002t0008g0049 others(11): Show |
17 | HG02155.hp1 HG02486.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.-29+2668T>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | chr12 | 88145155 | |||||||
| chr12:88145266 | C | G | 14 | a0002c0002t0008g0006 a0002c0002t0008g0048 a0002c0002t0008g0049 others(11): Show |
17 | HG02155.hp1 HG02486.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.-29+2779C>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | chr12 | 88145266 | |||||||
| chr12:88145309 | T | A | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG02486.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-29+2822T>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | chr12 | 88145309 | |||||||
| chr12:88145394 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-28-2894A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | chr12 | 88145394 | |||||||
| chr12:88145481 | C | T | 2 | a0005c0005t0001g0143 a0005c0005t0001g0144 |
2 | NA18960.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.-28-2807C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | chr12 | 88145481 | |||||||
| chr12:88145661 | T | C | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(163): Show |
203 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(200): Show |
intron_variant | MODIFIER | c.-28-2627T>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | chr12 | 88145661 | |||||||
| chr12:88146148 | A | T | 2 | a0002c0002t0012g0147 a0002c0002t0020g0148 |
2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-28-2140A>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | chr12 | 88146148 | |||||||
| chr12:88146422 | T | C | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(163): Show |
203 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(200): Show |
intron_variant | MODIFIER | c.-28-1866T>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | chr12 | 88146422 | |||||||
| chr12:88146433 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-28-1855A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | chr12 | 88146433 | |||||||
| chr12:88146554 | C | T | 3 | a0001c0001t0015g0041 a0001c0001t0015g0042 a0001c0001t0022g0043 |
3 | HG01884.hp2 HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-28-1734C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | chr12 | 88146554 | |||||||
| chr12:88146591 | T | TTG | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(122): Show |
157 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(154): Show |
intron_variant | MODIFIER | c.-28-1677_-28-1676d others(4): Show |
TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 88146591 | ||||||
| chr12:88146611 | G | GTATA | 5 | a0002c0002t0012g0053 a0002c0002t0012g0147 a0002c0002t0020g0148 others(2): Show |
5 | HG02486.hp2 HG02559.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-28-1666_-28-1663d others(6): Show |
TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 88146611 | ||||||
| chr12:88146611 | G | GTATATA | 7 | a0002c0002t0008g0006 a0002c0002t0008g0048 a0002c0002t0008g0049 others(4): Show |
10 | HG02155.hp1 HG02886.hp2 HG06807.hp2 others(7): Show |
intron_variant | MODIFIER | c.-28-1668_-28-1663d others(8): Show |
TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 88146611 | ||||||
| chr12:88146611 | G | GTGTA | 4 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(1): Show |
4 | HG02040.hp2 NA18960.hp1 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-1676_-28-1675i others(6): Show |
TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 88146611 | ||||||
| chr12:88146613 | A | G | 19 | a0001c0001t0001g0141 a0001c0001t0003g0008 a0001c0001t0003g0009 others(16): Show |
21 | HG01081.hp1 HG01109.hp2 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.-28-1675A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | chr12 | 88146613 | |||||||
| chr12:88146613 | ATATATAT others(15): Show |
A | 1 | a0002c0002t0008g0052 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-28-1665_-28-1644d others(24): Show |
TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 88146613 | ||||||
| chr12:88146615 | A | G | 2 | a0001c0001t0010g0037 a0001c0001t0023g0039 |
2 | HG02109.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-28-1673A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | chr12 | 88146615 | |||||||
| chr12:88146632 | T | C | 1 | a0001c0001t0001g0061 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-28-1656T>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | chr12 | 88146632 | |||||||
| chr12:88146644 | T | G | 6 | a0001c0001t0004g0005 a0001c0001t0004g0149 a0001c0001t0004g0151 others(3): Show |
9 | HG02572.hp2 HG02630.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.-28-1644T>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | chr12 | 88146644 | |||||||
| chr12:88146776 | G | A | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(179): Show |
223 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(220): Show |
intron_variant | MODIFIER | c.-28-1512G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | chr12 | 88146776 | |||||||
| chr12:88146988 | A | G | 4 | a0001c0001t0001g0018 a0001c0001t0007g0018 a0001c0001t0007g0135 others(1): Show |
4 | NA18966.hp1 NA19010.hp2 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-1300A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | chr12 | 88146988 | |||||||
| chr12:88147285 | G | A | 1 | a0001c0001t0002g0062 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-28-1003G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | chr12 | 88147285 | |||||||
| chr12:88147596 | A | G | 1 | a0001c0001t0001g0134 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-28-692A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | chr12 | 88147596 | |||||||
| chr12:88147690 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-28-598A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | chr12 | 88147690 | |||||||
| chr12:88147768 | G | GA | 17 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0027 others(14): Show |
19 | HG01109.hp2 HG01192.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.-28-510dupA | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr12 | 88147768 | ||||||
| chr12:88147809 | C | A | 1 | a0001c0001t0002g0010 | 2 | HG02698.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-28-479C>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | chr12 | 88147809 | |||||||
| chr12:88147809 | C | T | 2 | a0001c0001t0004g0156 a0001c0001t0004g0157 |
2 | HG02895.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-28-479C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | chr12 | 88147809 | |||||||
| chr12:88147818 | T | G | 16 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0023 others(13): Show |
28 | HG00741.hp1 HG01074.hp2 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.-28-470T>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | chr12 | 88147818 | |||||||
| chr12:88147841 | A | T | 2 | a0001c0001t0004g0156 a0001c0001t0004g0157 |
2 | HG02895.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-28-447A>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | chr12 | 88147841 | |||||||
| chr12:88147918 | T | C | 7 | a0001c0001t0004g0156 a0001c0001t0004g0157 a0001c0001t0004g0170 others(4): Show |
7 | HG02280.hp1 HG02615.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-28-370T>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | chr12 | 88147918 | |||||||
| chr12:88147973 | G | T | 1 | a0002c0002t0008g0051 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-28-315G>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | chr12 | 88147973 | |||||||
| chr12:88148091 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-28-197G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | chr12 | 88148091 | |||||||
| chr12:88148141 | G | A | 2 | a0001c0001t0005g0158 a0001c0001t0005g0159 |
2 | HG02055.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.-28-147G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | chr12 | 88148141 | |||||||
| chr12:88148143 | C | T | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(180): Show |
224 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(221): Show |
intron_variant | MODIFIER | c.-28-145C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | chr12 | 88148143 | |||||||
| chr12:88148154 | T | C | 1 | a0001c0001t0011g0071 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-28-134T>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 1/13 | chr12 | 88148154 | |||||||
| chr12:88148790 | G | C | 14 | a0001c0001t0004g0005 a0001c0001t0004g0149 a0001c0001t0004g0151 others(11): Show |
17 | HG02280.hp1 HG02572.hp2 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.189+286G>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 2/13 | chr12 | 88148790 | |||||||
| chr12:88148814 | G | A | 17 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0027 others(14): Show |
19 | HG01109.hp2 HG01192.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.189+310G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 2/13 | chr12 | 88148814 | |||||||
| chr12:88148821 | G | A | 4 | a0002c0002t0008g0006 a0002c0002t0008g0048 a0002c0002t0008g0051 others(1): Show |
7 | NA18949.hp1 NA18955.hp1 NA19004.hp2 others(4): Show |
intron_variant | MODIFIER | c.189+317G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 2/13 | chr12 | 88148821 | |||||||
| chr12:88148835 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.189+331C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 2/13 | chr12 | 88148835 | |||||||
| chr12:88149050 | A | T | 1 | a0001c0001t0010g0037 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.189+546A>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 2/13 | chr12 | 88149050 | |||||||
| chr12:88149166 | T | C | 1 | a0001c0001t0007g0135 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.189+662T>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 2/13 | chr12 | 88149166 | |||||||
| chr12:88149423 | C | T | 2 | a0002c0002t0027g0054 a0002c0002t0032g0055 |
2 | HG02486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.189+919C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 2/13 | chr12 | 88149423 | |||||||
| chr12:88149718 | G | A | 1 | a0001c0001t0009g0044 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.189+1214G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 2/13 | chr12 | 88149718 | |||||||
| chr12:88149774 | G | A | 3 | a0001c0001t0015g0041 a0001c0001t0015g0042 a0001c0001t0022g0043 |
3 | HG01884.hp2 HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.189+1270G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 2/13 | chr12 | 88149774 | |||||||
| chr12:88149899 | A | G | 1 | a0002c0002t0012g0053 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.189+1395A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 2/13 | chr12 | 88149899 | |||||||
| chr12:88149991 | G | T | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(163): Show |
203 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(200): Show |
intron_variant | MODIFIER | c.189+1487G>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 2/13 | chr12 | 88149991 | |||||||
| chr12:88150003 | T | G | 4 | a0001c0001t0001g0011 a0001c0001t0001g0057 a0001c0001t0001g0133 others(1): Show |
4 | HG00099.hp2 HG01106.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.189+1499T>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 2/13 | chr12 | 88150003 | |||||||
| chr12:88150120 | G | A | 1 | a0001c0001t0004g0149 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.189+1616G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 2/13 | chr12 | 88150120 | |||||||
| chr12:88150204 | A | G | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(163): Show |
203 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(200): Show |
intron_variant | MODIFIER | c.189+1700A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 2/13 | chr12 | 88150204 | |||||||
| chr12:88151191 | C | T | 1 | a0001c0001t0029g0131 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.190-2100C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 2/13 | chr12 | 88151191 | |||||||
| chr12:88151229 | G | A | 1 | a0001c0001t0039g0153 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.190-2062G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 2/13 | chr12 | 88151229 | |||||||
| chr12:88151232 | G | A | 1 | a0001c0001t0001g0012 | 2 | HG02129.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.190-2059G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 2/13 | chr12 | 88151232 | |||||||
| chr12:88151298 | T | C | 1 | a0001c0001t0003g0027 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.190-1993T>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 2/13 | chr12 | 88151298 | |||||||
| chr12:88151595 | G | A | 1 | a0001c0001t0003g0028 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.190-1696G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 2/13 | chr12 | 88151595 | |||||||
| chr12:88151677 | AAT | A | 4 | a0001c0001t0001g0011 a0001c0001t0001g0057 a0001c0001t0001g0133 others(1): Show |
4 | HG00099.hp2 HG01106.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.190-1612_190-1611d others(4): Show |
TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr12 | 88151677 | ||||||
| chr12:88152039 | C | A | 2 | a0001c0001t0001g0073 a0001c0001t0002g0072 |
2 | NA18947.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.190-1252C>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 2/13 | chr12 | 88152039 | |||||||
| chr12:88152082 | A | G | 7 | a0001c0001t0009g0044 a0001c0001t0009g0045 a0001c0001t0009g0046 others(4): Show |
7 | HG01884.hp2 HG02257.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.190-1209A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 2/13 | chr12 | 88152082 | |||||||
| chr12:88152209 | T | G | 1 | a0001c0001t0004g0170 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.190-1082T>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 2/13 | chr12 | 88152209 | |||||||
| chr12:88152371 | C | G | 1 | a0001c0001t0001g0130 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.190-920C>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 2/13 | chr12 | 88152371 | |||||||
| chr12:88152404 | C | A | 1 | a0001c0001t0002g0074 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.190-887C>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 2/13 | chr12 | 88152404 | |||||||
| chr12:88152738 | A | G | 1 | a0001c0001t0002g0069 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.190-553A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 2/13 | chr12 | 88152738 | |||||||
| chr12:88152999 | A | T | 7 | a0001c0001t0009g0044 a0001c0001t0009g0045 a0001c0001t0009g0046 others(4): Show |
7 | HG01884.hp2 HG02257.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.190-292A>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 2/13 | chr12 | 88152999 | |||||||
| chr12:88153205 | A | G | 67 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(64): Show |
80 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.190-86A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 2/13 | chr12 | 88153205 | |||||||
| chr12:88153215 | G | A | 1 | a0002c0002t0008g0183 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.190-76G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 2/13 | chr12 | 88153215 | |||||||
| chr12:88153546 | C | G | 2 | a0001c0001t0001g0095 a0001c0001t0002g0094 |
2 | NA18957.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.408+37C>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 3/13 | chr12 | 88153546 | |||||||
| chr12:88153583 | A | G | 18 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0023 others(15): Show |
30 | HG00741.hp1 HG01074.hp2 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.408+74A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 3/13 | chr12 | 88153583 | |||||||
| chr12:88153709 | A | T | 4 | a0001c0001t0009g0044 a0001c0001t0009g0045 a0001c0001t0009g0046 others(1): Show |
4 | HG02257.hp2 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.408+200A>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 3/13 | chr12 | 88153709 | |||||||
| chr12:88154231 | A | G | 17 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0027 others(14): Show |
19 | HG01109.hp2 HG01192.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.409-57A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 3/13 | chr12 | 88154231 | |||||||
| chr12:88154491 | G | A | 3 | a0001c0001t0015g0041 a0001c0001t0015g0042 a0001c0001t0022g0043 |
3 | HG01884.hp2 HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.508+104G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 4/13 | chr12 | 88154491 | |||||||
| chr12:88154785 | A | G | 17 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0027 others(14): Show |
19 | HG01109.hp2 HG01192.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.508+398A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 4/13 | chr12 | 88154785 | |||||||
| chr12:88154885 | T | C | 2 | a0001c0001t0001g0013 a0001c0001t0007g0075 |
3 | HG02109.hp1 HG02559.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.508+498T>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 4/13 | chr12 | 88154885 | |||||||
| chr12:88154930 | AT | A | 17 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0027 others(14): Show |
19 | HG01109.hp2 HG01192.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.508+550delT | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr12 | 88154930 | ||||||
| chr12:88155450 | C | A | 1 | a0001c0001t0014g0096 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.508+1063C>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 4/13 | chr12 | 88155450 | |||||||
| chr12:88155591 | T | A | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(125): Show |
160 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(157): Show |
intron_variant | MODIFIER | c.508+1204T>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 4/13 | chr12 | 88155591 | |||||||
| chr12:88155656 | A | G | 1 | a0001c0001t0002g0129 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.508+1269A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 4/13 | chr12 | 88155656 | |||||||
| chr12:88155912 | C | T | 17 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0027 others(14): Show |
19 | HG01109.hp2 HG01192.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.508+1525C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 4/13 | chr12 | 88155912 | |||||||
| chr12:88155967 | A | G | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(163): Show |
203 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(200): Show |
intron_variant | MODIFIER | c.508+1580A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 4/13 | chr12 | 88155967 | |||||||
| chr12:88155996 | C | G | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(163): Show |
203 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(200): Show |
intron_variant | MODIFIER | c.508+1609C>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 4/13 | chr12 | 88155996 | |||||||
| chr12:88156072 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.508+1685C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 4/13 | chr12 | 88156072 | |||||||
| chr12:88156180 | A | G | 1 | a0007c0008t0002g0127 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.508+1793A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 4/13 | chr12 | 88156180 | |||||||
| chr12:88156330 | C | T | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(125): Show |
160 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(157): Show |
intron_variant | MODIFIER | c.508+1943C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 4/13 | chr12 | 88156330 | |||||||
| chr12:88156379 | G | T | 7 | a0001c0001t0009g0044 a0001c0001t0009g0045 a0001c0001t0009g0046 others(4): Show |
7 | HG01884.hp2 HG02257.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.508+1992G>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 4/13 | chr12 | 88156379 | |||||||
| chr12:88156417 | T | C | 1 | a0001c0001t0017g0076 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.508+2030T>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 4/13 | chr12 | 88156417 | |||||||
| chr12:88156449 | A | C | 1 | a0001c0001t0002g0068 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.508+2062A>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 4/13 | chr12 | 88156449 | |||||||
| chr12:88156618 | A | G | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(125): Show |
160 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(157): Show |
intron_variant | MODIFIER | c.508+2231A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 4/13 | chr12 | 88156618 | |||||||
| chr12:88156637 | G | A | 1 | a0002c0002t0008g0183 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.508+2250G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 4/13 | chr12 | 88156637 | |||||||
| chr12:88156696 | T | TA | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(160): Show |
200 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(197): Show |
intron_variant | MODIFIER | c.508+2320dupA | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr12 | 88156696 | ||||||
| chr12:88156811 | G | GT | 11 | a0001c0001t0003g0038 a0002c0002t0008g0006 a0002c0002t0008g0048 others(8): Show |
14 | HG02155.hp1 HG02486.hp2 HG02886.hp2 others(11): Show |
intron_variant | MODIFIER | c.508+2441dupT | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr12 | 88156811 | ||||||
| chr12:88156811 | G | GTT | 70 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0011 others(67): Show |
89 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.508+2440_508+2441d others(4): Show |
TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr12 | 88156811 | ||||||
| chr12:88156811 | G | GTTT | 47 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0023 others(44): Show |
56 | HG00609.hp2 HG00735.hp1 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.508+2439_508+2441d others(5): Show |
TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr12 | 88156811 | ||||||
| chr12:88156811 | G | GTTTT | 11 | a0001c0001t0001g0004 a0001c0001t0001g0091 a0001c0001t0001g0095 others(8): Show |
15 | HG01109.hp1 HG01891.hp1 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.508+2438_508+2441d others(6): Show |
TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr12 | 88156811 | ||||||
| chr12:88156813 | T | G | 17 | a0001c0001t0004g0005 a0001c0001t0004g0149 a0001c0001t0004g0151 others(14): Show |
20 | HG01884.hp2 HG02280.hp1 HG02572.hp2 others(17): Show |
intron_variant | MODIFIER | c.508+2426T>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 4/13 | chr12 | 88156813 | |||||||
| chr12:88156815 | T | G | 1 | a0001c0001t0004g0156 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.508+2428T>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 4/13 | chr12 | 88156815 | |||||||
| chr12:88156991 | AT | A | 14 | a0002c0002t0008g0006 a0002c0002t0008g0048 a0002c0002t0008g0049 others(11): Show |
17 | HG02155.hp1 HG02486.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.508+2607delT | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr12 | 88156991 | ||||||
| chr12:88156994 | T | A | 14 | a0002c0002t0008g0006 a0002c0002t0008g0048 a0002c0002t0008g0049 others(11): Show |
17 | HG02155.hp1 HG02486.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.508+2607T>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 4/13 | chr12 | 88156994 | |||||||
| chr12:88157479 | A | G | 17 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0027 others(14): Show |
19 | HG01109.hp2 HG01192.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.509-2635A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 4/13 | chr12 | 88157479 | |||||||
| chr12:88157822 | G | A | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(163): Show |
203 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(200): Show |
intron_variant | MODIFIER | c.509-2292G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 4/13 | chr12 | 88157822 | |||||||
| chr12:88158010 | C | T | 1 | a0001c0001t0039g0153 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.509-2104C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 4/13 | chr12 | 88158010 | |||||||
| chr12:88158429 | A | AT | 14 | a0002c0002t0008g0006 a0002c0002t0008g0048 a0002c0002t0008g0049 others(11): Show |
17 | HG02155.hp1 HG02486.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.509-1683dupT | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr12 | 88158429 | ||||||
| chr12:88158677 | T | TATTCA | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(156): Show |
196 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(193): Show |
intron_variant | MODIFIER | c.509-1436_509-1432d others(7): Show |
TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr12 | 88158677 | ||||||
| chr12:88158880 | C | T | 18 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0023 others(15): Show |
30 | HG00741.hp1 HG01074.hp2 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.509-1234C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 4/13 | chr12 | 88158880 | |||||||
| chr12:88159040 | G | A | 32 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0023 others(29): Show |
45 | HG00609.hp2 HG00741.hp1 HG01074.hp2 others(42): Show |
intron_variant | MODIFIER | c.509-1074G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 4/13 | chr12 | 88159040 | |||||||
| chr12:88159155 | T | C | 1 | a0001c0001t0003g0038 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.509-959T>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 4/13 | chr12 | 88159155 | |||||||
| chr12:88159226 | A | G | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(156): Show |
196 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(193): Show |
intron_variant | MODIFIER | c.509-888A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 4/13 | chr12 | 88159226 | |||||||
| chr12:88159416 | G | A | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG02486.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.509-698G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 4/13 | chr12 | 88159416 | |||||||
| chr12:88159487 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.509-627C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 4/13 | chr12 | 88159487 | |||||||
| chr12:88159540 | G | A | 3 | a0001c0001t0015g0041 a0001c0001t0015g0042 a0001c0001t0022g0043 |
3 | HG01884.hp2 HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.509-574G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 4/13 | chr12 | 88159540 | |||||||
| chr12:88159640 | G | A | 17 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0027 others(14): Show |
19 | HG01109.hp2 HG01192.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.509-474G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 4/13 | chr12 | 88159640 | |||||||
| chr12:88159662 | TA | T | 14 | a0001c0001t0009g0044 a0001c0001t0033g0080 a0002c0002t0008g0006 others(11): Show |
17 | HG01496.hp1 HG02155.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.509-437delA | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr12 | 88159662 | ||||||
| chr12:88159672 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.509-442A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 4/13 | chr12 | 88159672 | |||||||
| chr12:88159683 | G | A | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(156): Show |
196 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(193): Show |
intron_variant | MODIFIER | c.509-431G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 4/13 | chr12 | 88159683 | |||||||
| chr12:88159813 | C | G | 14 | a0002c0002t0008g0006 a0002c0002t0008g0048 a0002c0002t0008g0049 others(11): Show |
17 | HG02155.hp1 HG02486.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.509-301C>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 4/13 | chr12 | 88159813 | |||||||
| chr12:88159918 | A | C | 17 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0027 others(14): Show |
19 | HG01109.hp2 HG01192.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.509-196A>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 4/13 | chr12 | 88159918 | |||||||
| chr12:88160968 | A | C | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(125): Show |
160 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(157): Show |
intron_variant | MODIFIER | c.797+117A>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 6/13 | chr12 | 88160968 | |||||||
| chr12:88161027 | G | A | 2 | a0002c0002t0027g0054 a0002c0002t0032g0055 |
2 | HG02486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.797+176G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 6/13 | chr12 | 88161027 | |||||||
| chr12:88161054 | A | G | 1 | a0001c0001t0013g0168 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.797+203A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 6/13 | chr12 | 88161054 | |||||||
| chr12:88161188 | T | C | 1 | a0005c0005t0001g0143 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.797+337T>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 6/13 | chr12 | 88161188 | |||||||
| chr12:88161217 | G | A | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(177): Show |
220 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(217): Show |
intron_variant | MODIFIER | c.797+366G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 6/13 | chr12 | 88161217 | |||||||
| chr12:88161334 | A | G | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(125): Show |
160 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(157): Show |
intron_variant | MODIFIER | c.797+483A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 6/13 | chr12 | 88161334 | |||||||
| chr12:88161376 | C | G | 3 | a0001c0001t0015g0041 a0001c0001t0015g0042 a0001c0001t0022g0043 |
3 | HG01884.hp2 HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.797+525C>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 6/13 | chr12 | 88161376 | |||||||
| chr12:88161395 | G | T | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(178): Show |
222 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(219): Show |
intron_variant | MODIFIER | c.797+544G>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 6/13 | chr12 | 88161395 | |||||||
| chr12:88161629 | C | T | 1 | a0001c0001t0007g0090 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.797+778C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 6/13 | chr12 | 88161629 | |||||||
| chr12:88161714 | T | G | 11 | a0001c0001t0006g0003 a0001c0001t0006g0077 a0001c0001t0006g0078 others(8): Show |
16 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.797+863T>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 6/13 | chr12 | 88161714 | |||||||
| chr12:88161857 | A | G | 1 | a0002c0002t0012g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.797+1006A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 6/13 | chr12 | 88161857 | |||||||
| chr12:88161891 | A | G | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(163): Show |
203 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(200): Show |
intron_variant | MODIFIER | c.797+1040A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 6/13 | chr12 | 88161891 | |||||||
| chr12:88162325 | T | G | 1 | a0001c0001t0001g0097 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.797+1474T>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 6/13 | chr12 | 88162325 | |||||||
| chr12:88162341 | T | C | 1 | a0001c0001t0005g0160 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.797+1490T>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 6/13 | chr12 | 88162341 | |||||||
| chr12:88162407 | T | C | 4 | a0001c0001t0009g0044 a0001c0001t0009g0045 a0001c0001t0009g0046 others(1): Show |
4 | HG02257.hp2 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.797+1556T>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 6/13 | chr12 | 88162407 | |||||||
| chr12:88162413 | A | C | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(156): Show |
196 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(193): Show |
intron_variant | MODIFIER | c.797+1562A>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 6/13 | chr12 | 88162413 | |||||||
| chr12:88162488 | A | G | 14 | a0001c0001t0004g0005 a0001c0001t0004g0149 a0001c0001t0004g0151 others(11): Show |
17 | HG02280.hp1 HG02572.hp2 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.797+1637A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 6/13 | chr12 | 88162488 | |||||||
| chr12:88162553 | C | T | 1 | a0001c0001t0029g0131 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.797+1702C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 6/13 | chr12 | 88162553 | |||||||
| chr12:88162669 | T | A | 1 | a0001c0001t0023g0039 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.797+1818T>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 6/13 | chr12 | 88162669 | |||||||
| chr12:88162808 | C | T | 1 | a0001c0001t0001g0017 | 2 | HG02622.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.797+1957C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 6/13 | chr12 | 88162808 | |||||||
| chr12:88162919 | C | CT | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(177): Show |
221 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(218): Show |
intron_variant | MODIFIER | c.797+2079dupT | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr12 | 88162919 | ||||||
| chr12:88162984 | C | T | 17 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0027 others(14): Show |
19 | HG01109.hp2 HG01192.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.797+2133C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 6/13 | chr12 | 88162984 | |||||||
| chr12:88163148 | T | C | 7 | a0001c0001t0009g0044 a0001c0001t0009g0045 a0001c0001t0009g0046 others(4): Show |
7 | HG01884.hp2 HG02257.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.797+2297T>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 6/13 | chr12 | 88163148 | |||||||
| chr12:88163176 | A | G | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(145): Show |
182 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(179): Show |
intron_variant | MODIFIER | c.797+2325A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 6/13 | chr12 | 88163176 | |||||||
| chr12:88163318 | G | A | 1 | a0001c0001t0001g0081 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.797+2467G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 6/13 | chr12 | 88163318 | |||||||
| chr12:88163387 | T | A | 17 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0027 others(14): Show |
19 | HG01109.hp2 HG01192.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.797+2536T>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 6/13 | chr12 | 88163387 | |||||||
| chr12:88163455 | A | G | 1 | a0001c0001t0002g0084 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.797+2604A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 6/13 | chr12 | 88163455 | |||||||
| chr12:88163552 | C | A | 3 | a0002c0002t0012g0146 a0002c0002t0012g0147 a0002c0002t0020g0148 |
3 | HG02559.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.797+2701C>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 6/13 | chr12 | 88163552 | |||||||
| chr12:88163680 | TC | T | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(125): Show |
160 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(157): Show |
intron_variant | MODIFIER | c.798-2649delC | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 6/13 | chr12 | 88163680 | |||||||
| chr12:88163735 | T | A | 1 | a0001c0001t0003g0029 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.798-2595T>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 6/13 | chr12 | 88163735 | |||||||
| chr12:88164053 | G | A | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(125): Show |
160 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(157): Show |
intron_variant | MODIFIER | c.798-2277G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 6/13 | chr12 | 88164053 | |||||||
| chr12:88164054 | T | G | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(125): Show |
160 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(157): Show |
intron_variant | MODIFIER | c.798-2276T>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 6/13 | chr12 | 88164054 | |||||||
| chr12:88164189 | C | CA | 13 | a0001c0001t0001g0023 a0001c0001t0001g0086 a0001c0001t0001g0098 others(10): Show |
13 | HG00639.hp2 HG01074.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.798-2119dupA | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr12 | 88164189 | ||||||
| chr12:88164189 | CA | C | 6 | a0001c0001t0002g0016 a0001c0001t0002g0062 a0001c0001t0004g0152 others(3): Show |
7 | HG02451.hp2 HG02976.hp1 NA18965.hp1 others(4): Show |
intron_variant | MODIFIER | c.798-2119delA | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr12 | 88164189 | ||||||
| chr12:88164777 | C | T | 4 | a0001c0001t0001g0011 a0001c0001t0001g0057 a0001c0001t0001g0133 others(1): Show |
4 | HG00099.hp2 HG01106.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.798-1553C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 6/13 | chr12 | 88164777 | |||||||
| chr12:88164857 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.798-1473A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 6/13 | chr12 | 88164857 | |||||||
| chr12:88164921 | G | A | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(163): Show |
203 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(200): Show |
intron_variant | MODIFIER | c.798-1409G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 6/13 | chr12 | 88164921 | |||||||
| chr12:88164962 | A | G | 1 | a0001c0001t0009g0046 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.798-1368A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 6/13 | chr12 | 88164962 | |||||||
| chr12:88165073 | C | T | 1 | a0001c0001t0001g0040 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.798-1257C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 6/13 | chr12 | 88165073 | |||||||
| chr12:88165214 | A | G | 1 | a0001c0001t0002g0129 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.798-1116A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 6/13 | chr12 | 88165214 | |||||||
| chr12:88165504 | A | T | 5 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(2): Show |
5 | HG02145.hp2 HG02615.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.798-826A>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 6/13 | chr12 | 88165504 | |||||||
| chr12:88165614 | A | G | 3 | a0002c0002t0012g0146 a0002c0002t0012g0147 a0002c0002t0020g0148 |
3 | HG02559.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.798-716A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 6/13 | chr12 | 88165614 | |||||||
| chr12:88165740 | G | T | 1 | a0002c0002t0012g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.798-590G>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 6/13 | chr12 | 88165740 | |||||||
| chr12:88165992 | T | C | 3 | a0001c0001t0015g0041 a0001c0001t0015g0042 a0001c0001t0022g0043 |
3 | HG01884.hp2 HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.798-338T>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 6/13 | chr12 | 88165992 | |||||||
| chr12:88166992 | G | GT | 6 | a0001c0001t0005g0022 a0001c0001t0005g0167 a0001c0001t0013g0022 others(3): Show |
6 | HG01071.hp2 HG02258.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1050+428dupT | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr12 | 88166992 | ||||||
| chr12:88166992 | GT | G | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(145): Show |
185 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(182): Show |
intron_variant | MODIFIER | c.1050+428delT | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr12 | 88166992 | ||||||
| chr12:88167103 | A | G | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(128): Show |
163 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(160): Show |
intron_variant | MODIFIER | c.1050+521A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 7/13 | chr12 | 88167103 | |||||||
| chr12:88167122 | C | T | 1 | a0001c0001t0002g0063 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1050+540C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 7/13 | chr12 | 88167122 | |||||||
| chr12:88167185 | A | G | 1 | a0001c0001t0038g0169 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1050+603A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 7/13 | chr12 | 88167185 | |||||||
| chr12:88167271 | G | A | 2 | a0001c0001t0005g0020 a0001c0001t0036g0020 |
2 | HG04228.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1050+689G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 7/13 | chr12 | 88167271 | |||||||
| chr12:88167509 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1050+927T>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 7/13 | chr12 | 88167509 | |||||||
| chr12:88167566 | T | G | 1 | a0002c0002t0031g0056 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1050+984T>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 7/13 | chr12 | 88167566 | |||||||
| chr12:88167579 | G | A | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(125): Show |
160 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(157): Show |
intron_variant | MODIFIER | c.1050+997G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 7/13 | chr12 | 88167579 | |||||||
| chr12:88167609 | ATACACAG others(19): Show |
A | 1 | a0001c0001t0039g0153 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1050+1058_1050+108 others(30): Show |
TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr12 | 88167609 | ||||||
| chr12:88167621 | C | T | 1 | a0001c0001t0006g0140 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1050+1039C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 7/13 | chr12 | 88167621 | |||||||
| chr12:88167669 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1050+1087T>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 7/13 | chr12 | 88167669 | |||||||
| chr12:88167702 | A | G | 5 | a0001c0001t0001g0007 a0001c0001t0001g0115 a0001c0001t0001g0134 others(2): Show |
6 | HG00642.hp1 HG01243.hp2 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.1050+1120A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 7/13 | chr12 | 88167702 | |||||||
| chr12:88168065 | G | A | 1 | a0001c0001t0022g0043 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1050+1483G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 7/13 | chr12 | 88168065 | |||||||
| chr12:88168310 | G | A | 2 | a0004c0003t0001g0100 a0004c0003t0001g0119 |
2 | HG02622.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1050+1728G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 7/13 | chr12 | 88168310 | |||||||
| chr12:88168380 | A | AT | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(156): Show |
196 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(193): Show |
intron_variant | MODIFIER | c.1050+1800dupT | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr12 | 88168380 | ||||||
| chr12:88168384 | A | T | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(156): Show |
196 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(193): Show |
intron_variant | MODIFIER | c.1050+1802A>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 7/13 | chr12 | 88168384 | |||||||
| chr12:88168444 | T | A | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(180): Show |
224 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(221): Show |
intron_variant | MODIFIER | c.1050+1862T>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 7/13 | chr12 | 88168444 | |||||||
| chr12:88168578 | C | G | 1 | a0001c0001t0022g0043 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1050+1996C>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 7/13 | chr12 | 88168578 | |||||||
| chr12:88168655 | G | C | 1 | a0001c0001t0023g0039 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1050+2073G>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 7/13 | chr12 | 88168655 | |||||||
| chr12:88168664 | G | C | 1 | a0001c0001t0006g0182 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1050+2082G>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 7/13 | chr12 | 88168664 | |||||||
| chr12:88168757 | A | G | 1 | a0001c0001t0038g0169 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1050+2175A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 7/13 | chr12 | 88168757 | |||||||
| chr12:88168795 | T | C | 11 | a0002c0002t0008g0006 a0002c0002t0008g0048 a0002c0002t0008g0049 others(8): Show |
14 | HG02155.hp1 HG02486.hp2 HG02886.hp2 others(11): Show |
intron_variant | MODIFIER | c.1050+2213T>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 7/13 | chr12 | 88168795 | |||||||
| chr12:88169067 | T | C | 14 | a0002c0002t0008g0006 a0002c0002t0008g0048 a0002c0002t0008g0049 others(11): Show |
17 | HG02155.hp1 HG02486.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.1050+2485T>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 7/13 | chr12 | 88169067 | |||||||
| chr12:88169091 | T | C | 17 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0027 others(14): Show |
19 | HG01109.hp2 HG01192.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.1050+2509T>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 7/13 | chr12 | 88169091 | |||||||
| chr12:88169289 | A | G | 3 | a0001c0001t0015g0041 a0001c0001t0015g0042 a0001c0001t0022g0043 |
3 | HG01884.hp2 HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1050+2707A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 7/13 | chr12 | 88169289 | |||||||
| chr12:88169314 | C | A | 1 | a0001c0001t0001g0095 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1050+2732C>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 7/13 | chr12 | 88169314 | |||||||
| chr12:88169357 | G | A | 7 | a0002c0002t0008g0006 a0002c0002t0008g0048 a0002c0002t0008g0049 others(4): Show |
10 | HG02155.hp1 HG06807.hp2 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.1050+2775G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 7/13 | chr12 | 88169357 | |||||||
| chr12:88169461 | C | T | 4 | a0001c0001t0009g0044 a0001c0001t0009g0045 a0001c0001t0009g0046 others(1): Show |
4 | HG02257.hp2 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1050+2879C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 7/13 | chr12 | 88169461 | |||||||
| chr12:88169488 | G | T | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(156): Show |
196 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(193): Show |
intron_variant | MODIFIER | c.1050+2906G>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 7/13 | chr12 | 88169488 | |||||||
| chr12:88169935 | CAGAAAAA others(14): Show |
C | 2 | a0002c0002t0012g0147 a0002c0002t0020g0148 |
2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1051-2652_1051-263 others(25): Show |
TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr12 | 88169935 | ||||||
| chr12:88169937 | GA | G | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(175): Show |
209 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(206): Show |
intron_variant | MODIFIER | c.1051-2647delA | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr12 | 88169937 | ||||||
| chr12:88169937 | GAA | G | 22 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0018 others(19): Show |
29 | HG00741.hp1 HG01074.hp1 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.1051-2648_1051-264 others(6): Show |
TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr12 | 88169937 | ||||||
| chr12:88169991 | A | G | 3 | a0002c0002t0012g0146 a0002c0002t0012g0147 a0002c0002t0020g0148 |
3 | HG02559.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1051-2606A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 7/13 | chr12 | 88169991 | |||||||
| chr12:88170002 | G | T | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(163): Show |
203 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(200): Show |
intron_variant | MODIFIER | c.1051-2595G>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 7/13 | chr12 | 88170002 | |||||||
| chr12:88170038 | G | A | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(125): Show |
160 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(157): Show |
intron_variant | MODIFIER | c.1051-2559G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 7/13 | chr12 | 88170038 | |||||||
| chr12:88170328 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1051-2269A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 7/13 | chr12 | 88170328 | |||||||
| chr12:88170374 | G | A | 4 | a0001c0001t0009g0044 a0001c0001t0009g0045 a0001c0001t0009g0046 others(1): Show |
4 | HG02257.hp2 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1051-2223G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 7/13 | chr12 | 88170374 | |||||||
| chr12:88170454 | C | T | 1 | a0001c0001t0010g0037 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1051-2143C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 7/13 | chr12 | 88170454 | |||||||
| chr12:88170556 | T | C | 1 | a0001c0001t0005g0161 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1051-2041T>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 7/13 | chr12 | 88170556 | |||||||
| chr12:88171022 | A | G | 40 | a0001c0001t0004g0005 a0001c0001t0004g0149 a0001c0001t0004g0151 others(37): Show |
44 | HG01071.hp2 HG01884.hp2 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.1051-1575A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 7/13 | chr12 | 88171022 | |||||||
| chr12:88171330 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1051-1267T>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 7/13 | chr12 | 88171330 | |||||||
| chr12:88171423 | A | G | 1 | a0001c0001t0002g0065 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1051-1174A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 7/13 | chr12 | 88171423 | |||||||
| chr12:88171440 | G | A | 8 | a0002c0002t0008g0006 a0002c0002t0008g0048 a0002c0002t0008g0049 others(5): Show |
11 | HG02155.hp1 HG02886.hp2 HG06807.hp2 others(8): Show |
intron_variant | MODIFIER | c.1051-1157G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 7/13 | chr12 | 88171440 | |||||||
| chr12:88171484 | C | T | 1 | a0001c0001t0001g0113 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1051-1113C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 7/13 | chr12 | 88171484 | |||||||
| chr12:88171502 | G | A | 33 | a0001c0001t0004g0005 a0001c0001t0004g0149 a0001c0001t0004g0151 others(30): Show |
37 | HG01071.hp2 HG01891.hp2 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.1051-1095G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 7/13 | chr12 | 88171502 | |||||||
| chr12:88171580 | A | G | 17 | a0001c0001t0015g0041 a0001c0001t0015g0042 a0001c0001t0022g0043 others(14): Show |
20 | HG01884.hp2 HG02155.hp1 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.1051-1017A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 7/13 | chr12 | 88171580 | |||||||
| chr12:88171588 | C | A | 1 | a0001c0001t0022g0043 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1051-1009C>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 7/13 | chr12 | 88171588 | |||||||
| chr12:88171601 | G | A | 14 | a0002c0002t0008g0006 a0002c0002t0008g0048 a0002c0002t0008g0049 others(11): Show |
17 | HG02155.hp1 HG02486.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.1051-996G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 7/13 | chr12 | 88171601 | |||||||
| chr12:88171650 | T | C | 33 | a0001c0001t0004g0005 a0001c0001t0004g0149 a0001c0001t0004g0151 others(30): Show |
37 | HG01071.hp2 HG01891.hp2 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.1051-947T>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 7/13 | chr12 | 88171650 | |||||||
| chr12:88172010 | A | G | 4 | a0001c0001t0009g0044 a0001c0001t0009g0045 a0001c0001t0009g0046 others(1): Show |
4 | HG02257.hp2 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1051-587A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 7/13 | chr12 | 88172010 | |||||||
| chr12:88172196 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1051-401A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 7/13 | chr12 | 88172196 | |||||||
| chr12:88172221 | A | G | 1 | a0001c0001t0001g0026 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1051-376A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 7/13 | chr12 | 88172221 | |||||||
| chr12:88172297 | C | T | 7 | a0001c0001t0009g0044 a0001c0001t0009g0045 a0001c0001t0009g0046 others(4): Show |
7 | HG01884.hp2 HG02257.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1051-300C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 7/13 | chr12 | 88172297 | |||||||
| chr12:88172456 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1051-141A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 7/13 | chr12 | 88172456 | |||||||
| chr12:88172557 | A | T | 17 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0027 others(14): Show |
19 | HG01109.hp2 HG01192.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.1051-40A>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 7/13 | chr12 | 88172557 | |||||||
| chr12:88172866 | C | G | 1 | a0001c0001t0038g0169 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1199+121C>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 8/13 | chr12 | 88172866 | |||||||
| chr12:88174168 | T | A | 1 | a0001c0001t0001g0082 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1200-439T>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 8/13 | chr12 | 88174168 | |||||||
| chr12:88174318 | G | A | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(195): Show |
239 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(236): Show |
intron_variant | MODIFIER | c.1200-289G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 8/13 | chr12 | 88174318 | |||||||
| chr12:88174496 | CAT | C | 3 | a0001c0001t0003g0009 a0001c0001t0003g0028 a0001c0001t0010g0009 |
4 | HG01109.hp2 HG02258.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.1200-108_1200-107d others(4): Show |
TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr12 | 88174496 | ||||||
| chr12:88175102 | T | C | 1 | a0001c0001t0022g0043 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1320+375T>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 9/13 | chr12 | 88175102 | |||||||
| chr12:88175113 | A | G | 1 | a0002c0002t0008g0050 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1320+386A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 9/13 | chr12 | 88175113 | |||||||
| chr12:88175169 | G | T | 1 | a0001c0001t0001g0141 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1320+442G>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 9/13 | chr12 | 88175169 | |||||||
| chr12:88175292 | C | T | 7 | a0002c0002t0008g0006 a0002c0002t0008g0048 a0002c0002t0008g0049 others(4): Show |
10 | HG02155.hp1 HG06807.hp2 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.1320+565C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 9/13 | chr12 | 88175292 | |||||||
| chr12:88175401 | A | G | 2 | a0002c0002t0012g0147 a0002c0002t0020g0148 |
2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1320+674A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 9/13 | chr12 | 88175401 | |||||||
| chr12:88175403 | T | G | 17 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0027 others(14): Show |
19 | HG01109.hp2 HG01192.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.1320+676T>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 9/13 | chr12 | 88175403 | |||||||
| chr12:88175523 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1321-685T>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 9/13 | chr12 | 88175523 | |||||||
| chr12:88176106 | C | T | 40 | a0001c0001t0004g0005 a0001c0001t0004g0149 a0001c0001t0004g0151 others(37): Show |
44 | HG01071.hp2 HG01884.hp2 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.1321-102C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 9/13 | chr12 | 88176106 | |||||||
| chr12:88176475 | C | T | 1 | a0001c0001t0015g0042 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1432+156C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88176475 | |||||||
| chr12:88176582 | G | A | 2 | a0001c0001t0016g0014 a0001c0001t0029g0131 |
3 | HG02056.hp1 NA18969.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1432+263G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88176582 | |||||||
| chr12:88176693 | T | C | 33 | a0001c0001t0004g0005 a0001c0001t0004g0149 a0001c0001t0004g0151 others(30): Show |
37 | HG01071.hp2 HG01891.hp2 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.1432+374T>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88176693 | |||||||
| chr12:88176782 | C | G | 2 | a0001c0001t0005g0165 a0001c0001t0005g0167 |
2 | HG01071.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.1432+463C>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88176782 | |||||||
| chr12:88176879 | A | G | 17 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0027 others(14): Show |
19 | HG01109.hp2 HG01192.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.1432+560A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88176879 | |||||||
| chr12:88176998 | A | C | 1 | a0001c0001t0013g0168 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1432+679A>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88176998 | |||||||
| chr12:88177192 | G | T | 17 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0027 others(14): Show |
19 | HG01109.hp2 HG01192.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.1432+873G>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88177192 | |||||||
| chr12:88177241 | G | A | 1 | a0001c0001t0003g0029 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1432+922G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88177241 | |||||||
| chr12:88177281 | G | A | 8 | a0002c0002t0008g0006 a0002c0002t0008g0048 a0002c0002t0008g0049 others(5): Show |
11 | HG02155.hp1 HG02886.hp2 HG06807.hp2 others(8): Show |
intron_variant | MODIFIER | c.1432+962G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88177281 | |||||||
| chr12:88177327 | C | CA | 8 | a0002c0002t0008g0006 a0002c0002t0008g0048 a0002c0002t0008g0049 others(5): Show |
11 | HG02155.hp1 HG02886.hp2 HG06807.hp2 others(8): Show |
intron_variant | MODIFIER | c.1432+1020dupA | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr12 | 88177327 | ||||||
| chr12:88177327 | CA | C | 17 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0027 others(14): Show |
19 | HG01109.hp2 HG01192.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.1432+1020delA | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr12 | 88177327 | ||||||
| chr12:88177380 | G | A | 4 | a0001c0001t0009g0044 a0001c0001t0009g0045 a0001c0001t0009g0046 others(1): Show |
4 | HG02257.hp2 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1432+1061G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88177380 | |||||||
| chr12:88177395 | T | C | 2 | a0001c0001t0001g0120 a0001c0001t0025g0102 |
2 | NA18944.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1432+1076T>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88177395 | |||||||
| chr12:88177609 | C | T | 2 | a0001c0001t0001g0015 a0001c0001t0019g0015 |
2 | HG01099.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1432+1290C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88177609 | |||||||
| chr12:88177712 | G | A | 4 | a0001c0001t0009g0044 a0001c0001t0009g0045 a0001c0001t0009g0046 others(1): Show |
4 | HG02257.hp2 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1432+1393G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88177712 | |||||||
| chr12:88177739 | A | T | 1 | a0001c0001t0016g0014 | 2 | NA18969.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1432+1420A>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88177739 | |||||||
| chr12:88177771 | T | A | 14 | a0002c0002t0008g0006 a0002c0002t0008g0048 a0002c0002t0008g0049 others(11): Show |
17 | HG02155.hp1 HG02486.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.1432+1452T>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88177771 | |||||||
| chr12:88177843 | T | A | 1 | a0001c0001t0007g0126 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1432+1524T>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88177843 | |||||||
| chr12:88178149 | A | G | 5 | a0001c0001t0004g0005 a0001c0001t0004g0149 a0001c0001t0004g0151 others(2): Show |
8 | HG02572.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1432+1830A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88178149 | |||||||
| chr12:88178321 | G | T | 2 | a0001c0001t0005g0021 a0001c0001t0035g0021 |
2 | HG01891.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1432+2002G>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88178321 | |||||||
| chr12:88178328 | G | A | 1 | a0001c0001t0006g0077 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1432+2009G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88178328 | |||||||
| chr12:88178627 | AC | A | 17 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0005g0022 others(14): Show |
17 | HG01071.hp2 HG01891.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1432+2312delC | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr12 | 88178627 | ||||||
| chr12:88178738 | A | G | 40 | a0001c0001t0004g0005 a0001c0001t0004g0149 a0001c0001t0004g0151 others(37): Show |
44 | HG01071.hp2 HG01884.hp2 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.1432+2419A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88178738 | |||||||
| chr12:88179473 | A | G | 1 | a0002c0002t0020g0148 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1432+3154A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88179473 | |||||||
| chr12:88179477 | G | A | 2 | a0001c0001t0001g0013 a0001c0001t0007g0075 |
3 | HG02109.hp1 HG02559.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1432+3158G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88179477 | |||||||
| chr12:88179527 | G | A | 2 | a0001c0001t0017g0076 a0001c0001t0017g0087 |
2 | HG00639.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1432+3208G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88179527 | |||||||
| chr12:88179721 | G | A | 1 | a0001c0001t0005g0161 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1432+3402G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88179721 | |||||||
| chr12:88179737 | C | T | 11 | a0002c0002t0008g0006 a0002c0002t0008g0048 a0002c0002t0008g0049 others(8): Show |
14 | HG02155.hp1 HG02486.hp2 HG02886.hp2 others(11): Show |
intron_variant | MODIFIER | c.1432+3418C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88179737 | |||||||
| chr12:88179764 | C | T | 124 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(121): Show |
152 | HG00099.hp1 HG00099.hp2 HG00609.hp2 others(149): Show |
intron_variant | MODIFIER | c.1432+3445C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88179764 | |||||||
| chr12:88179785 | A | G | 2 | a0002c0002t0012g0147 a0002c0002t0020g0148 |
2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1432+3466A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88179785 | |||||||
| chr12:88179802 | A | T | 6 | a0001c0001t0001g0025 a0001c0001t0001g0097 a0001c0001t0001g0098 others(3): Show |
6 | HG01074.hp1 HG01891.hp1 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.1432+3483A>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88179802 | |||||||
| chr12:88179867 | A | G | 1 | a0001c0001t0001g0179 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1432+3548A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88179867 | |||||||
| chr12:88179952 | G | A | 2 | a0001c0001t0017g0076 a0001c0001t0017g0087 |
2 | HG00639.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1432+3633G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88179952 | |||||||
| chr12:88180007 | C | T | 14 | a0002c0002t0008g0006 a0002c0002t0008g0048 a0002c0002t0008g0049 others(11): Show |
17 | HG02155.hp1 HG02486.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.1432+3688C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88180007 | |||||||
| chr12:88180073 | C | G | 14 | a0002c0002t0008g0006 a0002c0002t0008g0048 a0002c0002t0008g0049 others(11): Show |
17 | HG02155.hp1 HG02486.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.1432+3754C>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88180073 | |||||||
| chr12:88180168 | ACT | A | 17 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0027 others(14): Show |
19 | HG01109.hp2 HG01192.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.1432+3851_1432+385 others(6): Show |
TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr12 | 88180168 | ||||||
| chr12:88180279 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1432+3960C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88180279 | |||||||
| chr12:88180324 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1432+4005T>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88180324 | |||||||
| chr12:88180349 | T | C | 1 | a0001c0001t0002g0094 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1432+4030T>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88180349 | |||||||
| chr12:88180365 | G | A | 3 | a0001c0001t0015g0041 a0001c0001t0015g0042 a0001c0001t0022g0043 |
3 | HG01884.hp2 HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1432+4046G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88180365 | |||||||
| chr12:88180371 | G | C | 1 | a0001c0001t0014g0096 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1432+4052G>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88180371 | |||||||
| chr12:88180620 | G | A | 1 | a0002c0002t0020g0148 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1432+4301G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88180620 | |||||||
| chr12:88180709 | C | T | 17 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0027 others(14): Show |
19 | HG01109.hp2 HG01192.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.1432+4390C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88180709 | |||||||
| chr12:88180737 | T | C | 2 | a0002c0002t0012g0147 a0002c0002t0020g0148 |
2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1432+4418T>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88180737 | |||||||
| chr12:88180830 | A | G | 1 | a0002c0002t0012g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1432+4511A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88180830 | |||||||
| chr12:88180893 | T | A | 1 | a0001c0001t0001g0141 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1432+4574T>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88180893 | |||||||
| chr12:88180993 | A | T | 36 | a0001c0001t0004g0005 a0001c0001t0004g0149 a0001c0001t0004g0151 others(33): Show |
40 | HG01071.hp2 HG01884.hp2 HG01891.hp2 others(37): Show |
intron_variant | MODIFIER | c.1432+4674A>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88180993 | |||||||
| chr12:88181071 | T | C | 3 | a0001c0001t0015g0041 a0001c0001t0015g0042 a0001c0001t0022g0043 |
3 | HG01884.hp2 HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1432+4752T>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88181071 | |||||||
| chr12:88181073 | G | T | 1 | a0001c0001t0004g0170 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1432+4754G>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88181073 | |||||||
| chr12:88181334 | T | C | 1 | a0001c0001t0001g0061 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1432+5015T>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88181334 | |||||||
| chr12:88181573 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1432+5254C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88181573 | |||||||
| chr12:88181576 | G | A | 14 | a0002c0002t0008g0006 a0002c0002t0008g0048 a0002c0002t0008g0049 others(11): Show |
17 | HG02155.hp1 HG02486.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.1432+5257G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88181576 | |||||||
| chr12:88181746 | G | T | 1 | a0001c0001t0001g0122 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1432+5427G>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88181746 | |||||||
| chr12:88181760 | A | G | 1 | a0001c0001t0001g0109 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1432+5441A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88181760 | |||||||
| chr12:88181774 | A | G | 3 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0002g0084 |
3 | NA18960.hp1 NA19009.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.1432+5455A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88181774 | |||||||
| chr12:88181822 | T | C | 1 | a0001c0001t0001g0141 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1432+5503T>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88181822 | |||||||
| chr12:88181863 | G | A | 1 | a0002c0002t0020g0148 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1432+5544G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88181863 | |||||||
| chr12:88181895 | TG | T | 19 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0005g0022 others(16): Show |
20 | HG01071.hp2 HG01891.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.1432+5581delG | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr12 | 88181895 | ||||||
| chr12:88181910 | C | T | 1 | a0001c0001t0001g0108 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1432+5591C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88181910 | |||||||
| chr12:88182105 | A | T | 1 | a0005c0005t0001g0143 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1432+5786A>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88182105 | |||||||
| chr12:88182254 | G | A | 2 | a0001c0001t0005g0158 a0001c0001t0005g0159 |
2 | HG02055.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1432+5935G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88182254 | |||||||
| chr12:88182305 | C | T | 1 | a0001c0001t0001g0064 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1432+5986C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88182305 | |||||||
| chr12:88182378 | A | G | 71 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0027 others(68): Show |
80 | HG01071.hp2 HG01109.hp2 HG01192.hp1 others(77): Show |
intron_variant | MODIFIER | c.1432+6059A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88182378 | |||||||
| chr12:88182428 | G | T | 1 | a0001c0001t0001g0107 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1432+6109G>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88182428 | |||||||
| chr12:88182434 | C | T | 9 | a0001c0001t0003g0009 a0001c0001t0003g0028 a0001c0001t0003g0033 others(6): Show |
10 | HG01109.hp2 HG01192.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.1432+6115C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88182434 | |||||||
| chr12:88182633 | C | T | 17 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0005g0022 others(14): Show |
17 | HG01071.hp2 HG01891.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1433-6210C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88182633 | |||||||
| chr12:88182643 | T | A | 36 | a0001c0001t0004g0005 a0001c0001t0004g0149 a0001c0001t0004g0151 others(33): Show |
40 | HG01071.hp2 HG01884.hp2 HG01891.hp2 others(37): Show |
intron_variant | MODIFIER | c.1433-6200T>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88182643 | |||||||
| chr12:88182664 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1433-6179C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88182664 | |||||||
| chr12:88182938 | T | C | 14 | a0002c0002t0008g0006 a0002c0002t0008g0048 a0002c0002t0008g0049 others(11): Show |
17 | HG02155.hp1 HG02486.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.1433-5905T>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88182938 | |||||||
| chr12:88182986 | A | G | 1 | a0001c0001t0028g0088 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1433-5857A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88182986 | |||||||
| chr12:88183023 | G | A | 4 | a0001c0001t0009g0044 a0001c0001t0009g0045 a0001c0001t0009g0046 others(1): Show |
4 | HG02257.hp2 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1433-5820G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88183023 | |||||||
| chr12:88183345 | T | C | 1 | a0001c0001t0001g0137 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1433-5498T>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88183345 | |||||||
| chr12:88183391 | C | G | 7 | a0002c0002t0008g0006 a0002c0002t0008g0048 a0002c0002t0008g0049 others(4): Show |
10 | HG02155.hp1 HG06807.hp2 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.1433-5452C>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88183391 | |||||||
| chr12:88183857 | T | C | 1 | a0001c0001t0003g0028 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1433-4986T>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88183857 | |||||||
| chr12:88183877 | C | T | 1 | a0002c0002t0012g0147 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1433-4966C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88183877 | |||||||
| chr12:88183878 | T | C | 1 | a0001c0001t0003g0031 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1433-4965T>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88183878 | |||||||
| chr12:88183999 | G | A | 1 | a0002c0002t0031g0056 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1433-4844G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88183999 | |||||||
| chr12:88184064 | G | A | 1 | a0001c0001t0018g0019 | 2 | HG03209.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1433-4779G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88184064 | |||||||
| chr12:88184070 | T | C | 36 | a0001c0001t0004g0005 a0001c0001t0004g0149 a0001c0001t0004g0151 others(33): Show |
40 | HG01071.hp2 HG01884.hp2 HG01891.hp2 others(37): Show |
intron_variant | MODIFIER | c.1433-4773T>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88184070 | |||||||
| chr12:88184126 | C | T | 3 | a0001c0001t0005g0020 a0001c0001t0005g0164 a0001c0001t0036g0020 |
3 | HG04228.hp1 NA18947.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1433-4717C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88184126 | |||||||
| chr12:88184295 | C | G | 4 | a0001c0001t0009g0044 a0001c0001t0009g0045 a0001c0001t0009g0046 others(1): Show |
4 | HG02257.hp2 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1433-4548C>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88184295 | |||||||
| chr12:88184307 | A | G | 1 | a0001c0001t0002g0068 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1433-4536A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88184307 | |||||||
| chr12:88184425 | C | T | 4 | a0001c0001t0009g0044 a0001c0001t0009g0045 a0001c0001t0009g0046 others(1): Show |
4 | HG02257.hp2 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1433-4418C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88184425 | |||||||
| chr12:88184438 | C | T | 4 | a0001c0001t0001g0118 a0001c0001t0001g0128 a0001c0001t0001g0142 others(1): Show |
4 | HG01515.hp1 HG01975.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1433-4405C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88184438 | |||||||
| chr12:88184456 | C | T | 17 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0027 others(14): Show |
19 | HG01109.hp2 HG01192.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.1433-4387C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88184456 | |||||||
| chr12:88184566 | G | T | 5 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 others(2): Show |
5 | HG02145.hp2 HG02615.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1433-4277G>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88184566 | |||||||
| chr12:88184622 | T | G | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | NA18960.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.1433-4221T>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88184622 | |||||||
| chr12:88184909 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1433-3934C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88184909 | |||||||
| chr12:88184961 | A | G | 36 | a0001c0001t0004g0005 a0001c0001t0004g0149 a0001c0001t0004g0151 others(33): Show |
40 | HG01071.hp2 HG01884.hp2 HG01891.hp2 others(37): Show |
intron_variant | MODIFIER | c.1433-3882A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88184961 | |||||||
| chr12:88185195 | C | T | 1 | a0001c0001t0004g0151 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1433-3648C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88185195 | |||||||
| chr12:88185348 | T | G | 1 | a0001c0001t0009g0046 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1433-3495T>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88185348 | |||||||
| chr12:88185367 | T | G | 1 | a0001c0001t0003g0038 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1433-3476T>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88185367 | |||||||
| chr12:88185429 | A | G | 1 | a0002c0002t0012g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1433-3414A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88185429 | |||||||
| chr12:88185534 | G | A | 11 | a0002c0002t0008g0006 a0002c0002t0008g0048 a0002c0002t0008g0049 others(8): Show |
14 | HG02155.hp1 HG02486.hp2 HG02886.hp2 others(11): Show |
intron_variant | MODIFIER | c.1433-3309G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88185534 | |||||||
| chr12:88185598 | C | A | 1 | a0001c0001t0001g0098 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1433-3245C>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88185598 | |||||||
| chr12:88185706 | C | CTCCTGCC others(171): Show |
1 | a0001c0001t0033g0080 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1433-3124_1433-312 others(182): Show |
TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr12 | 88185706 | ||||||
| chr12:88185706 | C | CTCCTGCC others(180): Show |
1 | a0001c0001t0006g0079 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1433-3124_1433-312 others(191): Show |
TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr12 | 88185706 | ||||||
| chr12:88185721 | A | T | 33 | a0001c0001t0004g0005 a0001c0001t0004g0149 a0001c0001t0004g0151 others(30): Show |
37 | HG01071.hp2 HG01891.hp2 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.1433-3122A>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88185721 | |||||||
| chr12:88186497 | A | G | 21 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0057 others(18): Show |
27 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.1433-2346A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88186497 | |||||||
| chr12:88186573 | G | T | 3 | a0001c0001t0001g0099 a0001c0001t0001g0103 a0001c0001t0001g0106 |
3 | HG01934.hp1 HG01981.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.1433-2270G>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88186573 | |||||||
| chr12:88186993 | G | A | 19 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0005g0022 others(16): Show |
20 | HG01071.hp2 HG01891.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.1433-1850G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88186993 | |||||||
| chr12:88187117 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1433-1726T>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88187117 | |||||||
| chr12:88187146 | A | G | 1 | a0002c0002t0008g0050 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1433-1697A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88187146 | |||||||
| chr12:88187167 | TA | T | 28 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0057 others(25): Show |
37 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.1433-1661delA | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr12 | 88187167 | ||||||
| chr12:88187178 | A | AAAAAAG | 22 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0005g0022 others(19): Show |
23 | HG01071.hp2 HG01884.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.1433-1661_1433-166 others(10): Show |
TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr12 | 88187178 | ||||||
| chr12:88187178 | A | AAAAAG | 14 | a0001c0001t0004g0005 a0001c0001t0004g0149 a0001c0001t0004g0151 others(11): Show |
17 | HG02280.hp1 HG02572.hp2 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.1433-1663_1433-165 others(9): Show |
TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr12 | 88187178 | ||||||
| chr12:88187517 | G | GT | 4 | a0001c0001t0002g0066 a0001c0001t0002g0074 a0001c0001t0007g0110 others(1): Show |
4 | HG02080.hp2 HG04199.hp1 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.1433-1318dupT | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr12 | 88187517 | ||||||
| chr12:88187794 | A | G | 1 | a0001c0001t0016g0014 | 2 | NA18969.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1433-1049A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88187794 | |||||||
| chr12:88187829 | A | C | 36 | a0001c0001t0004g0005 a0001c0001t0004g0149 a0001c0001t0004g0151 others(33): Show |
40 | HG01071.hp2 HG01884.hp2 HG01891.hp2 others(37): Show |
intron_variant | MODIFIER | c.1433-1014A>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88187829 | |||||||
| chr12:88187839 | G | A | 36 | a0001c0001t0004g0005 a0001c0001t0004g0149 a0001c0001t0004g0151 others(33): Show |
40 | HG01071.hp2 HG01884.hp2 HG01891.hp2 others(37): Show |
intron_variant | MODIFIER | c.1433-1004G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88187839 | |||||||
| chr12:88188011 | T | A | 3 | a0001c0001t0015g0041 a0001c0001t0015g0042 a0001c0001t0022g0043 |
3 | HG01884.hp2 HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1433-832T>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88188011 | |||||||
| chr12:88188363 | T | C | 4 | a0001c0001t0009g0044 a0001c0001t0009g0045 a0001c0001t0009g0046 others(1): Show |
4 | HG02257.hp2 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1433-480T>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88188363 | |||||||
| chr12:88188407 | A | G | 14 | a0002c0002t0008g0006 a0002c0002t0008g0048 a0002c0002t0008g0049 others(11): Show |
17 | HG02155.hp1 HG02486.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.1433-436A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88188407 | |||||||
| chr12:88188509 | C | T | 14 | a0002c0002t0008g0006 a0002c0002t0008g0048 a0002c0002t0008g0049 others(11): Show |
17 | HG02155.hp1 HG02486.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.1433-334C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88188509 | |||||||
| chr12:88188826 | T | G | 33 | a0001c0001t0004g0005 a0001c0001t0004g0149 a0001c0001t0004g0151 others(30): Show |
37 | HG01071.hp2 HG01891.hp2 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.1433-17T>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 10/13 | chr12 | 88188826 | |||||||
| chr12:88189156 | C | T | 1 | a0001c0001t0002g0172 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1536+210C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 11/13 | chr12 | 88189156 | |||||||
| chr12:88189195 | G | A | 4 | a0001c0001t0009g0044 a0001c0001t0009g0045 a0001c0001t0009g0046 others(1): Show |
4 | HG02257.hp2 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1536+249G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 11/13 | chr12 | 88189195 | |||||||
| chr12:88189241 | C | A | 135 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(132): Show |
164 | HG00099.hp1 HG00099.hp2 HG00609.hp2 others(161): Show |
intron_variant | MODIFIER | c.1536+295C>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 11/13 | chr12 | 88189241 | |||||||
| chr12:88189268 | A | G | 1 | a0001c0001t0002g0074 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1536+322A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 11/13 | chr12 | 88189268 | |||||||
| chr12:88189414 | T | C | 33 | a0001c0001t0004g0005 a0001c0001t0004g0149 a0001c0001t0004g0151 others(30): Show |
37 | HG01071.hp2 HG01891.hp2 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.1536+468T>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 11/13 | chr12 | 88189414 | |||||||
| chr12:88189961 | A | G | 1 | a0002c0002t0012g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1537-492A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 11/13 | chr12 | 88189961 | |||||||
| chr12:88189967 | C | T | 1 | a0002c0002t0012g0053 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1537-486C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 11/13 | chr12 | 88189967 | |||||||
| chr12:88190662 | G | A | 1 | a0002c0002t0008g0049 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1706+40G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 12/13 | chr12 | 88190662 | |||||||
| chr12:88191057 | A | T | 2 | a0002c0002t0027g0054 a0002c0002t0032g0055 |
2 | HG02486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1706+435A>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 12/13 | chr12 | 88191057 | |||||||
| chr12:88191151 | C | T | 1 | a0001c0001t0003g0034 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1706+529C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 12/13 | chr12 | 88191151 | |||||||
| chr12:88191224 | G | C | 19 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0005g0022 others(16): Show |
20 | HG01071.hp2 HG01891.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.1706+602G>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 12/13 | chr12 | 88191224 | |||||||
| chr12:88191637 | G | A | 33 | a0001c0001t0004g0005 a0001c0001t0004g0149 a0001c0001t0004g0151 others(30): Show |
37 | HG01071.hp2 HG01891.hp2 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.1707-967G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 12/13 | chr12 | 88191637 | |||||||
| chr12:88191710 | C | CTGTT | 4 | a0001c0001t0006g0077 a0001c0001t0006g0078 a0001c0001t0006g0182 others(1): Show |
4 | HG00642.hp2 HG01934.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.1707-878_1707-875d others(6): Show |
TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr12 | 88191710 | ||||||
| chr12:88191710 | C | CTGTTTGT others(1): Show |
33 | a0001c0001t0004g0005 a0001c0001t0004g0149 a0001c0001t0004g0151 others(30): Show |
37 | HG01071.hp2 HG01891.hp2 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.1707-882_1707-875d others(10): Show |
TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr12 | 88191710 | ||||||
| chr12:88191710 | C | CTGTTTGT others(5): Show |
3 | a0001c0001t0015g0041 a0001c0001t0015g0042 a0001c0001t0022g0043 |
3 | HG01884.hp2 HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1707-886_1707-875d others(14): Show |
TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr12 | 88191710 | ||||||
| chr12:88191940 | C | T | 1 | a0002c0002t0012g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1707-664C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 12/13 | chr12 | 88191940 | |||||||
| chr12:88191984 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1707-620C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 12/13 | chr12 | 88191984 | |||||||
| chr12:88192014 | CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0001g0112 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1707-578_1707-564d others(17): Show |
TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr12 | 88192014 | ||||||
| chr12:88192028 | C | CTTTCTTT | 10 | a0002c0002t0008g0006 a0002c0002t0008g0048 a0002c0002t0008g0049 others(7): Show |
13 | HG02155.hp1 HG02486.hp2 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.1707-573_1707-572i others(9): Show |
TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr12 | 88192028 | ||||||
| chr12:88192028 | C | CTTTTTT | 20 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0027 others(17): Show |
22 | HG01109.hp2 HG01192.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.1707-569_1707-564d others(8): Show |
TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr12 | 88192028 | ||||||
| chr12:88192028 | C | CTTTTTTT | 28 | a0001c0001t0003g0031 a0001c0001t0004g0005 a0001c0001t0004g0149 others(25): Show |
32 | HG01071.hp2 HG01891.hp2 HG02257.hp1 others(29): Show |
intron_variant | MODIFIER | c.1707-570_1707-564d others(9): Show |
TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr12 | 88192028 | ||||||
| chr12:88192028 | C | T | 3 | a0001c0001t0004g0175 a0001c0001t0005g0158 a0001c0001t0005g0159 |
3 | HG02055.hp2 HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1707-576C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 12/13 | chr12 | 88192028 | |||||||
| chr12:88192051 | G | A | 36 | a0001c0001t0004g0005 a0001c0001t0004g0149 a0001c0001t0004g0151 others(33): Show |
40 | HG01071.hp2 HG01884.hp2 HG01891.hp2 others(37): Show |
intron_variant | MODIFIER | c.1707-553G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 12/13 | chr12 | 88192051 | |||||||
| chr12:88192142 | A | G | 1 | a0001c0001t0022g0043 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1707-462A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 12/13 | chr12 | 88192142 | |||||||
| chr12:88192295 | A | T | 1 | a0001c0001t0003g0033 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1707-309A>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 12/13 | chr12 | 88192295 | |||||||
| chr12:88192500 | G | GA | 70 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0027 others(67): Show |
79 | HG01071.hp2 HG01109.hp2 HG01192.hp1 others(76): Show |
intron_variant | MODIFIER | c.1707-96dupA | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr12 | 88192500 | ||||||
| chr12:88192980 | A | G | 17 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0027 others(14): Show |
19 | HG01109.hp2 HG01192.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.1933+150A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 13/13 | chr12 | 88192980 | |||||||
| chr12:88193004 | C | T | 3 | a0001c0001t0001g0017 a0004c0003t0001g0100 a0004c0003t0001g0119 |
4 | HG02622.hp1 HG02622.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1933+174C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 13/13 | chr12 | 88193004 | |||||||
| chr12:88193296 | C | T | 4 | a0001c0001t0009g0044 a0001c0001t0009g0045 a0001c0001t0009g0046 others(1): Show |
4 | HG02257.hp2 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1933+466C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 13/13 | chr12 | 88193296 | |||||||
| chr12:88193663 | C | T | 71 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0027 others(68): Show |
80 | HG01071.hp2 HG01109.hp2 HG01192.hp1 others(77): Show |
intron_variant | MODIFIER | c.1933+833C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 13/13 | chr12 | 88193663 | |||||||
| chr12:88193821 | A | C | 1 | a0002c0002t0012g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1933+991A>C | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 13/13 | chr12 | 88193821 | |||||||
| chr12:88193836 | C | T | 1 | a0001c0001t0010g0037 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1934-1002C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 13/13 | chr12 | 88193836 | |||||||
| chr12:88193925 | A | G | 1 | a0001c0001t0001g0178 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1934-913A>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 13/13 | chr12 | 88193925 | |||||||
| chr12:88194293 | C | T | 3 | a0001c0001t0015g0041 a0001c0001t0015g0042 a0001c0001t0022g0043 |
3 | HG01884.hp2 HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1934-545C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 13/13 | chr12 | 88194293 | |||||||
| chr12:88194411 | C | T | 71 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0027 others(68): Show |
80 | HG01071.hp2 HG01109.hp2 HG01192.hp1 others(77): Show |
intron_variant | MODIFIER | c.1934-427C>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 13/13 | chr12 | 88194411 | |||||||
| chr12:88194448 | G | A | 71 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0027 others(68): Show |
80 | HG01071.hp2 HG01109.hp2 HG01192.hp1 others(77): Show |
intron_variant | MODIFIER | c.1934-390G>A | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 13/13 | chr12 | 88194448 | |||||||
| chr12:88194462 | G | T | 19 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0005g0022 others(16): Show |
20 | HG01071.hp2 HG01891.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.1934-376G>T | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 13/13 | chr12 | 88194462 | |||||||
| chr12:88194541 | C | G | 3 | a0001c0001t0015g0041 a0001c0001t0015g0042 a0001c0001t0022g0043 |
3 | HG01884.hp2 HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1934-297C>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 13/13 | chr12 | 88194541 | |||||||
| chr12:88194758 | T | G | 1 | a0001c0001t0005g0150 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1934-80T>G | TMTC3 | ENSG00000139324.12 | transcript | ENST00000266712.11 | protein_coding | 13/13 | chr12 | 88194758 |