Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55002 |
| ensemblid | ENSG00000150403.18 |
| hgncid | 20329 |
| symbol | TMCO3 |
| name | transmembrane and coiled-coil domains 3 |
| refseq_nuc | NM_017905.6 |
| refseq_prot | NP_060375.4 |
| ensembl_nuc | ENST00000434316.7 |
| ensembl_prot | ENSP00000389399.2 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 113491021 |
| end | 113550229 |
| strand | + |
| ver | v1.2 |
| region | chr13:113491021-113550229 |
| region5000 | chr13:113486021-113555229 |
| regionname0 | TMCO3_chr13_113491021_113550229 |
| regionname5000 | TMCO3_chr13_113486021_113555229 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 677 | 205 | 32 | 43 | 97 | 11 | 20 | 72 | TMCO3_chr13_113486021_113555229 | TMCO3 | MKVLG others(672): Show |
chr13 | 113486021 | 113555229 |
| a0002 | 0/0 | 677 | 75 | 19 | 15 | 30 | 1 | 10 | 21 | TMCO3_chr13_113486021_113555229 | TMCO3 | MKVLG others(672): Show |
chr13 | 113486021 | 113555229 |
| a0003 | 0/0 | 677 | 74 | 28 | 13 | 25 | 2 | 6 | 19 | TMCO3_chr13_113486021_113555229 | TMCO3 | MKVLG others(672): Show |
chr13 | 113486021 | 113555229 |
| a0004 | 0/0 | 677 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | MKVLG others(672): Show |
chr13 | 113486021 | 113555229 |
| a0005 | 0/0 | 677 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | MKVLG others(672): Show |
chr13 | 113486021 | 113555229 |
| a0006 | 0/0 | 677 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TMCO3_chr13_113486021_113555229 | TMCO3 | MKVLG others(672): Show |
chr13 | 113486021 | 113555229 |
| a0007 | 0/0 | 677 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | MKVLG others(672): Show |
chr13 | 113486021 | 113555229 |
| a0008 | 0/0 | 677 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | MKVLG others(672): Show |
chr13 | 113486021 | 113555229 |
| a0009 | 0/0 | 677 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | MKVLG others(672): Show |
chr13 | 113486021 | 113555229 |
| a0010 | 0/0 | 677 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | MKVLG others(672): Show |
chr13 | 113486021 | 113555229 |
| a0011 | 0/0 | 677 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | MKVLG others(672): Show |
chr13 | 113486021 | 113555229 |
| a0012 | 0/0 | 677 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | MKVLG others(672): Show |
chr13 | 113486021 | 113555229 |
| a0013 | 0/0 | 677 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | MKVLG others(672): Show |
chr13 | 113486021 | 113555229 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2031 | 163 | 18 | 36 | 82 | 8 | 17 | TMCO3_chr13_113486021_113555229 | TMCO3 | ATGAA others(2026): Show |
chr13 | 113486021 | 113555229 | ||
| a0001c0005 | 0/0 | 2031 | 17 | 7 | 6 | 0 | 2 | 2 | TMCO3_chr13_113486021_113555229 | TMCO3 | ATGAA others(2026): Show |
chr13 | 113486021 | 113555229 | ||
| a0001c0006 | 0/0 | 2031 | 17 | 0 | 1 | 14 | 1 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | ATGAA others(2026): Show |
chr13 | 113486021 | 113555229 | ||
| a0001c0007 | 0/0 | 2031 | 4 | 4 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | ATGAA others(2026): Show |
chr13 | 113486021 | 113555229 | ||
| a0001c0009 | 0/0 | 2031 | 3 | 3 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | ATGAA others(2026): Show |
chr13 | 113486021 | 113555229 | ||
| a0001c0022 | 0/0 | 2031 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | ATGAA others(2026): Show |
chr13 | 113486021 | 113555229 | ||
| a0002c0003 | 0/0 | 2031 | 51 | 6 | 14 | 26 | 0 | 5 | TMCO3_chr13_113486021_113555229 | TMCO3 | ATGAA others(2026): Show |
chr13 | 113486021 | 113555229 | ||
| a0002c0004 | 0/0 | 2031 | 23 | 13 | 1 | 3 | 1 | 5 | TMCO3_chr13_113486021_113555229 | TMCO3 | ATGAA others(2026): Show |
chr13 | 113486021 | 113555229 | ||
| a0002c0019 | 0/0 | 2031 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | ATGAA others(2026): Show |
chr13 | 113486021 | 113555229 | ||
| a0003c0002 | 0/0 | 2031 | 71 | 27 | 12 | 24 | 2 | 6 | TMCO3_chr13_113486021_113555229 | TMCO3 | ATGAA others(2026): Show |
chr13 | 113486021 | 113555229 | ||
| a0003c0014 | 0/0 | 2031 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | ATGAA others(2026): Show |
chr13 | 113486021 | 113555229 | ||
| a0003c0016 | 0/0 | 2031 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | ATGAA others(2026): Show |
chr13 | 113486021 | 113555229 | ||
| a0003c0023 | 0/0 | 2031 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | ATGAA others(2026): Show |
chr13 | 113486021 | 113555229 | ||
| a0004c0008 | 0/0 | 2031 | 3 | 3 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | ATGAA others(2026): Show |
chr13 | 113486021 | 113555229 | ||
| a0005c0011 | 0/0 | 2031 | 2 | 0 | 0 | 2 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | ATGAA others(2026): Show |
chr13 | 113486021 | 113555229 | ||
| a0006c0010 | 0/0 | 2031 | 2 | 0 | 0 | 2 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | ATGAA others(2026): Show |
chr13 | 113486021 | 113555229 | ||
| a0007c0012 | 0/0 | 2031 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | ATGAA others(2026): Show |
chr13 | 113486021 | 113555229 | ||
| a0008c0018 | 0/0 | 2031 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | ATGAA others(2026): Show |
chr13 | 113486021 | 113555229 | ||
| a0009c0020 | 0/0 | 2031 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | ATGAA others(2026): Show |
chr13 | 113486021 | 113555229 | ||
| a0010c0015 | 0/0 | 2031 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | ATGAA others(2026): Show |
chr13 | 113486021 | 113555229 | ||
| a0011c0017 | 0/0 | 2031 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | ATGAA others(2026): Show |
chr13 | 113486021 | 113555229 | ||
| a0012c0013 | 0/0 | 2031 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | ATGAA others(2026): Show |
chr13 | 113486021 | 113555229 | ||
| a0013c0021 | 0/0 | 2031 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | ATGAA others(2026): Show |
chr13 | 113486021 | 113555229 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3058 | 144 | 14 | 33 | 70 | 8 | 17 | TMCO3_chr13_113486021_113555229 | TMCO3 | GGGAG others(3053): Show |
chr13 | 113486021 | 113555229 |
| a0001c0001t0004 | 0/0 | 3058 | 14 | 2 | 2 | 10 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | GGGAG others(3053): Show |
chr13 | 113486021 | 113555229 |
| a0001c0001t0009 | 0/0 | 3058 | 2 | 1 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | GGGAG others(3053): Show |
chr13 | 113486021 | 113555229 |
| a0001c0001t0011 | 0/0 | 3058 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | GGGAG others(3053): Show |
chr13 | 113486021 | 113555229 |
| a0001c0001t0012 | 0/0 | 3058 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | GGGAG others(3053): Show |
chr13 | 113486021 | 113555229 |
| a0001c0001t0013 | 0/0 | 3058 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | GGGAG others(3053): Show |
chr13 | 113486021 | 113555229 |
| a0001c0005t0001 | 0/0 | 3058 | 16 | 6 | 6 | 0 | 2 | 2 | TMCO3_chr13_113486021_113555229 | TMCO3 | GGGAG others(3053): Show |
chr13 | 113486021 | 113555229 |
| a0001c0005t0010 | 0/0 | 3058 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | GGGAG others(3053): Show |
chr13 | 113486021 | 113555229 |
| a0001c0006t0001 | 0/0 | 3058 | 17 | 0 | 1 | 14 | 1 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | GGGAG others(3053): Show |
chr13 | 113486021 | 113555229 |
| a0001c0007t0006 | 0/0 | 3058 | 4 | 4 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | GGGAG others(3053): Show |
chr13 | 113486021 | 113555229 |
| a0001c0009t0004 | 0/0 | 3058 | 3 | 3 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | GGGAG others(3053): Show |
chr13 | 113486021 | 113555229 |
| a0001c0022t0001 | 0/0 | 3058 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | GGGAG others(3053): Show |
chr13 | 113486021 | 113555229 |
| a0002c0003t0003 | 0/0 | 3058 | 51 | 6 | 14 | 26 | 0 | 5 | TMCO3_chr13_113486021_113555229 | TMCO3 | GGGAG others(3053): Show |
chr13 | 113486021 | 113555229 |
| a0002c0004t0004 | 0/0 | 3058 | 4 | 4 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | GGGAG others(3053): Show |
chr13 | 113486021 | 113555229 |
| a0002c0004t0005 | 0/0 | 3066 | 16 | 6 | 1 | 3 | 1 | 5 | TMCO3_chr13_113486021_113555229 | TMCO3 | GGGAG others(3061): Show |
chr13 | 113486021 | 113555229 |
| a0002c0004t0007 | 0/0 | 3066 | 3 | 3 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | GGGAG others(3061): Show |
chr13 | 113486021 | 113555229 |
| a0002c0019t0003 | 0/0 | 3058 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | GGGAG others(3053): Show |
chr13 | 113486021 | 113555229 |
| a0003c0002t0002 | 0/0 | 3058 | 71 | 27 | 12 | 24 | 2 | 6 | TMCO3_chr13_113486021_113555229 | TMCO3 | GGGAG others(3053): Show |
chr13 | 113486021 | 113555229 |
| a0003c0014t0004 | 0/0 | 3058 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | GGGAG others(3053): Show |
chr13 | 113486021 | 113555229 |
| a0003c0016t0002 | 0/0 | 3058 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | GGGAG others(3053): Show |
chr13 | 113486021 | 113555229 |
| a0003c0023t0002 | 0/0 | 3058 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | GGGAG others(3053): Show |
chr13 | 113486021 | 113555229 |
| a0004c0008t0004 | 0/0 | 3058 | 3 | 3 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | GGGAG others(3053): Show |
chr13 | 113486021 | 113555229 |
| a0005c0011t0008 | 0/0 | 3058 | 2 | 0 | 0 | 2 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | GGGAG others(3053): Show |
chr13 | 113486021 | 113555229 |
| a0006c0010t0002 | 0/0 | 3058 | 2 | 0 | 0 | 2 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | GGGAG others(3053): Show |
chr13 | 113486021 | 113555229 |
| a0007c0012t0001 | 0/0 | 3058 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | GGGAG others(3053): Show |
chr13 | 113486021 | 113555229 |
| a0008c0018t0004 | 0/0 | 3058 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | GGGAG others(3053): Show |
chr13 | 113486021 | 113555229 |
| a0009c0020t0003 | 0/0 | 3058 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | GGGAG others(3053): Show |
chr13 | 113486021 | 113555229 |
| a0010c0015t0002 | 0/0 | 3058 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | GGGAG others(3053): Show |
chr13 | 113486021 | 113555229 |
| a0011c0017t0001 | 0/0 | 3058 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | GGGAG others(3053): Show |
chr13 | 113486021 | 113555229 |
| a0012c0013t0001 | 0/0 | 3058 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | GGGAG others(3053): Show |
chr13 | 113486021 | 113555229 |
| a0013c0021t0002 | 0/0 | 3058 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | GGGAG others(3053): Show |
chr13 | 113486021 | 113555229 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 11 | 0 | 0 | 10 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0003 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0004 | 1/0 | 6 | 0 | 1 | 3 | 1 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0006 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0196 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0004g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0004g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0004g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0004g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0004g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0004g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0004g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0004g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0004g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0004g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0009g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0009g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0011g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0012g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0013g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0005t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0005t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0005t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0005t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0005t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0005t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0005t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0005t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0005t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0005t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0005t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0005t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0005t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0005t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0005t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0005t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0005t0010g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0006t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0006t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0006t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0006t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0006t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0006t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0006t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0006t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0006t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0006t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0006t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0006t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0006t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0006t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0006t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0006t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0007t0006g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0007t0006g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0007t0006g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0007t0006g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0009t0004g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0009t0004g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0009t0004g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0022t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0002 | 0/0 | 8 | 0 | 3 | 5 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0004t0004g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0004t0004g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0004t0004g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0004t0005g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0004t0005g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0004t0005g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0004t0005g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0004t0005g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0004t0005g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0004t0005g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0004t0005g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0004t0005g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0004t0005g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0004t0005g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0004t0005g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0004t0005g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0004t0005g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0004t0005g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0004t0005g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0004t0007g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0004t0007g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0019t0003g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0005 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0014 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0014t0004g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0016t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0023t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0004c0008t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0004c0008t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0004c0008t0004g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0005c0011t0008g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0005c0011t0008g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0006c0010t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0006c0010t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0007c0012t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0008c0018t0004g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0009c0020t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0010c0015t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0011c0017t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0012c0013t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0013c0021t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0162 | EUR | GBR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00099 | hp2 | a0002 | c0004 | t0005 | g0293 | EUR | GBR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0158 | EUR | GBR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0189 | EUR | GBR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00280 | hp1 | a0001 | c0006 | t0001 | g0236 | EUR | FIN | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00408 | hp1 | a0002 | c0003 | t0003 | g0241 | EAS | CHS | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00423 | hp1 | a0003 | c0002 | t0002 | g0049 | EAS | CHS | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00423 | hp2 | a0003 | c0002 | t0002 | g0071 | EAS | CHS | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00438 | hp2 | a0002 | c0003 | t0003 | g0245 | EAS | CHS | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00544 | hp1 | a0001 | c0001 | t0004 | g0018 | EAS | CHS | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00544 | hp2 | a0001 | c0006 | t0001 | g0234 | EAS | CHS | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00558 | hp1 | a0001 | c0001 | t0004 | g0094 | EAS | CHS | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00558 | hp2 | a0001 | c0006 | t0001 | g0218 | EAS | CHS | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00597 | hp1 | a0001 | c0001 | t0004 | g0095 | EAS | CHS | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00597 | hp2 | a0003 | c0002 | t0002 | g0059 | EAS | CHS | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00609 | hp1 | a0003 | c0002 | t0002 | g0008 | EAS | CHS | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00621 | hp1 | a0001 | c0006 | t0001 | g0223 | EAS | CHS | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00621 | hp2 | a0002 | c0019 | t0003 | g0002 | EAS | CHS | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00639 | hp1 | a0001 | c0001 | t0009 | g0304 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00673 | hp1 | a0001 | c0006 | t0001 | g0222 | EAS | CHS | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00673 | hp2 | a0003 | c0002 | t0002 | g0069 | EAS | CHS | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00733 | hp1 | a0001 | c0005 | t0001 | g0108 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00738 | hp1 | a0003 | c0002 | t0002 | g0048 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01069 | hp2 | a0003 | c0002 | t0002 | g0015 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01070 | hp2 | a0003 | c0002 | t0002 | g0078 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01071 | hp2 | a0003 | c0002 | t0002 | g0015 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01081 | hp1 | a0003 | c0002 | t0002 | g0005 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01099 | hp1 | a0002 | c0003 | t0003 | g0269 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01099 | hp2 | a0001 | c0005 | t0001 | g0231 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01106 | hp2 | a0001 | c0005 | t0001 | g0173 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01109 | hp1 | a0002 | c0003 | t0003 | g0259 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01168 | hp2 | a0003 | c0002 | t0002 | g0080 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01175 | hp1 | a0003 | c0002 | t0002 | g0005 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01243 | hp1 | a0003 | c0016 | t0002 | g0074 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01243 | hp2 | a0003 | c0002 | t0002 | g0038 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01255 | hp2 | a0002 | c0003 | t0003 | g0263 | AMR | CLM | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01256 | hp1 | a0003 | c0002 | t0002 | g0081 | AMR | CLM | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01257 | hp1 | a0001 | c0005 | t0001 | g0230 | AMR | CLM | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01261 | hp1 | a0002 | c0003 | t0003 | g0276 | AMR | CLM | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01346 | hp1 | a0003 | c0002 | t0002 | g0077 | AMR | CLM | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01346 | hp2 | a0002 | c0003 | t0003 | g0247 | AMR | CLM | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01358 | hp2 | a0001 | c0005 | t0001 | g0232 | AMR | CLM | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01361 | hp2 | a0003 | c0002 | t0002 | g0030 | AMR | CLM | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01515 | hp1 | a0003 | c0002 | t0002 | g0005 | EUR | IBS | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01515 | hp2 | a0001 | c0005 | t0001 | g0172 | EUR | IBS | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0023 | EUR | IBS | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01517 | hp2 | a0003 | c0002 | t0002 | g0005 | EUR | IBS | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0102 | AFR | ACB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01884 | hp2 | a0002 | c0004 | t0005 | g0300 | AFR | ACB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01891 | hp2 | a0003 | c0002 | t0002 | g0010 | AFR | ACB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01928 | hp1 | a0002 | c0003 | t0003 | g0260 | AMR | PEL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01928 | hp2 | a0002 | c0003 | t0003 | g0243 | AMR | PEL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01952 | hp1 | a0003 | c0002 | t0002 | g0065 | AMR | PEL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01952 | hp2 | a0002 | c0003 | t0003 | g0254 | AMR | PEL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01978 | hp2 | a0002 | c0003 | t0003 | g0266 | AMR | PEL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01981 | hp1 | a0002 | c0003 | t0003 | g0002 | AMR | PEL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01981 | hp2 | a0007 | c0012 | t0001 | g0197 | AMR | PEL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01993 | hp1 | a0002 | c0003 | t0003 | g0253 | AMR | PEL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01993 | hp2 | a0001 | c0001 | t0004 | g0096 | AMR | PEL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02015 | hp1 | a0002 | c0003 | t0003 | g0248 | EAS | KHV | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02027 | hp1 | a0005 | c0011 | t0008 | g0307 | EAS | KHV | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02027 | hp2 | a0001 | c0001 | t0004 | g0093 | EAS | KHV | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02071 | hp1 | a0002 | c0003 | t0003 | g0002 | EAS | KHV | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02080 | hp1 | a0001 | c0006 | t0001 | g0224 | EAS | KHV | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02080 | hp2 | a0002 | c0003 | t0003 | g0274 | EAS | KHV | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02129 | hp1 | a0001 | c0001 | t0004 | g0105 | EAS | KHV | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02129 | hp2 | a0005 | c0011 | t0008 | g0306 | EAS | KHV | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02132 | hp2 | a0003 | c0002 | t0002 | g0008 | EAS | KHV | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02135 | hp1 | a0002 | c0004 | t0005 | g0299 | EAS | KHV | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02135 | hp2 | a0001 | c0022 | t0001 | g0192 | EAS | KHV | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02145 | hp1 | a0002 | c0004 | t0004 | g0086 | AFR | ACB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02148 | hp2 | a0002 | c0003 | t0003 | g0251 | AMR | PEL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02165 | hp1 | a0002 | c0003 | t0003 | g0273 | EAS | CDX | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CDX | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02258 | hp1 | a0001 | c0005 | t0001 | g0175 | AFR | ACB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02258 | hp2 | a0004 | c0008 | t0004 | g0104 | AFR | ACB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02273 | hp1 | a0002 | c0003 | t0003 | g0002 | AMR | PEL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02273 | hp2 | a0001 | c0001 | t0004 | g0101 | AMR | PEL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02280 | hp1 | a0001 | c0007 | t0006 | g0280 | AFR | ACB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02280 | hp2 | a0001 | c0005 | t0010 | g0164 | AFR | ACB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02293 | hp1 | a0001 | c0005 | t0001 | g0110 | AMR | PEL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02293 | hp2 | a0001 | c0006 | t0001 | g0235 | AMR | PEL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02451 | hp1 | a0003 | c0002 | t0002 | g0034 | AFR | ACB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02451 | hp2 | a0002 | c0004 | t0007 | g0288 | AFR | ACB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02523 | hp2 | a0001 | c0001 | t0004 | g0098 | EAS | KHV | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02572 | hp1 | a0002 | c0004 | t0005 | g0286 | AFR | GWD | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02572 | hp2 | a0003 | c0002 | t0002 | g0036 | AFR | GWD | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02602 | hp1 | a0001 | c0005 | t0001 | g0186 | SAS | PJL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02615 | hp1 | a0002 | c0003 | t0003 | g0240 | AFR | GWD | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02622 | hp1 | a0003 | c0002 | t0002 | g0040 | AFR | GWD | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02622 | hp2 | a0003 | c0002 | t0002 | g0064 | AFR | GWD | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02630 | hp1 | a0001 | c0005 | t0001 | g0126 | AFR | GWD | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02630 | hp2 | a0003 | c0002 | t0002 | g0014 | AFR | GWD | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02647 | hp1 | a0002 | c0004 | t0005 | g0287 | AFR | GWD | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02698 | hp1 | a0002 | c0004 | t0005 | g0302 | SAS | PJL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02717 | hp1 | a0001 | c0009 | t0004 | g0282 | AFR | GWD | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02717 | hp2 | a0008 | c0018 | t0004 | g0085 | AFR | GWD | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02723 | hp1 | a0003 | c0002 | t0002 | g0066 | AFR | GWD | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02738 | hp2 | a0002 | c0004 | t0005 | g0295 | SAS | PJL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02809 | hp1 | a0003 | c0002 | t0002 | g0043 | AFR | GWD | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02809 | hp2 | a0003 | c0014 | t0004 | g0185 | AFR | GWD | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02818 | hp2 | a0003 | c0002 | t0002 | g0035 | AFR | GWD | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02922 | hp1 | a0009 | c0020 | t0003 | g0007 | AFR | ESN | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02922 | hp2 | a0001 | c0007 | t0006 | g0092 | AFR | ESN | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02965 | hp1 | a0002 | c0003 | t0003 | g0029 | AFR | ESN | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02965 | hp2 | a0002 | c0004 | t0007 | g0028 | AFR | ESN | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02970 | hp1 | a0004 | c0008 | t0004 | g0103 | AFR | ESN | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02970 | hp2 | a0003 | c0002 | t0002 | g0012 | AFR | ESN | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02976 | hp1 | a0003 | c0002 | t0002 | g0041 | AFR | ESN | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02976 | hp2 | a0002 | c0004 | t0005 | g0291 | AFR | ESN | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03017 | hp1 | a0001 | c0005 | t0001 | g0187 | SAS | PJL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03017 | hp2 | a0002 | c0003 | t0003 | g0261 | SAS | PJL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03041 | hp2 | a0003 | c0002 | t0002 | g0016 | AFR | GWD | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03098 | hp1 | a0010 | c0015 | t0002 | g0070 | AFR | MSL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03098 | hp2 | a0001 | c0005 | t0001 | g0174 | AFR | MSL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03130 | hp1 | a0003 | c0002 | t0002 | g0011 | AFR | ESN | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ESN | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03139 | hp1 | a0001 | c0005 | t0001 | g0214 | AFR | ESN | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03139 | hp2 | a0003 | c0002 | t0002 | g0075 | AFR | ESN | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03195 | hp1 | a0002 | c0003 | t0003 | g0007 | AFR | ESN | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03195 | hp2 | a0011 | c0017 | t0001 | g0284 | AFR | ESN | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03209 | hp1 | a0001 | c0007 | t0006 | g0090 | AFR | MSL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03209 | hp2 | a0002 | c0003 | t0003 | g0007 | AFR | MSL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03225 | hp1 | a0004 | c0008 | t0004 | g0089 | AFR | MSL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03225 | hp2 | a0002 | c0004 | t0004 | g0305 | AFR | MSL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03239 | hp2 | a0002 | c0003 | t0003 | g0244 | SAS | PJL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03453 | hp1 | a0003 | c0002 | t0002 | g0046 | AFR | MSL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03453 | hp2 | a0002 | c0003 | t0003 | g0007 | AFR | MSL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03486 | hp1 | a0002 | c0004 | t0004 | g0017 | AFR | MSL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03486 | hp2 | a0003 | c0002 | t0002 | g0052 | AFR | MSL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03491 | hp2 | a0003 | c0002 | t0002 | g0072 | SAS | PJL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0100 | AFR | ESN | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03516 | hp2 | a0001 | c0009 | t0004 | g0281 | AFR | ESN | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03579 | hp1 | a0003 | c0002 | t0002 | g0042 | AFR | MSL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03579 | hp2 | a0003 | c0002 | t0002 | g0032 | AFR | MSL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03654 | hp1 | a0002 | c0003 | t0003 | g0242 | SAS | PJL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03654 | hp2 | a0001 | c0006 | t0001 | g0227 | SAS | PJL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03688 | hp1 | a0003 | c0002 | t0002 | g0039 | SAS | STU | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03704 | hp2 | a0002 | c0003 | t0003 | g0255 | SAS | PJL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | BEB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | BEB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03927 | hp1 | a0002 | c0004 | t0005 | g0294 | SAS | BEB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03927 | hp2 | a0003 | c0002 | t0002 | g0068 | SAS | BEB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | BEB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03942 | hp2 | a0003 | c0002 | t0002 | g0033 | SAS | BEB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | BEB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG04184 | hp2 | a0002 | c0004 | t0005 | g0296 | SAS | BEB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | STU | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG04199 | hp2 | a0002 | c0004 | t0005 | g0292 | SAS | STU | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG04204 | hp1 | a0003 | c0002 | t0002 | g0047 | SAS | STU | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | STU | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG04228 | hp1 | a0002 | c0003 | t0003 | g0257 | SAS | STU | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG04228 | hp2 | a0003 | c0002 | t0002 | g0050 | SAS | STU | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18522 | hp1 | a0002 | c0003 | t0003 | g0239 | AFR | YRI | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18522 | hp2 | a0002 | c0004 | t0005 | g0289 | AFR | YRI | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18612 | hp1 | a0002 | c0003 | t0003 | g0258 | EAS | CHB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | CHB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18747 | hp1 | a0001 | c0006 | t0001 | g0228 | EAS | CHB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | CHB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18906 | hp1 | a0001 | c0005 | t0001 | g0176 | AFR | YRI | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18906 | hp2 | a0003 | c0002 | t0002 | g0011 | AFR | YRI | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18940 | hp1 | a0003 | c0002 | t0002 | g0053 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18940 | hp2 | a0002 | c0003 | t0003 | g0238 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18941 | hp1 | a0002 | c0003 | t0003 | g0002 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18942 | hp1 | a0001 | c0001 | t0004 | g0097 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18942 | hp2 | a0002 | c0003 | t0003 | g0271 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18943 | hp1 | a0001 | c0006 | t0001 | g0217 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18944 | hp1 | a0001 | c0006 | t0001 | g0226 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18946 | hp1 | a0002 | c0003 | t0003 | g0256 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18946 | hp2 | a0003 | c0002 | t0002 | g0013 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18947 | hp2 | a0003 | c0023 | t0002 | g0031 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18948 | hp2 | a0002 | c0004 | t0005 | g0301 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18950 | hp1 | a0002 | c0004 | t0005 | g0298 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18953 | hp1 | a0003 | c0002 | t0002 | g0083 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18953 | hp2 | a0002 | c0003 | t0003 | g0262 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18954 | hp1 | a0012 | c0013 | t0001 | g0020 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18962 | hp1 | a0002 | c0003 | t0003 | g0252 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18963 | hp2 | a0002 | c0003 | t0003 | g0002 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18964 | hp1 | a0002 | c0003 | t0003 | g0265 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18966 | hp1 | a0006 | c0010 | t0002 | g0055 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18968 | hp2 | a0001 | c0006 | t0001 | g0225 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18969 | hp1 | a0002 | c0003 | t0003 | g0002 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18972 | hp1 | a0001 | c0001 | t0012 | g0151 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18972 | hp2 | a0002 | c0003 | t0003 | g0246 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18974 | hp2 | a0001 | c0006 | t0001 | g0221 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18975 | hp2 | a0003 | c0002 | t0002 | g0076 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18977 | hp1 | a0002 | c0003 | t0003 | g0272 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18982 | hp2 | a0001 | c0001 | t0011 | g0019 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18983 | hp2 | a0003 | c0002 | t0002 | g0082 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18987 | hp2 | a0002 | c0003 | t0003 | g0270 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18990 | hp1 | a0001 | c0006 | t0001 | g0219 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18990 | hp2 | a0003 | c0002 | t0002 | g0062 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18993 | hp1 | a0003 | c0002 | t0002 | g0067 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18994 | hp1 | a0006 | c0010 | t0002 | g0008 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18994 | hp2 | a0003 | c0002 | t0002 | g0060 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18995 | hp2 | a0002 | c0003 | t0003 | g0275 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18997 | hp1 | a0002 | c0003 | t0003 | g0264 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18998 | hp2 | a0003 | c0002 | t0002 | g0014 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18999 | hp2 | a0002 | c0003 | t0003 | g0268 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19000 | hp1 | a0001 | c0006 | t0001 | g0220 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19001 | hp1 | a0002 | c0003 | t0003 | g0250 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19001 | hp2 | a0003 | c0002 | t0002 | g0061 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19002 | hp2 | a0003 | c0002 | t0002 | g0013 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19004 | hp1 | a0002 | c0003 | t0003 | g0267 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19007 | hp2 | a0001 | c0001 | t0004 | g0018 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19009 | hp1 | a0003 | c0002 | t0002 | g0054 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19010 | hp1 | a0001 | c0001 | t0004 | g0099 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19030 | hp1 | a0002 | c0004 | t0005 | g0290 | AFR | LWK | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19030 | hp2 | a0003 | c0002 | t0002 | g0010 | AFR | LWK | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | LWK | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19043 | hp2 | a0003 | c0002 | t0002 | g0012 | AFR | LWK | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19055 | hp2 | a0003 | c0002 | t0002 | g0057 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19060 | hp1 | a0003 | c0002 | t0002 | g0277 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19064 | hp1 | a0003 | c0002 | t0002 | g0278 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19064 | hp2 | a0001 | c0006 | t0001 | g0027 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19066 | hp1 | a0002 | c0003 | t0003 | g0002 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19075 | hp2 | a0003 | c0002 | t0002 | g0073 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19079 | hp2 | a0001 | c0006 | t0001 | g0027 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19080 | hp2 | a0003 | c0002 | t0002 | g0058 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19085 | hp1 | a0013 | c0021 | t0002 | g0056 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19090 | hp2 | a0002 | c0003 | t0003 | g0249 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19240 | hp1 | a0001 | c0007 | t0006 | g0091 | AFR | YRI | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19240 | hp2 | a0003 | c0002 | t0002 | g0016 | AFR | YRI | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ASW | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | ASW | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0023 | EUR | TSI | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0021 | EUR | TSI | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0021 | EUR | TSI | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA20805 | hp2 | a0001 | c0005 | t0001 | g0233 | EUR | TSI | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | GIH | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | GIH | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01123 | hp1 | a0002 | c0003 | t0003 | g0002 | AMR | CLM | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01123 | hp2 | a0002 | c0004 | t0005 | g0297 | AMR | CLM | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02109 | hp1 | a0001 | c0001 | t0013 | g0084 | AFR | ACB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02109 | hp2 | a0003 | c0002 | t0002 | g0079 | AFR | ACB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02486 | hp1 | a0002 | c0004 | t0007 | g0028 | AFR | ACB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02559 | hp1 | a0002 | c0004 | t0004 | g0017 | AFR | ACB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02559 | hp2 | a0003 | c0002 | t0002 | g0044 | AFR | ACB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03471 | hp1 | a0001 | c0001 | t0009 | g0303 | AFR | MSL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03471 | hp2 | a0003 | c0002 | t0002 | g0045 | AFR | MSL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | USA | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG06807 | hp2 | a0003 | c0002 | t0002 | g0037 | AFR | USA | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18955 | hp1 | a0003 | c0002 | t0002 | g0063 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18955 | hp2 | a0001 | c0001 | t0004 | g0229 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA20300 | hp1 | a0003 | c0002 | t0002 | g0051 | AFR | USA | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA20300 | hp2 | a0001 | c0009 | t0004 | g0283 | AFR | USA | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA21309 | hp1 | a0001 | c0005 | t0001 | g0109 | AFR | LWK | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | LWK | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0196 | REF | REF | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0004 | REF | REF | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:113495637 | C | T | 1 | a0005 | 2 | HG02027.hp1 HG02129.hp2 |
missense_variant | MODERATE | c.56C>T | p.Ala19Val | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 2/13 | 389/3058 | 56/2034 | 19/677 | chr13 | 113495637 | |||
| chr13:113495714 | C | G | 1 | a0013 | 1 | NA19085.hp1 | missense_variant | MODERATE | c.133C>G | p.Gln45Glu | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 2/13 | 466/3058 | 133/2034 | 45/677 | chr13 | 113495714 | |||
| chr13:113495804 | A | G | 1 | a0008 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.223A>G | p.Ile75Val | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 2/13 | 556/3058 | 223/2034 | 75/677 | chr13 | 113495804 | |||
| chr13:113495987 | C | T | 1 | a0004 | 3 | HG02258.hp2 HG02970.hp1 HG03225.hp1 |
missense_variant | MODERATE | c.406C>T | p.Arg136Trp | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 2/13 | 739/3058 | 406/2034 | 136/677 | chr13 | 113495987 | |||
| chr13:113498379 | A | G | 1 | a0006 | 2 | NA18966.hp1 NA18994.hp1 |
missense_variant | MODERATE | c.482A>G | p.Lys161Arg | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 3/13 | 815/3058 | 482/2034 | 161/677 | chr13 | 113498379 | |||
| chr13:113498415 | A | G | 1 | a0011 | 1 | HG03195.hp2 | missense_variant | MODERATE | c.518A>G | p.Gln173Arg | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 3/13 | 851/3058 | 518/2034 | 173/677 | chr13 | 113498415 | |||
| chr13:113503544 | C | G | 1 | a0009 | 1 | HG02922.hp1 | missense_variant | MODERATE | c.994C>G | p.Leu332Val | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/13 | 1327/3058 | 994/2034 | 332/677 | chr13 | 113503544 | |||
| chr13:113520695 | G | A | 1 | a0007 | 1 | HG01981.hp2 | missense_variant | MODERATE | c.1305G>A | p.Met435Ile | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/13 | 1638/3058 | 1305/2034 | 435/677 | chr13 | 113520695 | |||
| chr13:113520717 | G | A | 4 | a0003 a0006 a0010 others(1): Show |
78 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(75): Show |
missense_variant | MODERATE | c.1327G>A | p.Ala443Thr | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/13 | 1660/3058 | 1327/2034 | 443/677 | chr13 | 113520717 | |||
| chr13:113520723 | G | A | 3 | a0002 a0008 a0009 |
77 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(74): Show |
missense_variant | MODERATE | c.1333G>A | p.Ala445Thr | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/13 | 1666/3058 | 1333/2034 | 445/677 | chr13 | 113520723 | |||
| chr13:113534122 | G | A | 1 | a0012 | 1 | NA18954.hp1 | missense_variant | MODERATE | c.1421G>A | p.Cys474Tyr | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/13 | 1754/3058 | 1421/2034 | 474/677 | chr13 | 113534122 | |||
| chr13:113548438 | G | A | 1 | a0010 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.1906G>A | p.Val636Ile | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 12/13 | 2239/3058 | 1906/2034 | 636/677 | chr13 | 113548438 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:113495692 | C | T | 3 | a0001c0009 a0001c0022 a0003c0023 |
5 | HG02135.hp2 HG02717.hp1 HG03516.hp2 others(2): Show |
synonymous_variant | LOW | c.111C>T | p.Arg37Arg | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 2/13 | 444/3058 | 111/2034 | 37/677 | chr13 | 113495692 | |||
| chr13:113495792 | C | T | 3 | a0002c0003 a0002c0019 a0009c0020 |
53 | HG00408.hp1 HG00438.hp2 HG00621.hp2 others(50): Show |
synonymous_variant | LOW | c.211C>T | p.Leu71Leu | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 2/13 | 544/3058 | 211/2034 | 71/677 | chr13 | 113495792 | |||
| chr13:113498440 | C | T | 6 | a0003c0002 a0003c0016 a0003c0023 others(3): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
synonymous_variant | LOW | c.543C>T | p.Asp181Asp | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 3/13 | 876/3058 | 543/2034 | 181/677 | chr13 | 113498440 | |||
| chr13:113500104 | G | A | 6 | a0003c0002 a0003c0016 a0003c0023 others(3): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
synonymous_variant | LOW | c.771G>A | p.Lys257Lys | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 4/13 | 1104/3058 | 771/2034 | 257/677 | chr13 | 113500104 | |||
| chr13:113501778 | C | T | 8 | a0001c0006 a0003c0002 a0003c0016 others(5): Show |
96 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(93): Show |
synonymous_variant | LOW | c.843C>T | p.Ser281Ser | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 5/13 | 1176/3058 | 843/2034 | 281/677 | chr13 | 113501778 | |||
| chr13:113503531 | G | A | 1 | a0001c0005 | 17 | HG00733.hp1 HG01099.hp2 HG01106.hp2 others(14): Show |
synonymous_variant | LOW | c.981G>A | p.Gly327Gly | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/13 | 1314/3058 | 981/2034 | 327/677 | chr13 | 113503531 | |||
| chr13:113520651 | C | T | 1 | a0001c0007 | 4 | HG02280.hp1 HG02922.hp2 HG03209.hp1 others(1): Show |
synonymous_variant | LOW | c.1261C>T | p.Leu421Leu | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/13 | 1594/3058 | 1261/2034 | 421/677 | chr13 | 113520651 | |||
| chr13:113520689 | C | T | 10 | a0001c0006 a0001c0009 a0003c0002 others(7): Show |
100 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(97): Show |
synonymous_variant | LOW | c.1299C>T | p.Ala433Ala | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/13 | 1632/3058 | 1299/2034 | 433/677 | chr13 | 113520689 | |||
| chr13:113549475 | G | A | 1 | a0003c0016 | 1 | HG01243.hp1 | synonymous_variant | LOW | c.1971G>A | p.Pro657Pro | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 13/13 | 2304/3058 | 1971/2034 | 657/677 | chr13 | 113549475 | |||
| chr13:113549499 | G | A | 1 | a0002c0019 | 1 | HG00621.hp2 | synonymous_variant | LOW | c.1995G>A | p.Thr665Thr | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 13/13 | 2328/3058 | 1995/2034 | 665/677 | chr13 | 113549499 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:113491065 | G | C | 1 | a0001c0007t0006 | 4 | HG02280.hp1 HG02922.hp2 HG03209.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-289G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/13 | 4517 | chr13 | 113491065 | ||||||
| chr13:113491084 | C | G | 1 | a0001c0001t0009 | 2 | HG00639.hp1 HG03471.hp1 |
5_prime_UTR_variant | MODIFIER | c.-270C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/13 | 4498 | chr13 | 113491084 | ||||||
| chr13:113491087 | A | ACTCCCGG others(1): Show |
2 | a0002c0004t0005 a0002c0004t0007 |
19 | HG00099.hp2 HG01123.hp2 HG01884.hp2 others(16): Show |
5_prime_UTR_variant | MODIFIER | c.-253_-246dupGGCCTC others(2): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/13 | 4473 | INFO_REALIGN_3_PRIME | chr13 | 113491087 | |||||
| chr13:113491095 | C | A | 1 | a0001c0005t0010 | 1 | HG02280.hp2 | 5_prime_UTR_variant | MODIFIER | c.-259C>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/13 | 4487 | chr13 | 113491095 | ||||||
| chr13:113491133 | A | G | 2 | a0002c0004t0005 a0002c0004t0007 |
19 | HG00099.hp2 HG01123.hp2 HG01884.hp2 others(16): Show |
5_prime_UTR_variant | MODIFIER | c.-221A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/13 | 4449 | chr13 | 113491133 | ||||||
| chr13:113495576 | T | C | 6 | a0003c0002t0002 a0003c0016t0002 a0003c0023t0002 others(3): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
5_prime_UTR_variant | MODIFIER | c.-6T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 2/13 | 6 | chr13 | 113495576 | ||||||
| chr13:113549594 | G | C | 1 | a0001c0001t0011 | 1 | NA18982.hp2 | 3_prime_UTR_variant | MODIFIER | c.*56G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 13/13 | 56 | chr13 | 113549594 | ||||||
| chr13:113549694 | A | C | 1 | a0001c0001t0013 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*156A>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 13/13 | 156 | chr13 | 113549694 | ||||||
| chr13:113549722 | G | C | 1 | a0001c0001t0012 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*184G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 13/13 | 184 | chr13 | 113549722 | ||||||
| chr13:113549816 | T | G | 1 | a0002c0004t0007 | 3 | HG02451.hp2 HG02486.hp1 HG02965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*278T>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 13/13 | 278 | chr13 | 113549816 | ||||||
| chr13:113549860 | C | T | 14 | a0001c0001t0004 a0001c0001t0009 a0001c0009t0004 others(11): Show |
107 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*322C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 13/13 | 322 | chr13 | 113549860 | ||||||
| chr13:113549940 | A | G | 19 | a0001c0001t0004 a0001c0001t0009 a0001c0009t0004 others(16): Show |
179 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(176): Show |
3_prime_UTR_variant | MODIFIER | c.*402A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 13/13 | 402 | chr13 | 113549940 | ||||||
| chr13:113550054 | G | A | 5 | a0002c0003t0003 a0002c0004t0005 a0002c0004t0007 others(2): Show |
72 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*516G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 13/13 | 516 | chr13 | 113550054 | ||||||
| chr13:113550076 | G | A | 7 | a0001c0001t0004 a0001c0001t0009 a0001c0009t0004 others(4): Show |
28 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*538G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 13/13 | 538 | chr13 | 113550076 | ||||||
| chr13:113550119 | A | G | 1 | a0005c0011t0008 | 2 | HG02027.hp1 HG02129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*581A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 13/13 | 581 | chr13 | 113550119 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:113491280 | A | G | 23 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0002c0004t0004g0305 others(20): Show |
24 | HG00099.hp2 HG00639.hp1 HG01123.hp2 others(21): Show |
splice_region_variant&intron_variant | LOW | c.-81+7A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113491280 | |||||||
| chr13:113491299 | G | A | 65 | a0002c0003t0003g0029 a0003c0002t0002g0005 a0003c0002t0002g0008 others(62): Show |
76 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.-81+26G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113491299 | |||||||
| chr13:113491316 | CCCTTCCT others(81): Show |
C | 1 | a0001c0001t0001g0285 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-81+76_-81+163delC others(87): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr13 | 113491316 | ||||||
| chr13:113491380 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-81+107T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113491380 | |||||||
| chr13:113491423 | C | T | 2 | a0003c0002t0002g0082 a0003c0002t0002g0083 |
2 | NA18953.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.-81+150C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113491423 | |||||||
| chr13:113491441 | C | T | 2 | a0005c0011t0008g0306 a0005c0011t0008g0307 |
2 | HG02027.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.-81+168C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113491441 | |||||||
| chr13:113491572 | C | T | 1 | a0011c0017t0001g0284 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-81+299C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113491572 | |||||||
| chr13:113491592 | CT | C | 18 | a0002c0004t0005g0286 a0002c0004t0005g0287 a0002c0004t0005g0289 others(15): Show |
19 | HG00099.hp2 HG01123.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.-81+320delT | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113491592 | |||||||
| chr13:113491725 | G | C | 18 | a0002c0004t0005g0286 a0002c0004t0005g0287 a0002c0004t0005g0289 others(15): Show |
19 | HG00099.hp2 HG01123.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.-81+452G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113491725 | |||||||
| chr13:113491916 | C | T | 3 | a0001c0009t0004g0281 a0001c0009t0004g0282 a0001c0009t0004g0283 |
3 | HG02717.hp1 HG03516.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-81+643C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113491916 | |||||||
| chr13:113491938 | C | T | 1 | a0002c0004t0004g0305 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-81+665C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113491938 | |||||||
| chr13:113492019 | G | A | 2 | a0001c0001t0009g0303 a0001c0001t0009g0304 |
2 | HG00639.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-81+746G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113492019 | |||||||
| chr13:113492022 | T | G | 18 | a0002c0004t0005g0286 a0002c0004t0005g0287 a0002c0004t0005g0289 others(15): Show |
19 | HG00099.hp2 HG01123.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.-81+749T>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113492022 | |||||||
| chr13:113492231 | C | T | 1 | a0001c0007t0006g0280 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-81+958C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113492231 | |||||||
| chr13:113492306 | T | C | 1 | a0001c0001t0013g0084 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-81+1033T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113492306 | |||||||
| chr13:113492370 | C | A | 2 | a0001c0001t0009g0303 a0001c0001t0009g0304 |
2 | HG00639.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-81+1097C>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113492370 | |||||||
| chr13:113492398 | C | G | 1 | a0001c0001t0001g0279 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-81+1125C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113492398 | |||||||
| chr13:113492433 | A | G | 7 | a0003c0002t0002g0005 a0003c0002t0002g0016 a0003c0002t0002g0077 others(4): Show |
11 | HG01070.hp2 HG01081.hp1 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.-81+1160A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113492433 | |||||||
| chr13:113492578 | C | T | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.-81+1305C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113492578 | |||||||
| chr13:113492770 | C | G | 2 | a0005c0011t0008g0306 a0005c0011t0008g0307 |
2 | HG02027.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.-81+1497C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113492770 | |||||||
| chr13:113493016 | A | C | 18 | a0002c0004t0005g0286 a0002c0004t0005g0287 a0002c0004t0005g0289 others(15): Show |
19 | HG00099.hp2 HG01123.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.-81+1743A>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113493016 | |||||||
| chr13:113493104 | G | GT | 44 | a0002c0003t0003g0002 a0002c0003t0003g0007 a0002c0003t0003g0029 others(41): Show |
53 | HG00408.hp1 HG00438.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.-81+1834dupT | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr13 | 113493104 | ||||||
| chr13:113493263 | C | T | 18 | a0002c0004t0005g0286 a0002c0004t0005g0287 a0002c0004t0005g0289 others(15): Show |
19 | HG00099.hp2 HG01123.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.-81+1990C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113493263 | |||||||
| chr13:113493305 | C | T | 1 | a0001c0001t0001g0237 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-81+2032C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113493305 | |||||||
| chr13:113493359 | A | G | 2 | a0001c0006t0001g0235 a0001c0006t0001g0236 |
2 | HG00280.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.-81+2086A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113493359 | |||||||
| chr13:113493366 | C | T | 1 | a0002c0004t0004g0305 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-81+2093C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113493366 | |||||||
| chr13:113493405 | C | G | 1 | a0002c0003t0003g0029 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-80-2097C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113493405 | |||||||
| chr13:113493489 | C | G | 1 | a0001c0006t0001g0234 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-80-2013C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113493489 | |||||||
| chr13:113493494 | C | T | 4 | a0001c0005t0001g0230 a0001c0005t0001g0231 a0001c0005t0001g0232 others(1): Show |
4 | HG01099.hp2 HG01257.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.-80-2008C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113493494 | |||||||
| chr13:113493540 | A | G | 1 | a0001c0001t0004g0229 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-80-1962A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113493540 | |||||||
| chr13:113493551 | TGTGTACT others(13): Show |
T | 16 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(13): Show |
17 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(14): Show |
intron_variant | MODIFIER | c.-80-1933_-80-1914d others(22): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr13 | 113493551 | ||||||
| chr13:113493682 | T | C | 181 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0106 others(178): Show |
205 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.-80-1820T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113493682 | |||||||
| chr13:113493700 | T | G | 16 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(13): Show |
17 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(14): Show |
intron_variant | MODIFIER | c.-80-1802T>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113493700 | |||||||
| chr13:113493786 | T | A | 1 | a0001c0001t0001g0107 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-80-1716T>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113493786 | |||||||
| chr13:113493804 | C | CT | 11 | a0002c0004t0005g0292 a0002c0004t0005g0293 a0002c0004t0005g0294 others(8): Show |
11 | HG00099.hp2 HG01123.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.-80-1697dupT | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr13 | 113493804 | ||||||
| chr13:113493809 | A | C | 1 | a0001c0001t0001g0216 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-80-1693A>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113493809 | |||||||
| chr13:113494217 | T | C | 16 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(13): Show |
17 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(14): Show |
intron_variant | MODIFIER | c.-80-1285T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113494217 | |||||||
| chr13:113494298 | A | C | 2 | a0005c0011t0008g0306 a0005c0011t0008g0307 |
2 | HG02027.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.-80-1204A>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113494298 | |||||||
| chr13:113494324 | T | C | 3 | a0001c0009t0004g0281 a0001c0009t0004g0282 a0001c0009t0004g0283 |
3 | HG02717.hp1 HG03516.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-80-1178T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113494324 | |||||||
| chr13:113494342 | C | T | 1 | a0003c0002t0002g0076 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-80-1160C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113494342 | |||||||
| chr13:113494349 | C | A | 16 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(13): Show |
17 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(14): Show |
intron_variant | MODIFIER | c.-80-1153C>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113494349 | |||||||
| chr13:113494405 | T | C | 44 | a0002c0003t0003g0002 a0002c0003t0003g0007 a0002c0003t0003g0029 others(41): Show |
53 | HG00408.hp1 HG00438.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.-80-1097T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113494405 | |||||||
| chr13:113494490 | C | G | 1 | a0003c0002t0002g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-80-1012C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113494490 | |||||||
| chr13:113494526 | G | C | 2 | a0001c0001t0009g0303 a0001c0001t0009g0304 |
2 | HG00639.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-80-976G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113494526 | |||||||
| chr13:113494620 | G | A | 7 | a0001c0001t0001g0087 a0001c0009t0004g0281 a0001c0009t0004g0282 others(4): Show |
8 | HG02145.hp1 HG02559.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-80-882G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113494620 | |||||||
| chr13:113494637 | G | A | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.-80-865G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113494637 | |||||||
| chr13:113494655 | C | CAT | 125 | a0001c0001t0001g0088 a0001c0001t0013g0084 a0001c0006t0001g0027 others(122): Show |
144 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.-80-832_-80-831dup others(2): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr13 | 113494655 | ||||||
| chr13:113494655 | C | CATAT | 5 | a0002c0003t0003g0007 a0002c0003t0003g0238 a0002c0003t0003g0239 others(2): Show |
7 | HG02615.hp1 HG02922.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.-80-834_-80-831dup others(4): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr13 | 113494655 | ||||||
| chr13:113494668 | A | ATT | 3 | a0001c0001t0001g0087 a0002c0004t0004g0017 a0002c0004t0004g0086 |
4 | HG02145.hp1 HG02559.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-80-833_-80-832ins others(2): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr13 | 113494668 | ||||||
| chr13:113494670 | A | T | 3 | a0001c0001t0001g0087 a0002c0004t0004g0017 a0002c0004t0004g0086 |
4 | HG02145.hp1 HG02559.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-80-832A>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113494670 | |||||||
| chr13:113494731 | C | A | 26 | a0001c0001t0001g0088 a0001c0001t0001g0285 a0001c0001t0004g0018 others(23): Show |
27 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(24): Show |
intron_variant | MODIFIER | c.-80-771C>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113494731 | |||||||
| chr13:113494747 | A | G | 2 | a0005c0011t0008g0306 a0005c0011t0008g0307 |
2 | HG02027.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.-80-755A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113494747 | |||||||
| chr13:113494804 | G | A | 1 | a0002c0003t0003g0029 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-80-698G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113494804 | |||||||
| chr13:113494866 | C | T | 67 | a0002c0004t0005g0302 a0003c0002t0002g0005 a0003c0002t0002g0008 others(64): Show |
78 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.-80-636C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113494866 | |||||||
| chr13:113494867 | G | A | 1 | a0002c0004t0004g0305 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-80-635G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113494867 | |||||||
| chr13:113494890 | GT | G | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.-80-602delT | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr13 | 113494890 | ||||||
| chr13:113494956 | T | C | 6 | a0001c0001t0001g0087 a0001c0001t0009g0303 a0001c0001t0009g0304 others(3): Show |
7 | HG00639.hp1 HG02145.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-80-546T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113494956 | |||||||
| chr13:113494998 | G | A | 1 | a0001c0006t0001g0235 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-80-504G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113494998 | |||||||
| chr13:113495010 | G | A | 2 | a0001c0001t0001g0019 a0001c0001t0011g0019 |
2 | NA18950.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.-80-492G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113495010 | |||||||
| chr13:113495097 | G | C | 2 | a0001c0001t0009g0303 a0001c0001t0009g0304 |
2 | HG00639.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-80-405G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113495097 | |||||||
| chr13:113495109 | C | G | 2 | a0001c0001t0009g0303 a0001c0001t0009g0304 |
2 | HG00639.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-80-393C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113495109 | |||||||
| chr13:113495143 | C | A | 1 | a0002c0003t0003g0241 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-80-359C>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113495143 | |||||||
| chr13:113495145 | A | G | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.-80-357A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113495145 | |||||||
| chr13:113495203 | G | A | 89 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0006t0001g0027 others(86): Show |
101 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.-80-299G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113495203 | |||||||
| chr13:113495219 | C | A | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.-80-283C>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113495219 | |||||||
| chr13:113495230 | C | T | 1 | a0001c0001t0001g0215 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-80-272C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113495230 | |||||||
| chr13:113495318 | G | A | 1 | a0001c0001t0001g0285 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-80-184G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113495318 | |||||||
| chr13:113495388 | G | A | 3 | a0001c0005t0001g0108 a0001c0005t0001g0109 a0001c0005t0001g0110 |
3 | HG00733.hp1 HG02293.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-80-114G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113495388 | |||||||
| chr13:113495393 | A | G | 1 | a0001c0007t0006g0280 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-80-109A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113495393 | |||||||
| chr13:113495424 | T | C | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.-80-78T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113495424 | |||||||
| chr13:113495443 | A | G | 1 | a0001c0001t0001g0285 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-80-59A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113495443 | |||||||
| chr13:113495477 | A | G | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.-80-25A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113495477 | |||||||
| chr13:113495480 | T | C | 16 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(13): Show |
17 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(14): Show |
intron_variant | MODIFIER | c.-80-22T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 1/12 | chr13 | 113495480 | |||||||
| chr13:113496035 | A | AGAGAGGG others(15): Show |
1 | a0002c0003t0003g0242 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.444+26_444+47dupAG others(20): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr13 | 113496035 | ||||||
| chr13:113496043 | A | G | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.444+18A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 2/12 | chr13 | 113496043 | |||||||
| chr13:113496093 | C | T | 1 | a0001c0001t0001g0285 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.444+68C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 2/12 | chr13 | 113496093 | |||||||
| chr13:113496118 | C | G | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.444+93C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 2/12 | chr13 | 113496118 | |||||||
| chr13:113496127 | C | T | 1 | a0002c0004t0004g0305 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.444+102C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 2/12 | chr13 | 113496127 | |||||||
| chr13:113496277 | G | A | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.444+252G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 2/12 | chr13 | 113496277 | |||||||
| chr13:113496480 | A | G | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.444+455A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 2/12 | chr13 | 113496480 | |||||||
| chr13:113496535 | G | A | 133 | a0001c0001t0001g0087 a0002c0003t0003g0002 a0002c0003t0003g0007 others(130): Show |
155 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.444+510G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 2/12 | chr13 | 113496535 | |||||||
| chr13:113496706 | G | A | 1 | a0003c0002t0002g0030 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.444+681G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 2/12 | chr13 | 113496706 | |||||||
| chr13:113496744 | A | C | 2 | a0001c0001t0009g0303 a0001c0001t0009g0304 |
2 | HG00639.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.444+719A>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 2/12 | chr13 | 113496744 | |||||||
| chr13:113496865 | A | G | 1 | a0002c0004t0005g0301 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.444+840A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 2/12 | chr13 | 113496865 | |||||||
| chr13:113496954 | T | C | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.444+929T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 2/12 | chr13 | 113496954 | |||||||
| chr13:113497045 | C | T | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.444+1020C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 2/12 | chr13 | 113497045 | |||||||
| chr13:113497057 | C | T | 1 | a0002c0003t0003g0276 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.444+1032C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 2/12 | chr13 | 113497057 | |||||||
| chr13:113497191 | A | G | 1 | a0003c0016t0002g0074 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.445-1151A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 2/12 | chr13 | 113497191 | |||||||
| chr13:113497206 | G | T | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.445-1136G>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 2/12 | chr13 | 113497206 | |||||||
| chr13:113497255 | GCAGCTAT others(7): Show |
G | 1 | a0003c0002t0002g0073 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.445-1081_445-1068d others(16): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr13 | 113497255 | ||||||
| chr13:113497272 | G | T | 1 | a0002c0003t0003g0241 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.445-1070G>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 2/12 | chr13 | 113497272 | |||||||
| chr13:113497273 | C | T | 1 | a0002c0003t0003g0241 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.445-1069C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 2/12 | chr13 | 113497273 | |||||||
| chr13:113497363 | C | A | 44 | a0002c0003t0003g0002 a0002c0003t0003g0007 a0002c0003t0003g0029 others(41): Show |
53 | HG00408.hp1 HG00438.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.445-979C>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 2/12 | chr13 | 113497363 | |||||||
| chr13:113497415 | C | CAGCTCTG others(28): Show |
1 | a0008c0018t0004g0085 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.445-893_445-892ins others(35): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr13 | 113497415 | ||||||
| chr13:113497504 | C | CTGTGTGA others(12): Show |
1 | a0001c0005t0001g0214 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.445-816_445-798dup others(19): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr13 | 113497504 | ||||||
| chr13:113497545 | C | T | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.445-797C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 2/12 | chr13 | 113497545 | |||||||
| chr13:113497551 | T | C | 69 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0005t0001g0214 others(66): Show |
80 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.445-791T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 2/12 | chr13 | 113497551 | |||||||
| chr13:113497554 | T | TAGCTGTG others(10): Show |
66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.445-755_445-739dup others(17): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr13 | 113497554 | ||||||
| chr13:113497634 | T | A | 89 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0006t0001g0027 others(86): Show |
101 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.445-708T>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 2/12 | chr13 | 113497634 | |||||||
| chr13:113497869 | T | C | 69 | a0001c0009t0004g0281 a0001c0009t0004g0282 a0001c0009t0004g0283 others(66): Show |
80 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.445-473T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 2/12 | chr13 | 113497869 | |||||||
| chr13:113497893 | T | C | 1 | a0001c0006t0001g0217 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.445-449T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 2/12 | chr13 | 113497893 | |||||||
| chr13:113497930 | C | T | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.445-412C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 2/12 | chr13 | 113497930 | |||||||
| chr13:113497950 | T | C | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.445-392T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 2/12 | chr13 | 113497950 | |||||||
| chr13:113497959 | C | A | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.445-383C>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 2/12 | chr13 | 113497959 | |||||||
| chr13:113497977 | A | G | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.445-365A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 2/12 | chr13 | 113497977 | |||||||
| chr13:113498122 | T | C | 1 | a0002c0003t0003g0243 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.445-220T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 2/12 | chr13 | 113498122 | |||||||
| chr13:113498125 | C | A | 13 | a0001c0001t0001g0019 a0001c0001t0001g0111 a0001c0001t0001g0112 others(10): Show |
13 | NA18747.hp2 NA18950.hp2 NA18952.hp2 others(10): Show |
intron_variant | MODIFIER | c.445-217C>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 2/12 | chr13 | 113498125 | |||||||
| chr13:113498125 | C | T | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.445-217C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 2/12 | chr13 | 113498125 | |||||||
| chr13:113498202 | C | T | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.445-140C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 2/12 | chr13 | 113498202 | |||||||
| chr13:113498211 | C | G | 1 | a0003c0002t0002g0072 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.445-131C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 2/12 | chr13 | 113498211 | |||||||
| chr13:113498528 | G | T | 2 | a0005c0011t0008g0306 a0005c0011t0008g0307 |
2 | HG02027.hp1 HG02129.hp2 |
splice_region_variant&intron_variant | LOW | c.624+7G>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 3/12 | chr13 | 113498528 | |||||||
| chr13:113498543 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.624+22C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 3/12 | chr13 | 113498543 | |||||||
| chr13:113498600 | G | A | 2 | a0005c0011t0008g0306 a0005c0011t0008g0307 |
2 | HG02027.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.624+79G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 3/12 | chr13 | 113498600 | |||||||
| chr13:113498604 | A | G | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.624+83A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 3/12 | chr13 | 113498604 | |||||||
| chr13:113498613 | A | G | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.624+92A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 3/12 | chr13 | 113498613 | |||||||
| chr13:113498667 | ATT | A | 3 | a0001c0009t0004g0281 a0001c0009t0004g0282 a0001c0009t0004g0283 |
3 | HG02717.hp1 HG03516.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.624+148_624+149del others(2): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr13 | 113498667 | ||||||
| chr13:113498689 | T | C | 1 | a0003c0023t0002g0031 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.624+168T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 3/12 | chr13 | 113498689 | |||||||
| chr13:113498726 | G | C | 1 | a0004c0008t0004g0089 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.624+205G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 3/12 | chr13 | 113498726 | |||||||
| chr13:113498795 | C | A | 4 | a0002c0004t0005g0292 a0002c0004t0005g0293 a0002c0004t0005g0294 others(1): Show |
4 | HG00099.hp2 HG02698.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.624+274C>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 3/12 | chr13 | 113498795 | |||||||
| chr13:113498866 | T | C | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.624+345T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 3/12 | chr13 | 113498866 | |||||||
| chr13:113498878 | CAA | C | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.624+358_624+359del others(2): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 3/12 | chr13 | 113498878 | |||||||
| chr13:113498897 | CAG | C | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.624+377_624+378del others(2): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 3/12 | chr13 | 113498897 | |||||||
| chr13:113498903 | T | G | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.624+382T>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 3/12 | chr13 | 113498903 | |||||||
| chr13:113499033 | A | G | 89 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0006t0001g0027 others(86): Show |
101 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.624+512A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 3/12 | chr13 | 113499033 | |||||||
| chr13:113499135 | A | T | 21 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(18): Show |
22 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(19): Show |
intron_variant | MODIFIER | c.624+614A>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 3/12 | chr13 | 113499135 | |||||||
| chr13:113499156 | G | A | 1 | a0001c0001t0013g0084 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.624+635G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 3/12 | chr13 | 113499156 | |||||||
| chr13:113499156 | G | T | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.624+635G>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 3/12 | chr13 | 113499156 | |||||||
| chr13:113499273 | C | T | 181 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0106 others(178): Show |
205 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.625-685C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 3/12 | chr13 | 113499273 | |||||||
| chr13:113499374 | C | T | 23 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0006t0001g0027 others(20): Show |
24 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.625-584C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 3/12 | chr13 | 113499374 | |||||||
| chr13:113499397 | C | G | 16 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(13): Show |
17 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(14): Show |
intron_variant | MODIFIER | c.625-561C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 3/12 | chr13 | 113499397 | |||||||
| chr13:113499468 | T | C | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.625-490T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 3/12 | chr13 | 113499468 | |||||||
| chr13:113499488 | A | G | 1 | a0004c0008t0004g0089 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.625-470A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 3/12 | chr13 | 113499488 | |||||||
| chr13:113499531 | A | G | 1 | a0001c0001t0004g0105 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.625-427A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 3/12 | chr13 | 113499531 | |||||||
| chr13:113499624 | A | G | 1 | a0002c0004t0004g0305 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.625-334A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 3/12 | chr13 | 113499624 | |||||||
| chr13:113499692 | A | G | 8 | a0001c0001t0001g0003 a0001c0001t0001g0207 a0001c0001t0001g0208 others(5): Show |
14 | NA18945.hp1 NA18949.hp1 NA18954.hp2 others(11): Show |
intron_variant | MODIFIER | c.625-266A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 3/12 | chr13 | 113499692 | |||||||
| chr13:113499699 | C | T | 1 | a0003c0002t0002g0071 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.625-259C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 3/12 | chr13 | 113499699 | |||||||
| chr13:113499766 | A | G | 1 | a0001c0006t0001g0228 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.625-192A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 3/12 | chr13 | 113499766 | |||||||
| chr13:113499885 | T | C | 23 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0006t0001g0027 others(20): Show |
24 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.625-73T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 3/12 | chr13 | 113499885 | |||||||
| chr13:113499893 | G | A | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.625-65G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 3/12 | chr13 | 113499893 | |||||||
| chr13:113499915 | G | A | 16 | a0002c0004t0005g0286 a0002c0004t0005g0287 a0002c0004t0005g0289 others(13): Show |
17 | HG00099.hp2 HG01123.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.625-43G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 3/12 | chr13 | 113499915 | |||||||
| chr13:113500208 | A | G | 1 | a0010c0015t0002g0070 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.816+59A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 4/12 | chr13 | 113500208 | |||||||
| chr13:113500214 | G | A | 1 | a0001c0001t0001g0121 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.816+65G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 4/12 | chr13 | 113500214 | |||||||
| chr13:113500415 | G | A | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.816+266G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 4/12 | chr13 | 113500415 | |||||||
| chr13:113500559 | C | T | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.816+410C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 4/12 | chr13 | 113500559 | |||||||
| chr13:113500681 | G | A | 2 | a0003c0002t0002g0077 a0003c0002t0002g0078 |
2 | HG01070.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.816+532G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 4/12 | chr13 | 113500681 | |||||||
| chr13:113500686 | G | A | 2 | a0001c0001t0001g0122 a0001c0001t0001g0123 |
2 | HG01106.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.816+537G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 4/12 | chr13 | 113500686 | |||||||
| chr13:113500714 | A | G | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | NA18998.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.816+565A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 4/12 | chr13 | 113500714 | |||||||
| chr13:113500777 | G | A | 3 | a0001c0009t0004g0281 a0001c0009t0004g0282 a0001c0009t0004g0283 |
3 | HG02717.hp1 HG03516.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.816+628G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 4/12 | chr13 | 113500777 | |||||||
| chr13:113500808 | C | T | 1 | a0001c0001t0001g0206 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.816+659C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 4/12 | chr13 | 113500808 | |||||||
| chr13:113500861 | G | A | 45 | a0002c0003t0003g0002 a0002c0003t0003g0007 a0002c0003t0003g0238 others(42): Show |
54 | HG00408.hp1 HG00438.hp2 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.816+712G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 4/12 | chr13 | 113500861 | |||||||
| chr13:113500915 | C | G | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.816+766C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 4/12 | chr13 | 113500915 | |||||||
| chr13:113500925 | G | A | 1 | a0002c0003t0003g0244 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.816+776G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 4/12 | chr13 | 113500925 | |||||||
| chr13:113500942 | A | G | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.816+793A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 4/12 | chr13 | 113500942 | |||||||
| chr13:113501002 | A | G | 2 | a0003c0002t0002g0077 a0003c0002t0002g0078 |
2 | HG01070.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.817-750A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 4/12 | chr13 | 113501002 | |||||||
| chr13:113501030 | G | A | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.817-722G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 4/12 | chr13 | 113501030 | |||||||
| chr13:113501041 | A | T | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.817-711A>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 4/12 | chr13 | 113501041 | |||||||
| chr13:113501053 | G | A | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.817-699G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 4/12 | chr13 | 113501053 | |||||||
| chr13:113501096 | G | T | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.817-656G>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 4/12 | chr13 | 113501096 | |||||||
| chr13:113501148 | A | G | 1 | a0001c0001t0001g0205 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.817-604A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 4/12 | chr13 | 113501148 | |||||||
| chr13:113501209 | C | T | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.817-543C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 4/12 | chr13 | 113501209 | |||||||
| chr13:113501338 | T | A | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.817-414T>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 4/12 | chr13 | 113501338 | |||||||
| chr13:113501386 | G | C | 1 | a0008c0018t0004g0085 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.817-366G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 4/12 | chr13 | 113501386 | |||||||
| chr13:113501391 | T | C | 156 | a0001c0001t0001g0087 a0001c0001t0009g0303 a0001c0001t0009g0304 others(153): Show |
179 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.817-361T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 4/12 | chr13 | 113501391 | |||||||
| chr13:113501427 | C | T | 65 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(62): Show |
76 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.817-325C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 4/12 | chr13 | 113501427 | |||||||
| chr13:113501454 | G | A | 21 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(18): Show |
22 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(19): Show |
intron_variant | MODIFIER | c.817-298G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 4/12 | chr13 | 113501454 | |||||||
| chr13:113501459 | T | C | 65 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(62): Show |
76 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.817-293T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 4/12 | chr13 | 113501459 | |||||||
| chr13:113501568 | C | T | 1 | a0003c0002t0002g0081 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.817-184C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 4/12 | chr13 | 113501568 | |||||||
| chr13:113501614 | A | G | 2 | a0003c0002t0002g0068 a0003c0002t0002g0069 |
2 | HG00673.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.817-138A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 4/12 | chr13 | 113501614 | |||||||
| chr13:113501650 | G | A | 154 | a0001c0001t0001g0087 a0001c0006t0001g0027 a0001c0006t0001g0217 others(151): Show |
177 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.817-102G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 4/12 | chr13 | 113501650 | |||||||
| chr13:113501667 | C | T | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.817-85C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 4/12 | chr13 | 113501667 | |||||||
| chr13:113501725 | C | A | 2 | a0001c0001t0001g0124 a0001c0001t0001g0125 |
2 | NA18975.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.817-27C>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 4/12 | chr13 | 113501725 | |||||||
| chr13:113502022 | C | T | 21 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(18): Show |
22 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(19): Show |
intron_variant | MODIFIER | c.945+142C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 5/12 | chr13 | 113502022 | |||||||
| chr13:113502072 | C | T | 3 | a0001c0009t0004g0281 a0001c0009t0004g0282 a0001c0009t0004g0283 |
3 | HG02717.hp1 HG03516.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.945+192C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 5/12 | chr13 | 113502072 | |||||||
| chr13:113502158 | A | G | 49 | a0001c0001t0001g0087 a0002c0003t0003g0002 a0002c0003t0003g0007 others(46): Show |
59 | HG00408.hp1 HG00438.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.945+278A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 5/12 | chr13 | 113502158 | |||||||
| chr13:113502202 | G | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(83): Show |
102 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.945+322G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 5/12 | chr13 | 113502202 | |||||||
| chr13:113502217 | G | T | 18 | a0002c0004t0005g0286 a0002c0004t0005g0287 a0002c0004t0005g0289 others(15): Show |
19 | HG00099.hp2 HG01123.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.945+337G>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 5/12 | chr13 | 113502217 | |||||||
| chr13:113502300 | G | A | 48 | a0001c0001t0001g0087 a0002c0003t0003g0002 a0002c0003t0003g0007 others(45): Show |
58 | HG00408.hp1 HG00438.hp2 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.945+420G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 5/12 | chr13 | 113502300 | |||||||
| chr13:113502302 | C | T | 1 | a0003c0002t0002g0067 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.945+422C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 5/12 | chr13 | 113502302 | |||||||
| chr13:113502435 | G | A | 1 | a0001c0005t0001g0126 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.945+555G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 5/12 | chr13 | 113502435 | |||||||
| chr13:113502455 | C | T | 7 | a0002c0003t0003g0273 a0002c0003t0003g0274 a0002c0003t0003g0275 others(4): Show |
7 | HG01070.hp2 HG02080.hp2 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.945+575C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 5/12 | chr13 | 113502455 | |||||||
| chr13:113502456 | G | A | 18 | a0002c0004t0005g0286 a0002c0004t0005g0287 a0002c0004t0005g0289 others(15): Show |
19 | HG00099.hp2 HG01123.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.945+576G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 5/12 | chr13 | 113502456 | |||||||
| chr13:113502543 | A | T | 21 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(18): Show |
22 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(19): Show |
intron_variant | MODIFIER | c.945+663A>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 5/12 | chr13 | 113502543 | |||||||
| chr13:113502575 | G | A | 1 | a0002c0003t0003g0238 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.945+695G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 5/12 | chr13 | 113502575 | |||||||
| chr13:113502683 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.945+803G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 5/12 | chr13 | 113502683 | |||||||
| chr13:113502690 | G | A | 2 | a0001c0001t0009g0303 a0001c0001t0009g0304 |
2 | HG00639.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.946-806G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 5/12 | chr13 | 113502690 | |||||||
| chr13:113502728 | C | G | 2 | a0005c0011t0008g0306 a0005c0011t0008g0307 |
2 | HG02027.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.946-768C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 5/12 | chr13 | 113502728 | |||||||
| chr13:113502833 | C | A | 1 | a0003c0002t0002g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.946-663C>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 5/12 | chr13 | 113502833 | |||||||
| chr13:113502852 | C | G | 1 | a0011c0017t0001g0284 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.946-644C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 5/12 | chr13 | 113502852 | |||||||
| chr13:113502853 | G | A | 2 | a0001c0001t0009g0303 a0001c0001t0009g0304 |
2 | HG00639.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.946-643G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 5/12 | chr13 | 113502853 | |||||||
| chr13:113502862 | C | T | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.946-634C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 5/12 | chr13 | 113502862 | |||||||
| chr13:113502909 | G | A | 18 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(15): Show |
19 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(16): Show |
intron_variant | MODIFIER | c.946-587G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 5/12 | chr13 | 113502909 | |||||||
| chr13:113502936 | C | T | 18 | a0002c0004t0005g0286 a0002c0004t0005g0287 a0002c0004t0005g0289 others(15): Show |
19 | HG00099.hp2 HG01123.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.946-560C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 5/12 | chr13 | 113502936 | |||||||
| chr13:113502942 | G | A | 1 | a0001c0001t0001g0285 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.946-554G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 5/12 | chr13 | 113502942 | |||||||
| chr13:113502944 | C | A | 1 | a0010c0015t0002g0070 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.946-552C>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 5/12 | chr13 | 113502944 | |||||||
| chr13:113502971 | G | T | 16 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(13): Show |
17 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(14): Show |
intron_variant | MODIFIER | c.946-525G>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 5/12 | chr13 | 113502971 | |||||||
| chr13:113502986 | G | A | 18 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(15): Show |
19 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(16): Show |
intron_variant | MODIFIER | c.946-510G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 5/12 | chr13 | 113502986 | |||||||
| chr13:113502990 | G | A | 44 | a0002c0003t0003g0002 a0002c0003t0003g0007 a0002c0003t0003g0029 others(41): Show |
53 | HG00408.hp1 HG00438.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.946-506G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 5/12 | chr13 | 113502990 | |||||||
| chr13:113503057 | C | T | 1 | a0001c0001t0001g0087 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.946-439C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 5/12 | chr13 | 113503057 | |||||||
| chr13:113503074 | A | C | 1 | a0001c0001t0001g0088 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.946-422A>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 5/12 | chr13 | 113503074 | |||||||
| chr13:113503254 | G | T | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.946-242G>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 5/12 | chr13 | 113503254 | |||||||
| chr13:113503335 | C | T | 156 | a0001c0001t0001g0087 a0001c0001t0009g0303 a0001c0001t0009g0304 others(153): Show |
179 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.946-161C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 5/12 | chr13 | 113503335 | |||||||
| chr13:113503345 | T | TTG | 18 | a0001c0001t0001g0106 a0001c0001t0001g0199 a0001c0001t0001g0200 others(15): Show |
18 | HG00099.hp2 HG00735.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.946-113_946-112dup others(2): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr13 | 113503345 | ||||||
| chr13:113503345 | T | TTGTG | 5 | a0001c0001t0001g0188 a0001c0001t0009g0303 a0001c0001t0009g0304 others(2): Show |
5 | HG00639.hp1 HG02647.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.946-115_946-112dup others(4): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr13 | 113503345 | ||||||
| chr13:113503345 | T | TTGTGTG | 6 | a0001c0001t0001g0285 a0002c0004t0005g0289 a0002c0004t0005g0299 others(3): Show |
7 | HG01884.hp2 HG02135.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.946-117_946-112dup others(6): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr13 | 113503345 | ||||||
| chr13:113503345 | TTG | T | 27 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0165 others(24): Show |
27 | HG00733.hp1 HG00741.hp2 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.946-113_946-112del others(2): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr13 | 113503345 | ||||||
| chr13:113503345 | TTGTG | T | 49 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(46): Show |
65 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.946-115_946-112del others(4): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr13 | 113503345 | ||||||
| chr13:113503345 | TTGTGTG | T | 21 | a0001c0001t0001g0088 a0001c0001t0001g0127 a0001c0001t0001g0128 others(18): Show |
22 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(19): Show |
intron_variant | MODIFIER | c.946-117_946-112del others(6): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr13 | 113503345 | ||||||
| chr13:113503345 | TTGTGTGT others(1): Show |
T | 44 | a0001c0001t0001g0121 a0001c0001t0004g0093 a0001c0006t0001g0227 others(41): Show |
53 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.946-119_946-112del others(8): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr13 | 113503345 | ||||||
| chr13:113503345 | TTGTGTGT others(3): Show |
T | 19 | a0001c0001t0001g0087 a0001c0006t0001g0027 a0001c0006t0001g0217 others(16): Show |
21 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.946-121_946-112del others(10): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr13 | 113503345 | ||||||
| chr13:113503345 | TTGTGTGT others(5): Show |
T | 2 | a0002c0003t0003g0245 a0002c0003t0003g0246 |
2 | HG00438.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.946-123_946-112del others(12): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr13 | 113503345 | ||||||
| chr13:113503346 | TGTGTGTG | T | 64 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(61): Show |
75 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.946-149_946-143del others(7): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 5/12 | chr13 | 113503346 | |||||||
| chr13:113503352 | T | A | 1 | a0003c0002t0002g0033 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.946-144T>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 5/12 | chr13 | 113503352 | |||||||
| chr13:113503353 | G | C | 1 | a0003c0002t0002g0033 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.946-143G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 5/12 | chr13 | 113503353 | |||||||
| chr13:113503354 | T | A | 64 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(61): Show |
75 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.946-142T>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 5/12 | chr13 | 113503354 | |||||||
| chr13:113503355 | G | C | 64 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(61): Show |
75 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.946-141G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 5/12 | chr13 | 113503355 | |||||||
| chr13:113503409 | G | A | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.946-87G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 5/12 | chr13 | 113503409 | |||||||
| chr13:113503637 | G | T | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1038+49G>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113503637 | |||||||
| chr13:113503763 | G | T | 17 | a0001c0005t0001g0108 a0001c0005t0001g0109 a0001c0005t0001g0110 others(14): Show |
17 | HG00733.hp1 HG01099.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.1038+175G>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113503763 | |||||||
| chr13:113503779 | A | T | 18 | a0002c0004t0005g0286 a0002c0004t0005g0287 a0002c0004t0005g0289 others(15): Show |
19 | HG00099.hp2 HG01123.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.1038+191A>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113503779 | |||||||
| chr13:113504015 | G | A | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1038+427G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113504015 | |||||||
| chr13:113504044 | A | G | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1038+456A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113504044 | |||||||
| chr13:113504187 | G | A | 1 | a0001c0001t0001g0087 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1038+599G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113504187 | |||||||
| chr13:113504212 | T | C | 1 | a0001c0001t0001g0129 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1038+624T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113504212 | |||||||
| chr13:113504299 | T | C | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1038+711T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113504299 | |||||||
| chr13:113504305 | T | C | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1038+717T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113504305 | |||||||
| chr13:113504386 | A | C | 23 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0006t0001g0027 others(20): Show |
24 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.1038+798A>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113504386 | |||||||
| chr13:113504391 | C | A | 86 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0006t0001g0027 others(83): Show |
98 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1038+803C>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113504391 | |||||||
| chr13:113504396 | G | T | 3 | a0001c0009t0004g0281 a0001c0009t0004g0282 a0001c0009t0004g0283 |
3 | HG02717.hp1 HG03516.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1038+808G>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113504396 | |||||||
| chr13:113504412 | C | T | 84 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(81): Show |
96 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.1038+824C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113504412 | |||||||
| chr13:113504513 | G | A | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1038+925G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113504513 | |||||||
| chr13:113504582 | C | T | 1 | a0003c0014t0004g0185 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1038+994C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113504582 | |||||||
| chr13:113504585 | C | T | 135 | a0001c0001t0001g0087 a0001c0001t0009g0303 a0001c0001t0009g0304 others(132): Show |
157 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.1038+997C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113504585 | |||||||
| chr13:113504661 | C | T | 67 | a0001c0005t0001g0176 a0003c0002t0002g0005 a0003c0002t0002g0008 others(64): Show |
78 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.1038+1073C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113504661 | |||||||
| chr13:113504767 | G | T | 1 | a0001c0001t0001g0285 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1038+1179G>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113504767 | |||||||
| chr13:113504809 | A | C | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1038+1221A>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113504809 | |||||||
| chr13:113504821 | C | T | 2 | a0001c0001t0001g0121 a0001c0001t0001g0163 |
2 | HG02523.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.1038+1233C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113504821 | |||||||
| chr13:113504993 | C | T | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1038+1405C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113504993 | |||||||
| chr13:113505082 | G | A | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1038+1494G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113505082 | |||||||
| chr13:113505089 | A | G | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1038+1501A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113505089 | |||||||
| chr13:113505160 | T | C | 21 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(18): Show |
22 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(19): Show |
intron_variant | MODIFIER | c.1038+1572T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113505160 | |||||||
| chr13:113505167 | C | T | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1038+1579C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113505167 | |||||||
| chr13:113505200 | A | G | 18 | a0002c0004t0005g0286 a0002c0004t0005g0287 a0002c0004t0005g0289 others(15): Show |
19 | HG00099.hp2 HG01123.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.1038+1612A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113505200 | |||||||
| chr13:113505285 | A | G | 1 | a0002c0003t0003g0240 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1038+1697A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113505285 | |||||||
| chr13:113505315 | T | A | 1 | a0001c0001t0001g0199 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1038+1727T>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113505315 | |||||||
| chr13:113505449 | A | G | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1038+1861A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113505449 | |||||||
| chr13:113505455 | C | T | 1 | a0001c0001t0001g0087 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1038+1867C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113505455 | |||||||
| chr13:113505474 | G | A | 69 | a0001c0009t0004g0281 a0001c0009t0004g0282 a0001c0009t0004g0283 others(66): Show |
80 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.1038+1886G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113505474 | |||||||
| chr13:113505482 | C | G | 87 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(84): Show |
99 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.1038+1894C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113505482 | |||||||
| chr13:113505495 | G | T | 1 | a0001c0001t0004g0102 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1038+1907G>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113505495 | |||||||
| chr13:113505497 | A | T | 2 | a0001c0001t0009g0303 a0001c0001t0009g0304 |
2 | HG00639.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1038+1909A>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113505497 | |||||||
| chr13:113505557 | T | C | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1038+1969T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113505557 | |||||||
| chr13:113505588 | G | A | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1038+2000G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113505588 | |||||||
| chr13:113505590 | G | A | 2 | a0001c0001t0009g0303 a0001c0001t0009g0304 |
2 | HG00639.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1038+2002G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113505590 | |||||||
| chr13:113505665 | G | C | 5 | a0003c0002t0002g0010 a0003c0002t0002g0034 a0003c0002t0002g0035 others(2): Show |
6 | HG01891.hp2 HG02451.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1038+2077G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113505665 | |||||||
| chr13:113505678 | A | G | 3 | a0001c0009t0004g0281 a0001c0009t0004g0282 a0001c0009t0004g0283 |
3 | HG02717.hp1 HG03516.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1038+2090A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113505678 | |||||||
| chr13:113505694 | A | G | 2 | a0001c0001t0001g0124 a0001c0001t0001g0125 |
2 | NA18975.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.1038+2106A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113505694 | |||||||
| chr13:113505836 | C | G | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1038+2248C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113505836 | |||||||
| chr13:113505941 | A | G | 2 | a0002c0003t0003g0270 a0002c0003t0003g0271 |
2 | NA18942.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.1038+2353A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113505941 | |||||||
| chr13:113505993 | C | T | 6 | a0001c0005t0001g0126 a0001c0005t0001g0174 a0001c0005t0001g0175 others(3): Show |
6 | HG02258.hp1 HG02280.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1038+2405C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113505993 | |||||||
| chr13:113506077 | T | G | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1038+2489T>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113506077 | |||||||
| chr13:113506088 | G | GTCA | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1038+2503_1038+250 others(7): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr13 | 113506088 | ||||||
| chr13:113506100 | G | A | 21 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(18): Show |
22 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(19): Show |
intron_variant | MODIFIER | c.1038+2512G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113506100 | |||||||
| chr13:113506124 | G | A | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1038+2536G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113506124 | |||||||
| chr13:113506153 | C | T | 4 | a0001c0001t0001g0006 a0001c0001t0001g0160 a0001c0001t0001g0161 others(1): Show |
7 | HG00099.hp1 HG00741.hp1 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.1038+2565C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113506153 | |||||||
| chr13:113506154 | G | GCGTGGCT others(58): Show |
1 | a0008c0018t0004g0085 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1038+2592_1038+259 others(69): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr13 | 113506154 | ||||||
| chr13:113506154 | GCGTGGCT others(59): Show |
G | 1 | a0002c0004t0005g0291 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1038+2603_1038+266 others(70): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr13 | 113506154 | ||||||
| chr13:113506158 | GGCTGCCT others(124): Show |
G | 45 | a0002c0003t0003g0002 a0002c0003t0003g0007 a0002c0003t0003g0029 others(42): Show |
54 | HG00408.hp1 HG00438.hp2 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.1038+2593_1038+272 others(4): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr13 | 113506158 | ||||||
| chr13:113506173 | G | A | 21 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(18): Show |
22 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(19): Show |
intron_variant | MODIFIER | c.1038+2585G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113506173 | |||||||
| chr13:113506179 | AG | A | 43 | a0001c0001t0001g0087 a0001c0001t0009g0303 a0001c0001t0009g0304 others(40): Show |
46 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.1038+2593delG | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr13 | 113506179 | ||||||
| chr13:113506179 | AGGAGCCT others(60): Show |
A | 1 | a0002c0004t0004g0305 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1038+2593_1038+265 others(71): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr13 | 113506179 | ||||||
| chr13:113506184 | CCTGTTAC others(187): Show |
C | 65 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(62): Show |
76 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.1038+2603_1038+279 others(4): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr13 | 113506184 | ||||||
| chr13:113506191 | C | T | 45 | a0001c0001t0001g0087 a0001c0001t0009g0303 a0001c0001t0009g0304 others(42): Show |
48 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.1038+2603C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113506191 | |||||||
| chr13:113506191 | CGGGTGGG others(59): Show |
C | 2 | a0001c0001t0004g0096 a0001c0001t0004g0101 |
2 | HG01993.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.1038+2624_1038+268 others(70): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr13 | 113506191 | ||||||
| chr13:113506210 | G | A | 17 | a0002c0004t0005g0286 a0002c0004t0005g0287 a0002c0004t0005g0289 others(14): Show |
18 | HG00099.hp2 HG01123.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.1038+2622G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113506210 | |||||||
| chr13:113506212 | C | A | 1 | a0003c0016t0002g0074 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1038+2624C>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113506212 | |||||||
| chr13:113506220 | A | G | 18 | a0002c0004t0005g0286 a0002c0004t0005g0287 a0002c0004t0005g0289 others(15): Show |
19 | HG00099.hp2 HG01123.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.1038+2632A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113506220 | |||||||
| chr13:113506250 | C | CCTGTTAT others(57): Show |
2 | a0001c0001t0001g0142 a0001c0001t0001g0154 |
2 | NA18983.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.1038+2690_1038+275 others(68): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr13 | 113506250 | ||||||
| chr13:113506250 | CCTGTTAT others(121): Show |
C | 1 | a0003c0016t0002g0074 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1038+2703_1038+283 others(4): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr13 | 113506250 | ||||||
| chr13:113506289 | T | TG | 21 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(18): Show |
22 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(19): Show |
intron_variant | MODIFIER | c.1038+2702dupG | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr13 | 113506289 | ||||||
| chr13:113506313 | GGCTGTTA others(57): Show |
G | 1 | a0001c0001t0001g0129 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1038+2754_1038+281 others(68): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr13 | 113506313 | ||||||
| chr13:113506350 | AGTGGCTG others(58): Show |
A | 1 | a0001c0001t0001g0152 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1038+2786_1038+285 others(69): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr13 | 113506350 | ||||||
| chr13:113506417 | TG | T | 65 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(62): Show |
76 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.1038+2831delG | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr13 | 113506417 | ||||||
| chr13:113506529 | C | T | 2 | a0003c0002t0002g0277 a0003c0002t0002g0278 |
2 | NA19060.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1038+2941C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113506529 | |||||||
| chr13:113506554 | TGTGA | T | 57 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(54): Show |
68 | HG00423.hp1 HG00423.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.1038+2970_1038+297 others(8): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr13 | 113506554 | ||||||
| chr13:113506556 | TGA | T | 7 | a0003c0002t0002g0036 a0003c0002t0002g0050 a0003c0002t0002g0051 others(4): Show |
7 | HG00597.hp2 HG02572.hp2 HG04228.hp2 others(4): Show |
intron_variant | MODIFIER | c.1038+2970_1038+297 others(6): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr13 | 113506556 | ||||||
| chr13:113506558 | A | AGT | 50 | a0001c0001t0001g0001 a0001c0001t0001g0127 a0001c0001t0001g0128 others(47): Show |
59 | HG00408.hp1 HG00438.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.1038+2991_1038+299 others(6): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr13 | 113506558 | ||||||
| chr13:113506558 | A | AGTGT | 3 | a0002c0003t0003g0002 a0002c0004t0005g0290 a0002c0004t0005g0291 |
3 | HG01981.hp1 HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1038+2989_1038+299 others(8): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr13 | 113506558 | ||||||
| chr13:113506558 | A | AGTGTGTG others(1): Show |
3 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0222 |
3 | HG00673.hp1 NA18943.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1038+2985_1038+299 others(12): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr13 | 113506558 | ||||||
| chr13:113506558 | A | AGTGTGTG others(5): Show |
18 | a0001c0006t0001g0027 a0001c0006t0001g0218 a0001c0006t0001g0219 others(15): Show |
18 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(15): Show |
intron_variant | MODIFIER | c.1038+2981_1038+299 others(16): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr13 | 113506558 | ||||||
| chr13:113506558 | A | AGTGTGTG others(7): Show |
1 | a0001c0006t0001g0224 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1038+2979_1038+299 others(18): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr13 | 113506558 | ||||||
| chr13:113506595 | T | C | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1038+3007T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113506595 | |||||||
| chr13:113506597 | C | T | 16 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(13): Show |
17 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(14): Show |
intron_variant | MODIFIER | c.1038+3009C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113506597 | |||||||
| chr13:113506623 | C | T | 21 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(18): Show |
22 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(19): Show |
intron_variant | MODIFIER | c.1038+3035C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113506623 | |||||||
| chr13:113506668 | G | A | 1 | a0003c0002t0002g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1038+3080G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113506668 | |||||||
| chr13:113506713 | C | T | 21 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(18): Show |
22 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(19): Show |
intron_variant | MODIFIER | c.1038+3125C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113506713 | |||||||
| chr13:113506779 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1038+3191A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113506779 | |||||||
| chr13:113506847 | G | A | 1 | a0003c0002t0002g0038 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1038+3259G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113506847 | |||||||
| chr13:113506854 | T | C | 156 | a0001c0001t0001g0087 a0001c0001t0009g0303 a0001c0001t0009g0304 others(153): Show |
179 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.1038+3266T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113506854 | |||||||
| chr13:113506893 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1038+3305G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113506893 | |||||||
| chr13:113506939 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1039-3299C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113506939 | |||||||
| chr13:113506947 | T | C | 87 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(84): Show |
99 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.1039-3291T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113506947 | |||||||
| chr13:113506997 | G | A | 46 | a0002c0003t0003g0002 a0002c0003t0003g0007 a0002c0003t0003g0029 others(43): Show |
55 | HG00408.hp1 HG00438.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.1039-3241G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113506997 | |||||||
| chr13:113507067 | T | C | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1039-3171T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113507067 | |||||||
| chr13:113507149 | G | A | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1039-3089G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113507149 | |||||||
| chr13:113507150 | G | A | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1039-3088G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113507150 | |||||||
| chr13:113507208 | G | A | 21 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(18): Show |
22 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(19): Show |
intron_variant | MODIFIER | c.1039-3030G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113507208 | |||||||
| chr13:113507250 | G | GT | 44 | a0002c0003t0003g0002 a0002c0003t0003g0007 a0002c0003t0003g0029 others(41): Show |
53 | HG00408.hp1 HG00438.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1039-2983dupT | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr13 | 113507250 | ||||||
| chr13:113507360 | G | A | 1 | a0003c0002t0002g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1039-2878G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113507360 | |||||||
| chr13:113507504 | G | A | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1039-2734G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113507504 | |||||||
| chr13:113507544 | T | G | 21 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(18): Show |
22 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(19): Show |
intron_variant | MODIFIER | c.1039-2694T>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113507544 | |||||||
| chr13:113507560 | C | T | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1039-2678C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113507560 | |||||||
| chr13:113507645 | A | C | 1 | a0001c0001t0001g0120 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1039-2593A>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113507645 | |||||||
| chr13:113507718 | T | C | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1039-2520T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113507718 | |||||||
| chr13:113507732 | G | A | 2 | a0001c0001t0001g0189 a0002c0003t0003g0247 |
2 | HG00140.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.1039-2506G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113507732 | |||||||
| chr13:113507839 | G | A | 18 | a0002c0004t0005g0286 a0002c0004t0005g0287 a0002c0004t0005g0289 others(15): Show |
19 | HG00099.hp2 HG01123.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.1039-2399G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113507839 | |||||||
| chr13:113507855 | C | T | 2 | a0001c0001t0009g0303 a0001c0001t0009g0304 |
2 | HG00639.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1039-2383C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113507855 | |||||||
| chr13:113507968 | G | C | 87 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(84): Show |
99 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.1039-2270G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113507968 | |||||||
| chr13:113507995 | A | G | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1039-2243A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113507995 | |||||||
| chr13:113508018 | C | G | 3 | a0001c0001t0001g0087 a0002c0004t0004g0017 a0002c0004t0004g0086 |
4 | HG02145.hp1 HG02559.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1039-2220C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113508018 | |||||||
| chr13:113508025 | G | A | 1 | a0002c0004t0004g0305 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1039-2213G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113508025 | |||||||
| chr13:113508032 | G | A | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1039-2206G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113508032 | |||||||
| chr13:113508034 | G | A | 1 | a0003c0002t0002g0030 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1039-2204G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113508034 | |||||||
| chr13:113508088 | C | T | 2 | a0001c0001t0001g0088 a0001c0001t0001g0158 |
2 | HG00140.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1039-2150C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113508088 | |||||||
| chr13:113508117 | T | G | 156 | a0001c0001t0001g0087 a0001c0001t0009g0303 a0001c0001t0009g0304 others(153): Show |
179 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.1039-2121T>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113508117 | |||||||
| chr13:113508169 | A | G | 4 | a0001c0007t0006g0090 a0001c0007t0006g0091 a0001c0007t0006g0092 others(1): Show |
4 | HG02280.hp1 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1039-2069A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113508169 | |||||||
| chr13:113508257 | C | T | 2 | a0005c0011t0008g0306 a0005c0011t0008g0307 |
2 | HG02027.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.1039-1981C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113508257 | |||||||
| chr13:113508258 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1039-1980C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113508258 | |||||||
| chr13:113508264 | C | T | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1039-1974C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113508264 | |||||||
| chr13:113508279 | T | C | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1039-1959T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113508279 | |||||||
| chr13:113508320 | G | A | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1039-1918G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113508320 | |||||||
| chr13:113508407 | A | G | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1039-1831A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113508407 | |||||||
| chr13:113508411 | C | T | 3 | a0002c0004t0005g0286 a0002c0004t0005g0287 a0002c0004t0005g0289 |
3 | HG02572.hp1 HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1039-1827C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113508411 | |||||||
| chr13:113508487 | A | G | 179 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0285 others(176): Show |
203 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.1039-1751A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113508487 | |||||||
| chr13:113508526 | G | A | 2 | a0001c0001t0009g0303 a0001c0001t0009g0304 |
2 | HG00639.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1039-1712G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113508526 | |||||||
| chr13:113508565 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1039-1673G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113508565 | |||||||
| chr13:113508624 | A | T | 21 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(18): Show |
22 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(19): Show |
intron_variant | MODIFIER | c.1039-1614A>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113508624 | |||||||
| chr13:113508642 | T | G | 21 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(18): Show |
22 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(19): Show |
intron_variant | MODIFIER | c.1039-1596T>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113508642 | |||||||
| chr13:113508683 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1039-1555G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113508683 | |||||||
| chr13:113508683 | G | C | 1 | a0003c0002t0002g0034 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1039-1555G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113508683 | |||||||
| chr13:113508915 | G | A | 1 | a0001c0001t0001g0285 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1039-1323G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113508915 | |||||||
| chr13:113508998 | C | T | 1 | a0003c0002t0002g0066 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1039-1240C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113508998 | |||||||
| chr13:113509018 | G | A | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1039-1220G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113509018 | |||||||
| chr13:113509026 | C | T | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1039-1212C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113509026 | |||||||
| chr13:113509041 | A | G | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1039-1197A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113509041 | |||||||
| chr13:113509042 | C | CGCTGCCT others(45): Show |
66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1039-1196_1039-119 others(56): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113509042 | |||||||
| chr13:113509043 | A | G | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1039-1195A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113509043 | |||||||
| chr13:113509062 | G | A | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1039-1176G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113509062 | |||||||
| chr13:113509067 | T | C | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1039-1171T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113509067 | |||||||
| chr13:113509097 | C | T | 1 | a0001c0001t0013g0084 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1039-1141C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113509097 | |||||||
| chr13:113509115 | G | A | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1039-1123G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113509115 | |||||||
| chr13:113509148 | G | T | 1 | a0001c0001t0004g0101 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1039-1090G>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113509148 | |||||||
| chr13:113509188 | C | CCCTGGCG others(243): Show |
66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1039-1048_1039-104 others(254): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr13 | 113509188 | ||||||
| chr13:113509206 | G | C | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1039-1032G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113509206 | |||||||
| chr13:113509247 | C | CGCTGCCT others(91): Show |
66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1039-982_1039-981i others(100): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr13 | 113509247 | ||||||
| chr13:113509257 | C | T | 2 | a0005c0011t0008g0306 a0005c0011t0008g0307 |
2 | HG02027.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.1039-981C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113509257 | |||||||
| chr13:113509268 | C | T | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1039-970C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113509268 | |||||||
| chr13:113509273 | GGGCTTGG others(40): Show |
G | 1 | a0002c0004t0005g0289 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1039-935_1039-889d others(49): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr13 | 113509273 | ||||||
| chr13:113509303 | T | G | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1039-935T>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113509303 | |||||||
| chr13:113509312 | A | G | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1039-926A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113509312 | |||||||
| chr13:113509367 | T | C | 87 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(84): Show |
99 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.1039-871T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113509367 | |||||||
| chr13:113509387 | T | C | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1039-851T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113509387 | |||||||
| chr13:113509400 | G | GTGTATGT others(43): Show |
61 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0011 others(58): Show |
71 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.1039-837_1039-836i others(52): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr13 | 113509400 | ||||||
| chr13:113509400 | G | GTGTATGT others(94): Show |
5 | a0003c0002t0002g0010 a0003c0002t0002g0034 a0003c0002t0002g0035 others(2): Show |
6 | HG01891.hp2 HG02451.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1039-837_1039-836i others(103): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr13 | 113509400 | ||||||
| chr13:113509402 | C | G | 5 | a0003c0002t0002g0010 a0003c0002t0002g0034 a0003c0002t0002g0035 others(2): Show |
6 | HG01891.hp2 HG02451.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1039-836C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113509402 | |||||||
| chr13:113509404 | A | G | 13 | a0002c0004t0005g0292 a0002c0004t0005g0293 a0002c0004t0005g0294 others(10): Show |
14 | HG00099.hp2 HG01123.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1039-834A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113509404 | |||||||
| chr13:113509406 | G | A | 3 | a0001c0006t0001g0227 a0001c0006t0001g0235 a0001c0006t0001g0236 |
3 | HG00280.hp1 HG02293.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1039-832G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113509406 | |||||||
| chr13:113509426 | T | C | 67 | a0001c0006t0001g0218 a0003c0002t0002g0005 a0003c0002t0002g0008 others(64): Show |
78 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.1039-812T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113509426 | |||||||
| chr13:113509433 | GT | G | 67 | a0001c0006t0001g0218 a0003c0002t0002g0005 a0003c0002t0002g0008 others(64): Show |
78 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.1039-804delT | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113509433 | |||||||
| chr13:113509450 | C | CTATG | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1039-786_1039-783d others(6): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr13 | 113509450 | ||||||
| chr13:113509450 | C | CTATGTTG others(44): Show |
17 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0219 others(14): Show |
18 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(15): Show |
intron_variant | MODIFIER | c.1039-773_1039-772i others(53): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr13 | 113509450 | ||||||
| chr13:113509476 | G | A | 1 | a0003c0002t0002g0040 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1039-762G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113509476 | |||||||
| chr13:113509494 | C | T | 3 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0215 |
3 | HG01167.hp1 HG02738.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1039-744C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113509494 | |||||||
| chr13:113509520 | C | A | 2 | a0001c0001t0009g0303 a0001c0001t0009g0304 |
2 | HG00639.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1039-718C>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113509520 | |||||||
| chr13:113509530 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1039-708G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113509530 | |||||||
| chr13:113509533 | A | G | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1039-705A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113509533 | |||||||
| chr13:113509537 | A | G | 1 | a0002c0003t0003g0269 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1039-701A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113509537 | |||||||
| chr13:113509544 | G | A | 16 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(13): Show |
17 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(14): Show |
intron_variant | MODIFIER | c.1039-694G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113509544 | |||||||
| chr13:113509548 | C | T | 1 | a0002c0003t0003g0029 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1039-690C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113509548 | |||||||
| chr13:113509671 | C | T | 67 | a0002c0003t0003g0029 a0003c0002t0002g0005 a0003c0002t0002g0008 others(64): Show |
78 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.1039-567C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113509671 | |||||||
| chr13:113509683 | G | A | 1 | a0011c0017t0001g0284 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1039-555G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113509683 | |||||||
| chr13:113509712 | G | A | 1 | a0001c0001t0001g0200 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1039-526G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113509712 | |||||||
| chr13:113509716 | C | T | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1039-522C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113509716 | |||||||
| chr13:113509735 | C | T | 21 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(18): Show |
22 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(19): Show |
intron_variant | MODIFIER | c.1039-503C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113509735 | |||||||
| chr13:113509765 | G | A | 64 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(61): Show |
75 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.1039-473G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113509765 | |||||||
| chr13:113509784 | C | T | 47 | a0001c0001t0001g0087 a0002c0003t0003g0002 a0002c0003t0003g0007 others(44): Show |
57 | HG00408.hp1 HG00438.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.1039-454C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113509784 | |||||||
| chr13:113509885 | C | T | 21 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(18): Show |
22 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(19): Show |
intron_variant | MODIFIER | c.1039-353C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113509885 | |||||||
| chr13:113509937 | T | C | 1 | a0001c0001t0001g0165 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1039-301T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113509937 | |||||||
| chr13:113509962 | A | G | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1039-276A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113509962 | |||||||
| chr13:113510065 | C | T | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1039-173C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113510065 | |||||||
| chr13:113510086 | G | C | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1039-152G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113510086 | |||||||
| chr13:113510095 | A | G | 87 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(84): Show |
99 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.1039-143A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113510095 | |||||||
| chr13:113510116 | C | T | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1039-122C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113510116 | |||||||
| chr13:113510211 | T | C | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1039-27T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 6/12 | chr13 | 113510211 | |||||||
| chr13:113510496 | G | A | 4 | a0001c0005t0001g0230 a0001c0005t0001g0231 a0001c0005t0001g0232 others(1): Show |
4 | HG01099.hp2 HG01257.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.1225+72G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113510496 | |||||||
| chr13:113510528 | T | C | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1225+104T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113510528 | |||||||
| chr13:113510597 | C | T | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1225+173C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113510597 | |||||||
| chr13:113510619 | C | A | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1225+195C>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113510619 | |||||||
| chr13:113510769 | T | C | 1 | a0001c0001t0001g0178 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1225+345T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113510769 | |||||||
| chr13:113510791 | A | C | 1 | a0010c0015t0002g0070 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1225+367A>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113510791 | |||||||
| chr13:113510886 | G | C | 21 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(18): Show |
22 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(19): Show |
intron_variant | MODIFIER | c.1225+462G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113510886 | |||||||
| chr13:113510906 | C | A | 2 | a0001c0001t0004g0094 a0001c0001t0004g0095 |
2 | HG00558.hp1 HG00597.hp1 |
intron_variant | MODIFIER | c.1225+482C>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113510906 | |||||||
| chr13:113510935 | C | T | 87 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(84): Show |
99 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.1225+511C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113510935 | |||||||
| chr13:113510945 | G | A | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1225+521G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113510945 | |||||||
| chr13:113510951 | T | C | 16 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(13): Show |
17 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(14): Show |
intron_variant | MODIFIER | c.1225+527T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113510951 | |||||||
| chr13:113510970 | CTGCGGGG others(51): Show |
C | 1 | a0001c0001t0004g0100 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1225+573_1225+630d others(60): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr13 | 113510970 | ||||||
| chr13:113510974 | G | A | 2 | a0002c0003t0003g0241 a0002c0003t0003g0264 |
2 | HG00408.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.1225+550G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113510974 | |||||||
| chr13:113510997 | C | T | 87 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(84): Show |
99 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.1225+573C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113510997 | |||||||
| chr13:113510998 | A | G | 87 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(84): Show |
99 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.1225+574A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113510998 | |||||||
| chr13:113511003 | GA | G | 87 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(84): Show |
99 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.1225+581delA | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr13 | 113511003 | ||||||
| chr13:113511004 | AAGCCTAG others(50): Show |
A | 2 | a0001c0001t0009g0303 a0001c0001t0009g0304 |
2 | HG00639.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1225+631_1225+687d others(59): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr13 | 113511004 | ||||||
| chr13:113511055 | T | C | 87 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(84): Show |
99 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.1225+631T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113511055 | |||||||
| chr13:113511056 | G | A | 87 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(84): Show |
99 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.1225+632G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113511056 | |||||||
| chr13:113511061 | G | GA | 87 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(84): Show |
99 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.1225+638dupA | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr13 | 113511061 | ||||||
| chr13:113511063 | G | A | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1225+639G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113511063 | |||||||
| chr13:113511097 | C | G | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1225+673C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113511097 | |||||||
| chr13:113511116 | C | CGGAAACC others(109): Show |
13 | a0003c0002t0002g0005 a0003c0002t0002g0011 a0003c0002t0002g0012 others(10): Show |
19 | HG01070.hp2 HG01081.hp1 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.1225+729_1225+730i others(118): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr13 | 113511116 | ||||||
| chr13:113511116 | C | CGGAAACC others(109): Show |
52 | a0003c0002t0002g0008 a0003c0002t0002g0010 a0003c0002t0002g0013 others(49): Show |
57 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.1225+729_1225+730i others(118): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr13 | 113511116 | ||||||
| chr13:113511116 | C | CGGAAACC others(109): Show |
1 | a0003c0002t0002g0064 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1225+709_1225+710i others(118): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr13 | 113511116 | ||||||
| chr13:113511122 | CCT | C | 3 | a0002c0004t0005g0286 a0002c0004t0005g0287 a0002c0004t0005g0289 |
3 | HG02572.hp1 HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1225+699_1225+700d others(4): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113511122 | |||||||
| chr13:113511175 | A | G | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1225+751A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113511175 | |||||||
| chr13:113511242 | C | T | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1225+818C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113511242 | |||||||
| chr13:113511253 | T | C | 3 | a0001c0001t0001g0087 a0002c0004t0004g0017 a0002c0004t0004g0086 |
4 | HG02145.hp1 HG02559.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1225+829T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113511253 | |||||||
| chr13:113511384 | T | C | 1 | a0002c0004t0007g0288 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1225+960T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113511384 | |||||||
| chr13:113511448 | T | C | 67 | a0001c0001t0013g0084 a0003c0002t0002g0005 a0003c0002t0002g0008 others(64): Show |
78 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.1225+1024T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113511448 | |||||||
| chr13:113511516 | A | T | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1225+1092A>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113511516 | |||||||
| chr13:113511543 | G | C | 1 | a0001c0001t0001g0088 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1225+1119G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113511543 | |||||||
| chr13:113511548 | G | A | 2 | a0001c0001t0001g0107 a0001c0001t0001g0130 |
2 | HG02698.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1225+1124G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113511548 | |||||||
| chr13:113511599 | C | T | 2 | a0001c0001t0009g0303 a0001c0001t0009g0304 |
2 | HG00639.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1225+1175C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113511599 | |||||||
| chr13:113511755 | A | G | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1225+1331A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113511755 | |||||||
| chr13:113511774 | G | A | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1225+1350G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113511774 | |||||||
| chr13:113511820 | C | T | 16 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(13): Show |
17 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(14): Show |
intron_variant | MODIFIER | c.1225+1396C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113511820 | |||||||
| chr13:113511838 | C | T | 2 | a0001c0001t0009g0303 a0001c0001t0009g0304 |
2 | HG00639.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1225+1414C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113511838 | |||||||
| chr13:113511839 | G | A | 1 | a0001c0005t0001g0172 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1225+1415G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113511839 | |||||||
| chr13:113511839 | G | C | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1225+1415G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113511839 | |||||||
| chr13:113511908 | G | A | 1 | a0001c0001t0004g0100 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1225+1484G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113511908 | |||||||
| chr13:113511932 | C | G | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1225+1508C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113511932 | |||||||
| chr13:113511933 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1225+1509G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113511933 | |||||||
| chr13:113511939 | A | G | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1225+1515A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113511939 | |||||||
| chr13:113511941 | G | A | 67 | a0001c0001t0013g0084 a0003c0002t0002g0005 a0003c0002t0002g0008 others(64): Show |
78 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.1225+1517G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113511941 | |||||||
| chr13:113511943 | A | G | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1225+1519A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113511943 | |||||||
| chr13:113511959 | G | A | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1225+1535G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113511959 | |||||||
| chr13:113511961 | C | G | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1225+1537C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113511961 | |||||||
| chr13:113511962 | A | G | 2 | a0001c0001t0009g0303 a0001c0001t0009g0304 |
2 | HG00639.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1225+1538A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113511962 | |||||||
| chr13:113511969 | C | T | 67 | a0001c0005t0001g0233 a0003c0002t0002g0005 a0003c0002t0002g0008 others(64): Show |
78 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.1225+1545C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113511969 | |||||||
| chr13:113511970 | G | A | 2 | a0001c0001t0004g0096 a0001c0001t0004g0101 |
2 | HG01993.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.1225+1546G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113511970 | |||||||
| chr13:113511972 | A | G | 2 | a0001c0001t0001g0088 a0001c0001t0013g0084 |
2 | HG02109.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1225+1548A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113511972 | |||||||
| chr13:113512034 | G | C | 68 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(65): Show |
79 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.1225+1610G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113512034 | |||||||
| chr13:113512041 | T | C | 68 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(65): Show |
79 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.1225+1617T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113512041 | |||||||
| chr13:113512042 | T | C | 68 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(65): Show |
79 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.1225+1618T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113512042 | |||||||
| chr13:113512045 | AGTGTAGA others(68): Show |
A | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1225+1650_1225+172 others(79): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr13 | 113512045 | ||||||
| chr13:113512080 | T | TGGAGTCT others(214): Show |
1 | a0001c0001t0001g0191 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1225+1724_1225+194 others(225): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr13 | 113512080 | ||||||
| chr13:113512161 | C | T | 67 | a0001c0001t0001g0087 a0002c0003t0003g0002 a0002c0003t0003g0007 others(64): Show |
78 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.1225+1737C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113512161 | |||||||
| chr13:113512182 | C | G | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1225+1758C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113512182 | |||||||
| chr13:113512189 | C | T | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1225+1765C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113512189 | |||||||
| chr13:113512190 | C | T | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1225+1766C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113512190 | |||||||
| chr13:113512213 | G | GTA | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1225+1796_1225+179 others(6): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr13 | 113512213 | ||||||
| chr13:113512222 | C | T | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1225+1798C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113512222 | |||||||
| chr13:113512226 | C | T | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1225+1802C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113512226 | |||||||
| chr13:113512233 | G | T | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1225+1809G>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113512233 | |||||||
| chr13:113512235 | G | A | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1225+1811G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113512235 | |||||||
| chr13:113512241 | C | T | 3 | a0001c0009t0004g0281 a0001c0009t0004g0282 a0001c0009t0004g0283 |
3 | HG02717.hp1 HG03516.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1225+1817C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113512241 | |||||||
| chr13:113512266 | A | T | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1225+1842A>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113512266 | |||||||
| chr13:113512286 | GTA | G | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1225+1871_1225+187 others(6): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr13 | 113512286 | ||||||
| chr13:113512308 | T | G | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1225+1884T>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113512308 | |||||||
| chr13:113512310 | A | G | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1225+1886A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113512310 | |||||||
| chr13:113512341 | T | A | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1225+1917T>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113512341 | |||||||
| chr13:113512461 | C | T | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1225+2037C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113512461 | |||||||
| chr13:113512553 | A | G | 1 | a0001c0001t0004g0100 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1225+2129A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113512553 | |||||||
| chr13:113512603 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1225+2179C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113512603 | |||||||
| chr13:113512606 | A | G | 1 | a0001c0001t0009g0304 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1225+2182A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113512606 | |||||||
| chr13:113512617 | A | G | 2 | a0005c0011t0008g0306 a0005c0011t0008g0307 |
2 | HG02027.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.1225+2193A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113512617 | |||||||
| chr13:113512657 | G | T | 2 | a0001c0001t0001g0199 a0001c0001t0001g0204 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1225+2233G>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113512657 | |||||||
| chr13:113512729 | GGAGTGTA others(61): Show |
G | 55 | a0002c0003t0003g0002 a0002c0003t0003g0007 a0002c0003t0003g0029 others(52): Show |
64 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.1225+2322_1225+238 others(72): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr13 | 113512729 | ||||||
| chr13:113512746 | A | AGTCAGTA others(61): Show |
66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1225+2350_1225+235 others(72): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr13 | 113512746 | ||||||
| chr13:113512872 | A | G | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1225+2448A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113512872 | |||||||
| chr13:113512940 | A | T | 1 | a0001c0001t0001g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1225+2516A>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113512940 | |||||||
| chr13:113512998 | G | A | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1225+2574G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113512998 | |||||||
| chr13:113513003 | C | A | 1 | a0003c0002t0002g0068 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1225+2579C>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113513003 | |||||||
| chr13:113513099 | C | T | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1225+2675C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113513099 | |||||||
| chr13:113513154 | G | A | 1 | a0003c0002t0002g0072 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1225+2730G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113513154 | |||||||
| chr13:113513178 | G | C | 1 | a0003c0002t0002g0010 | 2 | HG01891.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1225+2754G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113513178 | |||||||
| chr13:113513234 | T | C | 1 | a0001c0001t0004g0102 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1225+2810T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113513234 | |||||||
| chr13:113513295 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1225+2871G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113513295 | |||||||
| chr13:113513312 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1225+2888C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113513312 | |||||||
| chr13:113513392 | CAG | C | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1225+2971_1225+297 others(6): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr13 | 113513392 | ||||||
| chr13:113513400 | G | T | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1225+2976G>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113513400 | |||||||
| chr13:113513414 | C | A | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1225+2990C>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113513414 | |||||||
| chr13:113513446 | A | G | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1225+3022A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113513446 | |||||||
| chr13:113513656 | G | A | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1225+3232G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113513656 | |||||||
| chr13:113513889 | C | A | 1 | a0001c0001t0001g0201 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1225+3465C>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113513889 | |||||||
| chr13:113513948 | C | T | 3 | a0001c0006t0001g0227 a0001c0006t0001g0235 a0001c0006t0001g0236 |
3 | HG00280.hp1 HG02293.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1225+3524C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113513948 | |||||||
| chr13:113513956 | C | G | 1 | a0001c0001t0001g0198 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1225+3532C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113513956 | |||||||
| chr13:113514132 | C | T | 55 | a0002c0003t0003g0002 a0002c0003t0003g0007 a0002c0003t0003g0029 others(52): Show |
64 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.1225+3708C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113514132 | |||||||
| chr13:113514162 | A | G | 21 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(18): Show |
22 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(19): Show |
intron_variant | MODIFIER | c.1225+3738A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113514162 | |||||||
| chr13:113514170 | T | C | 2 | a0001c0001t0001g0088 a0001c0001t0013g0084 |
2 | HG02109.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1225+3746T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113514170 | |||||||
| chr13:113514237 | T | TC | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1225+3813_1225+381 others(5): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113514237 | |||||||
| chr13:113514299 | C | T | 1 | a0002c0003t0003g0029 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1225+3875C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113514299 | |||||||
| chr13:113514331 | G | T | 1 | a0001c0001t0001g0163 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1225+3907G>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113514331 | |||||||
| chr13:113514427 | AAGGAAGA others(211): Show |
A | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1225+4072_1225+428 others(4): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr13 | 113514427 | ||||||
| chr13:113514454 | CGGGGTGC others(102): Show |
C | 22 | a0001c0001t0001g0201 a0001c0006t0001g0027 a0001c0006t0001g0217 others(19): Show |
23 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(20): Show |
intron_variant | MODIFIER | c.1225+4139_1225+424 others(4): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr13 | 113514454 | ||||||
| chr13:113514702 | C | T | 1 | a0002c0004t0004g0305 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1225+4278C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113514702 | |||||||
| chr13:113514804 | C | A | 2 | a0001c0001t0001g0132 a0001c0001t0001g0133 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1225+4380C>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113514804 | |||||||
| chr13:113514874 | G | T | 2 | a0005c0011t0008g0306 a0005c0011t0008g0307 |
2 | HG02027.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.1225+4450G>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113514874 | |||||||
| chr13:113515072 | T | C | 3 | a0001c0009t0004g0281 a0001c0009t0004g0282 a0001c0009t0004g0283 |
3 | HG02717.hp1 HG03516.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1225+4648T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113515072 | |||||||
| chr13:113515254 | G | C | 84 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(81): Show |
100 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.1225+4830G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113515254 | |||||||
| chr13:113515298 | A | G | 1 | a0001c0001t0001g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1225+4874A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113515298 | |||||||
| chr13:113515432 | C | T | 11 | a0003c0002t0002g0057 a0003c0002t0002g0058 a0003c0002t0002g0059 others(8): Show |
11 | HG00597.hp2 NA18953.hp1 NA18955.hp1 others(8): Show |
intron_variant | MODIFIER | c.1225+5008C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113515432 | |||||||
| chr13:113515435 | G | A | 1 | a0001c0001t0001g0134 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1225+5011G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113515435 | |||||||
| chr13:113515611 | G | C | 21 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(18): Show |
22 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(19): Show |
intron_variant | MODIFIER | c.1226-5005G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113515611 | |||||||
| chr13:113515618 | A | G | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1226-4998A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113515618 | |||||||
| chr13:113515666 | C | T | 16 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(13): Show |
17 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(14): Show |
intron_variant | MODIFIER | c.1226-4950C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113515666 | |||||||
| chr13:113515741 | A | G | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1226-4875A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113515741 | |||||||
| chr13:113515747 | C | T | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1226-4869C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113515747 | |||||||
| chr13:113515775 | C | T | 1 | a0002c0004t0004g0305 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1226-4841C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113515775 | |||||||
| chr13:113515839 | C | T | 4 | a0001c0007t0006g0090 a0001c0007t0006g0091 a0001c0007t0006g0092 others(1): Show |
4 | HG02280.hp1 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1226-4777C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113515839 | |||||||
| chr13:113515890 | C | CA | 24 | a0001c0001t0001g0009 a0001c0001t0001g0088 a0001c0001t0001g0111 others(21): Show |
26 | HG00609.hp2 HG00735.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.1226-4702dupA | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr13 | 113515890 | ||||||
| chr13:113515890 | CA | C | 122 | a0001c0001t0001g0087 a0001c0001t0001g0134 a0001c0001t0001g0205 others(119): Show |
143 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.1226-4702delA | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr13 | 113515890 | ||||||
| chr13:113515996 | G | A | 48 | a0001c0001t0001g0087 a0002c0003t0003g0002 a0002c0003t0003g0007 others(45): Show |
58 | HG00408.hp1 HG00438.hp2 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.1226-4620G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113515996 | |||||||
| chr13:113516173 | A | G | 2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | NA18963.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.1226-4443A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113516173 | |||||||
| chr13:113516497 | C | T | 1 | a0002c0004t0004g0305 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1226-4119C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113516497 | |||||||
| chr13:113516563 | CT | C | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1226-4052delT | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113516563 | |||||||
| chr13:113516565 | CA | C | 5 | a0001c0001t0001g0133 a0002c0003t0003g0250 a0002c0003t0003g0267 others(2): Show |
6 | HG01168.hp1 HG02559.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1226-4037delA | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr13 | 113516565 | ||||||
| chr13:113516566 | A | C | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1226-4050A>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113516566 | |||||||
| chr13:113516578 | A | G | 1 | a0002c0004t0004g0305 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1226-4038A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113516578 | |||||||
| chr13:113516579 | AG | A | 63 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0002c0003t0003g0002 others(60): Show |
73 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.1226-4036delG | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113516579 | |||||||
| chr13:113516580 | G | A | 23 | a0001c0001t0001g0087 a0001c0006t0001g0027 a0001c0006t0001g0217 others(20): Show |
24 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.1226-4036G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113516580 | |||||||
| chr13:113516626 | T | C | 3 | a0001c0001t0001g0087 a0002c0004t0004g0017 a0002c0004t0004g0086 |
4 | HG02145.hp1 HG02559.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1226-3990T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113516626 | |||||||
| chr13:113516755 | A | G | 2 | a0005c0011t0008g0306 a0005c0011t0008g0307 |
2 | HG02027.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.1226-3861A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113516755 | |||||||
| chr13:113517035 | C | T | 3 | a0001c0007t0006g0090 a0001c0007t0006g0091 a0001c0007t0006g0092 |
3 | HG02922.hp2 HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1226-3581C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113517035 | |||||||
| chr13:113517109 | C | T | 21 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(18): Show |
22 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(19): Show |
intron_variant | MODIFIER | c.1226-3507C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113517109 | |||||||
| chr13:113517282 | G | A | 16 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(13): Show |
17 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(14): Show |
intron_variant | MODIFIER | c.1226-3334G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113517282 | |||||||
| chr13:113517283 | A | G | 16 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(13): Show |
17 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(14): Show |
intron_variant | MODIFIER | c.1226-3333A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113517283 | |||||||
| chr13:113517325 | C | T | 1 | a0003c0002t0002g0066 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1226-3291C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113517325 | |||||||
| chr13:113517327 | G | T | 1 | a0001c0006t0001g0226 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1226-3289G>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113517327 | |||||||
| chr13:113517370 | C | T | 67 | a0001c0001t0001g0179 a0003c0002t0002g0005 a0003c0002t0002g0008 others(64): Show |
78 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.1226-3246C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113517370 | |||||||
| chr13:113517378 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1226-3238G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113517378 | |||||||
| chr13:113517382 | G | A | 191 | a0001c0001t0001g0022 a0001c0001t0001g0087 a0001c0001t0001g0088 others(188): Show |
215 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.1226-3234G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113517382 | |||||||
| chr13:113517384 | C | G | 2 | a0001c0001t0009g0303 a0001c0001t0009g0304 |
2 | HG00639.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1226-3232C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113517384 | |||||||
| chr13:113517387 | C | T | 1 | a0002c0003t0003g0275 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1226-3229C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113517387 | |||||||
| chr13:113517390 | G | A | 194 | a0001c0001t0001g0022 a0001c0001t0001g0087 a0001c0001t0001g0088 others(191): Show |
218 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.1226-3226G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113517390 | |||||||
| chr13:113517394 | G | A | 2 | a0002c0004t0007g0028 a0002c0004t0007g0288 |
3 | HG02451.hp2 HG02486.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1226-3222G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113517394 | |||||||
| chr13:113517419 | G | A | 2 | a0001c0001t0001g0106 a0011c0017t0001g0284 |
2 | HG03195.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1226-3197G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113517419 | |||||||
| chr13:113517419 | G | C | 1 | a0001c0001t0001g0136 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1226-3197G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113517419 | |||||||
| chr13:113517430 | G | A | 1 | a0001c0001t0001g0114 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1226-3186G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113517430 | |||||||
| chr13:113517474 | C | T | 68 | a0001c0001t0001g0114 a0001c0005t0001g0232 a0001c0005t0001g0233 others(65): Show |
78 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.1226-3142C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113517474 | |||||||
| chr13:113517479 | T | C | 73 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(70): Show |
83 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.1226-3137T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113517479 | |||||||
| chr13:113517480 | G | A | 55 | a0002c0003t0003g0002 a0002c0003t0003g0007 a0002c0003t0003g0029 others(52): Show |
64 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.1226-3136G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113517480 | |||||||
| chr13:113517502 | A | T | 267 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0020 others(264): Show |
305 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.1226-3114A>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113517502 | |||||||
| chr13:113517594 | T | A | 1 | a0001c0001t0009g0304 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1226-3022T>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113517594 | |||||||
| chr13:113517637 | G | T | 106 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0106 others(103): Show |
120 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.1226-2979G>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113517637 | |||||||
| chr13:113517850 | C | G | 2 | a0001c0001t0001g0129 a0001c0001t0004g0102 |
2 | HG01884.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.1226-2766C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113517850 | |||||||
| chr13:113518124 | A | G | 1 | a0002c0003t0003g0238 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1226-2492A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113518124 | |||||||
| chr13:113518239 | C | G | 1 | a0001c0001t0004g0100 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1226-2377C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113518239 | |||||||
| chr13:113518285 | A | C | 16 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(13): Show |
17 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(14): Show |
intron_variant | MODIFIER | c.1226-2331A>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113518285 | |||||||
| chr13:113518296 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1226-2320C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113518296 | |||||||
| chr13:113518384 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1226-2232G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113518384 | |||||||
| chr13:113518429 | C | T | 67 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(64): Show |
78 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.1226-2187C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113518429 | |||||||
| chr13:113518510 | T | G | 21 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(18): Show |
22 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(19): Show |
intron_variant | MODIFIER | c.1226-2106T>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113518510 | |||||||
| chr13:113518638 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1226-1978C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113518638 | |||||||
| chr13:113518654 | C | T | 1 | a0013c0021t0002g0056 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1226-1962C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113518654 | |||||||
| chr13:113518724 | C | A | 2 | a0001c0001t0001g0020 a0012c0013t0001g0020 |
2 | NA18947.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.1226-1892C>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113518724 | |||||||
| chr13:113518889 | A | G | 11 | a0002c0004t0005g0292 a0002c0004t0005g0293 a0002c0004t0005g0294 others(8): Show |
11 | HG00099.hp2 HG01123.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.1226-1727A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113518889 | |||||||
| chr13:113518906 | C | A | 1 | a0001c0001t0001g0138 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1226-1710C>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113518906 | |||||||
| chr13:113518917 | A | G | 88 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(85): Show |
100 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.1226-1699A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113518917 | |||||||
| chr13:113518921 | A | G | 88 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(85): Show |
100 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.1226-1695A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113518921 | |||||||
| chr13:113519044 | CT | C | 149 | a0001c0001t0001g0184 a0001c0001t0009g0303 a0001c0001t0009g0304 others(146): Show |
172 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.1226-1556delT | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr13 | 113519044 | ||||||
| chr13:113519066 | G | A | 1 | a0003c0016t0002g0074 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1226-1550G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113519066 | |||||||
| chr13:113519129 | C | T | 1 | a0001c0001t0001g0154 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1226-1487C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113519129 | |||||||
| chr13:113519131 | C | T | 3 | a0003c0002t0002g0011 a0003c0002t0002g0012 a0003c0002t0002g0044 |
5 | HG02559.hp2 HG02970.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1226-1485C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113519131 | |||||||
| chr13:113519190 | C | T | 3 | a0002c0003t0003g0250 a0002c0003t0003g0267 a0002c0003t0003g0268 |
3 | NA18999.hp2 NA19001.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1226-1426C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113519190 | |||||||
| chr13:113519265 | C | T | 1 | a0001c0001t0001g0215 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1226-1351C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113519265 | |||||||
| chr13:113519293 | A | G | 156 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0006t0001g0027 others(153): Show |
179 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.1226-1323A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113519293 | |||||||
| chr13:113519312 | C | T | 1 | a0002c0004t0004g0086 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1226-1304C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113519312 | |||||||
| chr13:113519347 | C | CT | 12 | a0001c0001t0001g0119 a0001c0001t0001g0152 a0001c0001t0001g0153 others(9): Show |
12 | HG01978.hp1 HG01978.hp2 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.1226-1254dupT | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr13 | 113519347 | ||||||
| chr13:113519347 | C | CTTT | 63 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(60): Show |
74 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.1226-1256_1226-125 others(7): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr13 | 113519347 | ||||||
| chr13:113519383 | C | T | 16 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(13): Show |
17 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(14): Show |
intron_variant | MODIFIER | c.1226-1233C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113519383 | |||||||
| chr13:113519384 | G | A | 3 | a0003c0002t0002g0033 a0003c0002t0002g0039 a0003c0002t0002g0050 |
3 | HG03688.hp1 HG03942.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1226-1232G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113519384 | |||||||
| chr13:113519615 | CTTGGTCA others(66): Show |
C | 65 | a0002c0003t0003g0002 a0002c0003t0003g0007 a0002c0003t0003g0029 others(62): Show |
76 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.1226-928_1226-856d others(75): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr13 | 113519615 | ||||||
| chr13:113519678 | CCAAGTCT others(139): Show |
C | 1 | a0002c0004t0005g0289 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1226-921_1226-776d others(2): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr13 | 113519678 | ||||||
| chr13:113519695 | ACACAGTG others(66): Show |
A | 1 | a0003c0002t0002g0051 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1226-915_1226-843d others(75): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr13 | 113519695 | ||||||
| chr13:113519826 | A | C | 65 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(62): Show |
76 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.1226-790A>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113519826 | |||||||
| chr13:113519830 | CTG | C | 3 | a0002c0004t0004g0017 a0002c0004t0004g0086 a0008c0018t0004g0085 |
4 | HG02145.hp1 HG02559.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1226-782_1226-781d others(4): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr13 | 113519830 | ||||||
| chr13:113519834 | G | C | 1 | a0002c0004t0005g0289 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1226-782G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113519834 | |||||||
| chr13:113519847 | A | C | 1 | a0002c0004t0005g0289 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1226-769A>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113519847 | |||||||
| chr13:113519968 | A | G | 88 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(85): Show |
100 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.1226-648A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113519968 | |||||||
| chr13:113519995 | G | A | 1 | a0001c0001t0004g0100 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1226-621G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113519995 | |||||||
| chr13:113520045 | A | C | 4 | a0003c0002t0002g0008 a0003c0002t0002g0049 a0006c0010t0002g0008 others(1): Show |
5 | HG00423.hp1 HG00609.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.1226-571A>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113520045 | |||||||
| chr13:113520090 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1226-526A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113520090 | |||||||
| chr13:113520203 | C | T | 21 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(18): Show |
22 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(19): Show |
intron_variant | MODIFIER | c.1226-413C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113520203 | |||||||
| chr13:113520260 | T | C | 88 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(85): Show |
100 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.1226-356T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113520260 | |||||||
| chr13:113520438 | C | T | 65 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(62): Show |
76 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.1226-178C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113520438 | |||||||
| chr13:113520440 | A | T | 88 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(85): Show |
100 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.1226-176A>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113520440 | |||||||
| chr13:113520456 | C | T | 8 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(5): Show |
9 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(6): Show |
intron_variant | MODIFIER | c.1226-160C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113520456 | |||||||
| chr13:113520457 | C | T | 1 | a0005c0011t0008g0307 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1226-159C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113520457 | |||||||
| chr13:113520462 | C | T | 1 | a0002c0004t0004g0086 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1226-154C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113520462 | |||||||
| chr13:113520483 | C | CA | 6 | a0001c0001t0001g0160 a0001c0001t0001g0195 a0001c0001t0004g0097 others(3): Show |
6 | HG01069.hp1 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1226-114dupA | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr13 | 113520483 | ||||||
| chr13:113520483 | C | CAA | 70 | a0001c0006t0001g0218 a0001c0006t0001g0219 a0001c0006t0001g0220 others(67): Show |
81 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.1226-115_1226-114d others(4): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr13 | 113520483 | ||||||
| chr13:113520483 | C | CAAA | 12 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0221 others(9): Show |
13 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(10): Show |
intron_variant | MODIFIER | c.1226-116_1226-114d others(5): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr13 | 113520483 | ||||||
| chr13:113520483 | CA | C | 11 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0118 others(8): Show |
11 | HG01099.hp1 HG01099.hp2 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.1226-114delA | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr13 | 113520483 | ||||||
| chr13:113520574 | T | G | 5 | a0001c0001t0001g0026 a0001c0001t0001g0189 a0001c0001t0001g0193 others(2): Show |
6 | HG00140.hp2 HG00733.hp2 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.1226-42T>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113520574 | |||||||
| chr13:113520794 | C | G | 55 | a0002c0003t0003g0002 a0002c0003t0003g0007 a0002c0003t0003g0029 others(52): Show |
64 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.1343+61C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113520794 | |||||||
| chr13:113520805 | C | A | 21 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(18): Show |
22 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(19): Show |
intron_variant | MODIFIER | c.1343+72C>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113520805 | |||||||
| chr13:113520847 | C | T | 1 | a0003c0016t0002g0074 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1343+114C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113520847 | |||||||
| chr13:113520882 | C | T | 1 | a0001c0001t0001g0149 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1343+149C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113520882 | |||||||
| chr13:113520915 | C | T | 21 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(18): Show |
22 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(19): Show |
intron_variant | MODIFIER | c.1343+182C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113520915 | |||||||
| chr13:113520985 | C | G | 67 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(64): Show |
78 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.1343+252C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113520985 | |||||||
| chr13:113521019 | G | A | 1 | a0003c0002t0002g0049 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1343+286G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113521019 | |||||||
| chr13:113521043 | T | C | 88 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(85): Show |
100 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.1343+310T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113521043 | |||||||
| chr13:113521072 | G | A | 67 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(64): Show |
78 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.1343+339G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113521072 | |||||||
| chr13:113521118 | C | CTG | 3 | a0001c0001t0001g0087 a0001c0001t0001g0148 a0001c0001t0001g0285 |
3 | HG02165.hp2 NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1343+399_1343+400d others(4): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr13 | 113521118 | ||||||
| chr13:113521122 | G | A | 1 | a0001c0001t0001g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1343+389G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113521122 | |||||||
| chr13:113521130 | G | C | 3 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0184 |
3 | HG01109.hp2 HG02615.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1343+397G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113521130 | |||||||
| chr13:113521217 | T | TG | 18 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(15): Show |
19 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(16): Show |
intron_variant | MODIFIER | c.1343+491dupG | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr13 | 113521217 | ||||||
| chr13:113521302 | G | A | 1 | a0002c0004t0004g0086 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1343+569G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113521302 | |||||||
| chr13:113521494 | G | C | 2 | a0003c0002t0002g0057 a0003c0002t0002g0059 |
2 | HG00597.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.1343+761G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113521494 | |||||||
| chr13:113521558 | A | G | 94 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0106 others(91): Show |
106 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.1343+825A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113521558 | |||||||
| chr13:113521561 | C | T | 2 | a0003c0002t0002g0048 a0003c0002t0002g0065 |
2 | HG00738.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.1343+828C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113521561 | |||||||
| chr13:113521713 | A | T | 88 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(85): Show |
100 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.1343+980A>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113521713 | |||||||
| chr13:113521839 | G | A | 1 | a0002c0003t0003g0251 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1343+1106G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113521839 | |||||||
| chr13:113521845 | T | C | 2 | a0001c0001t0001g0087 a0001c0001t0001g0285 |
2 | NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1343+1112T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113521845 | |||||||
| chr13:113521958 | T | C | 1 | a0001c0001t0001g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1343+1225T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113521958 | |||||||
| chr13:113522008 | T | G | 67 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(64): Show |
78 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.1343+1275T>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113522008 | |||||||
| chr13:113522050 | C | T | 85 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(82): Show |
97 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.1343+1317C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113522050 | |||||||
| chr13:113522093 | A | G | 2 | a0005c0011t0008g0306 a0005c0011t0008g0307 |
2 | HG02027.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.1343+1360A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113522093 | |||||||
| chr13:113522288 | G | A | 18 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(15): Show |
19 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(16): Show |
intron_variant | MODIFIER | c.1343+1555G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113522288 | |||||||
| chr13:113522353 | T | C | 1 | a0002c0003t0003g0029 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1343+1620T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113522353 | |||||||
| chr13:113522404 | G | C | 2 | a0001c0001t0009g0303 a0001c0001t0009g0304 |
2 | HG00639.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1343+1671G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113522404 | |||||||
| chr13:113522530 | C | T | 2 | a0001c0001t0001g0025 a0001c0001t0001g0216 |
3 | HG00639.hp2 HG01361.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1343+1797C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113522530 | |||||||
| chr13:113522531 | G | A | 70 | a0001c0009t0004g0281 a0001c0009t0004g0282 a0001c0009t0004g0283 others(67): Show |
81 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.1343+1798G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113522531 | |||||||
| chr13:113522575 | T | C | 156 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0006t0001g0027 others(153): Show |
179 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.1343+1842T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113522575 | |||||||
| chr13:113522617 | G | A | 2 | a0001c0001t0001g0106 a0011c0017t0001g0284 |
2 | HG03195.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1343+1884G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113522617 | |||||||
| chr13:113522635 | C | T | 67 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(64): Show |
78 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.1343+1902C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113522635 | |||||||
| chr13:113522639 | T | C | 67 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(64): Show |
78 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.1343+1906T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113522639 | |||||||
| chr13:113522653 | A | G | 67 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(64): Show |
78 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.1343+1920A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113522653 | |||||||
| chr13:113522693 | C | T | 1 | a0001c0001t0001g0210 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1343+1960C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113522693 | |||||||
| chr13:113522789 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1343+2056G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113522789 | |||||||
| chr13:113522859 | C | T | 69 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0003c0002t0002g0005 others(66): Show |
80 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.1343+2126C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113522859 | |||||||
| chr13:113522978 | T | C | 67 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(64): Show |
78 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.1343+2245T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113522978 | |||||||
| chr13:113523054 | G | A | 67 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(64): Show |
78 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.1343+2321G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113523054 | |||||||
| chr13:113523118 | C | CT | 90 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0001t0012g0151 others(87): Show |
102 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.1343+2396dupT | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr13 | 113523118 | ||||||
| chr13:113523136 | CTT | C | 67 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(64): Show |
78 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.1343+2405_1343+240 others(6): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr13 | 113523136 | ||||||
| chr13:113523152 | TAA | T | 4 | a0001c0007t0006g0090 a0001c0007t0006g0091 a0001c0007t0006g0092 others(1): Show |
4 | HG02280.hp1 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1343+2422_1343+242 others(6): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr13 | 113523152 | ||||||
| chr13:113523200 | T | G | 2 | a0005c0011t0008g0306 a0005c0011t0008g0307 |
2 | HG02027.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.1343+2467T>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113523200 | |||||||
| chr13:113523203 | T | G | 67 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(64): Show |
78 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.1343+2470T>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113523203 | |||||||
| chr13:113523212 | G | A | 1 | a0003c0002t0002g0051 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1343+2479G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113523212 | |||||||
| chr13:113523243 | T | G | 67 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(64): Show |
78 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.1343+2510T>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113523243 | |||||||
| chr13:113523259 | G | A | 1 | a0003c0002t0002g0030 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1343+2526G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113523259 | |||||||
| chr13:113523410 | C | T | 67 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(64): Show |
78 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.1343+2677C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113523410 | |||||||
| chr13:113523413 | T | C | 2 | a0001c0001t0001g0134 a0001c0001t0001g0206 |
2 | NA18612.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.1343+2680T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113523413 | |||||||
| chr13:113523519 | T | G | 1 | a0001c0001t0001g0138 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1343+2786T>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113523519 | |||||||
| chr13:113523536 | A | G | 67 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(64): Show |
78 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.1343+2803A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113523536 | |||||||
| chr13:113523907 | T | A | 156 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0006t0001g0027 others(153): Show |
179 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.1343+3174T>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113523907 | |||||||
| chr13:113524119 | TGTCA | T | 67 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(64): Show |
78 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.1343+3393_1343+339 others(8): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr13 | 113524119 | ||||||
| chr13:113524565 | G | A | 5 | a0001c0001t0001g0026 a0001c0001t0001g0189 a0001c0001t0001g0193 others(2): Show |
6 | HG00140.hp2 HG00733.hp2 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.1343+3832G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113524565 | |||||||
| chr13:113524668 | C | T | 2 | a0001c0001t0001g0088 a0001c0001t0013g0084 |
2 | HG02109.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1343+3935C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113524668 | |||||||
| chr13:113524681 | T | C | 67 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(64): Show |
78 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.1343+3948T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113524681 | |||||||
| chr13:113524704 | A | T | 13 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(10): Show |
14 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.1343+3971A>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113524704 | |||||||
| chr13:113524705 | T | A | 67 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(64): Show |
78 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.1343+3972T>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113524705 | |||||||
| chr13:113524915 | TTTTA | T | 67 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(64): Show |
78 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.1343+4186_1343+418 others(8): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr13 | 113524915 | ||||||
| chr13:113524934 | C | T | 4 | a0001c0001t0001g0087 a0001c0001t0001g0285 a0002c0004t0005g0298 others(1): Show |
4 | NA18948.hp2 NA18950.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1343+4201C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113524934 | |||||||
| chr13:113524989 | T | C | 67 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(64): Show |
78 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.1343+4256T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113524989 | |||||||
| chr13:113525051 | G | A | 67 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(64): Show |
78 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.1343+4318G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113525051 | |||||||
| chr13:113525192 | A | G | 1 | a0002c0004t0004g0086 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1343+4459A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113525192 | |||||||
| chr13:113525230 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1343+4497G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113525230 | |||||||
| chr13:113525247 | C | G | 1 | a0001c0001t0001g0135 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1343+4514C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113525247 | |||||||
| chr13:113525316 | T | C | 55 | a0002c0003t0003g0002 a0002c0003t0003g0007 a0002c0003t0003g0029 others(52): Show |
64 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.1343+4583T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113525316 | |||||||
| chr13:113525384 | A | G | 67 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(64): Show |
78 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.1343+4651A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113525384 | |||||||
| chr13:113525389 | G | A | 67 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(64): Show |
78 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.1343+4656G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113525389 | |||||||
| chr13:113525413 | G | A | 89 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0006t0001g0027 others(86): Show |
101 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.1343+4680G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113525413 | |||||||
| chr13:113525460 | C | T | 2 | a0001c0001t0009g0303 a0001c0001t0009g0304 |
2 | HG00639.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1343+4727C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113525460 | |||||||
| chr13:113525474 | C | A | 1 | a0001c0001t0004g0105 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1343+4741C>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113525474 | |||||||
| chr13:113525501 | T | G | 5 | a0001c0001t0001g0019 a0001c0001t0001g0113 a0001c0001t0001g0114 others(2): Show |
5 | NA18950.hp2 NA18982.hp2 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.1343+4768T>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113525501 | |||||||
| chr13:113525564 | GAGACGAC others(44): Show |
G | 9 | a0001c0001t0001g0021 a0001c0001t0001g0131 a0001c0001t0001g0136 others(6): Show |
10 | HG00741.hp2 HG01081.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.1343+4850_1343+490 others(55): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr13 | 113525564 | ||||||
| chr13:113525583 | G | T | 1 | a0002c0004t0005g0292 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1343+4850G>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113525583 | |||||||
| chr13:113525583 | GGTTATTC others(44): Show |
G | 1 | a0013c0021t0002g0056 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1343+4882_1343+493 others(55): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr13 | 113525583 | ||||||
| chr13:113525611 | A | G | 1 | a0002c0004t0005g0292 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1343+4878A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113525611 | |||||||
| chr13:113525615 | C | G | 67 | a0002c0004t0005g0292 a0003c0002t0002g0005 a0003c0002t0002g0008 others(64): Show |
78 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.1343+4882C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113525615 | |||||||
| chr13:113525619 | C | T | 2 | a0001c0001t0009g0303 a0001c0001t0009g0304 |
2 | HG00639.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1343+4886C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113525619 | |||||||
| chr13:113525624 | G | A | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1343+4891G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113525624 | |||||||
| chr13:113525634 | T | G | 1 | a0002c0004t0005g0292 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1343+4901T>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113525634 | |||||||
| chr13:113525653 | A | ATCATCAT others(95): Show |
3 | a0003c0002t0002g0060 a0003c0002t0002g0067 a0003c0002t0002g0076 |
3 | NA18975.hp2 NA18993.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.1343+4922_1343+492 others(106): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr13 | 113525653 | ||||||
| chr13:113525653 | A | ATCATCAT others(95): Show |
1 | a0003c0002t0002g0061 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1343+4922_1343+492 others(106): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr13 | 113525653 | ||||||
| chr13:113525659 | A | ATCGTAGG others(95): Show |
54 | a0003c0002t0002g0005 a0003c0002t0002g0010 a0003c0002t0002g0011 others(51): Show |
63 | HG00597.hp2 HG00673.hp2 HG00738.hp1 others(60): Show |
intron_variant | MODIFIER | c.1343+4928_1343+492 others(106): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr13 | 113525659 | ||||||
| chr13:113525659 | A | ATCGTAGG others(95): Show |
1 | a0003c0002t0002g0043 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1343+4928_1343+492 others(106): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr13 | 113525659 | ||||||
| chr13:113525659 | A | G | 5 | a0002c0004t0005g0292 a0003c0002t0002g0060 a0003c0002t0002g0061 others(2): Show |
5 | HG04199.hp2 NA18975.hp2 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.1343+4926A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113525659 | |||||||
| chr13:113525662 | A | G | 67 | a0002c0004t0005g0292 a0003c0002t0002g0005 a0003c0002t0002g0008 others(64): Show |
78 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.1343+4929A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113525662 | |||||||
| chr13:113525670 | C | G | 1 | a0002c0004t0005g0292 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1343+4937C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113525670 | |||||||
| chr13:113525675 | G | A | 1 | a0013c0021t0002g0056 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1343+4942G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113525675 | |||||||
| chr13:113525685 | T | G | 8 | a0002c0004t0005g0292 a0003c0002t0002g0008 a0003c0002t0002g0013 others(5): Show |
10 | HG00423.hp1 HG00423.hp2 HG00609.hp1 others(7): Show |
intron_variant | MODIFIER | c.1343+4952T>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113525685 | |||||||
| chr13:113525704 | A | ATCGTCGT others(44): Show |
3 | a0003c0002t0002g0013 a0003c0002t0002g0071 a0003c0002t0002g0073 |
4 | HG00423.hp2 NA18946.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.1343+4976_1343+497 others(55): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr13 | 113525704 | ||||||
| chr13:113525704 | A | ATCGTCGT others(95): Show |
4 | a0003c0002t0002g0008 a0003c0002t0002g0049 a0006c0010t0002g0008 others(1): Show |
5 | HG00423.hp1 HG00609.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.1343+4976_1343+497 others(106): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr13 | 113525704 | ||||||
| chr13:113525704 | A | G | 59 | a0003c0002t0002g0005 a0003c0002t0002g0010 a0003c0002t0002g0011 others(56): Show |
68 | HG00597.hp2 HG00673.hp2 HG00738.hp1 others(65): Show |
intron_variant | MODIFIER | c.1343+4971A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113525704 | |||||||
| chr13:113525710 | A | G | 68 | a0002c0003t0003g0243 a0002c0004t0005g0292 a0003c0002t0002g0005 others(65): Show |
79 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.1343+4977A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113525710 | |||||||
| chr13:113525736 | G | T | 3 | a0003c0002t0002g0013 a0003c0002t0002g0071 a0003c0002t0002g0073 |
4 | HG00423.hp2 NA18946.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.1343+5003G>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113525736 | |||||||
| chr13:113525755 | A | G | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1343+5022A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113525755 | |||||||
| chr13:113525772 | G | C | 68 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0003c0002t0002g0005 others(65): Show |
79 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.1343+5039G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113525772 | |||||||
| chr13:113525800 | C | A | 21 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(18): Show |
22 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(19): Show |
intron_variant | MODIFIER | c.1343+5067C>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113525800 | |||||||
| chr13:113525806 | A | G | 67 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(64): Show |
78 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.1343+5073A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113525806 | |||||||
| chr13:113525808 | C | T | 3 | a0001c0009t0004g0281 a0001c0009t0004g0282 a0001c0009t0004g0283 |
3 | HG02717.hp1 HG03516.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1343+5075C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113525808 | |||||||
| chr13:113525833 | G | T | 1 | a0001c0001t0001g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1343+5100G>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113525833 | |||||||
| chr13:113525838 | T | G | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1343+5105T>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113525838 | |||||||
| chr13:113525857 | A | ATCGTCGT others(44): Show |
14 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(11): Show |
15 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(12): Show |
intron_variant | MODIFIER | c.1343+5220_1343+527 others(55): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr13 | 113525857 | ||||||
| chr13:113525857 | A | G | 68 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(65): Show |
79 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.1343+5124A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113525857 | |||||||
| chr13:113525866 | G | T | 1 | a0003c0002t0002g0061 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1343+5133G>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113525866 | |||||||
| chr13:113525926 | G | A | 3 | a0001c0009t0004g0281 a0001c0009t0004g0282 a0001c0009t0004g0283 |
3 | HG02717.hp1 HG03516.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1343+5193G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113525926 | |||||||
| chr13:113525938 | C | G | 7 | a0002c0004t0005g0286 a0002c0004t0005g0287 a0002c0004t0005g0289 others(4): Show |
8 | HG02451.hp2 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1343+5205C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113525938 | |||||||
| chr13:113525965 | G | A | 16 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(13): Show |
17 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(14): Show |
intron_variant | MODIFIER | c.1343+5232G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113525965 | |||||||
| chr13:113525984 | CTGTGCCG others(44): Show |
C | 1 | a0013c0021t0002g0056 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1343+5271_1343+532 others(55): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr13 | 113525984 | ||||||
| chr13:113526004 | G | C | 67 | a0002c0004t0004g0305 a0003c0002t0002g0005 a0003c0002t0002g0008 others(64): Show |
78 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.1343+5271G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113526004 | |||||||
| chr13:113526019 | G | A | 2 | a0001c0001t0001g0001 a0001c0001t0001g0139 |
5 | HG00438.hp1 HG02132.hp1 NA18945.hp2 others(2): Show |
intron_variant | MODIFIER | c.1343+5286G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113526019 | |||||||
| chr13:113526035 | A | C | 66 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1343+5302A>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113526035 | |||||||
| chr13:113526041 | C | T | 2 | a0005c0011t0008g0306 a0005c0011t0008g0307 |
2 | HG02027.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.1343+5308C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113526041 | |||||||
| chr13:113526060 | C | T | 4 | a0001c0005t0001g0230 a0001c0005t0001g0231 a0001c0005t0001g0232 others(1): Show |
4 | HG01099.hp2 HG01257.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.1343+5327C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113526060 | |||||||
| chr13:113526063 | C | T | 55 | a0002c0003t0003g0002 a0002c0003t0003g0007 a0002c0003t0003g0029 others(52): Show |
64 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.1343+5330C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113526063 | |||||||
| chr13:113526082 | A | G | 1 | a0003c0002t0002g0015 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1343+5349A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113526082 | |||||||
| chr13:113526092 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1343+5359C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113526092 | |||||||
| chr13:113526131 | C | T | 67 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(64): Show |
78 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.1343+5398C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113526131 | |||||||
| chr13:113526255 | G | C | 2 | a0002c0003t0003g0253 a0002c0003t0003g0276 |
2 | HG01261.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.1343+5522G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113526255 | |||||||
| chr13:113526332 | G | A | 1 | a0002c0004t0004g0305 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1343+5599G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113526332 | |||||||
| chr13:113526355 | A | T | 1 | a0002c0004t0004g0086 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1343+5622A>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113526355 | |||||||
| chr13:113526371 | A | G | 67 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(64): Show |
78 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.1343+5638A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113526371 | |||||||
| chr13:113526380 | A | G | 16 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(13): Show |
17 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(14): Show |
intron_variant | MODIFIER | c.1343+5647A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113526380 | |||||||
| chr13:113526472 | T | C | 67 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(64): Show |
78 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.1343+5739T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113526472 | |||||||
| chr13:113526488 | G | A | 1 | a0006c0010t0002g0055 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1343+5755G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113526488 | |||||||
| chr13:113526499 | G | A | 2 | a0001c0001t0009g0303 a0001c0001t0009g0304 |
2 | HG00639.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1343+5766G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113526499 | |||||||
| chr13:113526628 | A | C | 3 | a0002c0003t0003g0273 a0002c0003t0003g0274 a0002c0003t0003g0275 |
3 | HG02080.hp2 HG02165.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1343+5895A>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113526628 | |||||||
| chr13:113526694 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1343+5961G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113526694 | |||||||
| chr13:113526745 | G | A | 1 | a0002c0004t0004g0305 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1343+6012G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113526745 | |||||||
| chr13:113526845 | G | A | 76 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(73): Show |
86 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1343+6112G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113526845 | |||||||
| chr13:113526854 | A | G | 65 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(62): Show |
76 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.1343+6121A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113526854 | |||||||
| chr13:113526881 | A | G | 1 | a0001c0001t0001g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1343+6148A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113526881 | |||||||
| chr13:113526926 | T | C | 2 | a0002c0004t0004g0017 a0002c0004t0004g0086 |
3 | HG02145.hp1 HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1343+6193T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113526926 | |||||||
| chr13:113526943 | G | A | 1 | a0001c0001t0004g0100 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1343+6210G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113526943 | |||||||
| chr13:113527001 | A | T | 67 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(64): Show |
78 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.1343+6268A>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113527001 | |||||||
| chr13:113527174 | T | G | 4 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0003c0002t0002g0277 others(1): Show |
4 | HG00639.hp1 HG03471.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.1343+6441T>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113527174 | |||||||
| chr13:113527181 | G | T | 156 | a0001c0001t0001g0181 a0001c0001t0009g0303 a0001c0001t0009g0304 others(153): Show |
178 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.1343+6448G>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113527181 | |||||||
| chr13:113527426 | C | G | 1 | a0001c0001t0001g0279 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1344-6619C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113527426 | |||||||
| chr13:113527470 | T | G | 1 | a0001c0007t0006g0280 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1344-6575T>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113527470 | |||||||
| chr13:113527471 | C | T | 16 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(13): Show |
17 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(14): Show |
intron_variant | MODIFIER | c.1344-6574C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113527471 | |||||||
| chr13:113527490 | G | T | 1 | a0001c0001t0001g0159 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1344-6555G>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113527490 | |||||||
| chr13:113527527 | A | C | 1 | a0001c0001t0001g0237 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1344-6518A>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113527527 | |||||||
| chr13:113527559 | C | G | 2 | a0001c0001t0001g0088 a0001c0001t0013g0084 |
2 | HG02109.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1344-6486C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113527559 | |||||||
| chr13:113527663 | T | G | 3 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0184 |
3 | HG01109.hp2 HG02615.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1344-6382T>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113527663 | |||||||
| chr13:113527695 | A | C | 1 | a0002c0003t0003g0264 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1344-6350A>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113527695 | |||||||
| chr13:113527777 | C | CCTT | 158 | a0001c0001t0001g0088 a0001c0001t0009g0303 a0001c0001t0009g0304 others(155): Show |
181 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.1344-6266_1344-626 others(7): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr13 | 113527777 | ||||||
| chr13:113527788 | G | A | 156 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0006t0001g0027 others(153): Show |
179 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.1344-6257G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113527788 | |||||||
| chr13:113527845 | G | A | 1 | a0001c0022t0001g0192 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1344-6200G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113527845 | |||||||
| chr13:113527894 | C | T | 1 | a0002c0004t0004g0305 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1344-6151C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113527894 | |||||||
| chr13:113527964 | G | T | 2 | a0001c0001t0001g0189 a0001c0001t0001g0194 |
2 | HG00140.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1344-6081G>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113527964 | |||||||
| chr13:113528050 | T | C | 1 | a0003c0002t0002g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1344-5995T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113528050 | |||||||
| chr13:113528081 | G | A | 2 | a0005c0011t0008g0306 a0005c0011t0008g0307 |
2 | HG02027.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.1344-5964G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113528081 | |||||||
| chr13:113528345 | A | G | 155 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0006t0001g0027 others(152): Show |
178 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.1344-5700A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113528345 | |||||||
| chr13:113528365 | T | A | 3 | a0004c0008t0004g0089 a0004c0008t0004g0103 a0004c0008t0004g0104 |
3 | HG02258.hp2 HG02970.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1344-5680T>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113528365 | |||||||
| chr13:113528548 | G | A | 2 | a0002c0004t0005g0290 a0002c0004t0005g0291 |
2 | HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1344-5497G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113528548 | |||||||
| chr13:113528691 | T | TAGAGGGT others(10): Show |
2 | a0003c0002t0002g0082 a0003c0002t0002g0083 |
2 | NA18953.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1344-5343_1344-534 others(21): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr13 | 113528691 | ||||||
| chr13:113528703 | G | A | 67 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(64): Show |
78 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.1344-5342G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113528703 | |||||||
| chr13:113528703 | GTGATAAG others(27): Show |
G | 7 | a0002c0004t0005g0286 a0002c0004t0005g0287 a0002c0004t0005g0289 others(4): Show |
8 | HG02451.hp2 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1344-5323_1344-529 others(38): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr13 | 113528703 | ||||||
| chr13:113528745 | A | T | 1 | a0001c0001t0001g0210 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1344-5300A>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113528745 | |||||||
| chr13:113528805 | C | T | 1 | a0003c0002t0002g0061 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1344-5240C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113528805 | |||||||
| chr13:113528806 | G | T | 5 | a0002c0004t0005g0286 a0002c0004t0005g0287 a0002c0004t0005g0289 others(2): Show |
6 | HG02451.hp2 HG02486.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1344-5239G>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113528806 | |||||||
| chr13:113528914 | G | A | 1 | a0003c0002t0002g0062 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1344-5131G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113528914 | |||||||
| chr13:113529050 | A | G | 67 | a0003c0002t0002g0005 a0003c0002t0002g0008 a0003c0002t0002g0010 others(64): Show |
78 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.1344-4995A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113529050 | |||||||
| chr13:113529074 | G | A | 1 | a0001c0005t0001g0108 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1344-4971G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113529074 | |||||||
| chr13:113529222 | C | T | 1 | a0001c0001t0013g0084 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1344-4823C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113529222 | |||||||
| chr13:113529235 | G | A | 2 | a0002c0004t0004g0017 a0002c0004t0004g0086 |
3 | HG02145.hp1 HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1344-4810G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113529235 | |||||||
| chr13:113529318 | C | T | 4 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0184 others(1): Show |
4 | HG01109.hp2 HG02615.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1344-4727C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113529318 | |||||||
| chr13:113529319 | A | C | 4 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0184 others(1): Show |
4 | HG01109.hp2 HG02615.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1344-4726A>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113529319 | |||||||
| chr13:113529321 | G | GC | 4 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0184 others(1): Show |
4 | HG01109.hp2 HG02615.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1344-4723dupC | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr13 | 113529321 | ||||||
| chr13:113529321 | GCTGTCAT others(62): Show |
G | 14 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(11): Show |
15 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(12): Show |
intron_variant | MODIFIER | c.1344-4714_1344-464 others(73): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr13 | 113529321 | ||||||
| chr13:113529376 | C | T | 1 | a0001c0001t0013g0084 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1344-4669C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113529376 | |||||||
| chr13:113529377 | G | T | 1 | a0002c0019t0003g0002 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1344-4668G>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113529377 | |||||||
| chr13:113529379 | A | G | 3 | a0001c0009t0004g0281 a0001c0009t0004g0282 a0001c0009t0004g0283 |
3 | HG02717.hp1 HG03516.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1344-4666A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113529379 | |||||||
| chr13:113529381 | C | T | 3 | a0001c0009t0004g0281 a0001c0009t0004g0282 a0001c0009t0004g0283 |
3 | HG02717.hp1 HG03516.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1344-4664C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113529381 | |||||||
| chr13:113529386 | T | C | 3 | a0001c0009t0004g0281 a0001c0009t0004g0282 a0001c0009t0004g0283 |
3 | HG02717.hp1 HG03516.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1344-4659T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113529386 | |||||||
| chr13:113529387 | C | A | 3 | a0001c0009t0004g0281 a0001c0009t0004g0282 a0001c0009t0004g0283 |
3 | HG02717.hp1 HG03516.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1344-4658C>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113529387 | |||||||
| chr13:113529400 | T | C | 5 | a0001c0001t0001g0088 a0001c0001t0013g0084 a0001c0009t0004g0281 others(2): Show |
5 | HG02109.hp1 HG02145.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1344-4645T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113529400 | |||||||
| chr13:113529404 | G | A | 5 | a0001c0005t0001g0126 a0001c0005t0001g0174 a0001c0005t0001g0175 others(2): Show |
5 | HG02258.hp1 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1344-4641G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113529404 | |||||||
| chr13:113529416 | T | A | 5 | a0001c0007t0006g0090 a0001c0007t0006g0091 a0001c0007t0006g0092 others(2): Show |
5 | HG02280.hp1 HG02922.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1344-4629T>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113529416 | |||||||
| chr13:113529421 | G | C | 1 | a0001c0001t0001g0116 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1344-4624G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113529421 | |||||||
| chr13:113529421 | G | T | 5 | a0001c0007t0006g0090 a0001c0007t0006g0091 a0001c0007t0006g0092 others(2): Show |
5 | HG02280.hp1 HG02922.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1344-4624G>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113529421 | |||||||
| chr13:113529432 | C | T | 5 | a0001c0007t0006g0090 a0001c0007t0006g0091 a0001c0007t0006g0092 others(2): Show |
5 | HG02280.hp1 HG02922.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1344-4613C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113529432 | |||||||
| chr13:113529446 | C | G | 60 | a0001c0001t0001g0146 a0001c0001t0001g0148 a0001c0001t0001g0182 others(57): Show |
70 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.1344-4599C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113529446 | |||||||
| chr13:113529446 | C | T | 7 | a0003c0002t0002g0013 a0003c0002t0002g0047 a0003c0002t0002g0048 others(4): Show |
8 | HG00423.hp2 HG00738.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.1344-4599C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113529446 | |||||||
| chr13:113529466 | C | T | 1 | a0002c0003t0003g0247 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1344-4579C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113529466 | |||||||
| chr13:113529486 | T | C | 6 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0002c0004t0004g0017 others(3): Show |
8 | HG00639.hp1 HG02145.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1344-4559T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113529486 | |||||||
| chr13:113529511 | A | G | 1 | a0002c0003t0003g0263 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1344-4534A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113529511 | |||||||
| chr13:113529520 | C | A | 2 | a0002c0004t0004g0017 a0002c0004t0004g0086 |
3 | HG02145.hp1 HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1344-4525C>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113529520 | |||||||
| chr13:113529530 | T | G | 13 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(10): Show |
14 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.1344-4515T>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113529530 | |||||||
| chr13:113529543 | G | A | 3 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0184 |
3 | HG01109.hp2 HG02615.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1344-4502G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113529543 | |||||||
| chr13:113529582 | A | G | 2 | a0001c0001t0004g0096 a0001c0001t0004g0101 |
2 | HG01993.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.1344-4463A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113529582 | |||||||
| chr13:113529598 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1344-4447T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113529598 | |||||||
| chr13:113529605 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1344-4440A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113529605 | |||||||
| chr13:113529607 | G | A | 1 | a0002c0004t0004g0305 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1344-4438G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113529607 | |||||||
| chr13:113529649 | C | CA | 55 | a0001c0001t0001g0019 a0001c0001t0011g0019 a0002c0003t0003g0002 others(52): Show |
64 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.1344-4384dupA | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr13 | 113529649 | ||||||
| chr13:113529745 | G | A | 2 | a0002c0003t0003g0252 a0002c0003t0003g0272 |
2 | NA18962.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.1344-4300G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113529745 | |||||||
| chr13:113529748 | C | T | 3 | a0002c0004t0007g0028 a0002c0004t0007g0288 a0003c0002t0002g0040 |
4 | HG02451.hp2 HG02486.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1344-4297C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113529748 | |||||||
| chr13:113529763 | G | A | 2 | a0002c0004t0004g0017 a0002c0004t0004g0086 |
3 | HG02145.hp1 HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1344-4282G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113529763 | |||||||
| chr13:113529818 | T | C | 1 | a0002c0003t0003g0270 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1344-4227T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113529818 | |||||||
| chr13:113529837 | C | A | 16 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(13): Show |
17 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(14): Show |
intron_variant | MODIFIER | c.1344-4208C>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113529837 | |||||||
| chr13:113529837 | C | G | 2 | a0005c0011t0008g0306 a0005c0011t0008g0307 |
2 | HG02027.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.1344-4208C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113529837 | |||||||
| chr13:113529880 | C | T | 1 | a0003c0002t0002g0047 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1344-4165C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113529880 | |||||||
| chr13:113530106 | G | A | 1 | a0002c0003t0003g0262 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1344-3939G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113530106 | |||||||
| chr13:113530122 | C | T | 2 | a0002c0004t0005g0286 a0002c0004t0005g0287 |
2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1344-3923C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113530122 | |||||||
| chr13:113530131 | A | T | 4 | a0001c0007t0006g0090 a0001c0007t0006g0091 a0001c0007t0006g0092 others(1): Show |
4 | HG02280.hp1 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1344-3914A>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113530131 | |||||||
| chr13:113530167 | G | A | 1 | a0001c0006t0001g0224 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1344-3878G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113530167 | |||||||
| chr13:113530223 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1344-3822G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113530223 | |||||||
| chr13:113530288 | G | T | 55 | a0002c0003t0003g0002 a0002c0003t0003g0007 a0002c0003t0003g0029 others(52): Show |
64 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.1344-3757G>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113530288 | |||||||
| chr13:113530399 | G | A | 4 | a0001c0001t0001g0129 a0001c0001t0001g0140 a0001c0001t0001g0166 others(1): Show |
4 | NA18943.hp2 NA18959.hp1 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1344-3646G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113530399 | |||||||
| chr13:113530416 | TAGA | T | 4 | a0001c0007t0006g0090 a0001c0007t0006g0091 a0001c0007t0006g0092 others(1): Show |
4 | HG02280.hp1 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1344-3624_1344-362 others(7): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr13 | 113530416 | ||||||
| chr13:113530566 | A | G | 1 | a0001c0001t0001g0177 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1344-3479A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113530566 | |||||||
| chr13:113530570 | C | T | 1 | a0002c0004t0005g0297 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1344-3475C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113530570 | |||||||
| chr13:113530643 | A | G | 1 | a0008c0018t0004g0085 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1344-3402A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113530643 | |||||||
| chr13:113530935 | G | A | 22 | a0001c0001t0001g0087 a0001c0001t0001g0285 a0001c0001t0004g0018 others(19): Show |
23 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.1344-3110G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113530935 | |||||||
| chr13:113530941 | C | T | 1 | a0007c0012t0001g0197 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1344-3104C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113530941 | |||||||
| chr13:113530952 | C | A | 1 | a0001c0001t0004g0229 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1344-3093C>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113530952 | |||||||
| chr13:113530985 | G | A | 2 | a0002c0004t0004g0017 a0002c0004t0004g0086 |
3 | HG02145.hp1 HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1344-3060G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113530985 | |||||||
| chr13:113530992 | A | G | 167 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(164): Show |
191 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.1344-3053A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113530992 | |||||||
| chr13:113531223 | G | A | 2 | a0001c0001t0001g0141 a0001c0001t0001g0171 |
2 | HG03492.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.1344-2822G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113531223 | |||||||
| chr13:113531251 | T | A | 1 | a0003c0002t0002g0011 | 2 | HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1344-2794T>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113531251 | |||||||
| chr13:113531251 | T | G | 152 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0006t0001g0027 others(149): Show |
174 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.1344-2794T>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113531251 | |||||||
| chr13:113531292 | C | T | 5 | a0002c0004t0005g0286 a0002c0004t0005g0287 a0002c0004t0005g0289 others(2): Show |
6 | HG02451.hp2 HG02486.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1344-2753C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113531292 | |||||||
| chr13:113531411 | C | T | 9 | a0002c0004t0004g0017 a0002c0004t0004g0086 a0002c0004t0005g0286 others(6): Show |
11 | HG02145.hp1 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1344-2634C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113531411 | |||||||
| chr13:113531490 | T | C | 158 | a0001c0001t0001g0088 a0001c0001t0009g0303 a0001c0001t0009g0304 others(155): Show |
181 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.1344-2555T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113531490 | |||||||
| chr13:113531492 | C | T | 2 | a0001c0001t0001g0087 a0001c0001t0001g0285 |
2 | NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1344-2553C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113531492 | |||||||
| chr13:113531507 | G | A | 18 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(15): Show |
19 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(16): Show |
intron_variant | MODIFIER | c.1344-2538G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113531507 | |||||||
| chr13:113531550 | G | A | 1 | a0002c0003t0003g0263 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1344-2495G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113531550 | |||||||
| chr13:113531637 | C | T | 1 | a0002c0003t0003g0261 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1344-2408C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113531637 | |||||||
| chr13:113531638 | G | C | 1 | a0001c0001t0013g0084 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1344-2407G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113531638 | |||||||
| chr13:113531660 | G | A | 3 | a0001c0009t0004g0281 a0001c0009t0004g0282 a0001c0009t0004g0283 |
3 | HG02717.hp1 HG03516.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1344-2385G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113531660 | |||||||
| chr13:113531680 | C | T | 1 | a0007c0012t0001g0197 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1344-2365C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113531680 | |||||||
| chr13:113531712 | C | T | 1 | a0001c0001t0001g0022 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1344-2333C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113531712 | |||||||
| chr13:113531797 | T | C | 70 | a0002c0004t0004g0305 a0002c0004t0005g0290 a0002c0004t0005g0291 others(67): Show |
81 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.1344-2248T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113531797 | |||||||
| chr13:113531863 | G | A | 68 | a0002c0004t0004g0305 a0003c0002t0002g0005 a0003c0002t0002g0008 others(65): Show |
79 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.1344-2182G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113531863 | |||||||
| chr13:113531883 | A | G | 1 | a0001c0007t0006g0280 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1344-2162A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113531883 | |||||||
| chr13:113531956 | C | A | 3 | a0001c0005t0001g0230 a0001c0005t0001g0231 a0001c0005t0001g0232 |
3 | HG01099.hp2 HG01257.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.1344-2089C>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113531956 | |||||||
| chr13:113531981 | TCTGCA | T | 7 | a0002c0004t0005g0286 a0002c0004t0005g0287 a0002c0004t0005g0289 others(4): Show |
8 | HG02451.hp2 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1344-2060_1344-205 others(9): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr13 | 113531981 | ||||||
| chr13:113532081 | A | G | 153 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0006t0001g0027 others(150): Show |
176 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.1344-1964A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113532081 | |||||||
| chr13:113532282 | C | G | 1 | a0001c0001t0004g0102 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1344-1763C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113532282 | |||||||
| chr13:113532351 | T | C | 153 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0006t0001g0027 others(150): Show |
176 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.1344-1694T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113532351 | |||||||
| chr13:113532444 | GC | G | 9 | a0002c0004t0004g0017 a0002c0004t0004g0086 a0002c0004t0005g0286 others(6): Show |
11 | HG02145.hp1 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1344-1600delC | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113532444 | |||||||
| chr13:113532485 | A | G | 182 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0106 others(179): Show |
206 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.1344-1560A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113532485 | |||||||
| chr13:113532669 | T | A | 2 | a0002c0003t0003g0245 a0002c0003t0003g0246 |
2 | HG00438.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.1344-1376T>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113532669 | |||||||
| chr13:113532744 | G | A | 1 | a0003c0002t0002g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1344-1301G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113532744 | |||||||
| chr13:113532753 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1344-1292T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113532753 | |||||||
| chr13:113532781 | T | G | 1 | a0002c0004t0004g0305 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1344-1264T>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113532781 | |||||||
| chr13:113532784 | TAAGTCGC others(104): Show |
T | 2 | a0001c0001t0001g0131 a0001c0001t0001g0145 |
2 | HG02015.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1344-1153_1344-104 others(4): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr13 | 113532784 | ||||||
| chr13:113532784 | TAAGTCGC others(212): Show |
T | 1 | a0001c0001t0001g0130 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1344-1091_1344-873 others(3): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr13 | 113532784 | ||||||
| chr13:113532789 | C | T | 1 | a0002c0004t0005g0294 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1344-1256C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113532789 | |||||||
| chr13:113532790 | G | A | 3 | a0001c0001t0001g0184 a0003c0002t0002g0005 a0003c0002t0002g0079 |
6 | HG01081.hp1 HG01175.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.1344-1255G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113532790 | |||||||
| chr13:113532824 | G | A | 1 | a0002c0004t0004g0017 | 2 | HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1344-1221G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113532824 | |||||||
| chr13:113532835 | C | CCTA | 18 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(15): Show |
19 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(16): Show |
intron_variant | MODIFIER | c.1344-1208_1344-120 others(7): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr13 | 113532835 | ||||||
| chr13:113532835 | CCTGAAGT others(50): Show |
C | 7 | a0002c0004t0005g0286 a0002c0004t0005g0287 a0002c0004t0005g0289 others(4): Show |
8 | HG02451.hp2 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1344-1153_1344-109 others(61): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr13 | 113532835 | ||||||
| chr13:113532843 | C | T | 66 | a0002c0004t0004g0305 a0003c0002t0002g0005 a0003c0002t0002g0008 others(63): Show |
77 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1344-1202C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113532843 | |||||||
| chr13:113532877 | C | T | 3 | a0001c0007t0006g0090 a0001c0007t0006g0091 a0001c0007t0006g0092 |
3 | HG02922.hp2 HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1344-1168C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113532877 | |||||||
| chr13:113532883 | C | CTCCCTCC others(47): Show |
1 | a0001c0001t0001g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1344-1154_1344-115 others(58): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr13 | 113532883 | ||||||
| chr13:113532889 | CCTA | C | 20 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0006t0001g0027 others(17): Show |
21 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(18): Show |
intron_variant | MODIFIER | c.1344-1153_1344-115 others(7): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr13 | 113532889 | ||||||
| chr13:113532892 | A | ACTGAAGT others(47): Show |
6 | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0001t0001g0189 others(3): Show |
7 | HG00140.hp2 HG00733.hp2 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.1344-988_1344-935d others(56): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr13 | 113532892 | ||||||
| chr13:113532892 | A | ACTGAAGT others(101): Show |
1 | a0003c0016t0002g0074 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1344-1092_1344-109 others(112): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr13 | 113532892 | ||||||
| chr13:113532892 | ACTGAAGT others(47): Show |
A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0171 |
2 | HG03492.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.1344-988_1344-935d others(56): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr13 | 113532892 | ||||||
| chr13:113532900 | C | T | 18 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(15): Show |
19 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(16): Show |
intron_variant | MODIFIER | c.1344-1145C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113532900 | |||||||
| chr13:113532946 | C | CCTGAAGT others(50): Show |
3 | a0003c0002t0002g0048 a0003c0002t0002g0065 a0003c0002t0002g0075 |
3 | HG00738.hp1 HG01952.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1344-1043_1344-104 others(61): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr13 | 113532946 | ||||||
| chr13:113532946 | C | CCTGAAGT others(104): Show |
1 | a0003c0002t0002g0038 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1344-1037_1344-103 others(115): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr13 | 113532946 | ||||||
| chr13:113532946 | C | CCTGAAGT others(104): Show |
61 | a0002c0004t0004g0305 a0003c0002t0002g0005 a0003c0002t0002g0008 others(58): Show |
72 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.1344-989_1344-988i others(113): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr13 | 113532946 | ||||||
| chr13:113532973 | G | A | 1 | a0008c0018t0004g0085 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1344-1072G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113532973 | |||||||
| chr13:113533000 | C | CCTA | 18 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(15): Show |
19 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(16): Show |
intron_variant | MODIFIER | c.1344-1043_1344-104 others(7): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr13 | 113533000 | ||||||
| chr13:113533000 | C | CCTGAAGT others(50): Show |
3 | a0001c0001t0001g0019 a0001c0001t0011g0019 a0003c0002t0002g0062 |
3 | NA18950.hp2 NA18982.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.1344-989_1344-988i others(59): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr13 | 113533000 | ||||||
| chr13:113533002 | T | TACTGAAG others(163): Show |
2 | a0001c0001t0009g0303 a0001c0001t0009g0304 |
2 | HG00639.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1344-1043_1344-104 others(174): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113533002 | |||||||
| chr13:113533002 | T | TTC | 7 | a0002c0004t0005g0286 a0002c0004t0005g0287 a0002c0004t0005g0289 others(4): Show |
8 | HG02451.hp2 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1344-1043_1344-104 others(6): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113533002 | |||||||
| chr13:113533003 | G | GAAGTCGC others(49): Show |
3 | a0002c0004t0004g0017 a0002c0004t0004g0086 a0008c0018t0004g0085 |
4 | HG02145.hp1 HG02559.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1344-989_1344-988i others(58): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr13 | 113533003 | ||||||
| chr13:113533003 | G | T | 9 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0002c0004t0005g0286 others(6): Show |
10 | HG00639.hp1 HG02451.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1344-1042G>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113533003 | |||||||
| chr13:113533053 | TCCTGAAG others(101): Show |
T | 1 | a0002c0003t0003g0260 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1344-988_1344-881d others(2): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr13 | 113533053 | ||||||
| chr13:113533056 | T | TTC | 18 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(15): Show |
19 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(16): Show |
intron_variant | MODIFIER | c.1344-989_1344-988i others(4): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113533056 | |||||||
| chr13:113533057 | G | T | 18 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(15): Show |
19 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(16): Show |
intron_variant | MODIFIER | c.1344-988G>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113533057 | |||||||
| chr13:113533082 | C | T | 54 | a0002c0003t0003g0002 a0002c0003t0003g0007 a0002c0003t0003g0029 others(51): Show |
63 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.1344-963C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113533082 | |||||||
| chr13:113533107 | T | TCCTGAAG others(98): Show |
1 | a0003c0002t0002g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1344-935_1344-934i others(107): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr13 | 113533107 | ||||||
| chr13:113533108 | CCTA | C | 18 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(15): Show |
19 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(16): Show |
intron_variant | MODIFIER | c.1344-934_1344-932d others(5): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr13 | 113533108 | ||||||
| chr13:113533111 | A | C | 1 | a0003c0002t0002g0032 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1344-934A>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113533111 | |||||||
| chr13:113533139 | C | T | 1 | a0001c0001t0013g0084 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1344-906C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113533139 | |||||||
| chr13:113533165 | C | T | 1 | a0002c0003t0003g0260 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1344-880C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113533165 | |||||||
| chr13:113533167 | T | TACTGAAG others(52): Show |
1 | a0002c0003t0003g0262 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1344-878_1344-877i others(61): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113533167 | |||||||
| chr13:113533167 | T | TTC | 131 | a0002c0003t0003g0002 a0002c0003t0003g0007 a0002c0003t0003g0029 others(128): Show |
153 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.1344-878_1344-877i others(4): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113533167 | |||||||
| chr13:113533168 | G | T | 132 | a0002c0003t0003g0002 a0002c0003t0003g0007 a0002c0003t0003g0029 others(129): Show |
154 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.1344-877G>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113533168 | |||||||
| chr13:113533173 | T | C | 179 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0285 others(176): Show |
203 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.1344-872T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113533173 | |||||||
| chr13:113533183 | G | A | 7 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0115 others(4): Show |
7 | NA18747.hp2 NA18952.hp2 NA18963.hp1 others(4): Show |
intron_variant | MODIFIER | c.1344-862G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113533183 | |||||||
| chr13:113533240 | GATCCCTT others(19): Show |
G | 134 | a0001c0005t0010g0164 a0002c0003t0003g0002 a0002c0003t0003g0007 others(131): Show |
156 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.1344-785_1344-760d others(28): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr13 | 113533240 | ||||||
| chr13:113533272 | T | C | 1 | a0001c0001t0004g0100 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1344-773T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113533272 | |||||||
| chr13:113533299 | C | T | 55 | a0002c0003t0003g0002 a0002c0003t0003g0007 a0002c0003t0003g0029 others(52): Show |
64 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.1344-746C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113533299 | |||||||
| chr13:113533452 | G | A | 8 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0115 others(5): Show |
8 | NA18747.hp2 NA18952.hp2 NA18963.hp1 others(5): Show |
intron_variant | MODIFIER | c.1344-593G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113533452 | |||||||
| chr13:113533486 | G | A | 135 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0002c0003t0003g0002 others(132): Show |
157 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.1344-559G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113533486 | |||||||
| chr13:113533648 | C | T | 18 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(15): Show |
19 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(16): Show |
intron_variant | MODIFIER | c.1344-397C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113533648 | |||||||
| chr13:113533658 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1344-387C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113533658 | |||||||
| chr13:113533795 | A | G | 1 | a0002c0004t0005g0291 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1344-250A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113533795 | |||||||
| chr13:113533799 | T | C | 265 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(262): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.1344-246T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113533799 | |||||||
| chr13:113533850 | C | T | 168 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(165): Show |
192 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.1344-195C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113533850 | |||||||
| chr13:113533922 | G | A | 4 | a0003c0002t0002g0033 a0003c0002t0002g0039 a0003c0002t0002g0050 others(1): Show |
4 | HG03098.hp1 HG03688.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.1344-123G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113533922 | |||||||
| chr13:113533945 | A | G | 18 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(15): Show |
19 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(16): Show |
intron_variant | MODIFIER | c.1344-100A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113533945 | |||||||
| chr13:113533976 | A | G | 151 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(148): Show |
174 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.1344-69A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113533976 | |||||||
| chr13:113533995 | T | C | 1 | a0001c0007t0006g0090 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1344-50T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113533995 | |||||||
| chr13:113534428 | G | A | 1 | a0001c0001t0001g0149 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1539+188G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113534428 | |||||||
| chr13:113534471 | A | G | 1 | a0003c0016t0002g0074 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1539+231A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113534471 | |||||||
| chr13:113534651 | C | T | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | HG01167.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1539+411C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113534651 | |||||||
| chr13:113534700 | G | T | 18 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(15): Show |
19 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(16): Show |
intron_variant | MODIFIER | c.1539+460G>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113534700 | |||||||
| chr13:113534736 | G | T | 2 | a0005c0011t0008g0306 a0005c0011t0008g0307 |
2 | HG02027.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.1539+496G>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113534736 | |||||||
| chr13:113534789 | CA | C | 174 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0285 others(171): Show |
198 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.1539+558delA | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr13 | 113534789 | ||||||
| chr13:113534807 | T | C | 265 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(262): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.1539+567T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113534807 | |||||||
| chr13:113534939 | T | C | 1 | a0008c0018t0004g0085 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1539+699T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113534939 | |||||||
| chr13:113534940 | G | T | 1 | a0008c0018t0004g0085 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1539+700G>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113534940 | |||||||
| chr13:113534952 | G | A | 1 | a0008c0018t0004g0085 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1539+712G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113534952 | |||||||
| chr13:113535007 | C | T | 19 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(16): Show |
20 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(17): Show |
intron_variant | MODIFIER | c.1539+767C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113535007 | |||||||
| chr13:113535164 | G | A | 2 | a0005c0011t0008g0306 a0005c0011t0008g0307 |
2 | HG02027.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.1539+924G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113535164 | |||||||
| chr13:113535303 | C | T | 172 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(169): Show |
196 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.1539+1063C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113535303 | |||||||
| chr13:113535353 | A | T | 2 | a0002c0004t0004g0017 a0002c0004t0004g0086 |
3 | HG02145.hp1 HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1539+1113A>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113535353 | |||||||
| chr13:113535430 | G | C | 16 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(13): Show |
17 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(14): Show |
intron_variant | MODIFIER | c.1539+1190G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113535430 | |||||||
| chr13:113535474 | T | C | 169 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(166): Show |
193 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.1539+1234T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113535474 | |||||||
| chr13:113535683 | C | T | 1 | a0003c0002t0002g0054 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1539+1443C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113535683 | |||||||
| chr13:113535686 | A | T | 1 | a0001c0001t0001g0158 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1539+1446A>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113535686 | |||||||
| chr13:113535689 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1539+1449G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113535689 | |||||||
| chr13:113535840 | G | A | 18 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(15): Show |
19 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(16): Show |
intron_variant | MODIFIER | c.1539+1600G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113535840 | |||||||
| chr13:113535921 | A | G | 18 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(15): Show |
19 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(16): Show |
intron_variant | MODIFIER | c.1539+1681A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113535921 | |||||||
| chr13:113536042 | A | G | 2 | a0001c0001t0001g0087 a0001c0001t0001g0285 |
2 | NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1539+1802A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113536042 | |||||||
| chr13:113536207 | G | A | 1 | a0005c0011t0008g0306 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1539+1967G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113536207 | |||||||
| chr13:113536246 | C | T | 2 | a0001c0001t0001g0088 a0001c0001t0001g0107 |
2 | HG02145.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.1539+2006C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113536246 | |||||||
| chr13:113536340 | C | CA | 167 | a0001c0001t0001g0088 a0001c0001t0004g0018 a0001c0001t0004g0093 others(164): Show |
190 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.1539+2112dupA | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr13 | 113536340 | ||||||
| chr13:113536340 | C | CAA | 7 | a0002c0004t0005g0286 a0002c0004t0005g0287 a0002c0004t0005g0289 others(4): Show |
8 | HG02451.hp2 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1539+2111_1539+211 others(6): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr13 | 113536340 | ||||||
| chr13:113536352 | A | T | 1 | a0001c0007t0006g0090 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1539+2112A>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113536352 | |||||||
| chr13:113536382 | A | G | 1 | a0003c0002t0002g0030 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1539+2142A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113536382 | |||||||
| chr13:113536398 | A | C | 169 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(166): Show |
193 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.1539+2158A>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113536398 | |||||||
| chr13:113536431 | G | C | 2 | a0001c0001t0001g0142 a0001c0001t0001g0154 |
2 | NA18983.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.1539+2191G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113536431 | |||||||
| chr13:113536489 | T | C | 1 | a0001c0001t0001g0163 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1539+2249T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113536489 | |||||||
| chr13:113536517 | C | T | 1 | a0001c0001t0001g0285 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1539+2277C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113536517 | |||||||
| chr13:113536654 | C | T | 1 | a0001c0001t0001g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1539+2414C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113536654 | |||||||
| chr13:113536899 | A | G | 80 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(77): Show |
91 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.1540-2458A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113536899 | |||||||
| chr13:113536989 | A | G | 1 | a0002c0003t0003g0259 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1540-2368A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113536989 | |||||||
| chr13:113537187 | A | C | 147 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(144): Show |
169 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.1540-2170A>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113537187 | |||||||
| chr13:113537376 | G | A | 67 | a0002c0004t0004g0305 a0003c0002t0002g0008 a0003c0002t0002g0010 others(64): Show |
75 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.1540-1981G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113537376 | |||||||
| chr13:113537396 | G | A | 22 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(19): Show |
24 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(21): Show |
intron_variant | MODIFIER | c.1540-1961G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113537396 | |||||||
| chr13:113537426 | G | A | 62 | a0002c0003t0003g0002 a0002c0003t0003g0007 a0002c0003t0003g0029 others(59): Show |
72 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.1540-1931G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113537426 | |||||||
| chr13:113537447 | G | A | 2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | NA18963.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.1540-1910G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113537447 | |||||||
| chr13:113537450 | G | A | 1 | a0001c0006t0001g0234 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1540-1907G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113537450 | |||||||
| chr13:113537474 | C | T | 3 | a0002c0003t0003g0250 a0002c0003t0003g0267 a0002c0003t0003g0268 |
3 | NA18999.hp2 NA19001.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1540-1883C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113537474 | |||||||
| chr13:113537531 | A | C | 12 | a0001c0001t0004g0096 a0001c0001t0004g0100 a0001c0001t0004g0101 others(9): Show |
13 | HG00639.hp1 HG01884.hp1 HG01993.hp2 others(10): Show |
intron_variant | MODIFIER | c.1540-1826A>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113537531 | |||||||
| chr13:113537672 | C | T | 2 | a0005c0011t0008g0306 a0005c0011t0008g0307 |
2 | HG02027.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.1540-1685C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113537672 | |||||||
| chr13:113537694 | T | G | 1 | a0001c0001t0001g0207 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1540-1663T>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113537694 | |||||||
| chr13:113537765 | G | A | 16 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(13): Show |
17 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(14): Show |
intron_variant | MODIFIER | c.1540-1592G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113537765 | |||||||
| chr13:113537810 | A | G | 179 | a0001c0001t0001g0087 a0001c0001t0001g0127 a0001c0001t0001g0128 others(176): Show |
203 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.1540-1547A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113537810 | |||||||
| chr13:113537831 | G | T | 3 | a0002c0003t0003g0273 a0002c0003t0003g0274 a0002c0003t0003g0275 |
3 | HG02080.hp2 HG02165.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1540-1526G>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113537831 | |||||||
| chr13:113537869 | C | T | 2 | a0005c0011t0008g0306 a0005c0011t0008g0307 |
2 | HG02027.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.1540-1488C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113537869 | |||||||
| chr13:113537888 | CGTGT | C | 62 | a0002c0003t0003g0002 a0002c0003t0003g0007 a0002c0003t0003g0029 others(59): Show |
72 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.1540-1461_1540-145 others(8): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr13 | 113537888 | ||||||
| chr13:113537889 | G | A | 20 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(17): Show |
22 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(19): Show |
intron_variant | MODIFIER | c.1540-1468G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113537889 | |||||||
| chr13:113537995 | GTGTGTAC others(19): Show |
G | 2 | a0002c0004t0007g0028 a0002c0004t0007g0288 |
3 | HG02451.hp2 HG02486.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1540-1347_1540-132 others(30): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr13 | 113537995 | ||||||
| chr13:113538007 | G | GTC | 170 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(167): Show |
193 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.1540-1349_1540-134 others(6): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr13 | 113538007 | ||||||
| chr13:113538078 | T | G | 174 | a0001c0001t0001g0087 a0001c0001t0001g0285 a0001c0001t0004g0018 others(171): Show |
198 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.1540-1279T>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113538078 | |||||||
| chr13:113538107 | G | A | 1 | a0013c0021t0002g0056 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1540-1250G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113538107 | |||||||
| chr13:113538115 | T | TTGTG | 62 | a0002c0003t0003g0002 a0002c0003t0003g0007 a0002c0003t0003g0029 others(59): Show |
72 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.1540-1241_1540-123 others(8): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr13 | 113538115 | ||||||
| chr13:113538162 | ATG | A | 6 | a0001c0005t0001g0126 a0001c0005t0001g0174 a0001c0005t0001g0175 others(3): Show |
6 | HG02258.hp1 HG02280.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1540-1191_1540-119 others(6): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr13 | 113538162 | ||||||
| chr13:113538221 | C | T | 156 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(153): Show |
179 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.1540-1136C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113538221 | |||||||
| chr13:113538222 | A | G | 172 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(169): Show |
196 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.1540-1135A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113538222 | |||||||
| chr13:113538240 | G | GTGCGTGT others(8): Show |
156 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(153): Show |
179 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.1540-1115_1540-111 others(19): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr13 | 113538240 | ||||||
| chr13:113538258 | C | T | 20 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(17): Show |
22 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(19): Show |
intron_variant | MODIFIER | c.1540-1099C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113538258 | |||||||
| chr13:113538354 | G | A | 2 | a0001c0005t0001g0186 a0001c0005t0001g0187 |
2 | HG02602.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1540-1003G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113538354 | |||||||
| chr13:113538447 | C | T | 1 | a0010c0015t0002g0070 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1540-910C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113538447 | |||||||
| chr13:113538481 | CAT | C | 3 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0013g0084 |
3 | HG02109.hp1 NA18982.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1540-875_1540-874d others(4): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113538481 | |||||||
| chr13:113538483 | T | C | 157 | a0001c0001t0001g0088 a0001c0001t0004g0018 a0001c0001t0004g0093 others(154): Show |
180 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(177): Show |
intron_variant | MODIFIER | c.1540-874T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113538483 | |||||||
| chr13:113538519 | G | C | 2 | a0001c0001t0001g0142 a0001c0001t0001g0154 |
2 | NA18983.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.1540-838G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113538519 | |||||||
| chr13:113538543 | C | G | 1 | a0008c0018t0004g0085 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1540-814C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113538543 | |||||||
| chr13:113538570 | G | C | 155 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(152): Show |
178 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.1540-787G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113538570 | |||||||
| chr13:113538595 | T | A | 156 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(153): Show |
179 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.1540-762T>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113538595 | |||||||
| chr13:113538606 | G | A | 4 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0198 others(1): Show |
6 | HG00639.hp2 HG01070.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1540-751G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113538606 | |||||||
| chr13:113538708 | ATGC | A | 68 | a0002c0004t0004g0305 a0003c0002t0002g0005 a0003c0002t0002g0008 others(65): Show |
79 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.1540-644_1540-642d others(5): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr13 | 113538708 | ||||||
| chr13:113538776 | C | T | 6 | a0001c0001t0001g0088 a0001c0001t0013g0084 a0001c0007t0006g0090 others(3): Show |
6 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1540-581C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113538776 | |||||||
| chr13:113538787 | C | T | 68 | a0002c0004t0004g0305 a0003c0002t0002g0005 a0003c0002t0002g0008 others(65): Show |
79 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.1540-570C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113538787 | |||||||
| chr13:113538864 | A | T | 2 | a0005c0011t0008g0306 a0005c0011t0008g0307 |
2 | HG02027.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.1540-493A>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113538864 | |||||||
| chr13:113538895 | C | T | 63 | a0001c0001t0004g0095 a0002c0003t0003g0002 a0002c0003t0003g0007 others(60): Show |
73 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.1540-462C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113538895 | |||||||
| chr13:113539013 | C | T | 1 | a0002c0004t0005g0296 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1540-344C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113539013 | |||||||
| chr13:113539099 | G | A | 1 | a0002c0004t0004g0086 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1540-258G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113539099 | |||||||
| chr13:113539210 | A | C | 172 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(169): Show |
196 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.1540-147A>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113539210 | |||||||
| chr13:113539232 | G | A | 60 | a0002c0003t0003g0002 a0002c0003t0003g0007 a0002c0003t0003g0029 others(57): Show |
70 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.1540-125G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113539232 | |||||||
| chr13:113539282 | C | T | 1 | a0001c0005t0001g0214 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1540-75C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 9/12 | chr13 | 113539282 | |||||||
| chr13:113539518 | T | A | 26 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(23): Show |
28 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.1690+11T>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113539518 | |||||||
| chr13:113539563 | C | T | 94 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(91): Show |
107 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.1690+56C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113539563 | |||||||
| chr13:113539580 | GCATA | G | 26 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(23): Show |
28 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.1690+74_1690+77del others(4): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113539580 | |||||||
| chr13:113539744 | A | T | 1 | a0001c0006t0001g0228 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1690+237A>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113539744 | |||||||
| chr13:113539753 | G | A | 62 | a0002c0003t0003g0002 a0002c0003t0003g0007 a0002c0003t0003g0029 others(59): Show |
72 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.1690+246G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113539753 | |||||||
| chr13:113539784 | A | C | 2 | a0001c0001t0001g0088 a0001c0001t0013g0084 |
2 | HG02109.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1690+277A>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113539784 | |||||||
| chr13:113540003 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1690+496G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113540003 | |||||||
| chr13:113540009 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1690+502C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113540009 | |||||||
| chr13:113540163 | TGTGTCTT others(86): Show |
T | 1 | a0001c0001t0001g0141 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1690+658_1690+750d others(95): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113540163 | ||||||
| chr13:113540188 | C | T | 1 | a0002c0003t0003g0262 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1690+681C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113540188 | |||||||
| chr13:113540189 | G | A | 1 | a0001c0001t0001g0208 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1690+682G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113540189 | |||||||
| chr13:113540208 | C | T | 1 | a0002c0003t0003g0258 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1690+701C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113540208 | |||||||
| chr13:113540209 | G | T | 2 | a0005c0011t0008g0306 a0005c0011t0008g0307 |
2 | HG02027.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.1690+702G>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113540209 | |||||||
| chr13:113540231 | C | T | 2 | a0002c0004t0004g0017 a0002c0004t0004g0086 |
3 | HG02145.hp1 HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1690+724C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113540231 | |||||||
| chr13:113540251 | A | G | 62 | a0002c0003t0003g0002 a0002c0003t0003g0007 a0002c0003t0003g0029 others(59): Show |
72 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.1690+744A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113540251 | |||||||
| chr13:113540591 | T | G | 1 | a0001c0001t0001g0190 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1690+1084T>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113540591 | |||||||
| chr13:113540618 | A | G | 26 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(23): Show |
28 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.1690+1111A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113540618 | |||||||
| chr13:113540649 | C | G | 62 | a0002c0003t0003g0002 a0002c0003t0003g0007 a0002c0003t0003g0029 others(59): Show |
72 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.1690+1142C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113540649 | |||||||
| chr13:113540658 | G | C | 1 | a0008c0018t0004g0085 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1690+1151G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113540658 | |||||||
| chr13:113540765 | G | A | 1 | a0002c0003t0003g0261 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1690+1258G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113540765 | |||||||
| chr13:113540793 | C | G | 2 | a0005c0011t0008g0306 a0005c0011t0008g0307 |
2 | HG02027.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.1690+1286C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113540793 | |||||||
| chr13:113540842 | G | A | 2 | a0001c0001t0001g0088 a0001c0001t0013g0084 |
2 | HG02109.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1690+1335G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113540842 | |||||||
| chr13:113540846 | G | A | 130 | a0002c0003t0003g0002 a0002c0003t0003g0007 a0002c0003t0003g0029 others(127): Show |
151 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.1690+1339G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113540846 | |||||||
| chr13:113541033 | G | T | 4 | a0001c0007t0006g0090 a0001c0007t0006g0091 a0001c0007t0006g0092 others(1): Show |
4 | HG02280.hp1 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1690+1526G>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541033 | |||||||
| chr13:113541057 | G | T | 1 | a0008c0018t0004g0085 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1690+1550G>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541057 | |||||||
| chr13:113541177 | G | C | 2 | a0005c0011t0008g0306 a0005c0011t0008g0307 |
2 | HG02027.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.1690+1670G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541177 | |||||||
| chr13:113541222 | CACGCACA others(50): Show |
C | 24 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(21): Show |
25 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(22): Show |
intron_variant | MODIFIER | c.1690+1756_1690+181 others(61): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113541222 | ||||||
| chr13:113541263 | C | T | 2 | a0002c0004t0004g0017 a0002c0004t0004g0086 |
3 | HG02145.hp1 HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1690+1756C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541263 | |||||||
| chr13:113541264 | G | A | 1 | a0010c0015t0002g0070 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1690+1757G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541264 | |||||||
| chr13:113541267 | A | T | 2 | a0002c0004t0004g0017 a0002c0004t0004g0086 |
3 | HG02145.hp1 HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1690+1760A>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541267 | |||||||
| chr13:113541275 | A | G | 2 | a0002c0004t0004g0017 a0002c0004t0004g0086 |
3 | HG02145.hp1 HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1690+1768A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541275 | |||||||
| chr13:113541278 | A | C | 2 | a0002c0004t0004g0017 a0002c0004t0004g0086 |
3 | HG02145.hp1 HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1690+1771A>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541278 | |||||||
| chr13:113541279 | T | C | 2 | a0002c0004t0004g0017 a0002c0004t0004g0086 |
3 | HG02145.hp1 HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1690+1772T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541279 | |||||||
| chr13:113541281 | C | T | 2 | a0002c0004t0004g0017 a0002c0004t0004g0086 |
3 | HG02145.hp1 HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1690+1774C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541281 | |||||||
| chr13:113541298 | C | G | 2 | a0002c0004t0004g0017 a0002c0004t0004g0086 |
3 | HG02145.hp1 HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1690+1791C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541298 | |||||||
| chr13:113541318 | G | A | 1 | a0001c0005t0001g0186 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1690+1811G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541318 | |||||||
| chr13:113541319 | C | T | 2 | a0002c0004t0004g0017 a0002c0004t0004g0086 |
3 | HG02145.hp1 HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1690+1812C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541319 | |||||||
| chr13:113541320 | T | C | 2 | a0002c0004t0004g0017 a0002c0004t0004g0086 |
3 | HG02145.hp1 HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1690+1813T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541320 | |||||||
| chr13:113541321 | G | C | 2 | a0002c0004t0004g0017 a0002c0004t0004g0086 |
3 | HG02145.hp1 HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1690+1814G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541321 | |||||||
| chr13:113541324 | T | A | 2 | a0002c0004t0004g0017 a0002c0004t0004g0086 |
3 | HG02145.hp1 HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1690+1817T>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541324 | |||||||
| chr13:113541332 | A | G | 154 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(151): Show |
176 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.1690+1825A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541332 | |||||||
| chr13:113541335 | C | A | 2 | a0002c0004t0004g0017 a0002c0004t0004g0086 |
3 | HG02145.hp1 HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1690+1828C>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541335 | |||||||
| chr13:113541336 | C | T | 2 | a0002c0004t0004g0017 a0002c0004t0004g0086 |
3 | HG02145.hp1 HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1690+1829C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541336 | |||||||
| chr13:113541338 | T | C | 2 | a0002c0004t0004g0017 a0002c0004t0004g0086 |
3 | HG02145.hp1 HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1690+1831T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541338 | |||||||
| chr13:113541355 | C | G | 24 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(21): Show |
25 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(22): Show |
intron_variant | MODIFIER | c.1690+1848C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541355 | |||||||
| chr13:113541370 | T | A | 2 | a0002c0004t0004g0017 a0002c0004t0004g0086 |
3 | HG02145.hp1 HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1690+1863T>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541370 | |||||||
| chr13:113541374 | T | C | 26 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(23): Show |
28 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.1690+1867T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541374 | |||||||
| chr13:113541376 | C | T | 24 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(21): Show |
25 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(22): Show |
intron_variant | MODIFIER | c.1690+1869C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541376 | |||||||
| chr13:113541378 | C | G | 2 | a0002c0004t0004g0017 a0002c0004t0004g0086 |
3 | HG02145.hp1 HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1690+1871C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541378 | |||||||
| chr13:113541403 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1690+1896A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541403 | |||||||
| chr13:113541403 | ATCGCTGA others(563): Show |
A | 1 | a0002c0003t0003g0257 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1690+1920_1690+248 others(4): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113541403 | ||||||
| chr13:113541405 | C | T | 22 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(19): Show |
23 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.1690+1898C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541405 | |||||||
| chr13:113541406 | G | A | 1 | a0001c0001t0001g0116 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1690+1899G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541406 | |||||||
| chr13:113541427 | A | T | 3 | a0001c0001t0001g0156 a0002c0004t0004g0017 a0002c0004t0004g0086 |
4 | HG01167.hp1 HG02145.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1690+1920A>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541427 | |||||||
| chr13:113541435 | GAGATATG others(164): Show |
G | 3 | a0001c0009t0004g0281 a0001c0009t0004g0282 a0001c0009t0004g0283 |
3 | HG02717.hp1 HG03516.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1690+1933_1690+210 others(4): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113541435 | ||||||
| chr13:113541440 | A | G | 26 | a0001c0001t0001g0107 a0001c0001t0001g0129 a0001c0001t0001g0130 others(23): Show |
28 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.1690+1933A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541440 | |||||||
| chr13:113541509 | CGCACACG others(50): Show |
C | 61 | a0002c0003t0003g0002 a0002c0003t0003g0007 a0002c0003t0003g0029 others(58): Show |
71 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.1690+2019_1690+207 others(61): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113541509 | ||||||
| chr13:113541517 | A | G | 2 | a0002c0004t0004g0017 a0002c0004t0004g0086 |
3 | HG02145.hp1 HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1690+2010A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541517 | |||||||
| chr13:113541519 | T | C | 24 | a0001c0001t0001g0106 a0001c0001t0004g0018 a0001c0001t0004g0093 others(21): Show |
26 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(23): Show |
intron_variant | MODIFIER | c.1690+2012T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541519 | |||||||
| chr13:113541547 | CTGAGTTG others(50): Show |
C | 19 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(16): Show |
20 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(17): Show |
intron_variant | MODIFIER | c.1690+2041_1690+209 others(61): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541547 | |||||||
| chr13:113541548 | T | C | 4 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0002c0004t0004g0017 others(1): Show |
5 | HG00639.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1690+2041T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541548 | |||||||
| chr13:113541552 | T | A | 4 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0002c0004t0004g0017 others(1): Show |
5 | HG00639.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1690+2045T>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541552 | |||||||
| chr13:113541560 | G | A | 4 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0002c0004t0004g0017 others(1): Show |
5 | HG00639.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1690+2053G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541560 | |||||||
| chr13:113541563 | C | A | 4 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0002c0004t0004g0017 others(1): Show |
5 | HG00639.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1690+2056C>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541563 | |||||||
| chr13:113541564 | C | T | 4 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0002c0004t0004g0017 others(1): Show |
5 | HG00639.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1690+2057C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541564 | |||||||
| chr13:113541566 | T | C | 6 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0009g0303 others(3): Show |
7 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.1690+2059T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541566 | |||||||
| chr13:113541573 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1690+2066G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541573 | |||||||
| chr13:113541574 | A | G | 4 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0002c0004t0004g0017 others(1): Show |
5 | HG00639.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1690+2067A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541574 | |||||||
| chr13:113541576 | T | C | 4 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0002c0004t0004g0017 others(1): Show |
5 | HG00639.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1690+2069T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541576 | |||||||
| chr13:113541583 | G | C | 4 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0002c0004t0004g0017 others(1): Show |
5 | HG00639.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1690+2076G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541583 | |||||||
| chr13:113541604 | T | C | 4 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0002c0004t0004g0017 others(1): Show |
5 | HG00639.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1690+2097T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541604 | |||||||
| chr13:113541606 | C | CAGATGTG others(50): Show |
1 | a0001c0007t0006g0280 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1690+2125_1690+212 others(61): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113541606 | ||||||
| chr13:113541606 | C | G | 23 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(20): Show |
25 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(22): Show |
intron_variant | MODIFIER | c.1690+2099C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541606 | |||||||
| chr13:113541631 | A | G | 24 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(21): Show |
26 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(23): Show |
intron_variant | MODIFIER | c.1690+2124A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541631 | |||||||
| chr13:113541633 | T | C | 35 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0135 others(32): Show |
37 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.1690+2126T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541633 | |||||||
| chr13:113541633 | T | TGCTGATC others(50): Show |
3 | a0001c0001t0001g0285 a0001c0007t0006g0090 a0001c0007t0006g0092 |
3 | HG02922.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1690+2147_1690+214 others(61): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113541633 | ||||||
| chr13:113541633 | T | TGCTGATC others(107): Show |
1 | a0001c0007t0006g0091 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1690+2147_1690+214 others(118): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113541633 | ||||||
| chr13:113541633 | T | TGCTGATC others(164): Show |
1 | a0001c0001t0001g0087 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1690+2147_1690+214 others(175): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113541633 | ||||||
| chr13:113541633 | T | TGCTGATC others(107): Show |
1 | a0003c0002t0002g0043 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1690+2147_1690+214 others(118): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113541633 | ||||||
| chr13:113541633 | T | TGCTGATC others(50): Show |
1 | a0001c0001t0001g0115 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1690+2409_1690+246 others(61): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113541633 | ||||||
| chr13:113541633 | T | TGCTGATG others(50): Show |
1 | a0001c0001t0001g0181 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1690+2132_1690+213 others(61): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113541633 | ||||||
| chr13:113541633 | TGCTGATC others(50): Show |
T | 10 | a0001c0001t0001g0106 a0001c0001t0001g0162 a0001c0001t0001g0188 others(7): Show |
10 | HG00099.hp1 HG00735.hp2 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.1690+2409_1690+246 others(61): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113541633 | ||||||
| chr13:113541633 | TGCTGATC others(164): Show |
T | 1 | a0011c0017t0001g0284 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1690+2295_1690+246 others(4): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113541633 | ||||||
| chr13:113541640 | C | G | 2 | a0001c0001t0001g0135 a0001c0001t0001g0144 |
2 | HG00408.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.1690+2133C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541640 | |||||||
| chr13:113541655 | T | A | 144 | a0001c0001t0001g0088 a0001c0001t0013g0084 a0001c0006t0001g0027 others(141): Show |
166 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.1690+2148T>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541655 | |||||||
| chr13:113541659 | C | T | 2 | a0002c0004t0004g0017 a0002c0004t0004g0086 |
3 | HG02145.hp1 HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1690+2152C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541659 | |||||||
| chr13:113541688 | A | G | 24 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(21): Show |
26 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(23): Show |
intron_variant | MODIFIER | c.1690+2181A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541688 | |||||||
| chr13:113541690 | C | T | 1 | a0003c0002t0002g0051 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1690+2183C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541690 | |||||||
| chr13:113541712 | T | A | 9 | a0002c0004t0005g0286 a0002c0004t0005g0287 a0002c0004t0005g0289 others(6): Show |
11 | HG01069.hp2 HG01071.hp2 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.1690+2205T>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541712 | |||||||
| chr13:113541716 | C | T | 1 | a0003c0002t0002g0059 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1690+2209C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541716 | |||||||
| chr13:113541719 | C | T | 1 | a0003c0002t0002g0059 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1690+2212C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541719 | |||||||
| chr13:113541738 | G | A | 1 | a0003c0002t0002g0059 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1690+2231G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541738 | |||||||
| chr13:113541743 | C | T | 63 | a0002c0004t0004g0305 a0003c0002t0002g0005 a0003c0002t0002g0008 others(60): Show |
73 | HG00423.hp1 HG00609.hp1 HG00673.hp2 others(70): Show |
intron_variant | MODIFIER | c.1690+2236C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541743 | |||||||
| chr13:113541745 | A | G | 26 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(23): Show |
28 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.1690+2238A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541745 | |||||||
| chr13:113541772 | C | T | 1 | a0003c0002t0002g0059 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1690+2265C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541772 | |||||||
| chr13:113541773 | C | T | 2 | a0002c0004t0004g0017 a0002c0004t0004g0086 |
3 | HG02145.hp1 HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1690+2266C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541773 | |||||||
| chr13:113541776 | C | T | 3 | a0002c0004t0004g0017 a0002c0004t0004g0086 a0003c0002t0002g0059 |
4 | HG00597.hp2 HG02145.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1690+2269C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541776 | |||||||
| chr13:113541799 | A | T | 1 | a0001c0001t0001g0141 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1690+2292A>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541799 | |||||||
| chr13:113541800 | C | T | 3 | a0003c0002t0002g0015 a0003c0002t0002g0030 a0003c0002t0002g0059 |
4 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.1690+2293C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541800 | |||||||
| chr13:113541802 | A | ATCGCTGA others(107): Show |
1 | a0001c0001t0001g0129 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1690+2351_1690+235 others(118): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113541802 | ||||||
| chr13:113541802 | A | G | 24 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(21): Show |
25 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(22): Show |
intron_variant | MODIFIER | c.1690+2295A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541802 | |||||||
| chr13:113541802 | ATCGCTGA others(335): Show |
A | 2 | a0002c0003t0003g0029 a0002c0004t0005g0290 |
2 | HG02965.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1690+2352_1690+269 others(4): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113541802 | ||||||
| chr13:113541829 | C | T | 2 | a0002c0004t0004g0017 a0002c0004t0004g0086 |
3 | HG02145.hp1 HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1690+2322C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541829 | |||||||
| chr13:113541831 | G | A | 8 | a0003c0002t0002g0013 a0003c0002t0002g0047 a0003c0002t0002g0048 others(5): Show |
9 | HG00738.hp1 HG01952.hp1 HG04204.hp1 others(6): Show |
intron_variant | MODIFIER | c.1690+2324G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541831 | |||||||
| chr13:113541833 | C | T | 3 | a0002c0004t0004g0017 a0002c0004t0004g0086 a0003c0002t0002g0059 |
4 | HG00597.hp2 HG02145.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1690+2326C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541833 | |||||||
| chr13:113541847 | G | A | 1 | a0003c0002t0002g0059 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1690+2340G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541847 | |||||||
| chr13:113541848 | A | C | 1 | a0003c0002t0002g0059 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1690+2341A>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541848 | |||||||
| chr13:113541849 | T | C | 1 | a0003c0002t0002g0059 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1690+2342T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541849 | |||||||
| chr13:113541857 | C | T | 2 | a0002c0004t0004g0017 a0002c0004t0004g0086 |
3 | HG02145.hp1 HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1690+2350C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541857 | |||||||
| chr13:113541859 | A | ATCGCTGA others(50): Show |
1 | a0001c0001t0001g0001 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1690+2408_1690+240 others(61): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113541859 | ||||||
| chr13:113541859 | A | ATCGCTGA others(107): Show |
5 | a0001c0001t0001g0107 a0001c0001t0001g0130 a0001c0001t0001g0139 others(2): Show |
5 | HG00438.hp1 HG01081.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.1690+2408_1690+240 others(118): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113541859 | ||||||
| chr13:113541859 | A | G | 27 | a0001c0001t0001g0106 a0001c0001t0001g0129 a0001c0001t0001g0188 others(24): Show |
28 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.1690+2352A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541859 | |||||||
| chr13:113541859 | ATCGCTGA others(278): Show |
A | 53 | a0002c0003t0003g0002 a0002c0003t0003g0007 a0002c0003t0003g0238 others(50): Show |
62 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.1690+2409_1690+269 others(4): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113541859 | ||||||
| chr13:113541861 | C | T | 1 | a0003c0002t0002g0059 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1690+2354C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541861 | |||||||
| chr13:113541887 | C | T | 18 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(15): Show |
19 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(16): Show |
intron_variant | MODIFIER | c.1690+2380C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541887 | |||||||
| chr13:113541890 | C | T | 21 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(18): Show |
23 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.1690+2383C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541890 | |||||||
| chr13:113541894 | A | T | 1 | a0003c0002t0002g0059 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1690+2387A>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541894 | |||||||
| chr13:113541900 | GGATGATA others(277): Show |
G | 1 | a0002c0003t0003g0249 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1690+2395_1690+267 others(4): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113541900 | ||||||
| chr13:113541904 | G | A | 2 | a0002c0004t0004g0017 a0002c0004t0004g0086 |
3 | HG02145.hp1 HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1690+2397G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541904 | |||||||
| chr13:113541905 | A | C | 2 | a0002c0004t0004g0017 a0002c0004t0004g0086 |
3 | HG02145.hp1 HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1690+2398A>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541905 | |||||||
| chr13:113541906 | T | C | 2 | a0002c0004t0004g0017 a0002c0004t0004g0086 |
3 | HG02145.hp1 HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1690+2399T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541906 | |||||||
| chr13:113541915 | G | A | 57 | a0002c0004t0004g0305 a0003c0002t0002g0005 a0003c0002t0002g0008 others(54): Show |
65 | HG00423.hp1 HG00609.hp1 HG00673.hp2 others(62): Show |
intron_variant | MODIFIER | c.1690+2408G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541915 | |||||||
| chr13:113541916 | A | ATCGCTGA others(164): Show |
2 | a0001c0005t0001g0108 a0001c0005t0001g0109 |
2 | HG00733.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1690+2465_1690+246 others(175): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113541916 | ||||||
| chr13:113541916 | A | ATCGCTGA others(50): Show |
3 | a0001c0001t0001g0026 a0001c0001t0001g0181 a0001c0001t0001g0182 |
4 | HG01167.hp2 HG01169.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1690+2850_1690+290 others(61): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113541916 | ||||||
| chr13:113541916 | A | ATCGCTGA others(107): Show |
38 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0020 others(35): Show |
49 | HG00140.hp1 HG00609.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.1690+2793_1690+290 others(118): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113541916 | ||||||
| chr13:113541916 | A | ATCGCTGA others(164): Show |
6 | a0001c0001t0001g0021 a0001c0001t0001g0135 a0001c0001t0001g0136 others(3): Show |
7 | HG00408.hp2 HG02602.hp2 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.1690+2736_1690+290 others(175): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113541916 | ||||||
| chr13:113541916 | A | G | 41 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(38): Show |
45 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.1690+2409A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541916 | |||||||
| chr13:113541916 | ATCGCTGA others(50): Show |
A | 2 | a0003c0002t0002g0079 a0003c0002t0002g0081 |
2 | HG01256.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1690+2850_1690+290 others(61): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113541916 | ||||||
| chr13:113541916 | ATCGCTGA others(107): Show |
A | 2 | a0001c0001t0001g0138 a0001c0001t0001g0145 |
2 | HG02015.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1690+2793_1690+290 others(4): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113541916 | ||||||
| chr13:113541916 | ATCGCTGA others(221): Show |
A | 5 | a0002c0004t0005g0286 a0002c0004t0005g0287 a0002c0004t0005g0289 others(2): Show |
6 | HG02451.hp2 HG02486.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1690+2679_1690+290 others(4): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113541916 | ||||||
| chr13:113541916 | ATCGCTGA others(278): Show |
A | 1 | a0003c0002t0002g0052 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1690+2622_1690+290 others(4): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113541916 | ||||||
| chr13:113541916 | ATCGCTGA others(335): Show |
A | 1 | a0003c0002t0002g0059 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1690+2565_1690+290 others(4): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113541916 | ||||||
| chr13:113541918 | C | T | 2 | a0002c0004t0004g0017 a0002c0004t0004g0086 |
3 | HG02145.hp1 HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1690+2411C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541918 | |||||||
| chr13:113541943 | C | T | 18 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(15): Show |
19 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(16): Show |
intron_variant | MODIFIER | c.1690+2436C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541943 | |||||||
| chr13:113541944 | C | T | 3 | a0005c0011t0008g0306 a0005c0011t0008g0307 a0008c0018t0004g0085 |
3 | HG02027.hp1 HG02129.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1690+2437C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541944 | |||||||
| chr13:113541947 | C | T | 23 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(20): Show |
25 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(22): Show |
intron_variant | MODIFIER | c.1690+2440C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541947 | |||||||
| chr13:113541951 | A | T | 2 | a0002c0004t0004g0017 a0002c0004t0004g0086 |
3 | HG02145.hp1 HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1690+2444A>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541951 | |||||||
| chr13:113541971 | C | T | 18 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(15): Show |
19 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(16): Show |
intron_variant | MODIFIER | c.1690+2464C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541971 | |||||||
| chr13:113541972 | G | A | 6 | a0003c0002t0002g0011 a0003c0002t0002g0012 a0003c0002t0002g0015 others(3): Show |
9 | HG00423.hp2 HG01069.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1690+2465G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541972 | |||||||
| chr13:113541973 | G | A | 33 | a0001c0001t0001g0088 a0001c0001t0001g0165 a0001c0001t0004g0018 others(30): Show |
38 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.1690+2466G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113541973 | |||||||
| chr13:113541973 | G | GTCGCTGA others(221): Show |
1 | a0003c0002t0002g0043 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1690+2493_1690+249 others(232): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113541973 | ||||||
| chr13:113542000 | C | T | 2 | a0005c0011t0008g0306 a0005c0011t0008g0307 |
2 | HG02027.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.1690+2493C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542000 | |||||||
| chr13:113542004 | C | T | 20 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(17): Show |
21 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(18): Show |
intron_variant | MODIFIER | c.1690+2497C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542004 | |||||||
| chr13:113542018 | G | A | 18 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(15): Show |
19 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(16): Show |
intron_variant | MODIFIER | c.1690+2511G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542018 | |||||||
| chr13:113542019 | A | C | 18 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(15): Show |
19 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(16): Show |
intron_variant | MODIFIER | c.1690+2512A>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542019 | |||||||
| chr13:113542020 | T | C | 18 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(15): Show |
19 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(16): Show |
intron_variant | MODIFIER | c.1690+2513T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542020 | |||||||
| chr13:113542028 | C | T | 3 | a0005c0011t0008g0306 a0005c0011t0008g0307 a0008c0018t0004g0085 |
3 | HG02027.hp1 HG02129.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1690+2521C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542028 | |||||||
| chr13:113542030 | G | A | 26 | a0001c0001t0001g0088 a0001c0001t0004g0018 a0001c0001t0004g0093 others(23): Show |
28 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.1690+2523G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542030 | |||||||
| chr13:113542030 | G | ATCGCTGA others(164): Show |
1 | a0001c0005t0001g0110 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1690+2522_1690+252 others(175): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542030 | |||||||
| chr13:113542032 | C | T | 18 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(15): Show |
19 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(16): Show |
intron_variant | MODIFIER | c.1690+2525C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542032 | |||||||
| chr13:113542036 | G | C | 2 | a0002c0004t0004g0017 a0002c0004t0004g0086 |
3 | HG02145.hp1 HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1690+2529G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542036 | |||||||
| chr13:113542058 | C | T | 64 | a0001c0009t0004g0281 a0001c0009t0004g0282 a0001c0009t0004g0283 others(61): Show |
73 | HG00423.hp1 HG00609.hp1 HG00673.hp2 others(70): Show |
intron_variant | MODIFIER | c.1690+2551C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542058 | |||||||
| chr13:113542061 | C | T | 83 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(80): Show |
92 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.1690+2554C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542061 | |||||||
| chr13:113542065 | A | T | 18 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(15): Show |
19 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(16): Show |
intron_variant | MODIFIER | c.1690+2558A>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542065 | |||||||
| chr13:113542075 | G | A | 5 | a0002c0004t0004g0017 a0002c0004t0004g0086 a0005c0011t0008g0306 others(2): Show |
6 | HG02027.hp1 HG02129.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1690+2568G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542075 | |||||||
| chr13:113542076 | A | C | 5 | a0002c0004t0004g0017 a0002c0004t0004g0086 a0005c0011t0008g0306 others(2): Show |
6 | HG02027.hp1 HG02129.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1690+2569A>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542076 | |||||||
| chr13:113542077 | T | C | 5 | a0002c0004t0004g0017 a0002c0004t0004g0086 a0005c0011t0008g0306 others(2): Show |
6 | HG02027.hp1 HG02129.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1690+2570T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542077 | |||||||
| chr13:113542080 | G | A | 59 | a0002c0004t0004g0305 a0003c0002t0002g0005 a0003c0002t0002g0008 others(56): Show |
67 | HG00423.hp1 HG00609.hp1 HG00673.hp2 others(64): Show |
intron_variant | MODIFIER | c.1690+2573G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542080 | |||||||
| chr13:113542087 | G | A | 86 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(83): Show |
96 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.1690+2580G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542087 | |||||||
| chr13:113542089 | C | T | 3 | a0005c0011t0008g0306 a0005c0011t0008g0307 a0008c0018t0004g0085 |
3 | HG02027.hp1 HG02129.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1690+2582C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542089 | |||||||
| chr13:113542114 | C | T | 62 | a0001c0009t0004g0281 a0001c0009t0004g0282 a0001c0009t0004g0283 others(59): Show |
70 | HG00423.hp1 HG00609.hp1 HG00673.hp2 others(67): Show |
intron_variant | MODIFIER | c.1690+2607C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542114 | |||||||
| chr13:113542115 | C | T | 6 | a0003c0002t0002g0011 a0003c0002t0002g0012 a0003c0002t0002g0015 others(3): Show |
9 | HG00423.hp2 HG01069.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1690+2608C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542115 | |||||||
| chr13:113542118 | C | T | 71 | a0001c0009t0004g0281 a0001c0009t0004g0282 a0001c0009t0004g0283 others(68): Show |
82 | HG00423.hp1 HG00423.hp2 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.1690+2611C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542118 | |||||||
| chr13:113542122 | A | ATGTGTGG others(107): Show |
8 | a0003c0002t0002g0060 a0003c0002t0002g0061 a0003c0002t0002g0062 others(5): Show |
8 | NA18953.hp1 NA18955.hp1 NA18975.hp2 others(5): Show |
intron_variant | MODIFIER | c.1690+2634_1690+263 others(118): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113542122 | ||||||
| chr13:113542122 | A | T | 3 | a0005c0011t0008g0306 a0005c0011t0008g0307 a0008c0018t0004g0085 |
3 | HG02027.hp1 HG02129.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1690+2615A>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542122 | |||||||
| chr13:113542137 | G | A | 6 | a0003c0002t0002g0011 a0003c0002t0002g0012 a0003c0002t0002g0015 others(3): Show |
9 | HG00423.hp2 HG01069.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1690+2630G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542137 | |||||||
| chr13:113542142 | C | T | 54 | a0001c0009t0004g0281 a0001c0009t0004g0282 a0001c0009t0004g0283 others(51): Show |
62 | HG00423.hp1 HG00609.hp1 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.1690+2635C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542142 | |||||||
| chr13:113542144 | G | A | 93 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(90): Show |
106 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.1690+2637G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542144 | |||||||
| chr13:113542146 | C | T | 1 | a0003c0002t0002g0051 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1690+2639C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542146 | |||||||
| chr13:113542150 | G | C | 18 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(15): Show |
19 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(16): Show |
intron_variant | MODIFIER | c.1690+2643G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542150 | |||||||
| chr13:113542163 | C | T | 2 | a0002c0004t0004g0017 a0002c0004t0004g0086 |
3 | HG02145.hp1 HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1690+2656C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542163 | |||||||
| chr13:113542171 | C | T | 6 | a0003c0002t0002g0011 a0003c0002t0002g0012 a0003c0002t0002g0015 others(3): Show |
9 | HG00423.hp2 HG01069.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1690+2664C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542171 | |||||||
| chr13:113542172 | C | CGCCGAGA others(109): Show |
1 | a0001c0001t0001g0141 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1690+2673_1690+267 others(120): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113542172 | ||||||
| chr13:113542172 | C | T | 18 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(15): Show |
19 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(16): Show |
intron_variant | MODIFIER | c.1690+2665C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542172 | |||||||
| chr13:113542175 | C | T | 61 | a0001c0001t0004g0099 a0001c0009t0004g0281 a0001c0009t0004g0282 others(58): Show |
72 | HG00423.hp1 HG00423.hp2 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.1690+2668C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542175 | |||||||
| chr13:113542186 | G | T | 1 | a0002c0003t0003g0249 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1690+2679G>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542186 | |||||||
| chr13:113542189 | G | A | 72 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(69): Show |
81 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.1690+2682G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542189 | |||||||
| chr13:113542190 | A | C | 72 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(69): Show |
81 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.1690+2683A>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542190 | |||||||
| chr13:113542191 | T | C | 72 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(69): Show |
81 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.1690+2684T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542191 | |||||||
| chr13:113542194 | G | A | 3 | a0001c0009t0004g0281 a0001c0009t0004g0282 a0001c0009t0004g0283 |
3 | HG02717.hp1 HG03516.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1690+2687G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542194 | |||||||
| chr13:113542199 | C | T | 6 | a0003c0002t0002g0011 a0003c0002t0002g0012 a0003c0002t0002g0015 others(3): Show |
9 | HG00423.hp2 HG01069.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1690+2692C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542199 | |||||||
| chr13:113542200 | G | A | 1 | a0003c0002t0002g0043 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1690+2693G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542200 | |||||||
| chr13:113542201 | G | A | 92 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(89): Show |
105 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.1690+2694G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542201 | |||||||
| chr13:113542203 | C | T | 54 | a0001c0009t0004g0281 a0001c0009t0004g0282 a0001c0009t0004g0283 others(51): Show |
62 | HG00423.hp1 HG00609.hp1 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.1690+2696C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542203 | |||||||
| chr13:113542207 | G | C | 31 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(28): Show |
33 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.1690+2700G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542207 | |||||||
| chr13:113542229 | C | T | 23 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(20): Show |
25 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(22): Show |
intron_variant | MODIFIER | c.1690+2722C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542229 | |||||||
| chr13:113542232 | C | T | 61 | a0001c0006t0001g0222 a0001c0009t0004g0281 a0001c0009t0004g0282 others(58): Show |
72 | HG00423.hp1 HG00423.hp2 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.1690+2725C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542232 | |||||||
| chr13:113542236 | A | ATGTGTGG others(50): Show |
6 | a0003c0002t0002g0011 a0003c0002t0002g0012 a0003c0002t0002g0015 others(3): Show |
9 | HG00423.hp2 HG01069.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1690+2738_1690+273 others(61): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113542236 | ||||||
| chr13:113542236 | A | T | 54 | a0001c0009t0004g0281 a0001c0009t0004g0282 a0001c0009t0004g0283 others(51): Show |
62 | HG00423.hp1 HG00609.hp1 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.1690+2729A>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542236 | |||||||
| chr13:113542246 | G | A | 23 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(20): Show |
25 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(22): Show |
intron_variant | MODIFIER | c.1690+2739G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542246 | |||||||
| chr13:113542247 | A | C | 23 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(20): Show |
25 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(22): Show |
intron_variant | MODIFIER | c.1690+2740A>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542247 | |||||||
| chr13:113542248 | T | C | 23 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(20): Show |
25 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(22): Show |
intron_variant | MODIFIER | c.1690+2741T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542248 | |||||||
| chr13:113542250 | C | T | 1 | a0003c0002t0002g0050 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1690+2743C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542250 | |||||||
| chr13:113542258 | G | A | 91 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(88): Show |
104 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.1690+2751G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542258 | |||||||
| chr13:113542260 | C | T | 16 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(13): Show |
17 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(14): Show |
intron_variant | MODIFIER | c.1690+2753C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542260 | |||||||
| chr13:113542286 | C | T | 62 | a0002c0003t0003g0002 a0002c0003t0003g0007 a0002c0003t0003g0029 others(59): Show |
72 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.1690+2779C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542286 | |||||||
| chr13:113542287 | G | A | 18 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(15): Show |
19 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(16): Show |
intron_variant | MODIFIER | c.1690+2780G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542287 | |||||||
| chr13:113542289 | C | T | 80 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(77): Show |
91 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.1690+2782C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542289 | |||||||
| chr13:113542308 | G | A | 7 | a0002c0004t0005g0286 a0002c0004t0005g0287 a0002c0004t0005g0289 others(4): Show |
8 | HG02451.hp2 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1690+2801G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542308 | |||||||
| chr13:113542311 | C | T | 1 | a0002c0003t0003g0272 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1690+2804C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542311 | |||||||
| chr13:113542315 | G | A | 147 | a0001c0001t0001g0087 a0001c0001t0004g0018 a0001c0001t0004g0093 others(144): Show |
170 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.1690+2808G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542315 | |||||||
| chr13:113542315 | G | GTCGCTGA others(50): Show |
1 | a0001c0001t0001g0285 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1690+2864_1690+286 others(61): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113542315 | ||||||
| chr13:113542315 | G | GTCGCTGA others(563): Show |
2 | a0001c0006t0001g0235 a0001c0006t0001g0236 |
2 | HG00280.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.1690+2838_1690+283 others(574): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113542315 | ||||||
| chr13:113542315 | G | GTCGCTGA others(563): Show |
1 | a0001c0006t0001g0227 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1690+2838_1690+283 others(574): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113542315 | ||||||
| chr13:113542315 | G | GTCGCTGA others(563): Show |
12 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(9): Show |
13 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(10): Show |
intron_variant | MODIFIER | c.1690+2838_1690+283 others(574): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113542315 | ||||||
| chr13:113542315 | G | GTCGCTGA others(449): Show |
1 | a0001c0006t0001g0222 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1690+2835_1690+283 others(460): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113542315 | ||||||
| chr13:113542321 | G | C | 61 | a0001c0009t0004g0281 a0001c0009t0004g0282 a0001c0009t0004g0283 others(58): Show |
72 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.1690+2814G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542321 | |||||||
| chr13:113542321 | G | GATCACTG others(278): Show |
1 | a0003c0002t0002g0043 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1690+2835_1690+283 others(289): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113542321 | ||||||
| chr13:113542332 | T | TGCTTTAT others(107): Show |
1 | a0001c0001t0001g0168 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1690+2906_1690+290 others(118): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113542332 | ||||||
| chr13:113542342 | C | T | 62 | a0002c0003t0003g0002 a0002c0003t0003g0007 a0002c0003t0003g0029 others(59): Show |
72 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.1690+2835C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542342 | |||||||
| chr13:113542343 | C | T | 1 | a0003c0002t0002g0052 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1690+2836C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542343 | |||||||
| chr13:113542346 | C | CGAGATGT others(278): Show |
1 | a0001c0001t0013g0084 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1690+2892_1690+289 others(289): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113542346 | ||||||
| chr13:113542346 | C | CGAGATGT others(164): Show |
1 | a0001c0001t0001g0088 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1690+2892_1690+289 others(175): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113542346 | ||||||
| chr13:113542346 | C | T | 1 | a0003c0002t0002g0052 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1690+2839C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542346 | |||||||
| chr13:113542364 | C | T | 1 | a0001c0009t0004g0283 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1690+2857C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542364 | |||||||
| chr13:113542370 | C | T | 2 | a0003c0002t0002g0277 a0003c0002t0002g0278 |
2 | NA19060.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1690+2863C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542370 | |||||||
| chr13:113542372 | G | A | 130 | a0002c0003t0003g0002 a0002c0003t0003g0007 a0002c0003t0003g0029 others(127): Show |
151 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.1690+2865G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542372 | |||||||
| chr13:113542529 | G | T | 62 | a0002c0003t0003g0002 a0002c0003t0003g0007 a0002c0003t0003g0029 others(59): Show |
72 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.1690+3022G>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542529 | |||||||
| chr13:113542550 | T | C | 22 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(19): Show |
24 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(21): Show |
intron_variant | MODIFIER | c.1690+3043T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542550 | |||||||
| chr13:113542611 | T | A | 60 | a0002c0003t0003g0002 a0002c0003t0003g0007 a0002c0003t0003g0029 others(57): Show |
70 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.1690+3104T>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542611 | |||||||
| chr13:113542653 | G | T | 1 | a0001c0005t0001g0109 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1690+3146G>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542653 | |||||||
| chr13:113542760 | T | A | 1 | a0002c0003t0003g0249 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1690+3253T>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542760 | |||||||
| chr13:113542799 | G | A | 1 | a0001c0001t0001g0210 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1690+3292G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542799 | |||||||
| chr13:113542826 | T | G | 62 | a0002c0003t0003g0002 a0002c0003t0003g0007 a0002c0003t0003g0029 others(59): Show |
72 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.1690+3319T>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542826 | |||||||
| chr13:113542856 | C | T | 1 | a0003c0002t0002g0047 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1690+3349C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542856 | |||||||
| chr13:113542903 | G | A | 6 | a0003c0002t0002g0010 a0003c0002t0002g0034 a0003c0002t0002g0035 others(3): Show |
7 | HG01891.hp2 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1690+3396G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542903 | |||||||
| chr13:113542937 | T | C | 126 | a0002c0003t0003g0002 a0002c0003t0003g0007 a0002c0003t0003g0029 others(123): Show |
146 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.1690+3430T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542937 | |||||||
| chr13:113542944 | CTCCTGAC others(23): Show |
C | 1 | a0002c0003t0003g0249 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1690+3439_1690+346 others(34): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113542944 | ||||||
| chr13:113542956 | A | G | 2 | a0003c0002t0002g0041 a0003c0002t0002g0042 |
2 | HG02976.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1690+3449A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542956 | |||||||
| chr13:113542982 | C | T | 15 | a0001c0001t0004g0096 a0001c0001t0004g0100 a0001c0001t0004g0101 others(12): Show |
16 | HG01884.hp1 HG01993.hp2 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.1690+3475C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542982 | |||||||
| chr13:113542993 | C | G | 2 | a0002c0003t0003g0274 a0002c0003t0003g0275 |
2 | HG02080.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.1690+3486C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542993 | |||||||
| chr13:113542995 | C | T | 2 | a0001c0001t0009g0303 a0001c0001t0009g0304 |
2 | HG00639.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1690+3488C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542995 | |||||||
| chr13:113542997 | G | T | 1 | a0001c0001t0001g0141 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1690+3490G>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542997 | |||||||
| chr13:113542999 | T | G | 1 | a0001c0001t0001g0141 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1690+3492T>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113542999 | |||||||
| chr13:113543000 | G | C | 1 | a0001c0001t0001g0141 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1690+3493G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543000 | |||||||
| chr13:113543006 | T | G | 1 | a0001c0001t0001g0141 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1690+3499T>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543006 | |||||||
| chr13:113543007 | G | A | 1 | a0001c0001t0001g0141 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1690+3500G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543007 | |||||||
| chr13:113543014 | T | C | 1 | a0001c0001t0001g0141 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1690+3507T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543014 | |||||||
| chr13:113543028 | C | T | 10 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0106 others(7): Show |
10 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1690+3521C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543028 | |||||||
| chr13:113543034 | T | TCCCGCCT others(44): Show |
1 | a0001c0001t0001g0141 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1690+3529_1690+353 others(55): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543034 | ||||||
| chr13:113543036 | CGT | C | 154 | a0001c0001t0001g0026 a0001c0001t0001g0116 a0001c0001t0004g0018 others(151): Show |
178 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.1690+3537_1690+353 others(6): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543036 | ||||||
| chr13:113543041 | G | C | 1 | a0003c0002t0002g0049 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1690+3534G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543041 | |||||||
| chr13:113543043 | GTGACCCC others(422): Show |
G | 1 | a0002c0003t0003g0261 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1690+3558_1691-380 others(4): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543043 | ||||||
| chr13:113543045 | G | A | 1 | a0002c0003t0003g0249 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1690+3538G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543045 | |||||||
| chr13:113543046 | A | C | 1 | a0002c0003t0003g0249 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1690+3539A>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543046 | |||||||
| chr13:113543053 | C | A | 1 | a0001c0001t0001g0141 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1690+3546C>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543053 | |||||||
| chr13:113543067 | C | CCCCAGCC others(68): Show |
1 | a0005c0011t0008g0307 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1690+3560_1690+356 others(79): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543067 | |||||||
| chr13:113543067 | C | T | 1 | a0002c0003t0003g0251 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1690+3560C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543067 | |||||||
| chr13:113543068 | T | C | 3 | a0002c0003t0003g0251 a0003c0002t0002g0049 a0005c0011t0008g0307 |
3 | HG00423.hp1 HG02027.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1690+3561T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543068 | |||||||
| chr13:113543077 | A | ACCTCTGT others(154): Show |
1 | a0002c0003t0003g0263 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1690+3578_1690+357 others(165): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543077 | ||||||
| chr13:113543077 | A | C | 2 | a0003c0002t0002g0036 a0005c0011t0008g0307 |
2 | HG02027.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1690+3570A>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543077 | |||||||
| chr13:113543080 | T | C | 2 | a0002c0003t0003g0251 a0003c0002t0002g0049 |
2 | HG00423.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1690+3573T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543080 | |||||||
| chr13:113543080 | T | TGTCCGTG others(151): Show |
1 | a0003c0002t0002g0036 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1690+3573_1690+357 others(162): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543080 | |||||||
| chr13:113543085 | C | G | 1 | a0003c0002t0002g0036 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1690+3578C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543085 | |||||||
| chr13:113543086 | T | C | 48 | a0001c0001t0001g0116 a0002c0003t0003g0002 a0002c0003t0003g0029 others(45): Show |
53 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.1690+3579T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543086 | |||||||
| chr13:113543087 | GT | G | 45 | a0001c0001t0001g0116 a0002c0003t0003g0002 a0002c0003t0003g0029 others(42): Show |
52 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.1690+3581delT | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543087 | |||||||
| chr13:113543089 | G | T | 1 | a0003c0002t0002g0036 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1690+3582G>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543089 | |||||||
| chr13:113543090 | AC | A | 44 | a0001c0001t0001g0116 a0002c0003t0003g0002 a0002c0003t0003g0241 others(41): Show |
51 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.1690+3588delC | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543090 | ||||||
| chr13:113543091 | C | CCCCCACC others(68): Show |
1 | a0001c0001t0001g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1690+3604_1690+360 others(79): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543091 | ||||||
| chr13:113543093 | C | A | 1 | a0002c0003t0003g0263 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1690+3586C>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543093 | |||||||
| chr13:113543093 | C | CCACCTCC others(70): Show |
1 | a0002c0003t0003g0029 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1690+3587_1690+358 others(81): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543093 | ||||||
| chr13:113543093 | C | CCCACCTC others(67): Show |
1 | a0001c0001t0001g0087 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1690+3606_1690+360 others(78): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543093 | ||||||
| chr13:113543093 | C | CCCACCTC others(76): Show |
5 | a0001c0001t0013g0084 a0003c0002t0002g0010 a0003c0002t0002g0034 others(2): Show |
6 | HG01891.hp2 HG02109.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1690+3604_1690+360 others(87): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543093 | ||||||
| chr13:113543093 | C | CCCACCTC others(150): Show |
1 | a0001c0001t0001g0285 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1690+3604_1690+360 others(161): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543093 | ||||||
| chr13:113543093 | C | CCCACCTC others(76): Show |
1 | a0001c0007t0006g0280 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1690+3604_1690+360 others(87): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543093 | ||||||
| chr13:113543104 | C | T | 1 | a0003c0002t0002g0036 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1690+3597C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543104 | |||||||
| chr13:113543107 | C | G | 1 | a0003c0002t0002g0049 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1690+3600C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543107 | |||||||
| chr13:113543114 | C | T | 2 | a0002c0003t0003g0251 a0002c0003t0003g0263 |
2 | HG01255.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.1690+3607C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543114 | |||||||
| chr13:113543115 | A | AGCCCTCC others(68): Show |
1 | a0001c0001t0004g0098 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1690+3638_1690+363 others(79): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543115 | ||||||
| chr13:113543115 | A | AGCCCTCC others(111): Show |
11 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0219 others(8): Show |
12 | HG00544.hp2 HG00621.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.1690+3638_1690+363 others(122): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543115 | ||||||
| chr13:113543115 | A | AGCCCTCC others(191): Show |
1 | a0001c0006t0001g0218 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1690+3638_1690+363 others(202): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543115 | ||||||
| chr13:113543115 | A | C | 87 | a0001c0001t0001g0087 a0001c0001t0001g0106 a0001c0001t0001g0150 others(84): Show |
99 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.1690+3608A>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543115 | |||||||
| chr13:113543115 | A | T | 47 | a0001c0001t0001g0116 a0001c0006t0001g0227 a0001c0006t0001g0235 others(44): Show |
54 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.1690+3608A>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543115 | |||||||
| chr13:113543122 | C | CCT | 4 | a0001c0001t0001g0087 a0001c0001t0001g0285 a0001c0007t0006g0280 others(1): Show |
4 | HG02280.hp1 NA19043.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.1690+3616_1690+361 others(6): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543122 | ||||||
| chr13:113543122 | C | CCTGTCCG others(109): Show |
11 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(8): Show |
12 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(9): Show |
intron_variant | MODIFIER | c.1690+3638_1690+363 others(120): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543122 | ||||||
| chr13:113543122 | C | CCTGTCCG others(190): Show |
1 | a0002c0004t0004g0086 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1690+3638_1690+363 others(201): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543122 | ||||||
| chr13:113543122 | C | CCTGTCCG others(271): Show |
1 | a0005c0011t0008g0306 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1690+3638_1690+363 others(282): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543122 | ||||||
| chr13:113543122 | C | CCTGTCCG others(34): Show |
2 | a0001c0009t0004g0281 a0001c0009t0004g0282 |
2 | HG02717.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1690+3638_1690+363 others(45): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543122 | ||||||
| chr13:113543122 | C | CCTGTCTG others(227): Show |
1 | a0001c0006t0001g0227 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1690+3620_1690+362 others(238): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543122 | ||||||
| chr13:113543122 | C | CCTGTCTG others(268): Show |
2 | a0001c0006t0001g0235 a0001c0006t0001g0236 |
2 | HG00280.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.1690+3620_1690+362 others(279): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543122 | ||||||
| chr13:113543122 | C | T | 1 | a0003c0002t0002g0049 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1690+3615C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543122 | |||||||
| chr13:113543128 | C | CGGACCCC others(33): Show |
1 | a0002c0003t0003g0274 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1690+3622_1690+362 others(44): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543128 | ||||||
| chr13:113543128 | C | T | 39 | a0001c0001t0001g0116 a0002c0003t0003g0002 a0002c0003t0003g0238 others(36): Show |
41 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.1690+3621C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543128 | |||||||
| chr13:113543132 | A | ACCACCTC others(104): Show |
2 | a0003c0002t0002g0277 a0003c0002t0002g0278 |
2 | NA19060.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1690+3638_1690+363 others(115): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543132 | ||||||
| chr13:113543132 | ACCACCTC others(35): Show |
A | 1 | a0002c0003t0003g0002 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1690+3639_1690+368 others(46): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543132 | ||||||
| chr13:113543132 | ACCACCTC others(274): Show |
A | 2 | a0003c0002t0002g0068 a0003c0002t0002g0069 |
2 | HG00673.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1690+3628_1691-388 others(4): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543132 | ||||||
| chr13:113543135 | A | C | 1 | a0008c0018t0004g0085 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1690+3628A>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543135 | |||||||
| chr13:113543138 | T | A | 1 | a0008c0018t0004g0085 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1690+3631T>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543138 | |||||||
| chr13:113543146 | G | C | 74 | a0001c0001t0001g0088 a0001c0001t0001g0116 a0001c0001t0009g0303 others(71): Show |
82 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.1690+3639G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543146 | |||||||
| chr13:113543148 | G | GCCCCACC others(218): Show |
2 | a0001c0001t0009g0303 a0001c0001t0009g0304 |
2 | HG00639.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1690+3645_1690+364 others(229): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543148 | ||||||
| chr13:113543148 | G | GCCCCCCG others(33): Show |
1 | a0001c0001t0001g0088 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1690+3652_1690+365 others(44): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543148 | ||||||
| chr13:113543148 | G | T | 1 | a0008c0018t0004g0085 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1690+3641G>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543148 | |||||||
| chr13:113543150 | C | CCCACCTC others(30): Show |
1 | a0002c0004t0004g0017 | 2 | HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1690+3645_1690+364 others(41): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543150 | ||||||
| chr13:113543150 | C | CCCACCTC others(29): Show |
1 | a0001c0006t0001g0226 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1690+3645_1690+364 others(40): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543150 | ||||||
| chr13:113543150 | C | T | 42 | a0001c0001t0001g0116 a0001c0006t0001g0235 a0001c0006t0001g0236 others(39): Show |
44 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(41): Show |
intron_variant | MODIFIER | c.1690+3643C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543150 | |||||||
| chr13:113543153 | C | T | 8 | a0002c0003t0003g0002 a0002c0003t0003g0243 a0002c0003t0003g0244 others(5): Show |
10 | HG00423.hp1 HG01261.hp1 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.1690+3646C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543153 | |||||||
| chr13:113543154 | C | T | 3 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0008c0018t0004g0085 |
3 | HG00639.hp1 HG02717.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1690+3647C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543154 | |||||||
| chr13:113543159 | T | C | 3 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0008c0018t0004g0085 |
3 | HG00639.hp1 HG02717.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1690+3652T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543159 | |||||||
| chr13:113543159 | TAC | T | 16 | a0001c0001t0001g0116 a0002c0003t0003g0238 a0002c0003t0003g0245 others(13): Show |
16 | HG00438.hp2 HG01952.hp2 HG02080.hp2 others(13): Show |
intron_variant | MODIFIER | c.1690+3653_1690+365 others(6): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543159 | |||||||
| chr13:113543160 | A | C | 55 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(52): Show |
63 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.1690+3653A>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543160 | |||||||
| chr13:113543163 | T | C | 16 | a0001c0001t0001g0116 a0002c0003t0003g0238 a0002c0003t0003g0245 others(13): Show |
16 | HG00438.hp2 HG01952.hp2 HG02080.hp2 others(13): Show |
intron_variant | MODIFIER | c.1690+3656T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543163 | |||||||
| chr13:113543163 | T | TGTCCGTG others(65): Show |
10 | a0002c0003t0003g0002 a0002c0003t0003g0243 a0002c0003t0003g0244 others(7): Show |
12 | HG00099.hp2 HG01261.hp1 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.1690+3656_1690+365 others(76): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543163 | |||||||
| chr13:113543163 | T | TGTCCGTG others(66): Show |
1 | a0002c0004t0005g0294 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1690+3656_1690+365 others(77): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543163 | |||||||
| chr13:113543163 | T | TGTCCGTG others(104): Show |
1 | a0002c0003t0003g0257 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1690+3656_1690+365 others(115): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543163 | |||||||
| chr13:113543163 | T | TGTCCGTG others(104): Show |
12 | a0002c0003t0003g0002 a0002c0003t0003g0242 a0002c0003t0003g0247 others(9): Show |
12 | HG01109.hp1 HG01123.hp2 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.1690+3656_1690+365 others(115): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543163 | |||||||
| chr13:113543163 | T | TGTCCGTG others(105): Show |
1 | a0002c0003t0003g0269 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1690+3656_1690+365 others(116): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543163 | |||||||
| chr13:113543163 | T | TGTCCGTG others(221): Show |
1 | a0002c0004t0005g0295 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1690+3656_1690+365 others(232): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543163 | |||||||
| chr13:113543163 | T | TGTCCGTG others(220): Show |
1 | a0002c0003t0003g0264 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1690+3656_1690+365 others(231): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543163 | |||||||
| chr13:113543163 | T | TGTCCGTG others(104): Show |
1 | a0002c0003t0003g0241 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1690+3656_1690+365 others(115): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543163 | |||||||
| chr13:113543163 | T | TGTCCGTG others(147): Show |
3 | a0002c0003t0003g0002 a0002c0003t0003g0266 a0002c0019t0003g0002 |
3 | HG00621.hp2 HG01123.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.1690+3656_1690+365 others(158): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543163 | |||||||
| chr13:113543163 | T | TGTCCGTG others(104): Show |
1 | a0002c0003t0003g0002 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1690+3656_1690+365 others(115): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543163 | |||||||
| chr13:113543165 | T | A | 1 | a0002c0003t0003g0249 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1690+3658T>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543165 | |||||||
| chr13:113543165 | T | C | 29 | a0002c0003t0003g0002 a0002c0003t0003g0241 a0002c0003t0003g0242 others(26): Show |
34 | HG00099.hp2 HG00408.hp1 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.1690+3658T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543165 | |||||||
| chr13:113543170 | G | GT | 71 | a0001c0001t0001g0116 a0001c0006t0001g0027 a0001c0006t0001g0217 others(68): Show |
78 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.1690+3663_1690+366 others(5): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543170 | |||||||
| chr13:113543170 | G | GTGACCAC others(68): Show |
2 | a0002c0003t0003g0002 a0002c0003t0003g0251 |
2 | HG01981.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1690+3663_1690+366 others(79): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543170 | |||||||
| chr13:113543170 | G | GTGACCAC others(68): Show |
1 | a0003c0002t0002g0049 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1690+3663_1690+366 others(79): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543170 | |||||||
| chr13:113543172 | A | AC | 31 | a0002c0003t0003g0002 a0002c0003t0003g0241 a0002c0003t0003g0242 others(28): Show |
37 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(34): Show |
intron_variant | MODIFIER | c.1690+3669dupC | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543172 | ||||||
| chr13:113543172 | A | ACCCCACC others(109): Show |
1 | a0003c0002t0002g0083 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1690+3687_1690+368 others(120): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543172 | ||||||
| chr13:113543172 | ACC | A | 29 | a0001c0001t0001g0116 a0001c0006t0001g0027 a0001c0006t0001g0217 others(26): Show |
30 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.1690+3668_1690+366 others(6): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543172 | ||||||
| chr13:113543174 | C | CACCTCCT others(72): Show |
3 | a0001c0007t0006g0090 a0001c0007t0006g0091 a0001c0007t0006g0092 |
3 | HG02922.hp2 HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1690+3667_1690+366 others(83): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543174 | |||||||
| chr13:113543174 | C | CACCTCCT others(505): Show |
1 | a0005c0011t0008g0307 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1690+3667_1690+366 others(516): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543174 | |||||||
| chr13:113543174 | C | CCCACCTC others(32): Show |
1 | a0001c0006t0001g0226 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1690+3687_1690+368 others(43): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543174 | ||||||
| chr13:113543174 | C | CCCACCTC others(71): Show |
1 | a0005c0011t0008g0306 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1690+3687_1690+368 others(82): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543174 | ||||||
| chr13:113543174 | C | CCCACCTC others(32): Show |
6 | a0001c0001t0004g0100 a0001c0001t0004g0102 a0001c0001t0009g0303 others(3): Show |
6 | HG00639.hp1 HG01884.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1690+3684_1690+368 others(43): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543174 | ||||||
| chr13:113543174 | C | CCCCACCT others(117): Show |
1 | a0002c0004t0005g0290 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1690+3669_1690+367 others(128): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543174 | ||||||
| chr13:113543174 | C | CCCCACCT others(117): Show |
1 | a0002c0004t0005g0291 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1690+3669_1690+367 others(128): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543174 | ||||||
| chr13:113543179 | C | T | 2 | a0002c0004t0005g0290 a0002c0004t0005g0291 |
2 | HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1690+3672C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543179 | |||||||
| chr13:113543181 | C | G | 2 | a0004c0008t0004g0089 a0008c0018t0004g0085 |
2 | HG02717.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1690+3674C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543181 | |||||||
| chr13:113543183 | T | A | 1 | a0002c0003t0003g0249 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1690+3676T>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543183 | |||||||
| chr13:113543188 | C | T | 1 | a0002c0003t0003g0249 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1690+3681C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543188 | |||||||
| chr13:113543189 | T | G | 1 | a0002c0003t0003g0249 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1690+3682T>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543189 | |||||||
| chr13:113543190 | G | C | 1 | a0002c0003t0003g0249 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1690+3683G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543190 | |||||||
| chr13:113543192 | C | T | 8 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(5): Show |
9 | HG00544.hp1 HG00558.hp1 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.1690+3685C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543192 | |||||||
| chr13:113543195 | T | C | 84 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(81): Show |
99 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.1690+3688T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543195 | |||||||
| chr13:113543196 | C | T | 71 | a0001c0009t0004g0281 a0001c0009t0004g0282 a0001c0009t0004g0283 others(68): Show |
83 | HG00423.hp2 HG00597.hp2 HG00738.hp1 others(80): Show |
intron_variant | MODIFIER | c.1690+3689C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543196 | |||||||
| chr13:113543201 | T | C | 1 | a0002c0003t0003g0249 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1690+3694T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543201 | |||||||
| chr13:113543202 | C | CCCTGTCC others(32): Show |
1 | a0002c0004t0004g0017 | 2 | HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1690+3698_1690+369 others(43): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543202 | ||||||
| chr13:113543202 | C | T | 1 | a0002c0003t0003g0249 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1690+3695C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543202 | |||||||
| chr13:113543203 | C | CCTGTGTG others(28): Show |
3 | a0002c0003t0003g0250 a0002c0003t0003g0267 a0002c0003t0003g0268 |
3 | NA18999.hp2 NA19001.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1690+3698_1690+369 others(39): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543203 | ||||||
| chr13:113543203 | CCT | C | 68 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(65): Show |
82 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.1690+3699_1690+370 others(6): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543203 | ||||||
| chr13:113543205 | T | C | 1 | a0002c0003t0003g0249 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1690+3698T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543205 | |||||||
| chr13:113543205 | T | TCTGTCCG others(190): Show |
1 | a0001c0001t0004g0099 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1690+3725_1690+372 others(201): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543205 | ||||||
| chr13:113543205 | T | TGTCCGTG others(188): Show |
2 | a0001c0001t0004g0096 a0001c0001t0004g0101 |
2 | HG01993.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.1690+3698_1690+369 others(199): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543205 | |||||||
| chr13:113543205 | T | TGTCCGTG others(30): Show |
1 | a0004c0008t0004g0089 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1690+3698_1690+369 others(41): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543205 | |||||||
| chr13:113543205 | T | TGTCCGTG others(267): Show |
1 | a0002c0003t0003g0254 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1690+3698_1690+369 others(278): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543205 | |||||||
| chr13:113543205 | T | TGTCCGTG others(189): Show |
1 | a0002c0003t0003g0263 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1690+3698_1690+369 others(200): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543205 | |||||||
| chr13:113543205 | T | TGTCTGTG others(108): Show |
1 | a0003c0002t0002g0061 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1690+3698_1690+369 others(119): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543205 | |||||||
| chr13:113543205 | T | TGTCTGTG others(146): Show |
1 | a0003c0002t0002g0036 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1690+3698_1690+369 others(157): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543205 | |||||||
| chr13:113543205 | T | TGTCTGTG others(277): Show |
2 | a0003c0002t0002g0277 a0003c0002t0002g0278 |
2 | NA19060.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1690+3698_1690+369 others(288): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543205 | |||||||
| chr13:113543205 | T | TGTCTGTG others(108): Show |
1 | a0002c0004t0007g0028 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1690+3698_1690+369 others(119): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543205 | |||||||
| chr13:113543205 | T | TGTCTGTG others(149): Show |
1 | a0003c0002t0002g0072 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1690+3698_1690+369 others(160): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543205 | |||||||
| chr13:113543205 | T | TGTCTGTG others(230): Show |
2 | a0003c0002t0002g0033 a0003c0002t0002g0039 |
2 | HG03688.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1690+3698_1690+369 others(241): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543205 | |||||||
| chr13:113543205 | T | TGTCTGTG others(107): Show |
43 | a0002c0003t0003g0029 a0002c0003t0003g0239 a0002c0004t0005g0286 others(40): Show |
46 | HG00423.hp2 HG00738.hp1 HG01070.hp2 others(43): Show |
intron_variant | MODIFIER | c.1690+3698_1690+369 others(118): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543205 | |||||||
| chr13:113543205 | T | TGTCTGTG others(310): Show |
1 | a0002c0004t0004g0305 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1690+3698_1690+369 others(321): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543205 | |||||||
| chr13:113543205 | T | TGTCTGTG others(223): Show |
1 | a0003c0002t0002g0011 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1690+3698_1690+369 others(234): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543205 | |||||||
| chr13:113543205 | T | TGTCTGTG others(106): Show |
1 | a0003c0002t0002g0013 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1690+3698_1690+369 others(117): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543205 | |||||||
| chr13:113543205 | T | TGTCTGTG others(110): Show |
1 | a0010c0015t0002g0070 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1690+3698_1690+369 others(121): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543205 | |||||||
| chr13:113543205 | T | TGTCTGTG others(108): Show |
2 | a0003c0002t0002g0059 a0003c0002t0002g0065 |
2 | HG00597.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.1690+3698_1690+369 others(119): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543205 | |||||||
| chr13:113543205 | T | TGTCTGTG others(146): Show |
1 | a0002c0004t0005g0301 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1690+3698_1690+369 others(157): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543205 | |||||||
| chr13:113543205 | T | TGTCTGTG others(262): Show |
1 | a0002c0004t0005g0298 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1690+3698_1690+369 others(273): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543205 | |||||||
| chr13:113543211 | C | T | 13 | a0002c0003t0003g0007 a0002c0003t0003g0240 a0003c0002t0002g0005 others(10): Show |
20 | HG01069.hp2 HG01071.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1690+3704C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543211 | |||||||
| chr13:113543215 | ACCACCTC others(191): Show |
A | 2 | a0002c0004t0007g0028 a0002c0004t0007g0288 |
2 | HG02451.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1690+3711_1691-388 others(4): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543215 | ||||||
| chr13:113543221 | T | A | 21 | a0002c0003t0003g0002 a0002c0003t0003g0007 a0002c0003t0003g0238 others(18): Show |
27 | HG01069.hp2 HG01071.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.1690+3714T>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543221 | |||||||
| chr13:113543229 | C | T | 3 | a0002c0003t0003g0250 a0002c0003t0003g0267 a0002c0003t0003g0268 |
3 | NA18999.hp2 NA19001.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1690+3722C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543229 | |||||||
| chr13:113543231 | G | C | 1 | a0003c0016t0002g0074 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1690+3724G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543231 | |||||||
| chr13:113543233 | G | C | 4 | a0001c0001t0001g0141 a0002c0003t0003g0250 a0002c0003t0003g0267 others(1): Show |
4 | NA18979.hp1 NA18999.hp2 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.1690+3726G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543233 | |||||||
| chr13:113543233 | G | T | 1 | a0008c0018t0004g0085 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1690+3726G>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543233 | |||||||
| chr13:113543238 | T | C | 3 | a0002c0003t0003g0250 a0002c0003t0003g0267 a0002c0003t0003g0268 |
3 | NA18999.hp2 NA19001.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1690+3731T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543238 | |||||||
| chr13:113543239 | A | G | 4 | a0002c0003t0003g0250 a0002c0003t0003g0267 a0002c0003t0003g0268 others(1): Show |
4 | HG02717.hp2 NA18999.hp2 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.1690+3732A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543239 | |||||||
| chr13:113543244 | C | A | 1 | a0008c0018t0004g0085 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1690+3737C>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543244 | |||||||
| chr13:113543248 | G | C | 4 | a0002c0003t0003g0250 a0002c0003t0003g0267 a0002c0003t0003g0268 others(1): Show |
4 | HG02717.hp2 NA18999.hp2 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.1690+3741G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543248 | |||||||
| chr13:113543251 | T | TCC | 3 | a0002c0003t0003g0250 a0002c0003t0003g0267 a0002c0003t0003g0268 |
3 | NA18999.hp2 NA19001.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1690+3744_1690+374 others(6): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543251 | |||||||
| chr13:113543252 | G | C | 1 | a0008c0018t0004g0085 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1690+3745G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543252 | |||||||
| chr13:113543253 | T | C | 1 | a0008c0018t0004g0085 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1690+3746T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543253 | |||||||
| chr13:113543254 | T | G | 4 | a0002c0003t0003g0250 a0002c0003t0003g0267 a0002c0003t0003g0268 others(1): Show |
4 | HG02717.hp2 NA18999.hp2 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.1690+3747T>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543254 | |||||||
| chr13:113543255 | A | AC | 5 | a0001c0001t0001g0141 a0001c0001t0012g0151 a0002c0003t0003g0249 others(2): Show |
5 | HG01099.hp1 HG03688.hp1 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.1690+3753dupC | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543255 | ||||||
| chr13:113543255 | A | G | 1 | a0008c0018t0004g0085 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1690+3748A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543255 | |||||||
| chr13:113543256 | C | A | 1 | a0008c0018t0004g0085 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1690+3749C>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543256 | |||||||
| chr13:113543269 | T | C | 6 | a0001c0001t0001g0088 a0001c0001t0001g0135 a0002c0003t0003g0250 others(3): Show |
6 | HG02145.hp2 HG02717.hp2 NA18999.hp2 others(3): Show |
intron_variant | MODIFIER | c.1690+3762T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543269 | |||||||
| chr13:113543273 | T | C | 2 | a0001c0007t0006g0090 a0011c0017t0001g0284 |
2 | HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1690+3766T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543273 | |||||||
| chr13:113543274 | G | GTGCCC | 3 | a0002c0003t0003g0250 a0002c0003t0003g0267 a0002c0003t0003g0268 |
3 | NA18999.hp2 NA19001.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1690+3767_1690+376 others(9): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543274 | |||||||
| chr13:113543276 | C | A | 3 | a0002c0003t0003g0250 a0002c0003t0003g0267 a0002c0003t0003g0268 |
3 | NA18999.hp2 NA19001.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1690+3769C>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543276 | |||||||
| chr13:113543276 | C | CCCCCCGT others(274): Show |
1 | a0003c0002t0002g0008 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1690+3772_1690+377 others(285): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543276 | ||||||
| chr13:113543276 | C | CCCCCCGT others(275): Show |
3 | a0003c0002t0002g0008 a0006c0010t0002g0008 a0006c0010t0002g0055 |
3 | HG00609.hp1 NA18966.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.1690+3772_1690+377 others(286): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543276 | ||||||
| chr13:113543278 | C | T | 3 | a0001c0007t0006g0091 a0001c0007t0006g0092 a0011c0017t0001g0284 |
3 | HG02922.hp2 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1690+3771C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543278 | |||||||
| chr13:113543279 | CACT | C | 17 | a0001c0001t0001g0025 a0001c0005t0001g0126 a0001c0005t0001g0174 others(14): Show |
20 | HG01243.hp1 HG01361.hp1 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.1690+3773_1690+377 others(7): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543279 | |||||||
| chr13:113543280 | A | ACTCTGTC others(83): Show |
1 | a0001c0001t0001g0285 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1690+3801_1690+380 others(94): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543280 | ||||||
| chr13:113543280 | A | C | 5 | a0001c0001t0001g0088 a0001c0007t0006g0090 a0001c0007t0006g0091 others(2): Show |
5 | HG02145.hp2 HG02922.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1690+3773A>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543280 | |||||||
| chr13:113543280 | A | T | 7 | a0002c0003t0003g0250 a0002c0003t0003g0267 a0002c0003t0003g0268 others(4): Show |
8 | HG00609.hp1 HG02132.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1690+3773A>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543280 | |||||||
| chr13:113543282 | T | C | 7 | a0002c0003t0003g0250 a0002c0003t0003g0267 a0002c0003t0003g0268 others(4): Show |
8 | HG00609.hp1 HG02132.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1690+3775T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543282 | |||||||
| chr13:113543284 | T | C | 17 | a0001c0001t0001g0025 a0001c0005t0001g0126 a0001c0005t0001g0174 others(14): Show |
20 | HG01243.hp1 HG01361.hp1 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.1690+3777T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543284 | |||||||
| chr13:113543287 | C | G | 6 | a0002c0003t0003g0250 a0002c0003t0003g0267 a0002c0003t0003g0268 others(3): Show |
7 | HG00609.hp1 HG02132.hp2 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.1690+3780C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543287 | |||||||
| chr13:113543288 | C | CGTGACCC others(77): Show |
1 | a0003c0002t0002g0071 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1690+3804_1690+380 others(88): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543288 | ||||||
| chr13:113543288 | C | CGTGACCC others(517): Show |
1 | a0003c0002t0002g0046 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1690+3871_1690+387 others(528): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543288 | ||||||
| chr13:113543288 | C | CGTGACCC others(35): Show |
2 | a0001c0001t0001g0150 a0002c0003t0003g0265 |
2 | NA18952.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.1690+3804_1690+380 others(46): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543288 | ||||||
| chr13:113543288 | C | CGTGACCC others(122): Show |
2 | a0003c0002t0002g0048 a0003c0002t0002g0065 |
2 | HG00738.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.1690+3801_1690+380 others(133): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543288 | ||||||
| chr13:113543288 | C | CGTGACCC others(122): Show |
1 | a0005c0011t0008g0306 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1690+3801_1690+380 others(133): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543288 | ||||||
| chr13:113543288 | C | CGTGACCC others(80): Show |
14 | a0002c0003t0003g0002 a0002c0003t0003g0244 a0002c0003t0003g0245 others(11): Show |
15 | HG00438.hp2 HG00621.hp2 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.1690+3801_1690+380 others(91): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543288 | ||||||
| chr13:113543288 | C | CGTGACCC others(159): Show |
15 | a0003c0002t0002g0013 a0003c0002t0002g0014 a0003c0002t0002g0033 others(12): Show |
16 | HG00423.hp1 HG02622.hp1 HG03491.hp2 others(13): Show |
intron_variant | MODIFIER | c.1690+3801_1690+380 others(170): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543288 | ||||||
| chr13:113543288 | C | CGTGACCC others(241): Show |
1 | a0013c0021t0002g0056 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1690+3801_1690+380 others(252): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543288 | ||||||
| chr13:113543288 | C | CGTGACCC others(77): Show |
4 | a0001c0001t0004g0018 a0001c0001t0004g0096 a0001c0001t0004g0101 others(1): Show |
4 | HG00544.hp1 HG01993.hp2 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.1690+3801_1690+380 others(88): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543288 | ||||||
| chr13:113543288 | C | CGTGACCC others(77): Show |
2 | a0003c0002t0002g0277 a0003c0002t0002g0278 |
2 | NA19060.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1690+3801_1690+380 others(88): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543288 | ||||||
| chr13:113543288 | C | CGTGACCC others(158): Show |
1 | a0003c0002t0002g0061 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1690+3801_1690+380 others(169): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543288 | ||||||
| chr13:113543288 | C | CGTGACCC others(77): Show |
2 | a0003c0002t0002g0044 a0003c0002t0002g0051 |
2 | HG02559.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1690+3801_1690+380 others(88): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543288 | ||||||
| chr13:113543288 | C | T | 6 | a0002c0003t0003g0250 a0002c0003t0003g0267 a0002c0003t0003g0268 others(3): Show |
7 | HG00609.hp1 HG02132.hp2 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.1690+3781C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543288 | |||||||
| chr13:113543289 | G | GTGACCCC others(446): Show |
1 | a0002c0003t0003g0002 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1690+3801_1690+380 others(457): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543289 | ||||||
| chr13:113543292 | AC | A | 4 | a0002c0004t0005g0286 a0002c0004t0005g0287 a0002c0004t0005g0289 others(1): Show |
4 | HG02486.hp1 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1690+3790delC | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543292 | ||||||
| chr13:113543295 | C | CCCACCTC others(401): Show |
1 | a0003c0002t0002g0083 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1690+3801_1690+380 others(412): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543295 | ||||||
| chr13:113543295 | C | CCCACCTC others(400): Show |
1 | a0003c0002t0002g0082 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1690+3801_1690+380 others(411): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543295 | ||||||
| chr13:113543295 | C | CCCACCTC others(116): Show |
2 | a0002c0004t0004g0305 a0003c0002t0002g0080 |
2 | HG01168.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1690+3801_1690+380 others(127): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543295 | ||||||
| chr13:113543295 | C | CCCACCTC others(278): Show |
1 | a0010c0015t0002g0070 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1690+3801_1690+380 others(289): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543295 | ||||||
| chr13:113543300 | CTCCTCCC others(35): Show |
C | 3 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0184 |
3 | HG01109.hp2 HG02615.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1690+3810_1690+385 others(46): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543300 | ||||||
| chr13:113543309 | C | T | 95 | a0001c0001t0001g0087 a0001c0001t0001g0106 a0001c0001t0004g0018 others(92): Show |
105 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1690+3802C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543309 | |||||||
| chr13:113543311 | G | C | 1 | a0003c0002t0002g0038 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1690+3804G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543311 | |||||||
| chr13:113543311 | G | GAC | 7 | a0001c0001t0001g0088 a0001c0006t0001g0219 a0001c0007t0006g0090 others(4): Show |
7 | HG02135.hp1 HG02145.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1690+3804_1690+380 others(6): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543311 | |||||||
| chr13:113543311 | G | GCC | 87 | a0001c0001t0001g0087 a0001c0001t0004g0018 a0001c0001t0004g0093 others(84): Show |
97 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.1690+3808_1690+380 others(6): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543311 | ||||||
| chr13:113543311 | G | GCCCCCCC others(160): Show |
1 | a0003c0002t0002g0059 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1690+3809_1690+381 others(171): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543311 | ||||||
| chr13:113543311 | G | GT | 6 | a0001c0009t0004g0281 a0001c0009t0004g0282 a0001c0009t0004g0283 others(3): Show |
6 | HG02717.hp1 HG03516.hp2 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.1690+3804_1690+380 others(5): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543311 | |||||||
| chr13:113543312 | C | G | 6 | a0001c0009t0004g0281 a0001c0009t0004g0282 a0001c0009t0004g0283 others(3): Show |
6 | HG02717.hp1 HG03516.hp2 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.1690+3805C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543312 | |||||||
| chr13:113543315 | C | CCCCGCCC others(160): Show |
1 | a0003c0002t0002g0047 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1690+3809_1690+381 others(171): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543315 | ||||||
| chr13:113543315 | C | CT | 11 | a0002c0003t0003g0007 a0002c0003t0003g0239 a0002c0003t0003g0240 others(8): Show |
16 | HG01081.hp1 HG01175.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.1690+3808_1690+380 others(5): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543315 | |||||||
| chr13:113543316 | C | T | 7 | a0001c0001t0001g0088 a0001c0006t0001g0219 a0001c0007t0006g0090 others(4): Show |
7 | HG02135.hp1 HG02145.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1690+3809C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543316 | |||||||
| chr13:113543317 | G | A | 6 | a0001c0009t0004g0281 a0001c0009t0004g0282 a0001c0009t0004g0283 others(3): Show |
6 | HG02717.hp1 HG03516.hp2 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.1690+3810G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543317 | |||||||
| chr13:113543317 | G | C | 1 | a0002c0003t0003g0249 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1690+3810G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543317 | |||||||
| chr13:113543321 | TCC | T | 3 | a0001c0009t0004g0281 a0001c0009t0004g0282 a0001c0009t0004g0283 |
3 | HG02717.hp1 HG03516.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1690+3816_1690+381 others(6): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543321 | ||||||
| chr13:113543323 | C | CCTGTCCG others(68): Show |
1 | a0002c0003t0003g0273 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1690+3818_1690+381 others(79): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543323 | ||||||
| chr13:113543323 | C | CCTGTCCG others(152): Show |
2 | a0003c0002t0002g0005 a0003c0023t0002g0031 |
5 | HG01081.hp1 HG01175.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.1690+3818_1690+381 others(163): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543323 | ||||||
| chr13:113543323 | C | CCTGTCCG others(384): Show |
1 | a0003c0002t0002g0011 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1690+3818_1690+381 others(395): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543323 | ||||||
| chr13:113543323 | CCT | C | 9 | a0002c0003t0003g0007 a0002c0003t0003g0239 a0002c0003t0003g0240 others(6): Show |
11 | HG01243.hp1 HG02080.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1690+3819_1690+382 others(6): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543323 | ||||||
| chr13:113543325 | T | TGTGTGTG others(149): Show |
1 | a0002c0004t0005g0301 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1690+3818_1690+381 others(160): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543325 | |||||||
| chr13:113543330 | G | C | 109 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0106 others(106): Show |
124 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.1690+3823G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543330 | |||||||
| chr13:113543331 | G | C | 107 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0106 others(104): Show |
118 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.1690+3824G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543331 | |||||||
| chr13:113543331 | G | T | 9 | a0001c0009t0004g0281 a0001c0009t0004g0282 a0001c0009t0004g0283 others(6): Show |
12 | HG01081.hp1 HG01175.hp1 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.1690+3824G>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543331 | |||||||
| chr13:113543335 | A | AC | 60 | a0001c0001t0001g0087 a0001c0001t0004g0100 a0001c0001t0004g0102 others(57): Show |
67 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.1690+3829dupC | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543335 | ||||||
| chr13:113543335 | A | ACCCCCAC others(35): Show |
1 | a0002c0003t0003g0002 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1690+3829_1690+383 others(46): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543335 | ||||||
| chr13:113543335 | A | ACCCCCAC others(36): Show |
1 | a0002c0004t0005g0286 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1690+3829_1690+383 others(47): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543335 | ||||||
| chr13:113543335 | A | ACCCCCAC others(115): Show |
1 | a0003c0002t0002g0073 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1690+3829_1690+383 others(126): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543335 | ||||||
| chr13:113543335 | A | ACCCCCTC others(75): Show |
1 | a0001c0007t0006g0280 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1690+3829_1690+383 others(86): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543335 | ||||||
| chr13:113543335 | A | ACCCCCTC others(33): Show |
23 | a0002c0004t0005g0287 a0002c0004t0005g0289 a0003c0002t0002g0010 others(20): Show |
25 | HG01070.hp2 HG01243.hp2 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.1690+3829_1690+383 others(44): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543335 | ||||||
| chr13:113543335 | A | ACCCCCTC others(29): Show |
1 | a0003c0002t0002g0016 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1690+3829_1690+383 others(40): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543335 | ||||||
| chr13:113543335 | A | ACCCCCTC others(33): Show |
1 | a0001c0001t0001g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1690+3829_1690+383 others(44): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543335 | ||||||
| chr13:113543335 | ACT | A | 28 | a0001c0001t0001g0088 a0001c0001t0004g0018 a0001c0001t0004g0093 others(25): Show |
31 | HG00558.hp1 HG00597.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.1690+3830_1690+383 others(6): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543335 | ||||||
| chr13:113543337 | T | C | 87 | a0001c0001t0001g0087 a0001c0001t0001g0106 a0001c0001t0004g0100 others(84): Show |
99 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.1690+3830T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543337 | |||||||
| chr13:113543340 | A | C | 21 | a0001c0001t0001g0088 a0001c0001t0004g0018 a0001c0001t0004g0093 others(18): Show |
22 | HG00558.hp1 HG00597.hp1 HG02027.hp2 others(19): Show |
intron_variant | MODIFIER | c.1690+3833A>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543340 | |||||||
| chr13:113543342 | T | C | 113 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0106 others(110): Show |
130 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.1690+3835T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543342 | |||||||
| chr13:113543342 | T | TTCCTCCC others(398): Show |
1 | a0003c0002t0002g0030 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1690+3857_1690+385 others(409): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543342 | ||||||
| chr13:113543342 | T | TTCCTCCC others(153): Show |
2 | a0003c0002t0002g0014 a0003c0002t0002g0049 |
2 | HG00423.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.1690+3871_1690+387 others(164): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543342 | ||||||
| chr13:113543351 | C | T | 5 | a0001c0001t0001g0087 a0001c0001t0013g0084 a0001c0006t0001g0221 others(2): Show |
5 | HG02027.hp1 HG02109.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.1690+3844C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543351 | |||||||
| chr13:113543353 | G | GA | 21 | a0001c0001t0004g0100 a0001c0001t0004g0102 a0001c0001t0009g0303 others(18): Show |
22 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(19): Show |
intron_variant | MODIFIER | c.1690+3846_1690+384 others(5): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543353 | |||||||
| chr13:113543353 | G | GC | 7 | a0001c0001t0001g0087 a0001c0001t0001g0117 a0001c0001t0001g0161 others(4): Show |
7 | HG00741.hp1 HG02027.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1690+3852dupC | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543353 | ||||||
| chr13:113543353 | GC | G | 9 | a0001c0001t0001g0106 a0001c0001t0001g0140 a0001c0007t0006g0280 others(6): Show |
9 | HG02280.hp1 HG03579.hp2 HG03927.hp1 others(6): Show |
intron_variant | MODIFIER | c.1690+3852delC | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543353 | ||||||
| chr13:113543354 | C | CG | 8 | a0002c0003t0003g0007 a0002c0003t0003g0239 a0002c0003t0003g0240 others(5): Show |
10 | HG01243.hp1 HG02080.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1690+3847_1690+384 others(5): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543354 | |||||||
| chr13:113543354 | C | G | 1 | a0002c0003t0003g0002 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1690+3847C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543354 | |||||||
| chr13:113543354 | C | T | 46 | a0001c0001t0001g0088 a0001c0001t0004g0018 a0001c0001t0004g0093 others(43): Show |
50 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.1690+3847C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543354 | |||||||
| chr13:113543355 | C | G | 46 | a0001c0001t0001g0088 a0001c0001t0004g0018 a0001c0001t0004g0093 others(43): Show |
50 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.1690+3848C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543355 | |||||||
| chr13:113543359 | C | T | 29 | a0001c0001t0004g0100 a0001c0001t0004g0102 a0001c0001t0009g0303 others(26): Show |
32 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.1690+3852C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543359 | |||||||
| chr13:113543360 | G | A | 54 | a0001c0001t0001g0088 a0001c0001t0004g0018 a0001c0001t0004g0093 others(51): Show |
60 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.1690+3853G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543360 | |||||||
| chr13:113543366 | C | CCT | 35 | a0001c0001t0001g0087 a0001c0001t0001g0106 a0001c0001t0004g0100 others(32): Show |
37 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.1690+3860_1690+386 others(6): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543366 | ||||||
| chr13:113543366 | C | T | 6 | a0001c0007t0006g0090 a0001c0007t0006g0091 a0001c0007t0006g0092 others(3): Show |
8 | HG01069.hp2 HG01071.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1690+3859C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543366 | |||||||
| chr13:113543371 | C | G | 59 | a0001c0001t0001g0088 a0001c0001t0001g0106 a0001c0001t0004g0018 others(56): Show |
66 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.1690+3864C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543371 | |||||||
| chr13:113543372 | C | G | 8 | a0001c0001t0001g0106 a0001c0007t0006g0280 a0002c0003t0003g0002 others(5): Show |
9 | HG02071.hp1 HG02280.hp1 HG03579.hp2 others(6): Show |
intron_variant | MODIFIER | c.1690+3865C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543372 | |||||||
| chr13:113543372 | C | T | 54 | a0001c0001t0001g0088 a0001c0001t0004g0018 a0001c0001t0004g0093 others(51): Show |
60 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.1690+3865C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543372 | |||||||
| chr13:113543375 | G | T | 7 | a0002c0003t0003g0007 a0002c0003t0003g0239 a0002c0003t0003g0240 others(4): Show |
9 | HG01243.hp1 HG02080.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1690+3868G>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543375 | |||||||
| chr13:113543376 | A | AC | 65 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0004g0018 others(62): Show |
72 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.1690+3873dupC | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543376 | ||||||
| chr13:113543376 | ACC | A | 20 | a0002c0004t0005g0286 a0003c0002t0002g0005 a0003c0002t0002g0008 others(17): Show |
22 | HG00423.hp2 HG00597.hp2 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.1690+3872_1690+387 others(6): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543376 | ||||||
| chr13:113543376 | ACCCCACC others(30): Show |
A | 2 | a0001c0009t0004g0282 a0001c0009t0004g0283 |
2 | HG02717.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1690+3895_1691-386 others(41): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543376 | ||||||
| chr13:113543378 | C | CACCTCCT others(33): Show |
25 | a0002c0004t0005g0287 a0002c0004t0005g0289 a0003c0002t0002g0005 others(22): Show |
29 | HG01070.hp2 HG01175.hp1 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.1690+3871_1690+387 others(44): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543378 | |||||||
| chr13:113543378 | C | CACCTCCT others(75): Show |
1 | a0002c0003t0003g0271 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1690+3871_1690+387 others(86): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543378 | |||||||
| chr13:113543378 | C | CACCTCCT others(610): Show |
1 | a0003c0002t0002g0050 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1690+3871_1690+387 others(621): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543378 | |||||||
| chr13:113543378 | C | CCCCTCCT others(75): Show |
7 | a0001c0001t0004g0100 a0001c0001t0004g0102 a0001c0001t0009g0303 others(4): Show |
7 | HG00639.hp1 HG01884.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1690+3873_1690+387 others(86): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543378 | ||||||
| chr13:113543378 | C | CCCCTCCT others(75): Show |
1 | a0005c0011t0008g0307 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1690+3873_1690+387 others(86): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543378 | ||||||
| chr13:113543378 | C | T | 8 | a0001c0001t0001g0106 a0001c0007t0006g0280 a0002c0003t0003g0002 others(5): Show |
9 | HG02071.hp1 HG02280.hp1 HG03579.hp2 others(6): Show |
intron_variant | MODIFIER | c.1690+3871C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543378 | |||||||
| chr13:113543379 | CCA | C | 8 | a0001c0001t0013g0084 a0001c0006t0001g0219 a0001c0006t0001g0224 others(5): Show |
8 | HG00280.hp1 HG00544.hp2 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.1690+3874_1690+387 others(6): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543379 | ||||||
| chr13:113543383 | C | T | 42 | a0001c0001t0001g0106 a0001c0001t0004g0100 a0001c0001t0004g0102 others(39): Show |
47 | HG00639.hp1 HG01070.hp2 HG01175.hp1 others(44): Show |
intron_variant | MODIFIER | c.1690+3876C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543383 | |||||||
| chr13:113543387 | T | TCCCCCTG others(1): Show |
10 | a0001c0001t0001g0087 a0001c0006t0001g0027 a0001c0006t0001g0217 others(7): Show |
11 | HG00558.hp2 HG00621.hp1 HG00673.hp1 others(8): Show |
intron_variant | MODIFIER | c.1690+3887_1690+388 others(12): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543387 | ||||||
| chr13:113543389 | C | T | 7 | a0002c0003t0003g0007 a0002c0003t0003g0239 a0002c0003t0003g0240 others(4): Show |
9 | HG01243.hp1 HG02080.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1690+3882C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543389 | |||||||
| chr13:113543393 | T | C | 4 | a0001c0006t0001g0227 a0002c0003t0003g0245 a0002c0003t0003g0246 others(1): Show |
4 | HG00438.hp2 HG02129.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.1690+3886T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543393 | |||||||
| chr13:113543393 | T | TGCCCCC | 41 | a0001c0001t0001g0088 a0001c0001t0004g0018 a0001c0001t0004g0093 others(38): Show |
46 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.1690+3890_1690+389 others(10): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543393 | ||||||
| chr13:113543394 | G | GTGC | 7 | a0001c0006t0001g0219 a0001c0006t0001g0224 a0001c0006t0001g0225 others(4): Show |
7 | HG00280.hp1 HG00544.hp2 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.1690+3887_1690+388 others(7): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543394 | |||||||
| chr13:113543394 | GCCCTCCC others(45): Show |
G | 1 | a0001c0001t0013g0084 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1690+3888_1691-385 others(56): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543394 | |||||||
| chr13:113543398 | T | A | 7 | a0001c0006t0001g0219 a0001c0006t0001g0224 a0001c0006t0001g0225 others(4): Show |
7 | HG00280.hp1 HG00544.hp2 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.1690+3891T>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543398 | |||||||
| chr13:113543398 | T | C | 56 | a0001c0001t0001g0106 a0001c0001t0004g0100 a0001c0001t0004g0102 others(53): Show |
64 | HG00639.hp1 HG01069.hp2 HG01070.hp2 others(61): Show |
intron_variant | MODIFIER | c.1690+3891T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543398 | |||||||
| chr13:113543400 | C | A | 8 | a0002c0003t0003g0007 a0002c0003t0003g0239 a0002c0003t0003g0240 others(5): Show |
10 | HG01243.hp1 HG02080.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1690+3893C>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543400 | |||||||
| chr13:113543400 | C | CCT | 6 | a0001c0006t0001g0219 a0001c0006t0001g0224 a0001c0006t0001g0225 others(3): Show |
6 | HG00280.hp1 HG00544.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.1690+3896_1691-389 others(6): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543400 | ||||||
| chr13:113543400 | C | CGCCCT | 47 | a0001c0001t0001g0106 a0001c0001t0004g0100 a0001c0001t0004g0102 others(44): Show |
52 | HG00639.hp1 HG01070.hp2 HG01175.hp1 others(49): Show |
intron_variant | MODIFIER | c.1690+3893_1690+389 others(9): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543400 | |||||||
| chr13:113543400 | C | CGCCCTCC others(79): Show |
1 | a0003c0002t0002g0015 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1690+3893_1690+389 others(90): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543400 | |||||||
| chr13:113543402 | T | C | 52 | a0001c0001t0001g0106 a0001c0001t0001g0170 a0001c0001t0004g0100 others(49): Show |
58 | HG00423.hp1 HG00639.hp1 HG00741.hp2 others(55): Show |
intron_variant | MODIFIER | c.1690+3895T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543402 | |||||||
| chr13:113543402 | T | TCTGTGGG others(34): Show |
6 | a0002c0003t0003g0002 a0002c0003t0003g0243 a0002c0003t0003g0253 others(3): Show |
8 | HG01261.hp1 HG01928.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.1691-3894_1691-389 others(45): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543402 | ||||||
| chr13:113543402 | T | TCTGTGGG others(34): Show |
33 | a0001c0001t0001g0088 a0001c0001t0004g0018 a0001c0001t0004g0093 others(30): Show |
33 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.1691-3894_1691-389 others(45): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543402 | ||||||
| chr13:113543406 | T | C | 4 | a0001c0001t0001g0170 a0001c0009t0004g0281 a0002c0004t0004g0305 others(1): Show |
4 | HG00423.hp1 HG00741.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1691-3894T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543406 | |||||||
| chr13:113543406 | TCCATGAC others(30): Show |
T | 7 | a0001c0001t0001g0004 a0001c0001t0001g0165 a0002c0003t0003g0238 others(4): Show |
7 | HG02074.hp1 HG02717.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1691-3865_1691-382 others(41): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543406 | ||||||
| chr13:113543407 | C | G | 9 | a0001c0006t0001g0219 a0001c0006t0001g0224 a0001c0006t0001g0225 others(6): Show |
12 | HG00280.hp1 HG00544.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.1691-3893C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543407 | |||||||
| chr13:113543408 | C | G | 2 | a0002c0004t0004g0017 a0003c0002t0002g0005 |
5 | HG01081.hp1 HG01515.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1691-3892C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543408 | |||||||
| chr13:113543408 | C | T | 7 | a0001c0006t0001g0219 a0001c0006t0001g0224 a0001c0006t0001g0225 others(4): Show |
7 | HG00280.hp1 HG00544.hp2 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.1691-3892C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543408 | |||||||
| chr13:113543409 | A | G | 147 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0106 others(144): Show |
165 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.1691-3891A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543409 | |||||||
| chr13:113543412 | AC | A | 90 | a0001c0001t0001g0088 a0001c0001t0001g0106 a0001c0001t0001g0113 others(87): Show |
103 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.1691-3883delC | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543412 | ||||||
| chr13:113543413 | C | CCCCCACC others(236): Show |
1 | a0003c0002t0002g0062 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1691-3870_1691-386 others(247): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543413 | ||||||
| chr13:113543413 | C | CCCCCACC others(358): Show |
2 | a0003c0002t0002g0048 a0003c0002t0002g0065 |
2 | HG00738.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.1691-3869_1691-386 others(369): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543413 | ||||||
| chr13:113543413 | C | CCCCCACC others(115): Show |
1 | a0003c0002t0002g0013 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1691-3866_1691-386 others(126): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543413 | ||||||
| chr13:113543413 | C | CCCCCACC others(76): Show |
4 | a0001c0001t0001g0087 a0001c0001t0004g0096 a0001c0001t0004g0101 others(1): Show |
4 | HG01993.hp2 HG02273.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1691-3866_1691-386 others(87): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543413 | ||||||
| chr13:113543413 | C | CCCCCACC others(121): Show |
1 | a0002c0003t0003g0256 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1691-3872_1691-387 others(132): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543413 | ||||||
| chr13:113543413 | C | CCCCCACC others(117): Show |
1 | a0005c0011t0008g0306 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1691-3872_1691-387 others(128): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543413 | ||||||
| chr13:113543413 | C | CCCCCACC others(242): Show |
2 | a0003c0002t0002g0033 a0003c0002t0002g0039 |
2 | HG03688.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1691-3872_1691-387 others(253): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543413 | ||||||
| chr13:113543413 | C | CCCCCACC others(118): Show |
8 | a0003c0002t0002g0057 a0003c0002t0002g0058 a0003c0002t0002g0059 others(5): Show |
8 | HG00597.hp2 HG03491.hp2 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.1691-3872_1691-387 others(129): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543413 | ||||||
| chr13:113543413 | C | CCCCCACC others(199): Show |
2 | a0003c0002t0002g0046 a0003c0002t0002g0047 |
2 | HG03453.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1691-3872_1691-387 others(210): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543413 | ||||||
| chr13:113543413 | C | CCCCCACC others(238): Show |
3 | a0002c0003t0003g0248 a0003c0002t0002g0067 a0003c0002t0002g0076 |
3 | HG02015.hp1 NA18975.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.1691-3872_1691-387 others(249): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543413 | ||||||
| chr13:113543413 | C | CCCCCACC others(199): Show |
1 | a0013c0021t0002g0056 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1691-3872_1691-387 others(210): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543413 | ||||||
| chr13:113543413 | C | CCCCCACC others(160): Show |
1 | a0003c0002t0002g0040 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1691-3872_1691-387 others(171): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543413 | ||||||
| chr13:113543413 | C | CCCCCACC others(202): Show |
2 | a0003c0002t0002g0008 a0003c0002t0002g0083 |
2 | HG02132.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.1691-3872_1691-387 others(213): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543413 | ||||||
| chr13:113543413 | C | CCCCCACC others(195): Show |
1 | a0003c0002t0002g0008 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1691-3872_1691-387 others(206): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543413 | ||||||
| chr13:113543413 | C | CCCCCACC others(194): Show |
1 | a0003c0002t0002g0071 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1691-3872_1691-387 others(205): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543413 | ||||||
| chr13:113543413 | C | CCCCCCAC others(365): Show |
1 | a0010c0015t0002g0070 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1691-3883_1691-388 others(376): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543413 | ||||||
| chr13:113543413 | C | CCCCCTCC others(73): Show |
2 | a0006c0010t0002g0008 a0006c0010t0002g0055 |
2 | NA18966.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.1691-3883_1691-388 others(84): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543413 | ||||||
| chr13:113543413 | C | CCCCCTCC others(154): Show |
1 | a0002c0004t0005g0286 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1691-3883_1691-388 others(165): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543413 | ||||||
| chr13:113543413 | C | CCCCCTCC others(115): Show |
1 | a0001c0006t0001g0227 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1691-3883_1691-388 others(126): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543413 | ||||||
| chr13:113543413 | CCCCCACC others(29): Show |
C | 1 | a0002c0003t0003g0249 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1691-3882_1691-384 others(40): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543413 | ||||||
| chr13:113543415 | C | CCCTCCTC others(76): Show |
9 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(6): Show |
10 | HG00558.hp2 HG00621.hp1 HG00673.hp1 others(7): Show |
intron_variant | MODIFIER | c.1691-3883_1691-388 others(87): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543415 | ||||||
| chr13:113543415 | C | T | 2 | a0002c0004t0004g0017 a0003c0002t0002g0005 |
5 | HG01081.hp1 HG01515.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1691-3885C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543415 | |||||||
| chr13:113543418 | A | T | 1 | a0002c0004t0004g0086 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1691-3882A>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543418 | |||||||
| chr13:113543420 | C | T | 11 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(8): Show |
15 | HG00558.hp2 HG00621.hp1 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.1691-3880C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543420 | |||||||
| chr13:113543421 | TCCTCCCC others(4): Show |
T | 3 | a0001c0001t0004g0018 a0003c0002t0002g0051 a0003c0002t0002g0277 |
3 | HG00544.hp1 NA19060.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1691-3865_1691-385 others(15): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543421 | ||||||
| chr13:113543424 | T | TCCCCTTG others(1): Show |
6 | a0002c0003t0003g0007 a0002c0003t0003g0239 a0002c0003t0003g0240 others(3): Show |
8 | HG01243.hp1 HG02615.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1691-3872_1691-387 others(12): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543424 | ||||||
| chr13:113543428 | C | T | 1 | a0002c0004t0004g0086 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1691-3872C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543428 | |||||||
| chr13:113543429 | C | G | 1 | a0002c0004t0004g0086 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1691-3871C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543429 | |||||||
| chr13:113543429 | C | T | 1 | a0003c0002t0002g0278 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1691-3871C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543429 | |||||||
| chr13:113543430 | T | C | 7 | a0001c0006t0001g0227 a0002c0003t0003g0007 a0002c0003t0003g0239 others(4): Show |
9 | HG01243.hp1 HG02615.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.1691-3870T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543430 | |||||||
| chr13:113543432 | C | A | 3 | a0001c0006t0001g0224 a0001c0006t0001g0225 a0001c0006t0001g0234 |
3 | HG00544.hp2 HG02080.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.1691-3868C>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543432 | |||||||
| chr13:113543432 | C | CCCATGAC others(8): Show |
1 | a0001c0009t0004g0281 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1691-3866_1691-386 others(19): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543432 | ||||||
| chr13:113543432 | C | CCCCCCCG others(389): Show |
1 | a0003c0002t0002g0278 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1691-3866_1691-386 others(400): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543432 | ||||||
| chr13:113543432 | C | CCCCCCGC others(141): Show |
1 | a0003c0002t0002g0013 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1691-3866_1691-386 others(152): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543432 | ||||||
| chr13:113543432 | C | CCCTCCCC others(19): Show |
1 | a0001c0001t0001g0009 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1691-3832_1691-380 others(30): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543432 | ||||||
| chr13:113543432 | CCCTCCCC others(19): Show |
C | 5 | a0001c0001t0001g0178 a0001c0005t0001g0172 a0001c0005t0001g0173 others(2): Show |
5 | HG01106.hp2 HG01515.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.1691-3832_1691-380 others(30): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543432 | ||||||
| chr13:113543433 | C | CCCCGCCC others(40): Show |
2 | a0001c0006t0001g0235 a0001c0006t0001g0236 |
2 | HG00280.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.1691-3866_1691-386 others(51): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543433 | ||||||
| chr13:113543435 | T | A | 2 | a0002c0003t0003g0274 a0002c0003t0003g0275 |
2 | HG02080.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.1691-3865T>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543435 | |||||||
| chr13:113543435 | T | C | 18 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(15): Show |
22 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(19): Show |
intron_variant | MODIFIER | c.1691-3865T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543435 | |||||||
| chr13:113543436 | C | A | 1 | a0002c0004t0004g0086 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1691-3864C>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543436 | |||||||
| chr13:113543437 | C | CGCCCT | 11 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(8): Show |
15 | HG00558.hp2 HG00621.hp1 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.1691-3863_1691-386 others(9): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543437 | |||||||
| chr13:113543437 | C | CGCCCTCC others(41): Show |
1 | a0003c0002t0002g0030 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1691-3863_1691-386 others(52): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543437 | |||||||
| chr13:113543437 | C | CTGCCCTC others(42): Show |
3 | a0001c0006t0001g0224 a0001c0006t0001g0225 a0001c0006t0001g0234 |
3 | HG00544.hp2 HG02080.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.1691-3863_1691-386 others(53): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543437 | |||||||
| chr13:113543437 | C | T | 2 | a0001c0006t0001g0235 a0001c0006t0001g0236 |
2 | HG00280.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.1691-3863C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543437 | |||||||
| chr13:113543439 | C | T | 70 | a0001c0001t0001g0087 a0001c0001t0001g0188 a0001c0001t0004g0018 others(67): Show |
76 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.1691-3861C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543439 | |||||||
| chr13:113543442 | G | C | 1 | a0001c0009t0004g0281 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1691-3858G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543442 | |||||||
| chr13:113543443 | C | T | 95 | a0001c0001t0001g0006 a0001c0001t0001g0087 a0001c0001t0001g0160 others(92): Show |
108 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.1691-3857C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543443 | |||||||
| chr13:113543444 | C | G | 4 | a0001c0006t0001g0219 a0002c0003t0003g0274 a0002c0003t0003g0275 others(1): Show |
4 | HG02080.hp2 HG02145.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.1691-3856C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543444 | |||||||
| chr13:113543445 | C | CCCCGCCC others(11): Show |
1 | a0001c0009t0004g0281 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1691-3855_1691-385 others(22): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543445 | |||||||
| chr13:113543445 | C | G | 1 | a0001c0006t0001g0219 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1691-3855C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543445 | |||||||
| chr13:113543445 | C | T | 3 | a0002c0003t0003g0274 a0002c0003t0003g0275 a0002c0004t0004g0086 |
3 | HG02080.hp2 HG02145.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1691-3855C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543445 | |||||||
| chr13:113543446 | A | G | 28 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(25): Show |
34 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.1691-3854A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543446 | |||||||
| chr13:113543449 | AC | A | 15 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(12): Show |
17 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(14): Show |
intron_variant | MODIFIER | c.1691-3846delC | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543449 | ||||||
| chr13:113543452 | C | A | 1 | a0001c0006t0001g0220 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1691-3848C>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543452 | |||||||
| chr13:113543452 | C | T | 1 | a0001c0006t0001g0219 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1691-3848C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543452 | |||||||
| chr13:113543453 | C | CCTCCTCC others(146): Show |
1 | a0003c0002t0002g0053 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1691-3846_1691-384 others(157): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543453 | ||||||
| chr13:113543455 | A | C | 1 | a0003c0002t0002g0005 | 3 | HG01081.hp1 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1691-3845A>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543455 | |||||||
| chr13:113543455 | A | T | 1 | a0001c0006t0001g0220 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1691-3845A>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543455 | |||||||
| chr13:113543457 | C | CCTCCTCC others(5): Show |
1 | a0001c0001t0001g0161 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1691-3843_1691-384 others(16): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543457 | |||||||
| chr13:113543457 | C | T | 2 | a0001c0006t0001g0219 a0002c0004t0004g0086 |
2 | HG02145.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.1691-3843C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543457 | |||||||
| chr13:113543458 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1691-3842T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543458 | |||||||
| chr13:113543458 | T | TCCTCCCC others(4): Show |
3 | a0001c0001t0001g0006 a0001c0001t0001g0160 a0001c0001t0001g0162 |
6 | HG00099.hp1 HG01069.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.1691-3839_1691-382 others(15): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543458 | ||||||
| chr13:113543458 | T | TGC | 1 | a0003c0002t0002g0005 | 3 | HG01081.hp1 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1691-3842_1691-384 others(6): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543458 | |||||||
| chr13:113543463 | C | T | 2 | a0001c0001t0013g0084 a0003c0016t0002g0074 |
2 | HG01243.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1691-3837C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543463 | |||||||
| chr13:113543465 | C | CCCGCCCT others(4): Show |
2 | a0001c0006t0001g0235 a0001c0006t0001g0236 |
2 | HG00280.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.1691-3834_1691-383 others(15): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543465 | ||||||
| chr13:113543465 | C | CCTGTGCC others(87): Show |
4 | a0002c0003t0003g0007 a0002c0003t0003g0239 a0002c0003t0003g0240 others(1): Show |
6 | HG02615.hp1 HG02922.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1691-3832_1691-383 others(98): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543465 | ||||||
| chr13:113543465 | C | T | 2 | a0001c0006t0001g0220 a0002c0003t0003g0255 |
2 | HG03704.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.1691-3835C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543465 | |||||||
| chr13:113543469 | C | CCCCCCGC others(9): Show |
2 | a0001c0006t0001g0219 a0002c0004t0004g0086 |
2 | HG02145.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.1691-3829_1691-382 others(20): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543469 | ||||||
| chr13:113543469 | C | CCCCCCGC others(45): Show |
2 | a0002c0003t0003g0274 a0002c0003t0003g0275 |
2 | HG02080.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.1691-3829_1691-382 others(56): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543469 | ||||||
| chr13:113543469 | C | CCCTCCCT others(4): Show |
12 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(9): Show |
14 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.1691-3829_1691-382 others(15): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543469 | ||||||
| chr13:113543469 | C | T | 9 | a0001c0001t0013g0084 a0001c0006t0001g0220 a0001c0006t0001g0235 others(6): Show |
11 | HG00280.hp1 HG02109.hp1 HG02293.hp2 others(8): Show |
intron_variant | MODIFIER | c.1691-3831C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543469 | |||||||
| chr13:113543470 | C | G | 1 | a0001c0001t0013g0084 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1691-3830C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543470 | |||||||
| chr13:113543471 | C | CCCACTCT others(88): Show |
1 | a0003c0016t0002g0074 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1691-3829_1691-382 others(99): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543471 | |||||||
| chr13:113543471 | C | T | 1 | a0001c0001t0013g0084 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1691-3829C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543471 | |||||||
| chr13:113543472 | A | G | 4 | a0001c0001t0013g0084 a0001c0006t0001g0219 a0002c0004t0004g0086 others(1): Show |
4 | HG01243.hp1 HG02109.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.1691-3828A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543472 | |||||||
| chr13:113543492 | C | G | 2 | a0001c0001t0001g0107 a0001c0001t0001g0130 |
2 | HG02698.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1691-3808C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543492 | |||||||
| chr13:113543493 | T | TC | 10 | a0001c0001t0001g0118 a0001c0001t0001g0122 a0001c0001t0001g0153 others(7): Show |
10 | HG00597.hp2 HG01106.hp1 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.1691-3801dupC | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113543493 | ||||||
| chr13:113543494 | C | G | 2 | a0001c0006t0001g0219 a0002c0003t0003g0266 |
2 | HG01978.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1691-3806C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543494 | |||||||
| chr13:113543497 | CCCGCCCT others(10): Show |
C | 1 | a0002c0003t0003g0266 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1691-3802_1691-378 others(21): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543497 | |||||||
| chr13:113543500 | G | C | 1 | a0001c0001t0001g0141 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1691-3800G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543500 | |||||||
| chr13:113543515 | G | A | 1 | a0002c0003t0003g0266 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1691-3785G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543515 | |||||||
| chr13:113543526 | T | C | 1 | a0002c0003t0003g0266 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1691-3774T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543526 | |||||||
| chr13:113543542 | C | T | 2 | a0002c0004t0004g0017 a0008c0018t0004g0085 |
3 | HG02559.hp1 HG02717.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1691-3758C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543542 | |||||||
| chr13:113543581 | A | T | 1 | a0001c0001t0001g0141 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1691-3719A>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543581 | |||||||
| chr13:113543582 | T | A | 1 | a0001c0001t0001g0141 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1691-3718T>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543582 | |||||||
| chr13:113543664 | A | G | 1 | a0002c0004t0004g0305 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1691-3636A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543664 | |||||||
| chr13:113543724 | G | A | 1 | a0001c0001t0004g0093 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1691-3576G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543724 | |||||||
| chr13:113543733 | A | C | 263 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(260): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.1691-3567A>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543733 | |||||||
| chr13:113543734 | G | A | 263 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(260): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.1691-3566G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543734 | |||||||
| chr13:113543908 | C | T | 2 | a0001c0001t0009g0303 a0001c0001t0009g0304 |
2 | HG00639.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1691-3392C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543908 | |||||||
| chr13:113543946 | C | G | 1 | a0002c0003t0003g0256 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1691-3354C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543946 | |||||||
| chr13:113543990 | G | A | 1 | a0001c0006t0001g0226 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1691-3310G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113543990 | |||||||
| chr13:113544004 | C | T | 2 | a0001c0001t0009g0303 a0001c0001t0009g0304 |
2 | HG00639.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1691-3296C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113544004 | |||||||
| chr13:113544022 | G | A | 2 | a0001c0006t0001g0221 a0001c0006t0001g0226 |
2 | NA18944.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.1691-3278G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113544022 | |||||||
| chr13:113544050 | G | A | 1 | a0003c0002t0002g0044 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1691-3250G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113544050 | |||||||
| chr13:113544075 | C | T | 1 | a0001c0001t0001g0024 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1691-3225C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113544075 | |||||||
| chr13:113544132 | G | A | 61 | a0002c0004t0004g0305 a0003c0002t0002g0005 a0003c0002t0002g0008 others(58): Show |
72 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.1691-3168G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113544132 | |||||||
| chr13:113544194 | T | C | 64 | a0001c0001t0001g0143 a0002c0003t0003g0002 a0002c0003t0003g0007 others(61): Show |
75 | HG00099.hp2 HG00408.hp1 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.1691-3106T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113544194 | |||||||
| chr13:113544219 | G | A | 60 | a0002c0003t0003g0002 a0002c0003t0003g0007 a0002c0003t0003g0029 others(57): Show |
70 | HG00099.hp2 HG00408.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.1691-3081G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113544219 | |||||||
| chr13:113544231 | G | A | 1 | a0001c0001t0001g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1691-3069G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113544231 | |||||||
| chr13:113544237 | G | A | 1 | a0001c0001t0013g0084 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1691-3063G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113544237 | |||||||
| chr13:113544248 | C | A | 1 | a0001c0006t0001g0227 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1691-3052C>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113544248 | |||||||
| chr13:113544325 | G | A | 1 | a0001c0001t0004g0102 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1691-2975G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113544325 | |||||||
| chr13:113544338 | G | A | 1 | a0008c0018t0004g0085 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1691-2962G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113544338 | |||||||
| chr13:113544393 | A | G | 123 | a0002c0003t0003g0002 a0002c0003t0003g0007 a0002c0003t0003g0029 others(120): Show |
144 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.1691-2907A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113544393 | |||||||
| chr13:113544410 | C | T | 26 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(23): Show |
28 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.1691-2890C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113544410 | |||||||
| chr13:113544428 | AGGTGGTC others(2): Show |
A | 26 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(23): Show |
28 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.1691-2871_1691-286 others(13): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113544428 | |||||||
| chr13:113544482 | C | T | 10 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0106 others(7): Show |
10 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1691-2818C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113544482 | |||||||
| chr13:113544521 | C | T | 54 | a0001c0001t0004g0101 a0002c0003t0003g0002 a0002c0003t0003g0007 others(51): Show |
63 | HG00099.hp2 HG00408.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.1691-2779C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113544521 | |||||||
| chr13:113544641 | G | A | 68 | a0002c0004t0004g0305 a0003c0002t0002g0005 a0003c0002t0002g0008 others(65): Show |
79 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.1691-2659G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113544641 | |||||||
| chr13:113544670 | C | T | 12 | a0001c0001t0004g0096 a0001c0001t0004g0100 a0001c0001t0004g0101 others(9): Show |
12 | HG00639.hp1 HG01884.hp1 HG01993.hp2 others(9): Show |
intron_variant | MODIFIER | c.1691-2630C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113544670 | |||||||
| chr13:113544844 | A | G | 4 | a0003c0002t0002g0033 a0003c0002t0002g0039 a0003c0002t0002g0050 others(1): Show |
4 | HG03688.hp1 HG03942.hp2 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.1691-2456A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113544844 | |||||||
| chr13:113544874 | G | T | 1 | a0001c0001t0001g0147 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1691-2426G>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113544874 | |||||||
| chr13:113544896 | C | T | 2 | a0002c0004t0004g0017 a0002c0004t0004g0086 |
3 | HG02145.hp1 HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1691-2404C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113544896 | |||||||
| chr13:113544902 | G | GT | 3 | a0001c0001t0001g0147 a0001c0001t0001g0161 a0001c0001t0012g0151 |
3 | HG00741.hp1 HG01081.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.1691-2394dupT | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113544902 | ||||||
| chr13:113544908 | C | T | 26 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(23): Show |
28 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.1691-2392C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113544908 | |||||||
| chr13:113544937 | C | T | 68 | a0002c0004t0004g0305 a0003c0002t0002g0005 a0003c0002t0002g0008 others(65): Show |
79 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.1691-2363C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113544937 | |||||||
| chr13:113544946 | A | C | 1 | a0001c0006t0001g0227 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1691-2354A>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113544946 | |||||||
| chr13:113545036 | T | TC | 4 | a0001c0001t0001g0154 a0001c0001t0001g0161 a0001c0001t0001g0201 others(1): Show |
4 | HG00741.hp1 HG01255.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.1691-2260dupC | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113545036 | ||||||
| chr13:113545040 | C | T | 2 | a0005c0011t0008g0306 a0005c0011t0008g0307 |
2 | HG02027.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.1691-2260C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113545040 | |||||||
| chr13:113545057 | A | ACC | 68 | a0002c0004t0004g0305 a0003c0002t0002g0005 a0003c0002t0002g0008 others(65): Show |
79 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.1691-2243_1691-224 others(6): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113545057 | |||||||
| chr13:113545100 | G | A | 5 | a0001c0001t0001g0106 a0001c0001t0001g0200 a0001c0001t0001g0201 others(2): Show |
5 | HG00735.hp2 HG01255.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1691-2200G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113545100 | |||||||
| chr13:113545127 | G | GC | 7 | a0001c0001t0001g0141 a0001c0001t0001g0157 a0001c0001t0004g0098 others(4): Show |
7 | HG00438.hp2 HG02523.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1691-2168dupC | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113545127 | ||||||
| chr13:113545180 | G | A | 1 | a0003c0002t0002g0080 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1691-2120G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113545180 | |||||||
| chr13:113545240 | C | T | 1 | a0003c0002t0002g0047 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1691-2060C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113545240 | |||||||
| chr13:113545297 | G | A | 3 | a0001c0001t0001g0024 a0001c0001t0001g0122 a0001c0001t0001g0123 |
4 | HG01106.hp1 HG01192.hp2 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.1691-2003G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113545297 | |||||||
| chr13:113545299 | T | A | 1 | a0003c0002t0002g0035 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1691-2001T>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113545299 | |||||||
| chr13:113545307 | C | CAGTT | 130 | a0002c0003t0003g0002 a0002c0003t0003g0007 a0002c0003t0003g0029 others(127): Show |
151 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.1691-1990_1691-198 others(8): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113545307 | ||||||
| chr13:113545335 | G | A | 2 | a0002c0003t0003g0245 a0002c0003t0003g0246 |
2 | HG00438.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.1691-1965G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113545335 | |||||||
| chr13:113545337 | A | G | 68 | a0002c0004t0004g0305 a0003c0002t0002g0005 a0003c0002t0002g0008 others(65): Show |
79 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.1691-1963A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113545337 | |||||||
| chr13:113545347 | G | C | 68 | a0002c0004t0004g0305 a0003c0002t0002g0005 a0003c0002t0002g0008 others(65): Show |
79 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.1691-1953G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113545347 | |||||||
| chr13:113545382 | T | C | 182 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0106 others(179): Show |
206 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.1691-1918T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113545382 | |||||||
| chr13:113545442 | G | A | 182 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0106 others(179): Show |
206 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.1691-1858G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113545442 | |||||||
| chr13:113545566 | C | T | 1 | a0002c0004t0005g0290 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1691-1734C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113545566 | |||||||
| chr13:113545567 | A | C | 1 | a0001c0001t0001g0161 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1691-1733A>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113545567 | |||||||
| chr13:113545570 | C | G | 1 | a0011c0017t0001g0284 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1691-1730C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113545570 | |||||||
| chr13:113545594 | A | G | 156 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(153): Show |
179 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.1691-1706A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113545594 | |||||||
| chr13:113545599 | TAGCTCAG others(58): Show |
T | 2 | a0001c0001t0009g0303 a0001c0001t0009g0304 |
2 | HG00639.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1691-1671_1691-160 others(69): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113545599 | ||||||
| chr13:113545632 | C | T | 1 | a0001c0001t0004g0102 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1691-1668C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113545632 | |||||||
| chr13:113545800 | G | A | 3 | a0001c0009t0004g0281 a0001c0009t0004g0282 a0001c0009t0004g0283 |
3 | HG02717.hp1 HG03516.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1691-1500G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113545800 | |||||||
| chr13:113545830 | C | T | 94 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(91): Show |
107 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.1691-1470C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113545830 | |||||||
| chr13:113545831 | A | G | 96 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(93): Show |
110 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.1691-1469A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113545831 | |||||||
| chr13:113545859 | G | A | 3 | a0002c0004t0005g0292 a0002c0004t0005g0293 a0002c0004t0005g0302 |
3 | HG00099.hp2 HG02698.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1691-1441G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113545859 | |||||||
| chr13:113545977 | AAGGGGAG others(7): Show |
A | 1 | a0001c0001t0001g0147 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1691-1321_1691-130 others(18): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113545977 | ||||||
| chr13:113545985 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1691-1315G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113545985 | |||||||
| chr13:113546144 | C | T | 1 | a0003c0014t0004g0185 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1691-1156C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113546144 | |||||||
| chr13:113546188 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1691-1112G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113546188 | |||||||
| chr13:113546350 | C | G | 1 | a0001c0001t0001g0161 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1691-950C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113546350 | |||||||
| chr13:113546352 | A | C | 1 | a0001c0001t0001g0161 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1691-948A>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113546352 | |||||||
| chr13:113546353 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1691-947G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113546353 | |||||||
| chr13:113546402 | T | C | 2 | a0001c0001t0001g0135 a0001c0001t0001g0144 |
2 | HG00408.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.1691-898T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113546402 | |||||||
| chr13:113546449 | T | C | 1 | a0001c0005t0001g0110 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1691-851T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113546449 | |||||||
| chr13:113546451 | G | A | 1 | a0003c0002t0002g0079 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1691-849G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113546451 | |||||||
| chr13:113546498 | C | T | 74 | a0002c0003t0003g0255 a0002c0004t0004g0017 a0002c0004t0004g0086 others(71): Show |
86 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.1691-802C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113546498 | |||||||
| chr13:113546598 | C | T | 1 | a0001c0001t0001g0143 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1691-702C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113546598 | |||||||
| chr13:113546666 | C | T | 2 | a0002c0004t0004g0017 a0002c0004t0004g0086 |
3 | HG02145.hp1 HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1691-634C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113546666 | |||||||
| chr13:113546667 | G | A | 5 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0191 others(2): Show |
7 | HG00639.hp2 HG01070.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1691-633G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113546667 | |||||||
| chr13:113546794 | G | GTGGGCAG others(12): Show |
20 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(17): Show |
21 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(18): Show |
intron_variant | MODIFIER | c.1691-505_1691-504i others(21): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113546794 | ||||||
| chr13:113546797 | C | T | 1 | a0001c0007t0006g0280 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1691-503C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113546797 | |||||||
| chr13:113546863 | G | A | 5 | a0002c0004t0005g0286 a0002c0004t0005g0287 a0002c0004t0005g0289 others(2): Show |
6 | HG02451.hp2 HG02486.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1691-437G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113546863 | |||||||
| chr13:113546881 | G | C | 1 | a0001c0001t0001g0191 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1691-419G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113546881 | |||||||
| chr13:113546938 | G | C | 1 | a0008c0018t0004g0085 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1691-362G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113546938 | |||||||
| chr13:113547012 | T | C | 61 | a0002c0003t0003g0002 a0002c0003t0003g0007 a0002c0003t0003g0029 others(58): Show |
72 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.1691-288T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113547012 | |||||||
| chr13:113547055 | T | C | 183 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0106 others(180): Show |
206 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.1691-245T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113547055 | |||||||
| chr13:113547136 | G | T | 1 | a0008c0018t0004g0085 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1691-164G>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113547136 | |||||||
| chr13:113547192 | G | A | 10 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0106 others(7): Show |
10 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1691-108G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113547192 | |||||||
| chr13:113547261 | T | A | 57 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(54): Show |
73 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.1691-39T>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | chr13 | 113547261 | |||||||
| chr13:113547277 | CGT | C | 2 | a0002c0004t0004g0017 a0002c0004t0004g0086 |
3 | HG02145.hp1 HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1691-20_1691-19del others(2): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr13 | 113547277 | ||||||
| chr13:113547427 | T | C | 183 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0106 others(180): Show |
207 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.1770+48T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 11/12 | chr13 | 113547427 | |||||||
| chr13:113547485 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1770+106C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 11/12 | chr13 | 113547485 | |||||||
| chr13:113547580 | C | G | 7 | a0002c0004t0005g0286 a0002c0004t0005g0287 a0002c0004t0005g0289 others(4): Show |
8 | HG02451.hp2 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1770+201C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 11/12 | chr13 | 113547580 | |||||||
| chr13:113547699 | G | C | 1 | a0002c0003t0003g0255 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1770+320G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 11/12 | chr13 | 113547699 | |||||||
| chr13:113547777 | T | A | 68 | a0002c0004t0004g0305 a0003c0002t0002g0005 a0003c0002t0002g0008 others(65): Show |
79 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.1770+398T>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 11/12 | chr13 | 113547777 | |||||||
| chr13:113547850 | T | A | 54 | a0002c0003t0003g0002 a0002c0003t0003g0007 a0002c0003t0003g0029 others(51): Show |
63 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.1771-453T>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 11/12 | chr13 | 113547850 | |||||||
| chr13:113547885 | TCCACCAG others(27): Show |
T | 64 | a0002c0004t0004g0305 a0003c0002t0002g0005 a0003c0002t0002g0008 others(61): Show |
75 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.1771-401_1771-368d others(36): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr13 | 113547885 | ||||||
| chr13:113547902 | A | G | 3 | a0003c0002t0002g0032 a0005c0011t0008g0306 a0005c0011t0008g0307 |
3 | HG02027.hp1 HG02129.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1771-401A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 11/12 | chr13 | 113547902 | |||||||
| chr13:113547919 | A | T | 1 | a0003c0002t0002g0036 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1771-384A>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 11/12 | chr13 | 113547919 | |||||||
| chr13:113547931 | T | G | 1 | a0001c0001t0001g0161 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1771-372T>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 11/12 | chr13 | 113547931 | |||||||
| chr13:113547971 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1771-332A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 11/12 | chr13 | 113547971 | |||||||
| chr13:113548024 | TGGGGCG | T | 69 | a0001c0007t0006g0090 a0002c0004t0004g0305 a0003c0002t0002g0005 others(66): Show |
80 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.1771-268_1771-263d others(8): Show |
TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr13 | 113548024 | ||||||
| chr13:113548036 | G | A | 1 | a0011c0017t0001g0284 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1771-267G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 11/12 | chr13 | 113548036 | |||||||
| chr13:113548042 | G | C | 1 | a0003c0016t0002g0074 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1771-261G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 11/12 | chr13 | 113548042 | |||||||
| chr13:113548069 | T | C | 1 | a0003c0002t0002g0079 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1771-234T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 11/12 | chr13 | 113548069 | |||||||
| chr13:113548129 | G | T | 8 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(5): Show |
9 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(6): Show |
intron_variant | MODIFIER | c.1771-174G>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 11/12 | chr13 | 113548129 | |||||||
| chr13:113548204 | C | T | 1 | a0001c0009t0004g0282 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1771-99C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 11/12 | chr13 | 113548204 | |||||||
| chr13:113548216 | G | C | 1 | a0001c0001t0001g0182 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1771-87G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 11/12 | chr13 | 113548216 | |||||||
| chr13:113548217 | T | C | 61 | a0002c0003t0003g0002 a0002c0003t0003g0007 a0002c0003t0003g0238 others(58): Show |
71 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.1771-86T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 11/12 | chr13 | 113548217 | |||||||
| chr13:113548234 | C | G | 61 | a0002c0003t0003g0002 a0002c0003t0003g0007 a0002c0003t0003g0238 others(58): Show |
71 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.1771-69C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 11/12 | chr13 | 113548234 | |||||||
| chr13:113548245 | G | A | 55 | a0001c0007t0006g0092 a0002c0003t0003g0002 a0002c0003t0003g0007 others(52): Show |
64 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.1771-58G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 11/12 | chr13 | 113548245 | |||||||
| chr13:113548247 | G | A | 1 | a0003c0002t0002g0073 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1771-56G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 11/12 | chr13 | 113548247 | |||||||
| chr13:113548260 | T | C | 145 | a0001c0001t0001g0170 a0001c0001t0004g0018 a0001c0001t0004g0093 others(142): Show |
166 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.1771-43T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 11/12 | chr13 | 113548260 | |||||||
| chr13:113548277 | A | G | 67 | a0002c0003t0003g0029 a0002c0004t0004g0305 a0003c0002t0002g0005 others(64): Show |
78 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.1771-26A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 11/12 | chr13 | 113548277 | |||||||
| chr13:113548292 | C | T | 1 | a0001c0007t0006g0091 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1771-11C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 11/12 | chr13 | 113548292 | |||||||
| chr13:113548293 | G | T | 1 | a0001c0006t0001g0227 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1771-10G>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 11/12 | chr13 | 113548293 | |||||||
| chr13:113548558 | G | C | 140 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0106 others(137): Show |
160 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.1920+106G>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 12/12 | chr13 | 113548558 | |||||||
| chr13:113548583 | G | T | 1 | a0002c0003t0003g0261 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1920+131G>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 12/12 | chr13 | 113548583 | |||||||
| chr13:113548598 | C | G | 1 | a0003c0016t0002g0074 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1920+146C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 12/12 | chr13 | 113548598 | |||||||
| chr13:113548651 | G | A | 62 | a0002c0003t0003g0002 a0002c0003t0003g0007 a0002c0003t0003g0029 others(59): Show |
72 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.1920+199G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 12/12 | chr13 | 113548651 | |||||||
| chr13:113548801 | G | A | 1 | a0001c0007t0006g0280 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1920+349G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 12/12 | chr13 | 113548801 | |||||||
| chr13:113548807 | C | G | 16 | a0001c0006t0001g0027 a0001c0006t0001g0217 a0001c0006t0001g0218 others(13): Show |
17 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(14): Show |
intron_variant | MODIFIER | c.1920+355C>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 12/12 | chr13 | 113548807 | |||||||
| chr13:113548859 | G | A | 1 | a0001c0001t0001g0209 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1920+407G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 12/12 | chr13 | 113548859 | |||||||
| chr13:113548876 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1920+424T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 12/12 | chr13 | 113548876 | |||||||
| chr13:113548892 | C | T | 2 | a0001c0001t0001g0150 a0001c0001t0012g0151 |
2 | NA18952.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.1920+440C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 12/12 | chr13 | 113548892 | |||||||
| chr13:113548917 | C | T | 3 | a0002c0003t0003g0007 a0002c0003t0003g0240 a0009c0020t0003g0007 |
5 | HG02615.hp1 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1920+465C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 12/12 | chr13 | 113548917 | |||||||
| chr13:113548938 | G | A | 4 | a0003c0002t0002g0008 a0003c0002t0002g0049 a0006c0010t0002g0008 others(1): Show |
5 | HG00423.hp1 HG00609.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.1920+486G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 12/12 | chr13 | 113548938 | |||||||
| chr13:113549108 | C | T | 88 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(85): Show |
100 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.1921-317C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 12/12 | chr13 | 113549108 | |||||||
| chr13:113549158 | G | A | 1 | a0003c0016t0002g0074 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1921-267G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 12/12 | chr13 | 113549158 | |||||||
| chr13:113549237 | C | T | 26 | a0001c0001t0004g0018 a0001c0001t0004g0093 a0001c0001t0004g0094 others(23): Show |
28 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.1921-188C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 12/12 | chr13 | 113549237 | |||||||
| chr13:113549264 | G | A | 62 | a0002c0003t0003g0002 a0002c0003t0003g0007 a0002c0003t0003g0029 others(59): Show |
72 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.1921-161G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 12/12 | chr13 | 113549264 | |||||||
| chr13:113549288 | A | G | 173 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0106 others(170): Show |
191 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.1921-137A>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 12/12 | chr13 | 113549288 | |||||||
| chr13:113549355 | C | T | 68 | a0002c0004t0004g0305 a0003c0002t0002g0005 a0003c0002t0002g0008 others(65): Show |
79 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.1921-70C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 12/12 | chr13 | 113549355 | |||||||
| chr13:113549405 | T | C | 2 | a0001c0001t0001g0087 a0001c0001t0001g0285 |
2 | NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1921-20T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 12/12 | chr13 | 113549405 |