| 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 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 677 | 205 | 32 | 43 | 97 | 11 | 20 | 72 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0002 | 0/0 | 677 | 75 | 19 | 15 | 30 | 1 | 10 | 21 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0003 | 0/0 | 677 | 74 | 28 | 13 | 25 | 2 | 6 | 19 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0004 | 0/0 | 677 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0005 | 0/0 | 677 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0006 | 0/0 | 677 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0007 | 0/0 | 677 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0008 | 0/0 | 677 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0009 | 0/0 | 677 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0010 | 0/0 | 677 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0011 | 0/0 | 677 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0012 | 0/0 | 677 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0013 | 0/0 | 677 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2034 | 163 | 18 | 36 | 82 | 8 | 17 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| c0002 | 0/0 | 2034 | 71 | 27 | 12 | 24 | 2 | 6 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| c0003 | 0/0 | 2034 | 51 | 6 | 14 | 26 | 0 | 5 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| c0004 | 0/0 | 2034 | 23 | 13 | 1 | 3 | 1 | 5 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| c0005 | 0/0 | 2034 | 17 | 7 | 6 | 0 | 2 | 2 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| c0006 | 0/0 | 2034 | 17 | 0 | 1 | 14 | 1 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| c0007 | 0/0 | 2034 | 4 | 4 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| c0008 | 0/0 | 2034 | 3 | 3 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| c0009 | 0/0 | 2034 | 3 | 3 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| c0010 | 0/0 | 2034 | 2 | 0 | 0 | 2 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| c0011 | 0/0 | 2034 | 2 | 0 | 0 | 2 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| c0012 | 0/0 | 2034 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| c0013 | 0/0 | 2034 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| c0014 | 0/0 | 2034 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| c0015 | 0/0 | 2034 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| c0016 | 0/0 | 2034 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| c0017 | 0/0 | 2034 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| c0018 | 0/0 | 2034 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| c0019 | 0/0 | 2034 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| c0020 | 0/0 | 2034 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| c0021 | 0/0 | 2034 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| c0022 | 0/0 | 2034 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| c0023 | 0/0 | 2034 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1025 | 181 | 21 | 41 | 86 | 11 | 20 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| t0002 | 0/0 | 1025 | 77 | 28 | 13 | 28 | 2 | 6 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| t0003 | 0/0 | 1025 | 53 | 7 | 14 | 27 | 0 | 5 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| t0004 | 0/0 | 1025 | 24 | 12 | 2 | 10 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| t0005 | 0/0 | 1033 | 16 | 6 | 1 | 3 | 1 | 5 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| t0006 | 0/0 | 1025 | 4 | 4 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| t0007 | 0/0 | 1033 | 3 | 3 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| t0008 | 0/0 | 1025 | 2 | 0 | 0 | 2 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| t0009 | 0/0 | 1025 | 2 | 2 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| t0010 | 0/0 | 1025 | 2 | 1 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| t0011 | 0/0 | 1025 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| t0012 | 0/0 | 1025 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| t0013 | 0/0 | 1025 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| t0014 | 0/0 | 1025 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0003 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0004 | 0/0 | 4 | 0 | 1 | 2 | 1 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0006 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0014 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0016 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0204 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0209 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2034 | 163 | 18 | 36 | 82 | 8 | 17 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0001c0005 | 0/0 | 2034 | 17 | 7 | 6 | 0 | 2 | 2 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0001c0006 | 0/0 | 2034 | 17 | 0 | 1 | 14 | 1 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0001c0007 | 0/0 | 2034 | 4 | 4 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0001c0009 | 0/0 | 2034 | 3 | 3 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0001c0022 | 0/0 | 2034 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0002c0003 | 0/0 | 2034 | 51 | 6 | 14 | 26 | 0 | 5 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0002c0004 | 0/0 | 2034 | 23 | 13 | 1 | 3 | 1 | 5 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0002c0019 | 0/0 | 2034 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0003c0002 | 0/0 | 2034 | 71 | 27 | 12 | 24 | 2 | 6 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0003c0014 | 0/0 | 2034 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0003c0016 | 0/0 | 2034 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0003c0023 | 0/0 | 2034 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0004c0008 | 0/0 | 2034 | 3 | 3 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0005c0010 | 0/0 | 2034 | 2 | 0 | 0 | 2 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0006c0011 | 0/0 | 2034 | 2 | 0 | 0 | 2 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0007c0021 | 0/0 | 2034 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0008c0012 | 0/0 | 2034 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0009c0013 | 0/0 | 2034 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0010c0015 | 0/0 | 2034 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0011c0020 | 0/0 | 2034 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0012c0017 | 0/0 | 2034 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0013c0018 | 0/0 | 2034 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | 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 | copy fasta | chr13 | 113486021 | 113555229 |
| a0001c0001t0004 | 0/0 | 3058 | 14 | 2 | 2 | 10 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0001c0001t0010 | 0/0 | 3058 | 2 | 1 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0001c0001t0012 | 0/0 | 3058 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0001c0001t0013 | 0/0 | 3058 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0001c0001t0014 | 0/0 | 3058 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0001c0005t0001 | 0/0 | 3058 | 16 | 6 | 6 | 0 | 2 | 2 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0001c0005t0011 | 0/0 | 3058 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0001c0006t0001 | 0/0 | 3058 | 17 | 0 | 1 | 14 | 1 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0001c0007t0006 | 0/0 | 3058 | 4 | 4 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0001c0009t0004 | 0/0 | 3058 | 3 | 3 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0001c0022t0001 | 0/0 | 3058 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0002c0003t0003 | 0/0 | 3058 | 51 | 6 | 14 | 26 | 0 | 5 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0002c0004t0004 | 0/0 | 3058 | 3 | 3 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0002c0004t0005 | 0/0 | 3066 | 16 | 6 | 1 | 3 | 1 | 5 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0002c0004t0007 | 0/0 | 3066 | 3 | 3 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0002c0004t0009 | 0/0 | 3058 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0002c0019t0003 | 0/0 | 3058 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0003c0002t0002 | 0/0 | 3058 | 71 | 27 | 12 | 24 | 2 | 6 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0003c0014t0009 | 0/0 | 3058 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0003c0016t0002 | 0/0 | 3058 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0003c0023t0002 | 0/0 | 3058 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0004c0008t0004 | 0/0 | 3058 | 3 | 3 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0005c0010t0002 | 0/0 | 3058 | 2 | 0 | 0 | 2 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0006c0011t0008 | 0/0 | 3058 | 2 | 0 | 0 | 2 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0007c0021t0002 | 0/0 | 3058 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0008c0012t0001 | 0/0 | 3058 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0009c0013t0001 | 0/0 | 3058 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0010c0015t0002 | 0/0 | 3058 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0011c0020t0003 | 0/0 | 3058 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0012c0017t0001 | 0/0 | 3058 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| a0013c0018t0004 | 0/0 | 3058 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | copy fasta | chr13 | 113486021 | 113555229 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0003 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0004 | 0/0 | 4 | 0 | 1 | 2 | 1 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 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 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0126 | 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 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0151 | 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 | 0 | 1 | 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 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0204 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0209 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0004g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0004g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0004g0104 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0004g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0004g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0010g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0010g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0012g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0013g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0001t0014g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0005t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0005t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0005t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0005t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0005t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0005t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0005t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0005t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0005t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0005t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0005t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0005t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0005t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0005t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0005t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0005t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0005t0011g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0006t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0006t0001g0233 | 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 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0006t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0006t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0006t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0006t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0006t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0006t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0006t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0006t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0006t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0006t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0006t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0006t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0006t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0007t0006g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0007t0006g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0007t0006g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0007t0006g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0009t0004g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0009t0004g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0009t0004g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0001c0022t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0264 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 1 | 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 | 1 | 0 | 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 | 1 | 0 | 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 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0003t0003g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0004t0004g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0004t0004g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0004t0005g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0004t0005g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0004t0005g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0004t0005g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0004t0005g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0004t0005g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0004t0005g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0004t0005g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0004t0005g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0004t0005g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0004t0005g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0004t0005g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0004t0005g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0004t0005g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0004t0005g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0004t0005g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0004t0007g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0004t0007g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0004t0007g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0004t0009g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0002c0019t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0006 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0031 | 0/0 | 1 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0048 | 0/0 | 1 | 1 | 0 | 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 |
| a0003c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0056 | 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 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0080 | 0/0 | 1 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0002t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0014t0009g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0016t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0003c0023t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0004c0008t0004g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0004c0008t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0004c0008t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0005c0010t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0005c0010t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0006c0011t0008g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0006c0011t0008g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0007c0021t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0008c0012t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0009c0013t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0010c0015t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0011c0020t0003g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0012c0017t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| a0013c0018t0004g0090 | 0/0 | 1 | 1 | 0 | 0 | 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 | g0174 | EUR | GBR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00099 | hp2 | a0002 | c0004 | t0005 | g0319 | EUR | GBR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0168 | EUR | GBR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0200 | EUR | GBR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00280 | hp1 | a0001 | c0006 | t0001 | g0253 | 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 | g0258 | EAS | CHS | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00423 | hp1 | a0003 | c0002 | t0002 | g0044 | EAS | CHS | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00423 | hp2 | a0003 | c0002 | t0002 | g0072 | EAS | CHS | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00438 | hp2 | a0002 | c0003 | t0003 | g0262 | EAS | CHS | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00544 | hp1 | a0001 | c0001 | t0004 | g0105 | EAS | CHS | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00544 | hp2 | a0001 | c0006 | t0001 | g0251 | EAS | CHS | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00558 | hp1 | a0001 | c0001 | t0004 | g0101 | EAS | CHS | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00558 | hp2 | a0001 | c0006 | t0001 | g0235 | EAS | CHS | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00597 | hp1 | a0001 | c0001 | t0004 | g0102 | EAS | CHS | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00597 | hp2 | a0003 | c0002 | t0002 | g0066 | EAS | CHS | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00609 | hp1 | a0003 | c0002 | t0002 | g0051 | EAS | CHS | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00621 | hp1 | a0001 | c0006 | t0001 | g0240 | EAS | CHS | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00621 | hp2 | a0002 | c0019 | t0003 | g0287 | EAS | CHS | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00639 | hp1 | a0001 | c0001 | t0010 | g0330 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00673 | hp1 | a0001 | c0006 | t0001 | g0234 | EAS | CHS | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00673 | hp2 | a0003 | c0002 | t0002 | g0070 | EAS | CHS | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00733 | hp1 | a0001 | c0005 | t0001 | g0115 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00738 | hp1 | a0003 | c0002 | t0002 | g0041 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01069 | hp2 | a0003 | c0002 | t0002 | g0010 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01070 | hp2 | a0003 | c0002 | t0002 | g0079 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01071 | hp2 | a0003 | c0002 | t0002 | g0010 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01081 | hp1 | a0003 | c0002 | t0002 | g0006 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01099 | hp1 | a0002 | c0003 | t0003 | g0292 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01099 | hp2 | a0001 | c0005 | t0001 | g0248 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01106 | hp2 | a0001 | c0005 | t0001 | g0185 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01109 | hp1 | a0002 | c0003 | t0003 | g0282 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01168 | hp2 | a0003 | c0002 | t0002 | g0084 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01175 | hp1 | a0003 | c0002 | t0002 | g0081 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01243 | hp1 | a0003 | c0016 | t0002 | g0075 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01243 | hp2 | a0003 | c0002 | t0002 | g0029 | AMR | PUR | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | CLM | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01255 | hp2 | a0002 | c0003 | t0003 | g0286 | AMR | CLM | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01256 | hp1 | a0003 | c0002 | t0002 | g0085 | AMR | CLM | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01257 | hp1 | a0001 | c0005 | t0001 | g0247 | AMR | CLM | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01261 | hp1 | a0002 | c0003 | t0003 | g0300 | AMR | CLM | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01346 | hp1 | a0003 | c0002 | t0002 | g0078 | AMR | CLM | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01346 | hp2 | a0002 | c0003 | t0003 | g0264 | 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 | g0249 | AMR | CLM | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01361 | hp2 | a0003 | c0002 | t0002 | g0022 | AMR | CLM | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | CLM | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01515 | hp1 | a0003 | c0002 | t0002 | g0006 | EUR | IBS | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01515 | hp2 | a0001 | c0005 | t0001 | g0184 | EUR | IBS | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01517 | hp2 | a0003 | c0002 | t0002 | g0006 | EUR | IBS | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0109 | AFR | ACB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01884 | hp2 | a0002 | c0004 | t0005 | g0326 | AFR | ACB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01891 | hp2 | a0003 | c0002 | t0002 | g0008 | AFR | ACB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01928 | hp1 | a0002 | c0003 | t0003 | g0283 | AMR | PEL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01928 | hp2 | a0002 | c0003 | t0003 | g0260 | AMR | PEL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01952 | hp1 | a0003 | c0002 | t0002 | g0060 | AMR | PEL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01952 | hp2 | a0002 | c0003 | t0003 | g0277 | AMR | PEL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01978 | hp2 | a0002 | c0003 | t0003 | g0289 | AMR | PEL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01981 | hp1 | a0002 | c0003 | t0003 | g0293 | AMR | PEL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01981 | hp2 | a0008 | c0012 | t0001 | g0210 | AMR | PEL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01993 | hp1 | a0002 | c0003 | t0003 | g0271 | AMR | PEL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01993 | hp2 | a0001 | c0001 | t0004 | g0099 | AMR | PEL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02015 | hp1 | a0002 | c0003 | t0003 | g0265 | EAS | KHV | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02027 | hp1 | a0006 | c0011 | t0008 | g0333 | EAS | KHV | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02027 | hp2 | a0001 | c0001 | t0004 | g0098 | EAS | KHV | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02071 | hp1 | a0002 | c0003 | t0003 | g0279 | 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 | g0203 | 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 | g0243 | EAS | KHV | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02080 | hp2 | a0002 | c0003 | t0003 | g0298 | EAS | KHV | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02129 | hp1 | a0001 | c0001 | t0004 | g0112 | EAS | KHV | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02129 | hp2 | a0006 | c0011 | t0008 | g0332 | EAS | KHV | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02132 | hp2 | a0003 | c0002 | t0002 | g0052 | EAS | KHV | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02135 | hp1 | a0002 | c0004 | t0005 | g0325 | EAS | KHV | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02135 | hp2 | a0001 | c0022 | t0001 | g0205 | EAS | KHV | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02145 | hp1 | a0002 | c0004 | t0004 | g0091 | AFR | ACB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PEL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02148 | hp2 | a0002 | c0003 | t0003 | g0269 | AMR | PEL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02165 | hp1 | a0002 | c0003 | t0003 | g0297 | EAS | CDX | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | CDX | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02258 | hp1 | a0001 | c0005 | t0001 | g0187 | AFR | ACB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02258 | hp2 | a0004 | c0008 | t0004 | g0111 | AFR | ACB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02273 | hp1 | a0002 | c0003 | t0003 | g0273 | AMR | PEL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02273 | hp2 | a0001 | c0001 | t0004 | g0100 | AMR | PEL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02280 | hp1 | a0001 | c0007 | t0006 | g0304 | AFR | ACB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02280 | hp2 | a0001 | c0005 | t0011 | g0176 | AFR | ACB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02293 | hp1 | a0001 | c0005 | t0001 | g0117 | AMR | PEL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02293 | hp2 | a0001 | c0006 | t0001 | g0252 | AMR | PEL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02451 | hp1 | a0003 | c0002 | t0002 | g0025 | AFR | ACB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02451 | hp2 | a0002 | c0004 | t0007 | g0313 | AFR | ACB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02523 | hp2 | a0001 | c0001 | t0004 | g0106 | EAS | KHV | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02572 | hp1 | a0002 | c0004 | t0005 | g0310 | AFR | GWD | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02572 | hp2 | a0003 | c0002 | t0002 | g0028 | AFR | GWD | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02602 | hp1 | a0001 | c0005 | t0001 | g0197 | SAS | PJL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02615 | hp1 | a0002 | c0003 | t0003 | g0257 | AFR | GWD | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02622 | hp1 | a0003 | c0002 | t0002 | g0031 | AFR | GWD | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02622 | hp2 | a0003 | c0002 | t0002 | g0059 | AFR | GWD | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02630 | hp1 | a0001 | c0005 | t0001 | g0133 | AFR | GWD | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02630 | hp2 | a0003 | c0002 | t0002 | g0045 | AFR | GWD | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02647 | hp1 | a0002 | c0004 | t0005 | g0311 | AFR | GWD | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02698 | hp1 | a0002 | c0004 | t0005 | g0328 | SAS | PJL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02717 | hp1 | a0001 | c0009 | t0004 | g0306 | AFR | GWD | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02717 | hp2 | a0013 | c0018 | t0004 | g0090 | AFR | GWD | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02723 | hp1 | a0003 | c0002 | t0002 | g0061 | AFR | GWD | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02738 | hp2 | a0002 | c0004 | t0005 | g0321 | SAS | PJL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02809 | hp1 | a0003 | c0002 | t0002 | g0034 | AFR | GWD | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02809 | hp2 | a0003 | c0014 | t0009 | g0196 | AFR | GWD | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02818 | hp2 | a0003 | c0002 | t0002 | g0026 | AFR | GWD | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02922 | hp1 | a0011 | c0020 | t0003 | g0005 | AFR | ESN | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02922 | hp2 | a0001 | c0007 | t0006 | g0097 | AFR | ESN | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02965 | hp1 | a0002 | c0003 | t0003 | g0021 | AFR | ESN | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02965 | hp2 | a0002 | c0004 | t0007 | g0314 | AFR | ESN | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02970 | hp1 | a0004 | c0008 | t0004 | g0110 | AFR | ESN | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02970 | hp2 | a0003 | c0002 | t0002 | g0009 | AFR | ESN | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02976 | hp1 | a0003 | c0002 | t0002 | g0032 | AFR | ESN | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02976 | hp2 | a0002 | c0004 | t0005 | g0317 | AFR | ESN | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03017 | hp1 | a0001 | c0005 | t0001 | g0198 | SAS | PJL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03017 | hp2 | a0002 | c0003 | t0003 | g0284 | SAS | PJL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03041 | hp2 | a0003 | c0002 | t0002 | g0082 | AFR | GWD | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03098 | hp1 | a0010 | c0015 | t0002 | g0071 | AFR | MSL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03098 | hp2 | a0001 | c0005 | t0001 | g0186 | AFR | MSL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03130 | hp1 | a0003 | c0002 | t0002 | g0036 | AFR | ESN | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | ESN | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03139 | hp1 | a0001 | c0005 | t0001 | g0229 | AFR | ESN | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03139 | hp2 | a0003 | c0002 | t0002 | g0076 | AFR | ESN | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03195 | hp1 | a0002 | c0003 | t0003 | g0005 | AFR | ESN | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03195 | hp2 | a0012 | c0017 | t0001 | g0308 | AFR | ESN | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03209 | hp1 | a0001 | c0007 | t0006 | g0095 | AFR | MSL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03209 | hp2 | a0002 | c0003 | t0003 | g0005 | AFR | MSL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03225 | hp1 | a0004 | c0008 | t0004 | g0094 | AFR | MSL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03225 | hp2 | a0002 | c0004 | t0009 | g0331 | AFR | MSL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03239 | hp2 | a0002 | c0003 | t0003 | g0261 | SAS | PJL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03453 | hp1 | a0003 | c0002 | t0002 | g0039 | AFR | MSL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03453 | hp2 | a0002 | c0003 | t0003 | g0005 | AFR | MSL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03486 | hp1 | a0002 | c0004 | t0004 | g0011 | AFR | MSL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03486 | hp2 | a0003 | c0002 | t0002 | g0048 | AFR | MSL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03491 | hp2 | a0003 | c0002 | t0002 | g0073 | SAS | PJL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0108 | AFR | ESN | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03516 | hp2 | a0001 | c0009 | t0004 | g0305 | AFR | ESN | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03579 | hp1 | a0003 | c0002 | t0002 | g0033 | AFR | MSL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03579 | hp2 | a0003 | c0002 | t0002 | g0024 | AFR | MSL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03654 | hp1 | a0002 | c0003 | t0003 | g0259 | SAS | PJL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03654 | hp2 | a0001 | c0006 | t0001 | g0244 | SAS | PJL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03688 | hp1 | a0003 | c0002 | t0002 | g0030 | 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 | g0139 | SAS | PJL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03704 | hp2 | a0002 | c0003 | t0003 | g0276 | SAS | PJL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | BEB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | BEB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03927 | hp1 | a0002 | c0004 | t0005 | g0320 | SAS | BEB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03927 | hp2 | a0003 | c0002 | t0002 | g0069 | SAS | BEB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | BEB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03942 | hp2 | a0003 | c0002 | t0002 | g0067 | SAS | BEB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | BEB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG04184 | hp2 | a0002 | c0004 | t0005 | g0322 | SAS | BEB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | STU | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG04199 | hp2 | a0002 | c0004 | t0005 | g0318 | SAS | STU | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG04204 | hp1 | a0003 | c0002 | t0002 | g0040 | SAS | STU | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | STU | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG04228 | hp1 | a0002 | c0003 | t0003 | g0280 | SAS | STU | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG04228 | hp2 | a0003 | c0002 | t0002 | g0062 | SAS | STU | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18522 | hp1 | a0002 | c0003 | t0003 | g0256 | AFR | YRI | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18522 | hp2 | a0002 | c0004 | t0005 | g0312 | AFR | YRI | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18612 | hp1 | a0002 | c0003 | t0003 | g0281 | EAS | CHB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | CHB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18747 | hp1 | a0001 | c0006 | t0001 | g0245 | EAS | CHB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18906 | hp1 | a0001 | c0005 | t0001 | g0188 | AFR | YRI | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18906 | hp2 | a0003 | c0002 | t0002 | g0035 | AFR | YRI | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18940 | hp1 | a0003 | c0002 | t0002 | g0047 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18940 | hp2 | a0002 | c0003 | t0003 | g0255 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18941 | hp1 | a0002 | c0003 | t0003 | g0020 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18942 | hp1 | a0001 | c0001 | t0004 | g0103 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18942 | hp2 | a0002 | c0003 | t0003 | g0295 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18943 | hp1 | a0001 | c0006 | t0001 | g0232 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18944 | hp1 | a0001 | c0006 | t0001 | g0242 | 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 | g0002 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18946 | hp1 | a0002 | c0003 | t0003 | g0274 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18946 | hp2 | a0003 | c0002 | t0002 | g0042 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18947 | hp2 | a0003 | c0023 | t0002 | g0023 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18948 | hp2 | a0002 | c0004 | t0005 | g0327 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18950 | hp1 | a0002 | c0004 | t0005 | g0324 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18953 | hp1 | a0003 | c0002 | t0002 | g0087 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18953 | hp2 | a0002 | c0003 | t0003 | g0285 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18954 | hp1 | a0009 | c0013 | t0001 | g0013 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18962 | hp1 | a0002 | c0003 | t0003 | g0270 | 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 | g0119 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18963 | hp2 | a0002 | c0003 | t0003 | g0272 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18964 | hp1 | a0002 | c0003 | t0003 | g0288 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18966 | hp1 | a0005 | c0010 | t0002 | g0050 | 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 | g0161 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18968 | hp2 | a0001 | c0006 | t0001 | g0241 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18969 | hp1 | a0002 | c0003 | t0003 | g0275 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18972 | hp1 | a0001 | c0001 | t0013 | g0163 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18972 | hp2 | a0002 | c0003 | t0003 | g0263 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18974 | hp2 | a0001 | c0006 | t0001 | g0239 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18975 | hp2 | a0003 | c0002 | t0002 | g0077 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18977 | hp1 | a0002 | c0003 | t0003 | g0296 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18982 | hp2 | a0001 | c0001 | t0012 | g0012 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18983 | hp2 | a0003 | c0002 | t0002 | g0086 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18987 | hp2 | a0002 | c0003 | t0003 | g0294 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18990 | hp1 | a0001 | c0006 | t0001 | g0236 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18990 | hp2 | a0003 | c0002 | t0002 | g0057 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18993 | hp1 | a0003 | c0002 | t0002 | g0068 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18994 | hp1 | a0005 | c0010 | t0002 | g0053 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18994 | hp2 | a0003 | c0002 | t0002 | g0055 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18995 | hp2 | a0002 | c0003 | t0003 | g0299 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18997 | hp1 | a0002 | c0003 | t0003 | g0266 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18998 | hp2 | a0003 | c0002 | t0002 | g0046 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18999 | hp2 | a0002 | c0003 | t0003 | g0291 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19000 | hp1 | a0001 | c0006 | t0001 | g0237 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19001 | hp1 | a0002 | c0003 | t0003 | g0268 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19001 | hp2 | a0003 | c0002 | t0002 | g0056 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19002 | hp2 | a0003 | c0002 | t0002 | g0043 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19004 | hp1 | a0002 | c0003 | t0003 | g0290 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0126 | 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 | g0147 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19007 | hp2 | a0001 | c0001 | t0004 | g0104 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19009 | hp1 | a0003 | c0002 | t0002 | g0049 | 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 | g0107 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19030 | hp1 | a0002 | c0004 | t0005 | g0316 | AFR | LWK | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19030 | hp2 | a0003 | c0002 | t0002 | g0008 | AFR | LWK | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | LWK | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19043 | hp2 | a0003 | c0002 | t0002 | g0009 | AFR | LWK | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19055 | hp2 | a0003 | c0002 | t0002 | g0064 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19060 | hp1 | a0003 | c0002 | t0002 | g0301 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19064 | hp1 | a0003 | c0002 | t0002 | g0302 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19064 | hp2 | a0001 | c0006 | t0001 | g0233 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19066 | hp1 | a0002 | c0003 | t0003 | g0020 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19075 | hp2 | a0003 | c0002 | t0002 | g0074 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19079 | hp2 | a0001 | c0006 | t0001 | g0238 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19080 | hp2 | a0003 | c0002 | t0002 | g0065 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19085 | hp1 | a0007 | c0021 | t0002 | g0054 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19090 | hp2 | a0002 | c0003 | t0003 | g0267 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19240 | hp1 | a0001 | c0007 | t0006 | g0096 | AFR | YRI | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA19240 | hp2 | a0003 | c0002 | t0002 | g0083 | AFR | YRI | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ASW | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | ASW | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | TSI | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | TSI | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | TSI | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA20805 | hp2 | a0001 | c0005 | t0001 | g0250 | EUR | TSI | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | GIH | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | GIH | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01123 | hp1 | a0002 | c0003 | t0003 | g0278 | AMR | CLM | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG01123 | hp2 | a0002 | c0004 | t0005 | g0323 | AMR | CLM | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02109 | hp1 | a0001 | c0001 | t0014 | g0089 | AFR | ACB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02109 | hp2 | a0003 | c0002 | t0002 | g0080 | AFR | ACB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02486 | hp1 | a0002 | c0004 | t0007 | g0315 | AFR | ACB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02559 | hp1 | a0002 | c0004 | t0004 | g0011 | AFR | ACB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG02559 | hp2 | a0003 | c0002 | t0002 | g0037 | AFR | ACB | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03471 | hp1 | a0001 | c0001 | t0010 | g0329 | AFR | MSL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG03471 | hp2 | a0003 | c0002 | t0002 | g0038 | AFR | MSL | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | USA | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| HG06807 | hp2 | a0003 | c0002 | t0002 | g0027 | AFR | USA | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18955 | hp1 | a0003 | c0002 | t0002 | g0058 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA18955 | hp2 | a0001 | c0001 | t0004 | g0246 | EAS | JPT | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA20300 | hp1 | a0003 | c0002 | t0002 | g0063 | AFR | USA | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA20300 | hp2 | a0001 | c0009 | t0004 | g0307 | AFR | USA | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA21309 | hp1 | a0001 | c0005 | t0001 | g0116 | AFR | LWK | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | LWK | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0209 | REF | REF | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0204 | REF | REF | TMCO3_chr13_113486021_113555229 | TMCO3 | chr13 | 113486021 | 113555229 |
| 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 | a0006 | 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 | a0007 | 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 | a0013 | 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 | a0005 | 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 | a0012 | 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 | a0011 | 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 | a0008 | 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 | a0003a0005a0007others(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 | a0002a0011a0013 | 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 | a0009 | 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 |
| 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 | a0001c0009a0001c0022a0003c0023 | 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 | a0002c0003a0002c0019a0011c0020 | 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 | a0003c0002a0003c0016a0003c0023others(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 | a0003c0002a0003c0016a0003c0023others(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 | a0001c0006a0003c0002a0003c0016others(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 | a0001c0006a0001c0009a0003c0002others(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 |
| 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 | a0001c0001t0010 | 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 | a0002c0004t0005a0002c0004t0007 | 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 | a0001c0005t0011 | 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 | a0002c0004t0005a0002c0004t0007 | 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 | a0003c0002t0002a0003c0016t0002a0003c0023t0002others(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 | a0001c0001t0012 | 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 | a0001c0001t0014 | 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 | a0001c0001t0013 | 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 | 15 | a0001c0001t0004a0001c0001t0010a0001c0009t0004others(12): 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 | 20 | a0001c0001t0004a0001c0001t0010a0001c0009t0004others(17): 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 | a0002c0003t0003a0002c0004t0005a0002c0004t0007others(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 | a0001c0001t0004a0001c0001t0010a0001c0009t0004others(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 | a0006c0011t0008 | 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 |
| 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 | 24 | a0001c0001t0010g0329a0001c0001t0010g0330a0002c0004t0005g0310others(21): 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 | 71 | a0002c0003t0003g0021a0003c0002t0002g0006a0003c0002t0002g0008others(68): 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 | a0001c0001t0001g0309 | 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 | a0001c0001t0001g0088 | 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 | a0003c0002t0002g0086a0003c0002t0002g0087 | 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 | a0006c0011t0008g0332a0006c0011t0008g0333 | 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 | a0012c0017t0001g0308 | 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 | 19 | a0002c0004t0005g0310a0002c0004t0005g0311a0002c0004t0005g0312others(16): 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 | 19 | a0002c0004t0005g0310a0002c0004t0005g0311a0002c0004t0005g0312others(16): 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 | a0001c0009t0004g0305a0001c0009t0004g0306a0001c0009t0004g0307 | 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 | a0002c0004t0009g0331 | 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 | a0001c0001t0010g0329a0001c0001t0010g0330 | 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 | 19 | a0002c0004t0005g0310a0002c0004t0005g0311a0002c0004t0005g0312others(16): 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 | a0001c0007t0006g0304 | 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 | a0001c0001t0014g0089 | 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 | a0001c0001t0010g0329a0001c0001t0010g0330 | 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 | a0001c0001t0001g0303 | 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 | 9 | a0003c0002t0002g0006a0003c0002t0002g0078a0003c0002t0002g0079others(6): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | a0006c0011t0008g0332a0006c0011t0008g0333 | 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 | 19 | a0002c0004t0005g0310a0002c0004t0005g0311a0002c0004t0005g0312others(16): 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 | 50 | a0002c0003t0003g0005a0002c0003t0003g0020a0002c0003t0003g0021others(47): 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 | 19 | a0002c0004t0005g0310a0002c0004t0005g0311a0002c0004t0005g0312others(16): 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 | a0001c0001t0001g0254 | 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 | a0001c0006t0001g0252a0001c0006t0001g0253 | 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 | a0002c0004t0009g0331 | 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 | a0002c0003t0003g0021 | 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 | a0001c0006t0001g0251 | 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 | a0001c0005t0001g0247a0001c0005t0001g0248a0001c0005t0001g0249others(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 | a0001c0001t0004g0246 | 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 | 17 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(14): 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 | 196 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0113others(193): 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 | 17 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(14): 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 | a0001c0001t0001g0114 | 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 | a0002c0004t0005g0318a0002c0004t0005g0319a0002c0004t0005g0320others(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 | a0001c0001t0001g0231 | 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 | 17 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(14): 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 | a0006c0011t0008g0332a0006c0011t0008g0333 | 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 | a0001c0009t0004g0305a0001c0009t0004g0306a0001c0009t0004g0307 | 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 | a0003c0002t0002g0077 | 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 | 17 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(14): 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 | 50 | a0002c0003t0003g0005a0002c0003t0003g0020a0002c0003t0003g0021others(47): 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 | a0003c0002t0002g0076 | 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 | a0001c0001t0010g0329a0001c0001t0010g0330 | 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 | a0001c0001t0001g0092a0001c0009t0004g0305a0001c0009t0004g0306others(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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 138 | a0001c0001t0001g0093a0001c0001t0014g0089a0001c0006t0001g0232others(135): 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 | a0002c0003t0003g0005a0002c0003t0003g0255a0002c0003t0003g0256others(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 | a0001c0001t0001g0092a0002c0004t0004g0011a0002c0004t0004g0091 | 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 | a0001c0001t0001g0092a0002c0004t0004g0011a0002c0004t0004g0091 | 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 | 27 | a0001c0001t0001g0093a0001c0001t0001g0309a0001c0001t0004g0098others(24): 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 | a0006c0011t0008g0332a0006c0011t0008g0333 | 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 | a0002c0003t0003g0021 | 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 | 73 | a0002c0004t0005g0328a0003c0002t0002g0006a0003c0002t0002g0008others(70): 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 | a0002c0004t0009g0331 | 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | a0001c0001t0001g0092a0001c0001t0010g0329a0001c0001t0010g0330others(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 | a0001c0006t0001g0252 | 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 | a0001c0001t0001g0012a0001c0001t0012g0012 | 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 | a0001c0001t0010g0329a0001c0001t0010g0330 | 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 | a0001c0001t0010g0329a0001c0001t0010g0330 | 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 | a0002c0003t0003g0258 | 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 96 | a0001c0001t0010g0329a0001c0001t0010g0330a0001c0006t0001g0232others(93): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | a0001c0001t0001g0230 | 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 | a0001c0001t0001g0309 | 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 | a0001c0005t0001g0115a0001c0005t0001g0116a0001c0005t0001g0117 | 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 | a0001c0007t0006g0304 | 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | a0001c0001t0001g0309 | 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 17 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(14): 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 | a0002c0003t0003g0259 | 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | a0001c0001t0001g0309 | 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | a0002c0004t0009g0331 | 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 146 | a0001c0001t0001g0092a0002c0003t0003g0005a0002c0003t0003g0020others(143): 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 | a0003c0002t0002g0022 | 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 | a0001c0001t0010g0329a0001c0001t0010g0330 | 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 | a0002c0004t0005g0327 | 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | a0002c0003t0003g0300 | 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 | a0003c0016t0002g0075 | 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | a0003c0002t0002g0074 | 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 | a0002c0003t0003g0258 | 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 | a0002c0003t0003g0258 | 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 | 50 | a0002c0003t0003g0005a0002c0003t0003g0020a0002c0003t0003g0021others(47): 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 | a0013c0018t0004g0090 | 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 | a0001c0005t0001g0229 | 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 75 | a0001c0001t0010g0329a0001c0001t0010g0330a0001c0005t0001g0229others(72): 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 |
72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 96 | a0001c0001t0010g0329a0001c0001t0010g0330a0001c0006t0001g0232others(93): 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 | 75 | a0001c0009t0004g0305a0001c0009t0004g0306a0001c0009t0004g0307others(72): 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 | a0001c0006t0001g0232 | 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | a0002c0003t0003g0260 | 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 | a0001c0001t0001g0012a0001c0001t0001g0118a0001c0001t0001g0119others(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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | a0003c0002t0002g0073 | 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 | a0006c0011t0008g0332a0006c0011t0008g0333 | 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 | a0001c0001t0001g0093 | 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 | a0006c0011t0008g0332a0006c0011t0008g0333 | 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | a0001c0009t0004g0305a0001c0009t0004g0306a0001c0009t0004g0307 | 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 | a0003c0023t0002g0023 | 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 | a0004c0008t0004g0094 | 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 | a0002c0004t0005g0318a0002c0004t0005g0319a0002c0004t0005g0320others(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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 96 | a0001c0001t0010g0329a0001c0001t0010g0330a0001c0006t0001g0232others(93): 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 | 22 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(19): 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 | a0001c0001t0014g0089 | 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 196 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0113others(193): 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 | 24 | a0001c0001t0010g0329a0001c0001t0010g0330a0001c0006t0001g0232others(21): 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 | 17 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(14): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | a0004c0008t0004g0094 | 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 | a0001c0001t0004g0112 | 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 | a0002c0004t0009g0331 | 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 | 10 | a0001c0001t0001g0002a0001c0001t0001g0220a0001c0001t0001g0221others(7): 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 | a0003c0002t0002g0072 | 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 | a0001c0006t0001g0245 | 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 | 24 | a0001c0001t0010g0329a0001c0001t0010g0330a0001c0006t0001g0232others(21): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 17 | a0002c0004t0005g0310a0002c0004t0005g0311a0002c0004t0005g0312others(14): 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 | a0010c0015t0002g0071 | 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 | a0001c0001t0001g0128 | 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | a0003c0002t0002g0078a0003c0002t0002g0079 | 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 | a0001c0001t0001g0129a0001c0001t0001g0130 | 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 | a0001c0001t0001g0227a0001c0001t0001g0228 | 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 | a0001c0009t0004g0305a0001c0009t0004g0306a0001c0009t0004g0307 | 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 | a0001c0001t0001g0219 | 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 | 51 | a0002c0003t0003g0005a0002c0003t0003g0020a0002c0003t0003g0255others(48): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | a0002c0003t0003g0261 | 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | a0003c0002t0002g0078a0003c0002t0002g0079 | 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | a0001c0001t0001g0218 | 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | a0013c0018t0004g0090 | 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 | 170 | a0001c0001t0001g0092a0001c0001t0010g0329a0001c0001t0010g0330others(167): 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 | 71 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(68): 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 | 22 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(19): 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 | 71 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(68): 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 | a0003c0002t0002g0085 | 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 | a0003c0002t0002g0069a0003c0002t0002g0070 | 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 | 168 | a0001c0001t0001g0092a0001c0006t0001g0232a0001c0006t0001g0233others(165): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | a0001c0001t0001g0131a0001c0001t0001g0132 | 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 | 22 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(19): 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 | a0001c0009t0004g0305a0001c0009t0004g0306a0001c0009t0004g0307 | 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 | 55 | a0001c0001t0001g0092a0002c0003t0003g0005a0002c0003t0003g0020others(52): 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 | 91 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(88): 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 | 19 | a0002c0004t0005g0310a0002c0004t0005g0311a0002c0004t0005g0312others(16): 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 | 54 | a0001c0001t0001g0092a0002c0003t0003g0005a0002c0003t0003g0020others(51): 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 | a0003c0002t0002g0068 | 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 | a0001c0005t0001g0133 | 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 | a0002c0003t0003g0297a0002c0003t0003g0298a0002c0003t0003g0299others(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 | 19 | a0002c0004t0005g0310a0002c0004t0005g0311a0002c0004t0005g0312others(16): 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 | 22 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(19): 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 | a0002c0003t0003g0255 | 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 | a0001c0001t0001g0231 | 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 | a0001c0001t0010g0329a0001c0001t0010g0330 | 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 | a0006c0011t0008g0332a0006c0011t0008g0333 | 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 | a0003c0002t0002g0024 | 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 | a0012c0017t0001g0308 | 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 | a0001c0001t0010g0329a0001c0001t0010g0330 | 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 19 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(16): 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 | 19 | a0002c0004t0005g0310a0002c0004t0005g0311a0002c0004t0005g0312others(16): 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 | a0001c0001t0001g0309 | 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 | a0010c0015t0002g0071 | 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 | 17 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(14): 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 | 19 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(16): 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 | 50 | a0002c0003t0003g0005a0002c0003t0003g0020a0002c0003t0003g0021others(47): 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 | a0001c0001t0001g0092 | 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 | a0001c0001t0001g0093 | 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 170 | a0001c0001t0001g0092a0001c0001t0010g0329a0001c0001t0010g0330others(167): 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 | a0001c0001t0001g0113a0001c0001t0001g0212a0001c0001t0001g0213others(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 | a0001c0001t0001g0199a0001c0001t0010g0329a0001c0001t0010g0330others(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 | 7 | a0001c0001t0001g0309a0002c0004t0005g0312a0002c0004t0005g0325others(4): 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 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0177others(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 | 54 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(51): 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 | 22 | a0001c0001t0001g0093a0001c0001t0001g0134a0001c0001t0001g0135others(19): 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 | 50 | a0001c0001t0001g0128a0001c0001t0004g0098a0001c0006t0001g0244others(47): 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 | 20 | a0001c0001t0001g0092a0001c0006t0001g0232a0001c0006t0001g0233others(17): 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 | a0002c0003t0003g0262a0002c0003t0003g0263 | 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 | 70 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(67): 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 | a0003c0002t0002g0067 | 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 | a0003c0002t0002g0067 | 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 | 70 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(67): 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 | 70 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(67): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | a0001c0005t0001g0115a0001c0005t0001g0116a0001c0005t0001g0117others(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 | 19 | a0002c0004t0005g0310a0002c0004t0005g0311a0002c0004t0005g0312others(16): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | a0001c0001t0001g0092 | 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 | a0001c0001t0001g0136 | 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 24 | a0001c0001t0010g0329a0001c0001t0010g0330a0001c0006t0001g0232others(21): 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 | 93 | a0001c0001t0010g0329a0001c0001t0010g0330a0001c0006t0001g0232others(90): 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 | a0001c0009t0004g0305a0001c0009t0004g0306a0001c0009t0004g0307 | 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 | 91 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(88): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | a0003c0014t0009g0196 | 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 | 148 | a0001c0001t0001g0092a0001c0001t0010g0329a0001c0001t0010g0330others(145): 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 | 73 | a0001c0005t0001g0188a0003c0002t0002g0006a0003c0002t0002g0008others(70): 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 | a0001c0001t0001g0309 | 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | a0001c0001t0001g0128a0001c0001t0001g0175 | 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 22 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(19): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 19 | a0002c0004t0005g0310a0002c0004t0005g0311a0002c0004t0005g0312others(16): 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 | a0002c0003t0003g0257 | 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 | a0001c0001t0001g0212 | 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | a0001c0001t0001g0092 | 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 | 75 | a0001c0009t0004g0305a0001c0009t0004g0306a0001c0009t0004g0307others(72): 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 | 94 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(91): 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 | a0001c0001t0004g0109 | 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 | a0001c0001t0010g0329a0001c0001t0010g0330 | 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | a0001c0001t0010g0329a0001c0001t0010g0330 | 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 | a0003c0002t0002g0008a0003c0002t0002g0025a0003c0002t0002g0026others(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 | a0001c0009t0004g0305a0001c0009t0004g0306a0001c0009t0004g0307 | 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 | a0001c0001t0001g0131a0001c0001t0001g0132 | 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | a0002c0003t0003g0294a0002c0003t0003g0295 | 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 | a0001c0005t0001g0133a0001c0005t0001g0186a0001c0005t0001g0187others(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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 22 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(19): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | a0001c0001t0001g0003a0001c0001t0001g0172a0001c0001t0001g0173others(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 | a0013c0018t0004g0090 | 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 | a0002c0004t0005g0317 | 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 | 51 | a0002c0003t0003g0005a0002c0003t0003g0020a0002c0003t0003g0021others(48): 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 | 22 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(19): 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 | 45 | a0001c0001t0001g0092a0001c0001t0010g0329a0001c0001t0010g0330others(42): 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 | a0002c0004t0009g0331 | 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 | 71 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(68): 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 | 47 | a0001c0001t0001g0092a0001c0001t0010g0329a0001c0001t0010g0330others(44): 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 | a0001c0001t0004g0099a0001c0001t0004g0100 | 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 | 18 | a0002c0004t0005g0310a0002c0004t0005g0311a0002c0004t0005g0312others(15): 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 | a0003c0016t0002g0075 | 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 | 19 | a0002c0004t0005g0310a0002c0004t0005g0311a0002c0004t0005g0312others(16): 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 | a0001c0001t0001g0137a0001c0001t0001g0138 | 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 | a0003c0016t0002g0075 | 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 | 22 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(19): 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 | a0001c0001t0001g0136 | 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 | a0001c0001t0001g0171 | 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 | 71 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(68): 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 | a0003c0002t0002g0301a0003c0002t0002g0302 | 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 | 63 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(60): 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 | a0003c0002t0002g0028a0003c0002t0002g0062a0003c0002t0002g0063others(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 | 56 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0170others(53): 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 | a0002c0003t0003g0293a0002c0004t0005g0316a0002c0004t0005g0317 | 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 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234 | 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 | a0001c0006t0001g0235a0001c0006t0001g0236a0001c0006t0001g0237others(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 | a0001c0006t0001g0243 | 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 17 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(14): 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 | 22 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(19): 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 | a0003c0002t0002g0076 | 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 | 22 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(19): 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 | a0001c0001t0001g0093 | 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 | a0003c0002t0002g0029 | 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 | 170 | a0001c0001t0001g0092a0001c0001t0010g0329a0001c0001t0010g0330others(167): 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 | a0001c0001t0001g0120 | 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 | a0001c0001t0001g0169 | 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 | 94 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(91): 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 | 52 | a0002c0003t0003g0005a0002c0003t0003g0020a0002c0003t0003g0021others(49): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 22 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(19): 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 | 50 | a0002c0003t0003g0005a0002c0003t0003g0020a0002c0003t0003g0021others(47): 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 | a0003c0002t0002g0024 | 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 22 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(19): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | a0001c0001t0001g0127 | 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | a0001c0001t0001g0200a0002c0003t0003g0264 | 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 | 19 | a0002c0004t0005g0310a0002c0004t0005g0311a0002c0004t0005g0312others(16): 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 | a0001c0001t0010g0329a0001c0001t0010g0330 | 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 | 94 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(91): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | a0001c0001t0001g0092a0002c0004t0004g0011a0002c0004t0004g0091 | 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 | a0002c0004t0009g0331 | 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | a0003c0002t0002g0022 | 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 | a0001c0001t0001g0093a0001c0001t0001g0168 | 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 | 170 | a0001c0001t0001g0092a0001c0001t0010g0329a0001c0001t0010g0330others(167): 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 | a0001c0007t0006g0095a0001c0007t0006g0096a0001c0007t0006g0097others(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 | a0006c0011t0008g0332a0006c0011t0008g0333 | 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 | a0001c0001t0001g0167 | 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | a0002c0004t0005g0310a0002c0004t0005g0311a0002c0004t0005g0312 | 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 | 194 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0309others(191): 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 | a0001c0001t0010g0329a0001c0001t0010g0330 | 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 | a0001c0001t0001g0093 | 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 | 22 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(19): 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 | 22 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(19): 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 | a0001c0001t0001g0189 | 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 | a0003c0002t0002g0025 | 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 | a0001c0001t0001g0309 | 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 | a0003c0002t0002g0061 | 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 |
72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | a0001c0001t0014g0089 | 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | a0001c0001t0004g0100 | 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 |
72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 |
72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | a0006c0011t0008g0332a0006c0011t0008g0333 | 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | a0002c0004t0005g0312 | 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 94 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(91): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 |
67 | a0003c0002t0002g0006a0003c0002t0002g0009a0003c0002t0002g0010others(64): 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 | a0003c0002t0002g0008a0003c0002t0002g0025a0003c0002t0002g0026others(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 | a0003c0002t0002g0008a0003c0002t0002g0025a0003c0002t0002g0026others(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 | 14 | a0002c0004t0005g0318a0002c0004t0005g0319a0002c0004t0005g0320others(11): 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 | a0001c0006t0001g0244a0001c0006t0001g0252a0001c0006t0001g0253 | 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 | 73 | a0001c0006t0001g0235a0003c0002t0002g0006a0003c0002t0002g0008others(70): 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 | 73 | a0001c0006t0001g0235a0003c0002t0002g0006a0003c0002t0002g0008others(70): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 |
18 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(15): 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 | a0003c0002t0002g0031 | 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 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0230 | 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 | a0001c0001t0010g0329a0001c0001t0010g0330 | 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 | a0001c0001t0001g0189 | 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | a0002c0003t0003g0292 | 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 | 17 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(14): 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 | a0002c0003t0003g0021 | 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 | 73 | a0002c0003t0003g0021a0003c0002t0002g0006a0003c0002t0002g0008others(70): 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 | a0012c0017t0001g0308 | 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 | a0001c0001t0001g0213 | 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 22 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(19): 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 | 70 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(67): 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 | 53 | a0001c0001t0001g0092a0002c0003t0003g0005a0002c0003t0003g0020others(50): 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 | 22 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(19): 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 | a0001c0001t0001g0177 | 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 94 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(91): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | a0001c0005t0001g0247a0001c0005t0001g0248a0001c0005t0001g0249others(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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | a0001c0001t0001g0190 | 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 | a0010c0015t0002g0071 | 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 | 22 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(19): 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 | a0001c0001t0004g0101a0001c0001t0004g0102 | 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 | 94 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(91): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 17 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(14): 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 | a0001c0001t0004g0108 | 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 | a0002c0003t0003g0258a0002c0003t0003g0266 | 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 | 94 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(91): 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 | 94 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(91): 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 | 94 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(91): 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 | a0001c0001t0010g0329a0001c0001t0010g0330 | 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 | 94 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(91): 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 | 94 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(91): 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 | 94 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(91): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 |
16 | a0003c0002t0002g0006a0003c0002t0002g0009a0003c0002t0002g0032others(13): 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 |
55 | a0003c0002t0002g0008a0003c0002t0002g0010a0003c0002t0002g0022others(52): 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 | a0003c0002t0002g0059 | 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 | a0002c0004t0005g0310a0002c0004t0005g0311a0002c0004t0005g0312 | 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | a0001c0001t0001g0092a0002c0004t0004g0011a0002c0004t0004g0091 | 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 | a0002c0004t0007g0313 | 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 | 73 | a0001c0001t0014g0089a0003c0002t0002g0006a0003c0002t0002g0008others(70): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | a0001c0001t0001g0093 | 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 | a0001c0001t0001g0114a0001c0001t0001g0139 | 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 | a0001c0001t0010g0329a0001c0001t0010g0330 | 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 17 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(14): 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 | a0001c0001t0010g0329a0001c0001t0010g0330 | 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 | a0001c0005t0001g0184 | 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | a0001c0001t0004g0108 | 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | a0001c0001t0001g0191 | 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 73 | a0001c0001t0014g0089a0003c0002t0002g0006a0003c0002t0002g0008others(70): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | a0001c0001t0010g0329a0001c0001t0010g0330 | 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 | 73 | a0001c0005t0001g0250a0003c0002t0002g0006a0003c0002t0002g0008others(70): 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 | a0001c0001t0004g0099a0001c0001t0004g0100 | 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 | a0001c0001t0001g0093a0001c0001t0014g0089 | 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 | 74 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(71): 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 | 74 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(71): 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 | 74 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(71): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | a0001c0001t0001g0201 | 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 | 74 | a0001c0001t0001g0092a0002c0003t0003g0005a0002c0003t0003g0020others(71): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | a0001c0009t0004g0305a0001c0009t0004g0306a0001c0009t0004g0307 | 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | a0001c0001t0004g0108 | 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 | a0001c0001t0001g0183 | 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 | a0001c0001t0010g0330 | 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 | a0006c0011t0008g0332a0006c0011t0008g0333 | 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 | a0001c0001t0001g0212a0001c0001t0001g0217 | 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 | 61 | a0002c0003t0003g0005a0002c0003t0003g0020a0002c0003t0003g0021others(58): 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 |
72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | a0001c0001t0001g0113 | 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | a0003c0002t0002g0069 | 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | a0003c0002t0002g0073 | 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 | a0003c0002t0002g0008 | 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 | a0001c0001t0004g0109 | 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 | a0001c0001t0001g0140 | 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 | a0001c0001t0001g0195 | 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | a0001c0001t0001g0214 | 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 | a0001c0006t0001g0244a0001c0006t0001g0252a0001c0006t0001g0253 | 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 | a0001c0001t0001g0211 | 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 | 61 | a0002c0003t0003g0005a0002c0003t0003g0020a0002c0003t0003g0021others(58): 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 | 22 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(19): 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 | a0001c0001t0001g0093a0001c0001t0014g0089 | 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | a0002c0003t0003g0021 | 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 | a0001c0001t0001g0175 | 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 23 | a0001c0001t0001g0214a0001c0006t0001g0232a0001c0006t0001g0233others(20): 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 | a0002c0004t0009g0331 | 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 | a0001c0001t0001g0141a0001c0001t0001g0142 | 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 | a0006c0011t0008g0332a0006c0011t0008g0333 | 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 | a0001c0009t0004g0305a0001c0009t0004g0306a0001c0009t0004g0307 | 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 | 89 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(86): 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 | a0001c0001t0001g0113 | 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 | a0003c0002t0002g0055a0003c0002t0002g0056a0003c0002t0002g0057others(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 | a0001c0001t0001g0143 | 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 | 22 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(19): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 17 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(14): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | a0002c0004t0009g0331 | 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 | a0001c0007t0006g0095a0001c0007t0006g0096a0001c0007t0006g0097others(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 | 26 | a0001c0001t0001g0093a0001c0001t0001g0118a0001c0001t0001g0121others(23): 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 | 134 | a0001c0001t0001g0092a0001c0001t0001g0143a0001c0001t0001g0218others(131): 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 | 54 | a0001c0001t0001g0092a0002c0003t0003g0005a0002c0003t0003g0020others(51): 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 | a0001c0001t0001g0118a0001c0001t0001g0119 | 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 | a0002c0004t0009g0331 | 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | a0001c0001t0001g0142a0002c0003t0003g0268a0002c0003t0003g0290others(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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | a0002c0004t0009g0331 | 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 | 70 | a0001c0001t0010g0329a0001c0001t0010g0330a0002c0003t0003g0005others(67): 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 | 24 | a0001c0001t0001g0092a0001c0006t0001g0232a0001c0006t0001g0233others(21): 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 | a0001c0001t0001g0092a0002c0004t0004g0011a0002c0004t0004g0091 | 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 | a0006c0011t0008g0332a0006c0011t0008g0333 | 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 | a0001c0007t0006g0095a0001c0007t0006g0096a0001c0007t0006g0097 | 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 | 22 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(19): 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 | 17 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(14): 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 | 17 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(14): 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 | a0003c0002t0002g0061 | 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 | a0001c0006t0001g0242 | 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 | 73 | a0001c0001t0001g0191a0003c0002t0002g0006a0003c0002t0002g0008others(70): 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 | a0001c0001t0001g0202 | 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 | 205 | a0001c0001t0001g0015a0001c0001t0001g0088a0001c0001t0001g0092others(202): 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 | a0001c0001t0010g0329a0001c0001t0010g0330 | 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 | a0002c0003t0003g0299 | 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 | 208 | a0001c0001t0001g0015a0001c0001t0001g0088a0001c0001t0001g0092others(205): 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 | 3 | a0002c0004t0007g0313a0002c0004t0007g0314a0002c0004t0007g0315 | 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 | a0001c0001t0001g0113a0012c0017t0001g0308 | 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 | a0001c0001t0001g0148 | 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 | a0001c0001t0001g0121 | 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 | 74 | a0001c0001t0001g0121a0001c0001t0001g0209a0001c0005t0001g0249others(71): Show | 79 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.1226-3142C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113517474 | ||||||
| chr13:113517479
|
T | C | 80 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(77): 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 | 61 | a0002c0003t0003g0005a0002c0003t0003g0020a0002c0003t0003g0021others(58): 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 | 288 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0013others(285): Show | 306 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(303): 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 | a0001c0001t0010g0330 | 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 | 114 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0113others(111): 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 | a0001c0001t0001g0136a0001c0001t0004g0109 | 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 | a0002c0003t0003g0255 | 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 | a0001c0001t0004g0108 | 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 | 17 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(14): 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 | a0001c0001t0001g0194 | 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 | a0001c0001t0001g0149 | 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 | 73 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(70): 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 | 22 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(19): 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 | a0001c0001t0001g0216 | 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 | a0007c0021t0002g0054 | 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 | a0001c0001t0001g0013a0009c0013t0001g0013 | 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 | a0002c0004t0005g0318a0002c0004t0005g0319a0002c0004t0005g0320others(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 | a0001c0001t0001g0150 | 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 | 95 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(92): 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 | 95 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(92): 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 | 163 | a0001c0001t0001g0195a0001c0001t0010g0329a0001c0001t0010g0330others(160): 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 | a0003c0016t0002g0075 | 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 | a0001c0001t0001g0138 | 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 | 4 | a0003c0002t0002g0009a0003c0002t0002g0035a0003c0002t0002g0036others(1): Show | 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 | a0002c0003t0003g0268a0002c0003t0003g0290a0002c0003t0003g0291 | 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 | a0001c0001t0001g0230 | 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 | 170 | a0001c0001t0010g0329a0001c0001t0010g0330a0001c0006t0001g0232others(167): 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 | a0002c0004t0004g0091 | 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 | a0001c0001t0001g0126a0001c0001t0001g0138a0001c0001t0001g0164others(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 | 69 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(66): 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 | 17 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(14): 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 | a0003c0002t0002g0030a0003c0002t0002g0062a0003c0002t0002g0067 | 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 | 72 | a0002c0003t0003g0005a0002c0003t0003g0020a0002c0003t0003g0021others(69): 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 | a0002c0004t0005g0312 | 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 | a0003c0002t0002g0063 | 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 | 71 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(68): 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 | a0002c0004t0004g0011a0002c0004t0004g0091a0013c0018t0004g0090 | 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 | a0002c0004t0005g0312 | 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 | a0002c0004t0005g0312 | 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 | 95 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(92): 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 | a0001c0001t0004g0108 | 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 | 5 | a0003c0002t0002g0044a0003c0002t0002g0051a0003c0002t0002g0052others(2): 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 | a0001c0001t0001g0177 | 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 | 22 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(19): 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 | 95 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(92): 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 | 71 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(68): 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 | 95 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(92): 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 | 9 | a0001c0001t0004g0098a0001c0001t0004g0101a0001c0001t0004g0102others(6): 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 | a0006c0011t0008g0333 | 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 | a0002c0004t0004g0091 | 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 | a0001c0001t0001g0172a0001c0001t0001g0208a0001c0001t0004g0103others(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 | 76 | a0001c0006t0001g0235a0001c0006t0001g0236a0001c0006t0001g0237others(73): 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 | 13 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(10): 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 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0125others(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 | 6 | a0001c0001t0001g0019a0001c0001t0001g0200a0001c0001t0001g0206others(3): Show | 7 | HG00140.hp2 HG00733.hp2 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.1226-42T>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 7/12 | chr13 | 113520574 | ||||||
| chr13:113520794
|
C | G | 61 | a0002c0003t0003g0005a0002c0003t0003g0020a0002c0003t0003g0021others(58): 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 | 22 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(19): 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 | a0003c0016t0002g0075 | 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 | a0001c0001t0001g0161 | 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 | 22 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(19): 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 | 73 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(70): 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 | a0003c0002t0002g0044 | 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 | 95 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(92): 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 | 73 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(70): 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 | a0001c0001t0001g0092a0001c0001t0001g0160a0001c0001t0001g0309 | 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 | a0001c0001t0001g0113 | 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 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0195 | 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 | 19 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(16): 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 | a0002c0004t0004g0091 | 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 | a0003c0002t0002g0064a0003c0002t0002g0066 | 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 | 102 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0113others(99): 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 | a0003c0002t0002g0041a0003c0002t0002g0060 | 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 | 95 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(92): 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 | a0002c0003t0003g0269 | 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 | a0001c0001t0001g0092a0001c0001t0001g0309 | 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 | a0001c0001t0001g0113 | 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 | 73 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(70): 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 | 92 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(89): 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 | a0006c0011t0008g0332a0006c0011t0008g0333 | 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 | 19 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(16): 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 | a0002c0003t0003g0021 | 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 | a0001c0001t0010g0329a0001c0001t0010g0330 | 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 | a0001c0001t0001g0018a0001c0001t0001g0231 | 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 | 76 | a0001c0009t0004g0305a0001c0009t0004g0306a0001c0009t0004g0307others(73): 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 | 170 | a0001c0001t0010g0329a0001c0001t0010g0330a0001c0006t0001g0232others(167): 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 | a0001c0001t0001g0113a0012c0017t0001g0308 | 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 | 73 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(70): 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 | 73 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(70): 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 | 73 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(70): 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 | a0001c0001t0001g0225 | 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 | a0001c0001t0001g0093 | 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 | 75 | a0001c0001t0010g0329a0001c0001t0010g0330a0003c0002t0002g0006others(72): 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 | 73 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(70): 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 | 73 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(70): 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 | 98 | a0001c0001t0010g0329a0001c0001t0010g0330a0001c0001t0013g0163others(95): 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 | 73 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(70): 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 | a0001c0007t0006g0095a0001c0007t0006g0096a0001c0007t0006g0097others(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 | a0006c0011t0008g0332a0006c0011t0008g0333 | 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 | 73 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(70): 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 | a0003c0002t0002g0063 | 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 | 73 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(70): 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 | a0003c0002t0002g0022 | 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 | 73 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(70): 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 | a0001c0001t0001g0143a0001c0001t0001g0219 | 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 | a0001c0001t0001g0150 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1343+2786T>G | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113523519 | ||||||
| chr13:113523520
|
G | A | 335 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(332): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.1343+2787G>A | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113523520 | ||||||
| chr13:113523536
|
A | G | 73 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(70): 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 | 170 | a0001c0001t0010g0329a0001c0001t0010g0330a0001c0006t0001g0232others(167): 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 | 73 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(70): 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 | 6 | a0001c0001t0001g0019a0001c0001t0001g0200a0001c0001t0001g0206others(3): Show | 7 | HG00140.hp2 HG00733.hp2 HG01167.hp2 others(4): 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 | a0001c0001t0001g0093a0001c0001t0014g0089 | 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 | 73 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(70): 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 | 14 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(11): 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 | 73 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(70): 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 | 73 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(70): 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 | a0001c0001t0001g0092a0001c0001t0001g0309a0002c0004t0005g0324others(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 | 73 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(70): 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 | 73 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(70): 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 | a0002c0004t0004g0091 | 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 | a0001c0001t0001g0215 | 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 | a0001c0001t0001g0147 | 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 | 61 | a0002c0003t0003g0005a0002c0003t0003g0020a0002c0003t0003g0021others(58): 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 | 73 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(70): 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 | 73 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(70): 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 | 97 | a0001c0001t0010g0329a0001c0001t0010g0330a0001c0006t0001g0232others(94): 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 | a0001c0001t0010g0329a0001c0001t0010g0330 | 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 | a0001c0001t0004g0112 | 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 | a0001c0001t0001g0012a0001c0001t0001g0120a0001c0001t0001g0121others(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 | a0001c0001t0001g0014a0001c0001t0001g0140a0001c0001t0001g0148others(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 | a0002c0004t0005g0318 | 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 | a0007c0021t0002g0054 | 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 | a0002c0004t0005g0318 | 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 | 73 | a0002c0004t0005g0318a0003c0002t0002g0006a0003c0002t0002g0008others(70): 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 | a0001c0001t0010g0329a0001c0001t0010g0330 | 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | a0002c0004t0005g0318 | 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 | a0003c0002t0002g0055a0003c0002t0002g0068a0003c0002t0002g0077 | 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 | a0003c0002t0002g0056 | 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 |
58 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(55): 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 | a0003c0002t0002g0034 | 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 | a0002c0004t0005g0318a0003c0002t0002g0055a0003c0002t0002g0056others(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 | 73 | a0002c0004t0005g0318a0003c0002t0002g0006a0003c0002t0002g0008others(70): 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 | a0002c0004t0005g0318 | 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 | a0007c0021t0002g0054 | 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 | 10 | a0002c0004t0005g0318a0003c0002t0002g0042a0003c0002t0002g0043others(7): 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 |
4 | a0003c0002t0002g0042a0003c0002t0002g0043a0003c0002t0002g0072others(1): Show | 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 |
5 | a0003c0002t0002g0044a0003c0002t0002g0051a0003c0002t0002g0052others(2): 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 | 63 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(60): 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 | 74 | a0002c0003t0003g0260a0002c0004t0005g0318a0003c0002t0002g0006others(71): 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 | 4 | a0003c0002t0002g0042a0003c0002t0002g0043a0003c0002t0002g0072others(1): Show | 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 74 | a0001c0001t0010g0329a0001c0001t0010g0330a0003c0002t0002g0006others(71): 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 | 22 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(19): 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 | 73 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(70): 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 | a0001c0009t0004g0305a0001c0009t0004g0306a0001c0009t0004g0307 | 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 | a0001c0001t0001g0113 | 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 |
15 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(12): 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 | 74 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(71): 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 | a0003c0002t0002g0056 | 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 | a0001c0009t0004g0305a0001c0009t0004g0306a0001c0009t0004g0307 | 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 | 8 | a0002c0004t0005g0310a0002c0004t0005g0311a0002c0004t0005g0312others(5): 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 | 17 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(14): 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 | a0007c0021t0002g0054 | 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 | 73 | a0002c0004t0009g0331a0003c0002t0002g0006a0003c0002t0002g0008others(70): 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 | 3 | a0001c0001t0001g0007a0001c0001t0001g0151a0001c0001t0001g0170 | 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 | 72 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | a0006c0011t0008g0332a0006c0011t0008g0333 | 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 | a0001c0005t0001g0247a0001c0005t0001g0248a0001c0005t0001g0249others(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 | 61 | a0002c0003t0003g0005a0002c0003t0003g0020a0002c0003t0003g0021others(58): 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 | a0003c0002t0002g0010 | 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 | a0001c0001t0001g0174 | 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 | 73 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(70): 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 | a0002c0003t0003g0271a0002c0003t0003g0300 | 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 | a0002c0004t0009g0331 | 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 | a0002c0004t0004g0091 | 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 | 73 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(70): 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 | 17 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(14): 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 | 73 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(70): 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 | a0005c0010t0002g0050 | 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 | a0001c0001t0010g0329a0001c0001t0010g0330 | 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 | a0002c0003t0003g0297a0002c0003t0003g0298a0002c0003t0003g0299 | 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 | a0001c0001t0001g0093 | 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 | a0002c0004t0009g0331 | 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 | 83 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(80): 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 | 71 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(68): 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 | a0001c0001t0001g0113 | 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 | a0002c0004t0004g0011a0002c0004t0004g0091 | 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 | a0001c0001t0004g0108 | 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 | 73 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(70): 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 | a0001c0001t0010g0329a0001c0001t0010g0330a0003c0002t0002g0301others(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 | 169 | a0001c0001t0001g0088a0001c0001t0010g0329a0001c0001t0010g0330others(166): 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 | a0001c0001t0001g0303 | 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 | a0001c0007t0006g0304 | 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 | 17 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(14): 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 | a0001c0001t0001g0169 | 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 | a0001c0001t0001g0254 | 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 | a0001c0001t0001g0093a0001c0001t0014g0089 | 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 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0195 | 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 | a0002c0003t0003g0266 | 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 | 172 | a0001c0001t0001g0093a0001c0001t0010g0329a0001c0001t0010g0330others(169): 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 | 170 | a0001c0001t0010g0329a0001c0001t0010g0330a0001c0006t0001g0232others(167): 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 | a0001c0022t0001g0205 | 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 | a0002c0004t0009g0331 | 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 | a0001c0001t0001g0200a0001c0001t0001g0207 | 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 | a0003c0002t0002g0024 | 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 | a0006c0011t0008g0332a0006c0011t0008g0333 | 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 | 169 | a0001c0001t0010g0329a0001c0001t0010g0330a0001c0006t0001g0232others(166): 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 | a0004c0008t0004g0094a0004c0008t0004g0110a0004c0008t0004g0111 | 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 | a0002c0004t0005g0316a0002c0004t0005g0317 | 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 | a0003c0002t0002g0086a0003c0002t0002g0087 | 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 | 73 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(70): 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 | 8 | a0002c0004t0005g0310a0002c0004t0005g0311a0002c0004t0005g0312others(5): 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 | a0001c0001t0001g0225 | 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 | a0003c0002t0002g0056 | 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 | 6 | a0002c0004t0005g0310a0002c0004t0005g0311a0002c0004t0005g0312others(3): 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 | a0003c0002t0002g0057 | 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 | 73 | a0003c0002t0002g0006a0003c0002t0002g0008a0003c0002t0002g0009others(70): 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 | a0001c0005t0001g0115 | 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 | a0001c0001t0014g0089 | 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 | a0002c0004t0004g0011a0002c0004t0004g0091 | 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 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0195others(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 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0195others(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 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0195others(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 | 15 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(12): 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 | a0001c0001t0014g0089 | 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 | a0002c0019t0003g0287 | 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 | a0001c0009t0004g0305a0001c0009t0004g0306a0001c0009t0004g0307 | 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 | a0001c0009t0004g0305a0001c0009t0004g0306a0001c0009t0004g0307 | 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 | a0001c0009t0004g0305a0001c0009t0004g0306a0001c0009t0004g0307 | 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 | a0001c0009t0004g0305a0001c0009t0004g0306a0001c0009t0004g0307 | 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 | a0001c0001t0001g0093a0001c0001t0014g0089a0001c0009t0004g0305others(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 | a0001c0005t0001g0133a0001c0005t0001g0186a0001c0005t0001g0187others(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 | a0001c0007t0006g0095a0001c0007t0006g0096a0001c0007t0006g0097others(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 | a0001c0001t0001g0123 | 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 | a0001c0007t0006g0095a0001c0007t0006g0096a0001c0007t0006g0097others(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 | a0001c0007t0006g0095a0001c0007t0006g0096a0001c0007t0006g0097others(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 | 66 | a0001c0001t0001g0158a0001c0001t0001g0160a0001c0001t0001g0193others(63): 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 | 8 | a0003c0002t0002g0040a0003c0002t0002g0041a0003c0002t0002g0042others(5): 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 | a0002c0003t0003g0264 | 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 | 7 | a0001c0001t0010g0329a0001c0001t0010g0330a0002c0004t0004g0011others(4): 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 | a0002c0003t0003g0286 | 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 | a0002c0004t0004g0011a0002c0004t0004g0091 | 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 | 14 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(11): 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 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0195 | 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 | a0001c0001t0004g0099a0001c0001t0004g0100 | 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 | a0001c0001t0001g0151 | 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 | a0001c0001t0001g0151 | 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 | a0002c0004t0009g0331 | 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 | 61 | a0001c0001t0001g0012a0001c0001t0012g0012a0002c0003t0003g0005others(58): 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 | a0002c0003t0003g0270a0002c0003t0003g0296 | 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 | 4 | a0002c0004t0007g0313a0002c0004t0007g0314a0002c0004t0007g0315others(1): Show | 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 | a0002c0004t0004g0011a0002c0004t0004g0091 | 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 | a0002c0003t0003g0294 | 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 | 17 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(14): 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 | a0006c0011t0008g0332a0006c0011t0008g0333 | 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 | a0003c0002t0002g0040 | 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 | a0002c0003t0003g0285 | 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 | a0002c0004t0005g0310a0002c0004t0005g0311 | 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 | a0001c0007t0006g0095a0001c0007t0006g0096a0001c0007t0006g0097others(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 | a0001c0006t0001g0243 | 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 | a0001c0001t0001g0189 | 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 | 61 | a0002c0003t0003g0005a0002c0003t0003g0020a0002c0003t0003g0021others(58): 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 | a0001c0001t0001g0136a0001c0001t0001g0152a0001c0001t0001g0178others(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 | a0001c0007t0006g0095a0001c0007t0006g0096a0001c0007t0006g0097others(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 | a0001c0001t0001g0189 | 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 | a0002c0004t0005g0323 | 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 | a0013c0018t0004g0090 | 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 | 23 | a0001c0001t0001g0092a0001c0001t0001g0309a0001c0001t0004g0098others(20): 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 | 2 | a0001c0001t0001g0209a0008c0012t0001g0210 | 2 | HG01981.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1344-3104C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113530941 | ||||||
| chr13:113530952
|
C | A | 1 | a0001c0001t0004g0246 | 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 | a0002c0004t0004g0011a0002c0004t0004g0091 | 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 | 182 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(179): 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 | a0001c0001t0001g0153a0001c0001t0001g0183 | 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 | 2 | a0003c0002t0002g0035a0003c0002t0002g0036 | 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 | 165 | a0001c0001t0010g0329a0001c0001t0010g0330a0001c0006t0001g0232others(162): 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 | 6 | a0002c0004t0005g0310a0002c0004t0005g0311a0002c0004t0005g0312others(3): 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 | 10 | a0002c0004t0004g0011a0002c0004t0004g0091a0002c0004t0005g0310others(7): 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 | 172 | a0001c0001t0001g0093a0001c0001t0010g0329a0001c0001t0010g0330others(169): 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 | a0001c0001t0001g0092a0001c0001t0001g0309 | 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 | 19 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(16): 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 | a0002c0003t0003g0286 | 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 | a0002c0003t0003g0284 | 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 | a0001c0001t0014g0089 | 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 | a0001c0009t0004g0305a0001c0009t0004g0306a0001c0009t0004g0307 | 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 | 2 | a0001c0001t0001g0209a0008c0012t0001g0210 | 2 | HG01981.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1344-2365C>T | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 8/12 | chr13 | 113531680 | ||||||
| chr13:113531712
|
C | T | 1 | a0001c0001t0001g0015 | 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 | 76 | a0002c0004t0005g0316a0002c0004t0005g0317a0002c0004t0009g0331others(73): 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 | 74 | a0002c0004t0009g0331a0003c0002t0002g0006a0003c0002t0002g0008others(71): 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 | a0001c0007t0006g0304 | 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 | a0001c0005t0001g0247a0001c0005t0001g0248a0001c0005t0001g0249 | 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 | 8 | a0002c0004t0005g0310a0002c0004t0005g0311a0002c0004t0005g0312others(5): 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 | 167 | a0001c0001t0010g0329a0001c0001t0010g0330a0001c0006t0001g0232others(164): 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 | a0001c0001t0004g0109 | 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 | 167 | a0001c0001t0010g0329a0001c0001t0010g0330a0001c0006t0001g0232others(164): 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 | 10 | a0002c0004t0004g0011a0002c0004t0004g0091a0002c0004t0005g0310others(7): 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 | 197 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0113others(194): 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 | a0002c0003t0003g0262a0002c0003t0003g0263 | 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 | a0003c0002t0002g0076 | 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 | a0001c0001t0001g0139 | 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 | a0002c0004t0009g0331 | 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 | a0001c0001t0001g0140a0001c0001t0001g0157 | 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 | a0001c0001t0001g0139 | 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 | a0002c0004t0005g0320 | 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 | 4 | a0001c0001t0001g0195a0003c0002t0002g0006a0003c0002t0002g0080others(1): Show | 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 | a0002c0004t0004g0011 | 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 | 19 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(16): 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 | 8 | a0002c0004t0005g0310a0002c0004t0005g0311a0002c0004t0005g0312others(5): 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 | 72 | a0002c0004t0009g0331a0003c0002t0002g0006a0003c0002t0002g0008others(69): 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 | a0001c0007t0006g0095a0001c0007t0006g0096a0001c0007t0006g0097 | 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 | a0001c0001t0001g0113 | 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 | 21 | a0001c0001t0010g0329a0001c0001t0010g0330a0001c0006t0001g0232others(18): 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 |
7 | a0001c0001t0001g0019a0001c0001t0001g0156a0001c0001t0001g0200others(4): Show | 8 | HG00140.hp2 HG00733.hp2 HG01167.hp2 others(5): 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 | a0003c0016t0002g0075 | 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 | a0001c0001t0001g0144a0001c0001t0001g0183 | 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 | 19 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(16): 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 | a0003c0002t0002g0041a0003c0002t0002g0060a0003c0002t0002g0076 | 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 | a0003c0002t0002g0029 | 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 |
67 | a0002c0004t0009g0331a0003c0002t0002g0006a0003c0002t0002g0008others(64): 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 | a0013c0018t0004g0090 | 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 | 19 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(16): 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 | a0001c0001t0001g0012a0001c0001t0012g0012a0003c0002t0002g0057 | 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 | a0001c0001t0010g0329a0001c0001t0010g0330 | 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 | 8 | a0002c0004t0005g0310a0002c0004t0005g0311a0002c0004t0005g0312others(5): 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 | a0002c0004t0004g0011a0002c0004t0004g0091a0013c0018t0004g0090 | 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 | 10 | a0001c0001t0010g0329a0001c0001t0010g0330a0002c0004t0005g0310others(7): 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 | a0002c0003t0003g0283 | 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 | 19 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(16): 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 | 19 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(16): 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 | 60 | a0002c0003t0003g0005a0002c0003t0003g0020a0002c0003t0003g0021others(57): 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 | a0003c0002t0002g0024 | 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 | 19 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(16): 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 | a0003c0002t0002g0024 | 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 | a0001c0001t0014g0089 | 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 | a0002c0003t0003g0283 | 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 | a0002c0003t0003g0285 | 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 | 144 | a0002c0003t0003g0005a0002c0003t0003g0020a0002c0003t0003g0021others(141): 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 | 145 | a0002c0003t0003g0005a0002c0003t0003g0020a0002c0003t0003g0021others(142): 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 | 194 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0309others(191): 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 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0122others(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 | 147 | a0001c0005t0011g0176a0002c0003t0003g0005a0002c0003t0003g0020others(144): 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 | a0001c0001t0004g0108 | 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 | 61 | a0002c0003t0003g0005a0002c0003t0003g0020a0002c0003t0003g0021others(58): 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 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0122others(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 | 148 | a0001c0001t0010g0329a0001c0001t0010g0330a0002c0003t0003g0005others(145): 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 | 19 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(16): 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 | a0001c0001t0001g0182 | 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 | a0002c0004t0005g0317 | 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 | 285 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(282): 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 | 183 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(180): 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 | a0003c0002t0002g0030a0003c0002t0002g0062a0003c0002t0002g0067others(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 | 19 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(16): 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 | 165 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(162): 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 | a0001c0007t0006g0095 | 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 | a0001c0001t0001g0161 | 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 | a0003c0016t0002g0075 | 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 | a0001c0001t0001g0165a0001c0001t0001g0166 | 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 | 19 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(16): 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 | a0006c0011t0008g0332a0006c0011t0008g0333 | 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 | 189 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0309others(186): 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 | 285 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(282): 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 | a0013c0018t0004g0090 | 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 | a0013c0018t0004g0090 | 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 | a0013c0018t0004g0090 | 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 | 20 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(17): 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 | a0006c0011t0008g0332a0006c0011t0008g0333 | 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 | 187 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(184): 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 | a0002c0004t0004g0011a0002c0004t0004g0091 | 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 | 17 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(14): 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 | 184 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(181): 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 | a0003c0002t0002g0049 | 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 | a0001c0001t0001g0168 | 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 | a0001c0001t0001g0168 | 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 | 19 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(16): 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 | 19 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(16): 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 | a0001c0001t0001g0092a0001c0001t0001g0309 | 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 | a0006c0011t0008g0332 | 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 | a0001c0001t0001g0093a0001c0001t0001g0114 | 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 | 181 | a0001c0001t0001g0093a0001c0001t0004g0098a0001c0001t0004g0099others(178): 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 | 8 | a0002c0004t0005g0310a0002c0004t0005g0311a0002c0004t0005g0312others(5): 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 | a0001c0007t0006g0095 | 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 | a0003c0002t0002g0022 | 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 | 184 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(181): 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 | a0001c0001t0001g0137a0001c0001t0001g0138 | 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 | a0001c0001t0001g0175 | 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 | a0001c0001t0001g0309 | 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 | a0001c0001t0001g0113 | 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 | 88 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(85): 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 | a0002c0003t0003g0282 | 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 | 161 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(158): 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 | 72 | a0002c0004t0009g0331a0003c0002t0002g0008a0003c0002t0002g0009others(69): 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 | 23 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(20): 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 | 69 | a0002c0003t0003g0005a0002c0003t0003g0020a0002c0003t0003g0021others(66): 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 | a0001c0001t0001g0118a0001c0001t0001g0119 | 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 | a0001c0006t0001g0251 | 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 | a0002c0003t0003g0268a0002c0003t0003g0290a0002c0003t0003g0291 | 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 | a0001c0001t0004g0099a0001c0001t0004g0100a0001c0001t0004g0108others(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 | a0006c0011t0008g0332a0006c0011t0008g0333 | 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 | a0001c0001t0001g0220 | 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 | 17 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(14): 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 | 194 | a0001c0001t0001g0092a0001c0001t0001g0134a0001c0001t0001g0135others(191): 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 | a0002c0003t0003g0297a0002c0003t0003g0298a0002c0003t0003g0299 | 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 | a0006c0011t0008g0332a0006c0011t0008g0333 | 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 | 69 | a0002c0003t0003g0005a0002c0003t0003g0020a0002c0003t0003g0021others(66): 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 | 21 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(18): 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 | 3 | a0002c0004t0007g0313a0002c0004t0007g0314a0002c0004t0007g0315 | 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 | 184 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(181): 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 | 189 | a0001c0001t0001g0092a0001c0001t0001g0309a0001c0001t0004g0098others(186): 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 | a0007c0021t0002g0054 | 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 | 69 | a0002c0003t0003g0005a0002c0003t0003g0020a0002c0003t0003g0021others(66): 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 | a0001c0005t0001g0133a0001c0005t0001g0186a0001c0005t0001g0187others(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 | 170 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(167): 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 | 187 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(184): 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 |
170 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(167): 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 | 21 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(18): 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 | a0001c0005t0001g0197a0001c0005t0001g0198 | 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 | a0010c0015t0002g0071 | 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 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0014g0089 | 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 | 171 | a0001c0001t0001g0093a0001c0001t0004g0098a0001c0001t0004g0099others(168): 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 | a0001c0001t0001g0137a0001c0001t0001g0138 | 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 | a0013c0018t0004g0090 | 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 | 169 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(166): 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 | 170 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(167): 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 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0211others(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 | 74 | a0002c0004t0009g0331a0003c0002t0002g0006a0003c0002t0002g0008others(71): 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 | a0001c0001t0001g0093a0001c0001t0014g0089a0001c0007t0006g0095others(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 | 74 | a0002c0004t0009g0331a0003c0002t0002g0006a0003c0002t0002g0008others(71): 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 | a0006c0011t0008g0332a0006c0011t0008g0333 | 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 | 70 | a0001c0001t0004g0102a0002c0003t0003g0005a0002c0003t0003g0020others(67): 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 | a0002c0004t0005g0322 | 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 | a0002c0004t0004g0091 | 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 | 187 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(184): 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 | 67 | a0002c0003t0003g0005a0002c0003t0003g0020a0002c0003t0003g0021others(64): 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 | a0001c0005t0001g0229 | 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 | 27 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(24): 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 | 101 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(98): 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 | 27 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(24): 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 | a0001c0006t0001g0245 | 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 | 69 | a0002c0003t0003g0005a0002c0003t0003g0020a0002c0003t0003g0021others(66): 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 | a0001c0001t0001g0093a0001c0001t0014g0089 | 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 | a0001c0001t0001g0177 | 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 | a0001c0001t0001g0191 | 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 | a0001c0001t0001g0153 | 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 | a0002c0003t0003g0285 | 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 | a0001c0001t0001g0221 | 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 | a0002c0003t0003g0281 | 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 | a0006c0011t0008g0332a0006c0011t0008g0333 | 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 | a0002c0004t0004g0011a0002c0004t0004g0091 | 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 | 69 | a0002c0003t0003g0005a0002c0003t0003g0020a0002c0003t0003g0021others(66): 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 | a0001c0001t0001g0202 | 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 | 27 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(24): 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 | 69 | a0002c0003t0003g0005a0002c0003t0003g0020a0002c0003t0003g0021others(66): 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 | a0013c0018t0004g0090 | 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 | a0002c0003t0003g0284 | 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 | a0006c0011t0008g0332a0006c0011t0008g0333 | 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 | a0001c0001t0001g0093a0001c0001t0014g0089 | 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 | 143 | a0002c0003t0003g0005a0002c0003t0003g0020a0002c0003t0003g0021others(140): 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 | a0001c0007t0006g0095a0001c0007t0006g0096a0001c0007t0006g0097others(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 | a0013c0018t0004g0090 | 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 | a0006c0011t0008g0332a0006c0011t0008g0333 | 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 | 25 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(22): 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 | a0002c0004t0004g0011a0002c0004t0004g0091 | 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 | a0010c0015t0002g0071 | 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 | a0002c0004t0004g0011a0002c0004t0004g0091 | 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 | a0002c0004t0004g0011a0002c0004t0004g0091 | 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 | a0002c0004t0004g0011a0002c0004t0004g0091 | 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 | a0002c0004t0004g0011a0002c0004t0004g0091 | 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 | a0002c0004t0004g0011a0002c0004t0004g0091 | 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 | a0002c0004t0004g0011a0002c0004t0004g0091 | 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 | a0001c0005t0001g0197 | 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 | a0002c0004t0004g0011a0002c0004t0004g0091 | 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 | a0002c0004t0004g0011a0002c0004t0004g0091 | 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 | a0002c0004t0004g0011a0002c0004t0004g0091 | 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 | a0002c0004t0004g0011a0002c0004t0004g0091 | 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 | 168 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(165): 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 | a0002c0004t0004g0011a0002c0004t0004g0091 | 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 | a0002c0004t0004g0011a0002c0004t0004g0091 | 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 | a0002c0004t0004g0011a0002c0004t0004g0091 | 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 | 25 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(22): 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 | a0002c0004t0004g0011a0002c0004t0004g0091 | 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 | 27 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(24): 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 | 25 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(22): 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 | a0002c0004t0004g0011a0002c0004t0004g0091 | 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 | a0001c0001t0001g0166 | 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 | a0002c0003t0003g0280 | 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 | 23 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(20): 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 | a0001c0001t0001g0123 | 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 | a0001c0001t0001g0166a0002c0004t0004g0011a0002c0004t0004g0091 | 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 | a0001c0009t0004g0305a0001c0009t0004g0306a0001c0009t0004g0307 | 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 | 27 | a0001c0001t0001g0114a0001c0001t0001g0136a0001c0001t0001g0139others(24): 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 | 68 | a0002c0003t0003g0005a0002c0003t0003g0020a0002c0003t0003g0021others(65): 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 | a0002c0004t0004g0011a0002c0004t0004g0091 | 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 | 25 | a0001c0001t0001g0113a0001c0001t0004g0098a0001c0001t0004g0099others(22): 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 | 20 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(17): 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 | a0001c0001t0010g0329a0001c0001t0010g0330a0002c0004t0004g0011others(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 | a0001c0001t0010g0329a0001c0001t0010g0330a0002c0004t0004g0011others(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 | a0001c0001t0010g0329a0001c0001t0010g0330a0002c0004t0004g0011others(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 | a0001c0001t0010g0329a0001c0001t0010g0330a0002c0004t0004g0011others(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 | a0001c0001t0010g0329a0001c0001t0010g0330a0002c0004t0004g0011others(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 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0010g0329others(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 | a0001c0001t0001g0157 | 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 | a0001c0001t0010g0329a0001c0001t0010g0330a0002c0004t0004g0011others(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 | a0001c0001t0010g0329a0001c0001t0010g0330a0002c0004t0004g0011others(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 | a0001c0001t0010g0329a0001c0001t0010g0330a0002c0004t0004g0011others(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 | a0001c0001t0010g0329a0001c0001t0010g0330a0002c0004t0004g0011others(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 | a0001c0007t0006g0304 | 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 | 24 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(21): 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 | 25 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(22): 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 | 36 | a0001c0001t0001g0145a0001c0001t0001g0147a0001c0001t0001g0154others(33): 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 | a0001c0001t0001g0309a0001c0007t0006g0095a0001c0007t0006g0097 | 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 | a0001c0007t0006g0096 | 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 | a0001c0001t0001g0092 | 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 | a0003c0002t0002g0034 | 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 | a0001c0001t0001g0122 | 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 | a0001c0001t0001g0088 | 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 | a0001c0001t0001g0113a0001c0001t0001g0174a0001c0001t0001g0199others(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 | a0012c0017t0001g0308 | 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 | a0001c0001t0001g0147a0001c0001t0001g0154 | 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 | 158 | a0001c0001t0001g0093a0001c0001t0014g0089a0001c0006t0001g0232others(155): 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 | a0002c0004t0004g0011a0002c0004t0004g0091 | 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 | 25 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(22): 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 | a0003c0002t0002g0063 | 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 | 10 | a0002c0004t0005g0310a0002c0004t0005g0311a0002c0004t0005g0312others(7): 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 | a0003c0002t0002g0066 | 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 | a0003c0002t0002g0066 | 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 | a0003c0002t0002g0066 | 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 | 69 | a0002c0004t0009g0331a0003c0002t0002g0006a0003c0002t0002g0008others(66): 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 | 27 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(24): 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 | a0003c0002t0002g0066 | 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 | a0002c0004t0004g0011a0002c0004t0004g0091 | 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 | a0002c0004t0004g0011a0002c0004t0004g0091a0003c0002t0002g0066 | 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 | a0001c0001t0001g0153 | 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 | a0003c0002t0002g0010a0003c0002t0002g0022a0003c0002t0002g0066 | 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 | a0001c0001t0001g0136 | 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 | 25 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(22): 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 | a0002c0003t0003g0021a0002c0004t0005g0316 | 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 | a0002c0004t0004g0011a0002c0004t0004g0091 | 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 | 9 | a0003c0002t0002g0040a0003c0002t0002g0041a0003c0002t0002g0042others(6): 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 | a0002c0004t0004g0011a0002c0004t0004g0091a0003c0002t0002g0066 | 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 | a0003c0002t0002g0066 | 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 | a0003c0002t0002g0066 | 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 | a0003c0002t0002g0066 | 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 | a0002c0004t0004g0011a0002c0004t0004g0091 | 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 | a0001c0001t0001g0156 | 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 | a0001c0001t0001g0114a0001c0001t0001g0139a0001c0001t0001g0151others(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 | 28 | a0001c0001t0001g0113a0001c0001t0001g0136a0001c0001t0001g0199others(25): 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 | 59 | a0002c0003t0003g0005a0002c0003t0003g0020a0002c0003t0003g0255others(56): 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 | a0003c0002t0002g0066 | 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 | 19 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(16): 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 | 22 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(19): 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 | a0003c0002t0002g0066 | 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 | a0002c0003t0003g0267 | 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 | a0002c0004t0004g0011a0002c0004t0004g0091 | 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 | a0002c0004t0004g0011a0002c0004t0004g0091 | 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 | a0002c0004t0004g0011a0002c0004t0004g0091 | 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 | 62 | a0002c0004t0009g0331a0003c0002t0002g0006a0003c0002t0002g0008others(59): 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 | a0001c0005t0001g0115a0001c0005t0001g0116 | 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 | a0001c0001t0001g0019a0001c0001t0001g0088a0001c0001t0001g0193 | 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 |
42 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0013others(39): 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 | a0001c0001t0001g0014a0001c0001t0001g0147a0001c0001t0001g0148others(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 | 42 | a0001c0001t0001g0003a0001c0001t0001g0092a0001c0001t0001g0113others(39): 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 | a0003c0002t0002g0080a0003c0002t0002g0085 | 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 | a0001c0001t0001g0150a0001c0001t0001g0157 | 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 | 6 | a0002c0004t0005g0310a0002c0004t0005g0311a0002c0004t0005g0312others(3): 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 | a0003c0002t0002g0048 | 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 | a0003c0002t0002g0066 | 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 | a0002c0004t0004g0011a0002c0004t0004g0091 | 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 | 19 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(16): 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 | a0006c0011t0008g0332a0006c0011t0008g0333a0013c0018t0004g0090 | 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 | 24 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(21): 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 | a0002c0004t0004g0011a0002c0004t0004g0091 | 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 | 19 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(16): 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 | 7 | a0003c0002t0002g0009a0003c0002t0002g0010a0003c0002t0002g0032others(4): 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 | 35 | a0001c0001t0001g0093a0001c0001t0001g0177a0001c0001t0004g0098others(32): 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 | a0003c0002t0002g0034 | 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 | a0006c0011t0008g0332a0006c0011t0008g0333 | 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 | 21 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(18): 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 | 19 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(16): 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 | 19 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(16): 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 | 19 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(16): 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 | a0006c0011t0008g0332a0006c0011t0008g0333a0013c0018t0004g0090 | 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 | 27 | a0001c0001t0001g0093a0001c0001t0004g0098a0001c0001t0004g0099others(24): 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 | a0001c0005t0001g0117 | 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 | 19 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(16): 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 | a0002c0004t0004g0011a0002c0004t0004g0091 | 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 | 69 | a0001c0009t0004g0305a0001c0009t0004g0306a0001c0009t0004g0307others(66): 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 | 89 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(86): 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 | 19 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(16): 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 | a0002c0004t0004g0011a0002c0004t0004g0091a0006c0011t0008g0332others(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 | a0002c0004t0004g0011a0002c0004t0004g0091a0006c0011t0008g0332others(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 | a0002c0004t0004g0011a0002c0004t0004g0091a0006c0011t0008g0332others(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 | 64 | a0002c0004t0009g0331a0003c0002t0002g0006a0003c0002t0002g0008others(61): 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 | 92 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(89): 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 | a0006c0011t0008g0332a0006c0011t0008g0333a0013c0018t0004g0090 | 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 | 67 | a0001c0009t0004g0305a0001c0009t0004g0306a0001c0009t0004g0307others(64): 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 | 7 | a0003c0002t0002g0009a0003c0002t0002g0010a0003c0002t0002g0032others(4): 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 | 77 | a0001c0009t0004g0305a0001c0009t0004g0306a0001c0009t0004g0307others(74): 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 | a0003c0002t0002g0055a0003c0002t0002g0056a0003c0002t0002g0057others(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 | a0006c0011t0008g0332a0006c0011t0008g0333a0013c0018t0004g0090 | 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 | 7 | a0003c0002t0002g0009a0003c0002t0002g0010a0003c0002t0002g0032others(4): 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 | 59 | a0001c0009t0004g0305a0001c0009t0004g0306a0001c0009t0004g0307others(56): 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 | 100 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(97): 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 | a0003c0002t0002g0063 | 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 | 19 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(16): 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 | a0002c0004t0004g0011a0002c0004t0004g0091 | 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 | 7 | a0003c0002t0002g0009a0003c0002t0002g0010a0003c0002t0002g0032others(4): 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 | a0001c0001t0001g0153 | 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 | 19 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(16): 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 | 67 | a0001c0001t0004g0107a0001c0009t0004g0305a0001c0009t0004g0306others(64): 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 | a0002c0003t0003g0267 | 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 | 78 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(75): 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 | 78 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(75): 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 | 78 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(75): 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 | a0001c0009t0004g0305a0001c0009t0004g0306a0001c0009t0004g0307 | 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 | 7 | a0003c0002t0002g0009a0003c0002t0002g0010a0003c0002t0002g0032others(4): 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 | a0003c0002t0002g0034 | 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 | 99 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(96): 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 | 59 | a0001c0009t0004g0305a0001c0009t0004g0306a0001c0009t0004g0307others(56): 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 | 32 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(29): 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 | 24 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(21): 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 | 67 | a0001c0006t0001g0234a0001c0009t0004g0305a0001c0009t0004g0306others(64): 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 |
7 | a0003c0002t0002g0009a0003c0002t0002g0010a0003c0002t0002g0032others(4): 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 | 59 | a0001c0009t0004g0305a0001c0009t0004g0306a0001c0009t0004g0307others(56): 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 | 24 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(21): 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 | 24 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(21): 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 | 24 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(21): 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 | a0003c0002t0002g0062 | 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 | 98 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(95): 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 | 17 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(14): 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 | 69 | a0002c0003t0003g0005a0002c0003t0003g0020a0002c0003t0003g0021others(66): 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 | 19 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(16): 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 | 88 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(85): 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 | 8 | a0002c0004t0005g0310a0002c0004t0005g0311a0002c0004t0005g0312others(5): 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 | a0002c0003t0003g0296 | 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 | 161 | a0001c0001t0001g0092a0001c0001t0004g0098a0001c0001t0004g0099others(158): 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 | a0001c0001t0001g0309 | 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 | a0001c0006t0001g0252a0001c0006t0001g0253 | 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 | a0001c0006t0001g0244 | 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 |
13 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0235others(10): 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 | a0001c0006t0001g0234 | 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 | 67 | a0001c0009t0004g0305a0001c0009t0004g0306a0001c0009t0004g0307others(64): 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 | a0003c0002t0002g0034 | 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 | a0001c0001t0001g0180 | 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 | 69 | a0002c0003t0003g0005a0002c0003t0003g0020a0002c0003t0003g0021others(66): 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 | a0003c0002t0002g0048 | 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 | a0001c0001t0014g0089 | 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 | a0001c0001t0001g0093 | 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 | a0003c0002t0002g0048 | 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 | a0001c0009t0004g0307 | 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 | a0003c0002t0002g0301a0003c0002t0002g0302 | 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 | 143 | a0002c0003t0003g0005a0002c0003t0003g0020a0002c0003t0003g0021others(140): 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 | 69 | a0002c0003t0003g0005a0002c0003t0003g0020a0002c0003t0003g0021others(66): 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 | 23 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(20): 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 | 67 | a0002c0003t0003g0005a0002c0003t0003g0020a0002c0003t0003g0021others(64): 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 | a0001c0005t0001g0116 | 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 | a0002c0003t0003g0267 | 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 | a0001c0001t0001g0225 | 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 | 69 | a0002c0003t0003g0005a0002c0003t0003g0020a0002c0003t0003g0021others(66): 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 | a0003c0002t0002g0040 | 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 | a0003c0002t0002g0008a0003c0002t0002g0025a0003c0002t0002g0026others(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 | 138 | a0002c0003t0003g0005a0002c0003t0003g0020a0002c0003t0003g0021others(135): 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 | a0002c0003t0003g0267 | 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 | a0003c0002t0002g0032a0003c0002t0002g0033 | 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 | a0001c0001t0004g0099a0001c0001t0004g0100a0001c0001t0004g0108others(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 | a0002c0003t0003g0298a0002c0003t0003g0299 | 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 | a0001c0001t0010g0329a0001c0001t0010g0330 | 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 | a0001c0001t0001g0153 | 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 | a0001c0001t0001g0153 | 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 | a0001c0001t0001g0153 | 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 | a0001c0001t0001g0153 | 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 | a0001c0001t0001g0153 | 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 | a0001c0001t0001g0153 | 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 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0113others(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 | a0001c0001t0001g0153 | 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 | 168 | a0001c0001t0001g0019a0001c0001t0001g0123a0001c0001t0004g0098others(165): 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 | a0003c0002t0002g0044 | 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 | a0002c0003t0003g0284 | 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 | a0002c0003t0003g0267 | 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 | a0002c0003t0003g0267 | 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 | a0001c0001t0001g0153 | 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 | a0006c0011t0008g0333 | 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 | a0002c0003t0003g0269 | 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 | a0002c0003t0003g0269a0003c0002t0002g0044a0006c0011t0008g0333 | 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 | a0002c0003t0003g0286 | 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 | a0003c0002t0002g0028a0006c0011t0008g0333 | 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 | a0002c0003t0003g0269a0003c0002t0002g0044 | 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 | a0003c0002t0002g0028 | 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 | a0003c0002t0002g0028 | 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 | 53 | a0001c0001t0001g0123a0002c0003t0003g0021a0002c0003t0003g0258others(50): 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 | 51 | a0001c0001t0001g0123a0002c0003t0003g0020a0002c0003t0003g0021others(48): 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 | a0003c0002t0002g0028 | 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 | 50 | a0001c0001t0001g0123a0002c0003t0003g0020a0002c0003t0003g0258others(47): 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 | a0001c0001t0001g0113 | 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 | a0002c0003t0003g0286 | 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 | a0002c0003t0003g0021 | 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 | a0001c0001t0001g0092 | 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 | a0001c0001t0014g0089a0003c0002t0002g0008a0003c0002t0002g0025others(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 | a0001c0001t0001g0309 | 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 | a0001c0007t0006g0304 | 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 | a0003c0002t0002g0028 | 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 | a0003c0002t0002g0044 | 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 | a0002c0003t0003g0269a0002c0003t0003g0286 | 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 | a0001c0001t0004g0106 | 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 |
12 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(9): 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 | a0001c0006t0001g0235 | 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 | 92 | a0001c0001t0001g0092a0001c0001t0001g0113a0001c0001t0001g0162others(89): 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 | 53 | a0001c0001t0001g0123a0001c0006t0001g0244a0001c0006t0001g0252others(50): 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 | a0001c0001t0001g0092a0001c0001t0001g0309a0001c0007t0006g0304others(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 |
12 | a0001c0001t0004g0098a0001c0001t0004g0101a0001c0001t0004g0102others(9): 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 | a0002c0004t0004g0091 | 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 | a0006c0011t0008g0332 | 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 | a0001c0009t0004g0305a0001c0009t0004g0306 | 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 | a0001c0006t0001g0244 | 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 | a0001c0006t0001g0252a0001c0006t0001g0253 | 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 | a0003c0002t0002g0044 | 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 | a0002c0003t0003g0298 | 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 | 41 | a0001c0001t0001g0123a0002c0003t0003g0255a0002c0003t0003g0258others(38): 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 | a0003c0002t0002g0301a0003c0002t0002g0302 | 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 | a0002c0003t0003g0272 | 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 | a0003c0002t0002g0069a0003c0002t0002g0070 | 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 | a0013c0018t0004g0090 | 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 | a0013c0018t0004g0090 | 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 | 80 | a0001c0001t0001g0093a0001c0001t0001g0123a0001c0001t0010g0329others(77): 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 | a0001c0001t0010g0329a0001c0001t0010g0330 | 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 | a0001c0001t0001g0093 | 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 | a0013c0018t0004g0090 | 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 | a0002c0004t0004g0011 | 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 | a0001c0006t0001g0242 | 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 | 44 | a0001c0001t0001g0123a0001c0006t0001g0252a0001c0006t0001g0253others(41): 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 | 9 | a0002c0003t0003g0020a0002c0003t0003g0260a0002c0003t0003g0261others(6): 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 | a0001c0001t0010g0329a0001c0001t0010g0330a0013c0018t0004g0090 | 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 | a0001c0001t0010g0329a0001c0001t0010g0330a0013c0018t0004g0090 | 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 | a0001c0001t0001g0123a0002c0003t0003g0255a0002c0003t0003g0262others(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 | 61 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(58): 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 | a0001c0001t0001g0123a0002c0003t0003g0255a0002c0003t0003g0262others(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 |
11 | a0002c0003t0003g0020a0002c0003t0003g0260a0002c0003t0003g0261others(8): 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 | a0002c0004t0005g0320 | 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 | a0002c0003t0003g0280 | 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 | a0002c0003t0003g0259a0002c0003t0003g0264a0002c0003t0003g0265others(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 | a0002c0003t0003g0292 | 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 | a0002c0004t0005g0321 | 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 | a0002c0003t0003g0266 | 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 | a0002c0003t0003g0258 | 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 | a0002c0003t0003g0278a0002c0003t0003g0289a0002c0019t0003g0287 | 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 | a0002c0003t0003g0279 | 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 | a0002c0003t0003g0267 | 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 | 33 | a0002c0003t0003g0020a0002c0003t0003g0258a0002c0003t0003g0259others(30): 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 | 76 | a0001c0001t0001g0123a0001c0006t0001g0232a0001c0006t0001g0233others(73): 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 | a0002c0003t0003g0269a0002c0003t0003g0293 | 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 | a0003c0002t0002g0044 | 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 | 36 | a0002c0003t0003g0020a0002c0003t0003g0258a0002c0003t0003g0259others(33): 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 | a0003c0002t0002g0087 | 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 | 30 | a0001c0001t0001g0123a0001c0006t0001g0232a0001c0006t0001g0233others(27): 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 | a0001c0007t0006g0095a0001c0007t0006g0096a0001c0007t0006g0097 | 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 | a0006c0011t0008g0333 | 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 | a0001c0006t0001g0242 | 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 | a0006c0011t0008g0332 | 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 | a0001c0001t0004g0108a0001c0001t0004g0109a0001c0001t0010g0329others(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 | a0002c0004t0005g0316 | 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 | a0002c0004t0005g0317 | 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 | a0002c0004t0005g0316a0002c0004t0005g0317 | 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 | a0004c0008t0004g0094a0013c0018t0004g0090 | 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 | a0002c0003t0003g0267 | 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 | a0002c0003t0003g0267 | 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 | a0002c0003t0003g0267 | 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 | a0002c0003t0003g0267 | 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 | 9 | a0001c0001t0004g0098a0001c0001t0004g0101a0001c0001t0004g0103others(6): 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 | 91 | a0001c0001t0004g0098a0001c0001t0004g0101a0001c0001t0004g0102others(88): 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 | 76 | a0001c0009t0004g0305a0001c0009t0004g0306a0001c0009t0004g0307others(73): 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 | a0002c0003t0003g0267 | 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 | a0002c0004t0004g0011 | 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 | a0002c0003t0003g0267 | 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 | a0002c0003t0003g0268a0002c0003t0003g0290a0002c0003t0003g0291 | 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 | 76 | a0001c0001t0004g0098a0001c0001t0004g0101a0001c0001t0004g0102others(73): 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 | a0002c0003t0003g0267 | 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 | a0001c0001t0004g0107 | 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 | a0001c0001t0004g0099a0001c0001t0004g0100 | 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 | a0004c0008t0004g0094 | 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 | a0002c0003t0003g0277 | 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 | a0002c0003t0003g0286 | 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 | a0003c0002t0002g0056 | 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 | a0003c0002t0002g0028 | 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 | a0003c0002t0002g0301a0003c0002t0002g0302 | 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 | a0002c0004t0007g0315 | 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 | a0003c0002t0002g0073 | 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 | a0003c0002t0002g0030a0003c0002t0002g0067 | 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 |
44 | a0002c0003t0003g0021a0002c0003t0003g0256a0002c0004t0005g0310others(41): 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 | a0002c0004t0009g0331 | 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 | a0003c0002t0002g0036 | 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 | a0003c0002t0002g0043 | 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 | a0010c0015t0002g0071 | 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 | a0003c0002t0002g0060a0003c0002t0002g0066 | 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 | a0002c0004t0005g0327 | 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 | a0002c0004t0005g0324 | 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 | 15 | a0002c0003t0003g0005a0002c0003t0003g0257a0003c0002t0002g0006others(12): 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 | a0002c0004t0007g0313a0002c0004t0007g0314 | 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 | 22 | a0002c0003t0003g0005a0002c0003t0003g0255a0002c0003t0003g0257others(19): 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 | a0002c0003t0003g0268a0002c0003t0003g0290a0002c0003t0003g0291 | 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 | a0003c0016t0002g0075 | 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 | a0001c0001t0001g0153a0002c0003t0003g0268a0002c0003t0003g0290others(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 | a0013c0018t0004g0090 | 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 | a0002c0003t0003g0268a0002c0003t0003g0290a0002c0003t0003g0291 | 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 | a0002c0003t0003g0268a0002c0003t0003g0290a0002c0003t0003g0291others(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 | a0013c0018t0004g0090 | 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 | a0002c0003t0003g0268a0002c0003t0003g0290a0002c0003t0003g0291others(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 | a0002c0003t0003g0268a0002c0003t0003g0290a0002c0003t0003g0291 | 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 | a0013c0018t0004g0090 | 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 | a0013c0018t0004g0090 | 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 | a0002c0003t0003g0268a0002c0003t0003g0290a0002c0003t0003g0291others(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 | a0001c0001t0001g0153a0001c0001t0013g0163a0002c0003t0003g0267others(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 | a0013c0018t0004g0090 | 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 | a0013c0018t0004g0090 | 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 | a0001c0001t0001g0093a0001c0001t0001g0147a0002c0003t0003g0268others(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 | a0001c0007t0006g0095a0012c0017t0001g0308 | 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 | a0002c0003t0003g0268a0002c0003t0003g0290a0002c0003t0003g0291 | 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 | a0002c0003t0003g0268a0002c0003t0003g0290a0002c0003t0003g0291 | 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 | a0003c0002t0002g0052 | 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 | a0003c0002t0002g0051a0005c0010t0002g0050a0005c0010t0002g0053 | 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 | a0001c0007t0006g0096a0001c0007t0006g0097a0012c0017t0001g0308 | 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 | a0001c0001t0001g0018a0001c0005t0001g0133a0001c0005t0001g0186others(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 | a0001c0001t0001g0309 | 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 | a0001c0001t0001g0093a0001c0007t0006g0095a0001c0007t0006g0096others(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 | 8 | a0002c0003t0003g0268a0002c0003t0003g0290a0002c0003t0003g0291others(5): 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 | 8 | a0002c0003t0003g0268a0002c0003t0003g0290a0002c0003t0003g0291others(5): 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 | a0001c0001t0001g0018a0001c0005t0001g0133a0001c0005t0001g0186others(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 | 7 | a0002c0003t0003g0268a0002c0003t0003g0290a0002c0003t0003g0291others(4): 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 | a0003c0002t0002g0072 | 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 | a0003c0002t0002g0039 | 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 | a0001c0001t0001g0162a0002c0003t0003g0288 | 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 | a0003c0002t0002g0041a0003c0002t0002g0060 | 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 | a0006c0011t0008g0332 | 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 | a0002c0003t0003g0020a0002c0003t0003g0261a0002c0003t0003g0262others(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 |
16 | a0003c0002t0002g0030a0003c0002t0002g0031a0003c0002t0002g0042others(13): 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 | a0007c0021t0002g0054 | 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 | a0001c0001t0004g0099a0001c0001t0004g0100a0001c0001t0004g0105others(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 | a0003c0002t0002g0301a0003c0002t0002g0302 | 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 | a0003c0002t0002g0056 | 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 | a0003c0002t0002g0037a0003c0002t0002g0063 | 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 | 7 | a0002c0003t0003g0268a0002c0003t0003g0290a0002c0003t0003g0291others(4): 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 | a0002c0003t0003g0278 | 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 | a0002c0004t0005g0310a0002c0004t0005g0311a0002c0004t0005g0312others(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 | a0003c0002t0002g0087 | 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 | a0003c0002t0002g0086 | 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 | a0002c0004t0009g0331a0003c0002t0002g0084 | 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 | a0010c0015t0002g0071 | 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 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0001g0195 | 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 | 101 | a0001c0001t0001g0092a0001c0001t0001g0113a0001c0001t0004g0098others(98): 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 | a0003c0002t0002g0029 | 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 | a0001c0001t0001g0093a0001c0006t0001g0236a0001c0007t0006g0095others(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 | 93 | a0001c0001t0001g0092a0001c0001t0004g0098a0001c0001t0004g0101others(90): 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 | a0003c0002t0002g0066 | 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 | a0001c0009t0004g0305a0001c0009t0004g0306a0001c0009t0004g0307others(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 | a0001c0009t0004g0305a0001c0009t0004g0306a0001c0009t0004g0307others(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 | a0003c0002t0002g0040 | 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 | 12 | a0002c0003t0003g0005a0002c0003t0003g0256a0002c0003t0003g0257others(9): 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 | a0001c0001t0001g0093a0001c0006t0001g0236a0001c0007t0006g0095others(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 | a0001c0009t0004g0305a0001c0009t0004g0306a0001c0009t0004g0307others(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 | a0002c0003t0003g0267 | 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 | a0001c0009t0004g0305a0001c0009t0004g0306a0001c0009t0004g0307 | 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 | a0002c0003t0003g0297 | 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 |
3 | a0003c0002t0002g0006a0003c0002t0002g0081a0003c0023t0002g0023 | 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 | a0003c0002t0002g0035 | 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 | a0002c0003t0003g0005a0002c0003t0003g0256a0002c0003t0003g0257others(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 | a0002c0004t0005g0327 | 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 | 117 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0113others(114): 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 | 113 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0113others(110): 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 | 10 | a0001c0009t0004g0305a0001c0009t0004g0306a0001c0009t0004g0307others(7): 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 | 65 | a0001c0001t0001g0092a0001c0001t0004g0108a0001c0001t0004g0109others(62): 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 | a0002c0003t0003g0275 | 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 | a0002c0004t0005g0310 | 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 | a0003c0002t0002g0074 | 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 | a0001c0007t0006g0304 | 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 | a0002c0004t0005g0311a0002c0004t0005g0312a0003c0002t0002g0008others(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 | a0003c0002t0002g0083 | 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 | a0001c0001t0001g0113 | 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 | a0001c0001t0001g0093a0001c0001t0004g0098a0001c0001t0004g0101others(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 | 95 | a0001c0001t0001g0092a0001c0001t0001g0113a0001c0001t0004g0108others(92): 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 | a0001c0001t0001g0093a0001c0001t0004g0098a0001c0001t0004g0101others(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 | 122 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0113others(119): 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 | a0003c0002t0002g0022 | 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 | a0003c0002t0002g0044a0003c0002t0002g0046 | 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 | a0001c0001t0001g0092a0001c0001t0014g0089a0001c0006t0001g0239others(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 | 22 | a0001c0001t0004g0108a0001c0001t0004g0109a0001c0001t0010g0329others(19): 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 | a0001c0001t0001g0092a0001c0001t0001g0124a0001c0001t0001g0173others(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 | a0001c0001t0001g0113a0001c0001t0001g0152a0001c0007t0006g0304others(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 | a0002c0003t0003g0005a0002c0003t0003g0256a0002c0003t0003g0257others(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 | a0002c0003t0003g0279 | 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 | 48 | a0001c0001t0001g0093a0001c0001t0004g0098a0001c0001t0004g0101others(45): 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 | 48 | a0001c0001t0001g0093a0001c0001t0004g0098a0001c0001t0004g0101others(45): 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 | 30 | a0001c0001t0004g0108a0001c0001t0004g0109a0001c0001t0010g0329others(27): 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 | 56 | a0001c0001t0001g0093a0001c0001t0004g0098a0001c0001t0004g0101others(53): 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 | 37 | a0001c0001t0001g0092a0001c0001t0001g0113a0001c0001t0004g0108others(34): 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 | a0001c0007t0006g0095a0001c0007t0006g0096a0001c0007t0006g0097others(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 | 63 | a0001c0001t0001g0093a0001c0001t0001g0113a0001c0001t0004g0098others(60): 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 | 9 | a0001c0001t0001g0113a0001c0007t0006g0304a0002c0003t0003g0275others(6): 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 | 56 | a0001c0001t0001g0093a0001c0001t0004g0098a0001c0001t0004g0101others(53): 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 | a0002c0003t0003g0005a0002c0003t0003g0256a0002c0003t0003g0257others(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 | 68 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0004g0098others(65): 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 | a0002c0004t0005g0310a0003c0002t0002g0006a0003c0002t0002g0030others(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 | a0001c0009t0004g0306a0001c0009t0004g0307 | 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 |
27 | a0002c0004t0005g0311a0002c0004t0005g0312a0003c0002t0002g0008others(24): 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 | a0002c0003t0003g0295 | 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 | a0003c0002t0002g0062 | 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 | a0001c0001t0004g0108a0001c0001t0004g0109a0001c0001t0010g0329others(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 | a0006c0011t0008g0333 | 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 | 9 | a0001c0001t0001g0113a0001c0007t0006g0304a0002c0003t0003g0275others(6): 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 | a0001c0001t0014g0089a0001c0006t0001g0236a0001c0006t0001g0241others(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 | 45 | a0001c0001t0001g0113a0001c0001t0004g0108a0001c0001t0004g0109others(42): 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 |
11 | a0001c0001t0001g0092a0001c0006t0001g0232a0001c0006t0001g0233others(8): 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 | a0002c0003t0003g0005a0002c0003t0003g0256a0002c0003t0003g0257others(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 | a0001c0006t0001g0244a0002c0003t0003g0262a0002c0003t0003g0263others(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 | 43 | a0001c0001t0001g0093a0001c0001t0004g0098a0001c0001t0004g0101others(40): 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 | a0001c0006t0001g0236a0001c0006t0001g0241a0001c0006t0001g0243others(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 | a0001c0001t0014g0089 | 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 | a0001c0006t0001g0236a0001c0006t0001g0241a0001c0006t0001g0243others(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 | 59 | a0001c0001t0001g0113a0001c0001t0004g0108a0001c0001t0004g0109others(56): 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 | a0002c0003t0003g0005a0002c0003t0003g0256a0002c0003t0003g0257others(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 | a0001c0006t0001g0236a0001c0006t0001g0241a0001c0006t0001g0243others(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 | 50 | a0001c0001t0001g0113a0001c0001t0004g0108a0001c0001t0004g0109others(47): 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 | a0003c0002t0002g0010 | 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 | 55 | a0001c0001t0001g0113a0001c0001t0001g0182a0001c0001t0004g0108others(52): 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 |
8 | a0002c0003t0003g0260a0002c0003t0003g0271a0002c0003t0003g0272others(5): 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 | a0001c0001t0001g0093a0001c0001t0004g0098a0001c0001t0004g0101others(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 | a0001c0001t0001g0182a0001c0009t0004g0305a0002c0004t0009g0331others(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 | a0001c0001t0001g0177a0001c0001t0001g0203a0002c0003t0003g0255others(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 | a0001c0006t0001g0236a0001c0006t0001g0241a0001c0006t0001g0243others(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 | a0002c0004t0004g0011a0003c0002t0002g0006 | 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 | a0001c0006t0001g0236a0001c0006t0001g0241a0001c0006t0001g0243others(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 | 157 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0113others(154): 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 | 97 | a0001c0001t0001g0093a0001c0001t0001g0113a0001c0001t0001g0120others(94): 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 | a0003c0002t0002g0057 | 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 | a0003c0002t0002g0041a0003c0002t0002g0060 | 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 | a0003c0002t0002g0043 | 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 | a0001c0001t0001g0092a0001c0001t0004g0099a0001c0001t0004g0100others(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 | a0002c0003t0003g0274 | 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 | a0006c0011t0008g0332 | 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 | a0003c0002t0002g0030a0003c0002t0002g0067 | 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 | a0003c0002t0002g0055a0003c0002t0002g0056a0003c0002t0002g0058others(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 | a0003c0002t0002g0039a0003c0002t0002g0040 | 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 | a0002c0003t0003g0265a0003c0002t0002g0068a0003c0002t0002g0077 | 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 | a0007c0021t0002g0054 | 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 | a0003c0002t0002g0031 | 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 | a0003c0002t0002g0052a0003c0002t0002g0087 | 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 | a0003c0002t0002g0051 | 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 | a0003c0002t0002g0072 | 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 | a0010c0015t0002g0071 | 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 | a0005c0010t0002g0050a0005c0010t0002g0053 | 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 | a0002c0004t0005g0310 | 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 | a0001c0006t0001g0244 | 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 | a0002c0003t0003g0267 | 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 |
10 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(7): 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 | a0002c0004t0004g0011a0003c0002t0002g0006 | 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 | a0002c0004t0004g0091 | 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 | 12 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(9): 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 | a0001c0001t0004g0105a0003c0002t0002g0063a0003c0002t0002g0301 | 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 | a0002c0003t0003g0005a0002c0003t0003g0256a0002c0003t0003g0257others(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 | a0002c0004t0004g0091 | 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 | a0002c0004t0004g0091 | 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 | a0003c0002t0002g0302 | 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 | a0001c0006t0001g0244a0002c0003t0003g0005a0002c0003t0003g0256others(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 | a0001c0006t0001g0241a0001c0006t0001g0243a0001c0006t0001g0251 | 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 | a0001c0009t0004g0305 | 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 | a0003c0002t0002g0302 | 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 | a0003c0002t0002g0042 | 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 | a0001c0001t0001g0145 | 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 | a0001c0001t0001g0190a0001c0005t0001g0184a0001c0005t0001g0185others(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 | a0001c0006t0001g0252a0001c0006t0001g0253 | 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 | a0002c0003t0003g0298a0002c0003t0003g0299 | 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 | 19 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(16): 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 | a0002c0004t0004g0091 | 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 | 12 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(9): 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 | a0003c0002t0002g0022 | 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 | a0001c0006t0001g0241a0001c0006t0001g0243a0001c0006t0001g0251 | 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 | a0001c0006t0001g0252a0001c0006t0001g0253 | 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 | 74 | a0001c0001t0001g0092a0001c0001t0001g0199a0001c0001t0004g0098others(71): 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 | a0001c0009t0004g0305 | 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 | 100 | a0001c0001t0001g0003a0001c0001t0001g0092a0001c0001t0001g0172others(97): 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 | a0001c0006t0001g0236a0002c0003t0003g0298a0002c0003t0003g0299others(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 | a0001c0009t0004g0305 | 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 | a0001c0006t0001g0236 | 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 | a0002c0003t0003g0298a0002c0003t0003g0299a0002c0004t0004g0091 | 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 | 29 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(26): 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 | 16 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(13): 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 | a0001c0006t0001g0237 | 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 | a0001c0006t0001g0236 | 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 | a0003c0002t0002g0047 | 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 | a0003c0002t0002g0006 | 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 | a0001c0006t0001g0237 | 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 | a0001c0001t0001g0173 | 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 | a0001c0006t0001g0236a0002c0004t0004g0091 | 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 | a0001c0001t0001g0173 | 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 | a0001c0001t0001g0003a0001c0001t0001g0172a0001c0001t0001g0174 | 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 | a0003c0002t0002g0006 | 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 | a0001c0001t0014g0089a0003c0016t0002g0075 | 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 | a0001c0006t0001g0252a0001c0006t0001g0253 | 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 | a0002c0003t0003g0005a0002c0003t0003g0256a0002c0003t0003g0257others(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 | a0001c0006t0001g0237a0002c0003t0003g0276 | 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 | a0001c0006t0001g0236a0002c0004t0004g0091 | 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 | a0002c0003t0003g0298a0002c0003t0003g0299 | 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 |
13 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(10): 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 | a0001c0001t0014g0089a0001c0006t0001g0237a0001c0006t0001g0252others(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 | a0001c0001t0014g0089 | 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 | a0003c0016t0002g0075 | 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 | a0001c0001t0014g0089 | 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 | a0001c0001t0014g0089a0001c0006t0001g0236a0002c0004t0004g0091others(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 | a0001c0001t0001g0114a0001c0001t0001g0139 | 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 | a0001c0001t0001g0125a0001c0001t0001g0129a0001c0001t0001g0164others(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 | a0001c0006t0001g0236a0002c0003t0003g0289 | 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 | a0002c0003t0003g0289 | 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 | a0001c0001t0001g0153 | 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 | a0002c0003t0003g0289 | 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 | a0002c0003t0003g0289 | 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 | a0002c0004t0004g0011a0013c0018t0004g0090 | 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 | a0001c0001t0001g0153 | 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 | a0001c0001t0001g0153 | 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 | a0002c0004t0009g0331 | 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 | a0001c0001t0004g0098 | 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 | 283 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(280): 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 | 283 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(280): 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 | a0001c0001t0010g0329a0001c0001t0010g0330 | 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 | a0002c0003t0003g0274 | 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 | a0001c0006t0001g0242 | 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 | a0001c0001t0010g0329a0001c0001t0010g0330 | 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 | a0001c0006t0001g0239a0001c0006t0001g0242 | 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 | a0003c0002t0002g0037 | 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 | a0001c0001t0001g0017 | 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 | 67 | a0002c0004t0009g0331a0003c0002t0002g0006a0003c0002t0002g0008others(64): 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 | 71 | a0001c0001t0001g0155a0002c0003t0003g0005a0002c0003t0003g0020others(68): 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 | 67 | a0002c0003t0003g0005a0002c0003t0003g0020a0002c0003t0003g0021others(64): 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 | a0001c0001t0001g0113 | 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 | a0001c0001t0014g0089 | 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 | a0001c0006t0001g0244 | 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 | a0001c0001t0004g0109 | 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 | a0013c0018t0004g0090 | 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 | 136 | a0002c0003t0003g0005a0002c0003t0003g0020a0002c0003t0003g0021others(133): 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 | 27 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(24): 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 | 27 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(24): 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 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0113others(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 | 60 | a0001c0001t0004g0100a0002c0003t0003g0005a0002c0003t0003g0020others(57): 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 | 74 | a0002c0004t0009g0331a0003c0002t0002g0006a0003c0002t0002g0008others(71): 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 | a0001c0001t0004g0099a0001c0001t0004g0100a0001c0001t0004g0108others(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 | a0003c0002t0002g0030a0003c0002t0002g0062a0003c0002t0002g0067others(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 | a0001c0001t0001g0159 | 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 | a0002c0004t0004g0011a0002c0004t0004g0091 | 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 | a0001c0001t0001g0159a0001c0001t0001g0173a0001c0001t0013g0163 | 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 | 27 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(24): 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 | 74 | a0002c0004t0009g0331a0003c0002t0002g0006a0003c0002t0002g0008others(71): 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 | a0001c0006t0001g0244 | 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 | a0001c0001t0001g0138a0001c0001t0001g0173a0001c0001t0001g0214others(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 | a0006c0011t0008g0332a0006c0011t0008g0333 | 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 | 74 | a0002c0004t0009g0331a0003c0002t0002g0006a0003c0002t0002g0008others(71): 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 | a0001c0001t0001g0113a0001c0001t0001g0213a0001c0001t0001g0214others(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 | a0001c0001t0001g0153a0001c0001t0001g0167a0001c0001t0004g0106others(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 | a0003c0002t0002g0084 | 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 | a0003c0002t0002g0040 | 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 | a0001c0001t0001g0017a0001c0001t0001g0129a0001c0001t0001g0130 | 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 | a0003c0002t0002g0026 | 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 | 143 | a0002c0003t0003g0005a0002c0003t0003g0020a0002c0003t0003g0021others(140): 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 | a0002c0003t0003g0262a0002c0003t0003g0263 | 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 | 74 | a0002c0004t0009g0331a0003c0002t0002g0006a0003c0002t0002g0008others(71): 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 | 74 | a0002c0004t0009g0331a0003c0002t0002g0006a0003c0002t0002g0008others(71): 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 | 197 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0113others(194): 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 | 197 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0113others(194): 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 | a0002c0004t0005g0316 | 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 | a0001c0001t0001g0173 | 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 | a0012c0017t0001g0308 | 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 | 170 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(167): 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 | a0001c0001t0010g0329a0001c0001t0010g0330 | 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 | a0001c0001t0004g0109 | 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 | a0001c0009t0004g0305a0001c0009t0004g0306a0001c0009t0004g0307 | 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 | 101 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(98): 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 | 104 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(101): 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 | a0002c0004t0005g0318a0002c0004t0005g0319a0002c0004t0005g0328 | 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 | a0001c0001t0001g0159 | 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 | a0001c0001t0001g0199 | 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 | a0003c0014t0009g0196 | 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 | a0001c0001t0001g0171 | 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 | a0001c0001t0001g0173 | 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 | a0001c0001t0001g0173 | 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 | a0001c0001t0001g0173 | 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 | a0001c0001t0001g0147a0001c0001t0001g0154 | 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 | a0001c0005t0001g0117 | 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 | a0003c0002t0002g0080 | 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 | 80 | a0002c0003t0003g0276a0002c0004t0004g0011a0002c0004t0004g0091others(77): 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 | a0001c0001t0001g0155 | 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 | a0002c0004t0004g0011a0002c0004t0004g0091 | 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 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0201others(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 |
21 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(18): 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 | a0001c0007t0006g0304 | 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 | 6 | a0002c0004t0005g0310a0002c0004t0005g0311a0002c0004t0005g0312others(3): 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 | a0001c0001t0001g0201 | 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 | a0013c0018t0004g0090 | 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 | 68 | a0002c0003t0003g0005a0002c0003t0003g0020a0002c0003t0003g0021others(65): 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 | 198 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0113others(195): 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 | a0013c0018t0004g0090 | 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 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0113others(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 | 62 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(59): 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 | a0002c0004t0004g0011a0002c0004t0004g0091 | 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 | 198 | a0001c0001t0001g0088a0001c0001t0001g0092a0001c0001t0001g0093others(195): 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 | a0001c0001t0001g0150 | 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 | 8 | a0002c0004t0005g0310a0002c0004t0005g0311a0002c0004t0005g0312others(5): 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 | a0002c0003t0003g0276 | 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 | 74 | a0002c0004t0009g0331a0003c0002t0002g0006a0003c0002t0002g0008others(71): 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 | 60 | a0002c0003t0003g0005a0002c0003t0003g0020a0002c0003t0003g0021others(57): 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 | 70 | a0002c0004t0009g0331a0003c0002t0002g0006a0003c0002t0002g0008others(67): 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 | a0003c0002t0002g0024a0006c0011t0008g0332a0006c0011t0008g0333 | 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 | a0003c0002t0002g0028 | 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 | a0001c0001t0001g0173 | 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 | a0001c0001t0001g0173 | 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 | 75 | a0001c0007t0006g0095a0002c0004t0009g0331a0003c0002t0002g0006others(72): 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 | a0012c0017t0001g0308 | 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 | a0003c0016t0002g0075 | 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 | a0003c0002t0002g0080 | 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 | 9 | a0001c0001t0004g0098a0001c0001t0004g0101a0001c0001t0004g0102others(6): 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 | a0001c0009t0004g0306 | 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 | a0001c0001t0001g0193 | 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 | 68 | a0002c0003t0003g0005a0002c0003t0003g0020a0002c0003t0003g0255others(65): 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 | 68 | a0002c0003t0003g0005a0002c0003t0003g0020a0002c0003t0003g0255others(65): 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 | 61 | a0001c0007t0006g0097a0002c0003t0003g0005a0002c0003t0003g0020others(58): 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 | a0003c0002t0002g0074 | 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 | 158 | a0001c0001t0001g0182a0001c0001t0004g0098a0001c0001t0004g0099others(155): 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 | 73 | a0002c0003t0003g0021a0002c0004t0009g0331a0003c0002t0002g0006others(70): 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 | a0001c0007t0006g0096 | 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 | a0001c0006t0001g0244 | 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 | 152 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0113others(149): 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 | a0002c0003t0003g0284 | 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 | a0003c0016t0002g0075 | 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 | 69 | a0002c0003t0003g0005a0002c0003t0003g0020a0002c0003t0003g0021others(66): 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 | a0001c0007t0006g0304 | 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 | 17 | a0001c0006t0001g0232a0001c0006t0001g0233a0001c0006t0001g0234others(14): 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 | a0001c0001t0001g0223 | 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 | a0001c0001t0001g0151 | 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 | a0001c0001t0001g0162a0001c0001t0013g0163 | 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 | a0002c0003t0003g0005a0002c0003t0003g0257a0011c0020t0003g0005 | 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 | 5 | a0003c0002t0002g0044a0003c0002t0002g0051a0003c0002t0002g0052others(2): 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 | 96 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(93): 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 | a0003c0016t0002g0075 | 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 | 27 | a0001c0001t0004g0098a0001c0001t0004g0099a0001c0001t0004g0100others(24): 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 | 69 | a0002c0003t0003g0005a0002c0003t0003g0020a0002c0003t0003g0021others(66): 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 | 185 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0113others(182): 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 | 74 | a0002c0004t0009g0331a0003c0002t0002g0006a0003c0002t0002g0008others(71): 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 | a0001c0001t0001g0092a0001c0001t0001g0309 | 2 | NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1921-20T>C | TMCO3 | ENSG00000150403.18 | transcript | ENST00000434316.7 | protein_coding | 12/12 | chr13 | 113549405 |