Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | MEEKK others(1931): Show |
chr17 | 77953703 | 78113822 |
| a0002 | 0/0 | 1936 | 39 | 9 | 4 | 23 | 1 | 2 | 18 | TNRC6C_chr17_77953703_78113822 | TNRC6C | MEEKK others(1931): Show |
chr17 | 77953703 | 78113822 |
| a0003 | 0/0 | 1455 | 5 | 1 | 1 | 1 | 0 | 2 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | MEEKK others(1450): Show |
chr17 | 77953703 | 78113822 |
| a0004 | 0/0 | 1936 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | TNRC6C_chr17_77953703_78113822 | TNRC6C | MEEKK others(1931): Show |
chr17 | 77953703 | 78113822 |
| a0005 | 0/0 | 1936 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | MEEKK others(1931): Show |
chr17 | 77953703 | 78113822 |
| a0006 | 0/0 | 1936 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | MEEKK others(1931): Show |
chr17 | 77953703 | 78113822 |
| a0007 | 0/0 | 1936 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | MEEKK others(1931): Show |
chr17 | 77953703 | 78113822 |
| a0008 | 0/0 | 1455 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | MEEKK others(1450): Show |
chr17 | 77953703 | 78113822 |
| a0009 | 0/0 | 1936 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | MEEKK others(1931): Show |
chr17 | 77953703 | 78113822 |
| a0010 | 0/0 | 1936 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | MEEKK others(1931): Show |
chr17 | 77953703 | 78113822 |
| a0011 | 0/0 | 1936 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | MEEKK others(1931): Show |
chr17 | 77953703 | 78113822 |
| a0012 | 0/0 | 1936 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | MEEKK others(1931): Show |
chr17 | 77953703 | 78113822 |
| a0013 | 0/0 | 1455 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | MEEKK others(1450): Show |
chr17 | 77953703 | 78113822 |
| a0014 | 0/0 | 1936 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | MEEKK others(1931): Show |
chr17 | 77953703 | 78113822 |
| a0015 | 0/0 | 1936 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | MEEKK others(1931): Show |
chr17 | 77953703 | 78113822 |
| a0016 | 0/0 | 1936 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | MEEKK others(1931): Show |
chr17 | 77953703 | 78113822 |
| a0017 | 0/0 | 1455 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | MEEKK others(1450): Show |
chr17 | 77953703 | 78113822 |
| a0018 | 0/0 | 1936 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | MEEKK others(1931): Show |
chr17 | 77953703 | 78113822 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 5808 | 140 | 35 | 30 | 59 | 4 | 11 | TNRC6C_chr17_77953703_78113822 | TNRC6C | ATGGA others(5803): Show |
chr17 | 77953703 | 78113822 | ||
| a0001c0002 | 0/1 | 5808 | 39 | 15 | 3 | 15 | 1 | 4 | TNRC6C_chr17_77953703_78113822 | TNRC6C | ATGGA others(5803): Show |
chr17 | 77953703 | 78113822 | ||
| a0001c0004 | 0/0 | 5808 | 11 | 11 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | ATGGA others(5803): Show |
chr17 | 77953703 | 78113822 | ||
| a0001c0005 | 0/0 | 5808 | 9 | 9 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | ATGGA others(5803): Show |
chr17 | 77953703 | 78113822 | ||
| a0001c0006 | 0/0 | 5808 | 5 | 0 | 1 | 1 | 0 | 3 | TNRC6C_chr17_77953703_78113822 | TNRC6C | ATGGA others(5803): Show |
chr17 | 77953703 | 78113822 | ||
| a0001c0007 | 0/0 | 5808 | 3 | 3 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | ATGGA others(5803): Show |
chr17 | 77953703 | 78113822 | ||
| a0001c0009 | 0/0 | 5808 | 3 | 0 | 3 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | ATGGA others(5803): Show |
chr17 | 77953703 | 78113822 | ||
| a0001c0029 | 0/0 | 5808 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | ATGGA others(5803): Show |
chr17 | 77953703 | 78113822 | ||
| a0002c0003 | 0/0 | 5808 | 36 | 7 | 4 | 23 | 1 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | ATGGA others(5803): Show |
chr17 | 77953703 | 78113822 | ||
| a0002c0014 | 0/0 | 5808 | 2 | 1 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | ATGGA others(5803): Show |
chr17 | 77953703 | 78113822 | ||
| a0002c0027 | 0/0 | 5808 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | ATGGA others(5803): Show |
chr17 | 77953703 | 78113822 | ||
| a0003c0012 | 0/0 | 5809 | 2 | 1 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | ATGGA others(5804): Show |
chr17 | 77953703 | 78113822 | ||
| a0003c0021 | 0/0 | 5809 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | ATGGA others(5804): Show |
chr17 | 77953703 | 78113822 | ||
| a0003c0022 | 0/0 | 5809 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | ATGGA others(5804): Show |
chr17 | 77953703 | 78113822 | ||
| a0003c0030 | 0/0 | 5809 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | ATGGA others(5804): Show |
chr17 | 77953703 | 78113822 | ||
| a0004c0008 | 0/0 | 5808 | 3 | 0 | 0 | 3 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | ATGGA others(5803): Show |
chr17 | 77953703 | 78113822 | ||
| a0005c0010 | 0/0 | 5808 | 2 | 1 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | ATGGA others(5803): Show |
chr17 | 77953703 | 78113822 | ||
| a0006c0011 | 0/0 | 5808 | 2 | 1 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | ATGGA others(5803): Show |
chr17 | 77953703 | 78113822 | ||
| a0007c0016 | 0/0 | 5808 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | ATGGA others(5803): Show |
chr17 | 77953703 | 78113822 | ||
| a0007c0028 | 0/0 | 5808 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | ATGGA others(5803): Show |
chr17 | 77953703 | 78113822 | ||
| a0008c0013 | 0/0 | 5809 | 2 | 0 | 0 | 2 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | ATGGA others(5804): Show |
chr17 | 77953703 | 78113822 | ||
| a0009c0018 | 0/0 | 5808 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | ATGGA others(5803): Show |
chr17 | 77953703 | 78113822 | ||
| a0010c0031 | 0/0 | 5808 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | ATGGA others(5803): Show |
chr17 | 77953703 | 78113822 | ||
| a0011c0015 | 0/0 | 5808 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | ATGGA others(5803): Show |
chr17 | 77953703 | 78113822 | ||
| a0012c0020 | 0/0 | 5808 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | ATGGA others(5803): Show |
chr17 | 77953703 | 78113822 | ||
| a0013c0017 | 0/0 | 5809 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | ATGGA others(5804): Show |
chr17 | 77953703 | 78113822 | ||
| a0014c0023 | 0/0 | 5808 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | ATGGA others(5803): Show |
chr17 | 77953703 | 78113822 | ||
| a0015c0019 | 0/0 | 5808 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | ATGGA others(5803): Show |
chr17 | 77953703 | 78113822 | ||
| a0016c0024 | 0/0 | 5808 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | ATGGA others(5803): Show |
chr17 | 77953703 | 78113822 | ||
| a0017c0026 | 0/0 | 5809 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | ATGGA others(5804): Show |
chr17 | 77953703 | 78113822 | ||
| a0018c0025 | 0/0 | 5808 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | ATGGA others(5803): Show |
chr17 | 77953703 | 78113822 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 10391 | 101 | 18 | 27 | 45 | 4 | 7 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10386): Show |
chr17 | 77953703 | 78113822 |
| a0001c0001t0004 | 0/0 | 10392 | 9 | 6 | 0 | 3 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10387): Show |
chr17 | 77953703 | 78113822 |
| a0001c0001t0008 | 0/0 | 10390 | 4 | 0 | 0 | 4 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10385): Show |
chr17 | 77953703 | 78113822 |
| a0001c0001t0014 | 0/0 | 10391 | 3 | 1 | 2 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10386): Show |
chr17 | 77953703 | 78113822 |
| a0001c0001t0015 | 0/0 | 10391 | 2 | 0 | 1 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10386): Show |
chr17 | 77953703 | 78113822 |
| a0001c0001t0016 | 0/0 | 10390 | 2 | 2 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10385): Show |
chr17 | 77953703 | 78113822 |
| a0001c0001t0018 | 0/0 | 10390 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10385): Show |
chr17 | 77953703 | 78113822 |
| a0001c0001t0020 | 0/0 | 10392 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10387): Show |
chr17 | 77953703 | 78113822 |
| a0001c0001t0028 | 0/0 | 10391 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10386): Show |
chr17 | 77953703 | 78113822 |
| a0001c0001t0029 | 0/0 | 10391 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10386): Show |
chr17 | 77953703 | 78113822 |
| a0001c0001t0034 | 0/0 | 10391 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10386): Show |
chr17 | 77953703 | 78113822 |
| a0001c0001t0035 | 0/0 | 10391 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10386): Show |
chr17 | 77953703 | 78113822 |
| a0001c0001t0036 | 1/0 | 10391 | 1 | 0 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10386): Show |
chr17 | 77953703 | 78113822 |
| a0001c0001t0040 | 0/0 | 10390 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10385): Show |
chr17 | 77953703 | 78113822 |
| a0001c0001t0041 | 0/0 | 10390 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10385): Show |
chr17 | 77953703 | 78113822 |
| a0001c0001t0042 | 0/0 | 10391 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10386): Show |
chr17 | 77953703 | 78113822 |
| a0001c0001t0045 | 0/0 | 10392 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10387): Show |
chr17 | 77953703 | 78113822 |
| a0001c0001t0048 | 0/0 | 10391 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10386): Show |
chr17 | 77953703 | 78113822 |
| a0001c0001t0049 | 0/0 | 10391 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10386): Show |
chr17 | 77953703 | 78113822 |
| a0001c0001t0051 | 0/0 | 10389 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10384): Show |
chr17 | 77953703 | 78113822 |
| a0001c0001t0052 | 0/0 | 10391 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10386): Show |
chr17 | 77953703 | 78113822 |
| a0001c0001t0057 | 0/0 | 10392 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10387): Show |
chr17 | 77953703 | 78113822 |
| a0001c0001t0060 | 0/0 | 10391 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10386): Show |
chr17 | 77953703 | 78113822 |
| a0001c0001t0061 | 0/0 | 10391 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10386): Show |
chr17 | 77953703 | 78113822 |
| a0001c0001t0062 | 0/0 | 10391 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10386): Show |
chr17 | 77953703 | 78113822 |
| a0001c0002t0002 | 0/0 | 10390 | 23 | 5 | 2 | 13 | 1 | 2 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10385): Show |
chr17 | 77953703 | 78113822 |
| a0001c0002t0012 | 0/0 | 10391 | 3 | 3 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10386): Show |
chr17 | 77953703 | 78113822 |
| a0001c0002t0013 | 0/0 | 10389 | 3 | 3 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10384): Show |
chr17 | 77953703 | 78113822 |
| a0001c0002t0017 | 0/0 | 10390 | 2 | 2 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10385): Show |
chr17 | 77953703 | 78113822 |
| a0001c0002t0030 | 0/0 | 10391 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10386): Show |
chr17 | 77953703 | 78113822 |
| a0001c0002t0033 | 0/0 | 10390 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10385): Show |
chr17 | 77953703 | 78113822 |
| a0001c0002t0038 | 0/0 | 10389 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10384): Show |
chr17 | 77953703 | 78113822 |
| a0001c0002t0044 | 0/0 | 10390 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10385): Show |
chr17 | 77953703 | 78113822 |
| a0001c0002t0047 | 0/0 | 10389 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10384): Show |
chr17 | 77953703 | 78113822 |
| a0001c0002t0056 | 0/0 | 10390 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10385): Show |
chr17 | 77953703 | 78113822 |
| a0001c0002t0058 | 0/0 | 10389 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10384): Show |
chr17 | 77953703 | 78113822 |
| a0001c0002t0059 | 0/1 | 10388 | 1 | 0 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10383): Show |
chr17 | 77953703 | 78113822 |
| a0001c0004t0005 | 0/0 | 10390 | 6 | 6 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10385): Show |
chr17 | 77953703 | 78113822 |
| a0001c0004t0010 | 0/0 | 10387 | 3 | 3 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10382): Show |
chr17 | 77953703 | 78113822 |
| a0001c0004t0023 | 0/0 | 10391 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10386): Show |
chr17 | 77953703 | 78113822 |
| a0001c0004t0025 | 0/0 | 10387 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10382): Show |
chr17 | 77953703 | 78113822 |
| a0001c0005t0001 | 0/0 | 10391 | 9 | 9 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10386): Show |
chr17 | 77953703 | 78113822 |
| a0001c0006t0007 | 0/0 | 10391 | 3 | 0 | 1 | 1 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10386): Show |
chr17 | 77953703 | 78113822 |
| a0001c0006t0031 | 0/0 | 10391 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10386): Show |
chr17 | 77953703 | 78113822 |
| a0001c0006t0032 | 0/0 | 10391 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10386): Show |
chr17 | 77953703 | 78113822 |
| a0001c0007t0011 | 0/0 | 10393 | 3 | 3 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10388): Show |
chr17 | 77953703 | 78113822 |
| a0001c0009t0015 | 0/0 | 10391 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10386): Show |
chr17 | 77953703 | 78113822 |
| a0001c0009t0018 | 0/0 | 10390 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10385): Show |
chr17 | 77953703 | 78113822 |
| a0001c0009t0043 | 0/0 | 10392 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10387): Show |
chr17 | 77953703 | 78113822 |
| a0001c0029t0001 | 0/0 | 10391 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10386): Show |
chr17 | 77953703 | 78113822 |
| a0002c0003t0003 | 0/0 | 10396 | 22 | 3 | 4 | 14 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10391): Show |
chr17 | 77953703 | 78113822 |
| a0002c0003t0006 | 0/0 | 10395 | 5 | 0 | 0 | 5 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10390): Show |
chr17 | 77953703 | 78113822 |
| a0002c0003t0009 | 0/0 | 10399 | 3 | 3 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10394): Show |
chr17 | 77953703 | 78113822 |
| a0002c0003t0019 | 0/0 | 10395 | 2 | 0 | 0 | 2 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10390): Show |
chr17 | 77953703 | 78113822 |
| a0002c0003t0021 | 0/0 | 10396 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10391): Show |
chr17 | 77953703 | 78113822 |
| a0002c0003t0024 | 0/0 | 10394 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10389): Show |
chr17 | 77953703 | 78113822 |
| a0002c0003t0054 | 0/0 | 10397 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10392): Show |
chr17 | 77953703 | 78113822 |
| a0002c0003t0055 | 0/0 | 10396 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10391): Show |
chr17 | 77953703 | 78113822 |
| a0002c0014t0001 | 0/0 | 10391 | 2 | 1 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10386): Show |
chr17 | 77953703 | 78113822 |
| a0002c0027t0003 | 0/0 | 10396 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10391): Show |
chr17 | 77953703 | 78113822 |
| a0003c0012t0001 | 0/0 | 10392 | 2 | 1 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10387): Show |
chr17 | 77953703 | 78113822 |
| a0003c0021t0002 | 0/0 | 10391 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10386): Show |
chr17 | 77953703 | 78113822 |
| a0003c0022t0020 | 0/0 | 10393 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10388): Show |
chr17 | 77953703 | 78113822 |
| a0003c0030t0007 | 0/0 | 10392 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10387): Show |
chr17 | 77953703 | 78113822 |
| a0004c0008t0001 | 0/0 | 10391 | 3 | 0 | 0 | 3 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10386): Show |
chr17 | 77953703 | 78113822 |
| a0005c0010t0037 | 0/0 | 10389 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10384): Show |
chr17 | 77953703 | 78113822 |
| a0005c0010t0050 | 0/0 | 10389 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10384): Show |
chr17 | 77953703 | 78113822 |
| a0006c0011t0001 | 0/0 | 10391 | 2 | 1 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10386): Show |
chr17 | 77953703 | 78113822 |
| a0007c0016t0001 | 0/0 | 10391 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10386): Show |
chr17 | 77953703 | 78113822 |
| a0007c0028t0022 | 0/0 | 10392 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10387): Show |
chr17 | 77953703 | 78113822 |
| a0008c0013t0003 | 0/0 | 10397 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10392): Show |
chr17 | 77953703 | 78113822 |
| a0008c0013t0021 | 0/0 | 10397 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10392): Show |
chr17 | 77953703 | 78113822 |
| a0009c0018t0001 | 0/0 | 10391 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10386): Show |
chr17 | 77953703 | 78113822 |
| a0010c0031t0039 | 0/0 | 10390 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10385): Show |
chr17 | 77953703 | 78113822 |
| a0011c0015t0026 | 0/0 | 10389 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10384): Show |
chr17 | 77953703 | 78113822 |
| a0012c0020t0046 | 0/0 | 10391 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10386): Show |
chr17 | 77953703 | 78113822 |
| a0013c0017t0027 | 0/0 | 10391 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10386): Show |
chr17 | 77953703 | 78113822 |
| a0014c0023t0002 | 0/0 | 10390 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10385): Show |
chr17 | 77953703 | 78113822 |
| a0015c0019t0001 | 0/0 | 10391 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10386): Show |
chr17 | 77953703 | 78113822 |
| a0016c0024t0053 | 0/0 | 10396 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10391): Show |
chr17 | 77953703 | 78113822 |
| a0017c0026t0002 | 0/0 | 10391 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10386): Show |
chr17 | 77953703 | 78113822 |
| a0018c0025t0001 | 0/0 | 10391 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | AGTTA others(10386): Show |
chr17 | 77953703 | 78113822 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 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 | 0 | 1 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0060 | 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 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0092 | 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 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 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 | 0 | 1 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 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 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0211 | 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 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0001g0224 | 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 | 1 | 0 | 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 |
| a0001c0001t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0004g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0004g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0004g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0004g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0004g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0004g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0008g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0008g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0008g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0008g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0014g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0014g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0014g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0015g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0015g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0016g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0016g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0018g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0020g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0028g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0029g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0034g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0035g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0036g0058 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0040g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0041g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0042g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0045g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0048g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0049g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0051g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0052g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0057g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0060g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0061g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0001t0062g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0002t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 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 |
| a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0012g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0012g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0012g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0013g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0013g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0013g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0017g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0017g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0030g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0033g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0038g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0044g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0047g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0056g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0058g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0002t0059g0229 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0004t0005g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0004t0005g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0004t0005g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0004t0005g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0004t0005g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0004t0005g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0004t0010g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0004t0010g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0004t0010g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0004t0023g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0004t0025g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0005t0001g0002 | 0/0 | 2 | 2 | 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 |
| a0001c0005t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0005t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0005t0001g0139 | 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 |
| a0001c0005t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0005t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0006t0007g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0006t0007g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0006t0007g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0006t0031g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0006t0032g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0007t0011g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0007t0011g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0007t0011g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0009t0015g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0009t0018g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0009t0043g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0001c0029t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0003g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0003g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0003g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0003g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0003g0153 | 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 |
| a0002c0003t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0003g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0003g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0006g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0006g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0006g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0006g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0006g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0009g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0009g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0009g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0019g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0019g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0021g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0024g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0054g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0003t0055g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0014t0001g0005 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0002c0027t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0003c0012t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0003c0012t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0003c0021t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0003c0022t0020g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0003c0030t0007g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0004c0008t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0004c0008t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0004c0008t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0005c0010t0037g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0005c0010t0050g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0006c0011t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0006c0011t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0007c0016t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0007c0028t0022g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0008c0013t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0008c0013t0021g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0009c0018t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0010c0031t0039g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0011c0015t0026g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0012c0020t0046g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0013c0017t0027g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0014c0023t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0015c0019t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0016c0024t0053g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0017c0026t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| a0018c0025t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 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 | g0045 | EUR | FIN | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0134 | EUR | FIN | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0085 | EUR | FIN | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG00323 | hp2 | a0001 | c0002 | t0002 | g0124 | EUR | FIN | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG00423 | hp2 | a0001 | c0002 | t0002 | g0109 | EAS | CHS | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG00558 | hp2 | a0001 | c0002 | t0002 | g0116 | EAS | CHS | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | CHS | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG00597 | hp2 | a0001 | c0002 | t0002 | g0110 | EAS | CHS | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG00673 | hp1 | a0001 | c0002 | t0002 | g0119 | EAS | CHS | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG00735 | hp1 | a0001 | c0009 | t0043 | g0155 | AMR | PUR | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01070 | hp1 | a0005 | c0010 | t0037 | g0037 | AMR | PUR | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01070 | hp2 | a0002 | c0003 | t0003 | g0003 | AMR | PUR | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01071 | hp2 | a0002 | c0003 | t0003 | g0003 | AMR | PUR | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01167 | hp1 | a0001 | c0009 | t0015 | g0142 | AMR | PUR | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01169 | hp1 | a0001 | c0009 | t0018 | g0170 | AMR | PUR | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01169 | hp2 | a0001 | c0001 | t0014 | g0021 | AMR | PUR | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01175 | hp1 | a0001 | c0001 | t0014 | g0020 | AMR | PUR | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01243 | hp2 | a0006 | c0011 | t0001 | g0162 | AMR | PUR | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01255 | hp1 | a0002 | c0003 | t0003 | g0207 | AMR | CLM | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01255 | hp2 | a0007 | c0016 | t0001 | g0081 | AMR | CLM | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | CLM | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01261 | hp1 | a0001 | c0002 | t0033 | g0182 | AMR | CLM | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01358 | hp2 | a0001 | c0001 | t0015 | g0052 | AMR | CLM | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01361 | hp2 | a0002 | c0003 | t0003 | g0176 | AMR | CLM | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01884 | hp1 | a0002 | c0003 | t0003 | g0007 | AFR | ACB | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01891 | hp1 | a0001 | c0001 | t0035 | g0068 | AFR | ACB | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01891 | hp2 | a0005 | c0010 | t0050 | g0067 | AFR | ACB | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01943 | hp1 | a0001 | c0006 | t0007 | g0253 | AMR | PEL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01952 | hp1 | a0001 | c0002 | t0002 | g0112 | AMR | PEL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01981 | hp2 | a0001 | c0002 | t0002 | g0113 | AMR | PEL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01993 | hp1 | a0003 | c0021 | t0002 | g0114 | AMR | PEL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG01993 | hp2 | a0001 | c0029 | t0001 | g0033 | AMR | PEL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02027 | hp1 | a0009 | c0018 | t0001 | g0100 | EAS | KHV | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02027 | hp2 | a0001 | c0001 | t0045 | g0106 | EAS | KHV | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02040 | hp1 | a0001 | c0001 | t0004 | g0086 | EAS | KHV | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02040 | hp2 | a0002 | c0003 | t0003 | g0004 | EAS | KHV | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02055 | hp1 | a0003 | c0012 | t0001 | g0217 | AFR | ACB | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02055 | hp2 | a0002 | c0003 | t0003 | g0169 | AFR | ACB | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02080 | hp1 | a0008 | c0013 | t0021 | g0012 | EAS | KHV | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02083 | hp1 | a0002 | c0003 | t0003 | g0013 | EAS | KHV | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02132 | hp1 | a0010 | c0031 | t0039 | g0050 | EAS | KHV | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02132 | hp2 | a0002 | c0003 | t0003 | g0004 | EAS | KHV | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02135 | hp1 | a0001 | c0001 | t0004 | g0027 | EAS | KHV | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02135 | hp2 | a0002 | c0003 | t0003 | g0192 | EAS | KHV | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0025 | AFR | ACB | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02145 | hp2 | a0001 | c0007 | t0011 | g0267 | AFR | ACB | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02155 | hp1 | a0001 | c0006 | t0007 | g0248 | EAS | CDX | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02155 | hp2 | a0001 | c0001 | t0048 | g0215 | EAS | CDX | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CDX | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02165 | hp2 | a0002 | c0003 | t0021 | g0181 | EAS | CDX | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02257 | hp1 | a0001 | c0001 | t0057 | g0230 | AFR | ACB | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02258 | hp1 | a0011 | c0015 | t0026 | g0261 | AFR | ACB | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | ACB | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02280 | hp1 | a0001 | c0002 | t0012 | g0234 | AFR | ACB | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02280 | hp2 | a0006 | c0011 | t0001 | g0161 | AFR | ACB | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02451 | hp1 | a0001 | c0005 | t0001 | g0139 | AFR | ACB | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02451 | hp2 | a0001 | c0002 | t0013 | g0057 | AFR | ACB | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02602 | hp1 | a0001 | c0002 | t0002 | g0111 | SAS | PJL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02615 | hp1 | a0013 | c0017 | t0027 | g0260 | AFR | GWD | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0268 | AFR | GWD | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02622 | hp1 | a0001 | c0001 | t0016 | g0263 | AFR | GWD | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02622 | hp2 | a0001 | c0004 | t0005 | g0239 | AFR | GWD | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02630 | hp1 | a0001 | c0005 | t0001 | g0147 | AFR | GWD | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02630 | hp2 | a0001 | c0002 | t0012 | g0232 | AFR | GWD | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02647 | hp1 | a0002 | c0003 | t0009 | g0237 | AFR | GWD | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02717 | hp1 | a0001 | c0004 | t0010 | g0259 | AFR | GWD | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02723 | hp1 | a0001 | c0001 | t0014 | g0016 | AFR | GWD | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0156 | AFR | GWD | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02738 | hp1 | a0003 | c0030 | t0007 | g0252 | SAS | PJL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02738 | hp2 | a0001 | c0002 | t0056 | g0125 | SAS | PJL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02809 | hp2 | a0001 | c0002 | t0012 | g0235 | AFR | GWD | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02818 | hp1 | a0001 | c0002 | t0002 | g0108 | AFR | GWD | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02818 | hp2 | a0001 | c0001 | t0029 | g0256 | AFR | GWD | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02886 | hp1 | a0001 | c0002 | t0013 | g0056 | AFR | GWD | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02886 | hp2 | a0001 | c0007 | t0011 | g0265 | AFR | GWD | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02895 | hp2 | a0002 | c0003 | t0009 | g0242 | AFR | GWD | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02896 | hp1 | a0001 | c0005 | t0001 | g0010 | AFR | GWD | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02896 | hp2 | a0001 | c0004 | t0023 | g0240 | AFR | GWD | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02922 | hp1 | a0001 | c0004 | t0005 | g0243 | AFR | ESN | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02922 | hp2 | a0007 | c0028 | t0022 | g0255 | AFR | ESN | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02965 | hp1 | a0001 | c0005 | t0001 | g0011 | AFR | ESN | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0088 | AFR | ESN | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0221 | AFR | ESN | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02970 | hp2 | a0002 | c0003 | t0009 | g0247 | AFR | ESN | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02976 | hp1 | a0001 | c0004 | t0005 | g0245 | AFR | ESN | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02976 | hp2 | a0001 | c0001 | t0061 | g0082 | AFR | ESN | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03041 | hp1 | a0001 | c0005 | t0001 | g0149 | AFR | GWD | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03041 | hp2 | a0001 | c0004 | t0010 | g0254 | AFR | GWD | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03098 | hp1 | a0001 | c0002 | t0002 | g0178 | AFR | MSL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03098 | hp2 | a0001 | c0001 | t0028 | g0236 | AFR | MSL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | ESN | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03130 | hp2 | a0001 | c0002 | t0038 | g0059 | AFR | ESN | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03139 | hp1 | a0001 | c0005 | t0001 | g0009 | AFR | ESN | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03139 | hp2 | a0002 | c0027 | t0003 | g0007 | AFR | ESN | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03209 | hp1 | a0001 | c0001 | t0016 | g0264 | AFR | MSL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | MSL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03225 | hp1 | a0001 | c0007 | t0011 | g0266 | AFR | MSL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03225 | hp2 | a0001 | c0001 | t0034 | g0186 | AFR | MSL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | MSL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03453 | hp2 | a0001 | c0004 | t0005 | g0241 | AFR | MSL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | MSL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03486 | hp2 | a0001 | c0005 | t0001 | g0148 | AFR | MSL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03490 | hp1 | a0002 | c0014 | t0001 | g0005 | SAS | PJL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03491 | hp1 | a0001 | c0006 | t0032 | g0249 | SAS | PJL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03491 | hp2 | a0001 | c0001 | t0018 | g0143 | SAS | PJL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03492 | hp2 | a0001 | c0001 | t0015 | g0144 | SAS | PJL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03516 | hp1 | a0001 | c0004 | t0025 | g0257 | AFR | ESN | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0151 | AFR | ESN | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03540 | hp1 | a0001 | c0001 | t0049 | g0048 | AFR | GWD | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03540 | hp2 | a0001 | c0002 | t0017 | g0233 | AFR | GWD | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03579 | hp1 | a0001 | c0002 | t0002 | g0121 | AFR | MSL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03579 | hp2 | a0001 | c0002 | t0017 | g0231 | AFR | MSL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03669 | hp1 | a0001 | c0002 | t0002 | g0122 | SAS | PJL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03927 | hp1 | a0002 | c0003 | t0003 | g0105 | SAS | BEB | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03927 | hp2 | a0001 | c0001 | t0051 | g0099 | SAS | BEB | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG04115 | hp1 | a0001 | c0002 | t0058 | g0228 | SAS | STU | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG04115 | hp2 | a0003 | c0012 | t0001 | g0024 | SAS | STU | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG04228 | hp1 | a0001 | c0006 | t0007 | g0250 | SAS | STU | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG04228 | hp2 | a0001 | c0001 | t0060 | g0043 | SAS | STU | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18522 | hp1 | a0001 | c0004 | t0005 | g0246 | AFR | YRI | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18522 | hp2 | a0014 | c0023 | t0002 | g0190 | AFR | YRI | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18747 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | CHB | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | CHB | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18906 | hp1 | a0001 | c0004 | t0010 | g0258 | AFR | YRI | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18906 | hp2 | a0001 | c0005 | t0001 | g0002 | AFR | YRI | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18939 | hp2 | a0002 | c0003 | t0003 | g0166 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18940 | hp1 | a0001 | c0002 | t0002 | g0195 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18942 | hp1 | a0015 | c0019 | t0001 | g0115 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18943 | hp1 | a0004 | c0008 | t0001 | g0094 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18943 | hp2 | a0001 | c0002 | t0002 | g0117 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18952 | hp2 | a0002 | c0003 | t0003 | g0152 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18953 | hp1 | a0008 | c0013 | t0003 | g0154 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18957 | hp1 | a0001 | c0002 | t0002 | g0118 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18957 | hp2 | a0001 | c0001 | t0004 | g0097 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18959 | hp1 | a0001 | c0001 | t0062 | g0019 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18960 | hp2 | a0002 | c0003 | t0006 | g0140 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18966 | hp1 | a0002 | c0003 | t0006 | g0150 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18968 | hp1 | a0001 | c0002 | t0047 | g0123 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18968 | hp2 | a0004 | c0008 | t0001 | g0076 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18969 | hp1 | a0002 | c0003 | t0003 | g0164 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18970 | hp2 | a0001 | c0002 | t0002 | g0196 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18971 | hp1 | a0002 | c0003 | t0019 | g0180 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18975 | hp2 | a0002 | c0003 | t0003 | g0128 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18978 | hp1 | a0003 | c0022 | t0020 | g0132 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18978 | hp2 | a0001 | c0001 | t0020 | g0062 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18982 | hp1 | a0001 | c0001 | t0008 | g0157 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18983 | hp1 | a0002 | c0003 | t0003 | g0014 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18983 | hp2 | a0001 | c0001 | t0040 | g0131 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18988 | hp1 | a0004 | c0008 | t0001 | g0075 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18988 | hp2 | a0002 | c0003 | t0003 | g0141 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18994 | hp2 | a0001 | c0002 | t0002 | g0208 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18998 | hp1 | a0001 | c0002 | t0002 | g0197 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19007 | hp1 | a0016 | c0024 | t0053 | g0061 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19007 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19012 | hp1 | a0002 | c0003 | t0019 | g0193 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | LWK | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19030 | hp2 | a0001 | c0002 | t0002 | g0179 | AFR | LWK | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19043 | hp1 | a0001 | c0005 | t0001 | g0002 | AFR | LWK | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19043 | hp2 | a0001 | c0002 | t0030 | g0262 | AFR | LWK | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19055 | hp1 | a0001 | c0002 | t0002 | g0194 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19057 | hp1 | a0002 | c0003 | t0003 | g0168 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19060 | hp1 | a0002 | c0003 | t0003 | g0153 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19062 | hp1 | a0001 | c0001 | t0052 | g0096 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19062 | hp2 | a0017 | c0026 | t0002 | g0120 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19063 | hp2 | a0001 | c0001 | t0008 | g0158 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19064 | hp2 | a0001 | c0002 | t0044 | g0001 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19065 | hp2 | a0002 | c0003 | t0006 | g0165 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19074 | hp1 | a0001 | c0001 | t0008 | g0090 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19074 | hp2 | a0001 | c0001 | t0008 | g0173 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19075 | hp1 | a0002 | c0003 | t0054 | g0160 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19077 | hp2 | a0002 | c0003 | t0003 | g0163 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19079 | hp1 | a0018 | c0025 | t0001 | g0079 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19079 | hp2 | a0002 | c0003 | t0003 | g0146 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19081 | hp1 | a0002 | c0003 | t0006 | g0127 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19089 | hp2 | a0002 | c0003 | t0006 | g0104 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19090 | hp1 | a0001 | c0001 | t0042 | g0175 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | YRI | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA19240 | hp2 | a0001 | c0002 | t0013 | g0073 | AFR | YRI | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ASW | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ASW | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0030 | EUR | TSI | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA20752 | hp2 | a0002 | c0003 | t0055 | g0167 | EUR | TSI | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA20905 | hp1 | a0001 | c0006 | t0031 | g0251 | SAS | GIH | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | GIH | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | ACB | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02486 | hp1 | a0001 | c0004 | t0005 | g0244 | AFR | ACB | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG02486 | hp2 | a0012 | c0020 | t0046 | g0049 | AFR | ACB | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03471 | hp1 | a0001 | c0002 | t0002 | g0177 | AFR | MSL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG03471 | hp2 | a0002 | c0003 | t0024 | g0238 | AFR | MSL | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG06807 | hp1 | a0002 | c0014 | t0001 | g0005 | AFR | USA | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| HG06807 | hp2 | a0001 | c0001 | t0041 | g0101 | AFR | USA | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | USA | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| NA20300 | hp2 | a0002 | c0003 | t0003 | g0184 | AFR | USA | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0059 | g0229 | REF | REF | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0036 | g0058 | REF | REF | TNRC6C_chr17_77953703_78113822 | TNRC6C | chr17 | 77953703 | 78113822 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:78049475 | G | A | 1 | a0011 | 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 | a0009 | 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 | a0015 | 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 | a0012 | 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 | a0007 a0011 a0013 |
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 | a0002 a0006 a0008 |
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 | a0017 | 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 | a0003 a0008 a0013 others(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 | a0014 | 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 | a0016 | 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 | a0018 | 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 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:78049188 | G | A | 3 | a0007c0016 a0011c0015 a0013c0017 |
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 | a0001c0006 a0003c0030 |
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 | a0001c0006 a0003c0030 |
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 | a0001c0006 a0001c0007 a0002c0003 others(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 | a0001c0002 a0001c0004 a0001c0006 others(9): Show |
100 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(97): 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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:77958767 | T | C | 20 | a0001c0001t0016 a0001c0001t0028 a0001c0001t0029 others(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 | a0001c0004t0005 a0001c0004t0023 a0002c0003t0009 others(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 | a0007c0028t0022 | 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 | a0001c0001t0062 | 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 | a0001c0001t0061 | 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 | a0001c0001t0034 a0001c0002t0033 |
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 | a0001c0001t0060 | 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 | a0001c0004t0005 a0001c0004t0023 a0002c0003t0009 others(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 | 76 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0008 others(73): Show |
268 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(265): 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 | 2 | a0001c0001t0057 a0001c0002t0058 |
2 | HG02257.hp1 HG04115.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 | a0001c0006t0007 a0001c0006t0031 a0001c0006t0032 others(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 | a0001c0004t0005 a0001c0004t0010 a0001c0004t0023 others(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 | a0010c0031t0039 | 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 | a0001c0002t0056 | 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 | a0001c0001t0014 | 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 | 15 | a0001c0001t0020 a0001c0002t0012 a0001c0002t0030 others(12): 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 | a0001c0001t0016 a0001c0001t0035 a0001c0001t0040 others(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 | a0001c0004t0025 | 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 | a0001c0001t0042 | 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 | 12 | a0001c0007t0011 a0002c0003t0003 a0002c0003t0006 others(9): 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 | a0001c0004t0005 a0001c0004t0010 a0001c0004t0023 others(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 | a0001c0001t0052 a0010c0031t0039 |
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 | a0007c0028t0022 | 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 | 34 | a0001c0001t0045 a0001c0002t0002 a0001c0002t0012 others(31): Show |
97 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(94): 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 | 23 | a0001c0001t0051 a0001c0002t0013 a0001c0002t0038 others(20): Show |
62 | HG01070.hp1 HG01070.hp2 HG01071.hp2 others(59): 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 | a0001c0001t0041 | 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 | a0001c0002t0038 | 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 | a0001c0001t0004 a0001c0001t0035 a0001c0001t0057 others(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 | 11 | a0002c0003t0003 a0002c0003t0006 a0002c0003t0009 others(8): 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 | a0001c0001t0049 | 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 | a0001c0002t0058 | 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 | a0001c0001t0008 a0001c0001t0018 a0001c0009t0018 others(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 | a0001c0001t0001 a0001c0001t0015 a0001c0001t0042 others(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 | a0001c0001t0015 a0001c0001t0018 a0001c0009t0015 others(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 | a0002c0003t0006 a0016c0024t0053 |
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 | a0001c0002t0012 a0001c0002t0017 a0002c0003t0024 |
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 | 16 | a0001c0001t0045 a0001c0002t0002 a0001c0002t0013 others(13): Show |
40 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(37): 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 | a0001c0001t0051 a0001c0004t0005 a0001c0004t0010 others(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 | a0012c0020t0046 | 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 | 14 | a0001c0004t0005 a0001c0004t0010 a0001c0004t0023 others(11): 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 | 15 | a0001c0001t0045 a0001c0002t0002 a0001c0002t0013 others(12): Show |
39 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(36): 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 | a0001c0002t0044 | 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 | a0007c0028t0022 | 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 | a0001c0001t0048 | 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 | a0001c0006t0007 a0001c0006t0032 a0003c0030t0007 |
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 | a0002c0003t0021 a0008c0013t0021 |
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 | a0002c0003t0055 | 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 | a0001c0001t0028 a0001c0007t0011 |
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 | a0001c0001t0016 a0001c0006t0032 |
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 | 14 | a0001c0002t0002 a0001c0002t0013 a0001c0002t0030 others(11): Show |
38 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(35): 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 | a0007c0028t0022 | 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 | a0005c0010t0037 | 1 | HG01070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3853C>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 23/23 | 3853 | chr17 | 78108698 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:77959448 | C | T | 1 | a0001c0001t0004g0268 | 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 | a0001c0001t0001g0008 | 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 | a0001c0005t0001g0009 a0001c0005t0001g0010 a0001c0005t0001g0011 |
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 | a0001c0007t0011g0265 a0001c0007t0011g0266 a0001c0007t0011g0267 |
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 | a0001c0001t0016g0263 a0001c0001t0016g0264 |
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 | a0001c0002t0030g0262 | 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 | a0008c0013t0021g0012 | 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 | 50 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(47): Show |
50 | HG01243.hp1 HG01257.hp2 HG01943.hp1 others(47): 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 | a0001c0001t0001g0216 | 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 | a0011c0015t0026g0261 a0013c0017t0027g0260 |
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 | a0001c0001t0016g0263 a0001c0001t0016g0264 a0001c0001t0028g0236 others(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 | a0001c0001t0016g0263 a0001c0001t0016g0264 a0001c0001t0028g0236 others(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 | a0001c0001t0028g0236 a0001c0004t0005g0239 a0001c0004t0005g0241 others(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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(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 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(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 | a0001c0001t0001g0198 | 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 | 6 | a0001c0002t0002g0001 a0001c0002t0002g0195 a0001c0002t0002g0196 others(3): 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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | a0001c0001t0028g0236 a0001c0004t0005g0239 a0001c0004t0005g0241 others(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 | a0001c0001t0028g0236 | 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 | 49 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(46): Show |
49 | HG01243.hp1 HG01257.hp2 HG01943.hp1 others(46): 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 | a0001c0002t0012g0232 a0001c0002t0012g0234 a0001c0002t0012g0235 others(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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | a0001c0001t0028g0236 | 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 | a0003c0030t0007g0252 | 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 | a0002c0003t0003g0013 | 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 | a0002c0003t0003g0014 | 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 | a0002c0003t0009g0247 | 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 | 162 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0107 others(159): Show |
168 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(165): 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 | a0001c0001t0028g0236 a0001c0004t0005g0239 a0001c0004t0005g0241 others(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 | a0011c0015t0026g0261 | 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 | a0001c0002t0030g0262 | 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 | a0001c0002t0002g0194 | 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 | a0001c0001t0028g0236 | 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 | a0002c0003t0019g0193 | 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 | 1 | a0001c0002t0058g0228 | 1 | HG04115.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 | a0011c0015t0026g0261 a0013c0017t0027g0260 |
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 | a0001c0001t0016g0263 a0001c0001t0016g0264 a0001c0001t0028g0236 others(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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | a0001c0001t0016g0263 a0001c0001t0016g0264 |
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 | a0001c0001t0016g0263 a0001c0001t0016g0264 a0001c0001t0028g0236 others(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 | a0001c0001t0028g0236 a0001c0004t0005g0239 a0001c0004t0005g0241 others(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 | a0001c0004t0005g0243 a0001c0004t0005g0244 a0001c0004t0005g0245 others(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 | a0001c0001t0016g0263 a0001c0001t0016g0264 a0001c0001t0028g0236 others(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 | a0002c0003t0003g0192 | 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 | a0001c0001t0001g0191 | 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 | a0002c0003t0003g0105 | 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 | a0001c0007t0011g0265 a0001c0007t0011g0266 a0001c0007t0011g0267 |
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 | 28 | a0001c0001t0001g0107 a0001c0001t0001g0199 a0001c0001t0045g0106 others(25): 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 | a0001c0001t0028g0236 a0001c0004t0005g0239 a0001c0004t0005g0241 others(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 | a0001c0001t0001g0126 a0001c0002t0012g0232 a0001c0002t0012g0234 others(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 | a0002c0003t0006g0127 | 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 | a0001c0001t0028g0236 a0001c0004t0005g0239 a0001c0004t0005g0241 others(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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0007t0011g0265 a0001c0007t0011g0266 a0001c0007t0011g0267 |
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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | a0001c0001t0028g0236 a0001c0004t0005g0239 a0001c0004t0005g0241 others(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 | a0014c0023t0002g0190 | 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 | a0001c0004t0010g0254 | 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 | a0002c0003t0006g0104 | 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 | a0001c0001t0028g0236 a0001c0002t0030g0262 a0001c0004t0005g0239 others(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 | a0001c0002t0002g0119 | 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 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 |
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 | a0002c0003t0003g0128 a0002c0003t0003g0192 |
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 | a0001c0001t0001g0103 | 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 | a0001c0001t0001g0103 | 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 | a0001c0001t0028g0236 | 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 | a0001c0001t0016g0264 | 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 | a0001c0001t0001g0183 a0001c0001t0001g0185 a0001c0001t0034g0186 others(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 | a0001c0001t0016g0263 a0001c0001t0016g0264 a0001c0001t0028g0236 others(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 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0133 others(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 | a0001c0002t0056g0125 | 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 | a0001c0001t0028g0236 a0011c0015t0026g0261 a0013c0017t0027g0260 |
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 | a0001c0001t0001g0102 | 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 | a0001c0001t0041g0101 | 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 | a0001c0001t0045g0106 | 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 | a0001c0002t0002g0197 | 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 | a0001c0002t0030g0262 | 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 | a0001c0001t0001g0216 | 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 | a0001c0001t0028g0236 a0001c0002t0030g0262 a0001c0004t0005g0239 others(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 | a0001c0001t0001g0015 | 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 | a0001c0001t0034g0186 | 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 | a0009c0018t0001g0100 | 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 | a0001c0004t0005g0243 | 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 | a0011c0015t0026g0261 | 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 | a0001c0001t0028g0236 a0001c0004t0005g0239 a0001c0004t0005g0241 others(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 | a0001c0001t0028g0236 | 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 | a0007c0028t0022g0255 | 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 | a0001c0001t0016g0263 a0001c0001t0016g0264 a0001c0001t0028g0236 others(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 | a0001c0001t0001g0107 | 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 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0014g0016 others(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 | a0001c0007t0011g0265 a0001c0007t0011g0266 a0001c0007t0011g0267 |
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 | 1 | a0001c0002t0058g0228 | 1 | HG04115.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 | a0001c0001t0016g0263 a0001c0001t0016g0264 |
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 | a0001c0005t0001g0139 | 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 | a0001c0001t0029g0256 a0001c0004t0010g0254 a0001c0004t0010g0258 others(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 | a0001c0001t0016g0263 a0001c0001t0016g0264 a0001c0001t0028g0236 others(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 | a0001c0002t0002g0108 | 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 | a0001c0001t0028g0236 a0001c0004t0005g0239 a0001c0004t0005g0241 others(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 | a0001c0001t0028g0236 a0001c0004t0005g0239 a0001c0004t0005g0241 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0062g0019 |
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 | 38 | a0001c0001t0016g0263 a0001c0001t0016g0264 a0001c0001t0028g0236 others(35): Show |
38 | HG01943.hp1 HG02145.hp2 HG02155.hp1 others(35): 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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | a0001c0001t0051g0099 | 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 | a0002c0003t0019g0180 a0002c0003t0021g0181 a0008c0013t0021g0012 |
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 | a0002c0003t0009g0237 | 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 | a0001c0001t0028g0236 | 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 | a0001c0001t0014g0020 | 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 | a0001c0001t0001g0206 a0001c0001t0001g0213 a0001c0001t0001g0214 others(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 | a0001c0001t0001g0205 | 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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | 162 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0085 others(159): Show |
168 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(165): 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 | a0001c0001t0001g0189 a0001c0001t0028g0236 a0001c0002t0002g0177 others(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 | a0001c0001t0001g0083 a0001c0001t0001g0084 |
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 | a0001c0001t0029g0256 a0001c0004t0010g0254 a0001c0004t0010g0258 others(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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | a0001c0001t0029g0256 a0001c0004t0010g0254 a0001c0004t0010g0258 others(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 | a0001c0001t0015g0144 a0001c0001t0018g0143 |
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 | a0001c0001t0001g0145 | 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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0001t0014g0021 | 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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | a0001c0001t0029g0256 a0001c0004t0010g0254 a0001c0004t0010g0258 others(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 | a0001c0002t0002g0124 a0001c0002t0002g0194 a0001c0002t0047g0123 |
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 | a0001c0001t0029g0256 a0001c0004t0010g0254 a0001c0004t0010g0258 others(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 | a0001c0001t0001g0098 a0001c0001t0061g0082 |
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 | a0007c0016t0001g0081 | 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 | a0001c0001t0029g0256 a0001c0004t0010g0254 a0001c0004t0010g0258 others(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 | a0001c0001t0028g0236 a0001c0004t0005g0239 a0001c0004t0005g0241 others(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 | a0001c0001t0028g0236 a0001c0004t0005g0239 a0001c0004t0005g0241 others(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 | a0001c0001t0028g0236 | 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 | a0002c0003t0003g0146 | 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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | a0001c0005t0001g0139 | 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 | 165 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0095 others(162): Show |
171 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(168): 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 | a0001c0002t0030g0262 | 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 | a0001c0001t0001g0022 | 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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0002t0030g0262 | 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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | a0001c0004t0005g0241 | 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 | a0001c0002t0012g0232 a0001c0002t0012g0234 a0001c0002t0012g0235 others(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 | a0001c0007t0011g0265 a0001c0007t0011g0266 a0001c0007t0011g0267 |
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 | a0001c0005t0001g0002 a0001c0005t0001g0147 a0001c0005t0001g0148 others(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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | 1 | a0001c0002t0058g0228 | 1 | HG04115.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 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0018 others(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 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0029 others(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 | a0001c0001t0001g0023 a0001c0001t0029g0256 a0001c0004t0005g0239 others(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 | 65 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0107 others(62): Show |
71 | HG00323.hp2 HG00558.hp2 HG00673.hp1 others(68): 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 | a0001c0002t0030g0262 a0001c0006t0007g0248 a0001c0006t0007g0250 others(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 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0133 others(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 | a0001c0001t0028g0236 | 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 | a0001c0001t0001g0080 | 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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | a0001c0006t0007g0248 | 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 | a0001c0001t0001g0015 a0001c0001t0001g0032 a0001c0001t0001g0054 |
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 | a0001c0001t0001g0053 a0001c0001t0014g0021 |
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 | a0001c0001t0016g0263 a0001c0001t0016g0264 a0001c0001t0028g0236 others(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 | a0002c0003t0054g0160 | 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 | a0001c0001t0001g0205 | 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 | a0001c0001t0028g0236 a0011c0015t0026g0261 a0013c0017t0027g0260 |
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 | a0001c0007t0011g0265 a0001c0007t0011g0266 a0001c0007t0011g0267 others(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 | a0018c0025t0001g0079 | 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 | a0001c0007t0011g0265 a0001c0007t0011g0266 a0001c0007t0011g0267 others(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 | a0001c0002t0002g0208 | 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 | a0001c0002t0056g0125 | 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 | a0001c0001t0001g0051 a0001c0001t0001g0077 a0001c0001t0001g0078 others(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 | a0001c0004t0025g0257 a0001c0006t0007g0248 a0001c0006t0007g0250 others(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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | 31 | a0001c0001t0001g0008 a0001c0001t0001g0054 a0001c0007t0011g0265 others(28): 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 | a0001c0002t0002g0124 | 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 | 106 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0107 others(103): 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 | a0001c0002t0030g0262 | 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 | a0001c0007t0011g0265 a0001c0007t0011g0266 a0001c0007t0011g0267 |
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 | a0001c0005t0001g0147 | 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 | a0001c0002t0002g0122 | 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 | a0001c0002t0030g0262 a0001c0006t0007g0248 a0001c0006t0007g0250 others(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 | a0001c0002t0030g0262 | 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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | a0001c0007t0011g0265 a0001c0007t0011g0266 a0001c0007t0011g0267 |
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 | a0001c0001t0028g0236 | 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 | a0001c0001t0001g0191 | 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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | a0001c0001t0042g0175 | 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 | a0001c0001t0041g0101 | 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 | a0001c0002t0012g0232 a0001c0002t0012g0234 a0001c0002t0012g0235 others(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 | a0006c0011t0001g0161 a0006c0011t0001g0162 |
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 | 1 | a0001c0002t0058g0228 | 1 | HG04115.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 | a0001c0001t0016g0263 a0001c0001t0016g0264 a0001c0001t0028g0236 others(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 | a0012c0020t0046g0049 | 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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | a0001c0001t0029g0256 a0001c0004t0010g0254 a0001c0004t0010g0258 others(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 | a0001c0001t0001g0031 | 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 | a0001c0001t0001g0074 a0004c0008t0001g0075 a0004c0008t0001g0076 others(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 | a0001c0002t0030g0262 | 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 | a0001c0029t0001g0033 a0007c0016t0001g0081 |
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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | a0001c0006t0032g0249 | 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 | a0001c0002t0002g0112 | 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 | a0001c0001t0001g0185 | 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 | a0002c0003t0009g0237 a0002c0003t0009g0242 |
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 | a0001c0007t0011g0265 a0001c0007t0011g0266 a0001c0007t0011g0267 |
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 | a0001c0001t0049g0048 | 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 | a0013c0017t0027g0260 | 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 | a0001c0002t0012g0232 a0001c0002t0012g0234 a0001c0002t0012g0235 others(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 | 1 | a0002c0014t0001g0005 | 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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | 162 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0107 others(159): Show |
168 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(165): 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 | a0001c0001t0029g0256 a0001c0004t0010g0254 a0001c0004t0010g0258 others(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 | a0001c0001t0051g0099 | 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 | a0001c0002t0002g0179 | 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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | 6 | a0001c0002t0002g0001 a0001c0002t0002g0195 a0001c0002t0002g0196 others(3): 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 | a0007c0028t0022g0255 | 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 | a0001c0002t0002g0110 a0001c0002t0002g0112 a0001c0002t0002g0113 others(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 | a0001c0001t0016g0263 a0001c0001t0016g0264 a0001c0001t0028g0236 others(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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | a0001c0001t0001g0047 | 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 | a0001c0002t0030g0262 | 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 | a0001c0001t0029g0256 a0001c0004t0010g0254 a0001c0004t0010g0258 others(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 | a0001c0001t0001g0046 a0001c0001t0015g0052 |
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 | a0001c0001t0014g0021 | 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 | a0001c0005t0001g0002 a0001c0005t0001g0147 a0001c0005t0001g0148 others(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 | a0002c0003t0054g0160 | 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 | 132 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0126 others(129): Show |
138 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(135): 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 | a0011c0015t0026g0261 | 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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0002c0003t0054g0160 | 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 | a0001c0002t0030g0262 | 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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | a0001c0002t0030g0262 a0007c0028t0022g0255 |
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 | a0001c0001t0028g0236 | 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 | 1 | a0001c0002t0058g0228 | 1 | HG04115.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 | a0001c0002t0017g0231 | 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 | a0001c0001t0001g0204 | 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 | a0001c0007t0011g0265 a0001c0007t0011g0266 a0001c0007t0011g0267 others(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 | a0001c0007t0011g0265 a0001c0007t0011g0266 a0001c0007t0011g0267 |
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 | a0001c0001t0001g0034 a0001c0001t0001g0183 a0001c0001t0001g0185 others(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 | a0001c0001t0029g0256 a0001c0004t0010g0254 a0001c0004t0010g0258 others(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 | ||||||
| chr17:77984875 | G | A | 1 | a0007c0028t0022g0255 | 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 | a0001c0001t0001g0209 | 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 | a0001c0002t0012g0232 a0001c0002t0012g0234 a0001c0002t0012g0235 others(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 | a0001c0001t0001g0087 | 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 | a0001c0001t0016g0263 a0001c0001t0016g0264 |
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 | a0001c0001t0016g0264 a0001c0004t0010g0258 a0001c0004t0025g0257 others(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 | a0001c0002t0030g0262 a0001c0006t0032g0249 a0001c0007t0011g0265 |
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 | a0001c0006t0007g0248 a0001c0006t0007g0253 a0001c0006t0031g0251 others(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 | a0001c0006t0007g0250 | 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 | a0001c0004t0005g0241 a0001c0004t0005g0243 a0001c0004t0005g0245 others(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 | a0001c0004t0005g0239 a0001c0004t0005g0244 a0002c0003t0024g0238 |
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 | a0001c0002t0012g0234 a0001c0002t0012g0235 a0001c0002t0017g0233 |
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 | a0001c0002t0017g0231 | 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 | a0001c0002t0012g0232 | 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 | a0013c0017t0027g0260 | 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 | a0001c0001t0028g0236 | 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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | a0001c0001t0016g0263 a0001c0001t0016g0264 a0001c0001t0028g0236 others(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 | 33 | a0001c0001t0001g0008 a0002c0003t0003g0003 a0002c0003t0003g0004 others(30): 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 | a0001c0001t0016g0263 a0001c0001t0016g0264 a0001c0001t0028g0236 others(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 | a0001c0001t0016g0263 a0001c0001t0016g0264 a0001c0001t0028g0236 others(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 | a0001c0001t0029g0256 a0001c0004t0010g0254 a0001c0004t0010g0258 others(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 | a0001c0001t0028g0236 a0001c0004t0005g0239 a0001c0004t0005g0241 others(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 | a0001c0002t0030g0262 a0007c0028t0022g0255 |
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 | a0001c0002t0002g0111 | 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 | a0001c0001t0001g0035 a0001c0001t0001g0055 |
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 | a0011c0015t0026g0261 a0013c0017t0027g0260 |
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 | 13 | a0001c0001t0001g0036 a0001c0001t0001g0047 a0001c0001t0001g0087 others(10): Show |
13 | HG01943.hp1 HG02145.hp1 HG02155.hp1 others(10): 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 | 228 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0015 others(225): 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 | a0001c0001t0028g0236 a0001c0002t0002g0194 a0001c0002t0030g0262 others(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 | a0001c0001t0028g0236 | 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 | a0001c0001t0051g0099 | 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 | a0001c0002t0030g0262 | 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 | a0001c0001t0001g0034 a0001c0001t0001g0039 a0001c0001t0001g0040 others(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 | a0001c0002t0002g0108 a0001c0002t0002g0121 |
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 | 11 | a0001c0001t0001g0006 a0001c0001t0001g0145 a0001c0001t0001g0159 others(8): 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 | a0001c0002t0030g0262 | 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 | 25 | a0001c0001t0001g0107 a0001c0001t0045g0106 a0001c0002t0002g0001 others(22): 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 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0198 |
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 | a0002c0003t0019g0180 a0002c0003t0021g0181 a0008c0013t0021g0012 |
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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | a0001c0002t0030g0262 a0007c0028t0022g0255 |
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 | a0001c0001t0028g0236 a0001c0004t0005g0239 a0001c0004t0005g0241 others(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 | a0001c0001t0001g0159 | 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 | a0001c0001t0029g0256 a0001c0004t0010g0254 a0001c0004t0010g0258 others(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 | a0001c0002t0030g0262 | 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 | a0001c0007t0011g0265 a0001c0007t0011g0266 a0001c0007t0011g0267 |
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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | a0001c0005t0001g0002 a0001c0005t0001g0009 a0001c0005t0001g0010 others(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 | 162 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0107 others(159): Show |
168 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(165): 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 | a0001c0002t0030g0262 | 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 | a0001c0001t0029g0256 a0001c0004t0010g0254 a0001c0004t0010g0258 others(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 | a0001c0002t0030g0262 | 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 | a0001c0002t0030g0262 | 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 | a0014c0023t0002g0190 | 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 | a0001c0001t0001g0126 | 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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | 1 | a0001c0002t0058g0228 | 1 | HG04115.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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | a0001c0004t0005g0239 | 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 | a0001c0006t0032g0249 | 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 | a0001c0002t0002g0110 | 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 | a0001c0007t0011g0265 a0001c0007t0011g0266 a0001c0007t0011g0267 |
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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0007t0011g0265 a0001c0007t0011g0266 a0001c0007t0011g0267 |
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 | a0001c0001t0016g0263 a0001c0001t0016g0264 a0001c0001t0028g0236 others(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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | a0001c0001t0001g0045 a0001c0001t0014g0020 |
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 | a0001c0002t0012g0232 a0001c0002t0012g0234 a0001c0002t0012g0235 others(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 | |||||||
| chr17:77991209 | A | C | 37 | a0001c0001t0016g0263 a0001c0001t0016g0264 a0001c0001t0028g0236 others(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 | a0001c0002t0030g0262 | 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 | a0001c0002t0002g0110 a0001c0002t0002g0112 a0001c0002t0002g0113 others(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 | a0001c0001t0028g0236 a0011c0015t0026g0261 a0013c0017t0027g0260 |
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 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0030 others(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 | a0007c0028t0022g0255 | 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 | a0011c0015t0026g0261 a0013c0017t0027g0260 |
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 | a0001c0001t0016g0263 a0001c0001t0016g0264 |
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 | 157 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0039 others(154): Show |
163 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(160): 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 | a0001c0001t0001g0093 | 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 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0001g0044 others(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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | a0001c0001t0028g0236 | 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 | a0001c0001t0001g0107 a0001c0001t0045g0106 a0015c0019t0001g0115 |
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 | a0001c0001t0001g0159 a0001c0001t0001g0172 |
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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | a0007c0028t0022g0255 | 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 | a0001c0002t0012g0232 a0001c0002t0012g0234 a0001c0002t0012g0235 others(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 | a0001c0001t0001g0022 | 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 | a0001c0001t0016g0263 a0001c0001t0016g0264 a0001c0001t0028g0236 others(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 | a0001c0004t0005g0243 a0001c0004t0005g0244 a0001c0004t0005g0245 others(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 | a0001c0002t0012g0232 a0001c0002t0012g0234 a0001c0002t0012g0235 others(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 | a0001c0001t0016g0263 a0001c0001t0016g0264 |
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 | a0001c0001t0001g0066 a0001c0001t0001g0077 |
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 | a0001c0001t0051g0099 | 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 | a0001c0005t0001g0002 a0001c0005t0001g0147 a0001c0005t0001g0148 others(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 | a0001c0007t0011g0265 a0001c0007t0011g0266 a0001c0007t0011g0267 |
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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0013c0017t0027g0260 | 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 | a0001c0001t0028g0236 a0001c0002t0030g0262 a0001c0004t0005g0239 others(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 | a0001c0001t0001g0029 | 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 | a0001c0001t0028g0236 a0001c0004t0005g0239 a0001c0004t0005g0241 others(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 | a0001c0002t0038g0059 | 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 | a0001c0006t0032g0249 | 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 | a0001c0001t0016g0263 a0001c0001t0016g0264 |
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 | a0001c0001t0001g0205 a0001c0007t0011g0267 |
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 | a0001c0002t0030g0262 | 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 | a0002c0003t0003g0141 | 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 | a0007c0016t0001g0081 | 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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | a0001c0002t0030g0262 | 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 | a0001c0001t0028g0236 a0001c0004t0005g0239 a0001c0004t0005g0241 others(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 | a0001c0001t0001g0089 | 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 | a0011c0015t0026g0261 a0013c0017t0027g0260 |
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 | a0001c0005t0001g0139 | 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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | 108 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0039 others(105): 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 | 38 | a0001c0001t0016g0263 a0001c0001t0016g0264 a0001c0001t0028g0236 others(35): Show |
38 | HG01943.hp1 HG02145.hp2 HG02155.hp1 others(35): 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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | a0001c0002t0012g0232 a0001c0002t0012g0234 a0001c0002t0012g0235 others(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 | a0001c0007t0011g0265 a0001c0007t0011g0266 a0001c0007t0011g0267 |
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 | a0001c0001t0028g0236 a0001c0001t0029g0256 a0001c0002t0030g0262 others(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 | a0001c0001t0001g0171 a0001c0009t0015g0142 a0001c0009t0018g0170 others(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 | a0001c0001t0028g0236 a0001c0002t0030g0262 |
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 | a0001c0001t0029g0256 a0001c0004t0010g0254 a0001c0004t0010g0258 others(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 | a0001c0001t0001g0095 | 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 | a0001c0001t0028g0236 a0001c0002t0030g0262 |
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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0001t0001g0200 | 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 | a0001c0001t0034g0186 | 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 | a0001c0002t0012g0232 a0001c0002t0012g0234 a0001c0002t0012g0235 others(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 | a0001c0002t0002g0110 | 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 | a0001c0001t0028g0236 a0001c0002t0030g0262 a0001c0004t0005g0239 others(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 | a0001c0005t0001g0002 a0001c0005t0001g0009 a0001c0005t0001g0010 others(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 | a0001c0001t0001g0053 | 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 | a0001c0001t0028g0236 a0001c0002t0030g0262 a0001c0004t0005g0239 others(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 | a0002c0003t0003g0105 | 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 | a0001c0002t0030g0262 | 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 | a0001c0002t0030g0262 | 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 | a0013c0017t0027g0260 | 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 | a0001c0002t0012g0232 a0001c0002t0012g0234 a0001c0002t0012g0235 others(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 | a0001c0007t0011g0265 a0001c0007t0011g0266 a0001c0007t0011g0267 |
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 | 33 | a0001c0001t0001g0008 a0002c0003t0003g0003 a0002c0003t0003g0004 others(30): 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 | a0013c0017t0027g0260 | 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 | a0001c0001t0001g0045 a0001c0001t0001g0218 a0001c0001t0001g0219 others(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 | a0001c0002t0002g0108 | 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 | a0001c0001t0001g0191 | 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 | a0002c0003t0003g0007 a0002c0003t0003g0184 a0002c0027t0003g0007 |
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 | a0001c0001t0001g0028 | 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 | a0001c0002t0012g0232 a0001c0002t0012g0234 a0001c0002t0012g0235 others(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 | a0007c0028t0022g0255 | 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 | a0001c0001t0001g0107 a0001c0001t0001g0129 a0001c0001t0045g0106 others(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 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0133 others(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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | 1 | a0001c0002t0058g0228 | 1 | HG04115.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 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0042 others(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 | 71 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0018 others(68): Show |
71 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(68): 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 | a0001c0001t0001g0044 a0001c0001t0001g0054 a0001c0001t0001g0093 others(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 | a0017c0026t0002g0120 | 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 | a0001c0002t0002g0124 | 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 | a0001c0001t0001g0130 a0002c0003t0003g0176 a0002c0003t0019g0180 |
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 | a0001c0001t0004g0088 a0001c0002t0012g0234 a0001c0002t0017g0233 |
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 | a0001c0001t0001g0023 a0002c0003t0003g0003 a0002c0003t0003g0014 others(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 | a0001c0001t0016g0263 a0001c0001t0016g0264 a0001c0002t0012g0232 others(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 | a0001c0001t0001g0126 a0001c0001t0001g0145 |
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 | 3 | a0001c0001t0028g0236 a0001c0002t0058g0228 a0013c0017t0027g0260 |
3 | HG02615.hp1 HG03098.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-37-3538A>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | chr17 | 78000632 | |||||||
| chr17:78000634 | A | C | 1 | a0013c0017t0027g0260 | 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 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0005t0001g0002 others(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 | 12 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(9): Show |
12 | HG01243.hp1 HG01257.hp2 HG02055.hp1 others(9): 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 | a0001c0001t0029g0256 a0001c0004t0010g0254 a0001c0004t0010g0258 others(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 | a0001c0007t0011g0265 a0001c0007t0011g0266 a0001c0007t0011g0267 |
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 | 30 | a0001c0001t0001g0107 a0001c0001t0045g0106 a0001c0002t0002g0001 others(27): 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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | a0001c0001t0001g0172 | 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 | a0001c0001t0029g0256 a0001c0004t0010g0254 a0001c0004t0010g0258 others(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 | a0001c0005t0001g0002 a0001c0005t0001g0009 a0001c0005t0001g0010 others(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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | a0001c0002t0030g0262 | 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 | a0002c0003t0003g0192 | 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 | 155 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0107 others(152): Show |
161 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(158): 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 | a0001c0001t0001g0209 | 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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0001t0001g0018 | 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 | a0001c0001t0001g0018 | 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 | a0001c0002t0002g0197 | 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 | 106 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0107 others(103): 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 | a0001c0001t0029g0256 a0001c0004t0010g0254 a0001c0004t0010g0258 others(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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | a0001c0006t0007g0253 | 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 | a0001c0001t0016g0263 a0001c0001t0016g0264 a0001c0001t0028g0236 others(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 | a0002c0003t0003g0176 | 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 | a0001c0001t0016g0263 a0001c0001t0016g0264 |
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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | a0001c0002t0030g0262 | 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 | a0007c0028t0022g0255 | 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 | a0001c0001t0029g0256 a0001c0004t0010g0254 a0001c0004t0010g0258 others(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 | a0001c0001t0001g0018 | 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 | 155 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0107 others(152): Show |
161 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(158): 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 | a0001c0001t0016g0263 a0001c0001t0016g0264 a0001c0001t0028g0236 |
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 | a0001c0001t0001g0018 | 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 | a0013c0017t0027g0260 | 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 | a0001c0002t0002g0208 | 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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0002c0003t0024g0238 | 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 | a0001c0005t0001g0002 a0001c0005t0001g0009 a0001c0005t0001g0010 others(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 | a0001c0001t0004g0025 a0001c0001t0004g0088 |
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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 others(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 | a0001c0004t0005g0241 | 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 | a0001c0001t0015g0144 | 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 | a0001c0001t0001g0095 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0029 others(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 | a0001c0001t0001g0047 a0001c0001t0001g0087 a0001c0001t0001g0200 others(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 | a0001c0001t0001g0018 | 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 | a0001c0001t0001g0034 a0001c0001t0001g0042 a0001c0001t0001g0044 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0041 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0032 others(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 | a0001c0001t0001g0069 a0001c0001t0001g0126 a0001c0001t0001g0183 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0072 a0001c0001t0001g0185 others(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 | 5 | a0001c0001t0001g0064 a0004c0008t0001g0075 a0004c0008t0001g0076 others(2): Show |
5 | HG01255.hp2 HG02083.hp2 NA18943.hp1 others(2): 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 | a0001c0001t0004g0268 | 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 | a0001c0001t0001g0226 a0001c0001t0008g0157 |
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 | a0001c0001t0001g0226 a0001c0001t0008g0157 |
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 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 others(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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0011c0015t0026g0261 a0013c0017t0027g0260 |
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 | a0002c0003t0019g0180 a0008c0013t0021g0012 |
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 | a0001c0007t0011g0265 a0001c0007t0011g0266 a0001c0007t0011g0267 |
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 | a0001c0001t0016g0263 | 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 | a0001c0001t0016g0264 | 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 | a0001c0006t0007g0248 | 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 | a0001c0005t0001g0002 a0001c0005t0001g0147 a0001c0005t0001g0149 others(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 | a0001c0001t0001g0226 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | a0001c0002t0030g0262 | 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 | a0001c0002t0030g0262 | 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 | a0001c0002t0030g0262 | 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 | a0011c0015t0026g0261 | 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 | a0013c0017t0027g0260 | 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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | a0001c0001t0016g0263 a0001c0001t0016g0264 a0001c0001t0028g0236 others(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 | a0001c0002t0030g0262 a0001c0004t0005g0239 a0001c0004t0005g0241 others(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 | a0001c0001t0001g0126 | 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 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0030 others(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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0071 a0001c0001t0001g0092 |
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 | a0011c0015t0026g0261 | 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 | a0001c0001t0001g0030 a0001c0001t0001g0199 a0001c0001t0060g0043 others(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 | a0001c0002t0030g0262 a0001c0004t0005g0239 a0001c0004t0005g0241 others(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 | 152 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0015 others(149): 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 | a0002c0003t0024g0238 a0007c0028t0022g0255 |
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 | a0001c0001t0001g0098 a0001c0001t0001g0187 a0001c0001t0014g0016 others(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 | a0001c0001t0001g0189 | 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 | a0002c0003t0003g0207 | 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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | a0011c0015t0026g0261 a0013c0017t0027g0260 |
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 | a0001c0001t0016g0264 | 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 | a0002c0003t0003g0105 | 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 | a0001c0001t0035g0068 | 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 | a0001c0002t0012g0232 a0001c0002t0012g0234 a0001c0002t0012g0235 others(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 | a0002c0003t0003g0003 a0002c0003t0054g0160 |
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 | a0001c0001t0001g0092 | 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 | a0001c0001t0041g0101 | 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 | a0001c0002t0012g0232 a0001c0002t0012g0234 a0001c0002t0012g0235 others(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 | a0001c0006t0007g0253 a0001c0006t0031g0251 |
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 | a0001c0001t0001g0205 | 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 | a0007c0028t0022g0255 | 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 | a0001c0001t0029g0256 a0001c0004t0010g0254 a0001c0004t0010g0258 others(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 | a0001c0002t0030g0262 a0001c0004t0005g0239 a0001c0004t0005g0241 others(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 | a0001c0001t0001g0077 | 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 | a0001c0001t0001g0077 | 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 | a0001c0001t0001g0077 | 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 | a0001c0001t0001g0077 | 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 | a0001c0001t0001g0077 | 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 | a0001c0001t0001g0077 | 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 | a0001c0001t0001g0077 | 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 | a0001c0001t0001g0077 | 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 | a0001c0001t0001g0077 | 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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | a0001c0001t0001g0206 | 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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0002t0030g0262 | 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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0005t0001g0149 | 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 | a0014c0023t0002g0190 | 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 | a0001c0002t0030g0262 | 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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | a0002c0003t0003g0013 | 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 | a0006c0011t0001g0161 a0006c0011t0001g0162 |
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 | a0001c0002t0030g0262 | 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 | a0002c0003t0003g0192 | 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 | a0001c0006t0032g0249 | 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 | a0001c0001t0001g0205 | 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 | a0001c0001t0016g0263 a0001c0001t0016g0264 |
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 | a0001c0007t0011g0265 a0001c0007t0011g0266 a0001c0007t0011g0267 |
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 | 33 | a0001c0001t0001g0008 a0002c0003t0003g0003 a0002c0003t0003g0004 others(30): 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 | a0001c0001t0001g0159 a0001c0001t0001g0172 |
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 | a0001c0001t0028g0236 a0001c0002t0030g0262 a0001c0004t0005g0239 others(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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | a0001c0002t0030g0262 | 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 | 25 | a0001c0001t0001g0107 a0001c0001t0045g0106 a0001c0002t0002g0001 others(22): 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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0013c0017t0027g0260 | 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 | a0001c0001t0001g0044 | 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 | a0001c0001t0028g0236 | 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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0002t0002g0111 | 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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | a0001c0002t0030g0262 a0001c0004t0005g0239 a0001c0004t0005g0241 others(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 | a0001c0002t0030g0262 a0001c0004t0005g0239 a0001c0004t0005g0241 others(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 | a0001c0001t0016g0263 a0001c0001t0016g0264 a0001c0001t0029g0256 others(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 | a0001c0001t0016g0263 a0001c0001t0016g0264 |
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 | a0001c0001t0028g0236 | 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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | a0001c0001t0040g0131 | 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 | a0001c0001t0028g0236 a0001c0002t0030g0262 a0001c0004t0005g0239 others(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 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0133 others(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 | a0001c0001t0001g0216 | 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 | a0001c0002t0030g0262 | 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 | a0001c0001t0004g0025 a0001c0001t0004g0088 |
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 | a0011c0015t0026g0261 a0013c0017t0027g0260 |
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 | a0001c0001t0001g0023 a0001c0001t0001g0093 |
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 | a0001c0001t0028g0236 | 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 | a0001c0002t0030g0262 a0001c0004t0005g0239 a0001c0004t0005g0241 others(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 | a0002c0003t0003g0176 | 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 | a0001c0001t0001g0070 a0001c0001t0001g0212 |
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 | a0001c0002t0030g0262 a0001c0004t0005g0239 a0001c0004t0005g0241 others(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 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0133 others(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 | a0001c0002t0012g0232 a0001c0002t0012g0234 a0001c0002t0012g0235 others(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 | a0013c0017t0027g0260 | 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 | a0002c0003t0003g0153 | 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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | a0014c0023t0002g0190 | 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 | a0001c0007t0011g0265 a0001c0007t0011g0266 a0001c0007t0011g0267 |
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 | a0001c0002t0030g0262 a0001c0004t0005g0239 a0001c0004t0005g0241 others(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 | a0001c0001t0001g0216 | 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 | a0001c0002t0030g0262 | 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 | a0001c0001t0029g0256 a0001c0004t0010g0254 a0001c0004t0010g0258 others(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 | a0014c0023t0002g0190 | 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 | a0001c0001t0001g0206 a0001c0001t0001g0213 a0001c0001t0001g0214 |
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 | a0001c0002t0002g0109 | 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 | a0001c0001t0028g0236 a0001c0002t0030g0262 a0001c0004t0005g0239 others(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 | a0001c0002t0012g0232 a0001c0002t0012g0234 a0001c0002t0012g0235 others(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 | a0001c0001t0001g0211 | 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 | 105 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0107 others(102): 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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0011c0015t0026g0261 a0013c0017t0027g0260 |
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 | 25 | a0001c0001t0001g0107 a0001c0001t0045g0106 a0001c0002t0002g0001 others(22): 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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0001t0035g0068 | 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 | a0001c0002t0012g0232 a0001c0002t0012g0234 a0001c0002t0012g0235 others(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 | a0001c0006t0032g0249 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0071 a0001c0001t0001g0083 others(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 | a0003c0021t0002g0114 | 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 | a0001c0002t0012g0232 a0001c0002t0012g0234 a0001c0002t0012g0235 others(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 | a0001c0001t0020g0062 | 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 | a0001c0001t0028g0236 | 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 | a0007c0028t0022g0255 | 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 | a0001c0001t0001g0044 | 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 | a0003c0012t0001g0024 | 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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0002t0030g0262 | 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 | a0001c0001t0016g0263 a0001c0001t0016g0264 |
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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0002t0012g0232 a0001c0002t0012g0234 a0001c0002t0012g0235 others(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 | a0001c0002t0012g0232 a0001c0002t0012g0234 a0001c0002t0012g0235 others(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 | a0001c0001t0001g0126 a0001c0001t0001g0187 a0001c0001t0001g0188 others(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 | a0001c0001t0001g0008 a0002c0003t0003g0003 a0002c0003t0003g0004 others(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 | a0001c0001t0049g0048 | 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 | a0002c0003t0006g0104 | 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 | a0011c0015t0026g0261 a0013c0017t0027g0260 |
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 | a0002c0003t0024g0238 | 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 | a0001c0001t0001g0026 | 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 | a0001c0002t0012g0232 a0001c0002t0012g0234 a0001c0002t0012g0235 others(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 | a0001c0001t0001g0200 | 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 | a0001c0002t0012g0232 a0001c0002t0012g0234 a0001c0002t0012g0235 others(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 | a0001c0001t0001g0136 a0003c0022t0020g0132 |
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 | 30 | a0001c0001t0001g0107 a0001c0001t0045g0106 a0001c0002t0002g0001 others(27): 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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | 1 | a0007c0016t0001g0081 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.86-10794A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | chr17 | 78020722 | |||||||
| chr17:78020773 | G | A | 35 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0001t0052g0096 | 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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0001t0001g0200 a0001c0001t0001g0201 |
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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | a0001c0002t0030g0262 a0011c0015t0026g0261 a0013c0017t0027g0260 |
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 | a0001c0002t0012g0232 a0001c0002t0012g0234 a0001c0002t0012g0235 others(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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0002t0002g0124 | 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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | a0001c0002t0030g0262 a0011c0015t0026g0261 a0013c0017t0027g0260 |
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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0007t0011g0265 a0001c0007t0011g0266 a0001c0007t0011g0267 |
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 | a0001c0002t0030g0262 | 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 | a0002c0003t0006g0127 | 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 | a0001c0001t0001g0026 | 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 | a0001c0002t0012g0232 a0001c0002t0012g0234 a0001c0002t0012g0235 others(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 | a0011c0015t0026g0261 a0013c0017t0027g0260 |
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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | a0001c0001t0016g0263 a0001c0001t0016g0264 |
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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0001t0051g0099 | 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 | a0001c0001t0001g0216 | 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 | a0001c0001t0001g0069 | 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 | a0001c0001t0001g0015 a0001c0001t0001g0032 a0001c0001t0001g0054 |
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 | a0002c0003t0003g0013 | 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 | a0002c0003t0003g0141 | 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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0007t0011g0265 | 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 | a0001c0001t0051g0099 | 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 | a0002c0003t0009g0247 | 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 | a0001c0001t0001g0159 a0001c0001t0001g0172 |
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 | a0014c0023t0002g0190 | 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 | a0001c0007t0011g0265 a0001c0007t0011g0266 a0001c0007t0011g0267 |
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 | a0001c0001t0001g0134 a0001c0001t0001g0138 |
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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | a0001c0001t0028g0236 | 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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0002t0030g0262 | 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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0002t0002g0117 | 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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0001t0001g0098 a0001c0001t0061g0082 |
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 | a0001c0002t0012g0232 a0001c0002t0012g0234 a0001c0002t0012g0235 others(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 | a0001c0005t0001g0002 a0001c0005t0001g0147 a0001c0005t0001g0148 others(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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | 6 | a0001c0002t0002g0001 a0001c0002t0002g0195 a0001c0002t0002g0196 others(3): 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 | a0001c0001t0001g0172 | 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 | a0002c0003t0003g0146 | 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 | a0001c0001t0028g0236 | 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 | a0002c0003t0009g0242 | 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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0001t0001g0183 a0001c0001t0028g0236 |
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 | a0001c0007t0011g0265 a0001c0007t0011g0266 a0001c0007t0011g0267 |
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 | a0001c0002t0002g0124 a0001c0002t0002g0194 a0001c0002t0047g0123 |
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 | a0011c0015t0026g0261 a0013c0017t0027g0260 |
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 | a0001c0001t0001g0206 a0001c0001t0001g0213 a0001c0001t0001g0214 |
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 | a0007c0028t0022g0255 | 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 | a0001c0002t0013g0073 | 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 | a0001c0001t0001g0044 a0001c0001t0001g0199 a0001c0002t0002g0112 others(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 | a0001c0001t0001g0060 a0001c0001t0001g0201 a0001c0001t0001g0218 others(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 | a0001c0001t0028g0236 a0001c0006t0007g0248 a0001c0006t0007g0250 others(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 | a0013c0017t0027g0260 | 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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | 107 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(104): 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 | 23 | a0001c0001t0001g0107 a0001c0001t0045g0106 a0001c0002t0002g0001 others(20): 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 | a0001c0001t0001g0211 | 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 | a0001c0001t0001g0054 | 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 | a0001c0001t0028g0236 a0001c0006t0007g0248 a0001c0006t0007g0250 others(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 | a0001c0001t0004g0027 a0001c0001t0004g0086 |
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 | a0007c0028t0022g0255 | 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 | a0002c0003t0009g0237 a0002c0003t0009g0242 a0002c0003t0009g0247 others(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 | a0007c0028t0022g0255 | 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 | a0002c0003t0009g0237 a0002c0003t0009g0242 a0002c0003t0009g0247 others(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 | a0011c0015t0026g0261 | 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 | a0002c0003t0009g0247 | 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 | a0007c0028t0022g0255 | 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 | a0001c0002t0012g0232 a0001c0002t0012g0234 a0001c0002t0012g0235 others(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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | 57 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(54): Show |
57 | HG01070.hp1 HG01243.hp1 HG01257.hp2 others(54): 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 | a0007c0028t0022g0255 | 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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | a0001c0001t0062g0019 | 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 | a0001c0001t0016g0263 a0001c0001t0016g0264 |
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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0218 a0001c0001t0001g0219 others(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 | a0001c0001t0001g0098 a0001c0001t0001g0216 a0001c0001t0004g0097 others(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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0222 others(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 | 120 | a0001c0001t0001g0006 a0001c0001t0001g0107 a0001c0001t0001g0126 others(117): Show |
126 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(123): 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 | a0001c0001t0029g0256 a0001c0004t0005g0239 a0001c0004t0005g0241 others(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 | a0007c0028t0022g0255 | 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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | a0001c0005t0001g0002 a0001c0005t0001g0147 a0001c0005t0001g0148 others(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 | a0002c0003t0009g0237 a0002c0003t0009g0242 a0002c0003t0009g0247 others(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 | a0001c0001t0029g0256 a0001c0004t0005g0239 a0001c0004t0005g0241 others(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 | a0011c0015t0026g0261 a0013c0017t0027g0260 |
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 | a0007c0028t0022g0255 | 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 | a0001c0001t0001g0085 | 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 | a0002c0003t0009g0237 a0002c0003t0009g0242 a0002c0003t0009g0247 others(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 | a0002c0003t0003g0013 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0017 others(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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0005t0001g0147 | 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 | a0002c0003t0009g0237 a0002c0003t0009g0242 a0002c0003t0009g0247 others(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 | a0001c0002t0013g0056 a0001c0002t0013g0073 |
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 | a0002c0003t0003g0168 | 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 | a0001c0002t0012g0232 a0001c0002t0012g0234 a0001c0002t0012g0235 others(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 | 168 | a0001c0001t0001g0006 a0001c0001t0001g0039 a0001c0001t0001g0060 others(165): Show |
174 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(171): 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 | a0001c0007t0011g0265 a0001c0007t0011g0266 a0001c0007t0011g0267 |
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 | a0001c0001t0001g0136 a0003c0022t0020g0132 |
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 | a0007c0016t0001g0081 | 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 | a0001c0006t0007g0250 a0003c0030t0007g0252 |
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 | a0002c0003t0009g0237 a0002c0003t0009g0242 a0002c0003t0009g0247 others(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 | a0001c0001t0028g0236 | 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 | a0001c0001t0028g0236 | 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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0001t0001g0145 a0001c0001t0001g0174 |
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 | a0002c0003t0009g0237 a0002c0003t0009g0242 a0002c0003t0009g0247 others(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 | a0007c0028t0022g0255 | 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 | a0001c0002t0002g0110 | 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 | a0001c0001t0001g0129 | 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 | a0001c0001t0061g0082 | 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 | a0001c0002t0012g0232 a0001c0002t0012g0234 a0001c0002t0012g0235 others(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 | a0001c0001t0028g0236 | 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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0002t0012g0232 a0001c0002t0012g0234 a0001c0002t0012g0235 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0018 others(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 | a0001c0001t0029g0256 a0001c0004t0005g0239 a0001c0004t0005g0241 others(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 | a0001c0001t0029g0256 a0001c0004t0005g0239 a0001c0004t0005g0241 others(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 | a0001c0001t0001g0041 | 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 | 108 | a0001c0001t0001g0006 a0001c0001t0001g0039 a0001c0001t0001g0060 others(105): 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 | a0001c0002t0002g0178 a0001c0005t0001g0009 a0001c0005t0001g0010 others(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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0002c0003t0009g0237 a0002c0003t0009g0242 a0002c0003t0009g0247 |
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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | a0011c0015t0026g0261 | 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 | a0006c0011t0001g0161 a0006c0011t0001g0162 |
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 | a0001c0001t0001g0036 a0001c0001t0001g0047 a0001c0001t0001g0087 |
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 | |||||||
| chr17:78035112 | G | T | 3 | a0001c0007t0011g0265 a0001c0007t0011g0266 a0001c0007t0011g0267 |
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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | 256 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0015 others(253): Show |
262 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(259): 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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0001t0029g0256 a0001c0004t0005g0239 a0001c0004t0005g0241 others(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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0002c0003t0003g0176 | 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 | a0011c0015t0026g0261 a0013c0017t0027g0260 |
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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0001t0001g0211 | 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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0001t0001g0204 | 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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | 32 | a0002c0003t0003g0003 a0002c0003t0003g0004 a0002c0003t0003g0013 others(29): 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 | a0001c0001t0028g0236 a0001c0007t0011g0265 a0001c0007t0011g0266 others(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 | a0017c0026t0002g0120 | 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 | a0001c0001t0001g0206 a0011c0015t0026g0261 a0013c0017t0027g0260 |
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 | a0002c0003t0009g0237 a0002c0003t0009g0242 a0002c0003t0009g0247 others(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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0004t0023g0240 | 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 | a0001c0005t0001g0002 a0001c0005t0001g0009 a0001c0005t0001g0010 others(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 | a0001c0001t0052g0096 | 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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0002t0012g0232 a0001c0002t0017g0231 a0001c0002t0017g0233 |
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 | a0001c0001t0028g0236 | 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 | a0001c0001t0028g0236 a0001c0007t0011g0265 a0001c0007t0011g0266 others(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 | 122 | a0001c0001t0001g0006 a0001c0001t0001g0039 a0001c0001t0001g0060 others(119): Show |
128 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(125): 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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0002t0012g0232 a0001c0002t0012g0234 a0001c0002t0012g0235 others(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 | a0001c0001t0001g0129 | 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 | a0001c0001t0001g0188 | 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 | 10 | a0001c0002t0013g0056 a0001c0002t0013g0057 a0001c0002t0013g0073 others(7): Show |
10 | HG01070.hp1 HG01884.hp1 HG01891.hp2 others(7): 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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0002c0003t0003g0184 | 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 | a0001c0002t0012g0232 a0001c0002t0012g0234 a0001c0002t0012g0235 others(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 | a0002c0003t0003g0141 | 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 | a0002c0003t0009g0247 | 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 | a0007c0028t0022g0255 | 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 | a0001c0001t0001g0036 a0001c0001t0001g0047 a0001c0001t0001g0087 |
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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0007c0028t0022g0255 | 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 | a0001c0005t0001g0139 | 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 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0030 others(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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0001t0028g0236 | 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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0005t0001g0009 | 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 | 10 | a0001c0002t0013g0056 a0001c0002t0013g0057 a0001c0002t0013g0073 others(7): Show |
10 | HG01070.hp1 HG01884.hp1 HG01891.hp2 others(7): 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 | a0001c0001t0001g0034 a0001c0001t0001g0041 a0001c0001t0001g0045 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0083 a0001c0001t0001g0084 others(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 | a0001c0001t0028g0236 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | a0001c0001t0028g0236 a0001c0007t0011g0265 a0001c0007t0011g0266 others(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 | a0001c0002t0012g0232 a0001c0002t0012g0234 a0001c0002t0012g0235 others(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 | a0001c0002t0030g0262 a0007c0028t0022g0255 |
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 | 162 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0015 others(159): 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 | 25 | a0001c0002t0002g0001 a0001c0002t0002g0108 a0001c0002t0002g0109 others(22): 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 | a0001c0001t0001g0064 | 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 | a0002c0003t0009g0237 a0002c0003t0009g0242 a0002c0003t0009g0247 others(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 | a0007c0028t0022g0255 | 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 | a0007c0028t0022g0255 | 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 | a0001c0002t0002g0111 | 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 | a0001c0001t0001g0060 | 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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0014c0023t0002g0190 | 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 | a0001c0001t0029g0256 a0001c0004t0005g0239 a0001c0004t0005g0241 others(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 | a0001c0001t0001g0085 | 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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | a0001c0001t0016g0263 | 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 | a0001c0007t0011g0265 a0001c0007t0011g0266 a0001c0007t0011g0267 |
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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0001t0001g0183 a0001c0001t0001g0185 a0001c0001t0001g0209 others(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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0007t0011g0265 a0001c0007t0011g0266 a0001c0007t0011g0267 |
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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | 36 | a0001c0001t0001g0028 a0001c0001t0001g0089 a0001c0001t0001g0136 others(33): Show |
36 | HG01070.hp1 HG01261.hp2 HG01891.hp2 others(33): 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 | a0001c0001t0016g0263 a0001c0001t0016g0264 a0001c0002t0012g0232 others(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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0001t0001g0054 | 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 | a0002c0003t0009g0237 a0002c0003t0009g0242 a0002c0003t0009g0247 others(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 | a0001c0002t0012g0232 a0001c0002t0012g0234 a0001c0002t0012g0235 others(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 | a0001c0007t0011g0265 a0001c0007t0011g0266 a0001c0007t0011g0267 |
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 | a0007c0028t0022g0255 | 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 | 29 | a0002c0003t0003g0003 a0002c0003t0003g0004 a0002c0003t0003g0013 others(26): 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 | a0001c0005t0001g0002 a0001c0005t0001g0009 a0001c0005t0001g0010 others(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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | 168 | a0001c0001t0001g0006 a0001c0001t0001g0039 a0001c0001t0001g0060 others(165): Show |
174 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(171): 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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | a0003c0021t0002g0114 | 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 | a0002c0003t0024g0238 | 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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | 32 | a0002c0003t0003g0003 a0002c0003t0003g0004 a0002c0003t0003g0013 others(29): 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 | a0001c0002t0038g0059 | 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 | a0001c0001t0001g0222 | 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 | a0001c0001t0001g0225 | 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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0006c0011t0001g0161 a0006c0011t0001g0162 |
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 | a0001c0001t0004g0027 | 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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | a0002c0003t0009g0237 a0002c0003t0009g0242 a0002c0003t0009g0247 others(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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0013c0017t0027g0260 | 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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0011c0015t0026g0261 | 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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | a0011c0015t0026g0261 | 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 | a0001c0001t0001g0074 a0004c0008t0001g0075 a0004c0008t0001g0076 others(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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0001t0015g0052 | 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 | a0001c0007t0011g0265 a0001c0007t0011g0266 a0001c0007t0011g0267 |
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 | a0014c0023t0002g0190 | 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 | a0002c0003t0003g0141 a0002c0003t0003g0163 a0002c0003t0019g0193 |
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 | a0001c0001t0001g0070 a0001c0001t0001g0212 |
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 | a0007c0028t0022g0255 | 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 | a0001c0001t0014g0021 | 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 | a0001c0001t0001g0098 a0001c0001t0001g0191 a0001c0001t0001g0218 others(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 | a0002c0003t0003g0164 | 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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0001t0014g0016 a0001c0001t0014g0020 a0001c0001t0014g0021 |
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 | a0001c0001t0001g0072 | 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 | a0001c0001t0001g0015 a0001c0001t0001g0032 a0001c0001t0001g0054 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0017 others(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 | 8 | a0001c0002t0013g0056 a0001c0002t0013g0057 a0001c0002t0013g0073 others(5): Show |
8 | HG01070.hp1 HG01891.hp2 HG02451.hp2 others(5): 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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | 59 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(56): 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 | a0001c0002t0012g0234 | 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 | 69 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(66): 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 | a0014c0023t0002g0190 | 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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0005c0010t0037g0037 a0005c0010t0050g0067 |
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 | a0002c0003t0003g0105 | 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 | a0001c0001t0008g0173 | 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 | a0001c0001t0001g0171 a0001c0009t0015g0142 a0001c0009t0018g0170 others(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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0002t0002g0121 | 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 | 38 | a0002c0003t0003g0003 a0002c0003t0003g0004 a0002c0003t0003g0007 others(35): 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 | a0001c0001t0001g0032 | 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 | a0001c0001t0001g0040 | 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 | a0002c0003t0009g0237 a0002c0003t0009g0242 |
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 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0174 others(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 | a0001c0007t0011g0265 a0001c0007t0011g0266 a0001c0007t0011g0267 |
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 | 8 | a0001c0002t0013g0056 a0001c0002t0013g0057 a0001c0002t0013g0073 others(5): Show |
8 | HG01070.hp1 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.3016+2429A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78053877 | |||||||
| chr17:78053978 | T | A | 39 | a0002c0003t0003g0003 a0002c0003t0003g0004 a0002c0003t0003g0007 others(36): 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 | 68 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(65): 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 | 43 | a0001c0007t0011g0265 a0001c0007t0011g0266 a0001c0007t0011g0267 others(40): 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 | a0002c0003t0024g0238 | 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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0001t0004g0025 a0001c0001t0004g0088 |
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 | a0003c0012t0001g0217 | 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 | 70 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(67): 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 | a0001c0007t0011g0265 a0001c0007t0011g0266 a0001c0007t0011g0267 |
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 | a0001c0007t0011g0265 a0001c0007t0011g0266 a0001c0007t0011g0267 |
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 | 7 | a0001c0002t0013g0056 a0001c0002t0013g0057 a0001c0002t0013g0073 others(4): Show |
7 | HG01070.hp1 HG01891.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.3016+3219C>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78054667 | |||||||
| chr17:78054695 | T | C | 75 | a0001c0001t0001g0006 a0001c0001t0001g0107 a0001c0001t0001g0126 others(72): 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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0001t0001g0035 a0001c0001t0001g0055 a0001c0001t0001g0070 others(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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | 81 | a0001c0001t0001g0006 a0001c0001t0001g0039 a0001c0001t0001g0060 others(78): 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 | 1 | a0001c0002t0058g0228 | 1 | HG04115.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 | a0001c0001t0028g0236 | 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 | a0001c0001t0052g0096 | 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 |
7 | a0001c0002t0013g0056 a0001c0002t0013g0057 a0001c0002t0013g0073 others(4): Show |
7 | HG01070.hp1 HG01891.hp2 HG02451.hp2 others(4): 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 | a0001c0001t0001g0017 a0001c0001t0001g0018 |
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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | a0002c0003t0055g0167 | 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 | 1 | a0002c0014t0001g0005 | 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 | a0001c0002t0002g0110 | 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 | a0001c0002t0013g0057 | 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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | 267 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0015 others(264): Show |
273 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(270): 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 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0089 others(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 | a0001c0002t0012g0232 a0001c0002t0012g0234 a0001c0002t0012g0235 others(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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | a0007c0028t0022g0255 a0011c0015t0026g0261 a0013c0017t0027g0260 |
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 | 39 | a0002c0003t0003g0003 a0002c0003t0003g0004 a0002c0003t0003g0007 others(36): 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 | a0002c0003t0003g0128 | 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 | a0002c0003t0003g0164 a0002c0003t0003g0207 a0002c0003t0006g0165 |
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 |
32 | a0002c0003t0003g0003 a0002c0003t0003g0004 a0002c0003t0003g0013 others(29): 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 | a0002c0003t0003g0007 a0002c0003t0003g0184 a0002c0027t0003g0007 |
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 | a0002c0003t0003g0153 a0002c0003t0003g0169 |
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 | 73 | a0001c0001t0001g0006 a0001c0001t0001g0107 a0001c0001t0001g0126 others(70): 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 | 7 | a0001c0002t0013g0056 a0001c0002t0013g0057 a0001c0002t0013g0073 others(4): Show |
7 | HG01070.hp1 HG01891.hp2 HG02451.hp2 others(4): 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 | a0011c0015t0026g0261 a0013c0017t0027g0260 |
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 | a0001c0001t0016g0263 a0001c0001t0016g0264 |
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 | a0007c0028t0022g0255 a0011c0015t0026g0261 a0013c0017t0027g0260 |
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 | a0002c0003t0003g0004 a0002c0003t0003g0014 a0002c0003t0003g0153 others(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 | a0001c0001t0001g0066 | 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 | a0001c0006t0032g0249 | 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 | 64 | a0001c0002t0012g0232 a0001c0002t0012g0234 a0001c0002t0012g0235 others(61): 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 | a0001c0002t0012g0232 a0001c0002t0012g0234 a0001c0002t0012g0235 others(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 | a0007c0028t0022g0255 a0011c0015t0026g0261 a0013c0017t0027g0260 |
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 | a0007c0028t0022g0255 a0011c0015t0026g0261 a0013c0017t0027g0260 |
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 | a0001c0001t0001g0028 a0001c0001t0001g0046 a0001c0001t0015g0052 |
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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | 7 | a0001c0002t0013g0056 a0001c0002t0013g0057 a0001c0002t0013g0073 others(4): Show |
7 | HG01070.hp1 HG01891.hp2 HG02451.hp2 others(4): 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 | a0007c0028t0022g0255 a0011c0015t0026g0261 a0013c0017t0027g0260 |
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 | 40 | a0002c0003t0003g0003 a0002c0003t0003g0004 a0002c0003t0003g0007 others(37): 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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0001t0016g0263 a0001c0001t0016g0264 |
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 | a0001c0001t0001g0214 | 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 | 40 | a0002c0003t0003g0003 a0002c0003t0003g0004 a0002c0003t0003g0007 others(37): 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 | a0007c0028t0022g0255 a0011c0015t0026g0261 a0013c0017t0027g0260 |
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 | a0001c0001t0001g0023 a0001c0001t0001g0070 a0001c0001t0001g0218 others(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 | 40 | a0002c0003t0003g0003 a0002c0003t0003g0004 a0002c0003t0003g0007 others(37): 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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | a0001c0002t0012g0232 a0001c0002t0012g0234 a0001c0002t0012g0235 others(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 | a0001c0001t0014g0016 | 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 | a0007c0028t0022g0255 a0011c0015t0026g0261 a0013c0017t0027g0260 |
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 | a0001c0001t0001g0040 a0001c0001t0001g0091 |
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 | a0001c0001t0001g0174 a0001c0001t0014g0016 a0001c0001t0014g0020 others(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 | 54 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(51): 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 | 43 | a0001c0007t0011g0265 a0001c0007t0011g0266 a0001c0007t0011g0267 others(40): 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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | a0001c0001t0001g0174 a0001c0001t0014g0016 a0001c0001t0014g0020 others(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 | a0001c0007t0011g0265 a0001c0007t0011g0266 a0001c0007t0011g0267 |
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 | a0001c0002t0012g0235 | 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 | a0001c0001t0001g0171 | 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 | a0001c0001t0001g0036 a0001c0001t0001g0078 a0001c0001t0001g0087 others(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 | a0001c0001t0001g0040 a0001c0001t0001g0065 a0001c0001t0001g0084 others(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 | 40 | a0002c0003t0003g0003 a0002c0003t0003g0004 a0002c0003t0003g0007 others(37): 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 | a0001c0001t0001g0074 | 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 | a0001c0002t0002g0111 | 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 | a0001c0004t0010g0254 a0001c0004t0010g0259 a0001c0004t0025g0257 |
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 | a0001c0001t0001g0174 a0001c0001t0014g0016 a0001c0001t0014g0020 |
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 | a0001c0007t0011g0265 a0001c0007t0011g0266 a0001c0007t0011g0267 |
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 | 40 | a0002c0003t0003g0003 a0002c0003t0003g0004 a0002c0003t0003g0007 others(37): 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 | a0001c0007t0011g0265 a0001c0007t0011g0266 a0001c0007t0011g0267 |
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 | 40 | a0002c0003t0003g0003 a0002c0003t0003g0004 a0002c0003t0003g0007 others(37): 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 | a0001c0001t0004g0221 | 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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | 63 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(60): 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 | a0007c0028t0022g0255 | 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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0001t0001g0183 a0001c0001t0001g0185 |
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 | a0001c0001t0001g0044 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3017-2430A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | chr17 | 78062292 | |||||||
| chr17:78062416 | A | T | 7 | a0001c0002t0013g0056 a0001c0002t0013g0057 a0001c0002t0013g0073 others(4): Show |
7 | HG01070.hp1 HG01891.hp2 HG02451.hp2 others(4): 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 | a0001c0007t0011g0265 a0001c0007t0011g0266 a0001c0007t0011g0267 |
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 | 88 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(85): Show |
91 | HG01070.hp1 HG01070.hp2 HG01071.hp2 others(88): 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 | a0001c0002t0012g0232 a0001c0002t0012g0234 a0001c0002t0012g0235 others(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 | a0001c0006t0007g0248 | 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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | a0007c0028t0022g0255 a0011c0015t0026g0261 a0013c0017t0027g0260 |
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 | a0003c0012t0001g0024 | 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 | a0001c0007t0011g0265 a0001c0007t0011g0266 a0001c0007t0011g0267 |
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 | a0002c0003t0003g0164 | 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 | a0001c0007t0011g0265 a0001c0007t0011g0266 a0001c0007t0011g0267 |
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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | a0001c0007t0011g0265 a0001c0007t0011g0266 a0001c0007t0011g0267 |
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 | a0002c0003t0003g0207 | 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 | a0011c0015t0026g0261 | 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 | 40 | a0002c0003t0003g0003 a0002c0003t0003g0004 a0002c0003t0003g0007 others(37): 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 | 57 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(54): 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 | 54 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(51): 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 | a0001c0001t0035g0068 | 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 | a0001c0029t0001g0033 | 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 | a0001c0006t0032g0249 | 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 | a0002c0003t0003g0007 a0002c0003t0003g0184 a0002c0027t0003g0007 |
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 | a0001c0007t0011g0265 a0001c0007t0011g0266 a0001c0007t0011g0267 |
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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | a0001c0001t0028g0236 | 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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | a0001c0001t0015g0144 a0001c0001t0018g0143 |
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 | 162 | a0001c0001t0001g0006 a0001c0001t0001g0107 a0001c0001t0001g0126 others(159): Show |
168 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.3232+548C>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 6/22 | chr17 | 78065485 | |||||||
| chr17:78065889 | T | C | 3 | a0001c0007t0011g0265 a0001c0007t0011g0266 a0001c0007t0011g0267 |
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 | a0001c0001t0001g0222 | 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 | 40 | a0002c0003t0003g0003 a0002c0003t0003g0004 a0002c0003t0003g0007 others(37): 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 | a0001c0001t0001g0064 | 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 | 80 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(77): Show |
83 | HG01070.hp1 HG01070.hp2 HG01071.hp2 others(80): 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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0017 others(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 | a0001c0007t0011g0265 a0001c0007t0011g0266 a0001c0007t0011g0267 |
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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | 40 | a0002c0003t0003g0003 a0002c0003t0003g0004 a0002c0003t0003g0007 others(37): 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 | a0007c0028t0022g0255 a0011c0015t0026g0261 a0013c0017t0027g0260 |
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 | a0001c0007t0011g0265 a0001c0007t0011g0266 a0001c0007t0011g0267 |
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 | a0001c0001t0001g0199 a0001c0001t0001g0202 a0001c0001t0001g0203 others(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 | 40 | a0002c0003t0003g0003 a0002c0003t0003g0004 a0002c0003t0003g0007 others(37): 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 | 40 | a0002c0003t0003g0003 a0002c0003t0003g0004 a0002c0003t0003g0007 others(37): 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 | 40 | a0002c0003t0003g0003 a0002c0003t0003g0004 a0002c0003t0003g0007 others(37): 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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | a0011c0015t0026g0261 a0013c0017t0027g0260 |
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 | a0001c0002t0012g0232 a0001c0002t0012g0234 a0001c0002t0012g0235 others(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 | a0011c0015t0026g0261 | 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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | a0001c0001t0001g0183 a0001c0001t0001g0185 a0001c0001t0034g0186 |
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 | a0008c0013t0021g0012 | 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 | 40 | a0002c0003t0003g0003 a0002c0003t0003g0004 a0002c0003t0003g0007 others(37): 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 | a0001c0006t0032g0249 | 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 | 40 | a0002c0003t0003g0003 a0002c0003t0003g0004 a0002c0003t0003g0007 others(37): 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 | 31 | a0001c0001t0001g0107 a0001c0001t0045g0106 a0001c0002t0002g0001 others(28): 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 | 39 | a0002c0003t0003g0003 a0002c0003t0003g0004 a0002c0003t0003g0007 others(36): 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 | a0001c0005t0001g0002 a0001c0005t0001g0009 a0001c0005t0001g0010 others(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 | 40 | a0002c0003t0003g0003 a0002c0003t0003g0004 a0002c0003t0003g0007 others(37): 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 | 40 | a0002c0003t0003g0003 a0002c0003t0003g0004 a0002c0003t0003g0007 others(37): 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 | 40 | a0002c0003t0003g0003 a0002c0003t0003g0004 a0002c0003t0003g0007 others(37): 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 | a0001c0002t0002g0111 | 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 | a0001c0001t0001g0136 a0001c0001t0020g0062 |
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 | a0001c0002t0013g0056 a0001c0002t0013g0057 a0001c0002t0013g0073 others(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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | a0001c0005t0001g0002 a0001c0005t0001g0147 a0001c0005t0001g0148 others(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 | 60 | a0001c0001t0001g0126 a0001c0001t0001g0129 a0001c0001t0001g0130 others(57): Show |
61 | HG00280.hp2 HG00597.hp2 HG00642.hp1 others(58): 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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | 10 | a0001c0001t0004g0221 a0001c0001t0057g0230 a0001c0002t0013g0056 others(7): Show |
10 | HG01070.hp1 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.3400-412A>T | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 7/22 | chr17 | 78070673 | |||||||
| chr17:78070825 | C | T | 27 | a0001c0001t0001g0006 a0001c0001t0001g0126 a0001c0001t0001g0145 others(24): Show |
29 | HG00735.hp1 HG01070.hp1 HG01071.hp1 others(26): 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 | a0002c0003t0009g0237 a0002c0003t0009g0242 |
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 | a0002c0003t0009g0237 a0002c0003t0009g0242 |
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 | a0002c0003t0003g0003 a0002c0003t0003g0004 a0002c0003t0003g0007 others(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 | 94 | a0001c0001t0001g0107 a0001c0001t0045g0106 a0001c0002t0002g0001 others(91): Show |
97 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(94): 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 | a0001c0005t0001g0002 a0001c0005t0001g0009 a0001c0005t0001g0010 others(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 | a0001c0001t0001g0214 | 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 | a0011c0015t0026g0261 a0013c0017t0027g0260 |
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 | a0001c0001t0016g0264 | 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 | a0001c0001t0001g0072 | 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 | a0002c0003t0003g0146 | 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 | a0001c0001t0016g0263 a0001c0001t0016g0264 |
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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | a0001c0001t0042g0175 | 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 | a0001c0005t0001g0002 a0001c0005t0001g0009 a0001c0005t0001g0010 others(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 | a0001c0001t0001g0035 a0001c0001t0001g0055 a0001c0001t0001g0070 others(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 | a0002c0003t0003g0003 a0002c0003t0003g0004 a0002c0003t0003g0007 others(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 | a0001c0002t0013g0057 | 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 | a0010c0031t0039g0050 | 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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0040 a0001c0001t0001g0041 others(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 | a0011c0015t0026g0261 | 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 | a0015c0019t0001g0115 | 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 | a0015c0019t0001g0115 | 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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | a0001c0001t0016g0263 | 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 | a0011c0015t0026g0261 | 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 | 7 | a0001c0002t0013g0056 a0001c0002t0013g0057 a0001c0002t0013g0073 others(4): Show |
7 | HG01070.hp1 HG01891.hp2 HG02451.hp2 others(4): 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 | a0001c0001t0035g0068 | 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 | a0001c0002t0033g0182 | 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 | a0001c0001t0042g0175 | 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 | a0002c0003t0003g0128 a0002c0003t0003g0192 |
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 | a0011c0015t0026g0261 | 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 | a0001c0001t0001g0074 a0004c0008t0001g0075 a0004c0008t0001g0076 others(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 | a0002c0003t0009g0247 | 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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | a0001c0002t0002g0112 a0001c0002t0002g0113 a0003c0021t0002g0114 |
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 | a0011c0015t0026g0261 | 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 | a0001c0002t0002g0112 a0001c0002t0002g0113 a0003c0021t0002g0114 |
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 | a0001c0001t0001g0185 | 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 | a0001c0005t0001g0139 | 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 | a0011c0015t0026g0261 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0031 a0001c0001t0001g0089 others(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 | 91 | a0001c0001t0001g0107 a0001c0001t0016g0263 a0001c0001t0016g0264 others(88): Show |
94 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(91): 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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | 100 | a0001c0001t0001g0107 a0001c0001t0045g0106 a0001c0002t0002g0001 others(97): Show |
103 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(100): 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 | a0001c0001t0001g0069 | 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 | a0011c0015t0026g0261 | 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 | a0001c0001t0060g0043 | 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 | a0011c0015t0026g0261 | 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 | a0014c0023t0002g0190 | 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 | a0001c0001t0001g0145 | 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 | 45 | a0001c0001t0001g0107 a0001c0001t0045g0106 a0001c0002t0002g0001 others(42): Show |
46 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(43): 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 | 45 | a0001c0001t0001g0107 a0001c0001t0045g0106 a0001c0002t0002g0001 others(42): Show |
46 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.3831+311G>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 11/22 | chr17 | 78077645 | |||||||
| chr17:78078115 | A | G | 51 | a0001c0001t0001g0107 a0001c0001t0045g0106 a0001c0002t0002g0001 others(48): Show |
52 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(49): 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 | a0011c0015t0026g0261 | 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 | a0002c0003t0006g0104 | 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 | a0001c0001t0001g0210 | 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 | a0001c0001t0004g0027 a0001c0001t0004g0086 |
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 | a0011c0015t0026g0261 | 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 | a0001c0004t0005g0241 | 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 | a0001c0001t0001g0145 | 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 | a0001c0001t0016g0263 a0001c0001t0016g0264 |
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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | 52 | a0001c0001t0001g0107 a0001c0001t0045g0106 a0001c0002t0002g0001 others(49): Show |
53 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(50): 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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | a0011c0015t0026g0261 | 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 | a0001c0002t0002g0177 a0001c0002t0002g0178 a0001c0002t0002g0179 others(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 | a0001c0004t0005g0241 | 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 | a0001c0001t0041g0101 | 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 | a0003c0012t0001g0024 | 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 | a0002c0003t0006g0104 | 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 | a0002c0003t0006g0104 | 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 | 38 | a0001c0001t0001g0107 a0001c0001t0045g0106 a0001c0002t0002g0001 others(35): Show |
39 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(36): 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 | a0001c0002t0012g0232 a0001c0002t0012g0234 a0001c0002t0012g0235 others(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 | a0002c0003t0006g0104 | 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 | a0001c0001t0062g0019 | 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 | 46 | a0001c0001t0001g0107 a0001c0001t0045g0106 a0001c0002t0002g0001 others(43): Show |
47 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.3979-1503A>G | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 12/22 | chr17 | 78081544 | |||||||
| chr17:78081619 | A | G | 183 | a0001c0001t0001g0006 a0001c0001t0001g0034 a0001c0001t0001g0039 others(180): Show |
189 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(186): 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 | a0002c0003t0003g0003 a0002c0003t0003g0004 a0002c0003t0003g0007 others(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 | a0001c0001t0001g0078 | 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 | a0001c0001t0001g0126 a0001c0001t0001g0187 a0001c0001t0001g0188 others(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 | a0001c0004t0010g0258 | 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 | 181 | a0001c0001t0001g0006 a0001c0001t0001g0034 a0001c0001t0001g0039 others(178): Show |
187 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(184): Show |
intron_variant | MODIFIER | c.3979-909T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 12/22 | chr17 | 78082138 | |||||||
| chr17:78082207 | A | C | 74 | a0001c0001t0001g0034 a0001c0001t0001g0039 a0001c0001t0001g0040 others(71): Show |
75 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(72): 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 | a0002c0003t0006g0104 | 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 | a0002c0003t0003g0003 a0002c0003t0003g0004 a0002c0003t0003g0007 others(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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | a0001c0001t0001g0053 | 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 | a0017c0026t0002g0120 | 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 | a0002c0003t0006g0140 a0002c0003t0006g0150 a0002c0003t0006g0165 |
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 | a0002c0003t0006g0104 | 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 | a0007c0016t0001g0081 | 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 | a0001c0002t0002g0195 | 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 | a0001c0002t0002g0195 | 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 | a0001c0002t0002g0195 | 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 | a0001c0002t0002g0195 | 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 | a0001c0001t0062g0019 | 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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | a0001c0001t0001g0070 a0001c0001t0001g0199 a0001c0001t0001g0200 others(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 | a0001c0002t0013g0057 | 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 | a0001c0001t0004g0025 a0001c0001t0004g0088 a0001c0001t0004g0151 others(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 | a0001c0001t0016g0263 a0001c0001t0016g0264 a0011c0015t0026g0261 others(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 | a0001c0001t0051g0099 | 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 | a0001c0002t0013g0056 a0001c0002t0013g0073 |
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 | 45 | a0001c0001t0001g0107 a0001c0001t0045g0106 a0001c0002t0002g0001 others(42): Show |
46 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(43): 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 | a0011c0015t0026g0261 a0013c0017t0027g0260 |
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 | a0001c0001t0029g0256 | 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 | a0002c0003t0003g0003 a0002c0003t0003g0004 a0002c0003t0003g0007 others(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 | 98 | a0001c0001t0001g0107 a0001c0001t0045g0106 a0001c0002t0002g0001 others(95): Show |
101 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(98): 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 | a0002c0003t0003g0004 | 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 | a0001c0001t0001g0220 | 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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | a0001c0001t0001g0137 a0001c0001t0040g0131 a0002c0003t0003g0003 others(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 | a0001c0001t0001g0022 | 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 | a0001c0001t0001g0064 | 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 | 38 | a0001c0001t0001g0107 a0001c0001t0045g0106 a0001c0002t0002g0001 others(35): Show |
39 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.4098+1303G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 13/22 | chr17 | 78084469 | |||||||
| chr17:78084589 | G | A | 65 | a0001c0001t0001g0006 a0001c0001t0001g0034 a0001c0001t0001g0039 others(62): 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 | a0001c0004t0023g0240 | 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 | 83 | a0001c0001t0001g0032 a0001c0001t0001g0107 a0001c0001t0045g0106 others(80): Show |
86 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(83): 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 | a0001c0002t0012g0232 a0001c0002t0012g0234 a0001c0002t0012g0235 others(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 | a0001c0002t0012g0232 a0001c0002t0012g0234 a0001c0002t0012g0235 others(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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | 91 | a0001c0001t0001g0107 a0001c0001t0045g0106 a0001c0002t0002g0001 others(88): Show |
94 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(91): 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 | 87 | a0001c0001t0001g0107 a0001c0001t0045g0106 a0001c0002t0002g0001 others(84): Show |
90 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(87): 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 | a0001c0001t0004g0221 | 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 | 103 | a0001c0001t0001g0107 a0001c0001t0016g0263 a0001c0001t0016g0264 others(100): Show |
106 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.4099-406T>C | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 13/22 | chr17 | 78086097 | |||||||
| chr17:78086317 | G | A | 45 | a0001c0001t0001g0107 a0001c0001t0045g0106 a0001c0002t0002g0001 others(42): Show |
46 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(43): 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 | a0001c0001t0001g0069 a0001c0001t0001g0129 a0001c0001t0001g0135 others(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 | a0001c0001t0001g0040 a0001c0001t0001g0055 a0001c0001t0001g0063 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0041 a0001c0001t0001g0060 others(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 | a0001c0001t0001g0039 a0001c0001t0001g0065 a0001c0001t0001g0080 others(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 | a0001c0006t0007g0248 | 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 | a0001c0006t0007g0250 | 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 | a0003c0030t0007g0252 | 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 | 39 | a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0032 others(36): 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 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0017 others(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 | a0002c0003t0003g0146 a0002c0003t0003g0153 a0002c0003t0003g0169 others(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 | a0002c0003t0003g0003 a0002c0003t0003g0004 a0002c0003t0003g0007 others(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 | 46 | a0001c0001t0001g0107 a0001c0001t0045g0106 a0001c0002t0002g0001 others(43): Show |
47 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(44): 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 | 1 | a0001c0001t0001g0006 | 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 | a0001c0007t0011g0266 | 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 | a0001c0001t0001g0145 | 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 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0030 others(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 | a0001c0001t0001g0093 | 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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | a0010c0031t0039g0050 | 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 | a0001c0001t0001g0216 | 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 | 11 | a0001c0001t0001g0006 a0001c0001t0008g0157 a0001c0001t0008g0158 others(8): 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 | a0001c0001t0004g0025 a0001c0001t0004g0088 a0001c0001t0004g0151 others(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 | 93 | a0001c0001t0001g0107 a0001c0001t0045g0106 a0001c0002t0002g0001 others(90): Show |
96 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(93): 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 | a0001c0001t0014g0020 | 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 | a0001c0001t0001g0038 a0001c0001t0001g0051 a0001c0001t0001g0069 others(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 | a0001c0002t0002g0196 | 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 | a0002c0003t0003g0003 a0002c0003t0003g0004 a0002c0003t0003g0007 others(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 | a0001c0001t0020g0062 | 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 | a0001c0001t0001g0135 | 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 | a0002c0003t0003g0003 a0002c0003t0003g0004 a0002c0003t0003g0007 others(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 | 93 | a0001c0001t0001g0107 a0001c0001t0045g0106 a0001c0002t0002g0001 others(90): Show |
96 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(93): 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 | a0002c0003t0003g0003 a0002c0003t0003g0004 a0002c0003t0003g0007 others(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 | a0014c0023t0002g0190 | 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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | a0001c0001t0001g0130 | 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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | a0001c0002t0002g0195 | 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 | a0001c0002t0017g0233 a0001c0006t0007g0248 a0001c0006t0007g0250 others(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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | a0001c0006t0032g0249 | 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 | a0001c0001t0001g0035 a0001c0001t0001g0047 a0001c0001t0001g0078 others(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 | 97 | a0001c0001t0001g0006 a0001c0001t0001g0034 a0001c0001t0001g0041 others(94): 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 | a0001c0001t0001g0145 a0001c0001t0001g0159 a0001c0001t0001g0172 others(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 | 46 | a0001c0001t0001g0107 a0001c0001t0045g0106 a0001c0002t0002g0001 others(43): Show |
47 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(44): 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 | a0001c0001t0035g0068 a0002c0003t0019g0180 |
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 | a0001c0001t0001g0174 a0001c0001t0014g0016 a0001c0001t0014g0020 others(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 | a0001c0002t0002g0177 a0001c0002t0002g0178 a0001c0002t0002g0179 others(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 | a0001c0002t0002g0177 a0001c0002t0002g0178 a0001c0002t0002g0179 |
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 | a0001c0001t0001g0126 | 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 | a0001c0001t0001g0017 a0001c0001t0001g0018 |
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 | 267 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0015 others(264): Show |
273 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(270): 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 | a0001c0001t0004g0268 | 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 | a0001c0002t0030g0262 | 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 | a0001c0001t0041g0101 | 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 | a0002c0003t0003g0003 a0002c0003t0003g0004 a0002c0003t0003g0007 others(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 | a0001c0001t0001g0202 | 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 | 7 | a0001c0002t0013g0056 a0001c0002t0013g0057 a0001c0002t0013g0073 others(4): Show |
7 | HG01070.hp1 HG01891.hp2 HG02451.hp2 others(4): 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 | a0002c0003t0003g0003 a0002c0003t0003g0004 a0002c0003t0003g0007 others(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 | a0001c0002t0030g0262 | 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 | a0001c0002t0030g0262 | 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 | a0001c0001t0029g0256 | 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 | a0001c0004t0005g0241 | 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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | a0001c0001t0004g0268 | 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 | 45 | a0001c0001t0045g0106 a0001c0002t0002g0001 a0001c0002t0002g0108 others(42): Show |
46 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(43): 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 | a0013c0017t0027g0260 | 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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | 60 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0017 others(57): Show |
60 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(57): 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 | a0001c0001t0057g0230 | 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 | a0002c0003t0003g0169 | 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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | a0002c0003t0003g0003 a0002c0003t0003g0004 a0002c0003t0003g0007 others(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 | 38 | a0001c0001t0045g0106 a0001c0002t0002g0001 a0001c0002t0002g0108 others(35): Show |
39 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(36): 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 | a0001c0002t0012g0232 a0001c0002t0012g0234 a0001c0002t0012g0235 others(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 | 44 | a0001c0001t0045g0106 a0001c0002t0002g0001 a0001c0002t0002g0108 others(41): Show |
45 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(42): 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 | a0001c0001t0001g0031 a0001c0001t0001g0095 |
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 | a0001c0001t0061g0082 | 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 | a0001c0001t0001g0074 | 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 | a0002c0003t0003g0176 a0002c0003t0055g0167 |
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 | a0001c0001t0001g0211 | 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 | 37 | a0001c0001t0045g0106 a0001c0002t0002g0001 a0001c0002t0002g0108 others(34): Show |
38 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(35): 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 | a0007c0028t0022g0255 | 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 | a0002c0003t0003g0146 | 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 | 44 | a0001c0001t0045g0106 a0001c0002t0002g0001 a0001c0002t0002g0108 others(41): Show |
45 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(42): 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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | a0001c0001t0001g0070 a0001c0001t0001g0212 |
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 | a0001c0002t0012g0232 a0001c0002t0012g0234 a0001c0002t0012g0235 others(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 | 52 | a0001c0001t0016g0263 a0001c0001t0016g0264 a0001c0001t0045g0106 others(49): Show |
53 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(50): 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 | a0007c0028t0022g0255 | 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 | 96 | a0001c0001t0016g0263 a0001c0001t0016g0264 a0001c0001t0045g0106 others(93): Show |
99 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(96): 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 | a0001c0001t0001g0015 | 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 | a0005c0010t0037g0037 | 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 | a0001c0001t0001g0040 a0001c0001t0001g0174 a0001c0001t0014g0016 others(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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | a0014c0023t0002g0190 | 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 | a0001c0001t0001g0051 a0001c0001t0001g0078 |
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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | a0002c0003t0006g0150 | 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 | a0011c0015t0026g0261 a0013c0017t0027g0260 |
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 | a0006c0011t0001g0161 a0006c0011t0001g0162 |
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 | 37 | a0001c0001t0045g0106 a0001c0002t0002g0001 a0001c0002t0002g0108 others(34): Show |
38 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(35): 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 | a0001c0001t0016g0263 a0001c0004t0005g0239 a0001c0004t0005g0241 others(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 | a0001c0001t0001g0200 | 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 | a0001c0001t0016g0263 a0001c0004t0005g0239 a0001c0004t0005g0241 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0039 a0001c0001t0001g0040 others(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 | a0001c0001t0008g0090 | 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 | a0001c0007t0011g0265 a0001c0007t0011g0266 a0001c0007t0011g0267 |
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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | a0001c0001t0001g0107 a0001c0001t0062g0019 a0015c0019t0001g0115 |
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 | a0001c0002t0030g0262 | 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 | 102 | a0001c0001t0001g0218 a0001c0001t0016g0263 a0001c0002t0002g0001 others(99): Show |
105 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(102): 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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | a0001c0002t0030g0262 a0001c0004t0005g0239 a0001c0004t0005g0241 others(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 | 174 | a0001c0001t0001g0006 a0001c0001t0001g0034 a0001c0001t0001g0040 others(171): Show |
180 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(177): 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 | a0001c0007t0011g0265 a0001c0007t0011g0266 a0001c0007t0011g0267 |
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 | 8 | a0001c0001t0001g0191 a0001c0002t0013g0056 a0001c0002t0013g0057 others(5): Show |
8 | HG01070.hp1 HG01071.hp1 HG01891.hp2 others(5): 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 | a0001c0001t0016g0264 | 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 | a0001c0001t0028g0236 | 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 | a0001c0001t0016g0263 a0007c0028t0022g0255 |
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 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 |
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 | a0008c0013t0021g0012 | 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 | a0001c0001t0016g0263 a0007c0028t0022g0255 |
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 | 50 | a0001c0001t0001g0006 a0001c0001t0001g0034 a0001c0001t0001g0040 others(47): 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 | a0001c0006t0007g0248 | 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 | a0001c0001t0001g0216 | 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 | 97 | a0001c0002t0002g0001 a0001c0002t0002g0108 a0001c0002t0002g0109 others(94): Show |
100 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(97): 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 | a0001c0002t0002g0111 | 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 | a0001c0002t0030g0262 | 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 | a0001c0002t0002g0122 | 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 | 101 | a0001c0001t0016g0263 a0001c0001t0016g0264 a0001c0002t0002g0001 others(98): Show |
104 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(101): 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 | a0007c0028t0022g0255 | 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 | a0001c0001t0001g0102 | 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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | a0001c0001t0001g0053 | 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 | a0007c0028t0022g0255 | 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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0039 a0001c0001t0001g0040 others(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 | 7 | a0001c0002t0013g0056 a0001c0002t0013g0057 a0001c0002t0013g0073 others(4): Show |
7 | HG01070.hp1 HG01891.hp2 HG02451.hp2 others(4): 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 | a0001c0001t0001g0206 | 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 | a0002c0003t0003g0013 | 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 | a0001c0002t0002g0110 | 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 | a0001c0001t0001g0223 | 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 | a0001c0001t0001g0028 a0001c0001t0001g0039 a0001c0001t0001g0042 others(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 | a0001c0004t0023g0240 a0001c0006t0007g0248 a0001c0006t0007g0250 others(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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | 53 | a0001c0001t0001g0006 a0001c0001t0001g0098 a0001c0001t0001g0126 others(50): 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 | 35 | a0001c0002t0002g0001 a0001c0002t0002g0108 a0001c0002t0002g0109 others(32): Show |
36 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(33): 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 | a0001c0001t0001g0036 a0001c0001t0001g0087 |
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 | a0001c0005t0001g0009 a0001c0005t0001g0010 a0001c0005t0001g0011 |
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 | 90 | a0001c0002t0002g0001 a0001c0002t0002g0108 a0001c0002t0002g0109 others(87): Show |
93 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(90): 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 | a0001c0002t0030g0262 | 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 | a0001c0001t0016g0263 a0001c0001t0016g0264 |
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 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0220 others(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 | a0001c0001t0008g0157 | 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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | a0007c0028t0022g0255 | 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 | a0011c0015t0026g0261 | 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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | 36 | a0001c0002t0002g0001 a0001c0002t0002g0108 a0001c0002t0002g0109 others(33): Show |
37 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.5240-916G>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 20/22 | chr17 | 78101558 | |||||||
| chr17:78101560 | T | C | 94 | a0001c0001t0016g0263 a0001c0001t0016g0264 a0001c0002t0002g0001 others(91): Show |
97 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(94): 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 | a0001c0001t0016g0263 a0001c0001t0016g0264 |
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 | a0001c0001t0001g0044 | 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 | a0001c0002t0012g0232 a0001c0002t0012g0234 a0001c0002t0012g0235 others(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 | a0001c0002t0002g0122 | 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 | a0001c0001t0028g0236 | 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 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0209 others(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 | a0001c0001t0028g0236 | 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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | 1 | a0001c0001t0001g0006 | 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 | 35 | a0001c0002t0002g0001 a0001c0002t0002g0108 a0001c0002t0002g0109 others(32): Show |
36 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(33): 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 | a0007c0028t0022g0255 | 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 | 42 | a0001c0002t0002g0001 a0001c0002t0002g0108 a0001c0002t0002g0109 others(39): Show |
43 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(40): 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 | a0001c0001t0001g0031 | 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 | a0001c0001t0004g0221 | 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 | 36 | a0001c0002t0002g0001 a0001c0002t0002g0108 a0001c0002t0002g0109 others(33): Show |
37 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(34): 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 | a0012c0020t0046g0049 | 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 | a0002c0003t0003g0003 a0002c0003t0003g0004 a0002c0003t0003g0007 others(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 | a0001c0005t0001g0002 a0001c0005t0001g0147 a0001c0005t0001g0148 others(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 | a0007c0016t0001g0081 | 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 | a0001c0001t0057g0230 | 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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | a0001c0001t0001g0103 | 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 | a0001c0002t0030g0262 | 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 | a0001c0004t0005g0239 a0001c0004t0005g0241 a0001c0004t0005g0243 others(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 | a0001c0006t0007g0248 a0001c0006t0007g0250 a0001c0006t0007g0253 others(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 | a0001c0001t0001g0133 | 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 | 1 | a0002c0014t0001g0005 | 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 | a0001c0001t0001g0137 | 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 | a0001c0001t0016g0263 a0001c0001t0016g0264 |
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 | a0001c0001t0001g0191 | 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 | a0001c0006t0007g0248 | 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 | a0001c0001t0014g0016 | 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 | a0001c0002t0030g0262 | 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 | a0001c0002t0030g0262 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.5451-32C>A | TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 22/22 | chr17 | 78104453 |