Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 114908 |
|---|---|
| ensemblid | ENSG00000152558.15 |
| hgncid | 30138 |
| symbol | TMEM123 |
| name | transmembrane protein 123 |
| refseq_nuc | NM_052932.3 |
| refseq_prot | NP_443164.2 |
| ensembl_nuc | ENST00000398136.7 |
| ensembl_prot | ENSP00000381204.2 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 102396332 |
| end | 102452765 |
| strand | - |
| ver | v1.2 |
| region | chr11:102396332-102452765 |
| region5000 | chr11:102391332-102457765 |
| regionname0 | TMEM123_chr11_102396332_102452765 |
| regionname5000 | TMEM123_chr11_102391332_102457765 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 208 | 185 | 80 | 38 | 32 | 9 | 24 | 18 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| a0002 | 0/0 | 208 | 9 | 1 | 5 | 0 | 1 | 2 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| a0003 | 0/0 | 208 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| a0004 | 0/0 | 208 | 4 | 1 | 1 | 0 | 0 | 2 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| a0005 | 0/0 | 208 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 627 | 177 | 73 | 38 | 31 | 9 | 24 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| c0002 | 0/0 | 627 | 9 | 1 | 5 | 0 | 1 | 2 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| c0003 | 0/0 | 627 | 5 | 4 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| c0004 | 0/0 | 627 | 5 | 5 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| c0005 | 0/0 | 627 | 4 | 1 | 1 | 0 | 0 | 2 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| c0006 | 0/0 | 627 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| c0007 | 0/0 | 627 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| c0008 | 0/0 | 627 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 2677 | 132 | 41 | 32 | 30 | 7 | 21 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| t0002 | 0/0 | 2677 | 10 | 9 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| t0003 | 0/0 | 2676 | 8 | 5 | 3 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| t0004 | 0/0 | 2677 | 5 | 4 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| t0005 | 0/0 | 2681 | 5 | 1 | 2 | 0 | 0 | 2 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| t0006 | 0/0 | 2677 | 5 | 4 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| t0007 | 0/0 | 2677 | 4 | 4 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| t0008 | 0/0 | 2646 | 4 | 4 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| t0009 | 0/0 | 2677 | 4 | 0 | 3 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| t0010 | 0/0 | 2673 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| t0011 | 0/0 | 2677 | 3 | 1 | 1 | 0 | 1 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| t0012 | 0/0 | 2677 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| t0013 | 1/0 | 2678 | 2 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| t0014 | 0/0 | 2677 | 2 | 0 | 1 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| t0015 | 0/0 | 2677 | 2 | 0 | 0 | 1 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| t0016 | 0/0 | 2677 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| t0017 | 0/0 | 2677 | 2 | 0 | 0 | 0 | 1 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| t0018 | 0/0 | 2677 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| t0019 | 0/0 | 2677 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| t0020 | 0/0 | 2677 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| t0021 | 0/0 | 2677 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| t0022 | 0/0 | 2677 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| t0023 | 0/0 | 2677 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| t0024 | 0/0 | 2646 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| t0025 | 0/0 | 2676 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| t0026 | 0/0 | 2677 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0004 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0009 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0189 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 627 | 177 | 73 | 38 | 31 | 9 | 24 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| a0001c0004 | 0/0 | 627 | 5 | 5 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| a0001c0006 | 0/0 | 627 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| a0001c0007 | 0/0 | 627 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| a0002c0002 | 0/0 | 627 | 9 | 1 | 5 | 0 | 1 | 2 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| a0003c0003 | 0/0 | 627 | 5 | 4 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| a0004c0005 | 0/0 | 627 | 4 | 1 | 1 | 0 | 0 | 2 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| a0005c0008 | 0/0 | 627 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3303 | 122 | 40 | 27 | 29 | 6 | 19 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| a0001c0001t0002 | 0/0 | 3303 | 10 | 9 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| a0001c0001t0003 | 0/0 | 3302 | 8 | 5 | 3 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| a0001c0001t0004 | 0/0 | 3303 | 5 | 4 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| a0001c0001t0007 | 0/0 | 3303 | 4 | 4 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| a0001c0001t0009 | 0/0 | 3303 | 4 | 0 | 3 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| a0001c0001t0010 | 0/0 | 3299 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| a0001c0001t0011 | 0/0 | 3303 | 3 | 1 | 1 | 0 | 1 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| a0001c0001t0013 | 1/0 | 3304 | 2 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| a0001c0001t0014 | 0/0 | 3303 | 2 | 0 | 1 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| a0001c0001t0015 | 0/0 | 3303 | 2 | 0 | 0 | 1 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| a0001c0001t0016 | 0/0 | 3303 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| a0001c0001t0017 | 0/0 | 3303 | 2 | 0 | 0 | 0 | 1 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| a0001c0001t0018 | 0/0 | 3303 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| a0001c0001t0019 | 0/0 | 3303 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| a0001c0001t0020 | 0/0 | 3303 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| a0001c0001t0021 | 0/0 | 3303 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| a0001c0001t0022 | 0/0 | 3303 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| a0001c0001t0023 | 0/0 | 3303 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| a0001c0001t0025 | 0/0 | 3302 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| a0001c0001t0026 | 0/0 | 3303 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| a0001c0004t0008 | 0/0 | 3272 | 4 | 4 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| a0001c0004t0024 | 0/0 | 3272 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| a0001c0006t0012 | 0/0 | 3303 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| a0001c0007t0001 | 0/0 | 3303 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| a0002c0002t0001 | 0/0 | 3303 | 9 | 1 | 5 | 0 | 1 | 2 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| a0003c0003t0006 | 0/0 | 3303 | 5 | 4 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| a0004c0005t0005 | 0/0 | 3307 | 4 | 1 | 1 | 0 | 0 | 2 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| a0005c0008t0005 | 0/0 | 3307 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | copy fasta | chr11 | 102391332 | 102457765 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0004 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0003g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0004g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0004g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0007g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0007g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0007g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0007g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0009g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0009g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0009g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0009g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0010g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0010g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0010g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0011g0009 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0011g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0013g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0013g0189 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0014g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0014g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0015g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0015g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0016g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0016g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0017g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0017g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0018g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0019g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0020g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0021g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0022g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0023g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0025g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0001t0026g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0004t0008g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0004t0008g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0004t0008g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0004t0008g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0004t0024g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0006t0012g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0006t0012g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0001c0007t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0002c0002t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0002c0002t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0003c0003t0006g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0003c0003t0006g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0003c0003t0006g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0004c0005t0005g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0004c0005t0005g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0004c0005t0005g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0004c0005t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| a0005c0008t0005g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0048 | EUR | FIN | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0099 | EUR | FIN | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG00323 | hp1 | a0001 | c0001 | t0017 | g0042 | EUR | FIN | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG00323 | hp2 | a0002 | c0002 | t0001 | g0138 | EUR | FIN | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | CHS | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG00639 | hp2 | a0001 | c0001 | t0011 | g0009 | AMR | PUR | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG00738 | hp1 | a0001 | c0001 | t0009 | g0056 | AMR | PUR | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | PUR | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG00741 | hp2 | a0001 | c0001 | t0013 | g0173 | AMR | PUR | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0091 | AMR | PUR | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0008 | AMR | PUR | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG01109 | hp1 | a0003 | c0003 | t0006 | g0011 | AMR | PUR | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG01109 | hp2 | a0004 | c0005 | t0005 | g0033 | AMR | PUR | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG01192 | hp2 | a0001 | c0001 | t0014 | g0044 | AMR | PUR | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0022 | AMR | PUR | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG01255 | hp2 | a0005 | c0008 | t0005 | g0041 | AMR | CLM | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG01261 | hp1 | a0001 | c0001 | t0009 | g0077 | AMR | CLM | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0006 | AMR | CLM | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | CLM | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0168 | AMR | CLM | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0060 | AMR | CLM | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG01516 | hp2 | a0001 | c0001 | t0011 | g0009 | EUR | IBS | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0134 | EUR | IBS | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0067 | EUR | IBS | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG01884 | hp2 | a0003 | c0003 | t0006 | g0001 | AFR | ACB | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG01928 | hp2 | a0002 | c0002 | t0001 | g0006 | AMR | PEL | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0149 | AMR | PEL | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02071 | hp1 | a0001 | c0007 | t0001 | g0154 | EAS | KHV | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02145 | hp1 | a0003 | c0003 | t0006 | g0001 | AFR | ACB | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | ACB | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CDX | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | CDX | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0025 | AFR | ACB | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02258 | hp1 | a0001 | c0006 | t0012 | g0030 | AFR | ACB | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | ACB | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02280 | hp2 | a0003 | c0003 | t0006 | g0001 | AFR | ACB | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02293 | hp1 | a0001 | c0001 | t0009 | g0076 | AMR | PEL | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02572 | hp1 | a0001 | c0006 | t0012 | g0029 | AFR | GWD | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0188 | AFR | GWD | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | GWD | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02630 | hp2 | a0001 | c0001 | t0018 | g0057 | AFR | GWD | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02683 | hp2 | a0001 | c0001 | t0015 | g0128 | SAS | PJL | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02698 | hp1 | a0004 | c0005 | t0005 | g0031 | SAS | PJL | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | GWD | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | GWD | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02723 | hp1 | a0001 | c0001 | t0010 | g0086 | AFR | GWD | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0160 | SAS | PJL | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02738 | hp2 | a0001 | c0001 | t0017 | g0116 | SAS | PJL | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02818 | hp2 | a0001 | c0001 | t0026 | g0194 | AFR | GWD | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02886 | hp2 | a0001 | c0001 | t0010 | g0087 | AFR | GWD | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02895 | hp1 | a0001 | c0001 | t0007 | g0017 | AFR | GWD | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02897 | hp1 | a0001 | c0001 | t0007 | g0016 | AFR | GWD | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ESN | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02922 | hp2 | a0001 | c0001 | t0011 | g0181 | AFR | ESN | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0191 | AFR | ESN | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02970 | hp1 | a0001 | c0004 | t0024 | g0177 | AFR | ESN | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ESN | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02976 | hp1 | a0003 | c0003 | t0006 | g0010 | AFR | ESN | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG03098 | hp1 | a0001 | c0001 | t0016 | g0186 | AFR | MSL | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | MSL | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0020 | AFR | ESN | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ESN | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG03139 | hp1 | a0001 | c0001 | t0016 | g0185 | AFR | ESN | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0193 | AFR | ESN | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG03209 | hp1 | a0001 | c0004 | t0008 | g0014 | AFR | MSL | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG03209 | hp2 | a0001 | c0001 | t0010 | g0085 | AFR | MSL | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | MSL | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | MSL | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | MSL | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | MSL | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | MSL | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG03492 | hp1 | a0001 | c0001 | t0009 | g0055 | SAS | PJL | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG03516 | hp1 | a0001 | c0001 | t0021 | g0172 | AFR | ESN | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | ESN | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG03669 | hp2 | a0002 | c0002 | t0001 | g0141 | SAS | PJL | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | BEB | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG03831 | hp2 | a0001 | c0001 | t0020 | g0179 | SAS | BEB | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | BEB | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG03834 | hp2 | a0001 | c0001 | t0014 | g0171 | SAS | BEB | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | BEB | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG03927 | hp2 | a0004 | c0005 | t0005 | g0032 | SAS | BEB | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | STU | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | STU | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| NA18522 | hp2 | a0001 | c0004 | t0008 | g0015 | AFR | YRI | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | YRI | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | YRI | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| NA18979 | hp2 | a0001 | c0001 | t0022 | g0184 | EAS | JPT | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| NA19003 | hp1 | a0001 | c0001 | t0015 | g0129 | EAS | JPT | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | LWK | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | LWK | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| NA19043 | hp1 | a0001 | c0001 | t0023 | g0187 | AFR | LWK | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0192 | AFR | LWK | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| NA19240 | hp1 | a0001 | c0001 | t0019 | g0123 | AFR | YRI | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0021 | AFR | YRI | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ASW | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| NA20129 | hp2 | a0004 | c0005 | t0005 | g0034 | AFR | ASW | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| NA20752 | hp1 | a0001 | c0001 | t0025 | g0190 | EUR | TSI | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0133 | EUR | TSI | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | GIH | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | GIH | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0078 | AFR | ACB | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0023 | AFR | ACB | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02559 | hp1 | a0002 | c0002 | t0001 | g0139 | AFR | ACB | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG03471 | hp1 | a0001 | c0004 | t0008 | g0013 | AFR | MSL | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | MSL | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG06807 | hp1 | a0001 | c0004 | t0008 | g0012 | AFR | USA | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| HG06807 | hp2 | a0001 | c0001 | t0007 | g0018 | AFR | USA | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | USA | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| NA20300 | hp2 | a0001 | c0001 | t0007 | g0019 | AFR | USA | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0004 | REF | REF | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0013 | g0189 | REF | REF | TMEM123_chr11_102391332_102457765 | TMEM123 | chr11 | 102391332 | 102457765 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:102401669
|
C | T | 1 | a0003 | 5 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(2): Show |
missense_variant | MODERATE | c.472G>A | p.Ala158Thr | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 4/5 | 614/3304 | 472/627 | 158/208 | chr11 | 102401669 | ||
| chr11:102402108
|
C | A | 2 | a0004a0005 | 5 | HG01109.hp2 HG01255.hp2 HG02698.hp1 others(2): Show |
missense_variant | MODERATE | c.256G>T | p.Val86Phe | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 3/5 | 398/3304 | 256/627 | 86/208 | chr11 | 102402108 | ||
| chr11:102402153
|
C | T | 1 | a0002 | 9 | HG00323.hp2 HG01346.hp1 HG01361.hp1 others(6): Show |
missense_variant | MODERATE | c.211G>A | p.Val71Met | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 3/5 | 353/3304 | 211/627 | 71/208 | chr11 | 102402153 | ||
| chr11:102452581
|
C | A | 1 | a0005 | 1 | HG01255.hp2 | missense_variant | MODERATE | c.43G>T | p.Gly15Trp | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 1/5 | 185/3304 | 43/627 | 15/208 | chr11 | 102452581 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:102401546
|
G | T | 5 | a0001c0004a0001c0006a0003c0003others(2): Show | 17 | HG01109.hp1 HG01109.hp2 HG01255.hp2 others(14): Show |
synonymous_variant | LOW | c.595C>A | p.Arg199Arg | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 4/5 | 737/3304 | 595/627 | 199/208 | chr11 | 102401546 | ||
| chr11:102401652
|
T | C | 1 | a0001c0007 | 1 | HG02071.hp1 | synonymous_variant | LOW | c.489A>G | p.Lys163Lys | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 4/5 | 631/3304 | 489/627 | 163/208 | chr11 | 102401652 | ||
| chr11:102401685
|
T | A | 1 | a0001c0006 | 2 | HG02258.hp1 HG02572.hp1 |
synonymous_variant | LOW | c.456A>T | p.Thr152Thr | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 4/5 | 598/3304 | 456/627 | 152/208 | chr11 | 102401685 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:102396367
|
A | T | 6 | a0001c0004t0008a0001c0004t0024a0001c0006t0012others(3): Show | 17 | HG01109.hp1 HG01109.hp2 HG01255.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2500T>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 5/5 | 2500 | chr11 | 102396367 | |||||
| chr11:102396436
|
T | G | 2 | a0001c0001t0007a0001c0001t0018 | 5 | HG02630.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2431A>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 5/5 | 2431 | chr11 | 102396436 | |||||
| chr11:102396523
|
A | T | 1 | a0001c0001t0020 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2344T>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 5/5 | 2344 | chr11 | 102396523 | |||||
| chr11:102396566
|
G | A | 1 | a0001c0001t0021 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2301C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 5/5 | 2301 | chr11 | 102396566 | |||||
| chr11:102396585
|
T | A | 1 | a0001c0001t0015 | 2 | HG02683.hp2 NA19003.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2282A>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 5/5 | 2282 | chr11 | 102396585 | |||||
| chr11:102396698
|
A | G | 1 | a0001c0001t0019 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2169T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 5/5 | 2169 | chr11 | 102396698 | |||||
| chr11:102396914
|
G | A | 1 | a0001c0001t0016 | 2 | HG03098.hp1 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1953C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 5/5 | 1953 | chr11 | 102396914 | |||||
| chr11:102396965
|
TTTAAAAG others(24): Show |
T | 2 | a0001c0004t0008a0001c0004t0024 | 5 | HG02970.hp1 HG03209.hp1 HG03471.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1871_*1901delGATA others(27): Show |
TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 5/5 | 1871 | chr11 | 102396965 | |||||
| chr11:102397089
|
C | T | 6 | a0001c0004t0008a0001c0004t0024a0001c0006t0012others(3): Show | 17 | HG01109.hp1 HG01109.hp2 HG01255.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1778G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 5/5 | 1778 | chr11 | 102397089 | |||||
| chr11:102397384
|
T | C | 1 | a0001c0001t0017 | 2 | HG00323.hp1 HG02738.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1483A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 5/5 | 1483 | chr11 | 102397384 | |||||
| chr11:102397636
|
G | A | 1 | a0003c0003t0006 | 5 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1231C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 5/5 | 1231 | chr11 | 102397636 | |||||
| chr11:102397700
|
G | GTGTT | 2 | a0004c0005t0005a0005c0008t0005 | 5 | HG01109.hp2 HG01255.hp2 HG02698.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1163_*1166dupAACA | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 5/5 | 1166 | chr11 | 102397700 | |||||
| chr11:102397749
|
G | A | 1 | a0001c0001t0022 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1118C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 5/5 | 1118 | chr11 | 102397749 | |||||
| chr11:102397796
|
T | A | 14 | a0001c0001t0002a0001c0001t0003a0001c0001t0007others(11): Show | 46 | HG00639.hp2 HG00738.hp2 HG01081.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*1071A>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 5/5 | 1071 | chr11 | 102397796 | |||||
| chr11:102397843
|
C | T | 1 | a0001c0001t0025 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1024G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 5/5 | 1024 | chr11 | 102397843 | |||||
| chr11:102397872
|
A | T | 1 | a0001c0001t0014 | 2 | HG01192.hp2 HG03834.hp2 |
3_prime_UTR_variant | MODIFIER | c.*995T>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 5/5 | 995 | chr11 | 102397872 | |||||
| chr11:102397897
|
C | G | 13 | a0001c0001t0002a0001c0001t0003a0001c0001t0007others(10): Show | 45 | HG00639.hp2 HG00738.hp2 HG01081.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*970G>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 5/5 | 970 | chr11 | 102397897 | |||||
| chr11:102398319
|
T | C | 2 | a0004c0005t0005a0005c0008t0005 | 5 | HG01109.hp2 HG01255.hp2 HG02698.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*548A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 5/5 | 548 | chr11 | 102398319 | |||||
| chr11:102398397
|
A | G | 1 | a0001c0001t0009 | 4 | HG00738.hp1 HG01261.hp1 HG02293.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*470T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 5/5 | 470 | chr11 | 102398397 | |||||
| chr11:102398401
|
T | C | 2 | a0004c0005t0005a0005c0008t0005 | 5 | HG01109.hp2 HG01255.hp2 HG02698.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*466A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 5/5 | 466 | chr11 | 102398401 | |||||
| chr11:102398531
|
TTCTG | T | 1 | a0001c0001t0010 | 3 | HG02723.hp1 HG02886.hp2 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*332_*335delCAGA | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 5/5 | 332 | chr11 | 102398531 | |||||
| chr11:102398620
|
T | G | 4 | a0001c0004t0008a0001c0004t0024a0001c0006t0012others(1): Show | 12 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*247A>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 5/5 | 247 | chr11 | 102398620 | |||||
| chr11:102398666
|
AG | A | 28 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(25): Show | 202 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(199): Show |
3_prime_UTR_variant | MODIFIER | c.*200delC | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 5/5 | 200 | chr11 | 102398666 | |||||
| chr11:102398729
|
CG | C | 2 | a0001c0001t0003a0001c0001t0025 | 9 | HG00738.hp2 HG01081.hp2 HG01099.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*137delC | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 5/5 | 137 | chr11 | 102398729 | |||||
| chr11:102452630
|
G | A | 1 | a0001c0001t0026 | 1 | HG02818.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-7C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 1/5 | chr11 | 102452630 | ||||||
| chr11:102452646
|
A | G | 8 | a0001c0001t0002a0001c0001t0004a0001c0001t0007others(5): Show | 35 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(32): Show |
5_prime_UTR_variant | MODIFIER | c.-23T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 1/5 | 23 | chr11 | 102452646 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:102398948
|
T | G | 9 | a0001c0001t0003g0008a0001c0001t0003g0078a0001c0001t0003g0091others(6): Show | 11 | HG00639.hp2 HG00738.hp2 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.603-57A>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 4/4 | chr11 | 102398948 | ||||||
| chr11:102399007
|
G | T | 5 | a0004c0005t0005g0031a0004c0005t0005g0032a0004c0005t0005g0033others(2): Show | 5 | HG01109.hp2 HG01255.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.603-116C>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 4/4 | chr11 | 102399007 | ||||||
| chr11:102399012
|
G | C | 15 | a0001c0004t0008g0012a0001c0004t0008g0013a0001c0004t0008g0014others(12): Show | 17 | HG01109.hp1 HG01109.hp2 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.603-121C>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 4/4 | chr11 | 102399012 | ||||||
| chr11:102399115
|
A | C | 2 | a0001c0006t0012g0029a0001c0006t0012g0030 | 2 | HG02258.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.603-224T>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 4/4 | chr11 | 102399115 | ||||||
| chr11:102399116
|
C | A | 2 | a0001c0006t0012g0029a0001c0006t0012g0030 | 2 | HG02258.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.603-225G>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 4/4 | chr11 | 102399116 | ||||||
| chr11:102399320
|
T | C | 23 | a0001c0001t0002g0024a0001c0001t0002g0039a0001c0001t0002g0040others(20): Show | 25 | HG01109.hp1 HG01109.hp2 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.603-429A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 4/4 | chr11 | 102399320 | ||||||
| chr11:102399410
|
A | G | 2 | a0001c0001t0007g0018a0001c0001t0007g0019 | 2 | HG06807.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.603-519T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 4/4 | chr11 | 102399410 | ||||||
| chr11:102399478
|
T | C | 46 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0046others(43): Show | 48 | HG00621.hp1 HG00621.hp2 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.603-587A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 4/4 | chr11 | 102399478 | ||||||
| chr11:102399543
|
A | G | 3 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0011g0181 | 3 | HG02922.hp2 HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.603-652T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 4/4 | chr11 | 102399543 | ||||||
| chr11:102399598
|
T | C | 8 | a0001c0004t0008g0012a0001c0004t0008g0013a0001c0004t0008g0014others(5): Show | 10 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.603-707A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 4/4 | chr11 | 102399598 | ||||||
| chr11:102399957
|
G | C | 8 | a0001c0001t0003g0008a0001c0001t0003g0078a0001c0001t0003g0091others(5): Show | 9 | HG00738.hp2 HG01081.hp2 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.603-1066C>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 4/4 | chr11 | 102399957 | ||||||
| chr11:102399970
|
CA | C | 188 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(185): Show | 198 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.603-1080delT | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 4/4 | chr11 | 102399970 | ||||||
| chr11:102399995
|
A | T | 1 | a0002c0002t0001g0160 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.603-1104T>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 4/4 | chr11 | 102399995 | ||||||
| chr11:102400001
|
C | A | 1 | a0002c0002t0001g0160 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.603-1110G>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 4/4 | chr11 | 102400001 | ||||||
| chr11:102400004
|
T | A | 1 | a0002c0002t0001g0160 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.603-1113A>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 4/4 | chr11 | 102400004 | ||||||
| chr11:102400005
|
T | C | 1 | a0002c0002t0001g0160 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.603-1114A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 4/4 | chr11 | 102400005 | ||||||
| chr11:102400008
|
G | A | 1 | a0002c0002t0001g0160 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.603-1117C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 4/4 | chr11 | 102400008 | ||||||
| chr11:102400009
|
T | A | 1 | a0002c0002t0001g0160 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.603-1118A>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 4/4 | chr11 | 102400009 | ||||||
| chr11:102400010
|
T | A | 1 | a0002c0002t0001g0160 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.603-1119A>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 4/4 | chr11 | 102400010 | ||||||
| chr11:102400011
|
T | C | 1 | a0002c0002t0001g0160 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.603-1120A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 4/4 | chr11 | 102400011 | ||||||
| chr11:102400014
|
G | A | 1 | a0002c0002t0001g0160 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.603-1123C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 4/4 | chr11 | 102400014 | ||||||
| chr11:102400015
|
T | A | 1 | a0002c0002t0001g0160 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.603-1124A>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 4/4 | chr11 | 102400015 | ||||||
| chr11:102400018
|
T | G | 1 | a0002c0002t0001g0160 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.603-1127A>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 4/4 | chr11 | 102400018 | ||||||
| chr11:102400025
|
A | T | 1 | a0002c0002t0001g0160 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.603-1134T>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 4/4 | chr11 | 102400025 | ||||||
| chr11:102400057
|
C | A | 1 | a0001c0001t0001g0156 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.603-1166G>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 4/4 | chr11 | 102400057 | ||||||
| chr11:102400089
|
G | A | 8 | a0001c0001t0003g0008a0001c0001t0003g0078a0001c0001t0003g0091others(5): Show | 9 | HG00738.hp2 HG01081.hp2 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.603-1198C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 4/4 | chr11 | 102400089 | ||||||
| chr11:102400245
|
T | C | 1 | a0001c0001t0001g0070 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.602+1294A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 4/4 | chr11 | 102400245 | ||||||
| chr11:102400569
|
T | G | 4 | a0002c0002t0001g0138a0002c0002t0001g0139a0002c0002t0001g0149others(1): Show | 4 | HG00323.hp2 HG01934.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.602+970A>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 4/4 | chr11 | 102400569 | ||||||
| chr11:102400704
|
T | C | 1 | a0001c0001t0026g0194 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.602+835A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 4/4 | chr11 | 102400704 | ||||||
| chr11:102400706
|
C | G | 1 | a0001c0001t0001g0047 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.602+833G>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 4/4 | chr11 | 102400706 | ||||||
| chr11:102400827
|
A | G | 1 | a0001c0001t0001g0080 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.602+712T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 4/4 | chr11 | 102400827 | ||||||
| chr11:102400902
|
CA | C | 10 | a0001c0004t0008g0012a0001c0004t0008g0013a0001c0004t0008g0014others(7): Show | 12 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.602+636delT | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 4/4 | chr11 | 102400902 | ||||||
| chr11:102400973
|
T | C | 1 | a0001c0001t0026g0194 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.602+566A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 4/4 | chr11 | 102400973 | ||||||
| chr11:102400984
|
G | A | 8 | a0001c0001t0002g0024a0001c0001t0002g0039a0001c0001t0002g0040others(5): Show | 8 | HG01346.hp2 HG02145.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.602+555C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 4/4 | chr11 | 102400984 | ||||||
| chr11:102400987
|
G | C | 4 | a0001c0001t0001g0140a0001c0001t0001g0143a0001c0001t0001g0144others(1): Show | 4 | HG01071.hp2 HG01175.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.602+552C>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 4/4 | chr11 | 102400987 | ||||||
| chr11:102401078
|
C | G | 5 | a0004c0005t0005g0031a0004c0005t0005g0032a0004c0005t0005g0033others(2): Show | 5 | HG01109.hp2 HG01255.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.602+461G>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 4/4 | chr11 | 102401078 | ||||||
| chr11:102401175
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.602+364A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 4/4 | chr11 | 102401175 | ||||||
| chr11:102401724
|
G | C | 1 | a0001c0001t0001g0136 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.449-32C>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 3/4 | chr11 | 102401724 | ||||||
| chr11:102401729
|
A | AT | 5 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0022others(2): Show | 5 | HG01243.hp1 HG02109.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.449-38dupA | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 3/4 | chr11 | 102401729 | ||||||
| chr11:102401729
|
AT | A | 15 | a0001c0001t0001g0111a0001c0001t0001g0176a0001c0001t0002g0024others(12): Show | 15 | HG01109.hp2 HG01255.hp2 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.449-38delA | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 3/4 | chr11 | 102401729 | ||||||
| chr11:102401729
|
ATT | A | 10 | a0001c0004t0008g0012a0001c0004t0008g0013a0001c0004t0008g0014others(7): Show | 12 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.449-39_449-38delAA | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 3/4 | chr11 | 102401729 | ||||||
| chr11:102401888
|
GA | G | 10 | a0001c0004t0008g0012a0001c0004t0008g0013a0001c0004t0008g0014others(7): Show | 12 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.448+27delT | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 3/4 | chr11 | 102401888 | ||||||
| chr11:102402329
|
A | G | 10 | a0001c0004t0008g0012a0001c0004t0008g0013a0001c0004t0008g0014others(7): Show | 12 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.158-123T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102402329 | ||||||
| chr11:102402381
|
A | G | 1 | a0001c0001t0001g0099 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.158-175T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102402381 | ||||||
| chr11:102402511
|
T | C | 1 | a0001c0001t0009g0076 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.158-305A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102402511 | ||||||
| chr11:102402569
|
G | C | 1 | a0004c0005t0005g0034 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.158-363C>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102402569 | ||||||
| chr11:102402666
|
T | A | 2 | a0001c0001t0001g0052a0001c0001t0001g0053 | 2 | HG01978.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.158-460A>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102402666 | ||||||
| chr11:102402962
|
T | C | 1 | a0001c0001t0001g0182 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.158-756A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102402962 | ||||||
| chr11:102402973
|
C | T | 10 | a0001c0004t0008g0012a0001c0004t0008g0013a0001c0004t0008g0014others(7): Show | 12 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.158-767G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102402973 | ||||||
| chr11:102402980
|
A | G | 1 | a0001c0001t0001g0175 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.158-774T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102402980 | ||||||
| chr11:102403072
|
A | G | 1 | a0001c0001t0001g0107 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.158-866T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102403072 | ||||||
| chr11:102403102
|
C | T | 1 | a0001c0001t0009g0077 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.158-896G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102403102 | ||||||
| chr11:102403305
|
C | T | 3 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097 | 3 | HG02622.hp2 HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.158-1099G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102403305 | ||||||
| chr11:102403359
|
G | T | 1 | a0001c0001t0001g0089 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.158-1153C>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102403359 | ||||||
| chr11:102403450
|
G | C | 24 | a0001c0001t0001g0121a0001c0001t0002g0024a0001c0001t0002g0039others(21): Show | 26 | HG01109.hp1 HG01109.hp2 HG01255.hp2 others(23): Show |
intron_variant | MODIFIER | c.158-1244C>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102403450 | ||||||
| chr11:102403706
|
T | C | 1 | a0001c0001t0009g0077 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.158-1500A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102403706 | ||||||
| chr11:102403913
|
A | G | 1 | a0001c0001t0026g0194 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.158-1707T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102403913 | ||||||
| chr11:102403997
|
A | G | 2 | a0001c0001t0001g0127a0001c0001t0001g0130 | 2 | HG02055.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.158-1791T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102403997 | ||||||
| chr11:102404531
|
A | C | 6 | a0001c0001t0001g0121a0004c0005t0005g0031a0004c0005t0005g0032others(3): Show | 6 | HG01109.hp2 HG01255.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.158-2325T>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102404531 | ||||||
| chr11:102404571
|
C | A | 24 | a0001c0001t0001g0121a0001c0001t0002g0024a0001c0001t0002g0039others(21): Show | 26 | HG01109.hp1 HG01109.hp2 HG01255.hp2 others(23): Show |
intron_variant | MODIFIER | c.158-2365G>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102404571 | ||||||
| chr11:102404620
|
A | G | 1 | a0001c0001t0001g0156 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.158-2414T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102404620 | ||||||
| chr11:102404624
|
G | T | 1 | a0001c0001t0001g0103 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.158-2418C>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102404624 | ||||||
| chr11:102404669
|
G | A | 2 | a0001c0001t0001g0059a0001c0001t0001g0132 | 2 | HG02523.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.158-2463C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102404669 | ||||||
| chr11:102404734
|
G | GGATTACA others(13): Show |
1 | a0001c0001t0002g0024 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.158-2548_158-2529d others(22): Show |
TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102404734 | ||||||
| chr11:102404889
|
A | G | 37 | a0001c0001t0001g0050a0001c0001t0001g0121a0001c0001t0001g0164others(34): Show | 41 | HG00639.hp2 HG00738.hp2 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.158-2683T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102404889 | ||||||
| chr11:102405055
|
C | CT | 9 | a0001c0001t0001g0121a0001c0001t0001g0180a0001c0001t0002g0036others(6): Show | 9 | HG01109.hp2 HG01255.hp2 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.158-2850dupA | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102405055 | ||||||
| chr11:102405206
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.158-3000C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102405206 | ||||||
| chr11:102405238
|
G | A | 3 | a0001c0001t0010g0085a0001c0001t0010g0086a0001c0001t0010g0087 | 3 | HG02723.hp1 HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.158-3032C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102405238 | ||||||
| chr11:102405336
|
G | A | 6 | a0001c0001t0001g0121a0004c0005t0005g0031a0004c0005t0005g0032others(3): Show | 6 | HG01109.hp2 HG01255.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.158-3130C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102405336 | ||||||
| chr11:102405386
|
C | T | 43 | a0001c0001t0001g0121a0001c0001t0001g0164a0001c0001t0002g0024others(40): Show | 46 | HG00738.hp2 HG01081.hp2 HG01099.hp1 others(43): Show |
intron_variant | MODIFIER | c.158-3180G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102405386 | ||||||
| chr11:102405602
|
G | A | 1 | a0001c0001t0002g0026 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.158-3396C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102405602 | ||||||
| chr11:102405934
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.158-3728C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102405934 | ||||||
| chr11:102406144
|
AG | A | 10 | a0001c0004t0008g0012a0001c0004t0008g0013a0001c0004t0008g0014others(7): Show | 12 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.158-3939delC | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102406144 | ||||||
| chr11:102406150
|
G | T | 10 | a0001c0004t0008g0012a0001c0004t0008g0013a0001c0004t0008g0014others(7): Show | 12 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.158-3944C>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102406150 | ||||||
| chr11:102406575
|
A | T | 1 | a0001c0001t0001g0120 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.158-4369T>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102406575 | ||||||
| chr11:102406739
|
C | T | 11 | a0001c0001t0001g0169a0001c0004t0008g0012a0001c0004t0008g0013others(8): Show | 13 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.158-4533G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102406739 | ||||||
| chr11:102406764
|
G | A | 1 | a0001c0001t0001g0054 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.158-4558C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102406764 | ||||||
| chr11:102406868
|
C | CA | 5 | a0001c0001t0001g0150a0001c0001t0001g0170a0001c0001t0001g0176others(2): Show | 5 | HG02132.hp2 HG02523.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.158-4663dupT | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102406868 | ||||||
| chr11:102406868
|
C | CAA | 6 | a0001c0001t0001g0121a0004c0005t0005g0031a0004c0005t0005g0032others(3): Show | 6 | HG01109.hp2 HG01255.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.158-4664_158-4663d others(4): Show |
TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102406868 | ||||||
| chr11:102406868
|
CA | C | 10 | a0001c0001t0001g0063a0001c0001t0001g0093a0001c0001t0001g0155others(7): Show | 10 | HG01081.hp2 HG01496.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.158-4663delT | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102406868 | ||||||
| chr11:102406868
|
CAA | C | 3 | a0003c0003t0006g0001a0003c0003t0006g0010a0003c0003t0006g0011 | 5 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.158-4664_158-4663d others(4): Show |
TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102406868 | ||||||
| chr11:102406928
|
A | C | 2 | a0001c0001t0002g0039a0001c0001t0002g0040 | 2 | HG02145.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.158-4722T>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102406928 | ||||||
| chr11:102406988
|
A | G | 1 | a0001c0001t0001g0069 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.158-4782T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102406988 | ||||||
| chr11:102407365
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.158-5159A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102407365 | ||||||
| chr11:102407514
|
A | G | 1 | a0001c0001t0001g0112 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.158-5308T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102407514 | ||||||
| chr11:102407603
|
A | T | 16 | a0001c0001t0001g0121a0001c0004t0008g0012a0001c0004t0008g0013others(13): Show | 18 | HG01109.hp1 HG01109.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.158-5397T>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102407603 | ||||||
| chr11:102407729
|
C | T | 2 | a0001c0001t0001g0058a0001c0001t0001g0176 | 2 | HG02132.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.158-5523G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102407729 | ||||||
| chr11:102407760
|
A | AT | 3 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0037 | 3 | HG02280.hp1 HG02622.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.158-5555dupA | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102407760 | ||||||
| chr11:102408126
|
CTATT | C | 4 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0052others(1): Show | 4 | HG00280.hp1 HG00639.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.158-5924_158-5921d others(6): Show |
TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102408126 | ||||||
| chr11:102408246
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.158-6040C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102408246 | ||||||
| chr11:102408363
|
T | A | 10 | a0001c0004t0008g0012a0001c0004t0008g0013a0001c0004t0008g0014others(7): Show | 12 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.158-6157A>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102408363 | ||||||
| chr11:102408425
|
A | C | 1 | a0001c0001t0003g0008 | 2 | HG00738.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.158-6219T>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102408425 | ||||||
| chr11:102408583
|
A | G | 6 | a0001c0001t0001g0003a0001c0001t0001g0061a0001c0001t0001g0105others(3): Show | 7 | HG02258.hp2 HG02559.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.158-6377T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102408583 | ||||||
| chr11:102408744
|
C | T | 4 | a0001c0001t0001g0108a0001c0001t0001g0113a0001c0001t0017g0042others(1): Show | 4 | HG00323.hp1 HG01361.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.158-6538G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102408744 | ||||||
| chr11:102409219
|
A | T | 3 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0011g0181 | 3 | HG02922.hp2 HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.158-7013T>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102409219 | ||||||
| chr11:102409375
|
A | G | 2 | a0001c0001t0001g0106a0001c0001t0001g0112 | 2 | HG03130.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.158-7169T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102409375 | ||||||
| chr11:102409551
|
TA | T | 10 | a0001c0004t0008g0012a0001c0004t0008g0013a0001c0004t0008g0014others(7): Show | 12 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.158-7346delT | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102409551 | ||||||
| chr11:102409568
|
T | C | 6 | a0001c0001t0001g0121a0004c0005t0005g0031a0004c0005t0005g0032others(3): Show | 6 | HG01109.hp2 HG01255.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.158-7362A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102409568 | ||||||
| chr11:102409743
|
G | A | 2 | a0001c0001t0001g0127a0001c0001t0001g0130 | 2 | HG02055.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.158-7537C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102409743 | ||||||
| chr11:102409778
|
T | C | 5 | a0001c0001t0007g0016a0001c0001t0007g0017a0001c0001t0007g0018others(2): Show | 5 | HG02630.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.158-7572A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102409778 | ||||||
| chr11:102409822
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.158-7616C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102409822 | ||||||
| chr11:102409897
|
C | CA | 27 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047others(24): Show | 28 | HG00280.hp1 HG00639.hp1 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.158-7692dupT | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102409897 | ||||||
| chr11:102410000
|
A | G | 10 | a0001c0004t0008g0012a0001c0004t0008g0013a0001c0004t0008g0014others(7): Show | 12 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.158-7794T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102410000 | ||||||
| chr11:102410020
|
A | C | 24 | a0001c0001t0001g0121a0001c0001t0002g0024a0001c0001t0002g0039others(21): Show | 26 | HG01109.hp1 HG01109.hp2 HG01255.hp2 others(23): Show |
intron_variant | MODIFIER | c.158-7814T>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102410020 | ||||||
| chr11:102410087
|
A | G | 1 | a0001c0001t0001g0099 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.158-7881T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102410087 | ||||||
| chr11:102410203
|
A | AGTTAAAG others(12): Show |
6 | a0001c0001t0001g0088a0001c0001t0001g0094a0001c0001t0001g0111others(3): Show | 6 | HG02647.hp2 HG02723.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.158-8016_158-7998d others(21): Show |
TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102410203 | ||||||
| chr11:102410313
|
A | T | 2 | a0001c0001t0001g0049a0001c0001t0001g0142 | 2 | HG01884.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.158-8107T>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102410313 | ||||||
| chr11:102410326
|
C | A | 1 | a0001c0001t0002g0024 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.158-8120G>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102410326 | ||||||
| chr11:102410406
|
C | A | 2 | a0001c0001t0017g0042a0001c0001t0017g0116 | 2 | HG00323.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.158-8200G>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102410406 | ||||||
| chr11:102410511
|
C | CA | 5 | a0001c0001t0001g0043a0001c0001t0002g0039a0001c0001t0002g0040others(2): Show | 5 | HG02145.hp2 HG02738.hp1 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.158-8306dupT | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102410511 | ||||||
| chr11:102410511
|
C | CAAAA | 8 | a0001c0004t0008g0012a0001c0004t0008g0013a0001c0004t0008g0014others(5): Show | 10 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.158-8309_158-8306d others(6): Show |
TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102410511 | ||||||
| chr11:102410511
|
C | CAAAAAA | 8 | a0001c0001t0001g0121a0001c0006t0012g0029a0001c0006t0012g0030others(5): Show | 8 | HG01109.hp2 HG01255.hp2 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.158-8311_158-8306d others(8): Show |
TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102410511 | ||||||
| chr11:102410578
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.158-8372A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102410578 | ||||||
| chr11:102410736
|
G | A | 7 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(4): Show | 7 | HG02280.hp1 HG02717.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.158-8530C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102410736 | ||||||
| chr11:102410883
|
T | C | 17 | a0001c0001t0001g0100a0001c0001t0001g0121a0001c0004t0008g0012others(14): Show | 19 | HG01109.hp1 HG01109.hp2 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.158-8677A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102410883 | ||||||
| chr11:102411398
|
T | G | 1 | a0001c0001t0002g0026 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.158-9192A>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102411398 | ||||||
| chr11:102411485
|
G | A | 2 | a0001c0001t0001g0151a0001c0001t0001g0155 | 2 | NA19076.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.158-9279C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102411485 | ||||||
| chr11:102411659
|
G | T | 1 | a0001c0001t0002g0026 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.158-9453C>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102411659 | ||||||
| chr11:102411721
|
G | A | 147 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(144): Show | 153 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.158-9515C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102411721 | ||||||
| chr11:102411739
|
A | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0051 | 2 | HG00741.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.158-9533T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102411739 | ||||||
| chr11:102412051
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.158-9845A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102412051 | ||||||
| chr11:102412060
|
T | G | 10 | a0001c0004t0008g0012a0001c0004t0008g0013a0001c0004t0008g0014others(7): Show | 12 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.158-9854A>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102412060 | ||||||
| chr11:102412288
|
C | T | 10 | a0001c0004t0008g0012a0001c0004t0008g0013a0001c0004t0008g0014others(7): Show | 12 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.158-10082G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102412288 | ||||||
| chr11:102412752
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.158-10546C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102412752 | ||||||
| chr11:102413329
|
C | T | 1 | a0001c0001t0026g0194 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.158-11123G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102413329 | ||||||
| chr11:102413350
|
A | G | 1 | a0001c0001t0001g0183 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.158-11144T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102413350 | ||||||
| chr11:102413356
|
T | C | 1 | a0001c0001t0001g0144 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.158-11150A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102413356 | ||||||
| chr11:102413388
|
T | G | 2 | a0001c0001t0001g0005a0001c0001t0001g0161 | 3 | HG02602.hp2 HG03831.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.158-11182A>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102413388 | ||||||
| chr11:102413456
|
A | C | 1 | a0001c0001t0016g0185 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.158-11250T>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102413456 | ||||||
| chr11:102413509
|
A | T | 1 | a0001c0001t0009g0077 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.158-11303T>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102413509 | ||||||
| chr11:102413934
|
T | G | 5 | a0001c0001t0007g0016a0001c0001t0007g0017a0001c0001t0007g0018others(2): Show | 5 | HG02630.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.158-11728A>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102413934 | ||||||
| chr11:102414067
|
A | G | 3 | a0001c0001t0001g0148a0001c0001t0001g0152a0001c0001t0001g0180 | 3 | HG02056.hp2 HG02083.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.158-11861T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102414067 | ||||||
| chr11:102414159
|
T | C | 10 | a0001c0004t0008g0012a0001c0004t0008g0013a0001c0004t0008g0014others(7): Show | 12 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.158-11953A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102414159 | ||||||
| chr11:102414171
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.158-11965T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102414171 | ||||||
| chr11:102414495
|
A | G | 3 | a0001c0004t0008g0012a0001c0004t0008g0013a0001c0004t0024g0177 | 3 | HG02970.hp1 HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.158-12289T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102414495 | ||||||
| chr11:102414789
|
C | A | 2 | a0001c0001t0004g0020a0001c0001t0004g0021 | 2 | HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.158-12583G>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102414789 | ||||||
| chr11:102414907
|
T | C | 5 | a0001c0001t0001g0088a0001c0001t0001g0094a0001c0001t0010g0085others(2): Show | 5 | HG02647.hp2 HG02723.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.158-12701A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102414907 | ||||||
| chr11:102414941
|
C | T | 1 | a0001c0001t0002g0026 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.158-12735G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102414941 | ||||||
| chr11:102415231
|
T | C | 1 | a0001c0001t0001g0090 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.158-13025A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102415231 | ||||||
| chr11:102415321
|
T | G | 1 | a0002c0002t0001g0141 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.158-13115A>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102415321 | ||||||
| chr11:102415914
|
TATTATC | T | 10 | a0001c0004t0008g0012a0001c0004t0008g0013a0001c0004t0008g0014others(7): Show | 12 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.158-13714_158-1370 others(10): Show |
TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102415914 | ||||||
| chr11:102415917
|
TATC | T | 175 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(172): Show | 181 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.158-13714_158-1371 others(7): Show |
TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102415917 | ||||||
| chr11:102415920
|
C | T | 8 | a0001c0001t0001g0164a0001c0001t0003g0008a0001c0001t0003g0188others(5): Show | 10 | HG00639.hp2 HG00738.hp2 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.158-13714G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102415920 | ||||||
| chr11:102416143
|
G | A | 4 | a0001c0001t0001g0108a0001c0001t0001g0113a0001c0001t0017g0042others(1): Show | 4 | HG00323.hp1 HG01361.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.158-13937C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102416143 | ||||||
| chr11:102416194
|
G | C | 2 | a0001c0001t0001g0103a0001c0001t0001g0111 | 2 | HG03195.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.158-13988C>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102416194 | ||||||
| chr11:102416336
|
A | G | 2 | a0001c0001t0002g0036a0001c0001t0002g0037 | 2 | HG02280.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.158-14130T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102416336 | ||||||
| chr11:102416589
|
TAATAA | T | 3 | a0003c0003t0006g0001a0003c0003t0006g0010a0003c0003t0006g0011 | 5 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.158-14388_158-1438 others(9): Show |
TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102416589 | ||||||
| chr11:102416639
|
C | G | 10 | a0001c0004t0008g0012a0001c0004t0008g0013a0001c0004t0008g0014others(7): Show | 12 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.158-14433G>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102416639 | ||||||
| chr11:102416736
|
A | G | 1 | a0001c0001t0002g0024 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.158-14530T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102416736 | ||||||
| chr11:102416990
|
C | G | 10 | a0001c0004t0008g0012a0001c0004t0008g0013a0001c0004t0008g0014others(7): Show | 12 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.158-14784G>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102416990 | ||||||
| chr11:102417041
|
A | C | 1 | a0001c0001t0001g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.158-14835T>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102417041 | ||||||
| chr11:102417042
|
G | C | 1 | a0001c0001t0015g0128 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.158-14836C>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102417042 | ||||||
| chr11:102417294
|
A | G | 1 | a0001c0001t0026g0194 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.158-15088T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102417294 | ||||||
| chr11:102417474
|
C | T | 1 | a0001c0001t0026g0194 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.158-15268G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102417474 | ||||||
| chr11:102417602
|
T | G | 2 | a0001c0001t0002g0036a0001c0001t0002g0037 | 2 | HG02280.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.158-15396A>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102417602 | ||||||
| chr11:102417727
|
C | T | 161 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(158): Show | 167 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.158-15521G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102417727 | ||||||
| chr11:102418070
|
G | GA | 187 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(184): Show | 196 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.158-15865dupT | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102418070 | ||||||
| chr11:102418231
|
T | C | 5 | a0004c0005t0005g0031a0004c0005t0005g0032a0004c0005t0005g0033others(2): Show | 5 | HG01109.hp2 HG01255.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.158-16025A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102418231 | ||||||
| chr11:102418323
|
C | T | 6 | a0001c0001t0001g0003a0001c0001t0001g0061a0001c0001t0001g0105others(3): Show | 7 | HG02258.hp2 HG02559.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.158-16117G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102418323 | ||||||
| chr11:102418856
|
C | G | 5 | a0001c0001t0007g0016a0001c0001t0007g0017a0001c0001t0007g0018others(2): Show | 5 | HG02630.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.158-16650G>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102418856 | ||||||
| chr11:102418997
|
C | A | 5 | a0001c0001t0007g0016a0001c0001t0007g0017a0001c0001t0007g0018others(2): Show | 5 | HG02630.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.158-16791G>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102418997 | ||||||
| chr11:102419870
|
G | A | 81 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0045others(78): Show | 84 | HG00280.hp1 HG00323.hp2 HG00621.hp2 others(81): Show |
intron_variant | MODIFIER | c.158-17664C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102419870 | ||||||
| chr11:102419871
|
C | A | 80 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0045others(77): Show | 83 | HG00280.hp1 HG00323.hp2 HG00621.hp2 others(80): Show |
intron_variant | MODIFIER | c.158-17665G>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102419871 | ||||||
| chr11:102420076
|
C | T | 1 | a0001c0001t0023g0187 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.158-17870G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102420076 | ||||||
| chr11:102420100
|
A | G | 5 | a0004c0005t0005g0031a0004c0005t0005g0032a0004c0005t0005g0033others(2): Show | 5 | HG01109.hp2 HG01255.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.158-17894T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102420100 | ||||||
| chr11:102420259
|
A | C | 1 | a0001c0001t0001g0106 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.158-18053T>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102420259 | ||||||
| chr11:102420285
|
T | C | 1 | a0001c0001t0004g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.158-18079A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102420285 | ||||||
| chr11:102420353
|
C | G | 1 | a0001c0001t0001g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.158-18147G>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102420353 | ||||||
| chr11:102420787
|
G | A | 1 | a0001c0001t0020g0179 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.158-18581C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102420787 | ||||||
| chr11:102420865
|
T | C | 1 | a0001c0001t0002g0026 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.158-18659A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102420865 | ||||||
| chr11:102420899
|
T | C | 4 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0002g0038others(1): Show | 4 | HG02717.hp2 HG02922.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.158-18693A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102420899 | ||||||
| chr11:102420980
|
G | A | 4 | a0001c0001t0001g0125a0001c0001t0001g0158a0001c0001t0001g0159others(1): Show | 4 | HG01070.hp1 HG02895.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.158-18774C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102420980 | ||||||
| chr11:102421155
|
G | A | 1 | a0001c0001t0004g0023 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.158-18949C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102421155 | ||||||
| chr11:102421215
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.158-19009G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102421215 | ||||||
| chr11:102421500
|
CAAAG | C | 2 | a0001c0001t0002g0039a0001c0001t0002g0040 | 2 | HG02145.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.158-19298_158-1929 others(8): Show |
TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102421500 | ||||||
| chr11:102421519
|
C | CA | 6 | a0001c0001t0001g0163a0001c0001t0001g0165a0001c0001t0007g0018others(3): Show | 6 | HG01934.hp2 HG03098.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.158-19314dupT | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102421519 | ||||||
| chr11:102421519
|
CA | C | 10 | a0001c0004t0008g0012a0001c0004t0008g0013a0001c0004t0008g0014others(7): Show | 12 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.158-19314delT | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102421519 | ||||||
| chr11:102421532
|
T | C | 8 | a0001c0001t0002g0024a0001c0001t0002g0039a0001c0001t0002g0040others(5): Show | 8 | HG01346.hp2 HG02145.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.158-19326A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102421532 | ||||||
| chr11:102421647
|
A | G | 1 | a0001c0001t0001g0153 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.158-19441T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102421647 | ||||||
| chr11:102421801
|
T | G | 4 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0002g0038others(1): Show | 4 | HG02717.hp2 HG02922.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.158-19595A>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102421801 | ||||||
| chr11:102421866
|
A | C | 8 | a0001c0001t0001g0059a0001c0001t0001g0131a0001c0001t0001g0132others(5): Show | 8 | HG00621.hp2 HG01169.hp1 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.158-19660T>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102421866 | ||||||
| chr11:102421975
|
T | C | 3 | a0001c0001t0010g0085a0001c0001t0010g0086a0001c0001t0010g0087 | 3 | HG02723.hp1 HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.158-19769A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102421975 | ||||||
| chr11:102422016
|
G | A | 1 | a0001c0001t0002g0026 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.158-19810C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102422016 | ||||||
| chr11:102422423
|
G | A | 1 | a0001c0001t0001g0132 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.158-20217C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102422423 | ||||||
| chr11:102422428
|
T | C | 15 | a0001c0004t0008g0012a0001c0004t0008g0013a0001c0004t0008g0014others(12): Show | 17 | HG01109.hp1 HG01109.hp2 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.158-20222A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102422428 | ||||||
| chr11:102422516
|
C | A | 2 | a0001c0001t0001g0103a0001c0001t0001g0111 | 2 | HG03195.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.158-20310G>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102422516 | ||||||
| chr11:102422763
|
A | G | 4 | a0001c0001t0001g0140a0001c0001t0001g0143a0001c0001t0001g0144others(1): Show | 4 | HG01071.hp2 HG01175.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.158-20557T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102422763 | ||||||
| chr11:102422871
|
G | C | 11 | a0001c0001t0002g0026a0001c0004t0008g0012a0001c0004t0008g0013others(8): Show | 13 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.158-20665C>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102422871 | ||||||
| chr11:102423010
|
A | G | 1 | a0001c0001t0001g0107 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.158-20804T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102423010 | ||||||
| chr11:102423316
|
C | T | 1 | a0001c0006t0012g0029 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.158-21110G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102423316 | ||||||
| chr11:102423348
|
C | T | 5 | a0004c0005t0005g0031a0004c0005t0005g0032a0004c0005t0005g0033others(2): Show | 5 | HG01109.hp2 HG01255.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.158-21142G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102423348 | ||||||
| chr11:102423492
|
T | G | 1 | a0004c0005t0005g0032 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.158-21286A>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102423492 | ||||||
| chr11:102423633
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.158-21427C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102423633 | ||||||
| chr11:102423823
|
A | G | 3 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097 | 3 | HG02622.hp2 HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.158-21617T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102423823 | ||||||
| chr11:102423972
|
A | T | 4 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(1): Show | 4 | HG02622.hp2 HG02965.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.158-21766T>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102423972 | ||||||
| chr11:102424217
|
C | G | 1 | a0001c0001t0013g0173 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.158-22011G>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102424217 | ||||||
| chr11:102424550
|
G | A | 2 | a0002c0002t0001g0006a0002c0002t0001g0060 | 3 | HG01346.hp1 HG01496.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.158-22344C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102424550 | ||||||
| chr11:102424621
|
G | A | 2 | a0004c0005t0005g0033a0004c0005t0005g0034 | 2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.158-22415C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102424621 | ||||||
| chr11:102424728
|
C | T | 4 | a0001c0001t0001g0125a0001c0001t0001g0158a0001c0001t0001g0159others(1): Show | 4 | HG01070.hp1 HG02895.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.158-22522G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102424728 | ||||||
| chr11:102424746
|
T | C | 15 | a0001c0004t0008g0012a0001c0004t0008g0013a0001c0004t0008g0014others(12): Show | 17 | HG01109.hp1 HG01109.hp2 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.158-22540A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102424746 | ||||||
| chr11:102424811
|
G | A | 14 | a0001c0001t0001g0063a0001c0001t0001g0093a0001c0001t0002g0024others(11): Show | 14 | HG01243.hp1 HG01346.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.158-22605C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102424811 | ||||||
| chr11:102425069
|
T | A | 1 | a0001c0001t0023g0187 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.158-22863A>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102425069 | ||||||
| chr11:102425140
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.158-22934C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102425140 | ||||||
| chr11:102425177
|
G | C | 5 | a0001c0004t0008g0012a0001c0004t0008g0013a0001c0004t0008g0014others(2): Show | 5 | HG02970.hp1 HG03209.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.158-22971C>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102425177 | ||||||
| chr11:102425244
|
T | C | 1 | a0001c0001t0002g0035 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.158-23038A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102425244 | ||||||
| chr11:102425293
|
A | G | 5 | a0004c0005t0005g0031a0004c0005t0005g0032a0004c0005t0005g0033others(2): Show | 5 | HG01109.hp2 HG01255.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.158-23087T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102425293 | ||||||
| chr11:102425339
|
T | C | 2 | a0001c0001t0001g0146a0001c0001t0001g0157 | 2 | HG02630.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.158-23133A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102425339 | ||||||
| chr11:102425350
|
A | T | 1 | a0001c0001t0003g0191 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.158-23144T>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102425350 | ||||||
| chr11:102425514
|
A | G | 1 | a0001c0006t0012g0029 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.157+23298T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102425514 | ||||||
| chr11:102425562
|
G | GT | 11 | a0001c0001t0001g0003a0001c0001t0001g0061a0001c0001t0001g0072others(8): Show | 12 | HG01099.hp2 HG02055.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.157+23249dupA | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102425562 | ||||||
| chr11:102425583
|
C | CT | 9 | a0001c0001t0001g0075a0001c0001t0001g0117a0001c0001t0002g0026others(6): Show | 9 | HG01255.hp2 HG01496.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.157+23228dupA | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102425583 | ||||||
| chr11:102425583
|
C | CTT | 6 | a0001c0001t0001g0098a0001c0001t0001g0100a0001c0001t0001g0102others(3): Show | 6 | HG01109.hp2 HG01261.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.157+23227_157+2322 others(6): Show |
TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102425583 | ||||||
| chr11:102425583
|
CT | C | 10 | a0001c0001t0001g0103a0001c0001t0019g0123a0001c0004t0008g0012others(7): Show | 12 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.157+23228delA | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102425583 | ||||||
| chr11:102425657
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.157+23155G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102425657 | ||||||
| chr11:102425784
|
T | C | 1 | a0001c0001t0002g0026 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.157+23028A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102425784 | ||||||
| chr11:102425868
|
G | A | 1 | a0001c0001t0002g0026 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.157+22944C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102425868 | ||||||
| chr11:102425957
|
T | C | 5 | a0004c0005t0005g0031a0004c0005t0005g0032a0004c0005t0005g0033others(2): Show | 5 | HG01109.hp2 HG01255.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.157+22855A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102425957 | ||||||
| chr11:102426280
|
A | G | 1 | a0002c0002t0001g0139 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.157+22532T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102426280 | ||||||
| chr11:102426451
|
CT | C | 15 | a0001c0001t0001g0155a0001c0004t0008g0012a0001c0004t0008g0013others(12): Show | 17 | HG01109.hp1 HG01109.hp2 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.157+22360delA | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102426451 | ||||||
| chr11:102426482
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.157+22330C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102426482 | ||||||
| chr11:102426510
|
G | C | 1 | a0001c0001t0001g0073 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.157+22302C>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102426510 | ||||||
| chr11:102426606
|
G | A | 1 | a0001c0001t0001g0124 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.157+22206C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102426606 | ||||||
| chr11:102426730
|
A | C | 1 | a0001c0001t0001g0099 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.157+22082T>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102426730 | ||||||
| chr11:102426756
|
G | A | 10 | a0001c0004t0008g0012a0001c0004t0008g0013a0001c0004t0008g0014others(7): Show | 12 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.157+22056C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102426756 | ||||||
| chr11:102426832
|
C | T | 1 | a0001c0001t0002g0026 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.157+21980G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102426832 | ||||||
| chr11:102426858
|
T | TC | 5 | a0001c0004t0008g0015a0003c0003t0006g0001a0003c0003t0006g0010others(2): Show | 7 | HG01109.hp1 HG01255.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.157+21953_157+2195 others(5): Show |
TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102426858 | ||||||
| chr11:102426858
|
TTC | T | 2 | a0001c0004t0008g0012a0001c0004t0024g0177 | 2 | HG02970.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.157+21952_157+2195 others(6): Show |
TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102426858 | ||||||
| chr11:102426859
|
T | C | 10 | a0001c0004t0008g0014a0001c0004t0008g0015a0003c0003t0006g0001others(7): Show | 12 | HG01109.hp1 HG01109.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.157+21953A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102426859 | ||||||
| chr11:102426859
|
T | TCCC | 22 | a0001c0001t0001g0049a0001c0001t0001g0069a0001c0001t0001g0088others(19): Show | 22 | HG01070.hp1 HG01257.hp1 HG01361.hp1 others(19): Show |
intron_variant | MODIFIER | c.157+21950_157+2195 others(7): Show |
TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102426859 | ||||||
| chr11:102426859
|
T | TCCCC | 49 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(46): Show | 53 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.157+21949_157+2195 others(8): Show |
TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102426859 | ||||||
| chr11:102426859
|
T | TCCCCC | 31 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0050others(28): Show | 31 | HG00621.hp2 HG00738.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.157+21948_157+2195 others(9): Show |
TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102426859 | ||||||
| chr11:102426859
|
T | TCCCCCC | 30 | a0001c0001t0001g0007a0001c0001t0001g0046a0001c0001t0001g0051others(27): Show | 31 | HG00621.hp1 HG00741.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.157+21947_157+2195 others(10): Show |
TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102426859 | ||||||
| chr11:102426859
|
T | TCCCCCCC | 12 | a0001c0001t0001g0003a0001c0001t0001g0061a0001c0001t0001g0074others(9): Show | 13 | HG01243.hp1 HG01257.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.157+21946_157+2195 others(11): Show |
TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102426859 | ||||||
| chr11:102426859
|
T | TCCCCCCC others(3): Show |
2 | a0001c0001t0001g0075a0001c0001t0001g0093 | 2 | HG03654.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.157+21943_157+2195 others(14): Show |
TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102426859 | ||||||
| chr11:102426869
|
C | CCCCCCCC others(3): Show |
1 | a0001c0001t0015g0129 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.157+21942_157+2194 others(14): Show |
TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102426869 | ||||||
| chr11:102426943
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.157+21869C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102426943 | ||||||
| chr11:102427068
|
T | G | 1 | a0001c0001t0001g0082 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.157+21744A>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102427068 | ||||||
| chr11:102427264
|
T | C | 1 | a0001c0001t0001g0183 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.157+21548A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102427264 | ||||||
| chr11:102427271
|
G | A | 186 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(183): Show | 195 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.157+21541C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102427271 | ||||||
| chr11:102427401
|
AAGAGAAG others(11): Show |
A | 1 | a0001c0001t0009g0076 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.157+21393_157+2141 others(22): Show |
TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102427401 | ||||||
| chr11:102427447
|
C | CT | 4 | a0001c0001t0001g0005a0001c0001t0001g0104a0001c0001t0001g0157others(1): Show | 5 | HG02602.hp1 HG02602.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.157+21364dupA | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102427447 | ||||||
| chr11:102427447
|
CT | C | 31 | a0001c0001t0001g0117a0001c0001t0001g0120a0001c0001t0001g0155others(28): Show | 31 | HG01109.hp2 HG01243.hp1 HG01255.hp2 others(28): Show |
intron_variant | MODIFIER | c.157+21364delA | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102427447 | ||||||
| chr11:102427447
|
CTTT | C | 10 | a0001c0004t0008g0012a0001c0004t0008g0013a0001c0004t0008g0014others(7): Show | 12 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.157+21362_157+2136 others(7): Show |
TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102427447 | ||||||
| chr11:102427512
|
A | G | 193 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(190): Show | 203 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.157+21300T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102427512 | ||||||
| chr11:102427516
|
T | G | 178 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(175): Show | 186 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.157+21296A>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102427516 | ||||||
| chr11:102427518
|
A | G | 193 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(190): Show | 203 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.157+21294T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102427518 | ||||||
| chr11:102427567
|
G | A | 4 | a0001c0001t0001g0156a0003c0003t0006g0001a0003c0003t0006g0010others(1): Show | 6 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.157+21245C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102427567 | ||||||
| chr11:102427745
|
G | A | 1 | a0001c0001t0001g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.157+21067C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102427745 | ||||||
| chr11:102427841
|
TA | T | 13 | a0001c0001t0001g0125a0001c0001t0002g0024a0001c0001t0002g0039others(10): Show | 13 | HG01243.hp1 HG01346.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.157+20970delT | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102427841 | ||||||
| chr11:102428037
|
A | AT | 5 | a0004c0005t0005g0031a0004c0005t0005g0032a0004c0005t0005g0033others(2): Show | 5 | HG01109.hp2 HG01255.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.157+20774dupA | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102428037 | ||||||
| chr11:102428447
|
G | A | 1 | a0001c0001t0023g0187 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.157+20365C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102428447 | ||||||
| chr11:102428465
|
CT | C | 10 | a0001c0004t0008g0012a0001c0004t0008g0013a0001c0004t0008g0014others(7): Show | 12 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.157+20346delA | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102428465 | ||||||
| chr11:102428475
|
T | A | 1 | a0001c0001t0001g0053 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.157+20337A>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102428475 | ||||||
| chr11:102428479
|
T | A | 1 | a0001c0001t0002g0035 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.157+20333A>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102428479 | ||||||
| chr11:102428612
|
A | C | 6 | a0001c0001t0001g0067a0001c0001t0001g0098a0001c0001t0023g0187others(3): Show | 8 | HG01109.hp1 HG01517.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.157+20200T>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102428612 | ||||||
| chr11:102428987
|
C | G | 1 | a0001c0001t0001g0133 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.157+19825G>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102428987 | ||||||
| chr11:102428989
|
T | A | 3 | a0001c0001t0001g0059a0001c0001t0001g0131a0001c0001t0001g0132 | 3 | HG00621.hp2 HG02523.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.157+19823A>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102428989 | ||||||
| chr11:102428990
|
G | A | 3 | a0001c0001t0001g0059a0001c0001t0001g0131a0001c0001t0001g0132 | 3 | HG00621.hp2 HG02523.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.157+19822C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102428990 | ||||||
| chr11:102429104
|
G | A | 1 | a0002c0002t0001g0139 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.157+19708C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102429104 | ||||||
| chr11:102429668
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.157+19144G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102429668 | ||||||
| chr11:102429707
|
T | C | 4 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0052others(1): Show | 4 | HG00280.hp1 HG00639.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.157+19105A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102429707 | ||||||
| chr11:102429922
|
G | T | 7 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0089others(4): Show | 7 | HG01081.hp2 HG01243.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.157+18890C>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102429922 | ||||||
| chr11:102430145
|
G | T | 155 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(152): Show | 162 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.157+18667C>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102430145 | ||||||
| chr11:102430353
|
T | C | 3 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0011g0181 | 3 | HG02922.hp2 HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.157+18459A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102430353 | ||||||
| chr11:102430460
|
T | C | 1 | a0001c0001t0002g0026 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.157+18352A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102430460 | ||||||
| chr11:102430768
|
G | C | 2 | a0001c0001t0001g0103a0001c0001t0001g0111 | 2 | HG03195.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.157+18044C>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102430768 | ||||||
| chr11:102431088
|
A | T | 1 | a0002c0002t0001g0168 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.157+17724T>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102431088 | ||||||
| chr11:102431128
|
T | C | 5 | a0001c0004t0008g0012a0001c0004t0008g0013a0001c0004t0008g0014others(2): Show | 5 | HG02970.hp1 HG03209.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.157+17684A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102431128 | ||||||
| chr11:102431159
|
G | A | 5 | a0004c0005t0005g0031a0004c0005t0005g0032a0004c0005t0005g0033others(2): Show | 5 | HG01109.hp2 HG01255.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.157+17653C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102431159 | ||||||
| chr11:102431170
|
T | TA | 9 | a0001c0001t0001g0132a0001c0004t0008g0012a0001c0004t0008g0013others(6): Show | 11 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.157+17641dupT | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102431170 | ||||||
| chr11:102431353
|
A | G | 3 | a0003c0003t0006g0001a0003c0003t0006g0010a0003c0003t0006g0011 | 5 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.157+17459T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102431353 | ||||||
| chr11:102431706
|
CAGTT | C | 4 | a0001c0001t0001g0125a0001c0001t0001g0158a0001c0001t0001g0159others(1): Show | 4 | HG01070.hp1 HG02895.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.157+17102_157+1710 others(8): Show |
TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102431706 | ||||||
| chr11:102431851
|
C | T | 1 | a0001c0001t0001g0183 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.157+16961G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102431851 | ||||||
| chr11:102431948
|
C | T | 1 | a0003c0003t0006g0010 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.157+16864G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102431948 | ||||||
| chr11:102432074
|
T | C | 7 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0089others(4): Show | 7 | HG01081.hp2 HG01243.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.157+16738A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102432074 | ||||||
| chr11:102432277
|
TCC | T | 3 | a0002c0002t0001g0138a0002c0002t0001g0139a0002c0002t0001g0160 | 3 | HG00323.hp2 HG02559.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.157+16533_157+1653 others(6): Show |
TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102432277 | ||||||
| chr11:102432290
|
T | C | 5 | a0004c0005t0005g0031a0004c0005t0005g0032a0004c0005t0005g0033others(2): Show | 5 | HG01109.hp2 HG01255.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.157+16522A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102432290 | ||||||
| chr11:102432479
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.157+16333G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102432479 | ||||||
| chr11:102432623
|
G | A | 2 | a0001c0001t0001g0059a0001c0001t0001g0132 | 2 | HG02523.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.157+16189C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102432623 | ||||||
| chr11:102432817
|
G | A | 2 | a0001c0001t0002g0039a0001c0001t0002g0040 | 2 | HG02145.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.157+15995C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102432817 | ||||||
| chr11:102432853
|
GGTCAAAG others(3894): Show |
G | 1 | a0001c0001t0013g0173 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.157+12058_157+1595 others(4): Show |
TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102432853 | ||||||
| chr11:102432855
|
T | C | 2 | a0001c0001t0001g0122a0001c0001t0019g0123 | 2 | HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.157+15957A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102432855 | ||||||
| chr11:102432945
|
G | A | 1 | a0001c0001t0001g0054 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.157+15867C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102432945 | ||||||
| chr11:102433015
|
C | A | 1 | a0001c0001t0002g0024 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.157+15797G>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102433015 | ||||||
| chr11:102433128
|
T | C | 5 | a0001c0004t0008g0012a0001c0004t0008g0013a0001c0004t0008g0014others(2): Show | 5 | HG02970.hp1 HG03209.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.157+15684A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102433128 | ||||||
| chr11:102433160
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.157+15652C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102433160 | ||||||
| chr11:102433325
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.157+15487G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102433325 | ||||||
| chr11:102433387
|
C | G | 8 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(5): Show | 8 | HG02280.hp1 HG02622.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.157+15425G>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102433387 | ||||||
| chr11:102433479
|
A | C | 186 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(183): Show | 195 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.157+15333T>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102433479 | ||||||
| chr11:102433742
|
G | A | 9 | a0001c0001t0002g0035a0001c0004t0008g0012a0001c0004t0008g0013others(6): Show | 11 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.157+15070C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102433742 | ||||||
| chr11:102433819
|
T | C | 3 | a0003c0003t0006g0001a0003c0003t0006g0010a0003c0003t0006g0011 | 5 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.157+14993A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102433819 | ||||||
| chr11:102433826
|
A | G | 5 | a0004c0005t0005g0031a0004c0005t0005g0032a0004c0005t0005g0033others(2): Show | 5 | HG01109.hp2 HG01255.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.157+14986T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102433826 | ||||||
| chr11:102433908
|
GT | G | 8 | a0001c0004t0008g0012a0001c0004t0008g0013a0001c0004t0008g0014others(5): Show | 10 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.157+14903delA | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102433908 | ||||||
| chr11:102433929
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.157+14883G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102433929 | ||||||
| chr11:102434002
|
C | T | 8 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(5): Show | 8 | HG00280.hp2 HG01261.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.157+14810G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102434002 | ||||||
| chr11:102434374
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.157+14438C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102434374 | ||||||
| chr11:102434410
|
A | G | 1 | a0001c0001t0001g0002 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.157+14402T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102434410 | ||||||
| chr11:102434464
|
T | C | 12 | a0001c0001t0002g0024a0001c0001t0002g0039a0001c0001t0002g0040others(9): Show | 12 | HG01243.hp1 HG01346.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.157+14348A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102434464 | ||||||
| chr11:102434469
|
T | C | 5 | a0004c0005t0005g0031a0004c0005t0005g0032a0004c0005t0005g0033others(2): Show | 5 | HG01109.hp2 HG01255.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.157+14343A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102434469 | ||||||
| chr11:102434758
|
G | A | 1 | a0001c0001t0002g0026 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.157+14054C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102434758 | ||||||
| chr11:102435022
|
A | G | 2 | a0001c0001t0001g0047a0001c0001t0001g0048 | 2 | HG00280.hp1 HG00639.hp1 |
intron_variant | MODIFIER | c.157+13790T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102435022 | ||||||
| chr11:102435041
|
C | T | 3 | a0002c0002t0001g0138a0002c0002t0001g0139a0002c0002t0001g0160 | 3 | HG00323.hp2 HG02559.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.157+13771G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102435041 | ||||||
| chr11:102435267
|
C | T | 6 | a0001c0001t0001g0004a0001c0001t0001g0133a0001c0001t0001g0134others(3): Show | 7 | HG01081.hp1 HG01433.hp1 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.157+13545G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102435267 | ||||||
| chr11:102435401
|
CA | C | 2 | a0001c0001t0002g0036a0001c0001t0002g0037 | 2 | HG02280.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.157+13410delT | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102435401 | ||||||
| chr11:102435806
|
C | A | 1 | a0001c0001t0026g0194 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.157+13006G>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102435806 | ||||||
| chr11:102435910
|
G | T | 5 | a0004c0005t0005g0031a0004c0005t0005g0032a0004c0005t0005g0033others(2): Show | 5 | HG01109.hp2 HG01255.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.157+12902C>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102435910 | ||||||
| chr11:102435932
|
C | T | 1 | a0001c0001t0001g0007 | 2 | NA18983.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.157+12880G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102435932 | ||||||
| chr11:102435938
|
G | A | 3 | a0001c0001t0002g0038a0001c0006t0012g0029a0001c0006t0012g0030 | 3 | HG02258.hp1 HG02572.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.157+12874C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102435938 | ||||||
| chr11:102435957
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.157+12855C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102435957 | ||||||
| chr11:102436072
|
T | TA | 23 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(20): Show | 25 | HG01109.hp1 HG01109.hp2 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.157+12739dupT | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102436072 | ||||||
| chr11:102436193
|
C | T | 12 | a0001c0001t0002g0024a0001c0001t0002g0039a0001c0001t0002g0040others(9): Show | 12 | HG01243.hp1 HG01346.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.157+12619G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102436193 | ||||||
| chr11:102436409
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.157+12403G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102436409 | ||||||
| chr11:102436423
|
A | G | 5 | a0001c0004t0008g0012a0001c0004t0008g0013a0001c0004t0008g0014others(2): Show | 5 | HG02970.hp1 HG03209.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.157+12389T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102436423 | ||||||
| chr11:102436431
|
G | A | 1 | a0001c0001t0004g0023 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.157+12381C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102436431 | ||||||
| chr11:102436492
|
T | C | 2 | a0001c0001t0002g0039a0001c0001t0002g0040 | 2 | HG02145.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.157+12320A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102436492 | ||||||
| chr11:102436612
|
C | G | 7 | a0001c0001t0001g0059a0001c0001t0001g0131a0001c0001t0001g0132others(4): Show | 7 | HG00621.hp2 HG01169.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.157+12200G>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102436612 | ||||||
| chr11:102436668
|
A | G | 5 | a0004c0005t0005g0031a0004c0005t0005g0032a0004c0005t0005g0033others(2): Show | 5 | HG01109.hp2 HG01255.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.157+12144T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102436668 | ||||||
| chr11:102436980
|
T | C | 1 | a0003c0003t0006g0011 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.157+11832A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102436980 | ||||||
| chr11:102437089
|
T | G | 18 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(15): Show | 20 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.157+11723A>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102437089 | ||||||
| chr11:102437138
|
G | T | 1 | a0001c0001t0001g0125 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.157+11674C>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102437138 | ||||||
| chr11:102437152
|
CCTCA | C | 15 | a0001c0001t0001g0054a0001c0001t0001g0095a0001c0001t0001g0096others(12): Show | 15 | HG01346.hp2 HG02055.hp2 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.157+11656_157+1165 others(8): Show |
TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102437152 | ||||||
| chr11:102437310
|
T | G | 1 | a0001c0001t0001g0058 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.157+11502A>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102437310 | ||||||
| chr11:102437322
|
G | A | 5 | a0004c0005t0005g0031a0004c0005t0005g0032a0004c0005t0005g0033others(2): Show | 5 | HG01109.hp2 HG01255.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.157+11490C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102437322 | ||||||
| chr11:102437413
|
G | A | 1 | a0002c0002t0001g0160 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.157+11399C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102437413 | ||||||
| chr11:102437457
|
C | CA | 11 | a0001c0001t0001g0054a0001c0001t0001g0088a0001c0001t0001g0094others(8): Show | 11 | HG01361.hp2 HG01934.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.157+11354dupT | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102437457 | ||||||
| chr11:102437475
|
AT | A | 21 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(18): Show | 21 | HG01109.hp2 HG01255.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.157+11336delA | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102437475 | ||||||
| chr11:102437476
|
T | A | 170 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(167): Show | 180 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.157+11336A>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102437476 | ||||||
| chr11:102437486
|
G | A | 1 | a0001c0001t0001g0174 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.157+11326C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102437486 | ||||||
| chr11:102437521
|
A | G | 1 | a0001c0001t0001g0124 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.157+11291T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102437521 | ||||||
| chr11:102437523
|
C | T | 2 | a0001c0001t0001g0122a0001c0001t0019g0123 | 2 | HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.157+11289G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102437523 | ||||||
| chr11:102437524
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.157+11288C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102437524 | ||||||
| chr11:102437572
|
T | C | 18 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(15): Show | 20 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.157+11240A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102437572 | ||||||
| chr11:102437642
|
T | C | 4 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0167others(1): Show | 4 | HG01169.hp1 HG01928.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.157+11170A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102437642 | ||||||
| chr11:102437684
|
G | A | 3 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097 | 3 | HG02622.hp2 HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.157+11128C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102437684 | ||||||
| chr11:102437709
|
A | G | 149 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(146): Show | 156 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.157+11103T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102437709 | ||||||
| chr11:102437728
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.157+11084T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102437728 | ||||||
| chr11:102438053
|
TTTA | T | 4 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0022others(1): Show | 4 | HG01243.hp1 HG02109.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.157+10756_157+1075 others(7): Show |
TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102438053 | ||||||
| chr11:102438143
|
A | G | 186 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(183): Show | 195 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.157+10669T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102438143 | ||||||
| chr11:102438155
|
G | A | 2 | a0001c0006t0012g0029a0001c0006t0012g0030 | 2 | HG02258.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.157+10657C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102438155 | ||||||
| chr11:102438194
|
A | T | 12 | a0001c0001t0002g0024a0001c0001t0002g0039a0001c0001t0002g0040others(9): Show | 12 | HG01243.hp1 HG01346.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.157+10618T>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102438194 | ||||||
| chr11:102438484
|
G | A | 1 | a0001c0001t0003g0091 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.157+10328C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102438484 | ||||||
| chr11:102438592
|
T | C | 3 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0011g0181 | 3 | HG02922.hp2 HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.157+10220A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102438592 | ||||||
| chr11:102438763
|
A | G | 5 | a0004c0005t0005g0031a0004c0005t0005g0032a0004c0005t0005g0033others(2): Show | 5 | HG01109.hp2 HG01255.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.157+10049T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102438763 | ||||||
| chr11:102438821
|
G | A | 1 | a0001c0001t0009g0056 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.157+9991C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102438821 | ||||||
| chr11:102438822
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.157+9990C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102438822 | ||||||
| chr11:102438897
|
C | T | 2 | a0001c0001t0004g0020a0001c0001t0004g0021 | 2 | HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.157+9915G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102438897 | ||||||
| chr11:102439095
|
C | T | 1 | a0001c0001t0002g0035 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.157+9717G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102439095 | ||||||
| chr11:102439116
|
C | G | 1 | a0001c0001t0001g0066 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.157+9696G>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102439116 | ||||||
| chr11:102439173
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.157+9639A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102439173 | ||||||
| chr11:102439177
|
T | A | 8 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(5): Show | 8 | HG02280.hp1 HG02622.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.157+9635A>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102439177 | ||||||
| chr11:102439324
|
T | C | 1 | a0001c0001t0001g0166 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.157+9488A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102439324 | ||||||
| chr11:102439346
|
T | A | 2 | a0001c0006t0012g0029a0001c0006t0012g0030 | 2 | HG02258.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.157+9466A>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102439346 | ||||||
| chr11:102439495
|
A | T | 5 | a0004c0005t0005g0031a0004c0005t0005g0032a0004c0005t0005g0033others(2): Show | 5 | HG01109.hp2 HG01255.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.157+9317T>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102439495 | ||||||
| chr11:102439525
|
CA | C | 3 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0011g0181 | 3 | HG02922.hp2 HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.157+9286delT | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102439525 | ||||||
| chr11:102439636
|
C | T | 2 | a0001c0001t0001g0119a0001c0001t0001g0120 | 2 | HG02257.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.157+9176G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102439636 | ||||||
| chr11:102439666
|
G | A | 1 | a0001c0001t0001g0058 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.157+9146C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102439666 | ||||||
| chr11:102439705
|
C | T | 1 | a0001c0001t0026g0194 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.157+9107G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102439705 | ||||||
| chr11:102439867
|
T | TG | 18 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(15): Show | 20 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.157+8944dupC | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102439867 | ||||||
| chr11:102440073
|
T | C | 3 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097 | 3 | HG02622.hp2 HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.157+8739A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102440073 | ||||||
| chr11:102440082
|
C | T | 5 | a0001c0004t0008g0012a0001c0004t0008g0013a0001c0004t0008g0014others(2): Show | 5 | HG02970.hp1 HG03209.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.157+8730G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102440082 | ||||||
| chr11:102440093
|
G | A | 1 | a0001c0001t0007g0019 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.157+8719C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102440093 | ||||||
| chr11:102440100
|
G | A | 2 | a0001c0001t0001g0045a0001c0001t0014g0044 | 2 | HG01175.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.157+8712C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102440100 | ||||||
| chr11:102440133
|
T | C | 2 | a0001c0006t0012g0029a0001c0006t0012g0030 | 2 | HG02258.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.157+8679A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102440133 | ||||||
| chr11:102440223
|
G | C | 12 | a0001c0001t0002g0024a0001c0001t0002g0039a0001c0001t0002g0040others(9): Show | 12 | HG01243.hp1 HG01346.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.157+8589C>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102440223 | ||||||
| chr11:102440343
|
C | T | 5 | a0004c0005t0005g0031a0004c0005t0005g0032a0004c0005t0005g0033others(2): Show | 5 | HG01109.hp2 HG01255.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.157+8469G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102440343 | ||||||
| chr11:102440505
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.157+8307C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102440505 | ||||||
| chr11:102440617
|
G | A | 3 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0011g0181 | 3 | HG02922.hp2 HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.157+8195C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102440617 | ||||||
| chr11:102440619
|
T | C | 12 | a0001c0001t0002g0024a0001c0001t0002g0039a0001c0001t0002g0040others(9): Show | 12 | HG01243.hp1 HG01346.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.157+8193A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102440619 | ||||||
| chr11:102440624
|
G | A | 1 | a0002c0002t0001g0168 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.157+8188C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102440624 | ||||||
| chr11:102440836
|
A | G | 1 | a0001c0001t0002g0026 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.157+7976T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102440836 | ||||||
| chr11:102441189
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.157+7623G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102441189 | ||||||
| chr11:102441198
|
T | C | 1 | a0001c0001t0001g0169 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.157+7614A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102441198 | ||||||
| chr11:102441401
|
G | A | 18 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(15): Show | 20 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.157+7411C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102441401 | ||||||
| chr11:102441439
|
G | A | 2 | a0001c0001t0001g0089a0001c0001t0001g0090 | 2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.157+7373C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102441439 | ||||||
| chr11:102441509
|
C | A | 1 | a0001c0001t0001g0170 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.157+7303G>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102441509 | ||||||
| chr11:102441509
|
CA | C | 9 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0004g0022others(6): Show | 9 | HG01243.hp1 HG02109.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.157+7302delT | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102441509 | ||||||
| chr11:102441723
|
A | C | 1 | a0001c0001t0003g0078 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.157+7089T>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102441723 | ||||||
| chr11:102441733
|
C | CA | 16 | a0001c0001t0001g0043a0001c0001t0001g0115a0001c0001t0001g0182others(13): Show | 16 | HG00323.hp1 HG00738.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.157+7078dupT | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102441733 | ||||||
| chr11:102441733
|
C | CAA | 8 | a0001c0001t0002g0040a0001c0001t0004g0020a0001c0001t0004g0021others(5): Show | 8 | HG01243.hp1 HG02109.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.157+7077_157+7078d others(4): Show |
TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102441733 | ||||||
| chr11:102442120
|
G | C | 1 | a0001c0001t0001g0117 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.157+6692C>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102442120 | ||||||
| chr11:102442240
|
CACA | C | 3 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0011g0181 | 3 | HG02922.hp2 HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.157+6569_157+6571d others(5): Show |
TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102442240 | ||||||
| chr11:102442247
|
A | G | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(148): Show | 158 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.157+6565T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102442247 | ||||||
| chr11:102442349
|
C | T | 1 | a0001c0001t0021g0172 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.157+6463G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102442349 | ||||||
| chr11:102442350
|
A | G | 1 | a0001c0001t0021g0172 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.157+6462T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102442350 | ||||||
| chr11:102442358
|
T | G | 1 | a0001c0001t0021g0172 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.157+6454A>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102442358 | ||||||
| chr11:102442393
|
C | T | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG02056.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.157+6419G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102442393 | ||||||
| chr11:102442539
|
C | T | 1 | a0001c0001t0026g0194 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.157+6273G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102442539 | ||||||
| chr11:102442553
|
A | G | 65 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(62): Show | 68 | HG00280.hp2 HG00323.hp1 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.157+6259T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102442553 | ||||||
| chr11:102442733
|
T | G | 1 | a0001c0001t0026g0194 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.157+6079A>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102442733 | ||||||
| chr11:102442900
|
T | C | 1 | a0001c0001t0002g0026 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.157+5912A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102442900 | ||||||
| chr11:102443002
|
A | G | 3 | a0001c0001t0007g0016a0001c0001t0007g0017a0001c0001t0018g0057 | 3 | HG02630.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.157+5810T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102443002 | ||||||
| chr11:102443104
|
G | GAA | 5 | a0001c0001t0003g0008a0001c0001t0003g0188a0001c0001t0003g0191others(2): Show | 6 | HG00738.hp2 HG01099.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.157+5706_157+5707d others(4): Show |
TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102443104 | ||||||
| chr11:102443210
|
T | C | 1 | a0001c0001t0003g0091 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.157+5602A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102443210 | ||||||
| chr11:102443528
|
A | ATT | 5 | a0004c0005t0005g0031a0004c0005t0005g0032a0004c0005t0005g0033others(2): Show | 5 | HG01109.hp2 HG01255.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.157+5282_157+5283d others(4): Show |
TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102443528 | ||||||
| chr11:102443546
|
C | T | 1 | a0001c0001t0026g0194 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.157+5266G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102443546 | ||||||
| chr11:102443638
|
G | A | 1 | a0001c0001t0009g0077 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.157+5174C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102443638 | ||||||
| chr11:102444011
|
A | G | 5 | a0004c0005t0005g0031a0004c0005t0005g0032a0004c0005t0005g0033others(2): Show | 5 | HG01109.hp2 HG01255.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.157+4801T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102444011 | ||||||
| chr11:102444051
|
A | G | 186 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(183): Show | 195 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.157+4761T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102444051 | ||||||
| chr11:102444089
|
G | A | 6 | a0001c0001t0002g0024a0004c0005t0005g0031a0004c0005t0005g0032others(3): Show | 6 | HG01109.hp2 HG01255.hp2 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.157+4723C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102444089 | ||||||
| chr11:102444140
|
G | A | 1 | a0001c0001t0002g0038 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.157+4672C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102444140 | ||||||
| chr11:102444178
|
C | T | 5 | a0004c0005t0005g0031a0004c0005t0005g0032a0004c0005t0005g0033others(2): Show | 5 | HG01109.hp2 HG01255.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.157+4634G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102444178 | ||||||
| chr11:102444221
|
C | A | 1 | a0001c0001t0013g0173 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.157+4591G>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102444221 | ||||||
| chr11:102444438
|
G | A | 5 | a0004c0005t0005g0031a0004c0005t0005g0032a0004c0005t0005g0033others(2): Show | 5 | HG01109.hp2 HG01255.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.157+4374C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102444438 | ||||||
| chr11:102444723
|
T | A | 5 | a0004c0005t0005g0031a0004c0005t0005g0032a0004c0005t0005g0033others(2): Show | 5 | HG01109.hp2 HG01255.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.157+4089A>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102444723 | ||||||
| chr11:102444822
|
T | C | 1 | a0001c0001t0001g0174 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.157+3990A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102444822 | ||||||
| chr11:102444837
|
C | A | 2 | a0001c0001t0002g0039a0001c0001t0002g0040 | 2 | HG02145.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.157+3975G>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102444837 | ||||||
| chr11:102444925
|
A | C | 1 | a0001c0001t0002g0035 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.157+3887T>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102444925 | ||||||
| chr11:102445078
|
C | T | 8 | a0001c0004t0008g0012a0001c0004t0008g0013a0001c0004t0008g0014others(5): Show | 10 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.157+3734G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102445078 | ||||||
| chr11:102445079
|
G | C | 1 | a0001c0001t0002g0024 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.157+3733C>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102445079 | ||||||
| chr11:102445120
|
C | T | 23 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(20): Show | 25 | HG01109.hp1 HG01109.hp2 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.157+3692G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102445120 | ||||||
| chr11:102445197
|
C | T | 10 | a0001c0004t0008g0012a0001c0004t0008g0013a0001c0004t0008g0014others(7): Show | 12 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.157+3615G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102445197 | ||||||
| chr11:102445327
|
C | T | 3 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0011g0181 | 3 | HG02922.hp2 HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.157+3485G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102445327 | ||||||
| chr11:102445333
|
GTCTC | G | 20 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0058others(17): Show | 22 | HG00621.hp1 HG00738.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.157+3475_157+3478d others(6): Show |
TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102445333 | ||||||
| chr11:102445374
|
T | A | 3 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0011g0181 | 3 | HG02922.hp2 HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.157+3438A>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102445374 | ||||||
| chr11:102445443
|
A | C | 1 | a0001c0001t0001g0063 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.157+3369T>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102445443 | ||||||
| chr11:102445627
|
G | T | 2 | a0001c0001t0016g0185a0001c0001t0016g0186 | 2 | HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.157+3185C>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102445627 | ||||||
| chr11:102445692
|
C | G | 11 | a0001c0001t0002g0026a0001c0004t0008g0012a0001c0004t0008g0013others(8): Show | 13 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.157+3120G>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102445692 | ||||||
| chr11:102445699
|
C | T | 2 | a0001c0006t0012g0029a0001c0006t0012g0030 | 2 | HG02258.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.157+3113G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102445699 | ||||||
| chr11:102445900
|
A | T | 150 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(147): Show | 156 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.157+2912T>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102445900 | ||||||
| chr11:102446147
|
T | C | 1 | a0001c0001t0001g0093 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.157+2665A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102446147 | ||||||
| chr11:102446386
|
G | C | 2 | a0001c0001t0001g0175a0001c0001t0001g0176 | 2 | HG02132.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.157+2426C>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102446386 | ||||||
| chr11:102446429
|
T | C | 2 | a0001c0001t0001g0175a0001c0001t0001g0176 | 2 | HG02132.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.157+2383A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102446429 | ||||||
| chr11:102446476
|
CA | C | 3 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097 | 3 | HG02622.hp2 HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.157+2335delT | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102446476 | ||||||
| chr11:102446532
|
T | A | 18 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(15): Show | 20 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.157+2280A>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102446532 | ||||||
| chr11:102446647
|
T | G | 1 | a0001c0001t0001g0094 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.157+2165A>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102446647 | ||||||
| chr11:102446678
|
G | C | 8 | a0001c0004t0008g0012a0001c0004t0008g0013a0001c0004t0008g0014others(5): Show | 10 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.157+2134C>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102446678 | ||||||
| chr11:102446717
|
A | C | 41 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0045others(38): Show | 43 | HG00621.hp1 HG00738.hp1 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.157+2095T>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102446717 | ||||||
| chr11:102446889
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.157+1923C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102446889 | ||||||
| chr11:102447456
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.157+1356G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102447456 | ||||||
| chr11:102447461
|
C | T | 3 | a0003c0003t0006g0001a0003c0003t0006g0010a0003c0003t0006g0011 | 5 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.157+1351G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102447461 | ||||||
| chr11:102447723
|
T | A | 8 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(5): Show | 8 | HG02280.hp1 HG02622.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.157+1089A>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102447723 | ||||||
| chr11:102447921
|
C | T | 1 | a0001c0001t0009g0055 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.157+891G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102447921 | ||||||
| chr11:102447957
|
A | T | 1 | a0001c0001t0001g0061 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.157+855T>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102447957 | ||||||
| chr11:102448237
|
T | C | 17 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(14): Show | 19 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.157+575A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102448237 | ||||||
| chr11:102448597
|
T | C | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(148): Show | 158 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.157+215A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 2/4 | chr11 | 102448597 | ||||||
| chr11:102449169
|
T | C | 13 | a0001c0001t0002g0024a0001c0001t0002g0039a0001c0001t0002g0040others(10): Show | 13 | HG01243.hp1 HG01346.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.101-301A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 1/4 | chr11 | 102449169 | ||||||
| chr11:102449243
|
C | T | 1 | a0002c0002t0001g0060 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.101-375G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 1/4 | chr11 | 102449243 | ||||||
| chr11:102449284
|
A | C | 1 | a0001c0001t0001g0059 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.101-416T>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 1/4 | chr11 | 102449284 | ||||||
| chr11:102449403
|
A | C | 1 | a0001c0001t0001g0058 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.101-535T>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 1/4 | chr11 | 102449403 | ||||||
| chr11:102449551
|
T | TA | 150 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(147): Show | 157 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.101-684dupT | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 1/4 | chr11 | 102449551 | ||||||
| chr11:102449822
|
C | T | 1 | a0001c0001t0026g0194 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.101-954G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 1/4 | chr11 | 102449822 | ||||||
| chr11:102449840
|
T | C | 8 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(5): Show | 8 | HG02280.hp1 HG02622.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.101-972A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 1/4 | chr11 | 102449840 | ||||||
| chr11:102449891
|
T | A | 1 | a0001c0001t0001g0180 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.101-1023A>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 1/4 | chr11 | 102449891 | ||||||
| chr11:102450010
|
G | A | 8 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0028others(5): Show | 8 | HG02280.hp1 HG02622.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.101-1142C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 1/4 | chr11 | 102450010 | ||||||
| chr11:102450472
|
T | C | 7 | a0001c0006t0012g0029a0001c0006t0012g0030a0004c0005t0005g0031others(4): Show | 7 | HG01109.hp2 HG01255.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.101-1604A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 1/4 | chr11 | 102450472 | ||||||
| chr11:102450703
|
T | C | 5 | a0004c0005t0005g0031a0004c0005t0005g0032a0004c0005t0005g0033others(2): Show | 5 | HG01109.hp2 HG01255.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+1821A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 1/4 | chr11 | 102450703 | ||||||
| chr11:102450753
|
C | G | 1 | a0001c0001t0003g0188 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.100+1771G>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 1/4 | chr11 | 102450753 | ||||||
| chr11:102450803
|
C | T | 7 | a0001c0004t0008g0012a0001c0004t0008g0013a0001c0004t0008g0014others(4): Show | 9 | HG01109.hp1 HG01884.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.100+1721G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 1/4 | chr11 | 102450803 | ||||||
| chr11:102450892
|
T | G | 1 | a0001c0001t0001g0182 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.100+1632A>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 1/4 | chr11 | 102450892 | ||||||
| chr11:102450937
|
C | A | 1 | a0001c0001t0001g0183 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.100+1587G>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 1/4 | chr11 | 102450937 | ||||||
| chr11:102450944
|
T | C | 5 | a0004c0005t0005g0031a0004c0005t0005g0032a0004c0005t0005g0033others(2): Show | 5 | HG01109.hp2 HG01255.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+1580A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 1/4 | chr11 | 102450944 | ||||||
| chr11:102451083
|
T | C | 1 | a0001c0001t0022g0184 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.100+1441A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 1/4 | chr11 | 102451083 | ||||||
| chr11:102451118
|
T | C | 1 | a0001c0001t0001g0007 | 2 | NA18983.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.100+1406A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 1/4 | chr11 | 102451118 | ||||||
| chr11:102451345
|
CT | C | 5 | a0004c0005t0005g0031a0004c0005t0005g0032a0004c0005t0005g0033others(2): Show | 5 | HG01109.hp2 HG01255.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+1178delA | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 1/4 | chr11 | 102451345 | ||||||
| chr11:102451438
|
A | G | 1 | a0001c0001t0001g0054 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.100+1086T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 1/4 | chr11 | 102451438 | ||||||
| chr11:102451728
|
A | G | 10 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047others(7): Show | 10 | HG00280.hp1 HG00639.hp1 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.100+796T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 1/4 | chr11 | 102451728 | ||||||
| chr11:102451879
|
C | A | 2 | a0001c0001t0016g0185a0001c0001t0016g0186 | 2 | HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.100+645G>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 1/4 | chr11 | 102451879 | ||||||
| chr11:102452319
|
T | C | 1 | a0001c0001t0023g0187 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.100+205A>G | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 1/4 | chr11 | 102452319 | ||||||
| chr11:102452371
|
T | G | 4 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0037others(1): Show | 4 | HG02280.hp1 HG02622.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+153A>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 1/4 | chr11 | 102452371 | ||||||
| chr11:102452387
|
G | A | 2 | a0001c0001t0002g0039a0001c0001t0002g0040 | 2 | HG02145.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.100+137C>T | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 1/4 | chr11 | 102452387 | ||||||
| chr11:102452429
|
C | T | 152 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(149): Show | 158 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.100+95G>A | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 1/4 | chr11 | 102452429 | ||||||
| chr11:102452453
|
A | G | 2 | a0001c0001t0001g0043a0001c0001t0017g0042 | 2 | HG00323.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.100+71T>C | TMEM123 | ENSG00000152558.15 | transcript | ENST00000398136.7 | protein_coding | 1/4 | chr11 | 102452453 |