Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 57690 |
|---|---|
| ensemblid | ENSG00000078687.18 |
| hgncid | 29318 |
| symbol | TNRC6C |
| name | trinucleotide repeat containing adaptor 6C |
| refseq_nuc | NM_001142640.2 |
| refseq_prot | NP_001136112.2 |
| ensembl_nuc | ENST00000696270.1 |
| ensembl_prot | ENSP00000512514.1 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 77958703 |
| end | 78108822 |
| strand | + |
| ver | v1.2 |
| region | chr17:77958703-78108822 |
| region5000 | chr17:77953703-78113822 |
| regionname0 | TNRC6C_chr17_77958703_78108822 |
| regionname5000 | TNRC6C_chr17_77953703_78113822 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1936 | 211 | 73 | 38 | 75 | 5 | 18 | 57 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0002 | 0/0 | 1936 | 39 | 9 | 4 | 23 | 1 | 2 | 18 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0003 | 0/0 | 1455 | 5 | 1 | 1 | 1 | 0 | 2 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0004 | 0/0 | 1936 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0005 | 0/0 | 1936 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0006 | 0/0 | 1936 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0007 | 0/0 | 1455 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0008 | 0/0 | 1936 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0009 | 0/0 | 1936 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0010 | 0/0 | 1936 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0011 | 0/0 | 1936 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0012 | 0/0 | 1936 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0013 | 0/0 | 1455 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0014 | 0/0 | 1936 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0015 | 0/0 | 1936 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0016 | 0/0 | 1936 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0017 | 0/0 | 1455 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0018 | 0/0 | 1936 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 5811 | 140 | 35 | 30 | 59 | 4 | 11 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| c0002 | 0/1 | 5811 | 39 | 15 | 3 | 15 | 1 | 4 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| c0003 | 0/0 | 5811 | 36 | 7 | 4 | 23 | 1 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| c0004 | 0/0 | 5811 | 11 | 11 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| c0005 | 0/0 | 5811 | 9 | 9 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| c0006 | 0/0 | 5811 | 5 | 0 | 1 | 1 | 0 | 3 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| c0007 | 0/0 | 5811 | 3 | 3 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| c0008 | 0/0 | 5811 | 3 | 0 | 0 | 3 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| c0009 | 0/0 | 5811 | 3 | 0 | 3 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| c0010 | 0/0 | 5811 | 2 | 1 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| c0011 | 0/0 | 5811 | 2 | 1 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| c0012 | 0/0 | 5812 | 2 | 1 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| c0013 | 0/0 | 5812 | 2 | 0 | 0 | 2 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| c0014 | 0/0 | 5811 | 2 | 1 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| c0015 | 0/0 | 5811 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| c0016 | 0/0 | 5811 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| c0017 | 0/0 | 5812 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| c0018 | 0/0 | 5811 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| c0019 | 0/0 | 5811 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| c0020 | 0/0 | 5811 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| c0021 | 0/0 | 5812 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| c0022 | 0/0 | 5812 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| c0023 | 0/0 | 5811 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| c0024 | 0/0 | 5811 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| c0025 | 0/0 | 5811 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| c0026 | 0/0 | 5812 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| c0027 | 0/0 | 5811 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| c0028 | 0/0 | 5811 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| c0029 | 0/0 | 5811 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| c0030 | 0/0 | 5812 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| c0031 | 0/0 | 5811 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 4581 | 111 | 24 | 26 | 49 | 4 | 8 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0002 | 0/0 | 4579 | 25 | 5 | 3 | 14 | 1 | 2 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0003 | 0/0 | 4585 | 23 | 4 | 4 | 14 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0004 | 0/0 | 4581 | 13 | 6 | 4 | 2 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0005 | 0/0 | 4582 | 9 | 6 | 0 | 3 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0006 | 0/0 | 4579 | 6 | 6 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0007 | 0/0 | 4584 | 5 | 0 | 0 | 5 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0008 | 0/0 | 4580 | 4 | 0 | 1 | 1 | 0 | 2 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0009 | 0/0 | 4580 | 4 | 0 | 0 | 4 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0010 | 0/0 | 4588 | 3 | 3 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0011 | 0/0 | 4576 | 3 | 3 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0012 | 0/0 | 4583 | 3 | 3 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0013 | 0/0 | 4580 | 3 | 3 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0014 | 0/0 | 4578 | 3 | 3 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0015 | 0/0 | 4581 | 3 | 1 | 2 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0016 | 0/0 | 4581 | 3 | 0 | 2 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0017 | 0/0 | 4580 | 2 | 2 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0018 | 0/0 | 4579 | 2 | 2 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0019 | 0/0 | 4580 | 2 | 0 | 1 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0020 | 0/0 | 4584 | 2 | 0 | 0 | 2 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0021 | 0/0 | 4582 | 2 | 0 | 0 | 2 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0022 | 0/0 | 4585 | 2 | 0 | 0 | 2 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0023 | 0/0 | 4582 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0024 | 0/0 | 4580 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0025 | 0/0 | 4583 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0026 | 0/0 | 4576 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0027 | 0/0 | 4579 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0028 | 0/0 | 4580 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0029 | 0/0 | 4581 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0030 | 0/0 | 4581 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0031 | 0/0 | 4580 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0032 | 0/0 | 4581 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0033 | 0/0 | 4580 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0034 | 0/0 | 4581 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0035 | 0/0 | 4579 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0036 | 0/0 | 4581 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0037 | 1/0 | 4581 | 1 | 0 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0038 | 0/0 | 4578 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0039 | 0/0 | 4578 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0040 | 0/0 | 4580 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0041 | 0/0 | 4580 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0042 | 0/0 | 4580 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0043 | 0/0 | 4581 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0044 | 0/0 | 4582 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0045 | 0/0 | 4580 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0046 | 0/0 | 4581 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0047 | 0/0 | 4581 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0048 | 0/0 | 4581 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0049 | 0/0 | 4579 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0050 | 0/0 | 4579 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0051 | 0/0 | 4581 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0052 | 0/0 | 4578 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0053 | 0/0 | 4578 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0054 | 0/0 | 4581 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0055 | 0/0 | 4586 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0056 | 0/0 | 4586 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0057 | 0/0 | 4586 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0058 | 0/0 | 4585 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0059 | 0/0 | 4579 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0060 | 0/0 | 4582 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0061 | 0/1 | 4578 | 1 | 0 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0062 | 0/0 | 4578 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0063 | 0/0 | 4581 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0064 | 0/0 | 4581 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| t0065 | 0/0 | 4581 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0056 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0232 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 5811 | 140 | 35 | 30 | 59 | 4 | 11 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0001c0002 | 0/1 | 5811 | 39 | 15 | 3 | 15 | 1 | 4 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0001c0004 | 0/0 | 5811 | 11 | 11 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0001c0005 | 0/0 | 5811 | 9 | 9 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0001c0006 | 0/0 | 5811 | 5 | 0 | 1 | 1 | 0 | 3 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0001c0007 | 0/0 | 5811 | 3 | 3 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0001c0009 | 0/0 | 5811 | 3 | 0 | 3 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0001c0029 | 0/0 | 5811 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0002c0003 | 0/0 | 5811 | 36 | 7 | 4 | 23 | 1 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0002c0014 | 0/0 | 5811 | 2 | 1 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0002c0027 | 0/0 | 5811 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0003c0012 | 0/0 | 5812 | 2 | 1 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0003c0021 | 0/0 | 5812 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0003c0022 | 0/0 | 5812 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0003c0030 | 0/0 | 5812 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0004c0008 | 0/0 | 5811 | 3 | 0 | 0 | 3 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0005c0010 | 0/0 | 5811 | 2 | 1 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0006c0011 | 0/0 | 5811 | 2 | 1 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0007c0013 | 0/0 | 5812 | 2 | 0 | 0 | 2 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0008c0016 | 0/0 | 5811 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0008c0028 | 0/0 | 5811 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0009c0015 | 0/0 | 5811 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0010c0031 | 0/0 | 5811 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0011c0018 | 0/0 | 5811 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0012c0019 | 0/0 | 5811 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0013c0026 | 0/0 | 5812 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0014c0025 | 0/0 | 5811 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0015c0024 | 0/0 | 5811 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0016c0023 | 0/0 | 5811 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0017c0017 | 0/0 | 5812 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0018c0020 | 0/0 | 5811 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 10391 | 90 | 13 | 23 | 43 | 4 | 7 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0001c0001t0004 | 0/0 | 10391 | 11 | 5 | 4 | 2 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0001c0001t0005 | 0/0 | 10392 | 9 | 6 | 0 | 3 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0001c0001t0009 | 0/0 | 10390 | 4 | 0 | 0 | 4 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0001c0001t0015 | 0/0 | 10391 | 3 | 1 | 2 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0001c0001t0016 | 0/0 | 10391 | 2 | 0 | 1 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0001c0001t0017 | 0/0 | 10390 | 2 | 2 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0001c0001t0019 | 0/0 | 10390 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0001c0001t0021 | 0/0 | 10392 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0001c0001t0029 | 0/0 | 10391 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0001c0001t0030 | 0/0 | 10391 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0001c0001t0034 | 0/0 | 10391 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0001c0001t0036 | 0/0 | 10391 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0001c0001t0037 | 1/0 | 10391 | 1 | 0 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0001c0001t0041 | 0/0 | 10390 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0001c0001t0042 | 0/0 | 10390 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0001c0001t0043 | 0/0 | 10391 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0001c0001t0047 | 0/0 | 10391 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0001c0001t0048 | 0/0 | 10391 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0001c0001t0049 | 0/0 | 10389 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0001c0001t0051 | 0/0 | 10391 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0001c0001t0054 | 0/0 | 10391 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0001c0001t0060 | 0/0 | 10392 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0001c0001t0063 | 0/0 | 10391 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0001c0001t0064 | 0/0 | 10391 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0001c0001t0065 | 0/0 | 10391 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0001c0002t0002 | 0/0 | 10389 | 23 | 5 | 2 | 13 | 1 | 2 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0001c0002t0013 | 0/0 | 10390 | 3 | 3 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0001c0002t0014 | 0/0 | 10388 | 3 | 3 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0001c0002t0018 | 0/0 | 10389 | 2 | 2 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0001c0002t0031 | 0/0 | 10390 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0001c0002t0035 | 0/0 | 10389 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0001c0002t0039 | 0/0 | 10388 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0001c0002t0050 | 0/0 | 10389 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0001c0002t0052 | 0/0 | 10388 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0001c0002t0059 | 0/0 | 10389 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0001c0002t0061 | 0/1 | 10388 | 1 | 0 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0001c0002t0062 | 0/0 | 10388 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0001c0004t0006 | 0/0 | 10389 | 6 | 6 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0001c0004t0011 | 0/0 | 10386 | 3 | 3 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0001c0004t0024 | 0/0 | 10390 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0001c0004t0026 | 0/0 | 10386 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0001c0005t0001 | 0/0 | 10391 | 9 | 9 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0001c0006t0008 | 0/0 | 10390 | 3 | 0 | 1 | 1 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0001c0006t0032 | 0/0 | 10391 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0001c0006t0033 | 0/0 | 10390 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0001c0007t0012 | 0/0 | 10393 | 3 | 3 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0001c0009t0016 | 0/0 | 10391 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0001c0009t0019 | 0/0 | 10390 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0001c0009t0044 | 0/0 | 10392 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0001c0029t0001 | 0/0 | 10391 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0002c0003t0003 | 0/0 | 10395 | 21 | 3 | 4 | 13 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0002c0003t0007 | 0/0 | 10394 | 5 | 0 | 0 | 5 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0002c0003t0010 | 0/0 | 10398 | 3 | 3 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0002c0003t0020 | 0/0 | 10394 | 2 | 0 | 0 | 2 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0002c0003t0022 | 0/0 | 10395 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0002c0003t0025 | 0/0 | 10393 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0002c0003t0056 | 0/0 | 10396 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0002c0003t0057 | 0/0 | 10396 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0002c0003t0058 | 0/0 | 10395 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0002c0014t0004 | 0/0 | 10391 | 2 | 1 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0002c0027t0003 | 0/0 | 10395 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0003c0012t0001 | 0/0 | 10392 | 2 | 1 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0003c0021t0002 | 0/0 | 10390 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0003c0022t0021 | 0/0 | 10393 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0003c0030t0008 | 0/0 | 10391 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0004c0008t0001 | 0/0 | 10391 | 3 | 0 | 0 | 3 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0005c0010t0038 | 0/0 | 10388 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0005c0010t0053 | 0/0 | 10388 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0006c0011t0001 | 0/0 | 10391 | 2 | 1 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0007c0013t0003 | 0/0 | 10396 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0007c0013t0022 | 0/0 | 10396 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0008c0016t0001 | 0/0 | 10391 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0008c0028t0023 | 0/0 | 10392 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0009c0015t0027 | 0/0 | 10389 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0010c0031t0040 | 0/0 | 10390 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0011c0018t0001 | 0/0 | 10391 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0012c0019t0001 | 0/0 | 10391 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0013c0026t0002 | 0/0 | 10390 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0014c0025t0001 | 0/0 | 10391 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0015c0024t0055 | 0/0 | 10396 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0016c0023t0045 | 0/0 | 10390 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0017c0017t0028 | 0/0 | 10391 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| a0018c0020t0046 | 0/0 | 10391 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | copy fasta | chr17 | 77953703 | 78113822 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0004g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0004g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0004g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0004g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0004g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0004g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0004g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0004g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0004g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0004g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0005g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0005g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0005g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0005g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0005g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0005g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0005g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0005g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0005g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0009g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0009g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0009g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0009g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0015g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0015g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0015g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0016g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0016g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0017g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0017g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0019g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0021g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0029g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0030g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0034g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0036g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0037g0056 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0041g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0042g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0043g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0047g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0048g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0049g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0051g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0054g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0060g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0063g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0064g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0065g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0013g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0013g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0013g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0014g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0014g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0014g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0018g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0018g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0031g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0035g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0039g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0050g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0052g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0059g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0061g0232 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0062g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0004t0006g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0004t0006g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0004t0006g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0004t0006g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0004t0006g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0004t0006g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0004t0011g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0004t0011g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0004t0011g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0004t0024g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0004t0026g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0005t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0005t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0005t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0005t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0005t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0005t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0005t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0005t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0006t0008g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0006t0008g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0006t0008g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0006t0032g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0006t0033g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0007t0012g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0007t0012g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0007t0012g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0009t0016g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0009t0019g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0009t0044g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0029t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0003g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0003g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0003g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0003g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0003g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0003g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0003g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0003g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0007g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0007g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0007g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0007g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0007g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0010g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0010g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0010g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0020g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0020g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0022g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0025g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0056g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0057g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0058g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0014t0004g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0014t0004g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0027t0003g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0003c0012t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0003c0012t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0003c0021t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0003c0022t0021g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0003c0030t0008g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0004c0008t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0004c0008t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0004c0008t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0005c0010t0038g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0005c0010t0053g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0006c0011t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0006c0011t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0007c0013t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0007c0013t0022g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0008c0016t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0008c0028t0023g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0009c0015t0027g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0010c0031t0040g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0011c0018t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0012c0019t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0013c0026t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0014c0025t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0015c0024t0055g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0016c0023t0045g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0017c0017t0028g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0018c0020t0046g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0043 | EUR | FIN | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0132 | EUR | FIN | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0083 | EUR | FIN | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG00323 | hp2 | a0001 | c0002 | t0002 | g0122 | EUR | FIN | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | CHS | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG00423 | hp2 | a0001 | c0002 | t0002 | g0108 | EAS | CHS | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG00558 | hp2 | a0001 | c0002 | t0002 | g0115 | EAS | CHS | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG00597 | hp2 | a0001 | c0002 | t0002 | g0109 | EAS | CHS | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG00673 | hp1 | a0001 | c0002 | t0002 | g0104 | EAS | CHS | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG00735 | hp1 | a0001 | c0009 | t0044 | g0153 | AMR | PUR | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01070 | hp1 | a0005 | c0010 | t0038 | g0035 | AMR | PUR | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01070 | hp2 | a0002 | c0003 | t0003 | g0002 | AMR | PUR | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01071 | hp1 | a0001 | c0001 | t0004 | g0193 | AMR | PUR | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01071 | hp2 | a0002 | c0003 | t0003 | g0002 | AMR | PUR | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01167 | hp1 | a0001 | c0009 | t0016 | g0140 | AMR | PUR | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01169 | hp1 | a0001 | c0009 | t0019 | g0171 | AMR | PUR | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01169 | hp2 | a0001 | c0001 | t0015 | g0019 | AMR | PUR | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01175 | hp1 | a0001 | c0001 | t0015 | g0018 | AMR | PUR | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01243 | hp2 | a0006 | c0011 | t0001 | g0160 | AMR | PUR | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01255 | hp1 | a0002 | c0003 | t0003 | g0210 | AMR | CLM | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01255 | hp2 | a0008 | c0016 | t0001 | g0079 | AMR | CLM | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | CLM | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01261 | hp1 | a0001 | c0002 | t0035 | g0184 | AMR | CLM | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01358 | hp2 | a0001 | c0001 | t0016 | g0050 | AMR | CLM | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01361 | hp2 | a0002 | c0003 | t0003 | g0178 | AMR | CLM | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0176 | AMR | CLM | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01884 | hp1 | a0002 | c0003 | t0003 | g0004 | AFR | ACB | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0189 | AFR | ACB | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01891 | hp1 | a0001 | c0001 | t0036 | g0066 | AFR | ACB | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01891 | hp2 | a0005 | c0010 | t0053 | g0065 | AFR | ACB | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01934 | hp2 | a0001 | c0001 | t0004 | g0143 | AMR | PEL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01943 | hp1 | a0001 | c0006 | t0008 | g0256 | AMR | PEL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01952 | hp1 | a0001 | c0002 | t0002 | g0111 | AMR | PEL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01981 | hp2 | a0001 | c0002 | t0002 | g0112 | AMR | PEL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01993 | hp1 | a0003 | c0021 | t0002 | g0113 | AMR | PEL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01993 | hp2 | a0001 | c0029 | t0001 | g0031 | AMR | PEL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02027 | hp1 | a0011 | c0018 | t0001 | g0098 | EAS | KHV | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02027 | hp2 | a0001 | c0001 | t0051 | g0105 | EAS | KHV | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02040 | hp1 | a0001 | c0001 | t0005 | g0084 | EAS | KHV | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02040 | hp2 | a0002 | c0003 | t0003 | g0003 | EAS | KHV | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02055 | hp1 | a0003 | c0012 | t0001 | g0220 | AFR | ACB | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02055 | hp2 | a0002 | c0003 | t0003 | g0167 | AFR | ACB | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02080 | hp1 | a0007 | c0013 | t0022 | g0010 | EAS | KHV | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02083 | hp1 | a0002 | c0003 | t0003 | g0011 | EAS | KHV | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02132 | hp1 | a0010 | c0031 | t0040 | g0048 | EAS | KHV | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02132 | hp2 | a0002 | c0003 | t0003 | g0003 | EAS | KHV | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02135 | hp1 | a0001 | c0001 | t0005 | g0026 | EAS | KHV | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02135 | hp2 | a0002 | c0003 | t0003 | g0194 | EAS | KHV | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02145 | hp1 | a0001 | c0001 | t0005 | g0023 | AFR | ACB | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02145 | hp2 | a0001 | c0007 | t0012 | g0270 | AFR | ACB | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02155 | hp1 | a0001 | c0006 | t0008 | g0251 | EAS | CDX | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02155 | hp2 | a0001 | c0001 | t0047 | g0218 | EAS | CDX | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CDX | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02165 | hp2 | a0002 | c0003 | t0022 | g0183 | EAS | CDX | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02257 | hp1 | a0001 | c0001 | t0060 | g0233 | AFR | ACB | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02258 | hp1 | a0009 | c0015 | t0027 | g0264 | AFR | ACB | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | ACB | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02280 | hp1 | a0001 | c0002 | t0013 | g0236 | AFR | ACB | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02280 | hp2 | a0006 | c0011 | t0001 | g0159 | AFR | ACB | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02293 | hp2 | a0001 | c0001 | t0004 | g0172 | AMR | PEL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02451 | hp1 | a0001 | c0005 | t0001 | g0137 | AFR | ACB | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02451 | hp2 | a0001 | c0002 | t0014 | g0055 | AFR | ACB | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02602 | hp1 | a0001 | c0002 | t0002 | g0110 | SAS | PJL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02615 | hp1 | a0017 | c0017 | t0028 | g0263 | AFR | GWD | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02615 | hp2 | a0001 | c0001 | t0005 | g0271 | AFR | GWD | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02622 | hp1 | a0001 | c0001 | t0017 | g0266 | AFR | GWD | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02622 | hp2 | a0001 | c0004 | t0006 | g0242 | AFR | GWD | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02630 | hp1 | a0001 | c0005 | t0001 | g0145 | AFR | GWD | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02630 | hp2 | a0001 | c0002 | t0013 | g0235 | AFR | GWD | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02647 | hp1 | a0002 | c0003 | t0010 | g0240 | AFR | GWD | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02717 | hp1 | a0001 | c0004 | t0011 | g0262 | AFR | GWD | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02723 | hp1 | a0001 | c0001 | t0015 | g0014 | AFR | GWD | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02723 | hp2 | a0001 | c0001 | t0005 | g0154 | AFR | GWD | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02738 | hp1 | a0003 | c0030 | t0008 | g0255 | SAS | PJL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02738 | hp2 | a0001 | c0002 | t0059 | g0123 | SAS | PJL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02809 | hp2 | a0001 | c0002 | t0013 | g0238 | AFR | GWD | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02818 | hp1 | a0001 | c0002 | t0002 | g0107 | AFR | GWD | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02818 | hp2 | a0001 | c0001 | t0030 | g0259 | AFR | GWD | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02886 | hp1 | a0001 | c0002 | t0014 | g0054 | AFR | GWD | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02886 | hp2 | a0001 | c0007 | t0012 | g0268 | AFR | GWD | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0191 | AFR | GWD | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02895 | hp2 | a0002 | c0003 | t0010 | g0245 | AFR | GWD | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02896 | hp1 | a0001 | c0005 | t0001 | g0008 | AFR | GWD | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02896 | hp2 | a0001 | c0004 | t0024 | g0243 | AFR | GWD | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02922 | hp1 | a0001 | c0004 | t0006 | g0246 | AFR | ESN | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02922 | hp2 | a0008 | c0028 | t0023 | g0258 | AFR | ESN | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02965 | hp1 | a0001 | c0005 | t0001 | g0009 | AFR | ESN | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0086 | AFR | ESN | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0224 | AFR | ESN | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02970 | hp2 | a0002 | c0003 | t0010 | g0250 | AFR | ESN | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02976 | hp1 | a0001 | c0004 | t0006 | g0248 | AFR | ESN | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02976 | hp2 | a0001 | c0001 | t0064 | g0080 | AFR | ESN | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03041 | hp1 | a0001 | c0005 | t0001 | g0146 | AFR | GWD | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03041 | hp2 | a0001 | c0004 | t0011 | g0257 | AFR | GWD | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03098 | hp1 | a0001 | c0002 | t0002 | g0179 | AFR | MSL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03098 | hp2 | a0001 | c0001 | t0029 | g0239 | AFR | MSL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ESN | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03130 | hp2 | a0001 | c0002 | t0039 | g0057 | AFR | ESN | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03139 | hp1 | a0001 | c0005 | t0001 | g0007 | AFR | ESN | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03139 | hp2 | a0002 | c0027 | t0003 | g0004 | AFR | ESN | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03209 | hp1 | a0001 | c0001 | t0017 | g0267 | AFR | MSL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | MSL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03225 | hp1 | a0001 | c0007 | t0012 | g0269 | AFR | MSL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03225 | hp2 | a0001 | c0001 | t0034 | g0188 | AFR | MSL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | MSL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03453 | hp2 | a0001 | c0004 | t0006 | g0244 | AFR | MSL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | MSL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03486 | hp2 | a0001 | c0005 | t0001 | g0147 | AFR | MSL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03490 | hp1 | a0002 | c0014 | t0004 | g0168 | SAS | PJL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03491 | hp1 | a0001 | c0006 | t0033 | g0252 | SAS | PJL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03491 | hp2 | a0001 | c0001 | t0019 | g0141 | SAS | PJL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03492 | hp2 | a0001 | c0001 | t0016 | g0142 | SAS | PJL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03516 | hp1 | a0001 | c0004 | t0026 | g0260 | AFR | ESN | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0149 | AFR | ESN | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03540 | hp1 | a0001 | c0001 | t0048 | g0046 | AFR | GWD | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03540 | hp2 | a0001 | c0002 | t0018 | g0237 | AFR | GWD | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03579 | hp1 | a0001 | c0002 | t0002 | g0119 | AFR | MSL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03579 | hp2 | a0001 | c0002 | t0018 | g0234 | AFR | MSL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03669 | hp1 | a0001 | c0002 | t0002 | g0120 | SAS | PJL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03927 | hp1 | a0002 | c0003 | t0003 | g0103 | SAS | BEB | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03927 | hp2 | a0001 | c0001 | t0049 | g0097 | SAS | BEB | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG04115 | hp1 | a0001 | c0002 | t0062 | g0231 | SAS | STU | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG04115 | hp2 | a0003 | c0012 | t0001 | g0022 | SAS | STU | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG04228 | hp1 | a0001 | c0006 | t0008 | g0253 | SAS | STU | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG04228 | hp2 | a0001 | c0001 | t0063 | g0042 | SAS | STU | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18522 | hp1 | a0001 | c0004 | t0006 | g0249 | AFR | YRI | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18522 | hp2 | a0016 | c0023 | t0045 | g0192 | AFR | YRI | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18747 | hp1 | a0001 | c0002 | t0002 | g0199 | EAS | CHB | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | CHB | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18906 | hp1 | a0001 | c0004 | t0011 | g0261 | AFR | YRI | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18906 | hp2 | a0001 | c0005 | t0001 | g0001 | AFR | YRI | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18939 | hp2 | a0002 | c0003 | t0003 | g0162 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18940 | hp1 | a0001 | c0002 | t0002 | g0197 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18942 | hp1 | a0012 | c0019 | t0001 | g0114 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18943 | hp1 | a0004 | c0008 | t0001 | g0092 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18943 | hp2 | a0001 | c0002 | t0002 | g0116 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18952 | hp2 | a0002 | c0003 | t0003 | g0151 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18953 | hp1 | a0007 | c0013 | t0003 | g0152 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18957 | hp1 | a0001 | c0002 | t0002 | g0117 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18957 | hp2 | a0001 | c0001 | t0005 | g0095 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18959 | hp1 | a0001 | c0001 | t0065 | g0017 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18960 | hp2 | a0002 | c0003 | t0007 | g0138 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18966 | hp1 | a0002 | c0003 | t0007 | g0148 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18968 | hp1 | a0001 | c0002 | t0052 | g0121 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18968 | hp2 | a0004 | c0008 | t0001 | g0074 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18969 | hp1 | a0002 | c0003 | t0003 | g0163 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18970 | hp2 | a0001 | c0002 | t0002 | g0198 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18971 | hp1 | a0002 | c0003 | t0020 | g0182 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18971 | hp2 | a0001 | c0001 | t0004 | g0175 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18975 | hp2 | a0002 | c0003 | t0003 | g0126 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18978 | hp1 | a0003 | c0022 | t0021 | g0130 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18978 | hp2 | a0001 | c0001 | t0021 | g0061 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18982 | hp1 | a0001 | c0001 | t0009 | g0155 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18983 | hp1 | a0002 | c0003 | t0003 | g0012 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18983 | hp2 | a0001 | c0001 | t0041 | g0129 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18988 | hp1 | a0004 | c0008 | t0001 | g0073 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18988 | hp2 | a0002 | c0003 | t0003 | g0139 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18994 | hp2 | a0001 | c0002 | t0002 | g0211 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18998 | hp1 | a0001 | c0002 | t0002 | g0200 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19007 | hp1 | a0015 | c0024 | t0055 | g0060 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19007 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19012 | hp1 | a0002 | c0003 | t0020 | g0195 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | LWK | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19030 | hp2 | a0001 | c0002 | t0002 | g0181 | AFR | LWK | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19043 | hp1 | a0001 | c0005 | t0001 | g0001 | AFR | LWK | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19043 | hp2 | a0001 | c0002 | t0031 | g0265 | AFR | LWK | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19055 | hp1 | a0001 | c0002 | t0002 | g0196 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19057 | hp1 | a0002 | c0003 | t0003 | g0165 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19060 | hp1 | a0002 | c0003 | t0056 | g0150 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19062 | hp1 | a0001 | c0001 | t0054 | g0094 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19062 | hp2 | a0013 | c0026 | t0002 | g0118 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19063 | hp2 | a0001 | c0001 | t0009 | g0156 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19064 | hp2 | a0001 | c0002 | t0050 | g0005 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19065 | hp2 | a0002 | c0003 | t0007 | g0164 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19070 | hp1 | a0001 | c0001 | t0004 | g0174 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19074 | hp1 | a0001 | c0001 | t0009 | g0088 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19074 | hp2 | a0001 | c0001 | t0009 | g0173 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19075 | hp1 | a0002 | c0003 | t0057 | g0158 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19077 | hp2 | a0002 | c0003 | t0003 | g0161 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19079 | hp1 | a0014 | c0025 | t0001 | g0077 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19079 | hp2 | a0002 | c0003 | t0003 | g0144 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19081 | hp1 | a0002 | c0003 | t0007 | g0125 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19089 | hp2 | a0002 | c0003 | t0007 | g0102 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19090 | hp1 | a0001 | c0001 | t0043 | g0177 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0190 | AFR | YRI | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19240 | hp2 | a0001 | c0002 | t0014 | g0071 | AFR | YRI | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ASW | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ASW | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0028 | EUR | TSI | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA20752 | hp2 | a0002 | c0003 | t0058 | g0166 | EUR | TSI | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA20905 | hp1 | a0001 | c0006 | t0032 | g0254 | SAS | GIH | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | GIH | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0124 | AFR | ACB | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | ACB | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02486 | hp1 | a0001 | c0004 | t0006 | g0247 | AFR | ACB | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02486 | hp2 | a0018 | c0020 | t0046 | g0047 | AFR | ACB | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03471 | hp1 | a0001 | c0002 | t0002 | g0180 | AFR | MSL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03471 | hp2 | a0002 | c0003 | t0025 | g0241 | AFR | MSL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG06807 | hp1 | a0002 | c0014 | t0004 | g0169 | AFR | USA | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG06807 | hp2 | a0001 | c0001 | t0042 | g0099 | AFR | USA | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0157 | AFR | USA | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA20300 | hp2 | a0002 | c0003 | t0003 | g0186 | AFR | USA | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0061 | g0232 | REF | REF | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0037 | g0056 | REF | REF | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:78049475
|
G | A | 1 | a0009 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.1043G>A | p.Gly348Asp | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/23 | 1646/10391 | 1043/5811 | 348/1936 | chr17 | 78049475 | ||
| chr17:78049495
|
A | T | 1 | a0010 | 1 | HG02132.hp1 | missense_variant | MODERATE | c.1063A>T | p.Thr355Ser | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/23 | 1666/10391 | 1063/5811 | 355/1936 | chr17 | 78049495 | ||
| chr17:78049796
|
G | A | 1 | a0005 | 2 | HG01070.hp1 HG01891.hp2 |
missense_variant | MODERATE | c.1364G>A | p.Ser455Asn | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/23 | 1967/10391 | 1364/5811 | 455/1936 | chr17 | 78049796 | ||
| chr17:78050321
|
G | A | 1 | a0011 | 1 | HG02027.hp1 | missense_variant | MODERATE | c.1889G>A | p.Arg630Gln | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/23 | 2492/10391 | 1889/5811 | 630/1936 | chr17 | 78050321 | ||
| chr17:78050531
|
G | C | 1 | a0012 | 1 | NA18942.hp1 | missense_variant | MODERATE | c.2099G>C | p.Gly700Ala | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/23 | 2702/10391 | 2099/5811 | 700/1936 | chr17 | 78050531 | ||
| chr17:78050542
|
G | A | 1 | a0018 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.2110G>A | p.Asp704Asn | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/23 | 2713/10391 | 2110/5811 | 704/1936 | chr17 | 78050542 | ||
| chr17:78050595
|
C | A | 1 | a0006 | 2 | HG01243.hp2 HG02280.hp2 |
missense_variant | MODERATE | c.2163C>A | p.Asn721Lys | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/23 | 2766/10391 | 2163/5811 | 721/1936 | chr17 | 78050595 | ||
| chr17:78050645
|
A | G | 3 | a0008a0009a0017 | 4 | HG01255.hp2 HG02258.hp1 HG02615.hp1 others(1): Show |
missense_variant | MODERATE | c.2213A>G | p.Asn738Ser | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/23 | 2816/10391 | 2213/5811 | 738/1936 | chr17 | 78050645 | ||
| chr17:78064785
|
C | G | 3 | a0002a0006a0007 | 43 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(40): Show |
missense_variant | MODERATE | c.3080C>G | p.Pro1027Arg | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 6/23 | 3683/10391 | 3080/5811 | 1027/1936 | chr17 | 78064785 | ||
| chr17:78086941
|
C | T | 1 | a0013 | 1 | NA19062.hp2 | missense_variant | MODERATE | c.4271C>T | p.Pro1424Leu | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 15/23 | 4874/10391 | 4271/5811 | 1424/1936 | chr17 | 78086941 | ||
| chr17:78086948
|
G | GC | 4 | a0003a0007a0013others(1): Show | 9 | HG01993.hp1 HG02055.hp1 HG02080.hp1 others(6): Show |
frameshift_variant | HIGH | c.4283dupC | p.Pro1429fs | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 15/23 | 4887/10391 | 4284/5811 | 1428/1936 | INFO_REALIGN_3_PRIME | chr17 | 78086948 | |
| chr17:78091484
|
G | A | 1 | a0004 | 3 | NA18943.hp1 NA18968.hp2 NA18988.hp1 |
missense_variant | MODERATE | c.4468G>A | p.Gly1490Ser | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 16/23 | 5071/10391 | 4468/5811 | 1490/1936 | chr17 | 78091484 | ||
| chr17:78093046
|
G | C | 1 | a0016 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.4705G>C | p.Ala1569Pro | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 17/23 | 5308/10391 | 4705/5811 | 1569/1936 | chr17 | 78093046 | ||
| chr17:78098399
|
G | T | 1 | a0015 | 1 | NA19007.hp1 | missense_variant | MODERATE | c.5101G>T | p.Ala1701Ser | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 20/23 | 5704/10391 | 5101/5811 | 1701/1936 | chr17 | 78098399 | ||
| chr17:78104601
|
C | T | 1 | a0014 | 1 | NA19079.hp1 | missense_variant | MODERATE | c.5567C>T | p.Ala1856Val | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 23/23 | 6170/10391 | 5567/5811 | 1856/1936 | chr17 | 78104601 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:78049188
|
G | A | 3 | a0008c0016a0009c0015a0017c0017 | 3 | HG01255.hp2 HG02258.hp1 HG02615.hp1 |
synonymous_variant | LOW | c.756G>A | p.Ala252Ala | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/23 | 1359/10391 | 756/5811 | 252/1936 | chr17 | 78049188 | ||
| chr17:78049725
|
C | T | 2 | a0001c0006a0003c0030 | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
synonymous_variant | LOW | c.1293C>T | p.His431His | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/23 | 1896/10391 | 1293/5811 | 431/1936 | chr17 | 78049725 | ||
| chr17:78050184
|
C | T | 1 | a0001c0004 | 11 | HG02486.hp1 HG02622.hp2 HG02717.hp1 others(8): Show |
synonymous_variant | LOW | c.1752C>T | p.Thr584Thr | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/23 | 2355/10391 | 1752/5811 | 584/1936 | chr17 | 78050184 | ||
| chr17:78050595
|
C | T | 1 | a0001c0029 | 1 | HG01993.hp2 | synonymous_variant | LOW | c.2163C>T | p.Asn721Asn | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/23 | 2766/10391 | 2163/5811 | 721/1936 | chr17 | 78050595 | ||
| chr17:78051168
|
G | A | 1 | a0001c0005 | 9 | HG02451.hp1 HG02630.hp1 HG02896.hp1 others(6): Show |
synonymous_variant | LOW | c.2736G>A | p.Lys912Lys | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/23 | 3339/10391 | 2736/5811 | 912/1936 | chr17 | 78051168 | ||
| chr17:78051396
|
G | T | 1 | a0001c0009 | 3 | HG00735.hp1 HG01167.hp1 HG01169.hp1 |
synonymous_variant | LOW | c.2964G>T | p.Pro988Pro | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/23 | 3567/10391 | 2964/5811 | 988/1936 | chr17 | 78051396 | ||
| chr17:78051402
|
G | A | 1 | a0001c0007 | 3 | HG02145.hp2 HG02886.hp2 HG03225.hp1 |
synonymous_variant | LOW | c.2970G>A | p.Pro990Pro | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/23 | 3573/10391 | 2970/5811 | 990/1936 | chr17 | 78051402 | ||
| chr17:78051411
|
C | T | 2 | a0001c0006a0003c0030 | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
synonymous_variant | LOW | c.2979C>T | p.Ala993Ala | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/23 | 3582/10391 | 2979/5811 | 993/1936 | chr17 | 78051411 | ||
| chr17:78064873
|
A | C | 11 | a0001c0006a0001c0007a0002c0003others(8): Show | 55 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(52): Show |
synonymous_variant | LOW | c.3168A>C | p.Ala1056Ala | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 6/23 | 3771/10391 | 3168/5811 | 1056/1936 | chr17 | 78064873 | ||
| chr17:78067761
|
A | C | 1 | a0001c0004 | 11 | HG02486.hp1 HG02622.hp2 HG02717.hp1 others(8): Show |
synonymous_variant | LOW | c.3237A>C | p.Ser1079Ser | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 7/23 | 3840/10391 | 3237/5811 | 1079/1936 | chr17 | 78067761 | ||
| chr17:78086858
|
G | A | 1 | a0002c0027 | 1 | HG03139.hp2 | synonymous_variant | LOW | c.4188G>A | p.Ala1396Ala | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 15/23 | 4791/10391 | 4188/5811 | 1396/1936 | chr17 | 78086858 | ||
| chr17:78093075
|
A | G | 1 | a0003c0022 | 1 | NA18978.hp1 | synonymous_variant | LOW | c.4734A>G | p.Lys1578Lys | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 17/23 | 5337/10391 | 4734/5811 | 1578/1936 | chr17 | 78093075 | ||
| chr17:78097785
|
T | C | 12 | a0001c0002a0001c0004a0001c0006others(9): Show | 101 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(98): Show |
synonymous_variant | LOW | c.4968T>C | p.Ser1656Ser | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 19/23 | 5571/10391 | 4968/5811 | 1656/1936 | chr17 | 78097785 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:77958767
|
T | C | 20 | a0001c0001t0017a0001c0001t0029a0001c0001t0030others(17): Show | 37 | HG01943.hp1 HG02145.hp2 HG02155.hp1 others(34): Show |
5_prime_UTR_variant | MODIFIER | c.-539T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/23 | 45440 | chr17 | 77958767 | |||||
| chr17:77958768
|
A | AGCC | 4 | a0001c0004t0006a0001c0004t0024a0002c0003t0010others(1): Show | 11 | HG02486.hp1 HG02622.hp2 HG02647.hp1 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-527_-525dupCCG | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/23 | 45425 | INFO_REALIGN_3_PRIME | chr17 | 77958768 | ||||
| chr17:77958781
|
G | A | 1 | a0008c0028t0023 | 1 | HG02922.hp2 | 5_prime_UTR_variant | MODIFIER | c.-525G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/23 | 45426 | chr17 | 77958781 | |||||
| chr17:77958855
|
C | T | 1 | a0001c0001t0065 | 1 | NA18959.hp1 | 5_prime_UTR_variant | MODIFIER | c.-451C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/23 | 45352 | chr17 | 77958855 | |||||
| chr17:77958878
|
A | G | 1 | a0001c0001t0064 | 1 | HG02976.hp2 | 5_prime_UTR_variant | MODIFIER | c.-428A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/23 | 45329 | chr17 | 77958878 | |||||
| chr17:77958936
|
T | A | 2 | a0001c0001t0034a0001c0002t0035 | 2 | HG01261.hp1 HG03225.hp2 |
5_prime_UTR_variant | MODIFIER | c.-370T>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/23 | 45271 | chr17 | 77958936 | |||||
| chr17:77958949
|
C | T | 1 | a0001c0001t0063 | 1 | HG04228.hp2 | 5_prime_UTR_variant | MODIFIER | c.-357C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/23 | 45258 | chr17 | 77958949 | |||||
| chr17:77959099
|
C | A | 4 | a0001c0004t0006a0001c0004t0024a0002c0003t0010others(1): Show | 11 | HG02486.hp1 HG02622.hp2 HG02647.hp1 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-207C>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/23 | 45108 | chr17 | 77959099 | |||||
| chr17:77959182
|
C | T | 79 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(76): Show | 269 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(266): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-124C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/23 | chr17 | 77959182 | ||||||
| chr17:77959194
|
C | G | 3 | a0001c0001t0060a0001c0002t0061a0001c0002t0062 | 3 | HG02257.hp1 HG04115.hp1 homoSapiens_chm13v2.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-112C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/23 | chr17 | 77959194 | ||||||
| chr17:77959198
|
C | T | 4 | a0001c0006t0008a0001c0006t0032a0001c0006t0033others(1): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-108C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/23 | 45009 | chr17 | 77959198 | |||||
| chr17:78104848
|
T | G | 8 | a0001c0004t0006a0001c0004t0011a0001c0004t0024others(5): Show | 17 | HG01943.hp1 HG02155.hp1 HG02486.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*3T>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 23/23 | 3 | chr17 | 78104848 | |||||
| chr17:78104858
|
T | C | 1 | a0010c0031t0040 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 23/23 | 13 | chr17 | 78104858 | |||||
| chr17:78104928
|
C | G | 1 | a0001c0002t0059 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*83C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 23/23 | 83 | chr17 | 78104928 | |||||
| chr17:78104995
|
G | A | 1 | a0001c0001t0015 | 3 | HG01169.hp2 HG01175.hp1 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*150G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 23/23 | 150 | chr17 | 78104995 | |||||
| chr17:78105113
|
A | AT | 16 | a0001c0001t0021a0001c0002t0013a0001c0002t0031others(13): Show | 44 | HG01070.hp2 HG01071.hp2 HG01255.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*284dupT | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 23/23 | 285 | INFO_REALIGN_3_PRIME | chr17 | 78105113 | ||||
| chr17:78105113
|
AT | A | 8 | a0001c0001t0017a0001c0001t0036a0001c0001t0041others(5): Show | 16 | HG01891.hp1 HG02486.hp1 HG02622.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*284delT | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 23/23 | 284 | INFO_REALIGN_3_PRIME | chr17 | 78105113 | ||||
| chr17:78105322
|
A | G | 1 | a0001c0004t0026 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*477A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 23/23 | 477 | chr17 | 78105322 | |||||
| chr17:78105380
|
C | A | 1 | a0001c0001t0043 | 1 | NA19090.hp1 | 3_prime_UTR_variant | MODIFIER | c.*535C>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 23/23 | 535 | chr17 | 78105380 | |||||
| chr17:78105634
|
A | AGT | 13 | a0001c0007t0012a0002c0003t0003a0002c0003t0007others(10): Show | 42 | HG01070.hp2 HG01071.hp2 HG01255.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*803_*804dupTG | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 23/23 | 805 | INFO_REALIGN_3_PRIME | chr17 | 78105634 | ||||
| chr17:78105634
|
AGT | A | 5 | a0001c0004t0006a0001c0004t0011a0001c0004t0024others(2): Show | 12 | HG02258.hp1 HG02486.hp1 HG02622.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*803_*804delTG | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 23/23 | 803 | INFO_REALIGN_3_PRIME | chr17 | 78105634 | ||||
| chr17:78105676
|
C | T | 2 | a0001c0001t0054a0010c0031t0040 | 2 | HG02132.hp1 NA19062.hp1 |
3_prime_UTR_variant | MODIFIER | c.*831C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 23/23 | 831 | chr17 | 78105676 | |||||
| chr17:78105779
|
G | A | 1 | a0008c0028t0023 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*934G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 23/23 | 934 | chr17 | 78105779 | |||||
| chr17:78106055
|
GA | G | 35 | a0001c0001t0051a0001c0002t0002a0001c0002t0013others(32): Show | 98 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*1224delA | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 23/23 | 1224 | INFO_REALIGN_3_PRIME | chr17 | 78106055 | ||||
| chr17:78106253
|
TA | T | 25 | a0001c0001t0049a0001c0002t0014a0001c0002t0039others(22): Show | 63 | HG01070.hp1 HG01070.hp2 HG01071.hp2 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*1421delA | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 23/23 | 1421 | INFO_REALIGN_3_PRIME | chr17 | 78106253 | ||||
| chr17:78106369
|
C | T | 1 | a0001c0001t0042 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1524C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 23/23 | 1524 | chr17 | 78106369 | |||||
| chr17:78106412
|
A | G | 1 | a0001c0002t0039 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1567A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 23/23 | 1567 | chr17 | 78106412 | |||||
| chr17:78106522
|
T | TA | 11 | a0001c0001t0005a0001c0001t0036a0001c0001t0060others(8): Show | 28 | HG00735.hp1 HG01891.hp1 HG01943.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1691dupA | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 23/23 | 1692 | INFO_REALIGN_3_PRIME | chr17 | 78106522 | ||||
| chr17:78106532
|
A | AAAC | 12 | a0002c0003t0003a0002c0003t0007a0002c0003t0010others(9): Show | 39 | HG01070.hp2 HG01071.hp2 HG01255.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*1689_*1690insCAA | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 23/23 | 1690 | INFO_REALIGN_3_PRIME | chr17 | 78106532 | ||||
| chr17:78106532
|
A | C | 1 | a0001c0001t0048 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1687A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 23/23 | 1687 | chr17 | 78106532 | |||||
| chr17:78106536
|
A | G | 1 | a0001c0002t0062 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1691A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 23/23 | 1691 | chr17 | 78106536 | |||||
| chr17:78106536
|
AC | A | 4 | a0001c0001t0009a0001c0001t0019a0001c0009t0019others(1): Show | 7 | HG01169.hp1 HG02615.hp1 HG03491.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1692delC | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 23/23 | 1692 | chr17 | 78106536 | |||||
| chr17:78106537
|
C | A | 7 | a0001c0001t0004a0001c0001t0016a0001c0001t0043others(4): Show | 19 | HG00735.hp1 HG01071.hp1 HG01167.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1692C>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 23/23 | 1692 | chr17 | 78106537 | |||||
| chr17:78106542
|
C | A | 5 | a0001c0001t0016a0001c0001t0019a0001c0009t0016others(2): Show | 6 | HG00735.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1697C>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 23/23 | 1697 | chr17 | 78106542 | |||||
| chr17:78106556
|
GA | G | 2 | a0002c0003t0007a0015c0024t0055 | 6 | NA18960.hp2 NA18966.hp1 NA19007.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1719delA | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 23/23 | 1719 | INFO_REALIGN_3_PRIME | chr17 | 78106556 | ||||
| chr17:78106881
|
AT | A | 3 | a0001c0002t0013a0001c0002t0018a0002c0003t0025 | 6 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2037delT | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 23/23 | 2037 | chr17 | 78106881 | |||||
| chr17:78106884
|
C | CA | 17 | a0001c0001t0051a0001c0002t0002a0001c0002t0014others(14): Show | 41 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*2055dupA | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 23/23 | 2056 | INFO_REALIGN_3_PRIME | chr17 | 78106884 | ||||
| chr17:78106884
|
CA | C | 5 | a0001c0001t0049a0001c0004t0006a0001c0004t0011others(2): Show | 12 | HG02132.hp1 HG02486.hp1 HG02622.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2055delA | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 23/23 | 2055 | INFO_REALIGN_3_PRIME | chr17 | 78106884 | ||||
| chr17:78107134
|
T | C | 1 | a0018c0020t0046 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2289T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 23/23 | 2289 | chr17 | 78107134 | |||||
| chr17:78107582
|
C | T | 15 | a0001c0004t0006a0001c0004t0011a0001c0004t0024others(12): Show | 49 | HG01070.hp2 HG01071.hp2 HG01255.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*2737C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 23/23 | 2737 | chr17 | 78107582 | |||||
| chr17:78107603
|
G | C | 16 | a0001c0001t0051a0001c0002t0002a0001c0002t0014others(13): Show | 40 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*2758G>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 23/23 | 2758 | chr17 | 78107603 | |||||
| chr17:78107679
|
G | A | 1 | a0001c0002t0050 | 1 | NA19064.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2834G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 23/23 | 2834 | chr17 | 78107679 | |||||
| chr17:78107778
|
C | T | 1 | a0008c0028t0023 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2933C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 23/23 | 2933 | chr17 | 78107778 | |||||
| chr17:78107835
|
T | C | 1 | a0001c0001t0047 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2990T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 23/23 | 2990 | chr17 | 78107835 | |||||
| chr17:78108035
|
C | T | 3 | a0001c0006t0008a0001c0006t0033a0003c0030t0008 | 5 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3190C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 23/23 | 3190 | chr17 | 78108035 | |||||
| chr17:78108125
|
C | T | 2 | a0002c0003t0022a0007c0013t0022 | 2 | HG02080.hp1 HG02165.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3280C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 23/23 | 3280 | chr17 | 78108125 | |||||
| chr17:78108257
|
C | T | 1 | a0002c0003t0058 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3412C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 23/23 | 3412 | chr17 | 78108257 | |||||
| chr17:78108292
|
T | C | 2 | a0001c0001t0029a0001c0007t0012 | 4 | HG02145.hp2 HG02886.hp2 HG03098.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3447T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 23/23 | 3447 | chr17 | 78108292 | |||||
| chr17:78108459
|
G | A | 2 | a0001c0001t0017a0001c0006t0033 | 3 | HG02622.hp1 HG03209.hp1 HG03491.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3614G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 23/23 | 3614 | chr17 | 78108459 | |||||
| chr17:78108492
|
CTG | C | 15 | a0001c0002t0002a0001c0002t0014a0001c0002t0031others(12): Show | 39 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*3649_*3650delGT | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 23/23 | 3649 | INFO_REALIGN_3_PRIME | chr17 | 78108492 | ||||
| chr17:78108562
|
C | G | 1 | a0008c0028t0023 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3717C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 23/23 | 3717 | chr17 | 78108562 | |||||
| chr17:78108698
|
C | G | 1 | a0005c0010t0038 | 1 | HG01070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3853C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 23/23 | 3853 | chr17 | 78108698 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:77959448
|
C | T | 1 | a0001c0001t0005g0271 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-38+180C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77959448 | ||||||
| chr17:77959723
|
G | A | 1 | a0001c0001t0001g0006 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-38+455G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77959723 | ||||||
| chr17:77959725
|
C | A | 3 | a0001c0005t0001g0007a0001c0005t0001g0008a0001c0005t0001g0009 | 3 | HG02896.hp1 HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-38+457C>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77959725 | ||||||
| chr17:77959756
|
C | G | 3 | a0001c0007t0012g0268a0001c0007t0012g0269a0001c0007t0012g0270 | 3 | HG02145.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-38+488C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77959756 | ||||||
| chr17:77959886
|
C | G | 2 | a0001c0001t0017g0266a0001c0001t0017g0267 | 2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-38+618C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77959886 | ||||||
| chr17:77959921
|
G | T | 1 | a0001c0002t0031g0265 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-38+653G>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77959921 | ||||||
| chr17:77959946
|
G | C | 1 | a0007c0013t0022g0010 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-38+678G>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77959946 | ||||||
| chr17:77959993
|
A | T | 51 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(48): Show | 51 | HG01243.hp1 HG01257.hp2 HG01943.hp1 others(48): Show |
intron_variant | MODIFIER | c.-38+725A>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77959993 | ||||||
| chr17:77960092
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-38+824C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77960092 | ||||||
| chr17:77960378
|
C | T | 2 | a0009c0015t0027g0264a0017c0017t0028g0263 | 2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.-38+1110C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77960378 | ||||||
| chr17:77960461
|
C | T | 37 | a0001c0001t0017g0266a0001c0001t0017g0267a0001c0001t0029g0239others(34): Show | 37 | HG01943.hp1 HG02145.hp2 HG02155.hp1 others(34): Show |
intron_variant | MODIFIER | c.-38+1193C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77960461 | ||||||
| chr17:77960630
|
A | G | 32 | a0001c0001t0017g0266a0001c0001t0017g0267a0001c0001t0029g0239others(29): Show | 32 | HG01943.hp1 HG02145.hp2 HG02155.hp1 others(29): Show |
intron_variant | MODIFIER | c.-38+1362A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77960630 | ||||||
| chr17:77960720
|
G | A | 20 | a0001c0001t0029g0239a0001c0004t0006g0242a0001c0004t0006g0244others(17): Show | 20 | HG01943.hp1 HG02155.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-38+1452G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77960720 | ||||||
| chr17:77960971
|
C | T | 6 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(3): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.-38+1703C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77960971 | ||||||
| chr17:77961157
|
C | CT | 15 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0204others(12): Show | 15 | HG01255.hp1 HG01943.hp1 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.-38+1906dupT | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 77961157 | |||||
| chr17:77961157
|
C | CTT | 7 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0214others(4): Show | 7 | HG00423.hp1 HG02155.hp2 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.-38+1905_-38+1906d others(4): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 77961157 | |||||
| chr17:77961244
|
C | T | 1 | a0001c0001t0001g0201 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-38+1976C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77961244 | ||||||
| chr17:77961270
|
C | T | 7 | a0001c0002t0002g0005a0001c0002t0002g0197a0001c0002t0002g0198others(4): Show | 7 | NA18747.hp1 NA18940.hp1 NA18970.hp2 others(4): Show |
intron_variant | MODIFIER | c.-38+2002C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77961270 | ||||||
| chr17:77961344
|
C | T | 6 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(3): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.-38+2076C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77961344 | ||||||
| chr17:77961387
|
T | C | 20 | a0001c0001t0029g0239a0001c0004t0006g0242a0001c0004t0006g0244others(17): Show | 20 | HG01943.hp1 HG02155.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-38+2119T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77961387 | ||||||
| chr17:77961406
|
T | G | 1 | a0001c0001t0029g0239 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-38+2138T>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77961406 | ||||||
| chr17:77961500
|
ACTGT | A | 50 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(47): Show | 50 | HG01243.hp1 HG01257.hp2 HG01943.hp1 others(47): Show |
intron_variant | MODIFIER | c.-38+2238_-38+2241d others(6): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 77961500 | |||||
| chr17:77961524
|
TAAC | T | 5 | a0001c0002t0013g0235a0001c0002t0013g0236a0001c0002t0013g0238others(2): Show | 5 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-38+2259_-38+2261d others(5): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 77961524 | |||||
| chr17:77961809
|
C | T | 11 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(8): Show | 11 | HG02486.hp1 HG02622.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.-38+2541C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77961809 | ||||||
| chr17:77961898
|
T | C | 1 | a0001c0001t0029g0239 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-38+2630T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77961898 | ||||||
| chr17:77962167
|
C | T | 1 | a0003c0030t0008g0255 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-38+2899C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77962167 | ||||||
| chr17:77962737
|
G | A | 1 | a0002c0003t0003g0011 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-38+3469G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77962737 | ||||||
| chr17:77962842
|
G | C | 1 | a0002c0003t0003g0012 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-38+3574G>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77962842 | ||||||
| chr17:77963397
|
A | G | 1 | a0002c0003t0010g0250 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-38+4129A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77963397 | ||||||
| chr17:77963743
|
A | C | 166 | a0001c0001t0001g0006a0001c0001t0001g0106a0001c0001t0001g0127others(163): Show | 169 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.-38+4475A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77963743 | ||||||
| chr17:77963878
|
C | A | 14 | a0001c0001t0029g0239a0001c0004t0006g0242a0001c0004t0006g0244others(11): Show | 14 | HG02258.hp1 HG02486.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.-38+4610C>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77963878 | ||||||
| chr17:77963976
|
A | G | 1 | a0009c0015t0027g0264 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-38+4708A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77963976 | ||||||
| chr17:77964038
|
G | A | 1 | a0001c0002t0031g0265 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-38+4770G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77964038 | ||||||
| chr17:77964126
|
G | T | 1 | a0001c0002t0002g0196 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-38+4858G>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77964126 | ||||||
| chr17:77964259
|
G | T | 1 | a0001c0001t0029g0239 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-38+4991G>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77964259 | ||||||
| chr17:77964444
|
A | T | 1 | a0002c0003t0020g0195 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-38+5176A>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77964444 | ||||||
| chr17:77964593
|
C | T | 2 | a0001c0002t0061g0232a0001c0002t0062g0231 | 2 | HG04115.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-38+5325C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77964593 | ||||||
| chr17:77964954
|
T | G | 2 | a0009c0015t0027g0264a0017c0017t0028g0263 | 2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.-38+5686T>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77964954 | ||||||
| chr17:77965059
|
A | G | 32 | a0001c0001t0017g0266a0001c0001t0017g0267a0001c0001t0029g0239others(29): Show | 32 | HG01943.hp1 HG02145.hp2 HG02155.hp1 others(29): Show |
intron_variant | MODIFIER | c.-38+5791A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77965059 | ||||||
| chr17:77965082
|
T | C | 6 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(3): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.-38+5814T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77965082 | ||||||
| chr17:77965352
|
G | A | 2 | a0001c0001t0017g0266a0001c0001t0017g0267 | 2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-38+6084G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77965352 | ||||||
| chr17:77965431
|
A | G | 37 | a0001c0001t0017g0266a0001c0001t0017g0267a0001c0001t0029g0239others(34): Show | 37 | HG01943.hp1 HG02145.hp2 HG02155.hp1 others(34): Show |
intron_variant | MODIFIER | c.-38+6163A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77965431 | ||||||
| chr17:77965454
|
C | A | 14 | a0001c0001t0029g0239a0001c0004t0006g0242a0001c0004t0006g0244others(11): Show | 14 | HG02258.hp1 HG02486.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.-38+6186C>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77965454 | ||||||
| chr17:77965746
|
C | G | 4 | a0001c0004t0006g0246a0001c0004t0006g0247a0001c0004t0006g0248others(1): Show | 4 | HG02486.hp1 HG02922.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-38+6478C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77965746 | ||||||
| chr17:77965787
|
G | T | 32 | a0001c0001t0017g0266a0001c0001t0017g0267a0001c0001t0029g0239others(29): Show | 32 | HG01943.hp1 HG02145.hp2 HG02155.hp1 others(29): Show |
intron_variant | MODIFIER | c.-38+6519G>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77965787 | ||||||
| chr17:77965792
|
C | G | 1 | a0002c0003t0003g0194 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-38+6524C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77965792 | ||||||
| chr17:77965914
|
C | T | 1 | a0001c0001t0004g0193 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-38+6646C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77965914 | ||||||
| chr17:77966418
|
G | A | 1 | a0002c0003t0003g0103 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-38+7150G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77966418 | ||||||
| chr17:77966430
|
C | A | 3 | a0001c0007t0012g0268a0001c0007t0012g0269a0001c0007t0012g0270 | 3 | HG02145.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-38+7162C>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77966430 | ||||||
| chr17:77966512
|
T | TA | 29 | a0001c0001t0001g0106a0001c0001t0001g0202a0001c0001t0051g0105others(26): Show | 29 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.-38+7245dupA | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 77966512 | |||||
| chr17:77966692
|
A | G | 14 | a0001c0001t0029g0239a0001c0004t0006g0242a0001c0004t0006g0244others(11): Show | 14 | HG02258.hp1 HG02486.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.-38+7424A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77966692 | ||||||
| chr17:77966806
|
C | A | 6 | a0001c0001t0004g0124a0001c0002t0013g0235a0001c0002t0013g0236others(3): Show | 6 | HG02109.hp1 HG02280.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-38+7538C>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77966806 | ||||||
| chr17:77966817
|
T | C | 1 | a0002c0003t0007g0125 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-38+7549T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77966817 | ||||||
| chr17:77966818
|
C | T | 14 | a0001c0001t0029g0239a0001c0004t0006g0242a0001c0004t0006g0244others(11): Show | 14 | HG02258.hp1 HG02486.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.-38+7550C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77966818 | ||||||
| chr17:77967108
|
G | A | 11 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(8): Show | 11 | HG01243.hp1 HG01257.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.-38+7840G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77967108 | ||||||
| chr17:77967110
|
G | A | 3 | a0001c0007t0012g0268a0001c0007t0012g0269a0001c0007t0012g0270 | 3 | HG02145.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-38+7842G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77967110 | ||||||
| chr17:77967136
|
T | C | 11 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(8): Show | 11 | HG02486.hp1 HG02622.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.-38+7868T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77967136 | ||||||
| chr17:77967269
|
A | C | 14 | a0001c0001t0029g0239a0001c0004t0006g0242a0001c0004t0006g0244others(11): Show | 14 | HG02258.hp1 HG02486.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.-38+8001A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77967269 | ||||||
| chr17:77967303
|
A | G | 1 | a0016c0023t0045g0192 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-38+8035A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77967303 | ||||||
| chr17:77967327
|
T | A | 1 | a0001c0004t0011g0257 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-38+8059T>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77967327 | ||||||
| chr17:77967347
|
A | G | 1 | a0002c0003t0007g0102 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-38+8079A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77967347 | ||||||
| chr17:77967401
|
CG | C | 15 | a0001c0001t0029g0239a0001c0002t0031g0265a0001c0004t0006g0242others(12): Show | 15 | HG02258.hp1 HG02486.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.-38+8141delG | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 77967401 | |||||
| chr17:77967402
|
G | A | 1 | a0001c0002t0002g0104 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-38+8134G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77967402 | ||||||
| chr17:77967403
|
G | T | 3 | a0001c0001t0004g0189a0001c0001t0004g0190a0001c0001t0004g0191 | 3 | HG01884.hp2 HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-38+8135G>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77967403 | ||||||
| chr17:77967548
|
G | A | 2 | a0002c0003t0003g0126a0002c0003t0003g0194 | 2 | HG02135.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.-38+8280G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77967548 | ||||||
| chr17:77967594
|
A | T | 1 | a0001c0001t0001g0101 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-38+8326A>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77967594 | ||||||
| chr17:77967634
|
G | A | 1 | a0001c0001t0001g0101 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-38+8366G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77967634 | ||||||
| chr17:77967656
|
A | C | 1 | a0001c0001t0029g0239 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-38+8388A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77967656 | ||||||
| chr17:77967780
|
A | G | 1 | a0001c0001t0017g0267 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-38+8512A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77967780 | ||||||
| chr17:77967832
|
A | G | 7 | a0001c0001t0001g0185a0001c0001t0001g0187a0001c0001t0034g0188others(4): Show | 7 | HG01261.hp1 HG01884.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.-38+8564A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77967832 | ||||||
| chr17:77968124
|
T | C | 37 | a0001c0001t0017g0266a0001c0001t0017g0267a0001c0001t0029g0239others(34): Show | 37 | HG01943.hp1 HG02145.hp2 HG02155.hp1 others(34): Show |
intron_variant | MODIFIER | c.-38+8856T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77968124 | ||||||
| chr17:77968160
|
G | A | 10 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0131others(7): Show | 10 | HG00280.hp2 HG00642.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.-38+8892G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77968160 | ||||||
| chr17:77968281
|
C | G | 1 | a0001c0002t0059g0123 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-38+9013C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77968281 | ||||||
| chr17:77968385
|
A | G | 3 | a0001c0001t0029g0239a0009c0015t0027g0264a0017c0017t0028g0263 | 3 | HG02258.hp1 HG02615.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-38+9117A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77968385 | ||||||
| chr17:77968396
|
C | T | 1 | a0001c0001t0001g0100 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-38+9128C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77968396 | ||||||
| chr17:77968539
|
A | T | 1 | a0001c0001t0042g0099 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-38+9271A>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77968539 | ||||||
| chr17:77968575
|
T | G | 1 | a0001c0001t0051g0105 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-38+9307T>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77968575 | ||||||
| chr17:77968591
|
C | T | 1 | a0001c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-38+9323C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77968591 | ||||||
| chr17:77968614
|
A | T | 1 | a0001c0002t0031g0265 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-38+9346A>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77968614 | ||||||
| chr17:77968710
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-38+9442G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77968710 | ||||||
| chr17:77968740
|
G | A | 21 | a0001c0001t0029g0239a0001c0002t0031g0265a0001c0004t0006g0242others(18): Show | 21 | HG01943.hp1 HG02155.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.-38+9472G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77968740 | ||||||
| chr17:77968747
|
T | G | 1 | a0001c0001t0001g0013 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-38+9479T>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77968747 | ||||||
| chr17:77968764
|
A | T | 1 | a0001c0001t0034g0188 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-38+9496A>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77968764 | ||||||
| chr17:77968842
|
C | T | 1 | a0011c0018t0001g0098 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-38+9574C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77968842 | ||||||
| chr17:77968850
|
T | A | 1 | a0001c0004t0006g0246 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-38+9582T>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77968850 | ||||||
| chr17:77968877
|
C | T | 1 | a0009c0015t0027g0264 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-38+9609C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77968877 | ||||||
| chr17:77968926
|
A | G | 14 | a0001c0001t0029g0239a0001c0004t0006g0242a0001c0004t0006g0244others(11): Show | 14 | HG02258.hp1 HG02486.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.-38+9658A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77968926 | ||||||
| chr17:77969024
|
A | T | 1 | a0001c0001t0029g0239 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-38+9756A>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77969024 | ||||||
| chr17:77969065
|
T | C | 1 | a0008c0028t0023g0258 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-38+9797T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77969065 | ||||||
| chr17:77969276
|
A | G | 37 | a0001c0001t0017g0266a0001c0001t0017g0267a0001c0001t0029g0239others(34): Show | 37 | HG01943.hp1 HG02145.hp2 HG02155.hp1 others(34): Show |
intron_variant | MODIFIER | c.-38+10008A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77969276 | ||||||
| chr17:77969294
|
G | A | 1 | a0001c0001t0001g0106 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-38+10026G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77969294 | ||||||
| chr17:77969326
|
T | A | 4 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0015g0014others(1): Show | 4 | HG00673.hp2 HG02165.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-38+10058T>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77969326 | ||||||
| chr17:77969546
|
G | A | 3 | a0001c0007t0012g0268a0001c0007t0012g0269a0001c0007t0012g0270 | 3 | HG02145.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-38+10278G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77969546 | ||||||
| chr17:77969720
|
C | G | 2 | a0001c0002t0061g0232a0001c0002t0062g0231 | 2 | HG04115.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-38+10452C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77969720 | ||||||
| chr17:77969795
|
A | G | 2 | a0001c0001t0017g0266a0001c0001t0017g0267 | 2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-38+10527A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77969795 | ||||||
| chr17:77970138
|
T | C | 1 | a0001c0005t0001g0137 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-38+10870T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77970138 | ||||||
| chr17:77970200
|
C | G | 5 | a0001c0001t0030g0259a0001c0004t0011g0257a0001c0004t0011g0261others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-38+10932C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77970200 | ||||||
| chr17:77970277
|
A | G | 37 | a0001c0001t0017g0266a0001c0001t0017g0267a0001c0001t0029g0239others(34): Show | 37 | HG01943.hp1 HG02145.hp2 HG02155.hp1 others(34): Show |
intron_variant | MODIFIER | c.-38+11009A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77970277 | ||||||
| chr17:77970283
|
T | C | 1 | a0001c0002t0002g0107 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-38+11015T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77970283 | ||||||
| chr17:77970385
|
A | G | 14 | a0001c0001t0029g0239a0001c0004t0006g0242a0001c0004t0006g0244others(11): Show | 14 | HG02258.hp1 HG02486.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.-38+11117A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77970385 | ||||||
| chr17:77970404
|
C | A | 14 | a0001c0001t0029g0239a0001c0004t0006g0242a0001c0004t0006g0244others(11): Show | 14 | HG02258.hp1 HG02486.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.-38+11136C>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77970404 | ||||||
| chr17:77970497
|
A | T | 3 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0065g0017 | 3 | HG00673.hp2 HG02165.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.-38+11229A>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77970497 | ||||||
| chr17:77970512
|
C | T | 39 | a0001c0001t0017g0266a0001c0001t0017g0267a0001c0001t0029g0239others(36): Show | 39 | HG01943.hp1 HG02145.hp2 HG02155.hp1 others(36): Show |
intron_variant | MODIFIER | c.-38+11244C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77970512 | ||||||
| chr17:77970626
|
T | A | 6 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(3): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.-38+11358T>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77970626 | ||||||
| chr17:77970673
|
A | G | 1 | a0001c0001t0049g0097 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-38+11405A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77970673 | ||||||
| chr17:77970870
|
A | G | 3 | a0002c0003t0020g0182a0002c0003t0022g0183a0007c0013t0022g0010 | 3 | HG02080.hp1 HG02165.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-38+11602A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77970870 | ||||||
| chr17:77970893
|
T | C | 1 | a0002c0003t0010g0240 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-38+11625T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77970893 | ||||||
| chr17:77971041
|
G | C | 1 | a0001c0001t0029g0239 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-38+11773G>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77971041 | ||||||
| chr17:77971103
|
T | C | 1 | a0001c0001t0015g0018 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-38+11835T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77971103 | ||||||
| chr17:77971150
|
C | T | 4 | a0001c0001t0001g0209a0001c0001t0001g0216a0001c0001t0001g0217others(1): Show | 4 | HG02155.hp2 NA18990.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38+11882C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77971150 | ||||||
| chr17:77971573
|
A | G | 1 | a0001c0001t0001g0208 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-38+12305A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77971573 | ||||||
| chr17:77971602
|
T | G | 11 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(8): Show | 11 | HG01243.hp1 HG01257.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.-38+12334T>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77971602 | ||||||
| chr17:77971867
|
TA | T | 166 | a0001c0001t0001g0006a0001c0001t0001g0083a0001c0001t0001g0085others(163): Show | 169 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.-38+12614delA | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 77971867 | |||||
| chr17:77971867
|
TAA | T | 14 | a0001c0001t0004g0191a0001c0001t0029g0239a0001c0002t0002g0179others(11): Show | 14 | HG01943.hp1 HG02155.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.-38+12613_-38+1261 others(6): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 77971867 | |||||
| chr17:77971939
|
C | T | 2 | a0001c0001t0001g0081a0001c0001t0001g0082 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-38+12671C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77971939 | ||||||
| chr17:77971971
|
AG | A | 5 | a0001c0001t0030g0259a0001c0004t0011g0257a0001c0004t0011g0261others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-38+12704delG | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77971971 | ||||||
| chr17:77972039
|
G | T | 6 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(3): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.-38+12771G>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77972039 | ||||||
| chr17:77972641
|
A | G | 5 | a0001c0001t0030g0259a0001c0004t0011g0257a0001c0004t0011g0261others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-38+13373A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77972641 | ||||||
| chr17:77972919
|
T | A | 2 | a0001c0001t0016g0142a0001c0001t0019g0141 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-38+13651T>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77972919 | ||||||
| chr17:77972957
|
G | A | 1 | a0001c0001t0004g0143 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-38+13689G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77972957 | ||||||
| chr17:77973045
|
A | G | 7 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(4): Show | 7 | HG02486.hp1 HG02622.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-38+13777A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77973045 | ||||||
| chr17:77973262
|
GA | G | 11 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(8): Show | 11 | HG02486.hp1 HG02622.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.-38+13999delA | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 77973262 | |||||
| chr17:77973287
|
ATTCT | A | 11 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(8): Show | 11 | HG01243.hp1 HG01257.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.-38+14023_-38+1402 others(8): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 77973287 | |||||
| chr17:77973411
|
G | A | 1 | a0001c0001t0015g0019 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-38+14143G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77973411 | ||||||
| chr17:77973644
|
C | A | 6 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(3): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.-38+14376C>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77973644 | ||||||
| chr17:77973737
|
A | G | 5 | a0001c0001t0030g0259a0001c0004t0011g0257a0001c0004t0011g0261others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-38+14469A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77973737 | ||||||
| chr17:77973749
|
GCAA | G | 3 | a0001c0002t0002g0122a0001c0002t0002g0196a0001c0002t0052g0121 | 3 | HG00323.hp2 NA18968.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.-38+14483_-38+1448 others(7): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 77973749 | |||||
| chr17:77974240
|
C | T | 6 | a0001c0001t0030g0259a0001c0004t0011g0257a0001c0004t0011g0261others(3): Show | 6 | HG01361.hp2 HG02717.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-38+14972C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77974240 | ||||||
| chr17:77974301
|
A | C | 2 | a0001c0001t0001g0096a0001c0001t0064g0080 | 2 | HG02976.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-38+15033A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77974301 | ||||||
| chr17:77974311
|
A | G | 1 | a0008c0016t0001g0079 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-38+15043A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77974311 | ||||||
| chr17:77974397
|
C | T | 5 | a0001c0001t0030g0259a0001c0004t0011g0257a0001c0004t0011g0261others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-38+15129C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77974397 | ||||||
| chr17:77974486
|
C | T | 14 | a0001c0001t0029g0239a0001c0004t0006g0242a0001c0004t0006g0244others(11): Show | 14 | HG02258.hp1 HG02486.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.-38+15218C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77974486 | ||||||
| chr17:77974492
|
A | C | 20 | a0001c0001t0029g0239a0001c0004t0006g0242a0001c0004t0006g0244others(17): Show | 20 | HG01943.hp1 HG02155.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-38+15224A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77974492 | ||||||
| chr17:77974493
|
A | C | 1 | a0001c0001t0029g0239 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-38+15225A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77974493 | ||||||
| chr17:77974527
|
G | A | 1 | a0002c0003t0003g0144 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-38+15259G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77974527 | ||||||
| chr17:77974816
|
G | T | 11 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(8): Show | 11 | HG02486.hp1 HG02622.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.-38+15548G>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77974816 | ||||||
| chr17:77974871
|
G | C | 1 | a0001c0005t0001g0137 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-38+15603G>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77974871 | ||||||
| chr17:77975016
|
G | GAAATT | 169 | a0001c0001t0001g0006a0001c0001t0001g0093a0001c0001t0001g0106others(166): Show | 172 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.-38+15752_-38+1575 others(9): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 77975016 | |||||
| chr17:77975130
|
C | G | 1 | a0001c0002t0031g0265 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-38+15862C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77975130 | ||||||
| chr17:77975133
|
T | G | 1 | a0001c0001t0001g0020 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-38+15865T>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77975133 | ||||||
| chr17:77975234
|
G | GT | 11 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(8): Show | 11 | HG01243.hp1 HG01257.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.-38+15975dupT | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 77975234 | |||||
| chr17:77975327
|
A | C | 1 | a0001c0002t0031g0265 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-38+16059A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77975327 | ||||||
| chr17:77975423
|
T | C | 11 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(8): Show | 11 | HG02486.hp1 HG02622.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.-38+16155T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77975423 | ||||||
| chr17:77975468
|
A | C | 1 | a0001c0004t0006g0244 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-38+16200A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77975468 | ||||||
| chr17:77975637
|
A | G | 5 | a0001c0002t0013g0235a0001c0002t0013g0236a0001c0002t0013g0238others(2): Show | 5 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-38+16369A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77975637 | ||||||
| chr17:77975845
|
G | T | 3 | a0001c0007t0012g0268a0001c0007t0012g0269a0001c0007t0012g0270 | 3 | HG02145.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-38+16577G>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77975845 | ||||||
| chr17:77975914
|
G | A | 4 | a0001c0005t0001g0001a0001c0005t0001g0145a0001c0005t0001g0146others(1): Show | 5 | HG02630.hp1 HG03041.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-38+16646G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77975914 | ||||||
| chr17:77976264
|
CA | C | 11 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(8): Show | 11 | HG02486.hp1 HG02622.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.-38+16997delA | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77976264 | ||||||
| chr17:77976755
|
C | G | 11 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(8): Show | 11 | HG01243.hp1 HG01257.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.-38+17487C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77976755 | ||||||
| chr17:77976802
|
G | A | 6 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(3): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.-38+17534G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77976802 | ||||||
| chr17:77976908
|
G | A | 2 | a0001c0002t0061g0232a0001c0002t0062g0231 | 2 | HG04115.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-38+17640G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77976908 | ||||||
| chr17:77976931
|
G | GA | 65 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(62): Show | 65 | HG00280.hp1 HG00423.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.-38+17692dupA | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 77976931 | |||||
| chr17:77976931
|
G | GAA | 24 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(21): Show | 24 | HG00323.hp1 HG01081.hp2 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.-38+17691_-38+1769 others(6): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 77976931 | |||||
| chr17:77976931
|
G | GAAA | 8 | a0001c0001t0001g0021a0001c0001t0030g0259a0001c0004t0006g0242others(5): Show | 8 | HG02258.hp1 HG02486.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-38+17690_-38+1769 others(7): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 77976931 | |||||
| chr17:77976931
|
GA | G | 69 | a0001c0001t0001g0006a0001c0001t0001g0106a0001c0001t0001g0170others(66): Show | 72 | HG00323.hp2 HG00558.hp2 HG00673.hp1 others(69): Show |
intron_variant | MODIFIER | c.-38+17692delA | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 77976931 | |||||
| chr17:77976931
|
GAAAAAAA | G | 7 | a0001c0002t0031g0265a0001c0006t0008g0251a0001c0006t0008g0253others(4): Show | 7 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.-38+17686_-38+1769 others(11): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 77976931 | |||||
| chr17:77976931
|
GAAAAAAA others(1): Show |
G | 10 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0131others(7): Show | 10 | HG00280.hp2 HG00642.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.-38+17685_-38+1769 others(12): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 77976931 | |||||
| chr17:77976931
|
GAAAAAAA others(4): Show |
G | 1 | a0001c0001t0029g0239 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-38+17682_-38+1769 others(15): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 77976931 | |||||
| chr17:77976931
|
GAAAAAAA others(5): Show |
G | 1 | a0001c0001t0001g0078 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-38+17681_-38+1769 others(16): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 77976931 | |||||
| chr17:77976957
|
A | C | 6 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(3): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.-38+17689A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77976957 | ||||||
| chr17:77976989
|
G | A | 1 | a0001c0006t0008g0251 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-38+17721G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77976989 | ||||||
| chr17:77977056
|
A | G | 3 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0052 | 3 | HG01496.hp2 HG01981.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.-38+17788A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77977056 | ||||||
| chr17:77977131
|
C | T | 2 | a0001c0001t0001g0051a0001c0001t0015g0019 | 2 | HG00642.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-38+17863C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77977131 | ||||||
| chr17:77977210
|
G | A | 37 | a0001c0001t0017g0266a0001c0001t0017g0267a0001c0001t0029g0239others(34): Show | 37 | HG01943.hp1 HG02145.hp2 HG02155.hp1 others(34): Show |
intron_variant | MODIFIER | c.-38+17942G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77977210 | ||||||
| chr17:77977235
|
T | G | 1 | a0002c0003t0057g0158 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-38+17967T>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77977235 | ||||||
| chr17:77977283
|
A | T | 1 | a0001c0001t0001g0208 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-38+18015A>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77977283 | ||||||
| chr17:77977318
|
C | T | 3 | a0001c0001t0029g0239a0009c0015t0027g0264a0017c0017t0028g0263 | 3 | HG02258.hp1 HG02615.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-38+18050C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77977318 | ||||||
| chr17:77977320
|
A | G | 4 | a0001c0007t0012g0268a0001c0007t0012g0269a0001c0007t0012g0270others(1): Show | 4 | HG02145.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38+18052A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77977320 | ||||||
| chr17:77977380
|
C | T | 1 | a0014c0025t0001g0077 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-38+18112C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77977380 | ||||||
| chr17:77977503
|
C | T | 4 | a0001c0007t0012g0268a0001c0007t0012g0269a0001c0007t0012g0270others(1): Show | 4 | HG02145.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38+18235C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77977503 | ||||||
| chr17:77977748
|
A | G | 1 | a0001c0002t0002g0211 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-38+18480A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77977748 | ||||||
| chr17:77977872
|
T | C | 1 | a0001c0002t0059g0123 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-38+18604T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77977872 | ||||||
| chr17:77977891
|
C | CT | 26 | a0001c0001t0001g0049a0001c0001t0001g0075a0001c0001t0001g0076others(23): Show | 26 | HG01106.hp2 HG01167.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.-38+18645dupT | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 77977891 | |||||
| chr17:77977891
|
C | CTT | 8 | a0001c0004t0026g0260a0001c0006t0008g0251a0001c0006t0008g0253others(5): Show | 8 | HG02155.hp1 HG02647.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-38+18644_-38+1864 others(6): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 77977891 | |||||
| chr17:77977891
|
C | CTTT | 10 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(7): Show | 10 | HG01943.hp1 HG02486.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-38+18643_-38+1864 others(7): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 77977891 | |||||
| chr17:77977891
|
CT | C | 32 | a0001c0001t0001g0006a0001c0001t0001g0052a0001c0007t0012g0268others(29): Show | 34 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.-38+18645delT | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 77977891 | |||||
| chr17:77977957
|
G | A | 1 | a0001c0002t0002g0122 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-38+18689G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77977957 | ||||||
| chr17:77978140
|
A | T | 109 | a0001c0001t0001g0006a0001c0001t0001g0106a0001c0001t0001g0127others(106): Show | 112 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.-38+18872A>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77978140 | ||||||
| chr17:77978218
|
A | G | 1 | a0001c0002t0031g0265 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-38+18950A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77978218 | ||||||
| chr17:77978312
|
A | G | 3 | a0001c0007t0012g0268a0001c0007t0012g0269a0001c0007t0012g0270 | 3 | HG02145.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-38+19044A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77978312 | ||||||
| chr17:77978446
|
G | A | 1 | a0001c0005t0001g0145 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-38+19178G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77978446 | ||||||
| chr17:77978705
|
C | T | 1 | a0001c0002t0002g0120 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-38+19437C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77978705 | ||||||
| chr17:77978967
|
C | T | 7 | a0001c0002t0031g0265a0001c0006t0008g0251a0001c0006t0008g0253others(4): Show | 7 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.-38+19699C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77978967 | ||||||
| chr17:77979077
|
A | C | 1 | a0001c0002t0031g0265 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-38+19809A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77979077 | ||||||
| chr17:77979234
|
G | A | 6 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(3): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.-38+19966G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77979234 | ||||||
| chr17:77979265
|
T | A | 3 | a0001c0007t0012g0268a0001c0007t0012g0269a0001c0007t0012g0270 | 3 | HG02145.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-38+19997T>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77979265 | ||||||
| chr17:77979475
|
T | C | 1 | a0001c0001t0029g0239 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-38+20207T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77979475 | ||||||
| chr17:77979749
|
A | T | 1 | a0001c0001t0004g0193 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-38+20481A>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77979749 | ||||||
| chr17:77979790
|
C | CA | 11 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(8): Show | 11 | HG01243.hp1 HG01257.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.-38+20526dupA | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 77979790 | |||||
| chr17:77979791
|
A | G | 11 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(8): Show | 11 | HG02486.hp1 HG02622.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.-38+20523A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77979791 | ||||||
| chr17:77979864
|
C | T | 1 | a0001c0001t0043g0177 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-38+20596C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77979864 | ||||||
| chr17:77979910
|
C | T | 1 | a0001c0001t0042g0099 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-38+20642C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77979910 | ||||||
| chr17:77980076
|
A | G | 5 | a0001c0002t0013g0235a0001c0002t0013g0236a0001c0002t0013g0238others(2): Show | 5 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-38+20808A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77980076 | ||||||
| chr17:77980137
|
G | A | 2 | a0006c0011t0001g0159a0006c0011t0001g0160 | 2 | HG01243.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.-38+20869G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77980137 | ||||||
| chr17:77980153
|
C | T | 2 | a0001c0002t0061g0232a0001c0002t0062g0231 | 2 | HG04115.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-38+20885C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77980153 | ||||||
| chr17:77980167
|
A | G | 37 | a0001c0001t0017g0266a0001c0001t0017g0267a0001c0001t0029g0239others(34): Show | 37 | HG01943.hp1 HG02145.hp2 HG02155.hp1 others(34): Show |
intron_variant | MODIFIER | c.-38+20899A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77980167 | ||||||
| chr17:77980195
|
A | G | 1 | a0018c0020t0046g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-38+20927A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77980195 | ||||||
| chr17:77980234
|
C | G | 7 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(4): Show | 7 | HG02486.hp1 HG02622.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-38+20966C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77980234 | ||||||
| chr17:77980260
|
T | C | 5 | a0001c0001t0030g0259a0001c0004t0011g0257a0001c0004t0011g0261others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-38+20992T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77980260 | ||||||
| chr17:77980304
|
C | T | 1 | a0001c0001t0001g0029 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-38+21036C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77980304 | ||||||
| chr17:77980576
|
C | CGTA | 4 | a0001c0001t0001g0072a0004c0008t0001g0073a0004c0008t0001g0074others(1): Show | 4 | NA18943.hp1 NA18968.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.-38+21308_-38+2130 others(7): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77980576 | ||||||
| chr17:77980734
|
C | G | 1 | a0001c0002t0031g0265 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-38+21466C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77980734 | ||||||
| chr17:77980765
|
G | A | 2 | a0001c0029t0001g0031a0008c0016t0001g0079 | 2 | HG01255.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.-38+21497G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77980765 | ||||||
| chr17:77980857
|
TG | T | 6 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(3): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.-38+21595delG | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 77980857 | |||||
| chr17:77980867
|
G | A | 1 | a0001c0006t0033g0252 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-38+21599G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77980867 | ||||||
| chr17:77981012
|
A | G | 1 | a0001c0002t0002g0111 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-38+21744A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77981012 | ||||||
| chr17:77981141
|
A | C | 1 | a0001c0001t0001g0187 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-38+21873A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77981141 | ||||||
| chr17:77981295
|
T | G | 2 | a0002c0003t0010g0240a0002c0003t0010g0245 | 2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-38+22027T>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77981295 | ||||||
| chr17:77981450
|
T | C | 3 | a0001c0007t0012g0268a0001c0007t0012g0269a0001c0007t0012g0270 | 3 | HG02145.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-38+22182T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77981450 | ||||||
| chr17:77981470
|
A | G | 1 | a0001c0001t0048g0046 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-38+22202A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77981470 | ||||||
| chr17:77981564
|
T | C | 1 | a0017c0017t0028g0263 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-38+22296T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77981564 | ||||||
| chr17:77981576
|
C | G | 5 | a0001c0002t0013g0235a0001c0002t0013g0236a0001c0002t0013g0238others(2): Show | 5 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-38+22308C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77981576 | ||||||
| chr17:77981761
|
C | G | 2 | a0002c0014t0004g0168a0002c0014t0004g0169 | 2 | HG03490.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-37-22409C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77981761 | ||||||
| chr17:77981881
|
TAGA | T | 11 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(8): Show | 11 | HG01243.hp1 HG01257.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.-37-22285_-37-2228 others(7): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 77981881 | |||||
| chr17:77981907
|
A | G | 166 | a0001c0001t0001g0006a0001c0001t0001g0106a0001c0001t0001g0127others(163): Show | 169 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.-37-22263A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77981907 | ||||||
| chr17:77982010
|
G | T | 5 | a0001c0001t0030g0259a0001c0004t0011g0257a0001c0004t0011g0261others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-37-22160G>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77982010 | ||||||
| chr17:77982039
|
A | G | 1 | a0001c0001t0049g0097 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-37-22131A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77982039 | ||||||
| chr17:77982078
|
C | G | 1 | a0001c0002t0002g0181 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-37-22092C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77982078 | ||||||
| chr17:77982225
|
C | T | 11 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(8): Show | 11 | HG02486.hp1 HG02622.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.-37-21945C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77982225 | ||||||
| chr17:77982270
|
G | A | 7 | a0001c0002t0002g0005a0001c0002t0002g0197a0001c0002t0002g0198others(4): Show | 7 | NA18747.hp1 NA18940.hp1 NA18970.hp2 others(4): Show |
intron_variant | MODIFIER | c.-37-21900G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77982270 | ||||||
| chr17:77982353
|
T | A | 1 | a0008c0028t0023g0258 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-37-21817T>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77982353 | ||||||
| chr17:77982430
|
G | C | 4 | a0001c0002t0002g0109a0001c0002t0002g0111a0001c0002t0002g0112others(1): Show | 4 | HG00597.hp2 HG01952.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37-21740G>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77982430 | ||||||
| chr17:77982687
|
T | C | 37 | a0001c0001t0017g0266a0001c0001t0017g0267a0001c0001t0029g0239others(34): Show | 37 | HG01943.hp1 HG02145.hp2 HG02155.hp1 others(34): Show |
intron_variant | MODIFIER | c.-37-21483T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77982687 | ||||||
| chr17:77982761
|
G | A | 6 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(3): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.-37-21409G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77982761 | ||||||
| chr17:77982957
|
C | G | 1 | a0001c0001t0001g0045 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-37-21213C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77982957 | ||||||
| chr17:77983099
|
G | T | 1 | a0001c0002t0031g0265 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-37-21071G>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77983099 | ||||||
| chr17:77983143
|
C | A | 5 | a0001c0001t0030g0259a0001c0004t0011g0257a0001c0004t0011g0261others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-37-21027C>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77983143 | ||||||
| chr17:77983644
|
A | G | 2 | a0001c0001t0001g0044a0001c0001t0016g0050 | 2 | HG01167.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.-37-20526A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77983644 | ||||||
| chr17:77983762
|
T | C | 1 | a0001c0001t0015g0019 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-37-20408T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77983762 | ||||||
| chr17:77983763
|
G | C | 4 | a0001c0005t0001g0001a0001c0005t0001g0145a0001c0005t0001g0146others(1): Show | 5 | HG02630.hp1 HG03041.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-37-20407G>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77983763 | ||||||
| chr17:77984137
|
T | C | 1 | a0002c0003t0057g0158 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-37-20033T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77984137 | ||||||
| chr17:77984356
|
TA | T | 136 | a0001c0001t0001g0006a0001c0001t0001g0127a0001c0001t0001g0128others(133): Show | 139 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.-37-19802delA | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 77984356 | |||||
| chr17:77984356
|
TAAAAAAA others(6): Show |
T | 1 | a0009c0015t0027g0264 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-37-19802_-37-1979 others(17): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 77984356 | |||||
| chr17:77984368
|
A | C | 18 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(15): Show | 18 | HG01243.hp1 HG01257.hp2 HG01943.hp1 others(15): Show |
intron_variant | MODIFIER | c.-37-19802A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77984368 | ||||||
| chr17:77984369
|
C | A | 18 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(15): Show | 18 | HG01243.hp1 HG01257.hp2 HG01943.hp1 others(15): Show |
intron_variant | MODIFIER | c.-37-19801C>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77984369 | ||||||
| chr17:77984370
|
A | C | 1 | a0002c0003t0057g0158 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-37-19800A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77984370 | ||||||
| chr17:77984377
|
A | C | 1 | a0001c0002t0031g0265 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-37-19793A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77984377 | ||||||
| chr17:77984380
|
A | C | 11 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(8): Show | 11 | HG02486.hp1 HG02622.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.-37-19790A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77984380 | ||||||
| chr17:77984503
|
G | A | 2 | a0001c0002t0031g0265a0008c0028t0023g0258 | 2 | HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-37-19667G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77984503 | ||||||
| chr17:77984579
|
G | A | 1 | a0001c0001t0029g0239 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-37-19591G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77984579 | ||||||
| chr17:77984683
|
C | G | 2 | a0001c0002t0061g0232a0001c0002t0062g0231 | 2 | HG04115.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-37-19487C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77984683 | ||||||
| chr17:77984701
|
G | A | 1 | a0001c0002t0018g0234 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-37-19469G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77984701 | ||||||
| chr17:77984702
|
G | A | 1 | a0001c0001t0001g0207 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-37-19468G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77984702 | ||||||
| chr17:77984796
|
G | A | 4 | a0001c0007t0012g0268a0001c0007t0012g0269a0001c0007t0012g0270others(1): Show | 4 | HG02145.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37-19374G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77984796 | ||||||
| chr17:77984827
|
C | T | 3 | a0001c0007t0012g0268a0001c0007t0012g0269a0001c0007t0012g0270 | 3 | HG02145.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-37-19343C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77984827 | ||||||
| chr17:77984828
|
G | GCA | 28 | a0001c0001t0001g0032a0001c0001t0001g0185a0001c0001t0001g0187others(25): Show | 29 | HG00558.hp1 HG01261.hp1 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.-37-19324_-37-1932 others(6): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 77984828 | |||||
| chr17:77984828
|
G | GCACA | 5 | a0001c0001t0030g0259a0001c0004t0011g0257a0001c0004t0011g0261others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-37-19326_-37-1932 others(8): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 77984828 | |||||
| chr17:77984844
|
A | G | 1 | a0001c0002t0061g0232 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-37-19326A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77984844 | ||||||
| chr17:77984875
|
G | A | 1 | a0008c0028t0023g0258 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-37-19295G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77984875 | ||||||
| chr17:77985083
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-37-19087G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77985083 | ||||||
| chr17:77985124
|
G | A | 5 | a0001c0002t0013g0235a0001c0002t0013g0236a0001c0002t0013g0238others(2): Show | 5 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-37-19046G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77985124 | ||||||
| chr17:77985143
|
T | G | 1 | a0001c0001t0001g0085 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-37-19027T>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77985143 | ||||||
| chr17:77985475
|
G | A | 2 | a0001c0001t0017g0266a0001c0001t0017g0267 | 2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-37-18695G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77985475 | ||||||
| chr17:77985601
|
C | CAAAAAAA others(3): Show |
5 | a0001c0001t0017g0267a0001c0004t0011g0261a0001c0004t0026g0260others(2): Show | 5 | HG02145.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-37-18563_-37-1855 others(14): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 77985601 | |||||
| chr17:77985601
|
C | CAAAAAAA others(4): Show |
3 | a0001c0002t0031g0265a0001c0006t0033g0252a0001c0007t0012g0268 | 3 | HG02886.hp2 HG03491.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-37-18564_-37-1855 others(15): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 77985601 | |||||
| chr17:77985601
|
C | CAAAAAAA others(5): Show |
5 | a0001c0006t0008g0251a0001c0006t0008g0256a0001c0006t0032g0254others(2): Show | 5 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.-37-18565_-37-1855 others(16): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 77985601 | |||||
| chr17:77985601
|
C | CAAAAAAA others(6): Show |
1 | a0001c0006t0008g0253 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-37-18566_-37-1855 others(17): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 77985601 | |||||
| chr17:77985601
|
C | CAAAAAAA others(10): Show |
9 | a0001c0004t0006g0244a0001c0004t0006g0246a0001c0004t0006g0248others(6): Show | 9 | HG02258.hp1 HG02647.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-37-18554_-37-1855 others(21): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 77985601 | |||||
| chr17:77985601
|
C | CAAAAAAA others(11): Show |
3 | a0001c0004t0006g0242a0001c0004t0006g0247a0002c0003t0025g0241 | 3 | HG02486.hp1 HG02622.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-37-18554_-37-1855 others(22): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 77985601 | |||||
| chr17:77985601
|
C | CAAAAAAA others(12): Show |
3 | a0001c0002t0013g0236a0001c0002t0013g0238a0001c0002t0018g0237 | 3 | HG02280.hp1 HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-37-18554_-37-1855 others(23): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 77985601 | |||||
| chr17:77985601
|
C | CAAAAAAA others(13): Show |
1 | a0001c0002t0018g0234 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-37-18554_-37-1855 others(24): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 77985601 | |||||
| chr17:77985601
|
C | CAAAAAAA others(14): Show |
1 | a0001c0002t0013g0235 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-37-18554_-37-1855 others(25): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 77985601 | |||||
| chr17:77985601
|
C | CAAAAAAA others(24): Show |
1 | a0017c0017t0028g0263 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-37-18554_-37-1855 others(35): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 77985601 | |||||
| chr17:77985603
|
A | AAAAAAAA others(16): Show |
1 | a0001c0001t0029g0239 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-37-18554_-37-1855 others(27): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 77985603 | |||||
| chr17:77985696
|
G | C | 11 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(8): Show | 11 | HG02486.hp1 HG02622.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.-37-18474G>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77985696 | ||||||
| chr17:77985796
|
A | G | 37 | a0001c0001t0017g0266a0001c0001t0017g0267a0001c0001t0029g0239others(34): Show | 37 | HG01943.hp1 HG02145.hp2 HG02155.hp1 others(34): Show |
intron_variant | MODIFIER | c.-37-18374A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77985796 | ||||||
| chr17:77986100
|
G | A | 34 | a0001c0001t0001g0006a0002c0003t0003g0002a0002c0003t0003g0003others(31): Show | 36 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.-37-18070G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77986100 | ||||||
| chr17:77986243
|
T | C | 37 | a0001c0001t0017g0266a0001c0001t0017g0267a0001c0001t0029g0239others(34): Show | 37 | HG01943.hp1 HG02145.hp2 HG02155.hp1 others(34): Show |
intron_variant | MODIFIER | c.-37-17927T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77986243 | ||||||
| chr17:77986272
|
A | G | 37 | a0001c0001t0017g0266a0001c0001t0017g0267a0001c0001t0029g0239others(34): Show | 37 | HG01943.hp1 HG02145.hp2 HG02155.hp1 others(34): Show |
intron_variant | MODIFIER | c.-37-17898A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77986272 | ||||||
| chr17:77986286
|
A | G | 5 | a0001c0001t0030g0259a0001c0004t0011g0257a0001c0004t0011g0261others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-37-17884A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77986286 | ||||||
| chr17:77986328
|
T | C | 14 | a0001c0001t0029g0239a0001c0004t0006g0242a0001c0004t0006g0244others(11): Show | 14 | HG02258.hp1 HG02486.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.-37-17842T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77986328 | ||||||
| chr17:77986353
|
T | C | 2 | a0001c0002t0031g0265a0008c0028t0023g0258 | 2 | HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-37-17817T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77986353 | ||||||
| chr17:77986368
|
G | A | 1 | a0001c0002t0002g0110 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-37-17802G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77986368 | ||||||
| chr17:77986370
|
G | A | 2 | a0001c0001t0001g0033a0001c0001t0001g0053 | 2 | HG01106.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-37-17800G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77986370 | ||||||
| chr17:77986371
|
C | T | 2 | a0009c0015t0027g0264a0017c0017t0028g0263 | 2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.-37-17799C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77986371 | ||||||
| chr17:77986426
|
A | AAAAG | 14 | a0001c0001t0001g0034a0001c0001t0001g0045a0001c0001t0001g0085others(11): Show | 14 | HG01943.hp1 HG02145.hp1 HG02155.hp1 others(11): Show |
intron_variant | MODIFIER | c.-37-17742_-37-1774 others(8): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 77986426 | |||||
| chr17:77986426
|
A | AAAG | 231 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0015others(228): Show | 234 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.-37-17732_-37-1773 others(7): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 77986426 | |||||
| chr17:77986426
|
A | AAG | 16 | a0001c0001t0029g0239a0001c0002t0002g0196a0001c0002t0031g0265others(13): Show | 16 | HG02258.hp1 HG02486.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.-37-17743_-37-1774 others(6): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 77986426 | |||||
| chr17:77986584
|
A | G | 1 | a0001c0001t0029g0239 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-37-17586A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77986584 | ||||||
| chr17:77986707
|
T | C | 1 | a0001c0001t0049g0097 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-37-17463T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77986707 | ||||||
| chr17:77987083
|
T | G | 1 | a0001c0002t0031g0265 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-37-17087T>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77987083 | ||||||
| chr17:77987492
|
T | C | 25 | a0001c0001t0001g0032a0001c0001t0001g0037a0001c0001t0001g0038others(22): Show | 25 | HG00558.hp1 HG00597.hp1 HG01934.hp1 others(22): Show |
intron_variant | MODIFIER | c.-37-16678T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77987492 | ||||||
| chr17:77987595
|
A | T | 2 | a0001c0002t0002g0107a0001c0002t0002g0119 | 2 | HG02818.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-37-16575A>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77987595 | ||||||
| chr17:77987736
|
C | T | 12 | a0001c0001t0004g0143a0001c0001t0004g0157a0001c0001t0004g0172others(9): Show | 12 | HG01496.hp1 HG01934.hp2 HG02293.hp2 others(9): Show |
intron_variant | MODIFIER | c.-37-16434C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77987736 | ||||||
| chr17:77987759
|
A | G | 1 | a0001c0002t0031g0265 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-37-16411A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77987759 | ||||||
| chr17:77987823
|
G | A | 26 | a0001c0001t0001g0106a0001c0001t0051g0105a0001c0002t0002g0005others(23): Show | 26 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.-37-16347G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77987823 | ||||||
| chr17:77987842
|
G | T | 3 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0201 | 3 | HG01081.hp2 HG02698.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-37-16328G>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77987842 | ||||||
| chr17:77987845
|
A | G | 3 | a0002c0003t0020g0182a0002c0003t0022g0183a0007c0013t0022g0010 | 3 | HG02080.hp1 HG02165.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-37-16325A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77987845 | ||||||
| chr17:77987939
|
C | CA | 6 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(3): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.-37-16228dupA | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 77987939 | |||||
| chr17:77987971
|
T | C | 2 | a0001c0002t0031g0265a0008c0028t0023g0258 | 2 | HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-37-16199T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77987971 | ||||||
| chr17:77987983
|
A | C | 14 | a0001c0001t0029g0239a0001c0004t0006g0242a0001c0004t0006g0244others(11): Show | 14 | HG02258.hp1 HG02486.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.-37-16187A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77987983 | ||||||
| chr17:77988180
|
C | T | 1 | a0001c0001t0004g0157 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-37-15990C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77988180 | ||||||
| chr17:77988192
|
T | C | 5 | a0001c0001t0030g0259a0001c0004t0011g0257a0001c0004t0011g0261others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-37-15978T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77988192 | ||||||
| chr17:77988264
|
A | G | 1 | a0001c0002t0031g0265 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-37-15906A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77988264 | ||||||
| chr17:77988279
|
T | C | 3 | a0001c0007t0012g0268a0001c0007t0012g0269a0001c0007t0012g0270 | 3 | HG02145.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-37-15891T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77988279 | ||||||
| chr17:77988376
|
T | TAC | 11 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(8): Show | 11 | HG02486.hp1 HG02622.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.-37-15780_-37-1577 others(6): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 77988376 | |||||
| chr17:77988690
|
T | A | 8 | a0001c0005t0001g0001a0001c0005t0001g0007a0001c0005t0001g0008others(5): Show | 9 | HG02451.hp1 HG02630.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.-37-15480T>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77988690 | ||||||
| chr17:77988903
|
A | G | 166 | a0001c0001t0001g0006a0001c0001t0001g0106a0001c0001t0001g0127others(163): Show | 169 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.-37-15267A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77988903 | ||||||
| chr17:77989009
|
G | T | 1 | a0001c0002t0031g0265 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-37-15161G>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77989009 | ||||||
| chr17:77989011
|
G | C | 5 | a0001c0001t0030g0259a0001c0004t0011g0257a0001c0004t0011g0261others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-37-15159G>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77989011 | ||||||
| chr17:77989206
|
C | T | 1 | a0001c0002t0031g0265 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-37-14964C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77989206 | ||||||
| chr17:77989328
|
T | G | 1 | a0001c0002t0031g0265 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-37-14842T>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77989328 | ||||||
| chr17:77989654
|
C | G | 1 | a0016c0023t0045g0192 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-37-14516C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77989654 | ||||||
| chr17:77989673
|
C | T | 1 | a0001c0001t0004g0124 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-37-14497C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77989673 | ||||||
| chr17:77989720
|
A | G | 11 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(8): Show | 11 | HG02486.hp1 HG02622.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.-37-14450A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77989720 | ||||||
| chr17:77989786
|
C | T | 2 | a0001c0002t0061g0232a0001c0002t0062g0231 | 2 | HG04115.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-37-14384C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77989786 | ||||||
| chr17:77990019
|
G | A | 6 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(3): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.-37-14151G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77990019 | ||||||
| chr17:77990118
|
C | T | 11 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(8): Show | 11 | HG02486.hp1 HG02622.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.-37-14052C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77990118 | ||||||
| chr17:77990155
|
T | A | 1 | a0001c0004t0006g0242 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-37-14015T>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77990155 | ||||||
| chr17:77990247
|
C | T | 1 | a0001c0006t0033g0252 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-37-13923C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77990247 | ||||||
| chr17:77990272
|
T | C | 1 | a0001c0002t0002g0109 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-37-13898T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77990272 | ||||||
| chr17:77990467
|
C | T | 3 | a0001c0007t0012g0268a0001c0007t0012g0269a0001c0007t0012g0270 | 3 | HG02145.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-37-13703C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77990467 | ||||||
| chr17:77990487
|
A | G | 11 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(8): Show | 11 | HG01243.hp1 HG01257.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.-37-13683A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77990487 | ||||||
| chr17:77990572
|
T | C | 3 | a0001c0007t0012g0268a0001c0007t0012g0269a0001c0007t0012g0270 | 3 | HG02145.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-37-13598T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77990572 | ||||||
| chr17:77990581
|
A | ATCT | 37 | a0001c0001t0017g0266a0001c0001t0017g0267a0001c0001t0029g0239others(34): Show | 37 | HG01943.hp1 HG02145.hp2 HG02155.hp1 others(34): Show |
intron_variant | MODIFIER | c.-37-13588_-37-1358 others(7): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 77990581 | |||||
| chr17:77990747
|
A | G | 7 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(4): Show | 7 | HG02486.hp1 HG02622.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-37-13423A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77990747 | ||||||
| chr17:77990840
|
C | T | 2 | a0001c0001t0001g0043a0001c0001t0015g0018 | 2 | HG00280.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.-37-13330C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77990840 | ||||||
| chr17:77990898
|
A | G | 7 | a0001c0002t0013g0235a0001c0002t0013g0236a0001c0002t0013g0238others(4): Show | 7 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-37-13272A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77990898 | ||||||
| chr17:77991119
|
G | A | 1 | a0001c0002t0061g0232 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-37-13051G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77991119 | ||||||
| chr17:77991209
|
A | C | 37 | a0001c0001t0017g0266a0001c0001t0017g0267a0001c0001t0029g0239others(34): Show | 37 | HG01943.hp1 HG02145.hp2 HG02155.hp1 others(34): Show |
intron_variant | MODIFIER | c.-37-12961A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77991209 | ||||||
| chr17:77991513
|
C | T | 1 | a0001c0002t0031g0265 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-37-12657C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77991513 | ||||||
| chr17:77991685
|
G | C | 4 | a0001c0002t0002g0109a0001c0002t0002g0111a0001c0002t0002g0112others(1): Show | 4 | HG00597.hp2 HG01952.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37-12485G>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77991685 | ||||||
| chr17:77991748
|
C | T | 3 | a0001c0001t0029g0239a0009c0015t0027g0264a0017c0017t0028g0263 | 3 | HG02258.hp1 HG02615.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-37-12422C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77991748 | ||||||
| chr17:77991904
|
G | A | 4 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0028others(1): Show | 4 | HG01081.hp2 HG01433.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37-12266G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77991904 | ||||||
| chr17:77991945
|
G | A | 1 | a0008c0028t0023g0258 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-37-12225G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77991945 | ||||||
| chr17:77992071
|
G | A | 2 | a0009c0015t0027g0264a0017c0017t0028g0263 | 2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.-37-12099G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77992071 | ||||||
| chr17:77992148
|
G | A | 2 | a0001c0001t0017g0266a0001c0001t0017g0267 | 2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-37-12022G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77992148 | ||||||
| chr17:77992201
|
TAAGATTA others(308): Show |
T | 161 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0106others(158): Show | 164 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.-37-11952_-37-1163 others(4): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 77992201 | |||||
| chr17:77992481
|
G | C | 1 | a0001c0001t0001g0090 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-37-11689G>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77992481 | ||||||
| chr17:77992497
|
C | CA | 15 | a0001c0001t0001g0025a0001c0001t0001g0029a0001c0001t0001g0040others(12): Show | 15 | HG00642.hp2 HG01167.hp2 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.-37-11652dupA | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 77992497 | |||||
| chr17:77992566
|
T | C | 11 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(8): Show | 11 | HG02486.hp1 HG02622.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.-37-11604T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77992566 | ||||||
| chr17:77992618
|
A | G | 6 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(3): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.-37-11552A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77992618 | ||||||
| chr17:77992707
|
G | T | 6 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(3): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.-37-11463G>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77992707 | ||||||
| chr17:77992715
|
C | T | 1 | a0001c0001t0029g0239 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-37-11455C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77992715 | ||||||
| chr17:77992804
|
G | C | 3 | a0001c0001t0001g0106a0001c0001t0051g0105a0012c0019t0001g0114 | 3 | HG02027.hp2 NA18942.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.-37-11366G>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77992804 | ||||||
| chr17:77992908
|
T | C | 2 | a0001c0001t0004g0157a0001c0001t0004g0172 | 2 | HG02293.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-37-11262T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77992908 | ||||||
| chr17:77992915
|
G | A | 6 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(3): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.-37-11255G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77992915 | ||||||
| chr17:77993029
|
G | A | 1 | a0008c0028t0023g0258 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-37-11141G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77993029 | ||||||
| chr17:77993110
|
C | T | 5 | a0001c0002t0013g0235a0001c0002t0013g0236a0001c0002t0013g0238others(2): Show | 5 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-37-11060C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77993110 | ||||||
| chr17:77993162
|
A | G | 1 | a0001c0001t0001g0020 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-37-11008A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77993162 | ||||||
| chr17:77993200
|
A | G | 37 | a0001c0001t0017g0266a0001c0001t0017g0267a0001c0001t0029g0239others(34): Show | 37 | HG01943.hp1 HG02145.hp2 HG02155.hp1 others(34): Show |
intron_variant | MODIFIER | c.-37-10970A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77993200 | ||||||
| chr17:77993254
|
G | A | 4 | a0001c0004t0006g0246a0001c0004t0006g0247a0001c0004t0006g0248others(1): Show | 4 | HG02486.hp1 HG02922.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37-10916G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77993254 | ||||||
| chr17:77993268
|
C | CT | 6 | a0001c0002t0013g0235a0001c0002t0013g0236a0001c0002t0013g0238others(3): Show | 7 | HG02040.hp2 HG02132.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-37-10894dupT | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 77993268 | |||||
| chr17:77993372
|
T | C | 2 | a0001c0001t0017g0266a0001c0001t0017g0267 | 2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-37-10798T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77993372 | ||||||
| chr17:77993400
|
A | G | 2 | a0001c0001t0001g0064a0001c0001t0001g0075 | 2 | HG01934.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.-37-10770A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77993400 | ||||||
| chr17:77993493
|
A | C | 1 | a0001c0001t0049g0097 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-37-10677A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77993493 | ||||||
| chr17:77993531
|
C | T | 4 | a0001c0005t0001g0001a0001c0005t0001g0145a0001c0005t0001g0146others(1): Show | 5 | HG02630.hp1 HG03041.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-37-10639C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77993531 | ||||||
| chr17:77993732
|
T | C | 3 | a0001c0007t0012g0268a0001c0007t0012g0269a0001c0007t0012g0270 | 3 | HG02145.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-37-10438T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77993732 | ||||||
| chr17:77993820
|
T | G | 11 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(8): Show | 11 | HG01243.hp1 HG01257.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.-37-10350T>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77993820 | ||||||
| chr17:77993840
|
G | T | 1 | a0017c0017t0028g0263 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-37-10330G>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77993840 | ||||||
| chr17:77993949
|
G | T | 15 | a0001c0001t0029g0239a0001c0002t0031g0265a0001c0004t0006g0242others(12): Show | 15 | HG02258.hp1 HG02486.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.-37-10221G>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77993949 | ||||||
| chr17:77994010
|
T | G | 1 | a0001c0001t0001g0027 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-37-10160T>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77994010 | ||||||
| chr17:77994017
|
AC | A | 14 | a0001c0001t0029g0239a0001c0004t0006g0242a0001c0004t0006g0244others(11): Show | 14 | HG02258.hp1 HG02486.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.-37-10149delC | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 77994017 | |||||
| chr17:77994067
|
C | T | 1 | a0001c0002t0039g0057 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-37-10103C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77994067 | ||||||
| chr17:77994124
|
C | T | 1 | a0001c0006t0033g0252 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-37-10046C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77994124 | ||||||
| chr17:77994487
|
A | C | 2 | a0001c0001t0017g0266a0001c0001t0017g0267 | 2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-37-9683A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77994487 | ||||||
| chr17:77994748
|
A | C | 2 | a0001c0001t0001g0208a0001c0007t0012g0270 | 2 | HG02145.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.-37-9422A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77994748 | ||||||
| chr17:77994806
|
C | T | 1 | a0001c0002t0031g0265 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-37-9364C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77994806 | ||||||
| chr17:77994854
|
T | C | 1 | a0002c0003t0003g0139 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-37-9316T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77994854 | ||||||
| chr17:77994876
|
T | C | 1 | a0008c0016t0001g0079 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-37-9294T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77994876 | ||||||
| chr17:77994961
|
A | G | 11 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(8): Show | 11 | HG02486.hp1 HG02622.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.-37-9209A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77994961 | ||||||
| chr17:77995205
|
C | T | 1 | a0001c0002t0031g0265 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-37-8965C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77995205 | ||||||
| chr17:77995336
|
C | T | 14 | a0001c0001t0029g0239a0001c0004t0006g0242a0001c0004t0006g0244others(11): Show | 14 | HG02258.hp1 HG02486.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.-37-8834C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77995336 | ||||||
| chr17:77995428
|
A | G | 1 | a0001c0001t0001g0087 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-37-8742A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77995428 | ||||||
| chr17:77995504
|
A | T | 2 | a0009c0015t0027g0264a0017c0017t0028g0263 | 2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.-37-8666A>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77995504 | ||||||
| chr17:77995562
|
G | A | 1 | a0001c0005t0001g0137 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-37-8608G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77995562 | ||||||
| chr17:77995721
|
TACAC | T | 6 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(3): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.-37-8434_-37-8431d others(6): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 77995721 | |||||
| chr17:77995735
|
C | G | 111 | a0001c0001t0001g0006a0001c0001t0001g0037a0001c0001t0001g0106others(108): Show | 114 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.-37-8435C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77995735 | ||||||
| chr17:77995942
|
C | A | 39 | a0001c0001t0017g0266a0001c0001t0017g0267a0001c0001t0029g0239others(36): Show | 39 | HG01943.hp1 HG02145.hp2 HG02155.hp1 others(36): Show |
intron_variant | MODIFIER | c.-37-8228C>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77995942 | ||||||
| chr17:77996013
|
C | T | 11 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(8): Show | 11 | HG02486.hp1 HG02622.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.-37-8157C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77996013 | ||||||
| chr17:77996074
|
AAAAC | A | 5 | a0001c0002t0013g0235a0001c0002t0013g0236a0001c0002t0013g0238others(2): Show | 5 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-37-8089_-37-8086d others(6): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 77996074 | |||||
| chr17:77996210
|
T | G | 3 | a0001c0007t0012g0268a0001c0007t0012g0269a0001c0007t0012g0270 | 3 | HG02145.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-37-7960T>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77996210 | ||||||
| chr17:77996612
|
A | G | 26 | a0001c0001t0029g0239a0001c0001t0030g0259a0001c0002t0031g0265others(23): Show | 26 | HG01943.hp1 HG02155.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.-37-7558A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77996612 | ||||||
| chr17:77996623
|
G | A | 4 | a0001c0001t0001g0170a0001c0009t0016g0140a0001c0009t0019g0171others(1): Show | 4 | HG00735.hp1 HG01167.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37-7547G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77996623 | ||||||
| chr17:77996811
|
G | T | 2 | a0001c0001t0029g0239a0001c0002t0031g0265 | 2 | HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-37-7359G>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77996811 | ||||||
| chr17:77996955
|
A | G | 5 | a0001c0001t0030g0259a0001c0004t0011g0257a0001c0004t0011g0261others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-37-7215A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77996955 | ||||||
| chr17:77996986
|
G | A | 1 | a0001c0001t0001g0093 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-37-7184G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77996986 | ||||||
| chr17:77997130
|
T | C | 2 | a0001c0001t0029g0239a0001c0002t0031g0265 | 2 | HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-37-7040T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77997130 | ||||||
| chr17:77997433
|
C | G | 11 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(8): Show | 11 | HG01243.hp1 HG01257.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.-37-6737C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77997433 | ||||||
| chr17:77997626
|
C | G | 1 | a0001c0001t0001g0203 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-37-6544C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77997626 | ||||||
| chr17:77997653
|
T | C | 1 | a0001c0001t0034g0188 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-37-6517T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77997653 | ||||||
| chr17:77997735
|
C | T | 5 | a0001c0002t0013g0235a0001c0002t0013g0236a0001c0002t0013g0238others(2): Show | 5 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-37-6435C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77997735 | ||||||
| chr17:77997745
|
C | G | 1 | a0001c0002t0002g0109 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-37-6425C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77997745 | ||||||
| chr17:77997780
|
G | A | 21 | a0001c0001t0029g0239a0001c0002t0031g0265a0001c0004t0006g0242others(18): Show | 21 | HG01943.hp1 HG02155.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.-37-6390G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77997780 | ||||||
| chr17:77997830
|
A | G | 8 | a0001c0005t0001g0001a0001c0005t0001g0007a0001c0005t0001g0008others(5): Show | 9 | HG02451.hp1 HG02630.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.-37-6340A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77997830 | ||||||
| chr17:77997899
|
C | A | 1 | a0001c0001t0001g0051 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-37-6271C>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77997899 | ||||||
| chr17:77997930
|
A | G | 15 | a0001c0001t0029g0239a0001c0002t0031g0265a0001c0004t0006g0242others(12): Show | 15 | HG02258.hp1 HG02486.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.-37-6240A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77997930 | ||||||
| chr17:77997978
|
A | C | 1 | a0002c0003t0003g0103 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-37-6192A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77997978 | ||||||
| chr17:77998080
|
C | G | 1 | a0001c0002t0031g0265 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-37-6090C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77998080 | ||||||
| chr17:77998769
|
T | C | 1 | a0001c0002t0031g0265 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-37-5401T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77998769 | ||||||
| chr17:77998866
|
A | G | 1 | a0017c0017t0028g0263 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-37-5304A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77998866 | ||||||
| chr17:77998965
|
G | T | 5 | a0001c0002t0013g0235a0001c0002t0013g0236a0001c0002t0013g0238others(2): Show | 5 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-37-5205G>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77998965 | ||||||
| chr17:77998972
|
C | T | 3 | a0001c0007t0012g0268a0001c0007t0012g0269a0001c0007t0012g0270 | 3 | HG02145.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-37-5198C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77998972 | ||||||
| chr17:77998992
|
A | G | 34 | a0001c0001t0001g0006a0002c0003t0003g0002a0002c0003t0003g0003others(31): Show | 36 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.-37-5178A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77998992 | ||||||
| chr17:77999094
|
T | C | 1 | a0017c0017t0028g0263 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-37-5076T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77999094 | ||||||
| chr17:77999126
|
G | A | 12 | a0001c0001t0001g0043a0001c0001t0001g0221a0001c0001t0001g0222others(9): Show | 12 | HG00280.hp1 HG01243.hp1 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-37-5044G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77999126 | ||||||
| chr17:77999258
|
C | T | 1 | a0001c0002t0002g0107 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-37-4912C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77999258 | ||||||
| chr17:77999274
|
C | T | 1 | a0001c0001t0004g0193 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-37-4896C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77999274 | ||||||
| chr17:77999366
|
A | G | 3 | a0002c0003t0003g0004a0002c0003t0003g0186a0002c0027t0003g0004 | 3 | HG01884.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-37-4804A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77999366 | ||||||
| chr17:77999401
|
A | T | 1 | a0001c0001t0001g0025 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-37-4769A>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77999401 | ||||||
| chr17:77999481
|
CGTT | C | 6 | a0001c0002t0013g0235a0001c0002t0013g0236a0001c0002t0013g0238others(3): Show | 6 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37-4671_-37-4669d others(5): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 77999481 | |||||
| chr17:77999513
|
G | A | 1 | a0008c0028t0023g0258 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-37-4657G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77999513 | ||||||
| chr17:77999597
|
G | A | 5 | a0001c0001t0001g0106a0001c0001t0001g0127a0001c0001t0051g0105others(2): Show | 5 | HG00558.hp2 HG02027.hp2 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.-37-4573G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77999597 | ||||||
| chr17:77999748
|
C | T | 10 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0131others(7): Show | 10 | HG00280.hp2 HG00642.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.-37-4422C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77999748 | ||||||
| chr17:77999789
|
G | A | 11 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(8): Show | 11 | HG02486.hp1 HG02622.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.-37-4381G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 77999789 | ||||||
| chr17:78000159
|
T | G | 2 | a0001c0002t0061g0232a0001c0002t0062g0231 | 2 | HG04115.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-37-4011T>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 78000159 | ||||||
| chr17:78000618
|
G | GC | 27 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0041others(24): Show | 27 | HG00323.hp1 HG00558.hp1 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.-37-3539dupC | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 78000618 | |||||
| chr17:78000618
|
G | GCC | 72 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(69): Show | 72 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.-37-3540_-37-3539d others(4): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 78000618 | |||||
| chr17:78000618
|
G | GCCC | 17 | a0001c0001t0001g0040a0001c0001t0001g0052a0001c0001t0001g0090others(14): Show | 17 | HG00673.hp1 HG01106.hp2 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.-37-3541_-37-3539d others(5): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 78000618 | |||||
| chr17:78000618
|
G | GCCCCCCC others(3): Show |
1 | a0013c0026t0002g0118 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-37-3548_-37-3539d others(12): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 78000618 | |||||
| chr17:78000618
|
G | GCCCCCCC others(4): Show |
1 | a0001c0002t0002g0122 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-37-3549_-37-3539d others(13): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 78000618 | |||||
| chr17:78000630
|
C | A | 3 | a0001c0001t0001g0128a0002c0003t0003g0178a0002c0003t0020g0182 | 3 | HG01081.hp1 HG01361.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-37-3540C>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 78000630 | ||||||
| chr17:78000630
|
C | CA | 3 | a0001c0001t0005g0086a0001c0002t0013g0236a0001c0002t0018g0237 | 3 | HG02280.hp1 HG02965.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-37-3540_-37-3539i others(3): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 78000630 | ||||||
| chr17:78000630
|
C | CACACA | 15 | a0001c0001t0001g0021a0002c0003t0003g0002a0002c0003t0003g0012others(12): Show | 16 | HG01070.hp2 HG01071.hp2 HG02080.hp1 others(13): Show |
intron_variant | MODIFIER | c.-37-3540_-37-3539i others(7): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 78000630 | ||||||
| chr17:78000630
|
C | CCA | 14 | a0001c0001t0017g0266a0001c0001t0017g0267a0001c0002t0013g0235others(11): Show | 14 | HG02486.hp1 HG02622.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.-37-3529_-37-3528d others(4): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 78000630 | |||||
| chr17:78000630
|
C | CCCCCCCC others(4): Show |
2 | a0001c0001t0004g0124a0001c0001t0004g0143 | 2 | HG01934.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.-37-3539_-37-3538i others(13): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | 78000630 | |||||
| chr17:78000632
|
A | C | 4 | a0001c0001t0029g0239a0001c0002t0061g0232a0001c0002t0062g0231others(1): Show | 4 | HG02615.hp1 HG03098.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37-3538A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 78000632 | ||||||
| chr17:78000634
|
A | C | 1 | a0017c0017t0028g0263 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-37-3536A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 78000634 | ||||||
| chr17:78000652
|
A | G | 6 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0005t0001g0001others(3): Show | 7 | HG02630.hp1 HG02717.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-37-3518A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 78000652 | ||||||
| chr17:78000860
|
T | A | 13 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(10): Show | 13 | HG01243.hp1 HG01257.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.-37-3310T>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 78000860 | ||||||
| chr17:78000921
|
A | G | 5 | a0001c0001t0030g0259a0001c0004t0011g0257a0001c0004t0011g0261others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-37-3249A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 78000921 | ||||||
| chr17:78001079
|
C | T | 3 | a0001c0007t0012g0268a0001c0007t0012g0269a0001c0007t0012g0270 | 3 | HG02145.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-37-3091C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 78001079 | ||||||
| chr17:78001226
|
C | T | 31 | a0001c0001t0001g0106a0001c0001t0051g0105a0001c0002t0002g0005others(28): Show | 31 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.-37-2944C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 78001226 | ||||||
| chr17:78001320
|
G | T | 11 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(8): Show | 11 | HG02486.hp1 HG02622.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.-37-2850G>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 78001320 | ||||||
| chr17:78001451
|
G | A | 6 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(3): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.-37-2719G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 78001451 | ||||||
| chr17:78001458
|
T | C | 1 | a0001c0001t0004g0172 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-37-2712T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 78001458 | ||||||
| chr17:78001569
|
G | C | 5 | a0001c0001t0030g0259a0001c0004t0011g0257a0001c0004t0011g0261others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-37-2601G>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 78001569 | ||||||
| chr17:78001939
|
T | G | 8 | a0001c0005t0001g0001a0001c0005t0001g0007a0001c0005t0001g0008others(5): Show | 9 | HG02451.hp1 HG02630.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.-37-2231T>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 78001939 | ||||||
| chr17:78002079
|
C | G | 11 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(8): Show | 11 | HG02486.hp1 HG02622.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.-37-2091C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 78002079 | ||||||
| chr17:78002208
|
A | G | 1 | a0001c0002t0031g0265 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-37-1962A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 78002208 | ||||||
| chr17:78002280
|
G | A | 1 | a0002c0003t0003g0194 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-37-1890G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 78002280 | ||||||
| chr17:78002289
|
A | G | 159 | a0001c0001t0001g0006a0001c0001t0001g0106a0001c0001t0001g0127others(156): Show | 162 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.-37-1881A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 78002289 | ||||||
| chr17:78002312
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-37-1858G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 78002312 | ||||||
| chr17:78002397
|
C | T | 11 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(8): Show | 11 | HG01243.hp1 HG01257.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.-37-1773C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 78002397 | ||||||
| chr17:78002469
|
A | C | 1 | a0001c0001t0001g0016 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-37-1701A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 78002469 | ||||||
| chr17:78002546
|
A | G | 1 | a0001c0001t0001g0016 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-37-1624A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 78002546 | ||||||
| chr17:78002650
|
T | C | 1 | a0001c0002t0002g0200 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-37-1520T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 78002650 | ||||||
| chr17:78002692
|
A | C | 109 | a0001c0001t0001g0006a0001c0001t0001g0106a0001c0001t0001g0127others(106): Show | 112 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.-37-1478A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 78002692 | ||||||
| chr17:78003035
|
G | T | 5 | a0001c0001t0030g0259a0001c0004t0011g0257a0001c0004t0011g0261others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-37-1135G>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 78003035 | ||||||
| chr17:78003123
|
C | G | 6 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(3): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.-37-1047C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 78003123 | ||||||
| chr17:78003318
|
A | C | 1 | a0001c0006t0008g0256 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-37-852A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 78003318 | ||||||
| chr17:78003353
|
A | C | 37 | a0001c0001t0017g0266a0001c0001t0017g0267a0001c0001t0029g0239others(34): Show | 37 | HG01943.hp1 HG02145.hp2 HG02155.hp1 others(34): Show |
intron_variant | MODIFIER | c.-37-817A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 78003353 | ||||||
| chr17:78003660
|
A | G | 1 | a0002c0003t0003g0178 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-37-510A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 78003660 | ||||||
| chr17:78003730
|
C | A | 2 | a0001c0001t0017g0266a0001c0001t0017g0267 | 2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-37-440C>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 78003730 | ||||||
| chr17:78003785
|
C | T | 6 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(3): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.-37-385C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 78003785 | ||||||
| chr17:78003818
|
C | T | 1 | a0001c0002t0031g0265 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-37-352C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 78003818 | ||||||
| chr17:78004061
|
G | T | 1 | a0008c0028t0023g0258 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-37-109G>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 78004061 | ||||||
| chr17:78004071
|
T | C | 5 | a0001c0001t0030g0259a0001c0004t0011g0257a0001c0004t0011g0261others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-37-99T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 78004071 | ||||||
| chr17:78004421
|
A | T | 1 | a0001c0001t0001g0016 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.63+152A>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 2/22 | chr17 | 78004421 | ||||||
| chr17:78004492
|
T | C | 159 | a0001c0001t0001g0006a0001c0001t0001g0106a0001c0001t0001g0127others(156): Show | 162 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.63+223T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 2/22 | chr17 | 78004492 | ||||||
| chr17:78004690
|
T | C | 3 | a0001c0001t0017g0266a0001c0001t0017g0267a0001c0001t0029g0239 | 3 | HG02622.hp1 HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.64-368T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 2/22 | chr17 | 78004690 | ||||||
| chr17:78004768
|
T | TTTAATGT others(16): Show |
1 | a0001c0001t0001g0016 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.64-289_64-267dupTT others(21): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr17 | 78004768 | |||||
| chr17:78004848
|
T | C | 1 | a0017c0017t0028g0263 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.64-210T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 2/22 | chr17 | 78004848 | ||||||
| chr17:78005048
|
T | C | 1 | a0001c0002t0002g0211 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.64-10T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 2/22 | chr17 | 78005048 | ||||||
| chr17:78005298
|
A | T | 11 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(8): Show | 11 | HG01243.hp1 HG01257.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.85+219A>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78005298 | ||||||
| chr17:78005360
|
T | G | 1 | a0002c0003t0025g0241 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.85+281T>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78005360 | ||||||
| chr17:78005399
|
A | G | 8 | a0001c0005t0001g0001a0001c0005t0001g0007a0001c0005t0001g0008others(5): Show | 9 | HG02451.hp1 HG02630.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.85+320A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78005399 | ||||||
| chr17:78006389
|
A | G | 2 | a0001c0001t0005g0023a0001c0001t0005g0086 | 2 | HG02145.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.85+1310A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78006389 | ||||||
| chr17:78006485
|
CTTCTTCT | C | 5 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(2): Show | 5 | HG01243.hp1 HG02258.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.85+1415_85+1421del others(7): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 78006485 | |||||
| chr17:78006488
|
CTTCT | C | 6 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(3): Show | 6 | HG01257.hp2 HG02055.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.85+1415_85+1418del others(4): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 78006488 | |||||
| chr17:78006489
|
TTCTTTCT others(14): Show |
T | 1 | a0001c0004t0006g0244 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.85+1412_85+1432del others(21): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 78006489 | |||||
| chr17:78006491
|
CTTTCTTC others(7): Show |
C | 1 | a0001c0001t0016g0142 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.85+1414_85+1427del others(14): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 78006491 | |||||
| chr17:78006492
|
T | TTCTTCTT others(4): Show |
1 | a0001c0001t0001g0093 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.85+1414_85+1415ins others(11): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 78006492 | |||||
| chr17:78006492
|
T | TTTC | 19 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0029others(16): Show | 19 | HG01081.hp2 HG01261.hp1 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.85+1480_85+1482dup others(3): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 78006492 | |||||
| chr17:78006492
|
T | TTTCTTC | 7 | a0001c0001t0001g0045a0001c0001t0001g0085a0001c0001t0001g0203others(4): Show | 7 | HG02080.hp2 HG02155.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.85+1477_85+1482dup others(6): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 78006492 | |||||
| chr17:78006492
|
T | TTTCTTCT others(3): Show |
1 | a0001c0001t0001g0016 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.85+1421_85+1422ins others(10): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 78006492 | |||||
| chr17:78006492
|
TTTC | T | 31 | a0001c0001t0001g0032a0001c0001t0001g0040a0001c0001t0001g0041others(28): Show | 31 | HG00280.hp1 HG00280.hp2 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.85+1480_85+1482del others(3): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 78006492 | |||||
| chr17:78006492
|
TTTCTTC | T | 26 | a0001c0001t0001g0006a0001c0001t0001g0033a0001c0001t0001g0038others(23): Show | 26 | HG00423.hp1 HG00423.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.85+1477_85+1482del others(6): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 78006492 | |||||
| chr17:78006492
|
TTTCTTCT others(2): Show |
T | 44 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0021others(41): Show | 44 | HG00642.hp1 HG00735.hp2 HG01071.hp1 others(41): Show |
intron_variant | MODIFIER | c.85+1474_85+1482del others(9): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 78006492 | |||||
| chr17:78006492
|
TTTCTTCT others(5): Show |
T | 31 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030others(28): Show | 32 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.85+1471_85+1482del others(12): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 78006492 | |||||
| chr17:78006492
|
TTTCTTCT others(8): Show |
T | 21 | a0001c0001t0001g0067a0001c0001t0001g0185a0001c0001t0001g0207others(18): Show | 22 | HG01257.hp1 HG01884.hp2 HG02027.hp1 others(19): Show |
intron_variant | MODIFIER | c.85+1468_85+1482del others(15): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 78006492 | |||||
| chr17:78006492
|
TTTCTTCT others(11): Show |
T | 15 | a0001c0001t0001g0044a0001c0001t0001g0069a0001c0001t0001g0187others(12): Show | 15 | HG01167.hp2 HG01243.hp2 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.85+1465_85+1482del others(18): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 78006492 | |||||
| chr17:78006492
|
TTTCTTCT others(14): Show |
T | 6 | a0001c0001t0001g0059a0001c0002t0061g0232a0004c0008t0001g0073others(3): Show | 6 | HG01255.hp2 HG02083.hp2 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.85+1462_85+1482del others(21): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 78006492 | |||||
| chr17:78006492
|
TTTCTTCT others(17): Show |
T | 1 | a0001c0001t0005g0271 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.85+1459_85+1482del others(24): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 78006492 | |||||
| chr17:78006494
|
T | C | 2 | a0001c0001t0001g0230a0001c0001t0009g0155 | 2 | HG02717.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.85+1415T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78006494 | ||||||
| chr17:78006495
|
C | T | 2 | a0001c0001t0001g0230a0001c0001t0009g0155 | 2 | HG02717.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.85+1416C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78006495 | ||||||
| chr17:78006499
|
TTC | T | 6 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(3): Show | 6 | HG01257.hp2 HG02055.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.85+1422_85+1423del others(2): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 78006499 | |||||
| chr17:78006502
|
TTC | T | 4 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(1): Show | 4 | HG01243.hp1 HG02258.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.85+1425_85+1426del others(2): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 78006502 | |||||
| chr17:78006530
|
T | C | 2 | a0009c0015t0027g0264a0017c0017t0028g0263 | 2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.85+1451T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78006530 | ||||||
| chr17:78006542
|
TCTTCTTC others(12): Show |
T | 2 | a0002c0003t0020g0182a0007c0013t0022g0010 | 2 | HG02080.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.85+1471_85+1489del others(19): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 78006542 | |||||
| chr17:78006543
|
CTTCTTCT others(4): Show |
C | 3 | a0001c0007t0012g0268a0001c0007t0012g0269a0001c0007t0012g0270 | 3 | HG02145.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.85+1465_85+1475del others(11): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78006543 | ||||||
| chr17:78006546
|
CTTCTTCT others(25): Show |
C | 1 | a0001c0001t0017g0266 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.85+1468_85+1499del others(32): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78006546 | ||||||
| chr17:78006549
|
CTTCTTCT others(22): Show |
C | 1 | a0001c0001t0017g0267 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.85+1471_85+1499del others(29): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78006549 | ||||||
| chr17:78006551
|
TCTTCTTC others(3): Show |
T | 1 | a0001c0006t0008g0251 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.85+1480_85+1489del others(10): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 78006551 | |||||
| chr17:78006552
|
CTT | C | 4 | a0001c0005t0001g0001a0001c0005t0001g0145a0001c0005t0001g0146others(1): Show | 5 | HG02615.hp1 HG02630.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.85+1474_85+1475del others(2): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78006552 | ||||||
| chr17:78006557
|
TCTTC | T | 4 | a0001c0001t0001g0230a0001c0006t0008g0253a0001c0006t0008g0256others(1): Show | 4 | HG01943.hp1 HG02717.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.85+1483_85+1486del others(4): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 78006557 | |||||
| chr17:78006559
|
T | C | 1 | a0001c0002t0031g0265 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.85+1480T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78006559 | ||||||
| chr17:78006561
|
C | T | 1 | a0001c0002t0031g0265 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.85+1482C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78006561 | ||||||
| chr17:78006578
|
T | C | 1 | a0001c0002t0031g0265 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.85+1499T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78006578 | ||||||
| chr17:78006583
|
T | C | 1 | a0009c0015t0027g0264 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.85+1504T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78006583 | ||||||
| chr17:78006583
|
T | TTCCTTCT others(10): Show |
1 | a0017c0017t0028g0263 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.85+1521_85+1537dup others(17): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 78006583 | |||||
| chr17:78006595
|
T | C | 11 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(8): Show | 11 | HG02486.hp1 HG02622.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.85+1516T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78006595 | ||||||
| chr17:78006620
|
T | C | 32 | a0001c0001t0017g0266a0001c0001t0017g0267a0001c0001t0029g0239others(29): Show | 32 | HG01943.hp1 HG02145.hp2 HG02155.hp1 others(29): Show |
intron_variant | MODIFIER | c.85+1541T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78006620 | ||||||
| chr17:78006632
|
C | CCTT | 24 | a0001c0002t0031g0265a0001c0004t0006g0242a0001c0004t0006g0244others(21): Show | 24 | HG01943.hp1 HG02145.hp2 HG02155.hp1 others(21): Show |
intron_variant | MODIFIER | c.85+1560_85+1562dup others(3): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 78006632 | |||||
| chr17:78006690
|
C | T | 1 | a0001c0001t0004g0124 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.85+1611C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78006690 | ||||||
| chr17:78006774
|
A | G | 7 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0028others(4): Show | 7 | HG00323.hp1 HG00735.hp2 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.85+1695A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78006774 | ||||||
| chr17:78006808
|
T | TTTTA | 9 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(6): Show | 9 | HG01243.hp1 HG01257.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.85+1749_85+1752dup others(4): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 78006808 | |||||
| chr17:78006808
|
T | TTTTATTT others(1): Show |
3 | a0001c0001t0001g0020a0001c0001t0001g0070a0001c0001t0001g0091 | 3 | HG02602.hp2 HG02698.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.85+1745_85+1752dup others(8): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 78006808 | |||||
| chr17:78006827
|
T | A | 1 | a0009c0015t0027g0264 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.85+1748T>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78006827 | ||||||
| chr17:78006828
|
A | T | 6 | a0001c0001t0001g0028a0001c0001t0001g0202a0001c0001t0063g0042others(3): Show | 6 | HG02258.hp1 HG03579.hp2 HG04228.hp2 others(3): Show |
intron_variant | MODIFIER | c.85+1749A>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78006828 | ||||||
| chr17:78006828
|
ATT | A | 12 | a0001c0002t0031g0265a0001c0004t0006g0242a0001c0004t0006g0244others(9): Show | 12 | HG02486.hp1 HG02615.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.85+1762_85+1763del others(2): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 78006828 | |||||
| chr17:78006832
|
T | A | 155 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0020others(152): Show | 158 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.85+1753T>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78006832 | ||||||
| chr17:78006834
|
T | A | 2 | a0002c0003t0025g0241a0008c0028t0023g0258 | 2 | HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.85+1755T>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78006834 | ||||||
| chr17:78006836
|
T | A | 9 | a0001c0001t0001g0096a0001c0001t0004g0189a0001c0001t0015g0014others(6): Show | 9 | HG01884.hp2 HG02622.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.85+1757T>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78006836 | ||||||
| chr17:78006841
|
T | C | 1 | a0001c0001t0004g0191 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.85+1762T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78006841 | ||||||
| chr17:78007029
|
G | A | 1 | a0002c0003t0003g0210 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.85+1950G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78007029 | ||||||
| chr17:78007081
|
G | A | 6 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(3): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.85+2002G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78007081 | ||||||
| chr17:78007200
|
T | C | 2 | a0009c0015t0027g0264a0017c0017t0028g0263 | 2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.85+2121T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78007200 | ||||||
| chr17:78007998
|
A | C | 1 | a0001c0001t0017g0267 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.85+2919A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78007998 | ||||||
| chr17:78008304
|
A | G | 1 | a0002c0003t0003g0103 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.85+3225A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78008304 | ||||||
| chr17:78008587
|
C | G | 1 | a0001c0001t0036g0066 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.85+3508C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78008587 | ||||||
| chr17:78008639
|
T | C | 5 | a0001c0002t0013g0235a0001c0002t0013g0236a0001c0002t0013g0238others(2): Show | 5 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.85+3560T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78008639 | ||||||
| chr17:78009239
|
A | C | 2 | a0002c0003t0003g0002a0002c0003t0057g0158 | 3 | HG01070.hp2 HG01071.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.85+4160A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78009239 | ||||||
| chr17:78009382
|
T | A | 1 | a0001c0001t0001g0091 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.85+4303T>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78009382 | ||||||
| chr17:78009596
|
C | T | 1 | a0001c0001t0042g0099 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.85+4517C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78009596 | ||||||
| chr17:78009697
|
G | A | 5 | a0001c0002t0013g0235a0001c0002t0013g0236a0001c0002t0013g0238others(2): Show | 5 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.85+4618G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78009697 | ||||||
| chr17:78009805
|
G | A | 2 | a0001c0006t0008g0256a0001c0006t0032g0254 | 2 | HG01943.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.85+4726G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78009805 | ||||||
| chr17:78009856
|
A | C | 1 | a0001c0001t0001g0208 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.85+4777A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78009856 | ||||||
| chr17:78009858
|
T | A | 1 | a0008c0028t0023g0258 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.85+4779T>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78009858 | ||||||
| chr17:78009915
|
A | T | 5 | a0001c0001t0030g0259a0001c0004t0011g0257a0001c0004t0011g0261others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.85+4836A>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78009915 | ||||||
| chr17:78009945
|
A | G | 14 | a0001c0002t0031g0265a0001c0004t0006g0242a0001c0004t0006g0244others(11): Show | 14 | HG02258.hp1 HG02486.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.85+4866A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78009945 | ||||||
| chr17:78010258
|
T | C | 1 | a0001c0001t0001g0075 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.85+5179T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78010258 | ||||||
| chr17:78010260
|
C | A | 1 | a0001c0001t0001g0075 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.85+5181C>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78010260 | ||||||
| chr17:78010261
|
G | C | 1 | a0001c0001t0001g0075 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.85+5182G>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78010261 | ||||||
| chr17:78010262
|
T | A | 1 | a0001c0001t0001g0075 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.85+5183T>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78010262 | ||||||
| chr17:78010263
|
T | C | 1 | a0001c0001t0001g0075 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.85+5184T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78010263 | ||||||
| chr17:78010264
|
C | G | 1 | a0001c0001t0001g0075 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.85+5185C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78010264 | ||||||
| chr17:78010266
|
G | C | 1 | a0001c0001t0001g0075 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.85+5187G>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78010266 | ||||||
| chr17:78010267
|
T | G | 1 | a0001c0001t0001g0075 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.85+5188T>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78010267 | ||||||
| chr17:78010268
|
T | A | 1 | a0001c0001t0001g0075 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.85+5189T>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78010268 | ||||||
| chr17:78010530
|
A | T | 6 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(3): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.85+5451A>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78010530 | ||||||
| chr17:78010723
|
T | C | 1 | a0001c0001t0001g0209 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.85+5644T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78010723 | ||||||
| chr17:78010805
|
CA | C | 11 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(8): Show | 11 | HG01243.hp1 HG01257.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.85+5734delA | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 78010805 | |||||
| chr17:78010821
|
A | G | 1 | a0001c0002t0031g0265 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.85+5742A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78010821 | ||||||
| chr17:78010857
|
G | A | 11 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(8): Show | 11 | HG01243.hp1 HG01257.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.85+5778G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78010857 | ||||||
| chr17:78010899
|
G | A | 1 | a0001c0005t0001g0146 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.85+5820G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78010899 | ||||||
| chr17:78011279
|
A | G | 1 | a0016c0023t0045g0192 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.85+6200A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78011279 | ||||||
| chr17:78011343
|
A | G | 1 | a0001c0002t0031g0265 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.85+6264A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78011343 | ||||||
| chr17:78011490
|
A | G | 6 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(3): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.85+6411A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78011490 | ||||||
| chr17:78011565
|
A | G | 1 | a0002c0003t0003g0011 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.85+6486A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78011565 | ||||||
| chr17:78011601
|
C | T | 2 | a0006c0011t0001g0159a0006c0011t0001g0160 | 2 | HG01243.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.85+6522C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78011601 | ||||||
| chr17:78011602
|
G | A | 1 | a0001c0002t0031g0265 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.85+6523G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78011602 | ||||||
| chr17:78011699
|
A | G | 1 | a0002c0003t0003g0194 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.85+6620A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78011699 | ||||||
| chr17:78011748
|
G | T | 1 | a0001c0006t0033g0252 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.85+6669G>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78011748 | ||||||
| chr17:78011774
|
G | A | 1 | a0001c0001t0001g0208 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.85+6695G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78011774 | ||||||
| chr17:78011800
|
A | G | 2 | a0001c0001t0017g0266a0001c0001t0017g0267 | 2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.85+6721A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78011800 | ||||||
| chr17:78011808
|
C | T | 3 | a0001c0007t0012g0268a0001c0007t0012g0269a0001c0007t0012g0270 | 3 | HG02145.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.85+6729C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78011808 | ||||||
| chr17:78011843
|
A | C | 34 | a0001c0001t0001g0006a0002c0003t0003g0002a0002c0003t0003g0003others(31): Show | 36 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.85+6764A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78011843 | ||||||
| chr17:78011967
|
G | C | 2 | a0001c0001t0004g0157a0001c0001t0004g0172 | 2 | HG02293.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.85+6888G>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78011967 | ||||||
| chr17:78012060
|
G | GCTTA | 15 | a0001c0001t0029g0239a0001c0002t0031g0265a0001c0004t0006g0242others(12): Show | 15 | HG02258.hp1 HG02486.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.85+6981_85+6982ins others(4): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78012060 | ||||||
| chr17:78012249
|
ATTAAC | A | 6 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(3): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.85+7175_85+7179del others(5): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 78012249 | |||||
| chr17:78012332
|
T | G | 13 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(10): Show | 13 | HG02258.hp1 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.85+7253T>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78012332 | ||||||
| chr17:78012355
|
A | G | 1 | a0001c0002t0031g0265 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.85+7276A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78012355 | ||||||
| chr17:78012404
|
C | T | 26 | a0001c0001t0001g0106a0001c0001t0051g0105a0001c0002t0002g0005others(23): Show | 26 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.85+7325C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78012404 | ||||||
| chr17:78012507
|
A | T | 20 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(17): Show | 20 | HG01243.hp1 HG01257.hp2 HG01943.hp1 others(17): Show |
intron_variant | MODIFIER | c.85+7428A>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78012507 | ||||||
| chr17:78012528
|
A | C | 1 | a0017c0017t0028g0263 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.85+7449A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78012528 | ||||||
| chr17:78012553
|
G | C | 1 | a0001c0001t0001g0040 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.85+7474G>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78012553 | ||||||
| chr17:78012575
|
T | C | 1 | a0001c0001t0029g0239 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.85+7496T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78012575 | ||||||
| chr17:78012576
|
A | G | 36 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(33): Show | 36 | HG01243.hp1 HG01257.hp2 HG01943.hp1 others(33): Show |
intron_variant | MODIFIER | c.85+7497A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78012576 | ||||||
| chr17:78012648
|
A | G | 1 | a0001c0002t0002g0110 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.85+7569A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78012648 | ||||||
| chr17:78012750
|
G | A | 6 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(3): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.85+7671G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78012750 | ||||||
| chr17:78012753
|
G | C | 6 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(3): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.85+7674G>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78012753 | ||||||
| chr17:78012952
|
C | G | 14 | a0001c0002t0031g0265a0001c0004t0006g0242a0001c0004t0006g0244others(11): Show | 14 | HG02258.hp1 HG02486.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.85+7873C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78012952 | ||||||
| chr17:78013113
|
C | CA | 14 | a0001c0002t0031g0265a0001c0004t0006g0242a0001c0004t0006g0244others(11): Show | 14 | HG02258.hp1 HG02486.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.85+8040dupA | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 78013113 | |||||
| chr17:78013223
|
G | A | 15 | a0001c0001t0017g0266a0001c0001t0017g0267a0001c0001t0030g0259others(12): Show | 15 | HG02145.hp2 HG02280.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.85+8144G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78013223 | ||||||
| chr17:78013582
|
G | C | 2 | a0001c0001t0017g0266a0001c0001t0017g0267 | 2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.85+8503G>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78013582 | ||||||
| chr17:78013704
|
A | G | 1 | a0001c0001t0029g0239 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.85+8625A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78013704 | ||||||
| chr17:78013718
|
C | CT | 7 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(4): Show | 7 | HG02486.hp1 HG02622.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.85+8640dupT | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 78013718 | |||||
| chr17:78013799
|
G | A | 1 | a0001c0001t0041g0129 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.85+8720G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78013799 | ||||||
| chr17:78014021
|
A | C | 15 | a0001c0001t0029g0239a0001c0002t0031g0265a0001c0004t0006g0242others(12): Show | 15 | HG02258.hp1 HG02486.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.85+8942A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78014021 | ||||||
| chr17:78014040
|
C | T | 10 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0131others(7): Show | 10 | HG00280.hp2 HG00642.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.85+8961C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78014040 | ||||||
| chr17:78014419
|
T | C | 1 | a0001c0001t0001g0219 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.85+9340T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78014419 | ||||||
| chr17:78014482
|
A | G | 1 | a0001c0002t0031g0265 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.85+9403A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78014482 | ||||||
| chr17:78014861
|
C | T | 2 | a0001c0001t0005g0023a0001c0001t0005g0086 | 2 | HG02145.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.85+9782C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78014861 | ||||||
| chr17:78014893
|
C | G | 2 | a0009c0015t0027g0264a0017c0017t0028g0263 | 2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.85+9814C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78014893 | ||||||
| chr17:78014981
|
G | T | 2 | a0001c0001t0001g0021a0001c0001t0001g0090 | 2 | NA18747.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.85+9902G>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78014981 | ||||||
| chr17:78015068
|
A | T | 1 | a0001c0001t0029g0239 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.85+9989A>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78015068 | ||||||
| chr17:78015218
|
C | T | 14 | a0001c0002t0031g0265a0001c0004t0006g0242a0001c0004t0006g0244others(11): Show | 14 | HG02258.hp1 HG02486.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.85+10139C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78015218 | ||||||
| chr17:78015281
|
C | T | 1 | a0002c0003t0003g0178 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.85+10202C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78015281 | ||||||
| chr17:78015282
|
G | A | 2 | a0001c0001t0001g0068a0001c0001t0001g0215 | 2 | NA18939.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.85+10203G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78015282 | ||||||
| chr17:78015413
|
ATT | A | 14 | a0001c0002t0031g0265a0001c0004t0006g0242a0001c0004t0006g0244others(11): Show | 14 | HG02258.hp1 HG02486.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.85+10338_85+10339d others(4): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 78015413 | |||||
| chr17:78015605
|
A | T | 10 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0131others(7): Show | 10 | HG00280.hp2 HG00642.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.85+10526A>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78015605 | ||||||
| chr17:78015691
|
C | T | 5 | a0001c0002t0013g0235a0001c0002t0013g0236a0001c0002t0013g0238others(2): Show | 5 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.85+10612C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78015691 | ||||||
| chr17:78015739
|
G | T | 1 | a0017c0017t0028g0263 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.85+10660G>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78015739 | ||||||
| chr17:78015792
|
A | T | 1 | a0002c0003t0056g0150 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.85+10713A>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78015792 | ||||||
| chr17:78015843
|
C | T | 11 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(8): Show | 11 | HG02486.hp1 HG02622.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.85+10764C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78015843 | ||||||
| chr17:78015970
|
G | A | 1 | a0016c0023t0045g0192 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.85+10891G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78015970 | ||||||
| chr17:78016153
|
C | G | 3 | a0001c0007t0012g0268a0001c0007t0012g0269a0001c0007t0012g0270 | 3 | HG02145.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.85+11074C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78016153 | ||||||
| chr17:78016173
|
T | C | 14 | a0001c0002t0031g0265a0001c0004t0006g0242a0001c0004t0006g0244others(11): Show | 14 | HG02258.hp1 HG02486.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.85+11094T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78016173 | ||||||
| chr17:78016201
|
G | C | 1 | a0001c0001t0001g0219 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.85+11122G>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78016201 | ||||||
| chr17:78016249
|
C | T | 1 | a0001c0002t0031g0265 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.85+11170C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78016249 | ||||||
| chr17:78016533
|
G | A | 5 | a0001c0001t0030g0259a0001c0004t0011g0257a0001c0004t0011g0261others(2): Show | 5 | HG02717.hp1 HG02818.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.85+11454G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78016533 | ||||||
| chr17:78016558
|
G | A | 1 | a0016c0023t0045g0192 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.85+11479G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78016558 | ||||||
| chr17:78016580
|
G | A | 3 | a0001c0001t0001g0209a0001c0001t0001g0216a0001c0001t0001g0217 | 3 | NA18990.hp2 NA19002.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.85+11501G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78016580 | ||||||
| chr17:78016606
|
T | A | 1 | a0001c0002t0002g0108 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.85+11527T>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78016606 | ||||||
| chr17:78016632
|
T | G | 15 | a0001c0001t0029g0239a0001c0002t0031g0265a0001c0004t0006g0242others(12): Show | 15 | HG02258.hp1 HG02486.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.85+11553T>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78016632 | ||||||
| chr17:78016728
|
T | C | 5 | a0001c0002t0013g0235a0001c0002t0013g0236a0001c0002t0013g0238others(2): Show | 5 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.85+11649T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78016728 | ||||||
| chr17:78016769
|
T | C | 1 | a0001c0001t0001g0214 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.85+11690T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78016769 | ||||||
| chr17:78016773
|
C | T | 107 | a0001c0001t0001g0006a0001c0001t0001g0106a0001c0001t0001g0127others(104): Show | 110 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.85+11694C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78016773 | ||||||
| chr17:78016856
|
G | A | 11 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(8): Show | 11 | HG01243.hp1 HG01257.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.85+11777G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78016856 | ||||||
| chr17:78017297
|
G | A | 2 | a0009c0015t0027g0264a0017c0017t0028g0263 | 2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.85+12218G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78017297 | ||||||
| chr17:78017306
|
C | T | 26 | a0001c0001t0001g0106a0001c0001t0051g0105a0001c0002t0002g0005others(23): Show | 26 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.85+12227C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78017306 | ||||||
| chr17:78017317
|
T | TC | 35 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(32): Show | 35 | HG01243.hp1 HG01257.hp2 HG01943.hp1 others(32): Show |
intron_variant | MODIFIER | c.85+12240dupC | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 78017317 | |||||
| chr17:78017334
|
G | C | 1 | a0001c0001t0036g0066 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.85+12255G>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78017334 | ||||||
| chr17:78017444
|
C | G | 5 | a0001c0002t0013g0235a0001c0002t0013g0236a0001c0002t0013g0238others(2): Show | 5 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.85+12365C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78017444 | ||||||
| chr17:78017461
|
A | G | 1 | a0001c0006t0033g0252 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.85+12382A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78017461 | ||||||
| chr17:78017565
|
T | TAGC | 5 | a0001c0001t0001g0020a0001c0001t0001g0070a0001c0001t0001g0081others(2): Show | 5 | HG02602.hp2 HG02698.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.85+12488_85+12490d others(5): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 78017565 | |||||
| chr17:78017917
|
C | T | 1 | a0003c0021t0002g0113 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.85+12838C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78017917 | ||||||
| chr17:78017966
|
G | A | 5 | a0001c0002t0013g0235a0001c0002t0013g0236a0001c0002t0013g0238others(2): Show | 5 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.85+12887G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78017966 | ||||||
| chr17:78018288
|
G | A | 1 | a0001c0001t0021g0061 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.85+13209G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78018288 | ||||||
| chr17:78018315
|
A | C | 1 | a0001c0001t0029g0239 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.86-13201A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78018315 | ||||||
| chr17:78018419
|
A | G | 1 | a0008c0028t0023g0258 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.86-13097A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78018419 | ||||||
| chr17:78018488
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.86-13028C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78018488 | ||||||
| chr17:78018508
|
A | G | 1 | a0003c0012t0001g0022 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.86-13008A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78018508 | ||||||
| chr17:78018541
|
G | T | 41 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(38): Show | 41 | HG01243.hp1 HG01257.hp2 HG02055.hp1 others(38): Show |
intron_variant | MODIFIER | c.86-12975G>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78018541 | ||||||
| chr17:78018543
|
G | C | 1 | a0001c0002t0031g0265 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.86-12973G>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78018543 | ||||||
| chr17:78018584
|
C | T | 2 | a0001c0001t0017g0266a0001c0001t0017g0267 | 2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.86-12932C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78018584 | ||||||
| chr17:78018954
|
A | G | 48 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(45): Show | 48 | HG01243.hp1 HG01257.hp2 HG01943.hp1 others(45): Show |
intron_variant | MODIFIER | c.86-12562A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78018954 | ||||||
| chr17:78018997
|
T | G | 5 | a0001c0002t0013g0235a0001c0002t0013g0236a0001c0002t0013g0238others(2): Show | 5 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.86-12519T>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78018997 | ||||||
| chr17:78018998
|
TTC | T | 5 | a0001c0002t0013g0235a0001c0002t0013g0236a0001c0002t0013g0238others(2): Show | 5 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.86-12516_86-12515d others(4): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 78018998 | |||||
| chr17:78019205
|
A | G | 9 | a0001c0001t0004g0124a0001c0001t0004g0189a0001c0001t0004g0190others(6): Show | 9 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.86-12311A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78019205 | ||||||
| chr17:78019330
|
A | C | 23 | a0001c0001t0001g0006a0002c0003t0003g0002a0002c0003t0003g0003others(20): Show | 25 | HG01070.hp2 HG01071.hp2 HG02040.hp2 others(22): Show |
intron_variant | MODIFIER | c.86-12186A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78019330 | ||||||
| chr17:78019547
|
A | G | 1 | a0001c0001t0048g0046 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.86-11969A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78019547 | ||||||
| chr17:78019662
|
G | T | 1 | a0002c0003t0007g0102 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.86-11854G>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78019662 | ||||||
| chr17:78019769
|
T | C | 2 | a0009c0015t0027g0264a0017c0017t0028g0263 | 2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.86-11747T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78019769 | ||||||
| chr17:78019796
|
G | A | 1 | a0002c0003t0025g0241 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.86-11720G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78019796 | ||||||
| chr17:78020151
|
C | T | 1 | a0001c0001t0001g0024 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.86-11365C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78020151 | ||||||
| chr17:78020273
|
C | T | 5 | a0001c0002t0013g0235a0001c0002t0013g0236a0001c0002t0013g0238others(2): Show | 5 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.86-11243C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78020273 | ||||||
| chr17:78020311
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.86-11205C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78020311 | ||||||
| chr17:78020355
|
A | C | 5 | a0001c0002t0013g0235a0001c0002t0013g0236a0001c0002t0013g0238others(2): Show | 5 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.86-11161A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78020355 | ||||||
| chr17:78020394
|
T | C | 2 | a0001c0001t0001g0134a0003c0022t0021g0130 | 2 | NA18964.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.86-11122T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78020394 | ||||||
| chr17:78020501
|
A | G | 31 | a0001c0001t0001g0106a0001c0001t0051g0105a0001c0002t0002g0005others(28): Show | 31 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.86-11015A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78020501 | ||||||
| chr17:78020639
|
G | C | 47 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(44): Show | 47 | HG01243.hp1 HG01257.hp2 HG01943.hp1 others(44): Show |
intron_variant | MODIFIER | c.86-10877G>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78020639 | ||||||
| chr17:78020722
|
A | G | 2 | a0001c0002t0061g0232a0008c0016t0001g0079 | 2 | HG01255.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.86-10794A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78020722 | ||||||
| chr17:78020773
|
G | A | 35 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(32): Show | 35 | HG01243.hp1 HG01257.hp2 HG01943.hp1 others(32): Show |
intron_variant | MODIFIER | c.86-10743G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78020773 | ||||||
| chr17:78021106
|
G | A | 47 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(44): Show | 47 | HG01243.hp1 HG01257.hp2 HG01943.hp1 others(44): Show |
intron_variant | MODIFIER | c.86-10410G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78021106 | ||||||
| chr17:78021311
|
C | T | 1 | a0001c0001t0054g0094 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.86-10205C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78021311 | ||||||
| chr17:78021384
|
G | A | 35 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(32): Show | 35 | HG01243.hp1 HG01257.hp2 HG01943.hp1 others(32): Show |
intron_variant | MODIFIER | c.86-10132G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78021384 | ||||||
| chr17:78021433
|
G | A | 2 | a0001c0001t0001g0203a0001c0001t0001g0206 | 2 | HG02080.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.86-10083G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78021433 | ||||||
| chr17:78021485
|
C | G | 6 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(3): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.86-10031C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78021485 | ||||||
| chr17:78021559
|
GTTAT | G | 3 | a0001c0002t0031g0265a0009c0015t0027g0264a0017c0017t0028g0263 | 3 | HG02258.hp1 HG02615.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.86-9950_86-9947del others(4): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 78021559 | |||||
| chr17:78021569
|
T | A | 5 | a0001c0002t0013g0235a0001c0002t0013g0236a0001c0002t0013g0238others(2): Show | 5 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.86-9947T>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78021569 | ||||||
| chr17:78021574
|
A | T | 24 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(21): Show | 24 | HG01243.hp1 HG01257.hp2 HG01943.hp1 others(21): Show |
intron_variant | MODIFIER | c.86-9942A>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78021574 | ||||||
| chr17:78021646
|
T | G | 1 | a0001c0002t0002g0122 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.86-9870T>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78021646 | ||||||
| chr17:78021895
|
A | C | 6 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(3): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.86-9621A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78021895 | ||||||
| chr17:78021971
|
T | C | 3 | a0001c0002t0031g0265a0009c0015t0027g0264a0017c0017t0028g0263 | 3 | HG02258.hp1 HG02615.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.86-9545T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78021971 | ||||||
| chr17:78022011
|
T | C | 47 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(44): Show | 47 | HG01243.hp1 HG01257.hp2 HG01943.hp1 others(44): Show |
intron_variant | MODIFIER | c.86-9505T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78022011 | ||||||
| chr17:78022218
|
T | G | 3 | a0001c0007t0012g0268a0001c0007t0012g0269a0001c0007t0012g0270 | 3 | HG02145.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.86-9298T>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78022218 | ||||||
| chr17:78022233
|
A | G | 1 | a0001c0002t0031g0265 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.86-9283A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78022233 | ||||||
| chr17:78022392
|
A | T | 1 | a0002c0003t0007g0125 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.86-9124A>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78022392 | ||||||
| chr17:78022434
|
A | G | 1 | a0001c0001t0001g0024 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.86-9082A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78022434 | ||||||
| chr17:78022527
|
T | C | 5 | a0001c0002t0013g0235a0001c0002t0013g0236a0001c0002t0013g0238others(2): Show | 5 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.86-8989T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78022527 | ||||||
| chr17:78022969
|
A | G | 2 | a0009c0015t0027g0264a0017c0017t0028g0263 | 2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.86-8547A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78022969 | ||||||
| chr17:78023156
|
G | A | 11 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(8): Show | 11 | HG02486.hp1 HG02622.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.86-8360G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78023156 | ||||||
| chr17:78023185
|
G | A | 2 | a0001c0001t0017g0266a0001c0001t0017g0267 | 2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.86-8331G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78023185 | ||||||
| chr17:78023260
|
G | A | 40 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(37): Show | 40 | HG01243.hp1 HG01257.hp2 HG02055.hp1 others(37): Show |
intron_variant | MODIFIER | c.86-8256G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78023260 | ||||||
| chr17:78023300
|
T | C | 1 | a0001c0001t0049g0097 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.86-8216T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78023300 | ||||||
| chr17:78023417
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.86-8099C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78023417 | ||||||
| chr17:78023760
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.86-7756C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78023760 | ||||||
| chr17:78023903
|
A | G | 3 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0052 | 3 | HG01496.hp2 HG01981.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.86-7613A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78023903 | ||||||
| chr17:78023997
|
C | G | 1 | a0002c0003t0003g0011 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.86-7519C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78023997 | ||||||
| chr17:78024018
|
G | C | 1 | a0002c0003t0003g0139 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.86-7498G>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78024018 | ||||||
| chr17:78024091
|
A | T | 40 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(37): Show | 40 | HG01243.hp1 HG01257.hp2 HG02055.hp1 others(37): Show |
intron_variant | MODIFIER | c.86-7425A>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78024091 | ||||||
| chr17:78024277
|
C | T | 1 | a0001c0007t0012g0268 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.86-7239C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78024277 | ||||||
| chr17:78024356
|
G | T | 1 | a0001c0001t0049g0097 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.86-7160G>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78024356 | ||||||
| chr17:78024529
|
G | A | 1 | a0002c0003t0010g0250 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.86-6987G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78024529 | ||||||
| chr17:78024656
|
C | T | 2 | a0001c0001t0004g0157a0001c0001t0004g0172 | 2 | HG02293.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.86-6860C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78024656 | ||||||
| chr17:78024711
|
A | G | 1 | a0016c0023t0045g0192 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.86-6805A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78024711 | ||||||
| chr17:78024750
|
T | G | 3 | a0001c0007t0012g0268a0001c0007t0012g0269a0001c0007t0012g0270 | 3 | HG02145.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.86-6766T>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78024750 | ||||||
| chr17:78024776
|
A | T | 2 | a0001c0001t0001g0132a0001c0001t0001g0136 | 2 | HG00280.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.86-6740A>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78024776 | ||||||
| chr17:78024884
|
T | TC | 6 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(3): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.86-6630dupC | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 78024884 | |||||
| chr17:78024889
|
G | C | 1 | a0001c0001t0029g0239 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.86-6627G>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78024889 | ||||||
| chr17:78024982
|
CG | C | 17 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(14): Show | 17 | HG01243.hp1 HG01257.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.86-6530delG | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 78024982 | |||||
| chr17:78025082
|
C | T | 1 | a0001c0002t0031g0265 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.86-6434C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78025082 | ||||||
| chr17:78025192
|
A | T | 47 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(44): Show | 47 | HG01243.hp1 HG01257.hp2 HG01943.hp1 others(44): Show |
intron_variant | MODIFIER | c.86-6324A>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78025192 | ||||||
| chr17:78025237
|
C | G | 1 | a0001c0002t0002g0116 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.86-6279C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78025237 | ||||||
| chr17:78025366
|
T | C | 27 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(24): Show | 27 | HG01243.hp1 HG01257.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.86-6150T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78025366 | ||||||
| chr17:78025573
|
G | A | 2 | a0001c0001t0001g0096a0001c0001t0064g0080 | 2 | HG02976.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.86-5943G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78025573 | ||||||
| chr17:78025801
|
T | C | 5 | a0001c0002t0013g0235a0001c0002t0013g0236a0001c0002t0013g0238others(2): Show | 5 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.86-5715T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78025801 | ||||||
| chr17:78026058
|
G | A | 4 | a0001c0005t0001g0001a0001c0005t0001g0145a0001c0005t0001g0146others(1): Show | 5 | HG02630.hp1 HG03041.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.86-5458G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78026058 | ||||||
| chr17:78026081
|
AG | A | 27 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(24): Show | 27 | HG01243.hp1 HG01257.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.86-5434delG | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78026081 | ||||||
| chr17:78026118
|
T | A | 27 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(24): Show | 27 | HG01243.hp1 HG01257.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.86-5398T>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78026118 | ||||||
| chr17:78026364
|
C | T | 7 | a0001c0002t0002g0005a0001c0002t0002g0197a0001c0002t0002g0198others(4): Show | 7 | NA18747.hp1 NA18940.hp1 NA18970.hp2 others(4): Show |
intron_variant | MODIFIER | c.86-5152C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78026364 | ||||||
| chr17:78026427
|
A | G | 1 | a0001c0001t0004g0172 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.86-5089A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78026427 | ||||||
| chr17:78026435
|
T | C | 1 | a0002c0003t0003g0144 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.86-5081T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78026435 | ||||||
| chr17:78026447
|
C | G | 1 | a0001c0001t0029g0239 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.86-5069C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78026447 | ||||||
| chr17:78026697
|
C | T | 1 | a0002c0003t0010g0245 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.86-4819C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78026697 | ||||||
| chr17:78026698
|
G | A | 18 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(15): Show | 18 | HG01243.hp1 HG01257.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.86-4818G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78026698 | ||||||
| chr17:78026762
|
G | T | 2 | a0001c0001t0001g0185a0001c0001t0029g0239 | 2 | HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.86-4754G>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78026762 | ||||||
| chr17:78026962
|
T | C | 3 | a0001c0007t0012g0268a0001c0007t0012g0269a0001c0007t0012g0270 | 3 | HG02145.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.86-4554T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78026962 | ||||||
| chr17:78027475
|
A | G | 3 | a0001c0002t0002g0122a0001c0002t0002g0196a0001c0002t0052g0121 | 3 | HG00323.hp2 NA18968.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.86-4041A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78027475 | ||||||
| chr17:78027607
|
A | C | 2 | a0009c0015t0027g0264a0017c0017t0028g0263 | 2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.86-3909A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78027607 | ||||||
| chr17:78027608
|
C | T | 3 | a0001c0001t0001g0209a0001c0001t0001g0216a0001c0001t0001g0217 | 3 | NA18990.hp2 NA19002.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.86-3908C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78027608 | ||||||
| chr17:78027614
|
G | T | 1 | a0008c0028t0023g0258 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.86-3902G>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78027614 | ||||||
| chr17:78027770
|
A | T | 1 | a0001c0002t0014g0071 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.86-3746A>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78027770 | ||||||
| chr17:78027903
|
G | GT | 5 | a0001c0001t0001g0040a0001c0001t0001g0202a0001c0002t0002g0111others(2): Show | 5 | HG01175.hp2 HG01261.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.86-3595dupT | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 78027903 | |||||
| chr17:78027903
|
GT | G | 35 | a0001c0001t0001g0058a0001c0001t0001g0206a0001c0001t0001g0221others(32): Show | 35 | HG01243.hp1 HG01257.hp2 HG02055.hp1 others(32): Show |
intron_variant | MODIFIER | c.86-3595delT | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 78027903 | |||||
| chr17:78027903
|
GTT | G | 12 | a0001c0001t0029g0239a0001c0006t0008g0251a0001c0006t0008g0253others(9): Show | 12 | HG01943.hp1 HG02155.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.86-3596_86-3595del others(2): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 78027903 | |||||
| chr17:78027922
|
G | A | 1 | a0017c0017t0028g0263 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.86-3594G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78027922 | ||||||
| chr17:78027931
|
T | C | 11 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(8): Show | 11 | HG01243.hp1 HG01257.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.86-3585T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78027931 | ||||||
| chr17:78027989
|
G | A | 18 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(15): Show | 18 | HG01243.hp1 HG01257.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.86-3527G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78027989 | ||||||
| chr17:78028089
|
A | G | 108 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(105): Show | 108 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.86-3427A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78028089 | ||||||
| chr17:78028100
|
G | A | 24 | a0001c0001t0001g0106a0001c0001t0051g0105a0001c0002t0002g0005others(21): Show | 24 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.86-3416G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78028100 | ||||||
| chr17:78028127
|
C | T | 1 | a0001c0001t0001g0214 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.86-3389C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78028127 | ||||||
| chr17:78028147
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.86-3369G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78028147 | ||||||
| chr17:78028289
|
G | A | 11 | a0001c0001t0029g0239a0001c0006t0008g0251a0001c0006t0008g0253others(8): Show | 11 | HG01943.hp1 HG02155.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.86-3227G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78028289 | ||||||
| chr17:78028434
|
T | A | 2 | a0001c0001t0005g0026a0001c0001t0005g0084 | 2 | HG02040.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.86-3082T>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78028434 | ||||||
| chr17:78028591
|
G | A | 1 | a0008c0028t0023g0258 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.86-2925G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78028591 | ||||||
| chr17:78028659
|
C | CA | 4 | a0002c0003t0010g0240a0002c0003t0010g0245a0002c0003t0010g0250others(1): Show | 4 | HG02647.hp1 HG02895.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.86-2855dupA | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 78028659 | |||||
| chr17:78028662
|
T | C | 1 | a0008c0028t0023g0258 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.86-2854T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78028662 | ||||||
| chr17:78028943
|
C | T | 4 | a0002c0003t0010g0240a0002c0003t0010g0245a0002c0003t0010g0250others(1): Show | 4 | HG02647.hp1 HG02895.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.86-2573C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78028943 | ||||||
| chr17:78029021
|
C | G | 1 | a0009c0015t0027g0264 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.86-2495C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78029021 | ||||||
| chr17:78029080
|
T | C | 1 | a0002c0003t0010g0250 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.86-2436T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78029080 | ||||||
| chr17:78029088
|
T | A | 1 | a0008c0028t0023g0258 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.86-2428T>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78029088 | ||||||
| chr17:78029227
|
C | T | 5 | a0001c0002t0013g0235a0001c0002t0013g0236a0001c0002t0013g0238others(2): Show | 5 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.86-2289C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78029227 | ||||||
| chr17:78029253
|
T | G | 11 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(8): Show | 11 | HG01243.hp1 HG01257.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.86-2263T>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78029253 | ||||||
| chr17:78029328
|
T | C | 58 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(55): Show | 58 | HG01070.hp1 HG01243.hp1 HG01257.hp2 others(55): Show |
intron_variant | MODIFIER | c.86-2188T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78029328 | ||||||
| chr17:78029385
|
A | G | 1 | a0008c0028t0023g0258 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.86-2131A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78029385 | ||||||
| chr17:78029472
|
A | G | 6 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(3): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.86-2044A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78029472 | ||||||
| chr17:78029502
|
C | G | 1 | a0001c0001t0065g0017 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.86-2014C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78029502 | ||||||
| chr17:78029570
|
G | T | 2 | a0001c0001t0017g0266a0001c0001t0017g0267 | 2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.86-1946G>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78029570 | ||||||
| chr17:78029623
|
A | T | 22 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(19): Show | 22 | HG01243.hp1 HG01257.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.86-1893A>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78029623 | ||||||
| chr17:78029772
|
AT | A | 18 | a0001c0001t0001g0087a0001c0001t0001g0221a0001c0001t0001g0222others(15): Show | 18 | HG01243.hp1 HG01257.hp2 HG01943.hp1 others(15): Show |
intron_variant | MODIFIER | c.86-1734delT | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 78029772 | |||||
| chr17:78029808
|
G | GAC | 7 | a0001c0001t0001g0096a0001c0001t0001g0219a0001c0001t0005g0095others(4): Show | 7 | HG00735.hp2 HG02976.hp2 NA18943.hp1 others(4): Show |
intron_variant | MODIFIER | c.86-1680_86-1679dup others(2): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 78029808 | |||||
| chr17:78029808
|
G | GACAC | 9 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0225others(6): Show | 9 | HG01243.hp1 HG01257.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.86-1682_86-1679dup others(4): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 78029808 | |||||
| chr17:78029808
|
GAC | G | 124 | a0001c0001t0001g0106a0001c0001t0001g0127a0001c0001t0001g0128others(121): Show | 127 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.86-1680_86-1679del others(2): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 78029808 | |||||
| chr17:78029808
|
GACAC | G | 26 | a0001c0001t0030g0259a0001c0004t0006g0242a0001c0004t0006g0244others(23): Show | 26 | HG01943.hp1 HG02145.hp2 HG02155.hp1 others(23): Show |
intron_variant | MODIFIER | c.86-1682_86-1679del others(4): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 78029808 | |||||
| chr17:78029819
|
A | T | 1 | a0008c0028t0023g0258 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.86-1697A>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78029819 | ||||||
| chr17:78029939
|
GTGA | G | 6 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(3): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.86-1575_86-1573del others(3): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 78029939 | |||||
| chr17:78030002
|
G | A | 4 | a0001c0005t0001g0001a0001c0005t0001g0145a0001c0005t0001g0146others(1): Show | 5 | HG02630.hp1 HG03041.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.86-1514G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78030002 | ||||||
| chr17:78030122
|
TACTACTG others(6): Show |
T | 4 | a0002c0003t0010g0240a0002c0003t0010g0245a0002c0003t0010g0250others(1): Show | 4 | HG02647.hp1 HG02895.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.86-1392_86-1380del others(13): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 78030122 | |||||
| chr17:78030192
|
C | T | 12 | a0001c0001t0030g0259a0001c0004t0006g0242a0001c0004t0006g0244others(9): Show | 12 | HG02486.hp1 HG02622.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.86-1324C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78030192 | ||||||
| chr17:78030218
|
C | A | 2 | a0009c0015t0027g0264a0017c0017t0028g0263 | 2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.86-1298C>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78030218 | ||||||
| chr17:78030242
|
C | T | 1 | a0008c0028t0023g0258 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.86-1274C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78030242 | ||||||
| chr17:78030254
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.86-1262A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78030254 | ||||||
| chr17:78030292
|
C | T | 4 | a0002c0003t0010g0240a0002c0003t0010g0245a0002c0003t0010g0250others(1): Show | 4 | HG02647.hp1 HG02895.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.86-1224C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78030292 | ||||||
| chr17:78030314
|
TTGTGTGT others(5): Show |
T | 1 | a0002c0003t0003g0011 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.86-1191_86-1180del others(12): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 78030314 | |||||
| chr17:78030325
|
C | CGT | 61 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0015others(58): Show | 61 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.86-1174_86-1173dup others(2): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | 78030325 | |||||
| chr17:78030325
|
C | T | 47 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(44): Show | 47 | HG01243.hp1 HG01257.hp2 HG01943.hp1 others(44): Show |
intron_variant | MODIFIER | c.86-1191C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78030325 | ||||||
| chr17:78030327
|
T | C | 46 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(43): Show | 46 | HG01243.hp1 HG01257.hp2 HG01943.hp1 others(43): Show |
intron_variant | MODIFIER | c.86-1189T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78030327 | ||||||
| chr17:78030414
|
G | A | 1 | a0001c0005t0001g0145 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.86-1102G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78030414 | ||||||
| chr17:78030484
|
C | T | 4 | a0002c0003t0010g0240a0002c0003t0010g0245a0002c0003t0010g0250others(1): Show | 4 | HG02647.hp1 HG02895.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.86-1032C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78030484 | ||||||
| chr17:78030537
|
T | C | 2 | a0001c0002t0014g0054a0001c0002t0014g0071 | 2 | HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.86-979T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78030537 | ||||||
| chr17:78030561
|
G | A | 1 | a0002c0003t0003g0165 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.86-955G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78030561 | ||||||
| chr17:78030575
|
A | G | 5 | a0001c0002t0013g0235a0001c0002t0013g0236a0001c0002t0013g0238others(2): Show | 5 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.86-941A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78030575 | ||||||
| chr17:78030590
|
T | C | 172 | a0001c0001t0001g0037a0001c0001t0001g0058a0001c0001t0001g0063others(169): Show | 175 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.86-926T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78030590 | ||||||
| chr17:78030817
|
G | A | 3 | a0001c0007t0012g0268a0001c0007t0012g0269a0001c0007t0012g0270 | 3 | HG02145.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.86-699G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78030817 | ||||||
| chr17:78030821
|
G | A | 2 | a0001c0001t0001g0134a0003c0022t0021g0130 | 2 | NA18964.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.86-695G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78030821 | ||||||
| chr17:78030840
|
C | T | 1 | a0008c0016t0001g0079 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.86-676C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78030840 | ||||||
| chr17:78031001
|
A | G | 2 | a0001c0006t0008g0253a0003c0030t0008g0255 | 2 | HG02738.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.86-515A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78031001 | ||||||
| chr17:78031117
|
A | G | 4 | a0002c0003t0010g0240a0002c0003t0010g0245a0002c0003t0010g0250others(1): Show | 4 | HG02647.hp1 HG02895.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.86-399A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78031117 | ||||||
| chr17:78031120
|
A | G | 1 | a0001c0001t0029g0239 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.86-396A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78031120 | ||||||
| chr17:78031122
|
G | A | 1 | a0001c0001t0029g0239 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.86-394G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78031122 | ||||||
| chr17:78031297
|
T | A | 30 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(27): Show | 30 | HG01243.hp1 HG01257.hp2 HG01943.hp1 others(27): Show |
intron_variant | MODIFIER | c.86-219T>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78031297 | ||||||
| chr17:78031961
|
A | G | 2 | a0001c0001t0004g0143a0001c0001t0004g0176 | 2 | HG01496.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.412+119A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78031961 | ||||||
| chr17:78031972
|
T | C | 4 | a0002c0003t0010g0240a0002c0003t0010g0245a0002c0003t0010g0250others(1): Show | 4 | HG02647.hp1 HG02895.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.412+130T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78031972 | ||||||
| chr17:78031986
|
G | A | 1 | a0008c0028t0023g0258 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.412+144G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78031986 | ||||||
| chr17:78032190
|
A | G | 1 | a0001c0002t0002g0109 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.412+348A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78032190 | ||||||
| chr17:78032321
|
C | G | 1 | a0001c0001t0001g0127 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.412+479C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78032321 | ||||||
| chr17:78032330
|
G | T | 1 | a0001c0001t0064g0080 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.412+488G>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78032330 | ||||||
| chr17:78032491
|
C | G | 5 | a0001c0002t0013g0235a0001c0002t0013g0236a0001c0002t0013g0238others(2): Show | 5 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.412+649C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78032491 | ||||||
| chr17:78032579
|
G | A | 1 | a0001c0001t0029g0239 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.412+737G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78032579 | ||||||
| chr17:78032775
|
G | C | 30 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(27): Show | 30 | HG01243.hp1 HG01257.hp2 HG01943.hp1 others(27): Show |
intron_variant | MODIFIER | c.412+933G>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78032775 | ||||||
| chr17:78032821
|
A | G | 5 | a0001c0002t0013g0235a0001c0002t0013g0236a0001c0002t0013g0238others(2): Show | 5 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.412+979A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78032821 | ||||||
| chr17:78033188
|
A | G | 39 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(36): Show | 39 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.412+1346A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78033188 | ||||||
| chr17:78033669
|
CA | C | 13 | a0001c0001t0030g0259a0001c0004t0006g0242a0001c0004t0006g0244others(10): Show | 13 | HG02135.hp2 HG02486.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.412+1838delA | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr17 | 78033669 | |||||
| chr17:78033796
|
A | C | 12 | a0001c0001t0030g0259a0001c0004t0006g0242a0001c0004t0006g0244others(9): Show | 12 | HG02486.hp1 HG02622.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.412+1954A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78033796 | ||||||
| chr17:78033944
|
C | T | 1 | a0001c0001t0001g0038 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.412+2102C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78033944 | ||||||
| chr17:78033947
|
G | A | 111 | a0001c0001t0001g0037a0001c0001t0001g0058a0001c0001t0001g0063others(108): Show | 114 | HG00280.hp2 HG00323.hp2 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.412+2105G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78033947 | ||||||
| chr17:78033970
|
A | G | 4 | a0001c0002t0002g0179a0001c0005t0001g0007a0001c0005t0001g0008others(1): Show | 4 | HG02896.hp1 HG02965.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.412+2128A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78033970 | ||||||
| chr17:78033986
|
C | G | 46 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(43): Show | 46 | HG01243.hp1 HG01257.hp2 HG01943.hp1 others(43): Show |
intron_variant | MODIFIER | c.412+2144C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78033986 | ||||||
| chr17:78034035
|
G | A | 25 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(22): Show | 25 | HG01243.hp1 HG01257.hp2 HG01943.hp1 others(22): Show |
intron_variant | MODIFIER | c.412+2193G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78034035 | ||||||
| chr17:78034144
|
C | A | 3 | a0002c0003t0010g0240a0002c0003t0010g0245a0002c0003t0010g0250 | 3 | HG02647.hp1 HG02895.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.412+2302C>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78034144 | ||||||
| chr17:78034601
|
C | T | 5 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(2): Show | 5 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.412+2759C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78034601 | ||||||
| chr17:78034836
|
G | A | 1 | a0009c0015t0027g0264 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.412+2994G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78034836 | ||||||
| chr17:78034842
|
G | A | 2 | a0006c0011t0001g0159a0006c0011t0001g0160 | 2 | HG01243.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.412+3000G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78034842 | ||||||
| chr17:78034924
|
G | A | 3 | a0001c0001t0001g0034a0001c0001t0001g0045a0001c0001t0001g0085 | 3 | NA18952.hp1 NA18970.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.412+3082G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78034924 | ||||||
| chr17:78035083
|
G | T | 1 | a0001c0002t0061g0232 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.412+3241G>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78035083 | ||||||
| chr17:78035112
|
G | T | 3 | a0001c0007t0012g0268a0001c0007t0012g0269a0001c0007t0012g0270 | 3 | HG02145.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.412+3270G>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78035112 | ||||||
| chr17:78035143
|
C | G | 11 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(8): Show | 11 | HG01243.hp1 HG01257.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.412+3301C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78035143 | ||||||
| chr17:78035144
|
C | T | 260 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0015others(257): Show | 263 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.412+3302C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78035144 | ||||||
| chr17:78035348
|
T | C | 32 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(29): Show | 32 | HG01243.hp1 HG01257.hp2 HG01943.hp1 others(29): Show |
intron_variant | MODIFIER | c.412+3506T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78035348 | ||||||
| chr17:78035585
|
G | C | 12 | a0001c0001t0030g0259a0001c0004t0006g0242a0001c0004t0006g0244others(9): Show | 12 | HG02486.hp1 HG02622.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.412+3743G>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78035585 | ||||||
| chr17:78035883
|
T | A | 47 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(44): Show | 47 | HG01243.hp1 HG01257.hp2 HG01943.hp1 others(44): Show |
intron_variant | MODIFIER | c.412+4041T>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78035883 | ||||||
| chr17:78035909
|
A | G | 1 | a0002c0003t0003g0178 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.412+4067A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78035909 | ||||||
| chr17:78036098
|
G | T | 2 | a0009c0015t0027g0264a0017c0017t0028g0263 | 2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.412+4256G>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78036098 | ||||||
| chr17:78036156
|
T | C | 32 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(29): Show | 32 | HG01243.hp1 HG01257.hp2 HG01943.hp1 others(29): Show |
intron_variant | MODIFIER | c.412+4314T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78036156 | ||||||
| chr17:78036226
|
G | A | 1 | a0001c0001t0001g0214 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.412+4384G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78036226 | ||||||
| chr17:78036236
|
C | T | 18 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(15): Show | 18 | HG01243.hp1 HG01257.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.412+4394C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78036236 | ||||||
| chr17:78036579
|
A | G | 1 | a0001c0001t0001g0207 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.412+4737A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78036579 | ||||||
| chr17:78036581
|
G | T | 26 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(23): Show | 26 | HG01243.hp1 HG01257.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.412+4739G>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78036581 | ||||||
| chr17:78036704
|
A | G | 33 | a0002c0003t0003g0002a0002c0003t0003g0003a0002c0003t0003g0011others(30): Show | 35 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.412+4862A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78036704 | ||||||
| chr17:78036741
|
T | C | 8 | a0001c0001t0029g0239a0001c0007t0012g0268a0001c0007t0012g0269others(5): Show | 8 | HG02145.hp2 HG02647.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.412+4899T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78036741 | ||||||
| chr17:78036745
|
G | A | 1 | a0013c0026t0002g0118 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.412+4903G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78036745 | ||||||
| chr17:78036797
|
G | A | 3 | a0001c0001t0001g0209a0009c0015t0027g0264a0017c0017t0028g0263 | 3 | HG02258.hp1 HG02615.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.412+4955G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78036797 | ||||||
| chr17:78036819
|
G | A | 4 | a0002c0003t0010g0240a0002c0003t0010g0245a0002c0003t0010g0250others(1): Show | 4 | HG02647.hp1 HG02895.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.412+4977G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78036819 | ||||||
| chr17:78036921
|
T | TA | 15 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(12): Show | 15 | HG01243.hp1 HG01257.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.412+5091dupA | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr17 | 78036921 | |||||
| chr17:78037056
|
A | G | 1 | a0001c0004t0024g0243 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.412+5214A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78037056 | ||||||
| chr17:78037154
|
G | A | 8 | a0001c0005t0001g0001a0001c0005t0001g0007a0001c0005t0001g0008others(5): Show | 9 | HG02451.hp1 HG02630.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.412+5312G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78037154 | ||||||
| chr17:78037216
|
C | T | 1 | a0001c0001t0054g0094 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.412+5374C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78037216 | ||||||
| chr17:78037253
|
A | G | 32 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(29): Show | 32 | HG01243.hp1 HG01257.hp2 HG01943.hp1 others(29): Show |
intron_variant | MODIFIER | c.412+5411A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78037253 | ||||||
| chr17:78037302
|
T | G | 3 | a0001c0002t0013g0235a0001c0002t0018g0234a0001c0002t0018g0237 | 3 | HG02630.hp2 HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.412+5460T>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78037302 | ||||||
| chr17:78037335
|
A | C | 1 | a0001c0001t0029g0239 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.412+5493A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78037335 | ||||||
| chr17:78037447
|
A | G | 8 | a0001c0001t0029g0239a0001c0007t0012g0268a0001c0007t0012g0269others(5): Show | 8 | HG02145.hp2 HG02647.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.412+5605A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78037447 | ||||||
| chr17:78037481
|
C | T | 126 | a0001c0001t0001g0037a0001c0001t0001g0058a0001c0001t0001g0063others(123): Show | 129 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.412+5639C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78037481 | ||||||
| chr17:78037512
|
TG | T | 24 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(21): Show | 24 | HG01243.hp1 HG01257.hp2 HG01943.hp1 others(21): Show |
intron_variant | MODIFIER | c.412+5672delG | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr17 | 78037512 | |||||
| chr17:78037815
|
T | C | 5 | a0001c0002t0013g0235a0001c0002t0013g0236a0001c0002t0013g0238others(2): Show | 5 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.412+5973T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78037815 | ||||||
| chr17:78037820
|
A | C | 1 | a0001c0001t0001g0127 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.412+5978A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78037820 | ||||||
| chr17:78037966
|
A | G | 1 | a0001c0001t0004g0190 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.412+6124A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78037966 | ||||||
| chr17:78038006
|
G | A | 11 | a0001c0002t0014g0054a0001c0002t0014g0055a0001c0002t0014g0071others(8): Show | 11 | HG01070.hp1 HG01884.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.412+6164G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78038006 | ||||||
| chr17:78038075
|
A | G | 32 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(29): Show | 32 | HG01243.hp1 HG01257.hp2 HG01943.hp1 others(29): Show |
intron_variant | MODIFIER | c.412+6233A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78038075 | ||||||
| chr17:78038117
|
A | C | 1 | a0002c0003t0003g0186 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.412+6275A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78038117 | ||||||
| chr17:78038197
|
G | A | 5 | a0001c0002t0013g0235a0001c0002t0013g0236a0001c0002t0013g0238others(2): Show | 5 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.412+6355G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78038197 | ||||||
| chr17:78038197
|
G | C | 1 | a0002c0003t0003g0139 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.412+6355G>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78038197 | ||||||
| chr17:78038227
|
C | T | 1 | a0002c0003t0010g0250 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.412+6385C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78038227 | ||||||
| chr17:78038250
|
A | G | 1 | a0008c0028t0023g0258 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.412+6408A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78038250 | ||||||
| chr17:78038265
|
A | G | 3 | a0001c0001t0001g0034a0001c0001t0001g0045a0001c0001t0001g0085 | 3 | NA18952.hp1 NA18970.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.412+6423A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78038265 | ||||||
| chr17:78038282
|
G | T | 47 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(44): Show | 47 | HG01243.hp1 HG01257.hp2 HG01943.hp1 others(44): Show |
intron_variant | MODIFIER | c.412+6440G>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78038282 | ||||||
| chr17:78038324
|
G | T | 1 | a0008c0028t0023g0258 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.412+6482G>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78038324 | ||||||
| chr17:78038412
|
G | A | 1 | a0001c0005t0001g0137 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.412+6570G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78038412 | ||||||
| chr17:78038489
|
C | T | 7 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0028others(4): Show | 7 | HG00323.hp1 HG00735.hp2 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.412+6647C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78038489 | ||||||
| chr17:78038501
|
A | G | 32 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(29): Show | 32 | HG01243.hp1 HG01257.hp2 HG01943.hp1 others(29): Show |
intron_variant | MODIFIER | c.412+6659A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78038501 | ||||||
| chr17:78038536
|
G | A | 1 | a0001c0001t0029g0239 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.412+6694G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78038536 | ||||||
| chr17:78038611
|
G | A | 18 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(15): Show | 18 | HG01243.hp1 HG01257.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.412+6769G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78038611 | ||||||
| chr17:78038658
|
G | A | 1 | a0001c0005t0001g0007 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.412+6816G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78038658 | ||||||
| chr17:78038673
|
C | T | 11 | a0001c0002t0014g0054a0001c0002t0014g0055a0001c0002t0014g0071others(8): Show | 11 | HG01070.hp1 HG01884.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.412+6831C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78038673 | ||||||
| chr17:78038678
|
C | CA | 36 | a0001c0001t0001g0032a0001c0001t0001g0038a0001c0001t0001g0043others(33): Show | 36 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.412+6856dupA | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr17 | 78038678 | |||||
| chr17:78038678
|
CA | C | 25 | a0001c0001t0001g0044a0001c0001t0001g0081a0001c0001t0001g0082others(22): Show | 25 | HG01070.hp1 HG01167.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.412+6856delA | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr17 | 78038678 | |||||
| chr17:78038678
|
CAA | C | 10 | a0001c0001t0029g0239a0001c0006t0008g0253a0001c0006t0008g0256others(7): Show | 10 | HG01943.hp1 HG02647.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.412+6855_412+6856d others(4): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr17 | 78038678 | |||||
| chr17:78038776
|
C | T | 8 | a0001c0001t0029g0239a0001c0007t0012g0268a0001c0007t0012g0269others(5): Show | 8 | HG02145.hp2 HG02647.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.412+6934C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78038776 | ||||||
| chr17:78039062
|
C | G | 5 | a0001c0002t0013g0235a0001c0002t0013g0236a0001c0002t0013g0238others(2): Show | 5 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.412+7220C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78039062 | ||||||
| chr17:78039157
|
G | A | 2 | a0001c0002t0031g0265a0008c0028t0023g0258 | 2 | HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.412+7315G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78039157 | ||||||
| chr17:78039309
|
GC | G | 164 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0015others(161): Show | 167 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.412+7479delC | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr17 | 78039309 | |||||
| chr17:78039309
|
GCC | G | 26 | a0001c0002t0002g0005a0001c0002t0002g0104a0001c0002t0002g0107others(23): Show | 26 | HG00323.hp2 HG00423.hp2 HG00597.hp2 others(23): Show |
intron_variant | MODIFIER | c.412+7478_412+7479d others(4): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr17 | 78039309 | |||||
| chr17:78039315
|
C | G | 1 | a0001c0001t0001g0059 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.412+7473C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78039315 | ||||||
| chr17:78039418
|
T | C | 4 | a0002c0003t0010g0240a0002c0003t0010g0245a0002c0003t0010g0250others(1): Show | 4 | HG02647.hp1 HG02895.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.412+7576T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78039418 | ||||||
| chr17:78039660
|
C | T | 1 | a0008c0028t0023g0258 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.412+7818C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78039660 | ||||||
| chr17:78039675
|
C | A | 1 | a0008c0028t0023g0258 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.412+7833C>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78039675 | ||||||
| chr17:78040105
|
A | G | 1 | a0001c0002t0002g0110 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.412+8263A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78040105 | ||||||
| chr17:78040941
|
C | T | 1 | a0001c0001t0001g0058 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.413-7904C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78040941 | ||||||
| chr17:78040946
|
A | G | 48 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(45): Show | 48 | HG01243.hp1 HG01257.hp2 HG01943.hp1 others(45): Show |
intron_variant | MODIFIER | c.413-7899A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78040946 | ||||||
| chr17:78041006
|
T | C | 1 | a0016c0023t0045g0192 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.413-7839T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78041006 | ||||||
| chr17:78041127
|
C | T | 12 | a0001c0001t0030g0259a0001c0004t0006g0242a0001c0004t0006g0244others(9): Show | 12 | HG02486.hp1 HG02622.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.413-7718C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78041127 | ||||||
| chr17:78041169
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.413-7676C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78041169 | ||||||
| chr17:78041371
|
G | A | 6 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(3): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.413-7474G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78041371 | ||||||
| chr17:78041497
|
A | T | 1 | a0001c0001t0017g0266 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.413-7348A>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78041497 | ||||||
| chr17:78041585
|
A | G | 3 | a0001c0007t0012g0268a0001c0007t0012g0269a0001c0007t0012g0270 | 3 | HG02145.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.413-7260A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78041585 | ||||||
| chr17:78041689
|
G | C | 11 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(8): Show | 11 | HG01243.hp1 HG01257.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.413-7156G>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78041689 | ||||||
| chr17:78041760
|
C | T | 5 | a0001c0001t0001g0185a0001c0001t0001g0187a0001c0001t0001g0212others(2): Show | 5 | HG00423.hp1 HG01261.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.413-7085C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78041760 | ||||||
| chr17:78041909
|
A | G | 19 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(16): Show | 19 | HG01243.hp1 HG01257.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.413-6936A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78041909 | ||||||
| chr17:78042310
|
G | A | 3 | a0001c0007t0012g0268a0001c0007t0012g0269a0001c0007t0012g0270 | 3 | HG02145.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.413-6535G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78042310 | ||||||
| chr17:78042361
|
A | G | 11 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(8): Show | 11 | HG01243.hp1 HG01257.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.413-6484A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78042361 | ||||||
| chr17:78042420
|
G | A | 6 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(3): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.413-6425G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78042420 | ||||||
| chr17:78042565
|
AT | A | 37 | a0001c0001t0001g0025a0001c0001t0001g0087a0001c0001t0001g0134others(34): Show | 37 | HG01070.hp1 HG01261.hp2 HG01891.hp2 others(34): Show |
intron_variant | MODIFIER | c.413-6264delT | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr17 | 78042565 | |||||
| chr17:78042565
|
ATT | A | 12 | a0001c0001t0017g0266a0001c0001t0017g0267a0001c0002t0013g0235others(9): Show | 12 | HG02145.hp2 HG02280.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.413-6265_413-6264d others(4): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr17 | 78042565 | |||||
| chr17:78042565
|
ATTT | A | 14 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(11): Show | 14 | HG01243.hp1 HG01257.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.413-6266_413-6264d others(5): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr17 | 78042565 | |||||
| chr17:78042722
|
A | G | 1 | a0001c0001t0001g0052 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.413-6123A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78042722 | ||||||
| chr17:78042728
|
A | G | 4 | a0002c0003t0010g0240a0002c0003t0010g0245a0002c0003t0010g0250others(1): Show | 4 | HG02615.hp1 HG02647.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.413-6117A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78042728 | ||||||
| chr17:78042824
|
G | A | 5 | a0001c0002t0013g0235a0001c0002t0013g0236a0001c0002t0013g0238others(2): Show | 5 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.413-6021G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78042824 | ||||||
| chr17:78042971
|
C | T | 3 | a0001c0007t0012g0268a0001c0007t0012g0269a0001c0007t0012g0270 | 3 | HG02145.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.413-5874C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78042971 | ||||||
| chr17:78043302
|
T | C | 1 | a0008c0028t0023g0258 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.413-5543T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78043302 | ||||||
| chr17:78043338
|
G | C | 30 | a0002c0003t0003g0002a0002c0003t0003g0003a0002c0003t0003g0011others(27): Show | 32 | HG01070.hp2 HG01071.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.413-5507G>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78043338 | ||||||
| chr17:78043385
|
G | A | 8 | a0001c0005t0001g0001a0001c0005t0001g0007a0001c0005t0001g0008others(5): Show | 9 | HG02451.hp1 HG02630.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.413-5460G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78043385 | ||||||
| chr17:78043533
|
G | A | 25 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(22): Show | 25 | HG01243.hp1 HG01257.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.413-5312G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78043533 | ||||||
| chr17:78043763
|
A | G | 172 | a0001c0001t0001g0037a0001c0001t0001g0058a0001c0001t0001g0063others(169): Show | 175 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.413-5082A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78043763 | ||||||
| chr17:78043859
|
C | T | 6 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(3): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.413-4986C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78043859 | ||||||
| chr17:78043915
|
A | G | 1 | a0003c0021t0002g0113 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.413-4930A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78043915 | ||||||
| chr17:78044002
|
G | C | 1 | a0002c0003t0025g0241 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.413-4843G>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78044002 | ||||||
| chr17:78044107
|
A | G | 11 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(8): Show | 11 | HG01243.hp1 HG01257.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.413-4738A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78044107 | ||||||
| chr17:78044175
|
A | G | 32 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(29): Show | 32 | HG01243.hp1 HG01257.hp2 HG01943.hp1 others(29): Show |
intron_variant | MODIFIER | c.413-4670A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78044175 | ||||||
| chr17:78044446
|
T | C | 32 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(29): Show | 32 | HG01243.hp1 HG01257.hp2 HG01943.hp1 others(29): Show |
intron_variant | MODIFIER | c.413-4399T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78044446 | ||||||
| chr17:78044449
|
G | C | 32 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(29): Show | 32 | HG01243.hp1 HG01257.hp2 HG01943.hp1 others(29): Show |
intron_variant | MODIFIER | c.413-4396G>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78044449 | ||||||
| chr17:78044501
|
A | G | 33 | a0002c0003t0003g0002a0002c0003t0003g0003a0002c0003t0003g0011others(30): Show | 35 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.413-4344A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78044501 | ||||||
| chr17:78044616
|
C | T | 1 | a0001c0002t0039g0057 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.413-4229C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78044616 | ||||||
| chr17:78044852
|
G | A | 1 | a0001c0001t0001g0225 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.413-3993G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78044852 | ||||||
| chr17:78044966
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.413-3879C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78044966 | ||||||
| chr17:78045051
|
G | T | 18 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(15): Show | 18 | HG01243.hp1 HG01257.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.413-3794G>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78045051 | ||||||
| chr17:78045146
|
G | A | 2 | a0006c0011t0001g0159a0006c0011t0001g0160 | 2 | HG01243.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.413-3699G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78045146 | ||||||
| chr17:78045487
|
C | T | 1 | a0001c0001t0005g0026 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.413-3358C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78045487 | ||||||
| chr17:78045491
|
G | A | 6 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(3): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.413-3354G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78045491 | ||||||
| chr17:78045551
|
C | CTT | 4 | a0002c0003t0010g0240a0002c0003t0010g0245a0002c0003t0010g0250others(1): Show | 4 | HG02647.hp1 HG02895.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.413-3293_413-3292i others(4): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr17 | 78045551 | |||||
| chr17:78045702
|
C | T | 18 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(15): Show | 18 | HG01243.hp1 HG01257.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.413-3143C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78045702 | ||||||
| chr17:78045737
|
C | T | 1 | a0017c0017t0028g0263 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.413-3108C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78045737 | ||||||
| chr17:78046002
|
G | A | 6 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(3): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.413-2843G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78046002 | ||||||
| chr17:78046014
|
C | G | 18 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(15): Show | 18 | HG01243.hp1 HG01257.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.413-2831C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78046014 | ||||||
| chr17:78046142
|
T | A | 11 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(8): Show | 11 | HG01243.hp1 HG01257.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.413-2703T>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78046142 | ||||||
| chr17:78046228
|
C | G | 1 | a0009c0015t0027g0264 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.413-2617C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78046228 | ||||||
| chr17:78046342
|
G | A | 32 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(29): Show | 32 | HG01243.hp1 HG01257.hp2 HG01943.hp1 others(29): Show |
intron_variant | MODIFIER | c.413-2503G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78046342 | ||||||
| chr17:78046389
|
G | A | 6 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(3): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.413-2456G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78046389 | ||||||
| chr17:78046398
|
G | A | 1 | a0009c0015t0027g0264 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.413-2447G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78046398 | ||||||
| chr17:78046469
|
C | T | 4 | a0001c0001t0001g0072a0004c0008t0001g0073a0004c0008t0001g0074others(1): Show | 4 | NA18943.hp1 NA18968.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.413-2376C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78046469 | ||||||
| chr17:78046576
|
A | G | 18 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(15): Show | 18 | HG01243.hp1 HG01257.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.413-2269A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78046576 | ||||||
| chr17:78047000
|
A | G | 1 | a0001c0001t0016g0050 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.413-1845A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78047000 | ||||||
| chr17:78047018
|
T | C | 3 | a0001c0007t0012g0268a0001c0007t0012g0269a0001c0007t0012g0270 | 3 | HG02145.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.413-1827T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78047018 | ||||||
| chr17:78047085
|
A | C | 1 | a0016c0023t0045g0192 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.413-1760A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78047085 | ||||||
| chr17:78047263
|
T | C | 3 | a0002c0003t0003g0139a0002c0003t0003g0161a0002c0003t0020g0195 | 3 | NA18988.hp2 NA19012.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.413-1582T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78047263 | ||||||
| chr17:78047316
|
C | T | 2 | a0001c0001t0001g0068a0001c0001t0001g0215 | 2 | NA18939.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.413-1529C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78047316 | ||||||
| chr17:78047919
|
G | A | 1 | a0008c0028t0023g0258 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.413-926G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78047919 | ||||||
| chr17:78047952
|
G | A | 1 | a0001c0001t0015g0019 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.413-893G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78047952 | ||||||
| chr17:78048153
|
AT | A | 45 | a0001c0001t0001g0096a0001c0001t0001g0221a0001c0001t0001g0222others(42): Show | 45 | HG01071.hp1 HG01243.hp1 HG01257.hp2 others(42): Show |
intron_variant | MODIFIER | c.413-680delT | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr17 | 78048153 | |||||
| chr17:78048419
|
C | A | 1 | a0002c0003t0003g0163 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.413-426C>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78048419 | ||||||
| chr17:78048465
|
T | C | 34 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(31): Show | 34 | HG01243.hp1 HG01255.hp2 HG01257.hp2 others(31): Show |
intron_variant | MODIFIER | c.413-380T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78048465 | ||||||
| chr17:78048486
|
C | T | 3 | a0001c0001t0015g0014a0001c0001t0015g0018a0001c0001t0015g0019 | 3 | HG01169.hp2 HG01175.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.413-359C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78048486 | ||||||
| chr17:78048497
|
C | G | 1 | a0001c0001t0001g0069 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.413-348C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78048497 | ||||||
| chr17:78048720
|
T | C | 3 | a0001c0001t0001g0013a0001c0001t0001g0030a0001c0001t0001g0052 | 3 | HG01496.hp2 HG01981.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.413-125T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | chr17 | 78048720 | ||||||
| chr17:78051480
|
T | TA | 59 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0015others(56): Show | 59 | HG00323.hp1 HG00423.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.3016+50dupA | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr17 | 78051480 | |||||
| chr17:78051480
|
TA | T | 9 | a0001c0002t0014g0054a0001c0002t0014g0055a0001c0002t0014g0071others(6): Show | 9 | HG01070.hp1 HG01891.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.3016+50delA | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr17 | 78051480 | |||||
| chr17:78051480
|
TAA | T | 21 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(18): Show | 21 | HG01255.hp2 HG01943.hp1 HG02155.hp1 others(18): Show |
intron_variant | MODIFIER | c.3016+49_3016+50del others(2): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr17 | 78051480 | |||||
| chr17:78051480
|
TAAA | T | 60 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(57): Show | 62 | HG01070.hp2 HG01071.hp2 HG01243.hp1 others(59): Show |
intron_variant | MODIFIER | c.3016+48_3016+50del others(3): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr17 | 78051480 | |||||
| chr17:78051524
|
A | G | 1 | a0001c0002t0013g0236 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3016+76A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78051524 | ||||||
| chr17:78051531
|
G | A | 70 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(67): Show | 72 | HG01070.hp2 HG01071.hp2 HG01243.hp1 others(69): Show |
intron_variant | MODIFIER | c.3016+83G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78051531 | ||||||
| chr17:78051656
|
A | G | 1 | a0016c0023t0045g0192 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3016+208A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78051656 | ||||||
| chr17:78051748
|
A | G | 22 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(19): Show | 22 | HG01243.hp1 HG01255.hp2 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.3016+300A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78051748 | ||||||
| chr17:78051975
|
A | G | 2 | a0005c0010t0038g0035a0005c0010t0053g0065 | 2 | HG01070.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.3016+527A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78051975 | ||||||
| chr17:78052216
|
G | C | 1 | a0002c0003t0003g0103 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3016+768G>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78052216 | ||||||
| chr17:78052234
|
T | G | 1 | a0001c0001t0009g0173 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.3016+786T>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78052234 | ||||||
| chr17:78052646
|
G | A | 4 | a0001c0001t0001g0170a0001c0009t0016g0140a0001c0009t0019g0171others(1): Show | 4 | HG00735.hp1 HG01167.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.3016+1198G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78052646 | ||||||
| chr17:78052751
|
TTGG | T | 18 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(15): Show | 18 | HG01243.hp1 HG01257.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.3016+1308_3016+131 others(7): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr17 | 78052751 | |||||
| chr17:78052865
|
A | G | 1 | a0001c0002t0002g0119 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3016+1417A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78052865 | ||||||
| chr17:78052914
|
G | A | 39 | a0002c0003t0003g0002a0002c0003t0003g0003a0002c0003t0003g0004others(36): Show | 41 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(38): Show |
intron_variant | MODIFIER | c.3016+1466G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78052914 | ||||||
| chr17:78052921
|
T | G | 1 | a0001c0001t0001g0030 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.3016+1473T>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78052921 | ||||||
| chr17:78053099
|
G | A | 1 | a0001c0001t0001g0039 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.3016+1651G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78053099 | ||||||
| chr17:78053192
|
G | A | 2 | a0002c0003t0010g0240a0002c0003t0010g0245 | 2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.3016+1744G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78053192 | ||||||
| chr17:78053294
|
G | A | 7 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0004g0176others(4): Show | 7 | HG00673.hp2 HG01169.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.3016+1846G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78053294 | ||||||
| chr17:78053607
|
C | T | 3 | a0001c0007t0012g0268a0001c0007t0012g0269a0001c0007t0012g0270 | 3 | HG02145.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3016+2159C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78053607 | ||||||
| chr17:78053877
|
A | G | 9 | a0001c0002t0014g0054a0001c0002t0014g0055a0001c0002t0014g0071others(6): Show | 9 | HG01070.hp1 HG01891.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.3016+2429A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78053877 | ||||||
| chr17:78053978
|
T | A | 40 | a0002c0003t0003g0002a0002c0003t0003g0003a0002c0003t0003g0004others(37): Show | 42 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(39): Show |
intron_variant | MODIFIER | c.3016+2530T>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78053978 | ||||||
| chr17:78054041
|
C | T | 69 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(66): Show | 71 | HG01070.hp2 HG01071.hp2 HG01243.hp1 others(68): Show |
intron_variant | MODIFIER | c.3016+2593C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78054041 | ||||||
| chr17:78054195
|
G | A | 44 | a0001c0007t0012g0268a0001c0007t0012g0269a0001c0007t0012g0270others(41): Show | 46 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(43): Show |
intron_variant | MODIFIER | c.3016+2747G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78054195 | ||||||
| chr17:78054289
|
CACTACTG others(32): Show |
C | 1 | a0002c0003t0025g0241 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3016+2888_3016+292 others(43): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr17 | 78054289 | |||||
| chr17:78054314
|
C | T | 11 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(8): Show | 11 | HG01243.hp1 HG01257.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.3016+2866C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78054314 | ||||||
| chr17:78054417
|
CACCACTG others(13): Show |
C | 2 | a0001c0001t0005g0023a0001c0001t0005g0086 | 2 | HG02145.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.3016+2989_3016+300 others(24): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr17 | 78054417 | |||||
| chr17:78054439
|
C | A | 1 | a0003c0012t0001g0220 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3016+2991C>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78054439 | ||||||
| chr17:78054457
|
T | C | 71 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(68): Show | 73 | HG01070.hp2 HG01071.hp2 HG01243.hp1 others(70): Show |
intron_variant | MODIFIER | c.3016+3009T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78054457 | ||||||
| chr17:78054495
|
T | A | 3 | a0001c0007t0012g0268a0001c0007t0012g0269a0001c0007t0012g0270 | 3 | HG02145.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3016+3047T>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78054495 | ||||||
| chr17:78054496
|
A | C | 3 | a0001c0007t0012g0268a0001c0007t0012g0269a0001c0007t0012g0270 | 3 | HG02145.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3016+3048A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78054496 | ||||||
| chr17:78054667
|
C | T | 8 | a0001c0002t0014g0054a0001c0002t0014g0055a0001c0002t0014g0071others(5): Show | 8 | HG01070.hp1 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.3016+3219C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78054667 | ||||||
| chr17:78054695
|
T | C | 77 | a0001c0001t0001g0106a0001c0001t0001g0127a0001c0001t0001g0128others(74): Show | 78 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.3016+3247T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78054695 | ||||||
| chr17:78054739
|
C | T | 18 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(15): Show | 18 | HG01243.hp1 HG01257.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.3016+3291C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78054739 | ||||||
| chr17:78054771
|
AC | A | 20 | a0001c0001t0001g0033a0001c0001t0001g0053a0001c0001t0001g0068others(17): Show | 20 | HG00423.hp1 HG01106.hp1 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.3016+3324delC | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78054771 | ||||||
| chr17:78054772
|
C | T | 6 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(3): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.3016+3324C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78054772 | ||||||
| chr17:78054848
|
A | G | 83 | a0001c0001t0001g0037a0001c0001t0001g0058a0001c0001t0001g0063others(80): Show | 84 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.3016+3400A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78054848 | ||||||
| chr17:78054876
|
A | G | 2 | a0001c0002t0061g0232a0001c0002t0062g0231 | 2 | HG04115.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.3016+3428A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78054876 | ||||||
| chr17:78054881
|
A | C | 1 | a0001c0001t0029g0239 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3016+3433A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78054881 | ||||||
| chr17:78054917
|
T | C | 1 | a0001c0001t0054g0094 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.3016+3469T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78054917 | ||||||
| chr17:78054917
|
T | TGCTACCA others(23): Show |
8 | a0001c0002t0014g0054a0001c0002t0014g0055a0001c0002t0014g0071others(5): Show | 8 | HG01070.hp1 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.3016+3530_3016+355 others(34): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr17 | 78054917 | |||||
| chr17:78054977
|
C | T | 2 | a0001c0001t0001g0015a0001c0001t0001g0016 | 2 | HG00673.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.3016+3529C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78054977 | ||||||
| chr17:78055022
|
G | C | 6 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(3): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.3016+3574G>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78055022 | ||||||
| chr17:78055055
|
C | T | 1 | a0002c0003t0058g0166 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.3016+3607C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78055055 | ||||||
| chr17:78055239
|
T | C | 2 | a0002c0014t0004g0168a0002c0014t0004g0169 | 2 | HG03490.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.3016+3791T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78055239 | ||||||
| chr17:78055325
|
G | A | 1 | a0001c0002t0002g0109 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.3016+3877G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78055325 | ||||||
| chr17:78055756
|
T | G | 1 | a0001c0002t0014g0055 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3016+4308T>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78055756 | ||||||
| chr17:78056158
|
C | CT | 11 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(8): Show | 11 | HG01243.hp1 HG01257.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.3016+4724dupT | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr17 | 78056158 | |||||
| chr17:78056231
|
T | C | 271 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0015others(268): Show | 274 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.3016+4783T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78056231 | ||||||
| chr17:78056467
|
C | CT | 15 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0087others(12): Show | 15 | HG02040.hp1 HG02135.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.3016+5033dupT | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr17 | 78056467 | |||||
| chr17:78056550
|
GC | G | 5 | a0001c0002t0013g0235a0001c0002t0013g0236a0001c0002t0013g0238others(2): Show | 5 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.3016+5104delC | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr17 | 78056550 | |||||
| chr17:78056573
|
C | T | 6 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(3): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.3016+5125C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78056573 | ||||||
| chr17:78056620
|
C | T | 3 | a0008c0028t0023g0258a0009c0015t0027g0264a0017c0017t0028g0263 | 3 | HG02258.hp1 HG02615.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.3016+5172C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78056620 | ||||||
| chr17:78056624
|
C | T | 40 | a0002c0003t0003g0002a0002c0003t0003g0003a0002c0003t0003g0004others(37): Show | 42 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(39): Show |
intron_variant | MODIFIER | c.3016+5176C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78056624 | ||||||
| chr17:78056825
|
G | A | 1 | a0002c0003t0003g0126 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3016+5377G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78056825 | ||||||
| chr17:78056854
|
T | TAATTCTC others(107): Show |
3 | a0002c0003t0003g0163a0002c0003t0003g0210a0002c0003t0007g0164 | 3 | HG01255.hp1 NA18969.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.3016+5417_3016+541 others(118): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr17 | 78056854 | |||||
| chr17:78056854
|
T | TAATTCTC others(108): Show |
33 | a0002c0003t0003g0002a0002c0003t0003g0003a0002c0003t0003g0011others(30): Show | 35 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.3016+5417_3016+541 others(119): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr17 | 78056854 | |||||
| chr17:78056854
|
T | TAATTCTC others(108): Show |
3 | a0002c0003t0003g0004a0002c0003t0003g0186a0002c0027t0003g0004 | 3 | HG01884.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.3016+5417_3016+541 others(119): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr17 | 78056854 | |||||
| chr17:78056854
|
T | TAATTCTC others(109): Show |
2 | a0002c0003t0003g0167a0002c0003t0056g0150 | 2 | HG02055.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.3016+5417_3016+541 others(120): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr17 | 78056854 | |||||
| chr17:78057079
|
G | A | 75 | a0001c0001t0001g0106a0001c0001t0001g0127a0001c0001t0001g0128others(72): Show | 76 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.3016+5631G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78057079 | ||||||
| chr17:78057140
|
TGTTAA | T | 8 | a0001c0002t0014g0054a0001c0002t0014g0055a0001c0002t0014g0071others(5): Show | 8 | HG01070.hp1 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.3016+5696_3016+570 others(9): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr17 | 78057140 | |||||
| chr17:78057203
|
T | A | 2 | a0009c0015t0027g0264a0017c0017t0028g0263 | 2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.3016+5755T>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78057203 | ||||||
| chr17:78057469
|
G | A | 2 | a0001c0001t0017g0266a0001c0001t0017g0267 | 2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3016+6021G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78057469 | ||||||
| chr17:78057608
|
G | C | 3 | a0008c0028t0023g0258a0009c0015t0027g0264a0017c0017t0028g0263 | 3 | HG02258.hp1 HG02615.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.3016+6160G>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78057608 | ||||||
| chr17:78057743
|
T | C | 5 | a0002c0003t0003g0003a0002c0003t0003g0012a0002c0003t0003g0165others(2): Show | 6 | HG02040.hp2 HG02132.hp2 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.3016+6295T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78057743 | ||||||
| chr17:78057768
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.3016+6320C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78057768 | ||||||
| chr17:78057825
|
T | G | 1 | a0001c0006t0033g0252 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.3016+6377T>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78057825 | ||||||
| chr17:78057825
|
T | TTG | 65 | a0001c0002t0013g0235a0001c0002t0013g0236a0001c0002t0013g0238others(62): Show | 67 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(64): Show |
intron_variant | MODIFIER | c.3016+6393_3016+639 others(6): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr17 | 78057825 | |||||
| chr17:78057859
|
A | G | 5 | a0001c0002t0013g0235a0001c0002t0013g0236a0001c0002t0013g0238others(2): Show | 5 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.3016+6411A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78057859 | ||||||
| chr17:78058023
|
C | G | 3 | a0008c0028t0023g0258a0009c0015t0027g0264a0017c0017t0028g0263 | 3 | HG02258.hp1 HG02615.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.3016+6575C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78058023 | ||||||
| chr17:78058126
|
C | G | 3 | a0008c0028t0023g0258a0009c0015t0027g0264a0017c0017t0028g0263 | 3 | HG02258.hp1 HG02615.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.3017-6596C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78058126 | ||||||
| chr17:78058290
|
G | A | 3 | a0001c0001t0001g0025a0001c0001t0001g0044a0001c0001t0016g0050 | 3 | HG01167.hp2 HG01261.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.3017-6432G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78058290 | ||||||
| chr17:78058350
|
T | C | 6 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(3): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.3017-6372T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78058350 | ||||||
| chr17:78058618
|
A | G | 8 | a0001c0002t0014g0054a0001c0002t0014g0055a0001c0002t0014g0071others(5): Show | 8 | HG01070.hp1 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.3017-6104A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78058618 | ||||||
| chr17:78058640
|
T | C | 3 | a0008c0028t0023g0258a0009c0015t0027g0264a0017c0017t0028g0263 | 3 | HG02258.hp1 HG02615.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.3017-6082T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78058640 | ||||||
| chr17:78058668
|
C | G | 41 | a0002c0003t0003g0002a0002c0003t0003g0003a0002c0003t0003g0004others(38): Show | 43 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.3017-6054C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78058668 | ||||||
| chr17:78058934
|
T | G | 11 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(8): Show | 11 | HG01243.hp1 HG01257.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.3017-5788T>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78058934 | ||||||
| chr17:78059028
|
C | A | 2 | a0001c0001t0017g0266a0001c0001t0017g0267 | 2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3017-5694C>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78059028 | ||||||
| chr17:78059232
|
T | G | 1 | a0001c0001t0001g0217 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.3017-5490T>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78059232 | ||||||
| chr17:78059466
|
G | A | 41 | a0002c0003t0003g0002a0002c0003t0003g0003a0002c0003t0003g0004others(38): Show | 43 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.3017-5256G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78059466 | ||||||
| chr17:78059719
|
C | G | 3 | a0008c0028t0023g0258a0009c0015t0027g0264a0017c0017t0028g0263 | 3 | HG02258.hp1 HG02615.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.3017-5003C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78059719 | ||||||
| chr17:78059846
|
C | CA | 27 | a0001c0001t0001g0021a0001c0001t0001g0068a0001c0001t0001g0221others(24): Show | 27 | HG01243.hp1 HG01257.hp2 HG01943.hp1 others(24): Show |
intron_variant | MODIFIER | c.3017-4859dupA | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr17 | 78059846 | |||||
| chr17:78059855
|
A | AG | 41 | a0002c0003t0003g0002a0002c0003t0003g0003a0002c0003t0003g0004others(38): Show | 43 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.3017-4867_3017-486 others(5): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78059855 | ||||||
| chr17:78059859
|
A | AG | 11 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(8): Show | 11 | HG02486.hp1 HG02622.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.3017-4863_3017-486 others(5): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78059859 | ||||||
| chr17:78059877
|
T | C | 5 | a0001c0002t0013g0235a0001c0002t0013g0236a0001c0002t0013g0238others(2): Show | 5 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.3017-4845T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78059877 | ||||||
| chr17:78059895
|
C | T | 1 | a0001c0001t0015g0014 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3017-4827C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78059895 | ||||||
| chr17:78060000
|
A | G | 3 | a0008c0028t0023g0258a0009c0015t0027g0264a0017c0017t0028g0263 | 3 | HG02258.hp1 HG02615.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.3017-4722A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78060000 | ||||||
| chr17:78060055
|
G | A | 2 | a0001c0001t0001g0039a0001c0001t0001g0089 | 2 | NA18959.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.3017-4667G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78060055 | ||||||
| chr17:78060055
|
G | T | 4 | a0001c0001t0004g0176a0001c0001t0015g0014a0001c0001t0015g0018others(1): Show | 4 | HG01169.hp2 HG01175.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.3017-4667G>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78060055 | ||||||
| chr17:78060063
|
T | C | 55 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(52): Show | 57 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(54): Show |
intron_variant | MODIFIER | c.3017-4659T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78060063 | ||||||
| chr17:78060072
|
G | A | 44 | a0001c0007t0012g0268a0001c0007t0012g0269a0001c0007t0012g0270others(41): Show | 46 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(43): Show |
intron_variant | MODIFIER | c.3017-4650G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78060072 | ||||||
| chr17:78060177
|
G | A | 6 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(3): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.3017-4545G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78060177 | ||||||
| chr17:78060189
|
G | A | 4 | a0001c0001t0004g0176a0001c0001t0015g0014a0001c0001t0015g0018others(1): Show | 4 | HG01169.hp2 HG01175.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.3017-4533G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78060189 | ||||||
| chr17:78060354
|
G | A | 3 | a0001c0007t0012g0268a0001c0007t0012g0269a0001c0007t0012g0270 | 3 | HG02145.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3017-4368G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78060354 | ||||||
| chr17:78060446
|
G | A | 1 | a0001c0002t0013g0238 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3017-4276G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78060446 | ||||||
| chr17:78060447
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3017-4275A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78060447 | ||||||
| chr17:78060468
|
C | CT | 14 | a0001c0001t0001g0034a0001c0001t0001g0076a0001c0001t0001g0085others(11): Show | 14 | HG01071.hp1 HG01934.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.3017-4233dupT | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr17 | 78060468 | |||||
| chr17:78060468
|
CT | C | 14 | a0001c0001t0001g0039a0001c0001t0001g0063a0001c0001t0001g0082others(11): Show | 14 | HG01993.hp2 HG02258.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.3017-4233delT | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr17 | 78060468 | |||||
| chr17:78060468
|
CTT | C | 41 | a0002c0003t0003g0002a0002c0003t0003g0003a0002c0003t0003g0004others(38): Show | 43 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.3017-4234_3017-423 others(6): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr17 | 78060468 | |||||
| chr17:78060612
|
A | G | 1 | a0001c0001t0001g0072 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.3017-4110A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78060612 | ||||||
| chr17:78060664
|
C | T | 1 | a0001c0002t0002g0110 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3017-4058C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78060664 | ||||||
| chr17:78060784
|
C | T | 3 | a0001c0004t0011g0257a0001c0004t0011g0262a0001c0004t0026g0260 | 3 | HG02717.hp1 HG03041.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.3017-3938C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78060784 | ||||||
| chr17:78061047
|
T | G | 3 | a0001c0001t0004g0176a0001c0001t0015g0014a0001c0001t0015g0018 | 3 | HG01175.hp1 HG01496.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.3017-3675T>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78061047 | ||||||
| chr17:78061142
|
G | C | 3 | a0001c0007t0012g0268a0001c0007t0012g0269a0001c0007t0012g0270 | 3 | HG02145.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3017-3580G>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78061142 | ||||||
| chr17:78061273
|
A | G | 41 | a0002c0003t0003g0002a0002c0003t0003g0003a0002c0003t0003g0004others(38): Show | 43 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.3017-3449A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78061273 | ||||||
| chr17:78061326
|
G | A | 3 | a0001c0007t0012g0268a0001c0007t0012g0269a0001c0007t0012g0270 | 3 | HG02145.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3017-3396G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78061326 | ||||||
| chr17:78061354
|
A | C | 41 | a0002c0003t0003g0002a0002c0003t0003g0003a0002c0003t0003g0004others(38): Show | 43 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.3017-3368A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78061354 | ||||||
| chr17:78061457
|
A | G | 1 | a0001c0001t0005g0224 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3017-3265A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78061457 | ||||||
| chr17:78061618
|
C | T | 14 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(11): Show | 14 | HG02145.hp2 HG02486.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.3017-3104C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78061618 | ||||||
| chr17:78061661
|
A | G | 64 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(61): Show | 66 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(63): Show |
intron_variant | MODIFIER | c.3017-3061A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78061661 | ||||||
| chr17:78061668
|
G | A | 1 | a0008c0028t0023g0258 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3017-3054G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78061668 | ||||||
| chr17:78061717
|
G | T | 14 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(11): Show | 14 | HG02145.hp2 HG02486.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.3017-3005G>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78061717 | ||||||
| chr17:78062103
|
A | T | 11 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(8): Show | 11 | HG01243.hp1 HG01257.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.3017-2619A>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78062103 | ||||||
| chr17:78062147
|
C | T | 2 | a0001c0001t0001g0185a0001c0001t0001g0187 | 2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3017-2575C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78062147 | ||||||
| chr17:78062292
|
A | G | 1 | a0001c0001t0001g0040 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3017-2430A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78062292 | ||||||
| chr17:78062351
|
T | TA | 272 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0015others(269): Show | 275 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(272): Show |
intron_variant | MODIFIER | c.3017-2369dupA | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr17 | 78062351 | |||||
| chr17:78062416
|
A | T | 8 | a0001c0002t0014g0054a0001c0002t0014g0055a0001c0002t0014g0071others(5): Show | 8 | HG01070.hp1 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.3017-2306A>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78062416 | ||||||
| chr17:78062429
|
C | A | 3 | a0001c0007t0012g0268a0001c0007t0012g0269a0001c0007t0012g0270 | 3 | HG02145.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3017-2293C>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78062429 | ||||||
| chr17:78062601
|
A | T | 90 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(87): Show | 92 | HG01070.hp1 HG01070.hp2 HG01071.hp2 others(89): Show |
intron_variant | MODIFIER | c.3017-2121A>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78062601 | ||||||
| chr17:78062656
|
T | C | 5 | a0001c0002t0013g0235a0001c0002t0013g0236a0001c0002t0013g0238others(2): Show | 5 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.3017-2066T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78062656 | ||||||
| chr17:78062795
|
G | C | 1 | a0001c0006t0008g0251 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.3017-1927G>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78062795 | ||||||
| chr17:78062824
|
C | T | 14 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(11): Show | 14 | HG02145.hp2 HG02486.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.3017-1898C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78062824 | ||||||
| chr17:78062836
|
C | G | 3 | a0008c0028t0023g0258a0009c0015t0027g0264a0017c0017t0028g0263 | 3 | HG02258.hp1 HG02615.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.3017-1886C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78062836 | ||||||
| chr17:78062974
|
G | A | 1 | a0003c0012t0001g0022 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3017-1748G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78062974 | ||||||
| chr17:78063138
|
C | T | 3 | a0001c0007t0012g0268a0001c0007t0012g0269a0001c0007t0012g0270 | 3 | HG02145.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3017-1584C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78063138 | ||||||
| chr17:78063258
|
T | C | 1 | a0002c0003t0003g0163 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.3017-1464T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78063258 | ||||||
| chr17:78063264
|
T | A | 3 | a0001c0007t0012g0268a0001c0007t0012g0269a0001c0007t0012g0270 | 3 | HG02145.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3017-1458T>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78063264 | ||||||
| chr17:78063310
|
C | T | 14 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(11): Show | 14 | HG02145.hp2 HG02486.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.3017-1412C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78063310 | ||||||
| chr17:78063333
|
T | C | 3 | a0001c0007t0012g0268a0001c0007t0012g0269a0001c0007t0012g0270 | 3 | HG02145.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3017-1389T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78063333 | ||||||
| chr17:78063460
|
C | T | 1 | a0002c0003t0003g0210 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.3017-1262C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78063460 | ||||||
| chr17:78063563
|
G | A | 1 | a0009c0015t0027g0264 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3017-1159G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78063563 | ||||||
| chr17:78063661
|
C | CAG | 41 | a0002c0003t0003g0002a0002c0003t0003g0003a0002c0003t0003g0004others(38): Show | 43 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.3017-1059_3017-105 others(6): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr17 | 78063661 | |||||
| chr17:78063701
|
A | G | 58 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(55): Show | 60 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(57): Show |
intron_variant | MODIFIER | c.3017-1021A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78063701 | ||||||
| chr17:78063703
|
A | G | 55 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(52): Show | 57 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(54): Show |
intron_variant | MODIFIER | c.3017-1019A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78063703 | ||||||
| chr17:78063799
|
T | C | 1 | a0001c0001t0036g0066 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3017-923T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78063799 | ||||||
| chr17:78063919
|
T | C | 1 | a0001c0029t0001g0031 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.3017-803T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78063919 | ||||||
| chr17:78063931
|
A | G | 1 | a0001c0006t0033g0252 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.3017-791A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78063931 | ||||||
| chr17:78064137
|
G | A | 3 | a0002c0003t0003g0004a0002c0003t0003g0186a0002c0027t0003g0004 | 3 | HG01884.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.3017-585G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78064137 | ||||||
| chr17:78064189
|
G | A | 3 | a0001c0007t0012g0268a0001c0007t0012g0269a0001c0007t0012g0270 | 3 | HG02145.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3017-533G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78064189 | ||||||
| chr17:78064230
|
G | A | 11 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(8): Show | 11 | HG02486.hp1 HG02622.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.3017-492G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78064230 | ||||||
| chr17:78065084
|
C | A | 1 | a0001c0001t0029g0239 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3232+147C>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 6/22 | chr17 | 78065084 | ||||||
| chr17:78065206
|
G | A | 9 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(6): Show | 9 | HG01943.hp1 HG02145.hp2 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.3232+269G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 6/22 | chr17 | 78065206 | ||||||
| chr17:78065245
|
G | A | 6 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(3): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.3232+308G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 6/22 | chr17 | 78065245 | ||||||
| chr17:78065358
|
G | GA | 7 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(4): Show | 7 | HG02486.hp1 HG02622.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.3232+432dupA | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr17 | 78065358 | |||||
| chr17:78065393
|
A | G | 2 | a0001c0001t0016g0142a0001c0001t0019g0141 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.3232+456A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 6/22 | chr17 | 78065393 | ||||||
| chr17:78065485
|
C | A | 166 | a0001c0001t0001g0106a0001c0001t0001g0127a0001c0001t0001g0128others(163): Show | 169 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.3232+548C>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 6/22 | chr17 | 78065485 | ||||||
| chr17:78065665
|
G | T | 1 | a0001c0002t0061g0232 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3232+728G>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 6/22 | chr17 | 78065665 | ||||||
| chr17:78065889
|
T | C | 3 | a0001c0007t0012g0268a0001c0007t0012g0269a0001c0007t0012g0270 | 3 | HG02145.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3232+952T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 6/22 | chr17 | 78065889 | ||||||
| chr17:78065911
|
A | G | 1 | a0001c0001t0001g0225 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3232+974A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 6/22 | chr17 | 78065911 | ||||||
| chr17:78066075
|
A | G | 41 | a0002c0003t0003g0002a0002c0003t0003g0003a0002c0003t0003g0004others(38): Show | 43 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.3232+1138A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 6/22 | chr17 | 78066075 | ||||||
| chr17:78066155
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.3232+1218C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 6/22 | chr17 | 78066155 | ||||||
| chr17:78066226
|
CA | C | 82 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(79): Show | 84 | HG01070.hp1 HG01070.hp2 HG01071.hp2 others(81): Show |
intron_variant | MODIFIER | c.3232+1306delA | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr17 | 78066226 | |||||
| chr17:78066326
|
G | A | 11 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(8): Show | 11 | HG01243.hp1 HG01257.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.3232+1389G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 6/22 | chr17 | 78066326 | ||||||
| chr17:78066347
|
T | C | 44 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0015others(41): Show | 44 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.3232+1410T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 6/22 | chr17 | 78066347 | ||||||
| chr17:78066382
|
C | T | 3 | a0001c0007t0012g0268a0001c0007t0012g0269a0001c0007t0012g0270 | 3 | HG02145.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3233-1375C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 6/22 | chr17 | 78066382 | ||||||
| chr17:78066415
|
C | T | 7 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(4): Show | 7 | HG02486.hp1 HG02622.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.3233-1342C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 6/22 | chr17 | 78066415 | ||||||
| chr17:78066654
|
A | G | 41 | a0002c0003t0003g0002a0002c0003t0003g0003a0002c0003t0003g0004others(38): Show | 43 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.3233-1103A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 6/22 | chr17 | 78066654 | ||||||
| chr17:78066724
|
A | G | 3 | a0008c0028t0023g0258a0009c0015t0027g0264a0017c0017t0028g0263 | 3 | HG02258.hp1 HG02615.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.3233-1033A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 6/22 | chr17 | 78066724 | ||||||
| chr17:78066841
|
A | G | 3 | a0001c0007t0012g0268a0001c0007t0012g0269a0001c0007t0012g0270 | 3 | HG02145.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3233-916A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 6/22 | chr17 | 78066841 | ||||||
| chr17:78066886
|
T | C | 5 | a0001c0001t0001g0202a0001c0001t0001g0204a0001c0001t0001g0205others(2): Show | 5 | NA18940.hp2 NA18957.hp2 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.3233-871T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 6/22 | chr17 | 78066886 | ||||||
| chr17:78066907
|
C | T | 41 | a0002c0003t0003g0002a0002c0003t0003g0003a0002c0003t0003g0004others(38): Show | 43 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.3233-850C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 6/22 | chr17 | 78066907 | ||||||
| chr17:78066966
|
A | G | 41 | a0002c0003t0003g0002a0002c0003t0003g0003a0002c0003t0003g0004others(38): Show | 43 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.3233-791A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 6/22 | chr17 | 78066966 | ||||||
| chr17:78067127
|
G | C | 41 | a0002c0003t0003g0002a0002c0003t0003g0003a0002c0003t0003g0004others(38): Show | 43 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.3233-630G>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 6/22 | chr17 | 78067127 | ||||||
| chr17:78067343
|
A | G | 14 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(11): Show | 14 | HG02145.hp2 HG02486.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.3233-414A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 6/22 | chr17 | 78067343 | ||||||
| chr17:78067436
|
A | C | 2 | a0009c0015t0027g0264a0017c0017t0028g0263 | 2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.3233-321A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 6/22 | chr17 | 78067436 | ||||||
| chr17:78067453
|
G | C | 5 | a0001c0002t0013g0235a0001c0002t0013g0236a0001c0002t0013g0238others(2): Show | 5 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.3233-304G>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 6/22 | chr17 | 78067453 | ||||||
| chr17:78067672
|
C | T | 1 | a0009c0015t0027g0264 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3233-85C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 6/22 | chr17 | 78067672 | ||||||
| chr17:78067673
|
G | A | 11 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(8): Show | 11 | HG02486.hp1 HG02622.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.3233-84G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 6/22 | chr17 | 78067673 | ||||||
| chr17:78067718
|
G | A | 3 | a0001c0001t0001g0185a0001c0001t0001g0187a0001c0001t0034g0188 | 3 | HG03209.hp2 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3233-39G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 6/22 | chr17 | 78067718 | ||||||
| chr17:78068002
|
A | G | 1 | a0007c0013t0022g0010 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.3399+79A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 7/22 | chr17 | 78068002 | ||||||
| chr17:78068406
|
G | A | 41 | a0002c0003t0003g0002a0002c0003t0003g0003a0002c0003t0003g0004others(38): Show | 43 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.3399+483G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 7/22 | chr17 | 78068406 | ||||||
| chr17:78068633
|
A | G | 1 | a0001c0006t0033g0252 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.3399+710A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 7/22 | chr17 | 78068633 | ||||||
| chr17:78068895
|
C | G | 41 | a0002c0003t0003g0002a0002c0003t0003g0003a0002c0003t0003g0004others(38): Show | 43 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.3399+972C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 7/22 | chr17 | 78068895 | ||||||
| chr17:78069041
|
G | C | 32 | a0001c0001t0001g0106a0001c0001t0051g0105a0001c0002t0002g0005others(29): Show | 32 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.3399+1118G>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 7/22 | chr17 | 78069041 | ||||||
| chr17:78069209
|
T | TA | 40 | a0002c0003t0003g0002a0002c0003t0003g0003a0002c0003t0003g0004others(37): Show | 42 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(39): Show |
intron_variant | MODIFIER | c.3399+1296dupA | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr17 | 78069209 | |||||
| chr17:78069595
|
G | A | 8 | a0001c0005t0001g0001a0001c0005t0001g0007a0001c0005t0001g0008others(5): Show | 9 | HG02451.hp1 HG02630.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.3400-1490G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 7/22 | chr17 | 78069595 | ||||||
| chr17:78069700
|
A | G | 41 | a0002c0003t0003g0002a0002c0003t0003g0003a0002c0003t0003g0004others(38): Show | 43 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.3400-1385A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 7/22 | chr17 | 78069700 | ||||||
| chr17:78069703
|
G | A | 41 | a0002c0003t0003g0002a0002c0003t0003g0003a0002c0003t0003g0004others(38): Show | 43 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.3400-1382G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 7/22 | chr17 | 78069703 | ||||||
| chr17:78069766
|
T | G | 41 | a0002c0003t0003g0002a0002c0003t0003g0003a0002c0003t0003g0004others(38): Show | 43 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.3400-1319T>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 7/22 | chr17 | 78069766 | ||||||
| chr17:78069816
|
G | A | 1 | a0001c0002t0002g0110 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3400-1269G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 7/22 | chr17 | 78069816 | ||||||
| chr17:78069994
|
A | G | 2 | a0001c0001t0001g0134a0001c0001t0021g0061 | 2 | NA18964.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.3400-1091A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 7/22 | chr17 | 78069994 | ||||||
| chr17:78070006
|
C | T | 6 | a0001c0002t0014g0054a0001c0002t0014g0055a0001c0002t0014g0071others(3): Show | 6 | HG01070.hp1 HG01891.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.3400-1079C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 7/22 | chr17 | 78070006 | ||||||
| chr17:78070128
|
A | G | 11 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(8): Show | 11 | HG02486.hp1 HG02622.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.3400-957A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 7/22 | chr17 | 78070128 | ||||||
| chr17:78070196
|
G | C | 4 | a0001c0005t0001g0001a0001c0005t0001g0145a0001c0005t0001g0146others(1): Show | 5 | HG02630.hp1 HG03041.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.3400-889G>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 7/22 | chr17 | 78070196 | ||||||
| chr17:78070493
|
A | T | 62 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0131others(59): Show | 62 | HG00280.hp2 HG00597.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.3400-592A>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 7/22 | chr17 | 78070493 | ||||||
| chr17:78070626
|
G | A | 10 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(7): Show | 10 | HG02486.hp1 HG02622.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.3400-459G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 7/22 | chr17 | 78070626 | ||||||
| chr17:78070673
|
A | T | 11 | a0001c0001t0005g0224a0001c0001t0060g0233a0001c0002t0014g0054others(8): Show | 11 | HG01070.hp1 HG01891.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.3400-412A>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 7/22 | chr17 | 78070673 | ||||||
| chr17:78070825
|
C | T | 30 | a0001c0001t0004g0124a0001c0001t0004g0143a0001c0001t0004g0157others(27): Show | 30 | HG00735.hp1 HG01070.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.3400-260C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 7/22 | chr17 | 78070825 | ||||||
| chr17:78070882
|
C | T | 2 | a0002c0003t0010g0240a0002c0003t0010g0245 | 2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.3400-203C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 7/22 | chr17 | 78070882 | ||||||
| chr17:78070885
|
G | A | 2 | a0002c0003t0010g0240a0002c0003t0010g0245 | 2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.3400-200G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 7/22 | chr17 | 78070885 | ||||||
| chr17:78071204
|
C | G | 36 | a0002c0003t0003g0002a0002c0003t0003g0003a0002c0003t0003g0004others(33): Show | 38 | HG01070.hp2 HG01071.hp2 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.3480+39C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 8/22 | chr17 | 78071204 | ||||||
| chr17:78071374
|
C | T | 96 | a0001c0001t0001g0106a0001c0001t0051g0105a0001c0002t0002g0005others(93): Show | 98 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.3480+209C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 8/22 | chr17 | 78071374 | ||||||
| chr17:78071548
|
C | T | 8 | a0001c0005t0001g0001a0001c0005t0001g0007a0001c0005t0001g0008others(5): Show | 9 | HG02451.hp1 HG02630.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.3480+383C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 8/22 | chr17 | 78071548 | ||||||
| chr17:78071619
|
C | T | 1 | a0001c0001t0001g0217 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.3480+454C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 8/22 | chr17 | 78071619 | ||||||
| chr17:78071626
|
G | A | 2 | a0009c0015t0027g0264a0017c0017t0028g0263 | 2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.3480+461G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 8/22 | chr17 | 78071626 | ||||||
| chr17:78071687
|
C | T | 1 | a0001c0001t0017g0267 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3480+522C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 8/22 | chr17 | 78071687 | ||||||
| chr17:78071726
|
A | G | 1 | a0001c0001t0001g0069 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.3480+561A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 8/22 | chr17 | 78071726 | ||||||
| chr17:78071781
|
G | C | 1 | a0002c0003t0003g0144 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.3480+616G>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 8/22 | chr17 | 78071781 | ||||||
| chr17:78071916
|
G | T | 2 | a0001c0001t0017g0266a0001c0001t0017g0267 | 2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3480+751G>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 8/22 | chr17 | 78071916 | ||||||
| chr17:78072251
|
T | A | 11 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(8): Show | 11 | HG02486.hp1 HG02622.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.3481-786T>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 8/22 | chr17 | 78072251 | ||||||
| chr17:78072968
|
T | C | 1 | a0001c0001t0043g0177 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.3481-69T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 8/22 | chr17 | 78072968 | ||||||
| chr17:78073335
|
C | G | 8 | a0001c0005t0001g0001a0001c0005t0001g0007a0001c0005t0001g0008others(5): Show | 9 | HG02451.hp1 HG02630.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.3538+241C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 9/22 | chr17 | 78073335 | ||||||
| chr17:78073336
|
C | T | 19 | a0001c0001t0001g0033a0001c0001t0001g0053a0001c0001t0001g0068others(16): Show | 19 | HG00423.hp1 HG01106.hp1 HG02080.hp2 others(16): Show |
intron_variant | MODIFIER | c.3538+242C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 9/22 | chr17 | 78073336 | ||||||
| chr17:78073692
|
A | G | 36 | a0002c0003t0003g0002a0002c0003t0003g0003a0002c0003t0003g0004others(33): Show | 38 | HG01070.hp2 HG01071.hp2 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.3538+598A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 9/22 | chr17 | 78073692 | ||||||
| chr17:78073817
|
G | A | 1 | a0001c0002t0014g0055 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3538+723G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 9/22 | chr17 | 78073817 | ||||||
| chr17:78074106
|
G | A | 1 | a0010c0031t0040g0048 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.3538+1012G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 9/22 | chr17 | 78074106 | ||||||
| chr17:78074175
|
AC | A | 6 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(3): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.3539-960delC | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 9/22 | chr17 | 78074175 | ||||||
| chr17:78074199
|
C | G | 30 | a0001c0001t0001g0032a0001c0001t0001g0038a0001c0001t0001g0039others(27): Show | 30 | HG00280.hp2 HG00558.hp1 HG00597.hp1 others(27): Show |
intron_variant | MODIFIER | c.3539-937C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 9/22 | chr17 | 78074199 | ||||||
| chr17:78074392
|
G | C | 1 | a0009c0015t0027g0264 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3539-744G>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 9/22 | chr17 | 78074392 | ||||||
| chr17:78074620
|
T | A | 1 | a0012c0019t0001g0114 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.3539-516T>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 9/22 | chr17 | 78074620 | ||||||
| chr17:78074640
|
G | A | 1 | a0012c0019t0001g0114 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.3539-496G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 9/22 | chr17 | 78074640 | ||||||
| chr17:78074644
|
A | C | 7 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(4): Show | 7 | HG01943.hp1 HG02155.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.3539-492A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 9/22 | chr17 | 78074644 | ||||||
| chr17:78074726
|
G | C | 1 | a0001c0001t0017g0266 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3539-410G>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 9/22 | chr17 | 78074726 | ||||||
| chr17:78074781
|
C | T | 1 | a0009c0015t0027g0264 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3539-355C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 9/22 | chr17 | 78074781 | ||||||
| chr17:78074878
|
G | A | 8 | a0001c0002t0014g0054a0001c0002t0014g0055a0001c0002t0014g0071others(5): Show | 8 | HG01070.hp1 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.3539-258G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 9/22 | chr17 | 78074878 | ||||||
| chr17:78074948
|
C | T | 1 | a0001c0001t0036g0066 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3539-188C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 9/22 | chr17 | 78074948 | ||||||
| chr17:78074957
|
T | C | 1 | a0001c0002t0035g0184 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3539-179T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 9/22 | chr17 | 78074957 | ||||||
| chr17:78075129
|
G | T | 1 | a0001c0001t0043g0177 | 1 | NA19090.hp1 | splice_region_variant&intron_variant | LOW | c.3539-7G>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 9/22 | chr17 | 78075129 | ||||||
| chr17:78075353
|
C | A | 2 | a0002c0003t0003g0126a0002c0003t0003g0194 | 2 | HG02135.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.3681+75C>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 10/22 | chr17 | 78075353 | ||||||
| chr17:78075624
|
G | A | 1 | a0009c0015t0027g0264 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3681+346G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 10/22 | chr17 | 78075624 | ||||||
| chr17:78075631
|
A | G | 4 | a0001c0001t0001g0072a0004c0008t0001g0073a0004c0008t0001g0074others(1): Show | 4 | NA18943.hp1 NA18968.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.3681+353A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 10/22 | chr17 | 78075631 | ||||||
| chr17:78075664
|
T | C | 1 | a0002c0003t0010g0250 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.3681+386T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 10/22 | chr17 | 78075664 | ||||||
| chr17:78075669
|
C | CT | 12 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(9): Show | 12 | HG02486.hp1 HG02615.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.3681+393dupT | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr17 | 78075669 | |||||
| chr17:78075690
|
G | A | 3 | a0001c0002t0002g0111a0001c0002t0002g0112a0003c0021t0002g0113 | 3 | HG01952.hp1 HG01981.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.3681+412G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 10/22 | chr17 | 78075690 | ||||||
| chr17:78075742
|
G | A | 1 | a0009c0015t0027g0264 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3681+464G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 10/22 | chr17 | 78075742 | ||||||
| chr17:78075747
|
G | A | 3 | a0001c0002t0002g0111a0001c0002t0002g0112a0003c0021t0002g0113 | 3 | HG01952.hp1 HG01981.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.3681+469G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 10/22 | chr17 | 78075747 | ||||||
| chr17:78075807
|
A | G | 1 | a0001c0001t0001g0187 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3681+529A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 10/22 | chr17 | 78075807 | ||||||
| chr17:78075966
|
C | T | 1 | a0001c0005t0001g0137 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3681+688C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 10/22 | chr17 | 78075966 | ||||||
| chr17:78076088
|
C | T | 1 | a0009c0015t0027g0264 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3681+810C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 10/22 | chr17 | 78076088 | ||||||
| chr17:78076215
|
CAAAAAAA others(12): Show |
C | 7 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0087others(4): Show | 7 | HG02040.hp1 HG02135.hp1 HG04228.hp2 others(4): Show |
intron_variant | MODIFIER | c.3681+950_3682-939d others(21): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr17 | 78076215 | |||||
| chr17:78076238
|
A | AG | 93 | a0001c0001t0001g0106a0001c0001t0017g0266a0001c0001t0017g0267others(90): Show | 95 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.3682-947_3682-946i others(3): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 10/22 | chr17 | 78076238 | ||||||
| chr17:78076239
|
A | G | 12 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(9): Show | 12 | HG02486.hp1 HG02615.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.3682-946A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 10/22 | chr17 | 78076239 | ||||||
| chr17:78076363
|
T | C | 102 | a0001c0001t0001g0106a0001c0001t0051g0105a0001c0002t0002g0005others(99): Show | 104 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.3682-822T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 10/22 | chr17 | 78076363 | ||||||
| chr17:78076475
|
T | G | 1 | a0001c0001t0001g0067 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.3682-710T>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 10/22 | chr17 | 78076475 | ||||||
| chr17:78076678
|
C | T | 1 | a0009c0015t0027g0264 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3682-507C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 10/22 | chr17 | 78076678 | ||||||
| chr17:78076692
|
T | C | 1 | a0001c0001t0063g0042 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3682-493T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 10/22 | chr17 | 78076692 | ||||||
| chr17:78076840
|
T | A | 1 | a0009c0015t0027g0264 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3682-345T>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 10/22 | chr17 | 78076840 | ||||||
| chr17:78076909
|
G | A | 1 | a0016c0023t0045g0192 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3682-276G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 10/22 | chr17 | 78076909 | ||||||
| chr17:78077024
|
C | T | 1 | a0001c0001t0004g0143 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.3682-161C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 10/22 | chr17 | 78077024 | ||||||
| chr17:78077098
|
C | CG | 47 | a0001c0001t0001g0106a0001c0001t0051g0105a0001c0002t0002g0005others(44): Show | 47 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.3682-86dupG | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr17 | 78077098 | |||||
| chr17:78077645
|
G | C | 47 | a0001c0001t0001g0106a0001c0001t0051g0105a0001c0002t0002g0005others(44): Show | 47 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.3831+311G>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 11/22 | chr17 | 78077645 | ||||||
| chr17:78078115
|
A | G | 53 | a0001c0001t0001g0106a0001c0001t0051g0105a0001c0002t0002g0005others(50): Show | 53 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.3831+781A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 11/22 | chr17 | 78078115 | ||||||
| chr17:78078156
|
T | C | 1 | a0009c0015t0027g0264 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3831+822T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 11/22 | chr17 | 78078156 | ||||||
| chr17:78078250
|
A | G | 1 | a0002c0003t0007g0102 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.3831+916A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 11/22 | chr17 | 78078250 | ||||||
| chr17:78078597
|
G | A | 1 | a0001c0001t0001g0213 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.3832-798G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 11/22 | chr17 | 78078597 | ||||||
| chr17:78078636
|
G | T | 2 | a0001c0001t0005g0026a0001c0001t0005g0084 | 2 | HG02040.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.3832-759G>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 11/22 | chr17 | 78078636 | ||||||
| chr17:78078876
|
A | T | 1 | a0009c0015t0027g0264 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3832-519A>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 11/22 | chr17 | 78078876 | ||||||
| chr17:78078908
|
T | A | 1 | a0001c0004t0006g0244 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3832-487T>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 11/22 | chr17 | 78078908 | ||||||
| chr17:78078916
|
C | A | 1 | a0001c0001t0004g0143 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.3832-479C>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 11/22 | chr17 | 78078916 | ||||||
| chr17:78078969
|
G | A | 2 | a0001c0001t0017g0266a0001c0001t0017g0267 | 2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3832-426G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 11/22 | chr17 | 78078969 | ||||||
| chr17:78078991
|
A | G | 6 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(3): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.3832-404A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 11/22 | chr17 | 78078991 | ||||||
| chr17:78079039
|
T | C | 54 | a0001c0001t0001g0106a0001c0001t0051g0105a0001c0002t0002g0005others(51): Show | 54 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.3832-356T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 11/22 | chr17 | 78079039 | ||||||
| chr17:78079121
|
G | C | 6 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(3): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.3832-274G>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 11/22 | chr17 | 78079121 | ||||||
| chr17:78079258
|
C | A | 1 | a0009c0015t0027g0264 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3832-137C>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 11/22 | chr17 | 78079258 | ||||||
| chr17:78079763
|
T | C | 4 | a0001c0002t0002g0179a0001c0002t0002g0180a0001c0002t0002g0181others(1): Show | 4 | HG01261.hp1 HG03098.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.3978+222T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 12/22 | chr17 | 78079763 | ||||||
| chr17:78080168
|
C | T | 1 | a0001c0004t0006g0244 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3978+627C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 12/22 | chr17 | 78080168 | ||||||
| chr17:78080169
|
G | A | 1 | a0001c0001t0042g0099 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3978+628G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 12/22 | chr17 | 78080169 | ||||||
| chr17:78080228
|
C | G | 1 | a0003c0012t0001g0022 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3978+687C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 12/22 | chr17 | 78080228 | ||||||
| chr17:78080311
|
T | G | 1 | a0002c0003t0007g0102 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.3978+770T>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 12/22 | chr17 | 78080311 | ||||||
| chr17:78080406
|
A | ATTGCACT others(29): Show |
1 | a0002c0003t0007g0102 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.3978+868_3978+903d others(38): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr17 | 78080406 | |||||
| chr17:78081097
|
C | T | 40 | a0001c0001t0001g0106a0001c0001t0051g0105a0001c0002t0002g0005others(37): Show | 40 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.3978+1556C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 12/22 | chr17 | 78081097 | ||||||
| chr17:78081272
|
T | G | 6 | a0001c0002t0013g0235a0001c0002t0013g0236a0001c0002t0013g0238others(3): Show | 6 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.3978+1731T>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 12/22 | chr17 | 78081272 | ||||||
| chr17:78081276
|
G | A | 1 | a0002c0003t0007g0102 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.3978+1735G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 12/22 | chr17 | 78081276 | ||||||
| chr17:78081417
|
T | C | 1 | a0001c0001t0065g0017 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.3979-1630T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 12/22 | chr17 | 78081417 | ||||||
| chr17:78081544
|
A | G | 48 | a0001c0001t0001g0106a0001c0001t0051g0105a0001c0002t0002g0005others(45): Show | 48 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.3979-1503A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 12/22 | chr17 | 78081544 | ||||||
| chr17:78081619
|
A | G | 187 | a0001c0001t0001g0032a0001c0001t0001g0037a0001c0001t0001g0038others(184): Show | 190 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(187): Show |
intron_variant | MODIFIER | c.3979-1428A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 12/22 | chr17 | 78081619 | ||||||
| chr17:78081813
|
G | T | 36 | a0002c0003t0003g0002a0002c0003t0003g0003a0002c0003t0003g0004others(33): Show | 38 | HG01070.hp2 HG01071.hp2 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.3979-1234G>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 12/22 | chr17 | 78081813 | ||||||
| chr17:78081872
|
C | G | 1 | a0001c0001t0001g0076 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3979-1175C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 12/22 | chr17 | 78081872 | ||||||
| chr17:78082027
|
A | G | 4 | a0001c0001t0004g0124a0001c0001t0004g0189a0001c0001t0004g0190others(1): Show | 4 | HG01884.hp2 HG02109.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.3979-1020A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 12/22 | chr17 | 78082027 | ||||||
| chr17:78082075
|
T | C | 1 | a0001c0004t0011g0261 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3979-972T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 12/22 | chr17 | 78082075 | ||||||
| chr17:78082138
|
T | C | 185 | a0001c0001t0001g0032a0001c0001t0001g0037a0001c0001t0001g0038others(182): Show | 188 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.3979-909T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 12/22 | chr17 | 78082138 | ||||||
| chr17:78082207
|
A | C | 76 | a0001c0001t0001g0032a0001c0001t0001g0037a0001c0001t0001g0038others(73): Show | 76 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.3979-840A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 12/22 | chr17 | 78082207 | ||||||
| chr17:78082256
|
T | G | 1 | a0002c0003t0007g0102 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.3979-791T>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 12/22 | chr17 | 78082256 | ||||||
| chr17:78082265
|
G | C | 36 | a0002c0003t0003g0002a0002c0003t0003g0003a0002c0003t0003g0004others(33): Show | 38 | HG01070.hp2 HG01071.hp2 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.3979-782G>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 12/22 | chr17 | 78082265 | ||||||
| chr17:78082297
|
G | A | 6 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(3): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.3979-750G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 12/22 | chr17 | 78082297 | ||||||
| chr17:78082358
|
A | G | 1 | a0001c0001t0001g0051 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.3979-689A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 12/22 | chr17 | 78082358 | ||||||
| chr17:78082377
|
A | G | 1 | a0013c0026t0002g0118 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.3979-670A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 12/22 | chr17 | 78082377 | ||||||
| chr17:78082400
|
T | G | 3 | a0002c0003t0007g0138a0002c0003t0007g0148a0002c0003t0007g0164 | 3 | NA18960.hp2 NA18966.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.3979-647T>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 12/22 | chr17 | 78082400 | ||||||
| chr17:78082407
|
A | T | 1 | a0002c0003t0007g0102 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.3979-640A>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 12/22 | chr17 | 78082407 | ||||||
| chr17:78082414
|
G | C | 1 | a0008c0016t0001g0079 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3979-633G>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 12/22 | chr17 | 78082414 | ||||||
| chr17:78082453
|
A | C | 1 | a0001c0002t0002g0197 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.3979-594A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 12/22 | chr17 | 78082453 | ||||||
| chr17:78082458
|
C | A | 1 | a0001c0002t0002g0197 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.3979-589C>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 12/22 | chr17 | 78082458 | ||||||
| chr17:78082463
|
T | A | 1 | a0001c0002t0002g0197 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.3979-584T>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 12/22 | chr17 | 78082463 | ||||||
| chr17:78082470
|
A | T | 1 | a0001c0002t0002g0197 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.3979-577A>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 12/22 | chr17 | 78082470 | ||||||
| chr17:78082550
|
G | A | 1 | a0001c0001t0065g0017 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.3979-497G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 12/22 | chr17 | 78082550 | ||||||
| chr17:78082687
|
TC | T | 11 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(8): Show | 11 | HG02486.hp1 HG02622.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.3979-356delC | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr17 | 78082687 | |||||
| chr17:78082699
|
G | A | 16 | a0001c0001t0001g0068a0001c0001t0001g0202a0001c0001t0001g0203others(13): Show | 16 | HG00423.hp1 HG02080.hp2 HG02155.hp2 others(13): Show |
intron_variant | MODIFIER | c.3979-348G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 12/22 | chr17 | 78082699 | ||||||
| chr17:78082817
|
G | T | 1 | a0001c0002t0014g0055 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3979-230G>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 12/22 | chr17 | 78082817 | ||||||
| chr17:78082918
|
A | G | 6 | a0001c0001t0005g0023a0001c0001t0005g0086a0001c0001t0005g0149others(3): Show | 6 | HG01891.hp1 HG02145.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.3979-129A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 12/22 | chr17 | 78082918 | ||||||
| chr17:78083175
|
A | T | 4 | a0001c0001t0017g0266a0001c0001t0017g0267a0009c0015t0027g0264others(1): Show | 4 | HG02258.hp1 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.4098+9A>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 13/22 | chr17 | 78083175 | ||||||
| chr17:78083198
|
C | G | 1 | a0001c0001t0049g0097 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.4098+32C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 13/22 | chr17 | 78083198 | ||||||
| chr17:78083327
|
T | C | 2 | a0001c0002t0014g0054a0001c0002t0014g0071 | 2 | HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.4098+161T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 13/22 | chr17 | 78083327 | ||||||
| chr17:78083670
|
C | A | 47 | a0001c0001t0001g0106a0001c0001t0051g0105a0001c0002t0002g0005others(44): Show | 47 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.4098+504C>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 13/22 | chr17 | 78083670 | ||||||
| chr17:78083823
|
T | A | 2 | a0009c0015t0027g0264a0017c0017t0028g0263 | 2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.4098+657T>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 13/22 | chr17 | 78083823 | ||||||
| chr17:78083838
|
C | A | 1 | a0001c0001t0030g0259 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.4098+672C>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 13/22 | chr17 | 78083838 | ||||||
| chr17:78084005
|
C | T | 36 | a0002c0003t0003g0002a0002c0003t0003g0003a0002c0003t0003g0004others(33): Show | 38 | HG01070.hp2 HG01071.hp2 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.4098+839C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 13/22 | chr17 | 78084005 | ||||||
| chr17:78084026
|
A | G | 100 | a0001c0001t0001g0106a0001c0001t0051g0105a0001c0002t0002g0005others(97): Show | 102 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.4098+860A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 13/22 | chr17 | 78084026 | ||||||
| chr17:78084140
|
C | T | 1 | a0002c0003t0003g0003 | 2 | HG02040.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.4098+974C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 13/22 | chr17 | 78084140 | ||||||
| chr17:78084219
|
G | A | 1 | a0001c0001t0001g0223 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.4098+1053G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 13/22 | chr17 | 78084219 | ||||||
| chr17:78084235
|
G | A | 11 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(8): Show | 11 | HG02486.hp1 HG02622.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.4098+1069G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 13/22 | chr17 | 78084235 | ||||||
| chr17:78084282
|
G | GA | 37 | a0001c0001t0001g0135a0001c0001t0041g0129a0002c0003t0003g0002others(34): Show | 39 | HG01070.hp2 HG01071.hp2 HG01255.hp1 others(36): Show |
intron_variant | MODIFIER | c.4098+1128dupA | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr17 | 78084282 | |||||
| chr17:78084351
|
C | G | 1 | a0001c0001t0001g0020 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.4098+1185C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 13/22 | chr17 | 78084351 | ||||||
| chr17:78084467
|
C | A | 1 | a0001c0001t0001g0059 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.4098+1301C>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 13/22 | chr17 | 78084467 | ||||||
| chr17:78084469
|
G | A | 40 | a0001c0001t0001g0106a0001c0001t0051g0105a0001c0002t0002g0005others(37): Show | 40 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.4098+1303G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 13/22 | chr17 | 78084469 | ||||||
| chr17:78084589
|
G | A | 67 | a0001c0001t0001g0032a0001c0001t0001g0037a0001c0001t0001g0038others(64): Show | 67 | HG00280.hp2 HG00558.hp1 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.4098+1423G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 13/22 | chr17 | 78084589 | ||||||
| chr17:78084615
|
C | A | 1 | a0001c0004t0024g0243 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.4098+1449C>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 13/22 | chr17 | 78084615 | ||||||
| chr17:78084621
|
C | CT | 85 | a0001c0001t0001g0030a0001c0001t0001g0106a0001c0001t0051g0105others(82): Show | 87 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.4098+1471dupT | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr17 | 78084621 | |||||
| chr17:78084692
|
G | A | 6 | a0001c0002t0013g0235a0001c0002t0013g0236a0001c0002t0013g0238others(3): Show | 6 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.4098+1526G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 13/22 | chr17 | 78084692 | ||||||
| chr17:78085728
|
G | A | 6 | a0001c0002t0013g0235a0001c0002t0013g0236a0001c0002t0013g0238others(3): Show | 6 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.4099-775G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 13/22 | chr17 | 78085728 | ||||||
| chr17:78085780
|
T | TTTG | 6 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(3): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.4099-722_4099-721i others(5): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr17 | 78085780 | |||||
| chr17:78085842
|
GT | G | 93 | a0001c0001t0001g0106a0001c0001t0051g0105a0001c0002t0002g0005others(90): Show | 95 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.4099-649delT | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr17 | 78085842 | |||||
| chr17:78085947
|
A | G | 89 | a0001c0001t0001g0106a0001c0001t0051g0105a0001c0002t0002g0005others(86): Show | 91 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.4099-556A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 13/22 | chr17 | 78085947 | ||||||
| chr17:78085966
|
T | C | 1 | a0001c0001t0005g0224 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.4099-537T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 13/22 | chr17 | 78085966 | ||||||
| chr17:78086097
|
T | C | 105 | a0001c0001t0001g0106a0001c0001t0017g0266a0001c0001t0017g0267others(102): Show | 107 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.4099-406T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 13/22 | chr17 | 78086097 | ||||||
| chr17:78086317
|
G | A | 47 | a0001c0001t0001g0106a0001c0001t0051g0105a0001c0002t0002g0005others(44): Show | 47 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.4099-186G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 13/22 | chr17 | 78086317 | ||||||
| chr17:78086328
|
T | TA | 12 | a0001c0001t0001g0067a0001c0001t0001g0127a0001c0001t0001g0133others(9): Show | 13 | HG00735.hp1 HG01167.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.4099-143dupA | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr17 | 78086328 | |||||
| chr17:78086328
|
T | TAA | 21 | a0001c0001t0001g0039a0001c0001t0001g0053a0001c0001t0001g0062others(18): Show | 21 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.4099-144_4099-143d others(4): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr17 | 78086328 | |||||
| chr17:78086328
|
T | TAAA | 19 | a0001c0001t0001g0032a0001c0001t0001g0038a0001c0001t0001g0058others(16): Show | 19 | HG00558.hp1 HG01243.hp1 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.4099-145_4099-143d others(5): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr17 | 78086328 | |||||
| chr17:78086328
|
T | TAAAA | 12 | a0001c0001t0001g0037a0001c0001t0001g0063a0001c0001t0001g0078others(9): Show | 12 | HG01106.hp2 HG02027.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.4099-146_4099-143d others(6): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr17 | 78086328 | |||||
| chr17:78086328
|
T | TAAAAAAA others(3): Show |
1 | a0001c0006t0008g0251 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.4099-152_4099-143d others(12): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr17 | 78086328 | |||||
| chr17:78086328
|
T | TAAAAAAA others(6): Show |
1 | a0001c0006t0008g0253 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.4099-155_4099-143d others(15): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr17 | 78086328 | |||||
| chr17:78086328
|
T | TAAAAAAA others(16): Show |
1 | a0003c0030t0008g0255 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.4099-165_4099-143d others(25): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr17 | 78086328 | |||||
| chr17:78086328
|
TA | T | 40 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0030others(37): Show | 40 | HG00423.hp1 HG00673.hp2 HG01175.hp1 others(37): Show |
intron_variant | MODIFIER | c.4099-143delA | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr17 | 78086328 | |||||
| chr17:78086328
|
TAA | T | 45 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0015others(42): Show | 45 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.4099-144_4099-143d others(4): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr17 | 78086328 | |||||
| chr17:78086328
|
TAAAAA | T | 7 | a0002c0003t0003g0144a0002c0003t0003g0167a0002c0003t0003g0178others(4): Show | 7 | HG01255.hp1 HG01361.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.4099-147_4099-143d others(7): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr17 | 78086328 | |||||
| chr17:78086328
|
TAAAAAA | T | 27 | a0002c0003t0003g0002a0002c0003t0003g0003a0002c0003t0003g0004others(24): Show | 29 | HG01070.hp2 HG01071.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.4099-148_4099-143d others(8): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr17 | 78086328 | |||||
| chr17:78086328
|
TAAAAAAA others(9): Show |
T | 48 | a0001c0001t0001g0106a0001c0001t0051g0105a0001c0002t0002g0005others(45): Show | 48 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.4099-158_4099-143d others(18): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr17 | 78086328 | |||||
| chr17:78086328
|
TAAAAAAA others(10): Show |
T | 2 | a0001c0001t0004g0174a0001c0001t0004g0175 | 2 | NA18971.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.4099-159_4099-143d others(19): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr17 | 78086328 | |||||
| chr17:78086330
|
A | G | 1 | a0001c0007t0012g0269 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4099-173A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 13/22 | chr17 | 78086330 | ||||||
| chr17:78086349
|
A | C | 1 | a0001c0001t0004g0143 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.4099-154A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 13/22 | chr17 | 78086349 | ||||||
| chr17:78086360
|
A | C | 4 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0028others(1): Show | 4 | HG01081.hp2 HG01433.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.4099-143A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 13/22 | chr17 | 78086360 | ||||||
| chr17:78086416
|
A | G | 1 | a0001c0001t0001g0090 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.4099-87A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 13/22 | chr17 | 78086416 | ||||||
| chr17:78086631
|
CCT | C | 11 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(8): Show | 11 | HG02486.hp1 HG02622.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.4182+46_4182+47del others(2): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 14/22 | chr17 | 78086631 | ||||||
| chr17:78087198
|
C | T | 1 | a0010c0031t0040g0048 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.4423+105C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 15/22 | chr17 | 78087198 | ||||||
| chr17:78087281
|
T | A | 1 | a0001c0001t0001g0219 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.4423+188T>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 15/22 | chr17 | 78087281 | ||||||
| chr17:78087357
|
A | G | 12 | a0001c0001t0004g0174a0001c0001t0004g0175a0001c0001t0009g0155others(9): Show | 12 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(9): Show |
intron_variant | MODIFIER | c.4423+264A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 15/22 | chr17 | 78087357 | ||||||
| chr17:78087372
|
C | A | 6 | a0001c0001t0005g0023a0001c0001t0005g0086a0001c0001t0005g0149others(3): Show | 6 | HG01891.hp1 HG02145.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.4423+279C>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 15/22 | chr17 | 78087372 | ||||||
| chr17:78087482
|
CA | C | 95 | a0001c0001t0001g0106a0001c0001t0051g0105a0001c0002t0002g0005others(92): Show | 97 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.4423+391delA | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr17 | 78087482 | |||||
| chr17:78087484
|
A | G | 1 | a0001c0001t0015g0018 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.4423+391A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 15/22 | chr17 | 78087484 | ||||||
| chr17:78087507
|
T | C | 4 | a0001c0001t0001g0036a0001c0001t0001g0049a0001c0001t0001g0067others(1): Show | 4 | HG01257.hp1 HG01361.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.4423+414T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 15/22 | chr17 | 78087507 | ||||||
| chr17:78087522
|
G | A | 1 | a0001c0002t0002g0198 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.4423+429G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 15/22 | chr17 | 78087522 | ||||||
| chr17:78087530
|
C | A | 36 | a0002c0003t0003g0002a0002c0003t0003g0003a0002c0003t0003g0004others(33): Show | 38 | HG01070.hp2 HG01071.hp2 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.4423+437C>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 15/22 | chr17 | 78087530 | ||||||
| chr17:78087664
|
G | A | 1 | a0001c0001t0021g0061 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.4423+571G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 15/22 | chr17 | 78087664 | ||||||
| chr17:78087796
|
C | G | 1 | a0001c0001t0001g0133 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.4423+703C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 15/22 | chr17 | 78087796 | ||||||
| chr17:78087798
|
C | G | 37 | a0002c0003t0003g0002a0002c0003t0003g0003a0002c0003t0003g0004others(34): Show | 39 | HG01070.hp2 HG01071.hp2 HG01255.hp1 others(36): Show |
intron_variant | MODIFIER | c.4423+705C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 15/22 | chr17 | 78087798 | ||||||
| chr17:78087937
|
C | T | 95 | a0001c0001t0001g0106a0001c0001t0051g0105a0001c0002t0002g0005others(92): Show | 97 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.4423+844C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 15/22 | chr17 | 78087937 | ||||||
| chr17:78088003
|
A | G | 36 | a0002c0003t0003g0002a0002c0003t0003g0003a0002c0003t0003g0004others(33): Show | 38 | HG01070.hp2 HG01071.hp2 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.4423+910A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 15/22 | chr17 | 78088003 | ||||||
| chr17:78088038
|
A | G | 1 | a0016c0023t0045g0192 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4423+945A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 15/22 | chr17 | 78088038 | ||||||
| chr17:78088273
|
C | T | 11 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(8): Show | 11 | HG02486.hp1 HG02622.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.4423+1180C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 15/22 | chr17 | 78088273 | ||||||
| chr17:78088363
|
T | G | 1 | a0001c0001t0001g0128 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.4423+1270T>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 15/22 | chr17 | 78088363 | ||||||
| chr17:78088460
|
C | A | 11 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(8): Show | 11 | HG02486.hp1 HG02622.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.4423+1367C>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 15/22 | chr17 | 78088460 | ||||||
| chr17:78088634
|
T | C | 1 | a0001c0002t0002g0197 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.4423+1541T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 15/22 | chr17 | 78088634 | ||||||
| chr17:78088661
|
G | A | 8 | a0001c0002t0018g0237a0001c0006t0008g0251a0001c0006t0008g0253others(5): Show | 8 | HG01255.hp1 HG01943.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.4423+1568G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 15/22 | chr17 | 78088661 | ||||||
| chr17:78088709
|
G | C | 6 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(3): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.4423+1616G>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 15/22 | chr17 | 78088709 | ||||||
| chr17:78088715
|
C | G | 1 | a0001c0006t0033g0252 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.4423+1622C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 15/22 | chr17 | 78088715 | ||||||
| chr17:78088959
|
C | CT | 16 | a0001c0001t0001g0033a0001c0001t0001g0045a0001c0001t0001g0076others(13): Show | 16 | HG01175.hp1 HG01358.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.4423+1892dupT | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr17 | 78088959 | |||||
| chr17:78088959
|
CT | C | 99 | a0001c0001t0001g0032a0001c0001t0001g0038a0001c0001t0001g0059others(96): Show | 101 | HG00280.hp2 HG00558.hp1 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.4423+1892delT | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr17 | 78088959 | |||||
| chr17:78088959
|
CTT | C | 8 | a0001c0001t0004g0143a0001c0001t0004g0157a0001c0001t0004g0172others(5): Show | 9 | HG01070.hp2 HG01071.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.4423+1891_4423+189 others(6): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr17 | 78088959 | |||||
| chr17:78088959
|
CTTTTTTT others(8): Show |
C | 48 | a0001c0001t0001g0106a0001c0001t0051g0105a0001c0002t0002g0005others(45): Show | 48 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.4423+1878_4423+189 others(19): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr17 | 78088959 | |||||
| chr17:78089023
|
G | A | 2 | a0001c0001t0036g0066a0002c0003t0020g0182 | 2 | HG01891.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.4423+1930G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 15/22 | chr17 | 78089023 | ||||||
| chr17:78089036
|
C | T | 4 | a0001c0001t0004g0176a0001c0001t0015g0014a0001c0001t0015g0018others(1): Show | 4 | HG01169.hp2 HG01175.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.4423+1943C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 15/22 | chr17 | 78089036 | ||||||
| chr17:78089067
|
A | C | 4 | a0001c0002t0002g0179a0001c0002t0002g0180a0001c0002t0002g0181others(1): Show | 4 | HG01261.hp1 HG03098.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.4423+1974A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 15/22 | chr17 | 78089067 | ||||||
| chr17:78089560
|
C | T | 3 | a0001c0002t0002g0179a0001c0002t0002g0180a0001c0002t0002g0181 | 3 | HG03098.hp1 HG03471.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.4424-1880C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 15/22 | chr17 | 78089560 | ||||||
| chr17:78089563
|
A | C | 1 | a0001c0001t0004g0124 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.4424-1877A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 15/22 | chr17 | 78089563 | ||||||
| chr17:78089597
|
T | C | 2 | a0001c0001t0001g0015a0001c0001t0001g0016 | 2 | HG00673.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.4424-1843T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 15/22 | chr17 | 78089597 | ||||||
| chr17:78089660
|
T | C | 271 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0015others(268): Show | 274 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.4424-1780T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 15/22 | chr17 | 78089660 | ||||||
| chr17:78089845
|
C | T | 1 | a0001c0001t0005g0271 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.4424-1595C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 15/22 | chr17 | 78089845 | ||||||
| chr17:78089953
|
G | A | 1 | a0001c0002t0031g0265 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4424-1487G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 15/22 | chr17 | 78089953 | ||||||
| chr17:78090138
|
G | A | 1 | a0001c0001t0042g0099 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.4424-1302G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 15/22 | chr17 | 78090138 | ||||||
| chr17:78090264
|
C | T | 37 | a0002c0003t0003g0002a0002c0003t0003g0003a0002c0003t0003g0004others(34): Show | 39 | HG01070.hp2 HG01071.hp2 HG01255.hp1 others(36): Show |
intron_variant | MODIFIER | c.4424-1176C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 15/22 | chr17 | 78090264 | ||||||
| chr17:78090319
|
G | A | 1 | a0001c0001t0001g0204 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.4424-1121G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 15/22 | chr17 | 78090319 | ||||||
| chr17:78090358
|
G | A | 8 | a0001c0002t0014g0054a0001c0002t0014g0055a0001c0002t0014g0071others(5): Show | 8 | HG01070.hp1 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.4424-1082G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 15/22 | chr17 | 78090358 | ||||||
| chr17:78090443
|
C | T | 37 | a0002c0003t0003g0002a0002c0003t0003g0003a0002c0003t0003g0004others(34): Show | 39 | HG01070.hp2 HG01071.hp2 HG01255.hp1 others(36): Show |
intron_variant | MODIFIER | c.4424-997C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 15/22 | chr17 | 78090443 | ||||||
| chr17:78090478
|
A | G | 1 | a0001c0002t0031g0265 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4424-962A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 15/22 | chr17 | 78090478 | ||||||
| chr17:78090480
|
G | A | 1 | a0001c0002t0031g0265 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4424-960G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 15/22 | chr17 | 78090480 | ||||||
| chr17:78090590
|
G | A | 1 | a0001c0001t0030g0259 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.4424-850G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 15/22 | chr17 | 78090590 | ||||||
| chr17:78090692
|
T | C | 1 | a0001c0004t0006g0244 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.4424-748T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 15/22 | chr17 | 78090692 | ||||||
| chr17:78090879
|
A | G | 43 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(40): Show | 45 | HG01070.hp2 HG01071.hp2 HG01255.hp1 others(42): Show |
intron_variant | MODIFIER | c.4424-561A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 15/22 | chr17 | 78090879 | ||||||
| chr17:78090928
|
G | C | 1 | a0001c0001t0005g0271 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.4424-512G>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 15/22 | chr17 | 78090928 | ||||||
| chr17:78091097
|
A | G | 47 | a0001c0001t0051g0105a0001c0002t0002g0005a0001c0002t0002g0104others(44): Show | 47 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.4424-343A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 15/22 | chr17 | 78091097 | ||||||
| chr17:78091258
|
G | A | 1 | a0017c0017t0028g0263 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.4424-182G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 15/22 | chr17 | 78091258 | ||||||
| chr17:78091280
|
T | C | 43 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(40): Show | 45 | HG01070.hp2 HG01071.hp2 HG01255.hp1 others(42): Show |
intron_variant | MODIFIER | c.4424-160T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 15/22 | chr17 | 78091280 | ||||||
| chr17:78091326
|
C | CA | 61 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0015others(58): Show | 61 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.4424-99dupA | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr17 | 78091326 | |||||
| chr17:78091412
|
C | T | 1 | a0001c0001t0060g0233 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.4424-28C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 15/22 | chr17 | 78091412 | ||||||
| chr17:78091423
|
C | T | 1 | a0002c0003t0003g0167 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4424-17C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 15/22 | chr17 | 78091423 | ||||||
| chr17:78091434
|
C | A | 7 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(4): Show | 7 | HG02486.hp1 HG02622.hp2 HG02896.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.4424-6C>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 15/22 | chr17 | 78091434 | ||||||
| chr17:78091659
|
G | T | 6 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(3): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.4591+52G>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 16/22 | chr17 | 78091659 | ||||||
| chr17:78091662
|
C | T | 5 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(2): Show | 5 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.4591+55C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 16/22 | chr17 | 78091662 | ||||||
| chr17:78091673
|
A | G | 37 | a0002c0003t0003g0002a0002c0003t0003g0003a0002c0003t0003g0004others(34): Show | 39 | HG01070.hp2 HG01071.hp2 HG01255.hp1 others(36): Show |
intron_variant | MODIFIER | c.4591+66A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 16/22 | chr17 | 78091673 | ||||||
| chr17:78092206
|
C | T | 40 | a0001c0001t0051g0105a0001c0002t0002g0005a0001c0002t0002g0104others(37): Show | 40 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.4591+599C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 16/22 | chr17 | 78092206 | ||||||
| chr17:78092215
|
C | T | 6 | a0001c0002t0013g0235a0001c0002t0013g0236a0001c0002t0013g0238others(3): Show | 6 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.4591+608C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 16/22 | chr17 | 78092215 | ||||||
| chr17:78092370
|
G | C | 46 | a0001c0001t0051g0105a0001c0002t0002g0005a0001c0002t0002g0104others(43): Show | 46 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.4592-563G>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 16/22 | chr17 | 78092370 | ||||||
| chr17:78092551
|
G | A | 2 | a0001c0001t0001g0029a0001c0001t0001g0093 | 2 | NA18964.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.4592-382G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 16/22 | chr17 | 78092551 | ||||||
| chr17:78092557
|
A | G | 1 | a0001c0001t0064g0080 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4592-376A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 16/22 | chr17 | 78092557 | ||||||
| chr17:78092706
|
C | T | 1 | a0001c0001t0001g0072 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.4592-227C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 16/22 | chr17 | 78092706 | ||||||
| chr17:78092741
|
T | A | 2 | a0002c0003t0003g0178a0002c0003t0058g0166 | 2 | HG01361.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.4592-192T>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 16/22 | chr17 | 78092741 | ||||||
| chr17:78093305
|
T | A | 1 | a0001c0001t0001g0214 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.4783+181T>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 17/22 | chr17 | 78093305 | ||||||
| chr17:78093377
|
C | G | 39 | a0001c0001t0051g0105a0001c0002t0002g0005a0001c0002t0002g0104others(36): Show | 39 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.4784-243C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 17/22 | chr17 | 78093377 | ||||||
| chr17:78093492
|
G | A | 1 | a0008c0028t0023g0258 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4784-128G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 17/22 | chr17 | 78093492 | ||||||
| chr17:78093552
|
T | C | 1 | a0002c0003t0003g0144 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.4784-68T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 17/22 | chr17 | 78093552 | ||||||
| chr17:78093553
|
T | C | 46 | a0001c0001t0051g0105a0001c0002t0002g0005a0001c0002t0002g0104others(43): Show | 46 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.4784-67T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 17/22 | chr17 | 78093553 | ||||||
| chr17:78093562
|
C | T | 6 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(3): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.4784-58C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 17/22 | chr17 | 78093562 | ||||||
| chr17:78093877
|
G | A | 6 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(3): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.4927+114G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 18/22 | chr17 | 78093877 | ||||||
| chr17:78093923
|
A | G | 2 | a0001c0001t0001g0068a0001c0001t0001g0215 | 2 | NA18939.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.4927+160A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 18/22 | chr17 | 78093923 | ||||||
| chr17:78093955
|
T | C | 6 | a0001c0002t0013g0235a0001c0002t0013g0236a0001c0002t0013g0238others(3): Show | 6 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.4927+192T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 18/22 | chr17 | 78093955 | ||||||
| chr17:78093982
|
CT | C | 54 | a0001c0001t0017g0266a0001c0001t0017g0267a0001c0001t0051g0105others(51): Show | 54 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.4927+234delT | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr17 | 78093982 | |||||
| chr17:78094062
|
C | T | 1 | a0008c0028t0023g0258 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4927+299C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 18/22 | chr17 | 78094062 | ||||||
| chr17:78094143
|
A | G | 98 | a0001c0001t0017g0266a0001c0001t0017g0267a0001c0001t0051g0105others(95): Show | 100 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.4927+380A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 18/22 | chr17 | 78094143 | ||||||
| chr17:78094184
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.4927+421G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 18/22 | chr17 | 78094184 | ||||||
| chr17:78094262
|
A | G | 1 | a0005c0010t0038g0035 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.4927+499A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 18/22 | chr17 | 78094262 | ||||||
| chr17:78094440
|
C | CT | 20 | a0001c0001t0001g0039a0001c0001t0004g0176a0001c0001t0015g0014others(17): Show | 21 | HG00673.hp1 HG01169.hp2 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.4927+693dupT | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr17 | 78094440 | |||||
| chr17:78094440
|
CTT | C | 46 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(43): Show | 48 | HG01070.hp2 HG01071.hp2 HG01255.hp1 others(45): Show |
intron_variant | MODIFIER | c.4927+692_4927+693d others(4): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr17 | 78094440 | |||||
| chr17:78094493
|
T | C | 1 | a0016c0023t0045g0192 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4927+730T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 18/22 | chr17 | 78094493 | ||||||
| chr17:78094498
|
G | A | 2 | a0001c0001t0001g0049a0001c0001t0001g0076 | 2 | HG01361.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.4927+735G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 18/22 | chr17 | 78094498 | ||||||
| chr17:78094683
|
G | A | 6 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(3): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.4927+920G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 18/22 | chr17 | 78094683 | ||||||
| chr17:78094692
|
G | A | 7 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(4): Show | 7 | HG02486.hp1 HG02622.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.4927+929G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 18/22 | chr17 | 78094692 | ||||||
| chr17:78094811
|
C | G | 1 | a0002c0003t0007g0148 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.4927+1048C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 18/22 | chr17 | 78094811 | ||||||
| chr17:78094955
|
G | A | 2 | a0009c0015t0027g0264a0017c0017t0028g0263 | 2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.4927+1192G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 18/22 | chr17 | 78094955 | ||||||
| chr17:78094967
|
C | G | 2 | a0006c0011t0001g0159a0006c0011t0001g0160 | 2 | HG01243.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.4927+1204C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 18/22 | chr17 | 78094967 | ||||||
| chr17:78095008
|
G | A | 39 | a0001c0001t0051g0105a0001c0002t0002g0005a0001c0002t0002g0104others(36): Show | 39 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.4927+1245G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 18/22 | chr17 | 78095008 | ||||||
| chr17:78095099
|
A | C | 50 | a0001c0001t0017g0266a0001c0004t0006g0242a0001c0004t0006g0244others(47): Show | 52 | HG01070.hp2 HG01071.hp2 HG01255.hp1 others(49): Show |
intron_variant | MODIFIER | c.4927+1336A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 18/22 | chr17 | 78095099 | ||||||
| chr17:78095234
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.4927+1471C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 18/22 | chr17 | 78095234 | ||||||
| chr17:78095407
|
G | A | 13 | a0001c0001t0017g0266a0001c0004t0006g0242a0001c0004t0006g0244others(10): Show | 13 | HG02486.hp1 HG02622.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.4927+1644G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 18/22 | chr17 | 78095407 | ||||||
| chr17:78095653
|
G | C | 35 | a0001c0001t0001g0032a0001c0001t0001g0037a0001c0001t0001g0038others(32): Show | 35 | HG00280.hp2 HG00558.hp1 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.4927+1890G>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 18/22 | chr17 | 78095653 | ||||||
| chr17:78095664
|
G | C | 1 | a0001c0001t0009g0088 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.4927+1901G>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 18/22 | chr17 | 78095664 | ||||||
| chr17:78095734
|
A | C | 3 | a0001c0007t0012g0268a0001c0007t0012g0269a0001c0007t0012g0270 | 3 | HG02145.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.4927+1971A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 18/22 | chr17 | 78095734 | ||||||
| chr17:78095812
|
C | G | 53 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(50): Show | 55 | HG01070.hp2 HG01071.hp2 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.4928-1933C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 18/22 | chr17 | 78095812 | ||||||
| chr17:78096180
|
A | G | 3 | a0001c0001t0001g0106a0001c0001t0065g0017a0012c0019t0001g0114 | 3 | NA18942.hp1 NA18948.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.4928-1565A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 18/22 | chr17 | 78096180 | ||||||
| chr17:78096250
|
C | T | 1 | a0001c0002t0031g0265 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4928-1495C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 18/22 | chr17 | 78096250 | ||||||
| chr17:78096264
|
T | G | 104 | a0001c0001t0001g0221a0001c0001t0017g0266a0001c0002t0002g0005others(101): Show | 106 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.4928-1481T>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 18/22 | chr17 | 78096264 | ||||||
| chr17:78096287
|
A | G | 6 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(3): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.4928-1458A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 18/22 | chr17 | 78096287 | ||||||
| chr17:78096453
|
T | G | 52 | a0001c0002t0031g0265a0001c0004t0006g0242a0001c0004t0006g0244others(49): Show | 54 | HG01070.hp2 HG01071.hp2 HG01255.hp1 others(51): Show |
intron_variant | MODIFIER | c.4928-1292T>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 18/22 | chr17 | 78096453 | ||||||
| chr17:78096472
|
G | C | 178 | a0001c0001t0001g0032a0001c0001t0001g0038a0001c0001t0001g0039others(175): Show | 181 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.4928-1273G>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 18/22 | chr17 | 78096472 | ||||||
| chr17:78096554
|
G | A | 3 | a0001c0007t0012g0268a0001c0007t0012g0269a0001c0007t0012g0270 | 3 | HG02145.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.4928-1191G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 18/22 | chr17 | 78096554 | ||||||
| chr17:78096623
|
A | G | 9 | a0001c0001t0004g0193a0001c0002t0014g0054a0001c0002t0014g0055others(6): Show | 9 | HG01070.hp1 HG01071.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.4928-1122A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 18/22 | chr17 | 78096623 | ||||||
| chr17:78096644
|
G | A | 1 | a0001c0001t0017g0267 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.4928-1101G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 18/22 | chr17 | 78096644 | ||||||
| chr17:78096657
|
G | T | 1 | a0001c0001t0029g0239 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4928-1088G>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 18/22 | chr17 | 78096657 | ||||||
| chr17:78097088
|
A | C | 2 | a0001c0001t0017g0266a0008c0028t0023g0258 | 2 | HG02622.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.4928-657A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 18/22 | chr17 | 78097088 | ||||||
| chr17:78097109
|
G | A | 3 | a0001c0001t0004g0189a0001c0001t0004g0190a0001c0001t0004g0191 | 3 | HG01884.hp2 HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.4928-636G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 18/22 | chr17 | 78097109 | ||||||
| chr17:78097156
|
G | A | 1 | a0007c0013t0022g0010 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.4928-589G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 18/22 | chr17 | 78097156 | ||||||
| chr17:78097208
|
T | C | 2 | a0001c0001t0017g0266a0008c0028t0023g0258 | 2 | HG02622.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.4928-537T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 18/22 | chr17 | 78097208 | ||||||
| chr17:78097288
|
GAAATACT others(1): Show |
G | 52 | a0001c0001t0001g0032a0001c0001t0001g0038a0001c0001t0001g0039others(49): Show | 52 | HG00280.hp2 HG00558.hp1 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.4928-452_4928-445d others(10): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr17 | 78097288 | |||||
| chr17:78097508
|
G | A | 1 | a0001c0006t0008g0251 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.4928-237G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 18/22 | chr17 | 78097508 | ||||||
| chr17:78097588
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.4928-157G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 18/22 | chr17 | 78097588 | ||||||
| chr17:78097596
|
T | C | 99 | a0001c0002t0002g0005a0001c0002t0002g0104a0001c0002t0002g0107others(96): Show | 101 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.4928-149T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 18/22 | chr17 | 78097596 | ||||||
| chr17:78097707
|
C | T | 1 | a0001c0002t0002g0110 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.4928-38C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 18/22 | chr17 | 78097707 | ||||||
| chr17:78097985
|
G | A | 1 | a0001c0002t0031g0265 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.5044+124G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 19/22 | chr17 | 78097985 | ||||||
| chr17:78098029
|
G | A | 1 | a0001c0002t0002g0120 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.5044+168G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 19/22 | chr17 | 78098029 | ||||||
| chr17:78098030
|
C | T | 103 | a0001c0001t0017g0266a0001c0001t0017g0267a0001c0002t0002g0005others(100): Show | 105 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.5044+169C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 19/22 | chr17 | 78098030 | ||||||
| chr17:78098248
|
G | A | 1 | a0008c0028t0023g0258 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.5045-95G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 19/22 | chr17 | 78098248 | ||||||
| chr17:78098562
|
C | T | 1 | a0001c0001t0001g0100 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.5239+25C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 20/22 | chr17 | 78098562 | ||||||
| chr17:78098883
|
C | A | 11 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(8): Show | 11 | HG02486.hp1 HG02622.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.5239+346C>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 20/22 | chr17 | 78098883 | ||||||
| chr17:78098907
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.5239+370C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 20/22 | chr17 | 78098907 | ||||||
| chr17:78098999
|
C | T | 1 | a0008c0028t0023g0258 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.5239+462C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 20/22 | chr17 | 78098999 | ||||||
| chr17:78099134
|
A | T | 6 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(3): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.5239+597A>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 20/22 | chr17 | 78099134 | ||||||
| chr17:78099364
|
A | G | 35 | a0001c0001t0001g0032a0001c0001t0001g0037a0001c0001t0001g0038others(32): Show | 35 | HG00280.hp2 HG00558.hp1 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.5239+827A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 20/22 | chr17 | 78099364 | ||||||
| chr17:78099371
|
C | T | 8 | a0001c0002t0014g0054a0001c0002t0014g0055a0001c0002t0014g0071others(5): Show | 8 | HG01070.hp1 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.5239+834C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 20/22 | chr17 | 78099371 | ||||||
| chr17:78100040
|
C | T | 1 | a0001c0001t0001g0209 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.5239+1503C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 20/22 | chr17 | 78100040 | ||||||
| chr17:78100178
|
A | C | 1 | a0002c0003t0003g0011 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.5239+1641A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 20/22 | chr17 | 78100178 | ||||||
| chr17:78100203
|
C | T | 1 | a0001c0002t0002g0109 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.5239+1666C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 20/22 | chr17 | 78100203 | ||||||
| chr17:78100420
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.5239+1883C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 20/22 | chr17 | 78100420 | ||||||
| chr17:78100770
|
C | CT | 14 | a0001c0001t0001g0025a0001c0001t0001g0037a0001c0001t0001g0041others(11): Show | 14 | HG00642.hp2 HG01261.hp2 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.5240-1682dupT | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr17 | 78100770 | |||||
| chr17:78100770
|
C | CTTT | 36 | a0001c0004t0024g0243a0001c0006t0008g0251a0001c0006t0008g0253others(33): Show | 38 | HG01070.hp2 HG01071.hp2 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.5240-1684_5240-168 others(7): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr17 | 78100770 | |||||
| chr17:78100770
|
C | CTTTT | 15 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(12): Show | 15 | HG02080.hp1 HG02165.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.5240-1685_5240-168 others(8): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr17 | 78100770 | |||||
| chr17:78100770
|
CT | C | 55 | a0001c0001t0001g0096a0001c0001t0001g0127a0001c0001t0001g0128others(52): Show | 56 | HG00735.hp1 HG01071.hp1 HG01081.hp1 others(53): Show |
intron_variant | MODIFIER | c.5240-1682delT | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr17 | 78100770 | |||||
| chr17:78100770
|
CTTTT | C | 37 | a0001c0002t0002g0005a0001c0002t0002g0104a0001c0002t0002g0107others(34): Show | 37 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.5240-1685_5240-168 others(8): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr17 | 78100770 | |||||
| chr17:78100771
|
T | C | 2 | a0001c0001t0001g0034a0001c0001t0001g0085 | 2 | NA18952.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.5240-1703T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 20/22 | chr17 | 78100771 | ||||||
| chr17:78100773
|
T | C | 3 | a0001c0005t0001g0007a0001c0005t0001g0008a0001c0005t0001g0009 | 3 | HG02896.hp1 HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.5240-1701T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 20/22 | chr17 | 78100773 | ||||||
| chr17:78100952
|
T | C | 92 | a0001c0002t0002g0005a0001c0002t0002g0104a0001c0002t0002g0107others(89): Show | 94 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.5240-1522T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 20/22 | chr17 | 78100952 | ||||||
| chr17:78101055
|
C | A | 1 | a0001c0002t0031g0265 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.5240-1419C>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 20/22 | chr17 | 78101055 | ||||||
| chr17:78101065
|
C | T | 2 | a0001c0001t0017g0266a0001c0001t0017g0267 | 2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.5240-1409C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 20/22 | chr17 | 78101065 | ||||||
| chr17:78101218
|
C | T | 10 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(7): Show | 10 | HG01243.hp1 HG01257.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.5240-1256C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 20/22 | chr17 | 78101218 | ||||||
| chr17:78101322
|
G | A | 1 | a0001c0001t0009g0155 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.5240-1152G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 20/22 | chr17 | 78101322 | ||||||
| chr17:78101328
|
G | C | 11 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(8): Show | 11 | HG02486.hp1 HG02622.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.5240-1146G>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 20/22 | chr17 | 78101328 | ||||||
| chr17:78101378
|
C | T | 1 | a0008c0028t0023g0258 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.5240-1096C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 20/22 | chr17 | 78101378 | ||||||
| chr17:78101418
|
C | T | 1 | a0009c0015t0027g0264 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.5240-1056C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 20/22 | chr17 | 78101418 | ||||||
| chr17:78101478
|
C | T | 6 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(3): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.5240-996C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 20/22 | chr17 | 78101478 | ||||||
| chr17:78101558
|
G | A | 38 | a0001c0002t0002g0005a0001c0002t0002g0104a0001c0002t0002g0107others(35): Show | 38 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.5240-916G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 20/22 | chr17 | 78101558 | ||||||
| chr17:78101560
|
T | C | 96 | a0001c0001t0017g0266a0001c0001t0017g0267a0001c0002t0002g0005others(93): Show | 98 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.5240-914T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 20/22 | chr17 | 78101560 | ||||||
| chr17:78101561
|
G | A | 2 | a0001c0001t0017g0266a0001c0001t0017g0267 | 2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.5240-913G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 20/22 | chr17 | 78101561 | ||||||
| chr17:78101573
|
A | G | 1 | a0001c0001t0001g0040 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.5240-901A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 20/22 | chr17 | 78101573 | ||||||
| chr17:78101608
|
T | C | 6 | a0001c0002t0013g0235a0001c0002t0013g0236a0001c0002t0013g0238others(3): Show | 6 | HG02280.hp1 HG02630.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.5240-866T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 20/22 | chr17 | 78101608 | ||||||
| chr17:78101626
|
C | T | 1 | a0001c0002t0002g0120 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.5240-848C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 20/22 | chr17 | 78101626 | ||||||
| chr17:78101681
|
A | C | 1 | a0001c0001t0029g0239 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5240-793A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 20/22 | chr17 | 78101681 | ||||||
| chr17:78101766
|
C | T | 5 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0212others(2): Show | 5 | HG00423.hp1 HG02155.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.5240-708C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 20/22 | chr17 | 78101766 | ||||||
| chr17:78101791
|
C | T | 1 | a0001c0001t0029g0239 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5240-683C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 20/22 | chr17 | 78101791 | ||||||
| chr17:78101874
|
G | A | 11 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(8): Show | 11 | HG02486.hp1 HG02622.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.5240-600G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 20/22 | chr17 | 78101874 | ||||||
| chr17:78101909
|
A | G | 2 | a0001c0001t0004g0174a0001c0001t0004g0175 | 2 | NA18971.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.5240-565A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 20/22 | chr17 | 78101909 | ||||||
| chr17:78101922
|
T | C | 37 | a0001c0002t0002g0005a0001c0002t0002g0104a0001c0002t0002g0107others(34): Show | 37 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.5240-552T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 20/22 | chr17 | 78101922 | ||||||
| chr17:78102025
|
G | A | 1 | a0008c0028t0023g0258 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.5240-449G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 20/22 | chr17 | 78102025 | ||||||
| chr17:78102100
|
A | G | 44 | a0001c0002t0002g0005a0001c0002t0002g0104a0001c0002t0002g0107others(41): Show | 44 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.5240-374A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 20/22 | chr17 | 78102100 | ||||||
| chr17:78102129
|
C | T | 1 | a0001c0001t0001g0029 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.5240-345C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 20/22 | chr17 | 78102129 | ||||||
| chr17:78102173
|
G | C | 1 | a0001c0001t0005g0224 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.5240-301G>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 20/22 | chr17 | 78102173 | ||||||
| chr17:78102420
|
G | A | 38 | a0001c0002t0002g0005a0001c0002t0002g0104a0001c0002t0002g0107others(35): Show | 38 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.5240-54G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 20/22 | chr17 | 78102420 | ||||||
| chr17:78102437
|
G | A | 1 | a0018c0020t0046g0047 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.5240-37G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 20/22 | chr17 | 78102437 | ||||||
| chr17:78102638
|
A | G | 36 | a0002c0003t0003g0002a0002c0003t0003g0003a0002c0003t0003g0004others(33): Show | 38 | HG01070.hp2 HG01071.hp2 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.5310+94A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 21/22 | chr17 | 78102638 | ||||||
| chr17:78102766
|
T | C | 4 | a0001c0005t0001g0001a0001c0005t0001g0145a0001c0005t0001g0146others(1): Show | 5 | HG02630.hp1 HG03041.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.5310+222T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 21/22 | chr17 | 78102766 | ||||||
| chr17:78102796
|
G | A | 1 | a0008c0016t0001g0079 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.5310+252G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 21/22 | chr17 | 78102796 | ||||||
| chr17:78102836
|
A | G | 1 | a0001c0001t0060g0233 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.5310+292A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 21/22 | chr17 | 78102836 | ||||||
| chr17:78102867
|
G | A | 47 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(44): Show | 49 | HG01070.hp2 HG01071.hp2 HG01255.hp1 others(46): Show |
intron_variant | MODIFIER | c.5310+323G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 21/22 | chr17 | 78102867 | ||||||
| chr17:78102904
|
G | A | 1 | a0001c0001t0001g0101 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.5310+360G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 21/22 | chr17 | 78102904 | ||||||
| chr17:78103001
|
G | A | 1 | a0001c0002t0031g0265 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.5311-413G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 21/22 | chr17 | 78103001 | ||||||
| chr17:78103139
|
C | T | 11 | a0001c0004t0006g0242a0001c0004t0006g0244a0001c0004t0006g0246others(8): Show | 11 | HG02486.hp1 HG02622.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.5311-275C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 21/22 | chr17 | 78103139 | ||||||
| chr17:78103217
|
G | A | 6 | a0001c0006t0008g0251a0001c0006t0008g0253a0001c0006t0008g0256others(3): Show | 6 | HG01943.hp1 HG02155.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.5311-197G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 21/22 | chr17 | 78103217 | ||||||
| chr17:78103254
|
T | G | 1 | a0001c0001t0001g0131 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.5311-160T>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 21/22 | chr17 | 78103254 | ||||||
| chr17:78103277
|
C | G | 2 | a0002c0014t0004g0168a0002c0014t0004g0169 | 2 | HG03490.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.5311-137C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 21/22 | chr17 | 78103277 | ||||||
| chr17:78103353
|
A | C | 1 | a0001c0001t0001g0135 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.5311-61A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 21/22 | chr17 | 78103353 | ||||||
| chr17:78103832
|
A | G | 2 | a0001c0001t0017g0266a0001c0001t0017g0267 | 2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.5450+279A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 22/22 | chr17 | 78103832 | ||||||
| chr17:78103916
|
C | T | 1 | a0001c0001t0004g0193 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.5450+363C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 22/22 | chr17 | 78103916 | ||||||
| chr17:78103921
|
C | T | 1 | a0001c0006t0008g0251 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.5450+368C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 22/22 | chr17 | 78103921 | ||||||
| chr17:78103980
|
G | A | 1 | a0001c0001t0015g0014 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.5450+427G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 22/22 | chr17 | 78103980 | ||||||
| chr17:78104279
|
T | A | 1 | a0001c0002t0031g0265 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.5451-206T>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 22/22 | chr17 | 78104279 | ||||||
| chr17:78104453
|
C | A | 1 | a0001c0002t0031g0265 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.5451-32C>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 22/22 | chr17 | 78104453 |