Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 943 |
| ensemblid | ENSG00000120949.15 |
| hgncid | 11923 |
| symbol | TNFRSF8 |
| name | TNF receptor superfamily member 8 |
| refseq_nuc | NM_001243.5 |
| refseq_prot | NP_001234.3 |
| ensembl_nuc | ENST00000263932.7 |
| ensembl_prot | ENSP00000263932.2 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 12063303 |
| end | 12144207 |
| strand | + |
| ver | v1.2 |
| region | chr1:12063303-12144207 |
| region5000 | chr1:12058303-12149207 |
| regionname0 | TNFRSF8_chr1_12063303_12144207 |
| regionname5000 | TNFRSF8_chr1_12058303_12149207 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 595 | 316 | 77 | 63 | 121 | 14 | 39 | 95 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | MRVLL others(590): Show |
chr1 | 12058303 | 12149207 |
| a0002 | 0/0 | 595 | 33 | 16 | 1 | 15 | 0 | 1 | 11 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | MRVLL others(590): Show |
chr1 | 12058303 | 12149207 |
| a0003 | 0/0 | 595 | 5 | 0 | 0 | 4 | 1 | 0 | 4 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | MRVLL others(590): Show |
chr1 | 12058303 | 12149207 |
| a0004 | 0/0 | 595 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | MRVLL others(590): Show |
chr1 | 12058303 | 12149207 |
| a0005 | 0/0 | 595 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | MRVLL others(590): Show |
chr1 | 12058303 | 12149207 |
| a0006 | 0/0 | 595 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | MRVLL others(590): Show |
chr1 | 12058303 | 12149207 |
| a0007 | 0/0 | 595 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | MRVLL others(590): Show |
chr1 | 12058303 | 12149207 |
| a0008 | 0/0 | 595 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | MRVLL others(590): Show |
chr1 | 12058303 | 12149207 |
| a0009 | 0/0 | 595 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | MRVLL others(590): Show |
chr1 | 12058303 | 12149207 |
| a0010 | 0/0 | 595 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | MRVLL others(590): Show |
chr1 | 12058303 | 12149207 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1785 | 147 | 30 | 35 | 51 | 9 | 20 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | ATGCG others(1780): Show |
chr1 | 12058303 | 12149207 | ||
| a0001c0002 | 0/0 | 1785 | 70 | 3 | 21 | 25 | 4 | 17 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | ATGCG others(1780): Show |
chr1 | 12058303 | 12149207 | ||
| a0001c0003 | 0/0 | 1785 | 61 | 26 | 7 | 27 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | ATGCG others(1780): Show |
chr1 | 12058303 | 12149207 | ||
| a0001c0004 | 0/0 | 1785 | 24 | 10 | 0 | 13 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | ATGCG others(1780): Show |
chr1 | 12058303 | 12149207 | ||
| a0001c0007 | 0/0 | 1785 | 3 | 3 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | ATGCG others(1780): Show |
chr1 | 12058303 | 12149207 | ||
| a0001c0009 | 0/0 | 1785 | 3 | 3 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | ATGCG others(1780): Show |
chr1 | 12058303 | 12149207 | ||
| a0001c0013 | 0/0 | 1785 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | ATGCG others(1780): Show |
chr1 | 12058303 | 12149207 | ||
| a0001c0014 | 0/0 | 1785 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | ATGCG others(1780): Show |
chr1 | 12058303 | 12149207 | ||
| a0001c0017 | 0/0 | 1785 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | ATGCG others(1780): Show |
chr1 | 12058303 | 12149207 | ||
| a0001c0018 | 0/0 | 1785 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | ATGCG others(1780): Show |
chr1 | 12058303 | 12149207 | ||
| a0001c0023 | 0/0 | 1785 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | ATGCG others(1780): Show |
chr1 | 12058303 | 12149207 | ||
| a0001c0025 | 0/0 | 1785 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | ATGCG others(1780): Show |
chr1 | 12058303 | 12149207 | ||
| a0001c0026 | 0/0 | 1785 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | ATGCG others(1780): Show |
chr1 | 12058303 | 12149207 | ||
| a0002c0005 | 0/0 | 1785 | 13 | 8 | 0 | 5 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | ATGCG others(1780): Show |
chr1 | 12058303 | 12149207 | ||
| a0002c0006 | 0/0 | 1785 | 11 | 3 | 1 | 6 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | ATGCG others(1780): Show |
chr1 | 12058303 | 12149207 | ||
| a0002c0010 | 0/0 | 1785 | 3 | 1 | 0 | 2 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | ATGCG others(1780): Show |
chr1 | 12058303 | 12149207 | ||
| a0002c0011 | 0/0 | 1785 | 3 | 1 | 0 | 2 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | ATGCG others(1780): Show |
chr1 | 12058303 | 12149207 | ||
| a0002c0012 | 0/0 | 1785 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | ATGCG others(1780): Show |
chr1 | 12058303 | 12149207 | ||
| a0002c0016 | 0/0 | 1785 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | ATGCG others(1780): Show |
chr1 | 12058303 | 12149207 | ||
| a0003c0008 | 0/0 | 1785 | 3 | 0 | 0 | 2 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | ATGCG others(1780): Show |
chr1 | 12058303 | 12149207 | ||
| a0003c0019 | 0/0 | 1785 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | ATGCG others(1780): Show |
chr1 | 12058303 | 12149207 | ||
| a0003c0027 | 0/0 | 1785 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | ATGCG others(1780): Show |
chr1 | 12058303 | 12149207 | ||
| a0004c0022 | 0/0 | 1785 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | ATGCG others(1780): Show |
chr1 | 12058303 | 12149207 | ||
| a0004c0028 | 0/0 | 1785 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | ATGCG others(1780): Show |
chr1 | 12058303 | 12149207 | ||
| a0005c0015 | 0/0 | 1785 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | ATGCG others(1780): Show |
chr1 | 12058303 | 12149207 | ||
| a0006c0021 | 0/0 | 1785 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | ATGCG others(1780): Show |
chr1 | 12058303 | 12149207 | ||
| a0007c0020 | 0/0 | 1785 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | ATGCG others(1780): Show |
chr1 | 12058303 | 12149207 | ||
| a0008c0029 | 0/0 | 1785 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | ATGCG others(1780): Show |
chr1 | 12058303 | 12149207 | ||
| a0009c0030 | 0/0 | 1785 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | ATGCG others(1780): Show |
chr1 | 12058303 | 12149207 | ||
| a0010c0024 | 0/0 | 1785 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | ATGCG others(1780): Show |
chr1 | 12058303 | 12149207 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3760 | 124 | 15 | 32 | 47 | 9 | 20 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0001c0001t0002 | 0/0 | 3760 | 3 | 3 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0001c0001t0004 | 0/0 | 3760 | 2 | 0 | 1 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0001c0001t0005 | 0/0 | 3760 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0001c0001t0006 | 0/0 | 3760 | 4 | 4 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0001c0001t0007 | 0/0 | 3760 | 4 | 4 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0001c0001t0008 | 0/0 | 3760 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0001c0001t0009 | 0/0 | 3760 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0001c0001t0011 | 0/0 | 3760 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0001c0001t0013 | 0/0 | 3760 | 2 | 0 | 2 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0001c0001t0016 | 0/0 | 3760 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0001c0001t0022 | 0/1 | 3760 | 1 | 0 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0001c0002t0001 | 0/0 | 3760 | 64 | 2 | 20 | 22 | 4 | 16 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0001c0002t0002 | 0/0 | 3760 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0001c0002t0004 | 0/0 | 3760 | 2 | 0 | 1 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0001c0002t0008 | 0/0 | 3760 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0001c0002t0011 | 0/0 | 3760 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0001c0002t0018 | 0/0 | 3760 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0001c0003t0001 | 0/0 | 3760 | 41 | 9 | 6 | 25 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0001c0003t0002 | 0/0 | 3760 | 4 | 4 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0001c0003t0003 | 0/0 | 3762 | 5 | 5 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3757): Show |
chr1 | 12058303 | 12149207 |
| a0001c0003t0005 | 0/0 | 3760 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0001c0003t0007 | 0/0 | 3760 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0001c0003t0008 | 0/0 | 3760 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0001c0003t0010 | 0/0 | 3760 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0001c0003t0012 | 0/0 | 3760 | 2 | 1 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0001c0003t0019 | 0/0 | 3760 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0001c0003t0020 | 0/0 | 3760 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0001c0003t0026 | 0/0 | 3760 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0001c0004t0001 | 0/0 | 3760 | 20 | 6 | 0 | 13 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0001c0004t0002 | 0/0 | 3760 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0001c0004t0003 | 0/0 | 3762 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3757): Show |
chr1 | 12058303 | 12149207 |
| a0001c0004t0010 | 0/0 | 3760 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0001c0004t0025 | 0/0 | 3760 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0001c0007t0001 | 0/0 | 3760 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0001c0007t0009 | 0/0 | 3760 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0001c0007t0015 | 0/0 | 3762 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3757): Show |
chr1 | 12058303 | 12149207 |
| a0001c0009t0001 | 0/0 | 3760 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0001c0009t0006 | 0/0 | 3760 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0001c0013t0001 | 0/0 | 3760 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0001c0014t0001 | 0/0 | 3760 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0001c0017t0014 | 0/0 | 3760 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0001c0018t0009 | 0/0 | 3760 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0001c0023t0001 | 0/0 | 3760 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0001c0025t0001 | 0/0 | 3760 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0001c0026t0001 | 0/0 | 3760 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0002c0005t0001 | 0/0 | 3760 | 7 | 2 | 0 | 5 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0002c0005t0002 | 0/0 | 3760 | 2 | 2 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0002c0005t0005 | 0/0 | 3760 | 3 | 3 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0002c0005t0006 | 0/0 | 3760 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0002c0006t0001 | 0/0 | 3760 | 9 | 2 | 1 | 5 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0002c0006t0003 | 0/0 | 3762 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3757): Show |
chr1 | 12058303 | 12149207 |
| a0002c0006t0008 | 0/0 | 3760 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0002c0010t0001 | 0/0 | 3760 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0002c0010t0024 | 0/0 | 3762 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3757): Show |
chr1 | 12058303 | 12149207 |
| a0002c0011t0001 | 0/0 | 3760 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0002c0011t0004 | 0/0 | 3760 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0002c0012t0001 | 0/0 | 3760 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0002c0012t0023 | 0/0 | 3760 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0002c0016t0004 | 0/0 | 3760 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0003c0008t0001 | 0/0 | 3760 | 2 | 0 | 0 | 2 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0003c0008t0017 | 0/0 | 3760 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0003c0019t0004 | 0/0 | 3760 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0003c0027t0001 | 0/0 | 3760 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0004c0022t0001 | 0/0 | 3760 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0004c0028t0021 | 0/0 | 3760 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0005c0015t0001 | 0/0 | 3760 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0006c0021t0001 | 0/0 | 3760 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0007c0020t0001 | 0/0 | 3760 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0008c0029t0001 | 0/0 | 3760 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0009c0030t0001 | 0/0 | 3760 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| a0010c0024t0001 | 0/0 | 3760 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | CTGAG others(3755): Show |
chr1 | 12058303 | 12149207 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0071 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0004g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0005g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0006g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0006g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0006g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0006g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0007g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0007g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0007g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0007g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0008g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0008g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0009g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0009g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0011g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0013g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0013g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0016g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0001t0022g0072 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0004g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0004g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0008g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0011g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0002t0018g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0005g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0005g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0007g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0008g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0010g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0010g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0012g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0012g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0019g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0020g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0003t0026g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0004t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0004t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0004t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0004t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0004t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0004t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0004t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0004t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0004t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0004t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0004t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0004t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0004t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0004t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0004t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0004t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0004t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0004t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0004t0001g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0004t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0004t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0004t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0004t0010g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0004t0025g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0007t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0007t0009g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0007t0015g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0009t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0009t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0009t0006g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0013t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0013t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0014t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0017t0014g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0018t0009g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0023t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0025t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0001c0026t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0005t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0005t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0005t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0005t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0005t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0005t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0005t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0005t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0005t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0005t0005g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0005t0005g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0005t0005g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0005t0006g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0006t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0006t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0006t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0006t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0006t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0006t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0006t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0006t0001g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0006t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0006t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0006t0008g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0010t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0010t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0010t0024g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0011t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0011t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0011t0004g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0012t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0012t0023g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0002c0016t0004g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0003c0008t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0003c0008t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0003c0008t0017g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0003c0019t0004g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0003c0027t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0004c0022t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0004c0028t0021g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0005c0015t0001g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0006c0021t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0007c0020t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0008c0029t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0009c0030t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| a0010c0024t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0017 | t0014 | g0265 | EUR | GBR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0269 | EUR | GBR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0054 | EUR | FIN | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0114 | EUR | FIN | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0065 | EUR | FIN | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0078 | EUR | FIN | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG00438 | hp1 | a0001 | c0003 | t0001 | g0085 | EAS | CHS | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0333 | EAS | CHS | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG00544 | hp1 | a0002 | c0005 | t0001 | g0051 | EAS | CHS | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG00544 | hp2 | a0002 | c0006 | t0008 | g0162 | EAS | CHS | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG00558 | hp1 | a0001 | c0003 | t0001 | g0062 | EAS | CHS | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG00558 | hp2 | a0001 | c0014 | t0001 | g0101 | EAS | CHS | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG00597 | hp1 | a0002 | c0006 | t0001 | g0081 | EAS | CHS | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG00597 | hp2 | a0001 | c0002 | t0018 | g0097 | EAS | CHS | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG00609 | hp1 | a0001 | c0004 | t0001 | g0267 | EAS | CHS | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG00609 | hp2 | a0001 | c0003 | t0001 | g0064 | EAS | CHS | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0134 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG00642 | hp2 | a0001 | c0003 | t0001 | g0139 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG00738 | hp2 | a0001 | c0003 | t0001 | g0076 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0043 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG00741 | hp2 | a0001 | c0003 | t0001 | g0077 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01069 | hp1 | a0001 | c0001 | t0013 | g0205 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01071 | hp1 | a0001 | c0001 | t0013 | g0182 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0033 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01106 | hp2 | a0005 | c0015 | t0001 | g0350 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0351 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01109 | hp2 | a0001 | c0002 | t0004 | g0042 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01167 | hp2 | a0001 | c0003 | t0012 | g0199 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0314 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01175 | hp2 | a0006 | c0021 | t0001 | g0154 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01243 | hp1 | a0002 | c0006 | t0001 | g0222 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0256 | AMR | PUR | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | CLM | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01255 | hp2 | a0001 | c0003 | t0001 | g0102 | AMR | CLM | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0032 | AMR | CLM | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | CLM | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | CLM | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | CLM | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0316 | AMR | CLM | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0312 | AMR | CLM | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0334 | AMR | CLM | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0128 | AMR | CLM | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0309 | AMR | CLM | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | CLM | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0160 | EUR | IBS | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01515 | hp2 | a0007 | c0020 | t0001 | g0019 | EUR | IBS | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0048 | EUR | IBS | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0098 | EUR | IBS | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0174 | EUR | IBS | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0099 | EUR | IBS | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01884 | hp1 | a0001 | c0003 | t0003 | g0211 | AFR | ACB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01884 | hp2 | a0001 | c0003 | t0001 | g0252 | AFR | ACB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01891 | hp1 | a0001 | c0003 | t0012 | g0236 | AFR | ACB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01891 | hp2 | a0002 | c0010 | t0024 | g0354 | AFR | ACB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01928 | hp1 | a0001 | c0003 | t0001 | g0315 | AMR | PEL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0308 | AMR | PEL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0294 | AMR | PEL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0298 | AMR | PEL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0255 | AMR | PEL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0331 | AMR | PEL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0109 | AMR | PEL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0295 | AMR | PEL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0307 | AMR | PEL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02004 | hp1 | a0001 | c0001 | t0004 | g0177 | AMR | PEL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0270 | AMR | PEL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02015 | hp2 | a0001 | c0004 | t0001 | g0322 | EAS | KHV | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | KHV | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02040 | hp2 | a0001 | c0003 | t0001 | g0249 | EAS | KHV | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02055 | hp1 | a0002 | c0005 | t0005 | g0210 | AFR | ACB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02055 | hp2 | a0001 | c0001 | t0009 | g0234 | AFR | ACB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | KHV | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0045 | EAS | KHV | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0016 | EAS | KHV | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02074 | hp2 | a0001 | c0004 | t0001 | g0135 | EAS | KHV | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02080 | hp1 | a0001 | c0003 | t0001 | g0341 | EAS | KHV | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0317 | EAS | KHV | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0053 | EAS | KHV | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02145 | hp1 | a0001 | c0009 | t0001 | g0360 | AFR | ACB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ACB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0095 | EAS | CDX | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02165 | hp2 | a0001 | c0003 | t0001 | g0057 | EAS | CDX | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02257 | hp1 | a0001 | c0003 | t0007 | g0301 | AFR | ACB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02257 | hp2 | a0001 | c0004 | t0001 | g0196 | AFR | ACB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02258 | hp2 | a0001 | c0004 | t0010 | g0202 | AFR | ACB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0116 | AMR | PEL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0297 | AMR | PEL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0344 | AFR | ACB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0218 | AFR | ACB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02293 | hp1 | a0001 | c0003 | t0001 | g0007 | AMR | PEL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0107 | AMR | PEL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0172 | AFR | ACB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02451 | hp2 | a0001 | c0003 | t0001 | g0217 | AFR | ACB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02523 | hp1 | a0002 | c0010 | t0001 | g0146 | EAS | KHV | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02523 | hp2 | a0001 | c0004 | t0001 | g0320 | EAS | KHV | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02572 | hp1 | a0001 | c0004 | t0001 | g0165 | AFR | GWD | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02572 | hp2 | a0001 | c0003 | t0001 | g0167 | AFR | GWD | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02615 | hp1 | a0001 | c0001 | t0007 | g0193 | AFR | GWD | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02615 | hp2 | a0001 | c0001 | t0005 | g0355 | AFR | GWD | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02622 | hp1 | a0001 | c0001 | t0006 | g0150 | AFR | GWD | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02622 | hp2 | a0001 | c0007 | t0001 | g0215 | AFR | GWD | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02630 | hp1 | a0001 | c0003 | t0001 | g0219 | AFR | GWD | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02630 | hp2 | a0001 | c0003 | t0003 | g0208 | AFR | GWD | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0338 | SAS | PJL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02717 | hp1 | a0001 | c0001 | t0007 | g0198 | AFR | GWD | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02717 | hp2 | a0001 | c0004 | t0002 | g0169 | AFR | GWD | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02723 | hp1 | a0001 | c0001 | t0007 | g0192 | AFR | GWD | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02723 | hp2 | a0001 | c0002 | t0002 | g0147 | AFR | GWD | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0035 | SAS | PJL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0254 | SAS | PJL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02809 | hp1 | a0001 | c0003 | t0001 | g0253 | AFR | GWD | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02809 | hp2 | a0001 | c0004 | t0001 | g0088 | AFR | GWD | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02818 | hp1 | a0001 | c0003 | t0005 | g0223 | AFR | GWD | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | GWD | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02895 | hp1 | a0001 | c0003 | t0002 | g0200 | AFR | GWD | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02895 | hp2 | a0001 | c0003 | t0003 | g0225 | AFR | GWD | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02896 | hp2 | a0001 | c0004 | t0001 | g0168 | AFR | GWD | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02897 | hp1 | a0001 | c0003 | t0003 | g0226 | AFR | GWD | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02922 | hp1 | a0001 | c0003 | t0001 | g0091 | AFR | ESN | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02922 | hp2 | a0001 | c0003 | t0001 | g0153 | AFR | ESN | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02965 | hp1 | a0001 | c0003 | t0026 | g0161 | AFR | ESN | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ESN | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02970 | hp1 | a0001 | c0003 | t0001 | g0313 | AFR | ESN | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | ESN | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02976 | hp1 | a0001 | c0009 | t0001 | g0359 | AFR | ESN | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02976 | hp2 | a0002 | c0005 | t0002 | g0235 | AFR | ESN | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03041 | hp1 | a0001 | c0003 | t0002 | g0214 | AFR | GWD | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03041 | hp2 | a0001 | c0001 | t0006 | g0148 | AFR | GWD | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03098 | hp2 | a0002 | c0006 | t0001 | g0155 | AFR | MSL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03130 | hp1 | a0002 | c0006 | t0003 | g0149 | AFR | ESN | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03130 | hp2 | a0001 | c0007 | t0009 | g0357 | AFR | ESN | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03139 | hp1 | a0001 | c0001 | t0009 | g0089 | AFR | ESN | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03139 | hp2 | a0001 | c0018 | t0009 | g0261 | AFR | ESN | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03195 | hp1 | a0002 | c0006 | t0001 | g0170 | AFR | ESN | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03195 | hp2 | a0002 | c0005 | t0001 | g0227 | AFR | ESN | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03225 | hp1 | a0001 | c0007 | t0015 | g0189 | AFR | MSL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03225 | hp2 | a0001 | c0003 | t0005 | g0092 | AFR | MSL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0305 | SAS | PJL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03453 | hp1 | a0001 | c0009 | t0006 | g0171 | AFR | MSL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03453 | hp2 | a0002 | c0005 | t0005 | g0230 | AFR | MSL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03486 | hp1 | a0001 | c0004 | t0001 | g0352 | AFR | MSL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03486 | hp2 | a0001 | c0003 | t0019 | g0207 | AFR | MSL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0029 | SAS | PJL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0108 | SAS | PJL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0271 | SAS | PJL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | ESN | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03516 | hp2 | a0002 | c0005 | t0005 | g0232 | AFR | ESN | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03540 | hp1 | a0001 | c0003 | t0003 | g0152 | AFR | GWD | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03540 | hp2 | a0001 | c0001 | t0007 | g0216 | AFR | GWD | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03579 | hp1 | a0002 | c0005 | t0002 | g0206 | AFR | MSL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03579 | hp2 | a0001 | c0004 | t0003 | g0220 | AFR | MSL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0311 | SAS | PJL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0129 | SAS | PJL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0318 | SAS | STU | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0022 | SAS | STU | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0112 | SAS | PJL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0264 | SAS | PJL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03710 | hp2 | a0002 | c0006 | t0001 | g0347 | SAS | PJL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0031 | SAS | BEB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0332 | SAS | BEB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0010 | SAS | BEB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | BEB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | BEB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0339 | SAS | BEB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0131 | SAS | BEB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03942 | hp2 | a0001 | c0004 | t0001 | g0348 | SAS | BEB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG04115 | hp1 | a0001 | c0002 | t0004 | g0260 | SAS | STU | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | STU | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG04184 | hp1 | a0001 | c0003 | t0001 | g0082 | SAS | BEB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0340 | SAS | BEB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0055 | SAS | STU | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | STU | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0268 | SAS | STU | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0110 | SAS | STU | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | YRI | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0224 | AFR | YRI | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18612 | hp1 | a0001 | c0004 | t0001 | g0291 | EAS | CHB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18612 | hp2 | a0001 | c0003 | t0001 | g0024 | EAS | CHB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18906 | hp1 | a0001 | c0003 | t0002 | g0213 | AFR | YRI | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18906 | hp2 | a0001 | c0003 | t0010 | g0259 | AFR | YRI | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18939 | hp1 | a0004 | c0022 | t0001 | g0002 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18941 | hp1 | a0001 | c0002 | t0011 | g0285 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18942 | hp1 | a0002 | c0005 | t0001 | g0094 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18942 | hp2 | a0001 | c0003 | t0020 | g0073 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18947 | hp1 | a0001 | c0004 | t0001 | g0132 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18947 | hp2 | a0001 | c0004 | t0001 | g0142 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0176 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18950 | hp2 | a0001 | c0003 | t0001 | g0319 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18953 | hp2 | a0001 | c0003 | t0001 | g0284 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18956 | hp1 | a0002 | c0005 | t0001 | g0349 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18956 | hp2 | a0001 | c0004 | t0001 | g0164 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18957 | hp2 | a0002 | c0006 | t0001 | g0090 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18960 | hp1 | a0001 | c0003 | t0001 | g0310 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18960 | hp2 | a0001 | c0023 | t0001 | g0061 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18969 | hp1 | a0002 | c0011 | t0001 | g0303 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18969 | hp2 | a0003 | c0027 | t0001 | g0060 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18970 | hp1 | a0003 | c0008 | t0001 | g0105 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18972 | hp1 | a0001 | c0026 | t0001 | g0337 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18972 | hp2 | a0001 | c0003 | t0001 | g0181 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18973 | hp1 | a0001 | c0004 | t0001 | g0069 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0302 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18974 | hp1 | a0001 | c0002 | t0001 | g0306 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18974 | hp2 | a0001 | c0003 | t0001 | g0321 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18978 | hp1 | a0001 | c0003 | t0001 | g0288 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18979 | hp2 | a0001 | c0003 | t0001 | g0023 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18980 | hp1 | a0001 | c0004 | t0001 | g0283 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18980 | hp2 | a0001 | c0001 | t0008 | g0362 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18983 | hp1 | a0002 | c0011 | t0001 | g0292 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18983 | hp2 | a0001 | c0003 | t0001 | g0025 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0266 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18985 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18989 | hp1 | a0001 | c0003 | t0001 | g0276 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18989 | hp2 | a0001 | c0003 | t0001 | g0179 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18990 | hp1 | a0001 | c0002 | t0008 | g0212 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18993 | hp1 | a0008 | c0029 | t0001 | g0240 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0323 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18994 | hp2 | a0001 | c0001 | t0008 | g0163 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18997 | hp2 | a0001 | c0003 | t0001 | g0145 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18999 | hp1 | a0001 | c0003 | t0001 | g0143 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0239 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19002 | hp1 | a0001 | c0004 | t0001 | g0070 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19007 | hp2 | a0001 | c0001 | t0011 | g0282 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19009 | hp2 | a0004 | c0028 | t0021 | g0113 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19010 | hp1 | a0003 | c0019 | t0004 | g0017 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19011 | hp1 | a0002 | c0005 | t0001 | g0121 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19030 | hp1 | a0001 | c0004 | t0025 | g0356 | AFR | LWK | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19030 | hp2 | a0001 | c0003 | t0001 | g0237 | AFR | LWK | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0166 | AFR | LWK | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19043 | hp2 | a0002 | c0016 | t0004 | g0228 | AFR | LWK | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19056 | hp1 | a0001 | c0003 | t0001 | g0111 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19056 | hp2 | a0001 | c0004 | t0001 | g0052 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19063 | hp2 | a0001 | c0003 | t0001 | g0281 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19064 | hp1 | a0002 | c0005 | t0001 | g0084 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19064 | hp2 | a0009 | c0030 | t0001 | g0120 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19065 | hp2 | a0001 | c0003 | t0001 | g0185 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19066 | hp1 | a0001 | c0003 | t0001 | g0324 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19066 | hp2 | a0003 | c0008 | t0001 | g0087 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19067 | hp1 | a0001 | c0002 | t0001 | g0140 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19067 | hp2 | a0001 | c0001 | t0004 | g0026 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19070 | hp1 | a0002 | c0006 | t0001 | g0056 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19070 | hp2 | a0001 | c0013 | t0001 | g0251 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19074 | hp1 | a0002 | c0006 | t0001 | g0361 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19082 | hp1 | a0001 | c0013 | t0001 | g0280 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19082 | hp2 | a0001 | c0003 | t0008 | g0204 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19083 | hp1 | a0001 | c0004 | t0001 | g0186 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19085 | hp2 | a0002 | c0010 | t0001 | g0345 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19089 | hp1 | a0001 | c0003 | t0001 | g0336 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19089 | hp2 | a0001 | c0002 | t0001 | g0243 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19090 | hp1 | a0001 | c0003 | t0001 | g0123 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19091 | hp2 | a0002 | c0006 | t0001 | g0021 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19240 | hp1 | a0001 | c0001 | t0006 | g0248 | AFR | YRI | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA19240 | hp2 | a0010 | c0024 | t0001 | g0238 | AFR | YRI | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ASW | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA20129 | hp2 | a0002 | c0011 | t0004 | g0221 | AFR | ASW | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA20752 | hp1 | a0003 | c0008 | t0017 | g0009 | EUR | TSI | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0067 | EUR | TSI | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0180 | EUR | TSI | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0130 | EUR | TSI | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02109 | hp1 | a0002 | c0005 | t0006 | g0209 | AFR | ACB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02109 | hp2 | a0001 | c0001 | t0006 | g0358 | AFR | ACB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02486 | hp2 | a0001 | c0004 | t0001 | g0036 | AFR | ACB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02559 | hp1 | a0002 | c0005 | t0001 | g0059 | AFR | ACB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0188 | AFR | ACB | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03471 | hp1 | a0002 | c0012 | t0023 | g0353 | AFR | MSL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG03471 | hp2 | a0001 | c0003 | t0010 | g0195 | AFR | MSL | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG06807 | hp1 | a0001 | c0001 | t0016 | g0194 | AFR | USA | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| HG06807 | hp2 | a0001 | c0003 | t0002 | g0197 | AFR | USA | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA21309 | hp1 | a0002 | c0012 | t0001 | g0178 | AFR | LWK | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| NA21309 | hp2 | a0001 | c0025 | t0001 | g0231 | AFR | LWK | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0022 | g0072 | REF | REF | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0071 | REF | REF | TNFRSF8_chr1_12058303_12149207 | TNFRSF8 | chr1 | 12058303 | 12149207 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:12104394 | A | G | 1 | a0010 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.284A>G | p.Lys95Arg | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/15 | 580/3760 | 284/1788 | 95/595 | chr1 | 12104394 | |||
| chr1:12115610 | A | G | 1 | a0009 | 1 | NA19064.hp2 | missense_variant | MODERATE | c.827A>G | p.Asn276Ser | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/15 | 1123/3760 | 827/1788 | 276/595 | chr1 | 12115610 | |||
| chr1:12115723 | C | T | 1 | a0008 | 1 | NA18993.hp1 | missense_variant | MODERATE | c.940C>T | p.Pro314Ser | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/15 | 1236/3760 | 940/1788 | 314/595 | chr1 | 12115723 | |||
| chr1:12126001 | A | G | 3 | a0002 a0004 a0005 |
36 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(33): Show |
missense_variant | MODERATE | c.1204A>G | p.Ser402Gly | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 11/15 | 1500/3760 | 1204/1788 | 402/595 | chr1 | 12126001 | |||
| chr1:12138248 | C | T | 1 | a0006 | 1 | HG01175.hp2 | missense_variant | MODERATE | c.1355C>T | p.Ser452Leu | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/15 | 1651/3760 | 1355/1788 | 452/595 | chr1 | 12138248 | |||
| chr1:12138290 | A | G | 1 | a0005 | 1 | HG01106.hp2 | missense_variant | MODERATE | c.1397A>G | p.Gln466Arg | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/15 | 1693/3760 | 1397/1788 | 466/595 | chr1 | 12138290 | |||
| chr1:12138305 | C | A | 2 | a0003 a0004 |
7 | NA18939.hp1 NA18969.hp2 NA18970.hp1 others(4): Show |
missense_variant | MODERATE | c.1412C>A | p.Thr471Asn | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/15 | 1708/3760 | 1412/1788 | 471/595 | chr1 | 12138305 | |||
| chr1:12138370 | G | A | 1 | a0007 | 1 | HG01515.hp2 | missense_variant | MODERATE | c.1477G>A | p.Gly493Ser | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/15 | 1773/3760 | 1477/1788 | 493/595 | chr1 | 12138370 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:12097147 | G | A | 1 | a0001c0014 | 1 | HG00558.hp2 | synonymous_variant | LOW | c.198G>A | p.Arg66Arg | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/15 | 494/3760 | 198/1788 | 66/595 | chr1 | 12097147 | |||
| chr1:12104380 | C | T | 11 | a0001c0002 a0001c0004 a0001c0009 others(8): Show |
109 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(106): Show |
splice_region_variant&synonymous_variant | LOW | c.270C>T | p.Asp90Asp | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/15 | 566/3760 | 270/1788 | 90/595 | chr1 | 12104380 | |||
| chr1:12110155 | G | A | 1 | a0001c0025 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.627G>A | p.Thr209Thr | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 6/15 | 923/3760 | 627/1788 | 209/595 | chr1 | 12110155 | |||
| chr1:12111992 | G | A | 4 | a0001c0009 a0002c0012 a0002c0016 others(1): Show |
7 | HG01106.hp2 HG02145.hp1 HG02976.hp1 others(4): Show |
synonymous_variant | LOW | c.771G>A | p.Thr257Thr | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/15 | 1067/3760 | 771/1788 | 257/595 | chr1 | 12111992 | |||
| chr1:12123315 | G | A | 1 | a0001c0017 | 1 | HG00140.hp1 | synonymous_variant | LOW | c.978G>A | p.Ala326Ala | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 9/15 | 1274/3760 | 978/1788 | 326/595 | chr1 | 12123315 | |||
| chr1:12123781 | C | T | 2 | a0001c0013 a0001c0023 |
3 | NA18960.hp2 NA19070.hp2 NA19082.hp1 |
synonymous_variant | LOW | c.1107C>T | p.Ser369Ser | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/15 | 1403/3760 | 1107/1788 | 369/595 | chr1 | 12123781 | |||
| chr1:12135604 | G | A | 2 | a0001c0007 a0001c0018 |
4 | HG02622.hp2 HG03130.hp2 HG03139.hp2 others(1): Show |
synonymous_variant | LOW | c.1326G>A | p.Arg442Arg | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/15 | 1622/3760 | 1326/1788 | 442/595 | chr1 | 12135604 | |||
| chr1:12138240 | T | C | 13 | a0001c0003 a0001c0004 a0001c0007 others(10): Show |
111 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(108): Show |
synonymous_variant | LOW | c.1347T>C | p.Ser449Ser | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/15 | 1643/3760 | 1347/1788 | 449/595 | chr1 | 12138240 | |||
| chr1:12138315 | C | T | 1 | a0001c0026 | 1 | NA18972.hp1 | synonymous_variant | LOW | c.1422C>T | p.Ser474Ser | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/15 | 1718/3760 | 1422/1788 | 474/595 | chr1 | 12138315 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:12063319 | C | T | 1 | a0001c0003t0026 | 1 | HG02965.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-280C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/15 | chr1 | 12063319 | |||||||
| chr1:12063442 | G | T | 4 | a0001c0001t0008 a0001c0002t0008 a0001c0003t0008 others(1): Show |
5 | HG00544.hp2 NA18980.hp2 NA18990.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-157G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/15 | 157 | chr1 | 12063442 | ||||||
| chr1:12063566 | G | T | 2 | a0001c0004t0025 a0002c0010t0024 |
2 | HG01891.hp2 NA19030.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-33G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/15 | chr1 | 12063566 | |||||||
| chr1:12142705 | C | G | 1 | a0002c0012t0023 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*174C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 15/15 | 174 | chr1 | 12142705 | ||||||
| chr1:12142731 | G | A | 1 | a0002c0012t0023 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*200G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 15/15 | 200 | chr1 | 12142731 | ||||||
| chr1:12142774 | G | A | 2 | a0001c0001t0011 a0001c0002t0011 |
2 | NA18941.hp1 NA19007.hp2 |
3_prime_UTR_variant | MODIFIER | c.*243G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 15/15 | 243 | chr1 | 12142774 | ||||||
| chr1:12142835 | G | A | 1 | a0001c0017t0014 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*304G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 15/15 | 304 | chr1 | 12142835 | ||||||
| chr1:12142897 | C | T | 3 | a0001c0001t0006 a0001c0009t0006 a0002c0005t0006 |
6 | HG02109.hp1 HG02109.hp2 HG02622.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*366C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 15/15 | 366 | chr1 | 12142897 | ||||||
| chr1:12142996 | G | A | 1 | a0001c0007t0015 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*465G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 15/15 | 465 | chr1 | 12142996 | ||||||
| chr1:12143101 | G | A | 3 | a0001c0001t0009 a0001c0007t0009 a0001c0018t0009 |
4 | HG02055.hp2 HG03130.hp2 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*570G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 15/15 | 570 | chr1 | 12143101 | ||||||
| chr1:12143138 | A | G | 8 | a0001c0001t0004 a0001c0002t0004 a0001c0003t0010 others(5): Show |
11 | HG01109.hp2 HG02004.hp1 HG02258.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*607A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 15/15 | 607 | chr1 | 12143138 | ||||||
| chr1:12143320 | C | T | 1 | a0001c0001t0013 | 2 | HG01069.hp1 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*789C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 15/15 | 789 | chr1 | 12143320 | ||||||
| chr1:12143418 | A | G | 1 | a0002c0012t0023 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*887A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 15/15 | 887 | chr1 | 12143418 | ||||||
| chr1:12143451 | T | C | 1 | a0004c0028t0021 | 1 | NA19009.hp2 | 3_prime_UTR_variant | MODIFIER | c.*920T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 15/15 | 920 | chr1 | 12143451 | ||||||
| chr1:12143542 | A | ACG | 5 | a0001c0003t0003 a0001c0004t0003 a0001c0007t0015 others(2): Show |
9 | HG01884.hp1 HG01891.hp2 HG02630.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1013_*1014dupGC | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 15/15 | 1015 | INFO_REALIGN_3_PRIME | chr1 | 12143542 | |||||
| chr1:12143544 | G | C | 14 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0009 others(11): Show |
25 | HG01167.hp2 HG01891.hp1 HG02055.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1013G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 15/15 | 1013 | chr1 | 12143544 | ||||||
| chr1:12143598 | A | C | 1 | a0001c0003t0020 | 1 | NA18942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1067A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 15/15 | 1067 | chr1 | 12143598 | ||||||
| chr1:12143705 | C | T | 1 | a0001c0003t0019 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1174C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 15/15 | 1174 | chr1 | 12143705 | ||||||
| chr1:12143718 | G | C | 1 | a0001c0003t0012 | 2 | HG01167.hp2 HG01891.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1187G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 15/15 | 1187 | chr1 | 12143718 | ||||||
| chr1:12143815 | C | T | 3 | a0001c0001t0005 a0001c0003t0005 a0002c0005t0005 |
6 | HG02055.hp1 HG02615.hp2 HG02818.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1284C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 15/15 | 1284 | chr1 | 12143815 | ||||||
| chr1:12143817 | G | C | 1 | a0003c0008t0017 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1286G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 15/15 | 1286 | chr1 | 12143817 | ||||||
| chr1:12143821 | G | A | 14 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0007 others(11): Show |
28 | HG01167.hp2 HG01891.hp1 HG02055.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1290G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 15/15 | 1290 | chr1 | 12143821 | ||||||
| chr1:12144010 | G | A | 1 | a0001c0002t0018 | 1 | HG00597.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1479G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 15/15 | 1479 | chr1 | 12144010 | ||||||
| chr1:12144123 | A | C | 2 | a0001c0003t0010 a0001c0004t0010 |
3 | HG02258.hp2 HG03471.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1592A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 15/15 | 1592 | chr1 | 12144123 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:12063756 | G | T | 1 | a0001c0001t0008g0362 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.63+95G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12063756 | |||||||
| chr1:12063968 | G | A | 18 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(15): Show |
18 | HG01074.hp2 HG01192.hp2 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.63+307G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12063968 | |||||||
| chr1:12064003 | C | T | 1 | a0002c0006t0001g0361 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.63+342C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12064003 | |||||||
| chr1:12064090 | C | G | 8 | a0001c0001t0005g0355 a0001c0001t0006g0358 a0001c0004t0025g0356 others(5): Show |
8 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.63+429C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12064090 | |||||||
| chr1:12064145 | A | T | 3 | a0001c0001t0001g0351 a0001c0004t0001g0352 a0005c0015t0001g0350 |
3 | HG01106.hp2 HG01109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.63+484A>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12064145 | |||||||
| chr1:12064157 | G | A | 3 | a0001c0001t0001g0351 a0001c0004t0001g0352 a0005c0015t0001g0350 |
3 | HG01106.hp2 HG01109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.63+496G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12064157 | |||||||
| chr1:12064202 | A | G | 115 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0244 others(112): Show |
115 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.63+541A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12064202 | |||||||
| chr1:12064448 | C | T | 1 | a0001c0001t0009g0234 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.63+787C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12064448 | |||||||
| chr1:12064486 | ACCATAGT others(5): Show |
A | 20 | a0001c0001t0001g0229 a0001c0001t0001g0233 a0001c0001t0002g0218 others(17): Show |
20 | HG01243.hp1 HG02055.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.63+827_63+838delCA others(10): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12064486 | ||||||
| chr1:12064544 | G | A | 4 | a0001c0003t0001g0237 a0001c0003t0012g0236 a0002c0005t0002g0235 others(1): Show |
4 | HG01891.hp1 HG02976.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+883G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12064544 | |||||||
| chr1:12064778 | C | G | 2 | a0001c0003t0002g0213 a0001c0003t0002g0214 |
2 | HG03041.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.63+1117C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12064778 | |||||||
| chr1:12064949 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.63+1288G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12064949 | |||||||
| chr1:12065064 | C | T | 1 | a0001c0002t0008g0212 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.63+1403C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12065064 | |||||||
| chr1:12065078 | C | CT | 61 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 others(58): Show |
61 | HG00544.hp2 HG00738.hp1 HG01071.hp1 others(58): Show |
intron_variant | MODIFIER | c.63+1439dupT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12065078 | ||||||
| chr1:12065078 | C | CTT | 16 | a0001c0001t0001g0229 a0001c0001t0001g0244 a0001c0001t0001g0351 others(13): Show |
16 | HG01069.hp1 HG01106.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.63+1438_63+1439dup others(2): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12065078 | ||||||
| chr1:12065078 | C | CTTT | 95 | a0001c0001t0001g0233 a0001c0001t0001g0245 a0001c0001t0001g0246 others(92): Show |
95 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.63+1437_63+1439dup others(3): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12065078 | ||||||
| chr1:12065078 | C | CTTTT | 16 | a0001c0001t0001g0335 a0001c0001t0001g0338 a0001c0001t0001g0342 others(13): Show |
16 | HG02080.hp1 HG02280.hp1 HG02698.hp2 others(13): Show |
intron_variant | MODIFIER | c.63+1436_63+1439dup others(4): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12065078 | ||||||
| chr1:12065078 | CT | C | 7 | a0001c0001t0001g0020 a0001c0002t0001g0022 a0001c0003t0001g0023 others(4): Show |
7 | HG01515.hp2 HG03471.hp1 HG03688.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+1439delT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12065078 | ||||||
| chr1:12065111 | C | T | 4 | a0001c0001t0001g0203 a0001c0003t0003g0208 a0002c0005t0005g0210 others(1): Show |
4 | HG02055.hp1 HG02109.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+1450C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12065111 | |||||||
| chr1:12065163 | A | C | 7 | a0001c0001t0001g0201 a0001c0001t0007g0198 a0001c0003t0002g0197 others(4): Show |
7 | HG01167.hp2 HG01192.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+1502A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12065163 | |||||||
| chr1:12065167 | C | A | 1 | a0001c0003t0026g0161 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.63+1506C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12065167 | |||||||
| chr1:12065190 | C | T | 158 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0173 others(155): Show |
158 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(155): Show |
intron_variant | MODIFIER | c.63+1529C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12065190 | |||||||
| chr1:12065303 | G | A | 1 | a0001c0001t0001g0245 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.63+1642G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12065303 | |||||||
| chr1:12065352 | G | A | 114 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0244 others(111): Show |
114 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.63+1691G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12065352 | |||||||
| chr1:12065611 | T | C | 3 | a0001c0001t0001g0351 a0001c0004t0001g0352 a0005c0015t0001g0350 |
3 | HG01106.hp2 HG01109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.63+1950T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12065611 | |||||||
| chr1:12065655 | T | C | 1 | a0001c0001t0001g0246 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.63+1994T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12065655 | |||||||
| chr1:12065714 | C | A | 5 | a0001c0001t0008g0163 a0001c0001t0008g0362 a0001c0002t0008g0212 others(2): Show |
5 | HG00544.hp2 NA18980.hp2 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+2053C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12065714 | |||||||
| chr1:12065779 | T | C | 7 | a0001c0001t0001g0203 a0001c0001t0002g0218 a0001c0001t0007g0216 others(4): Show |
7 | HG02055.hp1 HG02109.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+2118T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12065779 | |||||||
| chr1:12065857 | C | G | 8 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0007g0192 others(5): Show |
8 | HG02257.hp2 HG02615.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.63+2196C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12065857 | |||||||
| chr1:12066084 | A | G | 3 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 |
3 | HG01099.hp1 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.63+2423A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12066084 | |||||||
| chr1:12066142 | G | A | 1 | a0002c0006t0001g0361 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.63+2481G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12066142 | |||||||
| chr1:12066153 | G | A | 3 | a0001c0001t0001g0229 a0001c0003t0001g0219 a0001c0004t0003g0220 |
3 | HG02630.hp1 HG03516.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.63+2492G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12066153 | |||||||
| chr1:12066308 | T | A | 118 | a0001c0001t0001g0241 a0001c0001t0001g0244 a0001c0001t0001g0245 others(115): Show |
118 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.63+2647T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12066308 | |||||||
| chr1:12066308 | T | TA | 7 | a0001c0001t0001g0201 a0001c0001t0007g0198 a0001c0003t0002g0197 others(4): Show |
7 | HG01167.hp2 HG01192.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+2657dupA | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12066308 | ||||||
| chr1:12066309 | A | T | 2 | a0001c0002t0001g0018 a0003c0019t0004g0017 |
2 | NA18985.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.63+2648A>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12066309 | |||||||
| chr1:12066350 | T | A | 1 | a0002c0006t0001g0170 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.63+2689T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12066350 | |||||||
| chr1:12066350 | T | TA | 3 | a0001c0001t0001g0159 a0001c0003t0026g0161 a0001c0009t0006g0171 |
3 | HG02965.hp1 HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.63+2693dupA | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12066350 | ||||||
| chr1:12066354 | A | AT | 41 | a0001c0001t0001g0160 a0001c0001t0001g0173 a0001c0001t0001g0174 others(38): Show |
41 | HG00438.hp2 HG00738.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.63+2710dupT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12066354 | ||||||
| chr1:12066354 | AT | A | 6 | a0001c0001t0001g0028 a0001c0001t0001g0203 a0001c0001t0001g0247 others(3): Show |
6 | HG02647.hp2 HG03491.hp2 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+2710delT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12066354 | ||||||
| chr1:12066501 | T | C | 1 | a0001c0003t0001g0219 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.63+2840T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12066501 | |||||||
| chr1:12066505 | C | A | 1 | a0001c0001t0001g0203 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.63+2844C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12066505 | |||||||
| chr1:12066593 | T | C | 1 | a0001c0001t0006g0248 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.63+2932T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12066593 | |||||||
| chr1:12066599 | C | T | 5 | a0001c0001t0008g0163 a0001c0001t0008g0362 a0001c0002t0008g0212 others(2): Show |
5 | HG00544.hp2 NA18980.hp2 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+2938C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12066599 | |||||||
| chr1:12066600 | A | G | 189 | a0001c0001t0001g0151 a0001c0001t0001g0159 a0001c0001t0001g0160 others(186): Show |
189 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(186): Show |
intron_variant | MODIFIER | c.63+2939A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12066600 | |||||||
| chr1:12066642 | C | T | 7 | a0001c0001t0002g0224 a0001c0003t0003g0225 a0001c0003t0003g0226 others(4): Show |
7 | HG02895.hp2 HG02897.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+2981C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12066642 | |||||||
| chr1:12066706 | G | A | 1 | a0001c0003t0001g0249 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.63+3045G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12066706 | |||||||
| chr1:12066720 | T | G | 3 | a0001c0001t0002g0224 a0001c0003t0003g0225 a0001c0003t0003g0226 |
3 | HG02895.hp2 HG02897.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.63+3059T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12066720 | |||||||
| chr1:12066797 | T | C | 118 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0244 others(115): Show |
118 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.63+3136T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12066797 | |||||||
| chr1:12066823 | T | C | 7 | a0001c0001t0002g0224 a0001c0003t0003g0225 a0001c0003t0003g0226 others(4): Show |
7 | HG02895.hp2 HG02897.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+3162T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12066823 | |||||||
| chr1:12066992 | C | T | 3 | a0001c0001t0002g0224 a0001c0003t0003g0225 a0001c0003t0003g0226 |
3 | HG02895.hp2 HG02897.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.63+3331C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12066992 | |||||||
| chr1:12066993 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.63+3332G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12066993 | |||||||
| chr1:12067075 | C | T | 1 | a0001c0007t0009g0357 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.63+3414C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12067075 | |||||||
| chr1:12067092 | C | T | 3 | a0001c0001t0002g0224 a0001c0003t0003g0225 a0001c0003t0003g0226 |
3 | HG02895.hp2 HG02897.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.63+3431C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12067092 | |||||||
| chr1:12067205 | G | C | 20 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0174 others(17): Show |
20 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.63+3544G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12067205 | |||||||
| chr1:12067209 | C | T | 4 | a0001c0001t0008g0163 a0001c0001t0008g0362 a0001c0003t0008g0204 others(1): Show |
4 | HG00544.hp2 NA18980.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+3548C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12067209 | |||||||
| chr1:12067236 | C | T | 1 | a0001c0003t0026g0161 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.63+3575C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12067236 | |||||||
| chr1:12067255 | C | G | 1 | a0001c0002t0001g0188 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.63+3594C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12067255 | |||||||
| chr1:12067414 | C | T | 3 | a0001c0001t0006g0358 a0001c0009t0001g0359 a0001c0009t0001g0360 |
3 | HG02109.hp2 HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.63+3753C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12067414 | |||||||
| chr1:12067457 | G | T | 4 | a0001c0001t0001g0144 a0001c0003t0001g0143 a0001c0003t0001g0145 others(1): Show |
4 | HG02523.hp1 NA18966.hp2 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+3796G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12067457 | |||||||
| chr1:12067550 | A | G | 1 | a0001c0001t0002g0172 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.63+3889A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12067550 | |||||||
| chr1:12067562 | G | A | 4 | a0001c0001t0008g0163 a0001c0001t0008g0362 a0001c0003t0008g0204 others(1): Show |
4 | HG00544.hp2 NA18980.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+3901G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12067562 | |||||||
| chr1:12067646 | C | T | 1 | a0001c0003t0026g0161 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.63+3985C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12067646 | |||||||
| chr1:12067654 | T | C | 1 | a0008c0029t0001g0240 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.63+3993T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12067654 | |||||||
| chr1:12067713 | C | T | 1 | a0001c0003t0026g0161 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.63+4052C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12067713 | |||||||
| chr1:12067760 | C | T | 7 | a0001c0001t0002g0224 a0001c0003t0003g0225 a0001c0003t0003g0226 others(4): Show |
7 | HG02895.hp2 HG02897.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+4099C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12067760 | |||||||
| chr1:12067818 | A | G | 1 | a0001c0004t0001g0142 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.63+4157A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12067818 | |||||||
| chr1:12067875 | C | T | 3 | a0001c0001t0001g0241 a0001c0004t0001g0348 a0002c0006t0001g0347 |
3 | HG03710.hp2 HG03942.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.63+4214C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12067875 | |||||||
| chr1:12067903 | C | CG | 130 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0028 others(127): Show |
130 | HG00140.hp1 HG00140.hp2 HG00609.hp1 others(127): Show |
intron_variant | MODIFIER | c.63+4251dupG | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12067903 | ||||||
| chr1:12067903 | C | CGG | 48 | a0001c0001t0001g0159 a0001c0001t0001g0173 a0001c0001t0001g0183 others(45): Show |
48 | HG00438.hp2 HG00738.hp1 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.63+4250_63+4251dup others(2): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12067903 | ||||||
| chr1:12067903 | C | G | 15 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0002g0218 others(12): Show |
15 | HG02055.hp1 HG02109.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.63+4242C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12067903 | |||||||
| chr1:12067912 | G | GT | 3 | a0001c0001t0001g0241 a0001c0004t0001g0348 a0002c0006t0001g0347 |
3 | HG03710.hp2 HG03942.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.63+4251_63+4252ins others(1): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12067912 | |||||||
| chr1:12068101 | G | C | 2 | a0001c0001t0001g0030 a0001c0001t0001g0124 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.63+4440G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12068101 | |||||||
| chr1:12068183 | A | T | 1 | a0001c0001t0001g0203 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.63+4522A>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12068183 | |||||||
| chr1:12068222 | G | A | 7 | a0001c0001t0001g0201 a0001c0001t0007g0198 a0001c0003t0002g0197 others(4): Show |
7 | HG01167.hp2 HG01192.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+4561G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12068222 | |||||||
| chr1:12068235 | A | G | 1 | a0001c0003t0001g0123 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.63+4574A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12068235 | |||||||
| chr1:12068246 | T | C | 1 | a0001c0002t0001g0031 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.63+4585T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12068246 | |||||||
| chr1:12068378 | A | G | 59 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0098 others(56): Show |
59 | HG00280.hp2 HG00558.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.63+4717A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12068378 | |||||||
| chr1:12068441 | G | A | 117 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0244 others(114): Show |
117 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.63+4780G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12068441 | |||||||
| chr1:12068876 | C | CT | 46 | a0001c0001t0001g0096 a0001c0001t0001g0098 a0001c0001t0001g0099 others(43): Show |
46 | HG00280.hp2 HG00558.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.63+5228dupT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12068876 | ||||||
| chr1:12068935 | G | A | 1 | a0001c0025t0001g0231 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.63+5274G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12068935 | |||||||
| chr1:12068998 | A | G | 1 | a0003c0008t0001g0087 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.63+5337A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12068998 | |||||||
| chr1:12069117 | C | T | 1 | a0001c0003t0026g0161 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.63+5456C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12069117 | |||||||
| chr1:12069167 | G | T | 1 | a0001c0001t0009g0234 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.63+5506G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12069167 | |||||||
| chr1:12069170 | C | CT | 16 | a0001c0001t0001g0012 a0001c0001t0001g0083 a0001c0001t0001g0086 others(13): Show |
16 | HG00438.hp1 HG00597.hp1 HG02056.hp1 others(13): Show |
intron_variant | MODIFIER | c.63+5536dupT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12069170 | ||||||
| chr1:12069170 | CT | C | 20 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0332 others(17): Show |
20 | HG00438.hp2 HG00741.hp1 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.63+5536delT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12069170 | ||||||
| chr1:12069170 | CTT | C | 134 | a0001c0001t0001g0003 a0001c0001t0001g0034 a0001c0001t0001g0037 others(131): Show |
134 | HG00140.hp1 HG00140.hp2 HG00609.hp1 others(131): Show |
intron_variant | MODIFIER | c.63+5535_63+5536del others(2): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12069170 | ||||||
| chr1:12069170 | CTTT | C | 86 | a0001c0001t0001g0096 a0001c0001t0001g0098 a0001c0001t0001g0099 others(83): Show |
86 | HG00280.hp2 HG00558.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.63+5534_63+5536del others(3): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12069170 | ||||||
| chr1:12069170 | CTTTTTTT others(6): Show |
C | 2 | a0001c0001t0002g0172 a0002c0005t0002g0206 |
2 | HG02451.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.63+5524_63+5536del others(13): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12069170 | ||||||
| chr1:12069170 | CTTTTTTT others(7): Show |
C | 3 | a0001c0002t0001g0166 a0001c0004t0001g0165 a0001c0004t0001g0168 |
3 | HG02572.hp1 HG02896.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.63+5523_63+5536del others(14): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12069170 | ||||||
| chr1:12069248 | A | G | 116 | a0001c0001t0001g0096 a0001c0001t0001g0098 a0001c0001t0001g0099 others(113): Show |
116 | HG00280.hp2 HG00544.hp2 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.63+5587A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12069248 | |||||||
| chr1:12069367 | C | T | 6 | a0001c0001t0001g0151 a0001c0001t0006g0150 a0001c0003t0001g0153 others(3): Show |
6 | HG02622.hp1 HG02647.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+5706C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12069367 | |||||||
| chr1:12069424 | C | A | 6 | a0001c0001t0001g0344 a0001c0001t0006g0248 a0001c0003t0001g0252 others(3): Show |
6 | HG01884.hp1 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+5763C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12069424 | |||||||
| chr1:12069471 | C | T | 1 | a0001c0004t0001g0164 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.63+5810C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12069471 | |||||||
| chr1:12069509 | C | T | 1 | a0001c0001t0001g0330 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.63+5848C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12069509 | |||||||
| chr1:12069593 | T | C | 1 | a0001c0003t0026g0161 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.63+5932T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12069593 | |||||||
| chr1:12069717 | C | T | 1 | a0001c0002t0001g0188 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.63+6056C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12069717 | |||||||
| chr1:12069718 | G | A | 8 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0007g0192 others(5): Show |
8 | HG02257.hp2 HG02615.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.63+6057G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12069718 | |||||||
| chr1:12069816 | A | C | 1 | a0002c0006t0001g0347 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.63+6155A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12069816 | |||||||
| chr1:12069875 | T | C | 1 | a0001c0002t0001g0254 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.63+6214T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12069875 | |||||||
| chr1:12069881 | C | T | 1 | a0001c0025t0001g0231 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.63+6220C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12069881 | |||||||
| chr1:12069912 | G | A | 16 | a0001c0001t0001g0160 a0001c0001t0001g0174 a0001c0001t0001g0175 others(13): Show |
16 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.63+6251G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12069912 | |||||||
| chr1:12069992 | G | T | 1 | a0001c0001t0001g0332 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.63+6331G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12069992 | |||||||
| chr1:12069994 | C | T | 132 | a0001c0001t0001g0003 a0001c0001t0001g0034 a0001c0001t0001g0037 others(129): Show |
132 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.63+6333C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12069994 | |||||||
| chr1:12070013 | T | C | 1 | a0002c0006t0001g0021 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.63+6352T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12070013 | |||||||
| chr1:12070145 | TG | T | 231 | a0001c0001t0001g0003 a0001c0001t0001g0034 a0001c0001t0001g0037 others(228): Show |
231 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.63+6490delG | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12070145 | ||||||
| chr1:12070159 | A | G | 181 | a0001c0001t0001g0003 a0001c0001t0001g0034 a0001c0001t0001g0037 others(178): Show |
181 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(178): Show |
intron_variant | MODIFIER | c.63+6498A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12070159 | |||||||
| chr1:12070161 | TGGG | T | 181 | a0001c0001t0001g0003 a0001c0001t0001g0034 a0001c0001t0001g0037 others(178): Show |
181 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(178): Show |
intron_variant | MODIFIER | c.63+6504_63+6506del others(3): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12070161 | ||||||
| chr1:12070205 | T | C | 2 | a0001c0001t0007g0216 a0001c0003t0001g0217 |
2 | HG02451.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.63+6544T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12070205 | |||||||
| chr1:12070395 | C | T | 2 | a0001c0001t0001g0300 a0001c0001t0001g0330 |
2 | NA18962.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.63+6734C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12070395 | |||||||
| chr1:12070460 | C | T | 206 | a0001c0001t0001g0003 a0001c0001t0001g0034 a0001c0001t0001g0037 others(203): Show |
206 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.63+6799C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12070460 | |||||||
| chr1:12070504 | A | G | 3 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 |
3 | HG01099.hp1 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.63+6843A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12070504 | |||||||
| chr1:12070525 | A | G | 5 | a0001c0001t0002g0172 a0001c0002t0001g0166 a0001c0004t0001g0165 others(2): Show |
5 | HG02451.hp1 HG02572.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+6864A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12070525 | |||||||
| chr1:12070557 | C | G | 1 | a0001c0003t0001g0153 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.63+6896C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12070557 | |||||||
| chr1:12070641 | T | C | 8 | a0001c0001t0002g0218 a0001c0001t0007g0216 a0001c0002t0001g0188 others(5): Show |
8 | HG02055.hp1 HG02109.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.63+6980T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12070641 | |||||||
| chr1:12070712 | C | T | 1 | a0001c0003t0001g0153 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.63+7051C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12070712 | |||||||
| chr1:12070754 | T | C | 1 | a0002c0005t0001g0349 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.63+7093T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12070754 | |||||||
| chr1:12071152 | C | T | 6 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(3): Show |
6 | HG01257.hp1 HG01258.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+7491C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12071152 | |||||||
| chr1:12071235 | T | G | 12 | a0001c0001t0001g0203 a0001c0001t0002g0218 a0001c0001t0007g0216 others(9): Show |
12 | HG01243.hp1 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.63+7574T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12071235 | |||||||
| chr1:12071265 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.63+7604C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12071265 | |||||||
| chr1:12071332 | G | A | 1 | a0001c0001t0001g0044 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.63+7671G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12071332 | |||||||
| chr1:12071423 | A | G | 1 | a0001c0001t0001g0300 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.63+7762A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12071423 | |||||||
| chr1:12071447 | A | T | 1 | a0001c0001t0001g0079 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.63+7786A>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12071447 | |||||||
| chr1:12071551 | G | C | 1 | a0001c0001t0001g0300 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.63+7890G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12071551 | |||||||
| chr1:12071624 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.63+7963C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12071624 | |||||||
| chr1:12071632 | C | T | 1 | a0001c0025t0001g0231 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.63+7971C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12071632 | |||||||
| chr1:12071651 | C | T | 1 | a0001c0001t0001g0011 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.63+7990C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12071651 | |||||||
| chr1:12071684 | C | T | 3 | a0001c0001t0002g0224 a0001c0003t0003g0225 a0001c0003t0003g0226 |
3 | HG02895.hp2 HG02897.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.63+8023C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12071684 | |||||||
| chr1:12071713 | G | A | 127 | a0001c0001t0001g0003 a0001c0001t0001g0034 a0001c0001t0001g0037 others(124): Show |
127 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.63+8052G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12071713 | |||||||
| chr1:12071733 | T | C | 1 | a0002c0005t0002g0206 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.63+8072T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12071733 | |||||||
| chr1:12072108 | G | A | 1 | a0001c0025t0001g0231 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.63+8447G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12072108 | |||||||
| chr1:12072362 | G | A | 3 | a0001c0001t0002g0224 a0001c0003t0003g0225 a0001c0003t0003g0226 |
3 | HG02895.hp2 HG02897.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.63+8701G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12072362 | |||||||
| chr1:12072521 | G | C | 1 | a0001c0025t0001g0231 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.63+8860G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12072521 | |||||||
| chr1:12072575 | G | A | 74 | a0001c0001t0001g0040 a0001c0001t0001g0096 a0001c0001t0001g0098 others(71): Show |
74 | HG00280.hp2 HG00558.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.63+8914G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12072575 | |||||||
| chr1:12072663 | T | C | 3 | a0002c0005t0001g0227 a0002c0005t0005g0232 a0002c0016t0004g0228 |
3 | HG03195.hp2 HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.63+9002T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12072663 | |||||||
| chr1:12072668 | G | A | 1 | a0001c0002t0001g0045 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.63+9007G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12072668 | |||||||
| chr1:12072736 | T | C | 3 | a0001c0003t0005g0223 a0002c0006t0001g0222 a0002c0011t0004g0221 |
3 | HG01243.hp1 HG02818.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.63+9075T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12072736 | |||||||
| chr1:12072828 | C | T | 8 | a0001c0002t0001g0166 a0001c0002t0001g0188 a0001c0003t0003g0225 others(5): Show |
8 | HG02257.hp2 HG02559.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.63+9167C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12072828 | |||||||
| chr1:12072876 | G | A | 1 | a0001c0001t0001g0011 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.63+9215G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12072876 | |||||||
| chr1:12072877 | G | A | 3 | a0001c0003t0005g0223 a0002c0006t0001g0222 a0002c0011t0004g0221 |
3 | HG01243.hp1 HG02818.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.63+9216G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12072877 | |||||||
| chr1:12072988 | G | A | 1 | a0001c0001t0001g0344 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.63+9327G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12072988 | |||||||
| chr1:12073026 | G | A | 1 | a0001c0001t0001g0305 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.63+9365G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12073026 | |||||||
| chr1:12073100 | C | T | 8 | a0001c0001t0001g0151 a0001c0001t0006g0148 a0001c0001t0006g0150 others(5): Show |
8 | HG02622.hp1 HG02647.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.63+9439C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12073100 | |||||||
| chr1:12073107 | A | C | 1 | a0001c0002t0001g0078 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.63+9446A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12073107 | |||||||
| chr1:12073264 | A | AAAACAAA others(5): Show |
6 | a0001c0003t0005g0223 a0002c0005t0001g0227 a0002c0005t0005g0232 others(3): Show |
6 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+9605_63+9616dup others(12): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12073264 | ||||||
| chr1:12073284 | C | A | 1 | a0001c0001t0001g0305 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.63+9623C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12073284 | |||||||
| chr1:12073371 | G | A | 6 | a0001c0003t0005g0223 a0002c0005t0001g0227 a0002c0005t0005g0232 others(3): Show |
6 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+9710G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12073371 | |||||||
| chr1:12073417 | A | G | 6 | a0001c0003t0005g0223 a0002c0005t0001g0227 a0002c0005t0005g0232 others(3): Show |
6 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+9756A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12073417 | |||||||
| chr1:12073439 | TTTTCTTC others(24): Show |
T | 6 | a0001c0003t0005g0223 a0002c0005t0001g0227 a0002c0005t0005g0232 others(3): Show |
6 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+9781_63+9811del others(31): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12073439 | ||||||
| chr1:12073476 | C | T | 6 | a0001c0003t0005g0223 a0002c0005t0001g0227 a0002c0005t0005g0232 others(3): Show |
6 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+9815C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12073476 | |||||||
| chr1:12073478 | T | C | 6 | a0001c0003t0005g0223 a0002c0005t0001g0227 a0002c0005t0005g0232 others(3): Show |
6 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+9817T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12073478 | |||||||
| chr1:12073483 | T | TC | 6 | a0001c0003t0005g0223 a0002c0005t0001g0227 a0002c0005t0005g0232 others(3): Show |
6 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+9823dupC | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12073483 | ||||||
| chr1:12073548 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.63+9887C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12073548 | |||||||
| chr1:12073592 | C | CT | 6 | a0001c0001t0002g0172 a0001c0001t0002g0224 a0001c0002t0001g0032 others(3): Show |
6 | HG01256.hp1 HG02257.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+9943dupT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12073592 | ||||||
| chr1:12073592 | CT | C | 7 | a0001c0003t0001g0336 a0001c0003t0005g0223 a0002c0005t0001g0227 others(4): Show |
7 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+9943delT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12073592 | ||||||
| chr1:12073596 | T | C | 1 | a0001c0001t0001g0046 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.63+9935T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12073596 | |||||||
| chr1:12073696 | C | T | 5 | a0001c0001t0001g0293 a0001c0001t0001g0342 a0001c0003t0001g0341 others(2): Show |
5 | HG02080.hp1 NA18969.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+10035C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12073696 | |||||||
| chr1:12073735 | A | G | 19 | a0001c0001t0001g0233 a0001c0001t0002g0218 a0001c0001t0002g0224 others(16): Show |
19 | HG02055.hp1 HG02109.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.63+10074A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12073735 | |||||||
| chr1:12073750 | C | T | 2 | a0001c0001t0001g0342 a0001c0003t0001g0341 |
2 | HG02080.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.63+10089C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12073750 | |||||||
| chr1:12073757 | C | A | 3 | a0001c0003t0003g0225 a0001c0003t0003g0226 a0001c0004t0001g0196 |
3 | HG02257.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.63+10096C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12073757 | |||||||
| chr1:12073770 | A | G | 3 | a0001c0003t0005g0223 a0002c0006t0001g0222 a0002c0011t0004g0221 |
3 | HG01243.hp1 HG02818.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.63+10109A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12073770 | |||||||
| chr1:12073801 | G | A | 6 | a0001c0003t0005g0223 a0002c0005t0001g0227 a0002c0005t0005g0232 others(3): Show |
6 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+10140G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12073801 | |||||||
| chr1:12073810 | G | A | 4 | a0001c0001t0002g0172 a0001c0003t0003g0225 a0001c0003t0003g0226 others(1): Show |
4 | HG02257.hp2 HG02451.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+10149G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12073810 | |||||||
| chr1:12073887 | C | T | 6 | a0001c0003t0005g0223 a0002c0005t0001g0227 a0002c0005t0005g0232 others(3): Show |
6 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+10226C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12073887 | |||||||
| chr1:12073888 | A | G | 6 | a0001c0003t0005g0223 a0002c0005t0001g0227 a0002c0005t0005g0232 others(3): Show |
6 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+10227A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12073888 | |||||||
| chr1:12073892 | A | G | 173 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0037 others(170): Show |
173 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(170): Show |
intron_variant | MODIFIER | c.63+10231A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12073892 | |||||||
| chr1:12073929 | G | A | 6 | a0001c0003t0005g0223 a0002c0005t0001g0227 a0002c0005t0005g0232 others(3): Show |
6 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+10268G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12073929 | |||||||
| chr1:12073953 | C | T | 1 | a0001c0007t0001g0215 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.63+10292C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12073953 | |||||||
| chr1:12073954 | G | A | 1 | a0001c0003t0002g0213 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.63+10293G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12073954 | |||||||
| chr1:12074156 | G | A | 1 | a0001c0003t0002g0213 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.64-10308G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12074156 | |||||||
| chr1:12074163 | TGCTAAAA others(7): Show |
T | 6 | a0001c0003t0005g0223 a0002c0005t0001g0227 a0002c0005t0005g0232 others(3): Show |
6 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-10297_64-10284d others(16): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12074163 | ||||||
| chr1:12074171 | C | T | 2 | a0001c0002t0001g0306 a0001c0004t0001g0291 |
2 | NA18612.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.64-10293C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12074171 | |||||||
| chr1:12074217 | A | G | 6 | a0001c0003t0005g0223 a0002c0005t0001g0227 a0002c0005t0005g0232 others(3): Show |
6 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-10247A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12074217 | |||||||
| chr1:12074282 | T | C | 1 | a0002c0006t0001g0170 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.64-10182T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12074282 | |||||||
| chr1:12074373 | G | A | 1 | a0001c0003t0002g0214 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.64-10091G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12074373 | |||||||
| chr1:12074479 | T | C | 6 | a0001c0003t0005g0223 a0002c0005t0001g0227 a0002c0005t0005g0232 others(3): Show |
6 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-9985T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12074479 | |||||||
| chr1:12074526 | C | T | 7 | a0001c0001t0001g0272 a0001c0001t0001g0296 a0001c0001t0001g0297 others(4): Show |
7 | HG01099.hp2 HG01257.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-9938C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12074526 | |||||||
| chr1:12074527 | G | T | 1 | a0001c0001t0001g0305 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.64-9937G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12074527 | |||||||
| chr1:12074565 | C | G | 3 | a0001c0001t0001g0122 a0001c0002t0001g0117 a0001c0002t0001g0118 |
3 | NA18962.hp1 NA19063.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.64-9899C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12074565 | |||||||
| chr1:12074633 | A | G | 8 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(5): Show |
8 | HG00741.hp1 HG01074.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.64-9831A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12074633 | |||||||
| chr1:12074701 | T | A | 8 | a0001c0001t0001g0201 a0001c0001t0007g0198 a0001c0003t0001g0091 others(5): Show |
8 | HG01167.hp2 HG01192.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.64-9763T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12074701 | |||||||
| chr1:12074743 | A | G | 5 | a0001c0001t0001g0293 a0001c0001t0001g0342 a0001c0003t0001g0341 others(2): Show |
5 | HG02080.hp1 NA18969.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-9721A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12074743 | |||||||
| chr1:12074779 | GTGTT | G | 6 | a0001c0001t0001g0173 a0001c0003t0001g0237 a0001c0003t0002g0200 others(3): Show |
6 | HG01891.hp1 HG02145.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-9671_64-9668del others(4): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12074779 | ||||||
| chr1:12074874 | G | A | 8 | a0001c0001t0001g0151 a0001c0001t0006g0148 a0001c0001t0006g0150 others(5): Show |
8 | HG02622.hp1 HG02647.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.64-9590G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12074874 | |||||||
| chr1:12075093 | G | A | 173 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0037 others(170): Show |
173 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(170): Show |
intron_variant | MODIFIER | c.64-9371G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12075093 | |||||||
| chr1:12075198 | T | C | 6 | a0001c0003t0005g0223 a0002c0005t0001g0227 a0002c0005t0005g0232 others(3): Show |
6 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-9266T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12075198 | |||||||
| chr1:12075241 | C | CA | 9 | a0001c0001t0001g0151 a0001c0001t0006g0148 a0001c0001t0006g0150 others(6): Show |
9 | HG02622.hp1 HG02647.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.64-9213dupA | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12075241 | ||||||
| chr1:12075251 | A | AT | 116 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0037 others(113): Show |
116 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.64-9198dupT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12075251 | ||||||
| chr1:12075268 | A | T | 85 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0037 others(82): Show |
85 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.64-9196A>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12075268 | |||||||
| chr1:12075291 | G | A | 3 | a0001c0003t0003g0225 a0001c0003t0003g0226 a0001c0004t0001g0196 |
3 | HG02257.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.64-9173G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12075291 | |||||||
| chr1:12075300 | G | A | 6 | a0001c0003t0005g0223 a0002c0005t0001g0227 a0002c0005t0005g0232 others(3): Show |
6 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-9164G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12075300 | |||||||
| chr1:12075319 | T | C | 6 | a0001c0003t0005g0223 a0002c0005t0001g0227 a0002c0005t0005g0232 others(3): Show |
6 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-9145T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12075319 | |||||||
| chr1:12075341 | T | C | 6 | a0001c0003t0005g0223 a0002c0005t0001g0227 a0002c0005t0005g0232 others(3): Show |
6 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-9123T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12075341 | |||||||
| chr1:12075352 | C | T | 6 | a0001c0003t0005g0223 a0002c0005t0001g0227 a0002c0005t0005g0232 others(3): Show |
6 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-9112C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12075352 | |||||||
| chr1:12075354 | G | T | 76 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0037 others(73): Show |
76 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.64-9110G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12075354 | |||||||
| chr1:12075362 | G | A | 6 | a0001c0003t0005g0223 a0002c0005t0001g0227 a0002c0005t0005g0232 others(3): Show |
6 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-9102G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12075362 | |||||||
| chr1:12075383 | T | G | 6 | a0001c0003t0005g0223 a0002c0005t0001g0227 a0002c0005t0005g0232 others(3): Show |
6 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-9081T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12075383 | |||||||
| chr1:12075414 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.64-9050G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12075414 | |||||||
| chr1:12075469 | A | G | 169 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0037 others(166): Show |
169 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(166): Show |
intron_variant | MODIFIER | c.64-8995A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12075469 | |||||||
| chr1:12075574 | C | T | 6 | a0001c0003t0005g0223 a0002c0005t0001g0227 a0002c0005t0005g0232 others(3): Show |
6 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-8890C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12075574 | |||||||
| chr1:12075647 | A | T | 1 | a0001c0001t0001g0305 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.64-8817A>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12075647 | |||||||
| chr1:12075680 | C | T | 1 | a0001c0002t0001g0116 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.64-8784C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12075680 | |||||||
| chr1:12075739 | C | T | 6 | a0001c0003t0005g0223 a0002c0005t0001g0227 a0002c0005t0005g0232 others(3): Show |
6 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-8725C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12075739 | |||||||
| chr1:12075761 | C | T | 11 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0287 others(8): Show |
11 | HG02040.hp2 NA18955.hp2 NA18971.hp1 others(8): Show |
intron_variant | MODIFIER | c.64-8703C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12075761 | |||||||
| chr1:12075835 | G | C | 52 | a0001c0001t0001g0138 a0001c0001t0001g0151 a0001c0001t0001g0159 others(49): Show |
52 | HG00738.hp1 HG01081.hp1 HG01106.hp2 others(49): Show |
intron_variant | MODIFIER | c.64-8629G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12075835 | |||||||
| chr1:12075859 | A | T | 52 | a0001c0001t0001g0138 a0001c0001t0001g0151 a0001c0001t0001g0159 others(49): Show |
52 | HG00738.hp1 HG01081.hp1 HG01106.hp2 others(49): Show |
intron_variant | MODIFIER | c.64-8605A>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12075859 | |||||||
| chr1:12075913 | T | C | 6 | a0001c0003t0005g0223 a0002c0005t0001g0227 a0002c0005t0005g0232 others(3): Show |
6 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-8551T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12075913 | |||||||
| chr1:12075921 | C | T | 6 | a0001c0003t0005g0223 a0002c0005t0001g0227 a0002c0005t0005g0232 others(3): Show |
6 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-8543C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12075921 | |||||||
| chr1:12075992 | C | T | 6 | a0001c0001t0001g0286 a0001c0001t0001g0325 a0001c0002t0001g0018 others(3): Show |
6 | HG00438.hp2 HG02056.hp2 NA18985.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-8472C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12075992 | |||||||
| chr1:12076086 | C | CTCT | 77 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0037 others(74): Show |
77 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.64-8377_64-8376ins others(3): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12076086 | ||||||
| chr1:12076087 | T | TC | 4 | a0001c0003t0005g0223 a0002c0005t0001g0227 a0002c0005t0005g0232 others(1): Show |
4 | HG02818.hp1 HG03195.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-8377_64-8376ins others(1): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12076087 | |||||||
| chr1:12076088 | T | C | 2 | a0002c0006t0001g0222 a0002c0011t0004g0221 |
2 | HG01243.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.64-8376T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12076088 | |||||||
| chr1:12076097 | C | CT | 69 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0037 others(66): Show |
69 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.64-8362dupT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12076097 | ||||||
| chr1:12076097 | C | T | 6 | a0001c0003t0005g0223 a0002c0005t0001g0227 a0002c0005t0005g0232 others(3): Show |
6 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-8367C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12076097 | |||||||
| chr1:12076097 | CTTTTTCT others(7): Show |
C | 86 | a0001c0001t0001g0138 a0001c0001t0001g0151 a0001c0001t0001g0159 others(83): Show |
86 | HG00738.hp1 HG01081.hp1 HG01106.hp2 others(83): Show |
intron_variant | MODIFIER | c.64-8361_64-8348del others(14): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12076097 | ||||||
| chr1:12076099 | T | C | 1 | a0001c0003t0005g0223 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.64-8365T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12076099 | |||||||
| chr1:12076100 | T | C | 5 | a0002c0005t0001g0227 a0002c0005t0005g0232 a0002c0006t0001g0222 others(2): Show |
5 | HG01243.hp1 HG03195.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-8364T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12076100 | |||||||
| chr1:12076102 | TC | T | 3 | a0001c0003t0003g0225 a0001c0003t0003g0226 a0001c0004t0001g0196 |
3 | HG02257.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.64-8361delC | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12076102 | |||||||
| chr1:12076103 | C | T | 82 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0037 others(79): Show |
82 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.64-8361C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12076103 | |||||||
| chr1:12076132 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.64-8332C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12076132 | |||||||
| chr1:12076196 | G | A | 6 | a0001c0003t0005g0223 a0002c0005t0001g0227 a0002c0005t0005g0232 others(3): Show |
6 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-8268G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12076196 | |||||||
| chr1:12076203 | C | T | 1 | a0001c0003t0001g0085 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.64-8261C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12076203 | |||||||
| chr1:12076336 | G | A | 75 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0037 others(72): Show |
75 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.64-8128G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12076336 | |||||||
| chr1:12076442 | T | G | 1 | a0002c0006t0001g0170 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.64-8022T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12076442 | |||||||
| chr1:12076670 | T | C | 5 | a0001c0001t0001g0293 a0001c0001t0001g0342 a0001c0003t0001g0341 others(2): Show |
5 | HG02080.hp1 NA18969.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-7794T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12076670 | |||||||
| chr1:12076732 | T | C | 1 | a0001c0025t0001g0231 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.64-7732T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12076732 | |||||||
| chr1:12076865 | G | T | 1 | a0002c0006t0001g0170 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.64-7599G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12076865 | |||||||
| chr1:12076895 | G | T | 2 | a0001c0001t0001g0300 a0001c0001t0001g0330 |
2 | NA18962.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.64-7569G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12076895 | |||||||
| chr1:12076931 | A | G | 6 | a0001c0003t0005g0223 a0002c0005t0001g0227 a0002c0005t0005g0232 others(3): Show |
6 | HG01243.hp1 HG02818.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-7533A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12076931 | |||||||
| chr1:12077008 | C | A | 6 | a0001c0001t0002g0224 a0001c0002t0001g0166 a0001c0002t0001g0188 others(3): Show |
6 | HG02559.hp2 HG02572.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-7456C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12077008 | |||||||
| chr1:12077011 | G | A | 1 | a0001c0003t0002g0213 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.64-7453G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12077011 | |||||||
| chr1:12077022 | T | C | 1 | a0002c0006t0003g0149 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.64-7442T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12077022 | |||||||
| chr1:12077124 | G | A | 1 | a0002c0006t0001g0170 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.64-7340G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12077124 | |||||||
| chr1:12077197 | T | C | 1 | a0001c0004t0001g0135 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.64-7267T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12077197 | |||||||
| chr1:12077254 | T | C | 7 | a0001c0003t0005g0223 a0001c0007t0001g0215 a0002c0005t0001g0227 others(4): Show |
7 | HG01243.hp1 HG02622.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-7210T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12077254 | |||||||
| chr1:12077261 | A | G | 7 | a0001c0003t0005g0223 a0001c0007t0001g0215 a0002c0005t0001g0227 others(4): Show |
7 | HG01243.hp1 HG02622.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-7203A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12077261 | |||||||
| chr1:12077302 | G | A | 3 | a0001c0003t0005g0223 a0002c0006t0001g0222 a0002c0011t0004g0221 |
3 | HG01243.hp1 HG02818.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.64-7162G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12077302 | |||||||
| chr1:12077303 | G | C | 7 | a0001c0003t0005g0223 a0001c0007t0001g0215 a0002c0005t0001g0227 others(4): Show |
7 | HG01243.hp1 HG02622.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-7161G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12077303 | |||||||
| chr1:12077382 | G | A | 1 | a0001c0002t0001g0188 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.64-7082G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12077382 | |||||||
| chr1:12077546 | A | C | 76 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0020 others(73): Show |
76 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.64-6918A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12077546 | |||||||
| chr1:12077625 | A | G | 1 | a0001c0001t0001g0258 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.64-6839A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12077625 | |||||||
| chr1:12077640 | G | A | 3 | a0001c0003t0003g0225 a0001c0003t0003g0226 a0001c0004t0001g0196 |
3 | HG02257.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.64-6824G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12077640 | |||||||
| chr1:12077736 | C | A | 7 | a0001c0003t0005g0223 a0001c0007t0001g0215 a0002c0005t0001g0227 others(4): Show |
7 | HG01243.hp1 HG02622.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-6728C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12077736 | |||||||
| chr1:12077822 | G | A | 1 | a0001c0025t0001g0231 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.64-6642G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12077822 | |||||||
| chr1:12077868 | GT | G | 164 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0020 others(161): Show |
164 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(161): Show |
intron_variant | MODIFIER | c.64-6582delT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12077868 | ||||||
| chr1:12077883 | A | T | 1 | a0002c0006t0001g0170 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.64-6581A>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12077883 | |||||||
| chr1:12077892 | C | T | 1 | a0001c0001t0001g0318 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.64-6572C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12077892 | |||||||
| chr1:12077973 | C | T | 19 | a0001c0001t0001g0233 a0001c0001t0002g0218 a0001c0001t0002g0224 others(16): Show |
19 | HG02055.hp1 HG02109.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.64-6491C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12077973 | |||||||
| chr1:12078043 | T | C | 8 | a0001c0003t0005g0223 a0001c0003t0010g0259 a0001c0007t0001g0215 others(5): Show |
8 | HG01243.hp1 HG02622.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-6421T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078043 | |||||||
| chr1:12078110 | G | A | 1 | a0002c0005t0002g0206 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.64-6354G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078110 | |||||||
| chr1:12078137 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.64-6327C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078137 | |||||||
| chr1:12078140 | G | A | 8 | a0001c0003t0005g0223 a0001c0003t0010g0259 a0001c0007t0001g0215 others(5): Show |
8 | HG01243.hp1 HG02622.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-6324G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078140 | |||||||
| chr1:12078149 | C | G | 1 | a0001c0003t0001g0217 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.64-6315C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078149 | |||||||
| chr1:12078280 | T | A | 8 | a0001c0003t0005g0223 a0001c0003t0010g0259 a0001c0007t0001g0215 others(5): Show |
8 | HG01243.hp1 HG02622.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-6184T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078280 | |||||||
| chr1:12078294 | T | A | 22 | a0001c0001t0001g0151 a0001c0001t0001g0173 a0001c0001t0006g0148 others(19): Show |
22 | HG01243.hp1 HG01891.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.64-6170T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078294 | |||||||
| chr1:12078359 | T | C | 8 | a0001c0003t0005g0223 a0001c0003t0010g0259 a0001c0007t0001g0215 others(5): Show |
8 | HG01243.hp1 HG02622.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-6105T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078359 | |||||||
| chr1:12078388 | A | G | 6 | a0001c0001t0001g0173 a0001c0003t0001g0237 a0001c0003t0002g0200 others(3): Show |
6 | HG01891.hp1 HG02145.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-6076A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078388 | |||||||
| chr1:12078409 | T | C | 157 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0020 others(154): Show |
157 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(154): Show |
intron_variant | MODIFIER | c.64-6055T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078409 | |||||||
| chr1:12078437 | G | A | 1 | a0005c0015t0001g0350 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.64-6027G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078437 | |||||||
| chr1:12078437 | G | T | 1 | a0001c0002t0001g0015 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.64-6027G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078437 | |||||||
| chr1:12078438 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.64-6026C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078438 | |||||||
| chr1:12078512 | C | T | 1 | a0001c0003t0001g0217 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.64-5952C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078512 | |||||||
| chr1:12078539 | G | C | 1 | a0001c0002t0001g0340 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.64-5925G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078539 | |||||||
| chr1:12078545 | C | T | 8 | a0001c0003t0005g0223 a0001c0003t0010g0259 a0001c0007t0001g0215 others(5): Show |
8 | HG01243.hp1 HG02622.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-5919C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078545 | |||||||
| chr1:12078572 | A | G | 75 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(72): Show |
75 | HG00280.hp2 HG00642.hp1 HG00738.hp2 others(72): Show |
intron_variant | MODIFIER | c.64-5892A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078572 | |||||||
| chr1:12078626 | C | T | 1 | a0001c0004t0001g0196 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.64-5838C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078626 | |||||||
| chr1:12078630 | A | G | 192 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(189): Show |
192 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.64-5834A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078630 | |||||||
| chr1:12078696 | C | T | 8 | a0001c0003t0005g0223 a0001c0003t0010g0259 a0001c0007t0001g0215 others(5): Show |
8 | HG01243.hp1 HG02622.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-5768C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078696 | |||||||
| chr1:12078744 | G | A | 23 | a0001c0001t0001g0138 a0001c0001t0001g0159 a0001c0001t0001g0201 others(20): Show |
23 | HG01109.hp1 HG01167.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.64-5720G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078744 | |||||||
| chr1:12078758 | C | A | 1 | a0001c0003t0002g0213 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.64-5706C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078758 | |||||||
| chr1:12078761 | C | A | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5703C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078761 | |||||||
| chr1:12078761 | C | T | 1 | a0001c0001t0002g0172 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.64-5703C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078761 | |||||||
| chr1:12078763 | G | C | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5701G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078763 | |||||||
| chr1:12078767 | A | C | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5697A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078767 | |||||||
| chr1:12078769 | T | A | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5695T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078769 | |||||||
| chr1:12078770 | G | C | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5694G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078770 | |||||||
| chr1:12078771 | G | A | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5693G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078771 | |||||||
| chr1:12078772 | G | A | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5692G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078772 | |||||||
| chr1:12078774 | T | G | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5690T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078774 | |||||||
| chr1:12078780 | T | G | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5684T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078780 | |||||||
| chr1:12078781 | T | A | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5683T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078781 | |||||||
| chr1:12078783 | T | G | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5681T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078783 | |||||||
| chr1:12078784 | T | A | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5680T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078784 | |||||||
| chr1:12078787 | C | A | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5677C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078787 | |||||||
| chr1:12078788 | T | A | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5676T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078788 | |||||||
| chr1:12078790 | T | A | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5674T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078790 | |||||||
| chr1:12078791 | T | G | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5673T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078791 | |||||||
| chr1:12078795 | A | G | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5669A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078795 | |||||||
| chr1:12078796 | T | A | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5668T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078796 | |||||||
| chr1:12078797 | T | G | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5667T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078797 | |||||||
| chr1:12078801 | T | C | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5663T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078801 | |||||||
| chr1:12078804 | G | T | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5660G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078804 | |||||||
| chr1:12078806 | TATGGAAA others(6): Show |
T | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5657_64-5645del others(13): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078806 | |||||||
| chr1:12078821 | G | T | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5643G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078821 | |||||||
| chr1:12078824 | C | T | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5640C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078824 | |||||||
| chr1:12078826 | A | C | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5638A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078826 | |||||||
| chr1:12078827 | G | T | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5637G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078827 | |||||||
| chr1:12078829 | A | C | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5635A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078829 | |||||||
| chr1:12078831 | T | C | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5633T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078831 | |||||||
| chr1:12078832 | T | C | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5632T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078832 | |||||||
| chr1:12078833 | G | T | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5631G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078833 | |||||||
| chr1:12078835 | A | C | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5629A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078835 | |||||||
| chr1:12078836 | C | G | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5628C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078836 | |||||||
| chr1:12078839 | C | G | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5625C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078839 | |||||||
| chr1:12078842 | T | G | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5622T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078842 | |||||||
| chr1:12078843 | C | T | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5621C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078843 | |||||||
| chr1:12078846 | C | T | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5618C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078846 | |||||||
| chr1:12078848 | C | G | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.64-5616C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078848 | |||||||
| chr1:12078899 | T | C | 10 | a0001c0001t0001g0257 a0001c0001t0008g0163 a0001c0001t0008g0362 others(7): Show |
10 | HG01243.hp2 HG01433.hp2 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.64-5565T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078899 | |||||||
| chr1:12078998 | C | T | 1 | a0001c0003t0010g0259 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.64-5466C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12078998 | |||||||
| chr1:12079150 | G | A | 1 | a0001c0001t0001g0273 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.64-5314G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12079150 | |||||||
| chr1:12079193 | T | A | 1 | a0001c0001t0002g0172 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.64-5271T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12079193 | |||||||
| chr1:12079447 | C | T | 2 | a0001c0001t0001g0159 a0001c0009t0006g0171 |
2 | HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.64-5017C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12079447 | |||||||
| chr1:12079448 | G | A | 2 | a0001c0004t0025g0356 a0002c0010t0024g0354 |
2 | HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.64-5016G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12079448 | |||||||
| chr1:12079729 | T | C | 1 | a0001c0003t0010g0259 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.64-4735T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12079729 | |||||||
| chr1:12079898 | A | G | 8 | a0001c0003t0005g0223 a0001c0003t0010g0259 a0001c0007t0001g0215 others(5): Show |
8 | HG01243.hp1 HG02622.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-4566A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12079898 | |||||||
| chr1:12079949 | A | ATT | 9 | a0001c0001t0001g0151 a0001c0001t0006g0148 a0001c0001t0006g0150 others(6): Show |
9 | HG02622.hp1 HG02647.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.64-4499_64-4498dup others(2): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12079949 | ||||||
| chr1:12079949 | AT | A | 140 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(137): Show |
140 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.64-4498delT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12079949 | ||||||
| chr1:12079949 | ATT | A | 13 | a0001c0001t0001g0233 a0001c0001t0001g0244 a0001c0001t0002g0218 others(10): Show |
13 | HG01168.hp2 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.64-4499_64-4498del others(2): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12079949 | ||||||
| chr1:12079949 | ATTT | A | 11 | a0001c0001t0001g0257 a0001c0001t0008g0163 a0001c0001t0008g0362 others(8): Show |
11 | HG01243.hp2 HG01433.hp2 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.64-4500_64-4498del others(3): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12079949 | ||||||
| chr1:12079952 | T | A | 3 | a0001c0003t0005g0223 a0002c0006t0001g0222 a0002c0011t0004g0221 |
3 | HG01243.hp1 HG02818.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.64-4512T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12079952 | |||||||
| chr1:12079974 | G | C | 1 | a0002c0010t0001g0345 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.64-4490G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12079974 | |||||||
| chr1:12080060 | C | T | 6 | a0001c0001t0002g0224 a0001c0002t0001g0166 a0001c0004t0001g0165 others(3): Show |
6 | HG02572.hp1 HG02896.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-4404C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12080060 | |||||||
| chr1:12080239 | G | A | 5 | a0001c0001t0002g0224 a0001c0002t0001g0166 a0001c0004t0001g0165 others(2): Show |
5 | HG02572.hp1 HG02896.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-4225G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12080239 | |||||||
| chr1:12080276 | T | C | 1 | a0001c0001t0001g0175 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.64-4188T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12080276 | |||||||
| chr1:12080379 | T | C | 6 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0124 others(3): Show |
6 | HG01081.hp2 HG01175.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-4085T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12080379 | |||||||
| chr1:12080508 | T | C | 5 | a0001c0003t0001g0237 a0001c0003t0002g0200 a0001c0003t0012g0236 others(2): Show |
5 | HG01891.hp1 HG02895.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-3956T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12080508 | |||||||
| chr1:12080519 | G | A | 1 | a0001c0003t0026g0161 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.64-3945G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12080519 | |||||||
| chr1:12080531 | C | T | 70 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0020 others(67): Show |
70 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.64-3933C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12080531 | |||||||
| chr1:12080614 | A | G | 1 | a0001c0003t0001g0219 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.64-3850A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12080614 | |||||||
| chr1:12080667 | C | T | 1 | a0002c0005t0002g0206 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.64-3797C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12080667 | |||||||
| chr1:12080681 | C | T | 8 | a0001c0003t0005g0223 a0001c0003t0010g0259 a0001c0007t0001g0215 others(5): Show |
8 | HG01243.hp1 HG02622.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-3783C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12080681 | |||||||
| chr1:12080812 | A | C | 11 | a0001c0001t0001g0151 a0001c0001t0002g0172 a0001c0001t0006g0148 others(8): Show |
11 | HG02257.hp2 HG02451.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.64-3652A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12080812 | |||||||
| chr1:12080839 | C | T | 8 | a0001c0001t0001g0201 a0001c0001t0007g0198 a0001c0003t0001g0091 others(5): Show |
8 | HG01167.hp2 HG01192.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.64-3625C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12080839 | |||||||
| chr1:12080924 | C | T | 2 | a0001c0001t0008g0163 a0001c0001t0008g0362 |
2 | NA18980.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.64-3540C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12080924 | |||||||
| chr1:12081126 | C | T | 1 | a0001c0003t0002g0213 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.64-3338C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12081126 | |||||||
| chr1:12081264 | G | A | 2 | a0001c0001t0007g0216 a0001c0003t0001g0217 |
2 | HG02451.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.64-3200G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12081264 | |||||||
| chr1:12081285 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.64-3179A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12081285 | |||||||
| chr1:12081332 | A | C | 8 | a0001c0003t0005g0223 a0001c0003t0010g0259 a0001c0007t0001g0215 others(5): Show |
8 | HG01243.hp1 HG02622.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-3132A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12081332 | |||||||
| chr1:12081368 | C | T | 1 | a0001c0002t0001g0317 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.64-3096C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12081368 | |||||||
| chr1:12081404 | A | G | 173 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(170): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.64-3060A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12081404 | |||||||
| chr1:12081458 | C | A | 1 | a0001c0003t0010g0259 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.64-3006C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12081458 | |||||||
| chr1:12081546 | G | A | 10 | a0001c0001t0001g0257 a0001c0001t0008g0163 a0001c0001t0008g0362 others(7): Show |
10 | HG01243.hp2 HG01433.hp2 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.64-2918G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12081546 | |||||||
| chr1:12081657 | C | CA | 94 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(91): Show |
94 | HG00280.hp2 HG00642.hp1 HG00738.hp1 others(91): Show |
intron_variant | MODIFIER | c.64-2795dupA | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12081657 | ||||||
| chr1:12081819 | A | G | 188 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(185): Show |
188 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.64-2645A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12081819 | |||||||
| chr1:12081943 | G | C | 2 | a0001c0001t0001g0342 a0001c0003t0001g0341 |
2 | HG02080.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.64-2521G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12081943 | |||||||
| chr1:12081944 | CCTCTTGC others(19): Show |
C | 46 | a0001c0001t0001g0048 a0001c0001t0001g0138 a0001c0001t0001g0159 others(43): Show |
46 | HG00738.hp1 HG01081.hp1 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.64-2457_64-2432del others(26): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12081944 | ||||||
| chr1:12081947 | C | T | 2 | a0001c0001t0001g0342 a0001c0003t0001g0341 |
2 | HG02080.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.64-2517C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12081947 | |||||||
| chr1:12082060 | T | C | 174 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(171): Show |
174 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.64-2404T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12082060 | |||||||
| chr1:12082064 | C | G | 7 | a0001c0001t0001g0173 a0001c0001t0002g0224 a0001c0002t0001g0166 others(4): Show |
7 | HG02145.hp2 HG02572.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.64-2400C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12082064 | |||||||
| chr1:12082168 | A | G | 70 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0020 others(67): Show |
70 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.64-2296A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12082168 | |||||||
| chr1:12082186 | T | A | 70 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0020 others(67): Show |
70 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.64-2278T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12082186 | |||||||
| chr1:12082195 | A | G | 1 | a0002c0005t0005g0210 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.64-2269A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12082195 | |||||||
| chr1:12082247 | A | G | 1 | a0001c0001t0001g0173 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.64-2217A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12082247 | |||||||
| chr1:12082268 | G | A | 2 | a0001c0003t0001g0153 a0001c0003t0001g0167 |
2 | HG02572.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.64-2196G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12082268 | |||||||
| chr1:12082451 | C | T | 1 | a0003c0008t0001g0087 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.64-2013C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12082451 | |||||||
| chr1:12082549 | C | CA | 157 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(154): Show |
157 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(154): Show |
intron_variant | MODIFIER | c.64-1901dupA | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12082549 | ||||||
| chr1:12082549 | C | CAA | 20 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0173 others(17): Show |
20 | HG00642.hp1 HG01109.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.64-1902_64-1901dup others(2): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 12082549 | ||||||
| chr1:12082561 | A | AC | 4 | a0001c0001t0001g0269 a0001c0001t0001g0342 a0001c0002t0001g0316 others(1): Show |
4 | HG00140.hp2 HG01261.hp1 HG02080.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-1903_64-1902ins others(1): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12082561 | |||||||
| chr1:12082564 | C | A | 9 | a0001c0002t0001g0306 a0001c0003t0001g0237 a0001c0003t0002g0200 others(6): Show |
9 | HG01891.hp1 HG01891.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.64-1900C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12082564 | |||||||
| chr1:12082584 | C | A | 4 | a0001c0003t0005g0223 a0002c0005t0001g0094 a0002c0006t0001g0222 others(1): Show |
4 | HG01243.hp1 HG02818.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-1880C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12082584 | |||||||
| chr1:12082596 | C | T | 9 | a0001c0001t0001g0351 a0001c0001t0005g0355 a0001c0001t0006g0248 others(6): Show |
9 | HG01109.hp1 HG01884.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.64-1868C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12082596 | |||||||
| chr1:12082615 | G | A | 7 | a0001c0001t0001g0173 a0001c0001t0002g0224 a0001c0002t0001g0166 others(4): Show |
7 | HG02145.hp2 HG02572.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.64-1849G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12082615 | |||||||
| chr1:12082623 | G | A | 1 | a0001c0003t0001g0336 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.64-1841G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12082623 | |||||||
| chr1:12082641 | C | T | 95 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(92): Show |
95 | HG00280.hp2 HG00642.hp1 HG00738.hp1 others(92): Show |
intron_variant | MODIFIER | c.64-1823C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12082641 | |||||||
| chr1:12082943 | C | A | 8 | a0001c0003t0005g0223 a0001c0003t0010g0259 a0001c0007t0001g0215 others(5): Show |
8 | HG01243.hp1 HG02622.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-1521C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12082943 | |||||||
| chr1:12083103 | A | G | 1 | a0001c0003t0001g0315 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.64-1361A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12083103 | |||||||
| chr1:12083167 | G | T | 8 | a0001c0001t0001g0201 a0001c0001t0007g0198 a0001c0003t0001g0091 others(5): Show |
8 | HG01167.hp2 HG01192.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.64-1297G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12083167 | |||||||
| chr1:12083318 | G | A | 8 | a0001c0003t0005g0223 a0001c0003t0010g0259 a0001c0007t0001g0215 others(5): Show |
8 | HG01243.hp1 HG02622.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-1146G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12083318 | |||||||
| chr1:12083399 | C | T | 1 | a0002c0005t0002g0206 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.64-1065C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12083399 | |||||||
| chr1:12083411 | C | T | 7 | a0001c0001t0001g0286 a0001c0001t0001g0325 a0001c0002t0001g0018 others(4): Show |
7 | HG00438.hp2 HG02056.hp2 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.64-1053C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12083411 | |||||||
| chr1:12083623 | G | T | 95 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(92): Show |
95 | HG00280.hp2 HG00642.hp1 HG00738.hp1 others(92): Show |
intron_variant | MODIFIER | c.64-841G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12083623 | |||||||
| chr1:12083760 | A | G | 1 | a0001c0003t0001g0179 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.64-704A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12083760 | |||||||
| chr1:12083855 | C | T | 10 | a0001c0001t0001g0257 a0001c0001t0008g0163 a0001c0001t0008g0362 others(7): Show |
10 | HG01243.hp2 HG01433.hp2 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.64-609C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12083855 | |||||||
| chr1:12083884 | G | A | 8 | a0001c0003t0005g0223 a0001c0003t0010g0259 a0001c0007t0001g0215 others(5): Show |
8 | HG01243.hp1 HG02622.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-580G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12083884 | |||||||
| chr1:12083913 | C | T | 1 | a0003c0019t0004g0017 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.64-551C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12083913 | |||||||
| chr1:12083950 | G | A | 2 | a0001c0003t0003g0225 a0001c0003t0003g0226 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.64-514G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12083950 | |||||||
| chr1:12084064 | C | T | 1 | a0001c0003t0010g0259 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.64-400C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12084064 | |||||||
| chr1:12084162 | A | G | 177 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(174): Show |
177 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.64-302A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12084162 | |||||||
| chr1:12084355 | C | A | 8 | a0001c0003t0005g0223 a0001c0003t0010g0259 a0001c0007t0001g0215 others(5): Show |
8 | HG01243.hp1 HG02622.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-109C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12084355 | |||||||
| chr1:12084363 | T | C | 2 | a0001c0001t0008g0163 a0001c0001t0008g0362 |
2 | NA18980.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.64-101T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12084363 | |||||||
| chr1:12084364 | A | G | 1 | a0001c0002t0001g0118 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.64-100A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12084364 | |||||||
| chr1:12084377 | G | A | 46 | a0001c0001t0001g0048 a0001c0001t0001g0138 a0001c0001t0001g0159 others(43): Show |
46 | HG00738.hp1 HG01081.hp1 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.64-87G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12084377 | |||||||
| chr1:12084377 | G | T | 1 | a0001c0004t0001g0164 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.64-87G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 1/14 | chr1 | 12084377 | |||||||
| chr1:12084563 | C | T | 1 | a0001c0001t0001g0141 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.151+12C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12084563 | |||||||
| chr1:12084586 | G | A | 4 | a0001c0001t0001g0030 a0001c0001t0001g0124 a0001c0001t0001g0160 others(1): Show |
4 | HG01256.hp2 HG01258.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.151+35G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12084586 | |||||||
| chr1:12084605 | T | A | 69 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0020 others(66): Show |
69 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.151+54T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12084605 | |||||||
| chr1:12084610 | C | T | 69 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0020 others(66): Show |
69 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.151+59C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12084610 | |||||||
| chr1:12084729 | G | T | 1 | a0002c0006t0001g0090 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.151+178G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12084729 | |||||||
| chr1:12084744 | CTG | C | 69 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0020 others(66): Show |
69 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.151+197_151+198del others(2): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12084744 | ||||||
| chr1:12085007 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.151+456C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12085007 | |||||||
| chr1:12085044 | T | A | 12 | a0001c0001t0001g0257 a0001c0001t0001g0342 a0001c0001t0008g0163 others(9): Show |
12 | HG01243.hp2 HG01433.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.151+493T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12085044 | |||||||
| chr1:12085167 | A | G | 1 | a0001c0004t0001g0196 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.151+616A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12085167 | |||||||
| chr1:12085256 | A | G | 8 | a0001c0003t0005g0223 a0001c0003t0010g0259 a0001c0007t0001g0215 others(5): Show |
8 | HG01243.hp1 HG02622.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.151+705A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12085256 | |||||||
| chr1:12085274 | C | T | 1 | a0001c0001t0001g0011 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.151+723C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12085274 | |||||||
| chr1:12085307 | G | A | 186 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(183): Show |
186 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.151+756G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12085307 | |||||||
| chr1:12085614 | T | C | 8 | a0001c0003t0005g0223 a0001c0003t0010g0259 a0001c0007t0001g0215 others(5): Show |
8 | HG01243.hp1 HG02622.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.151+1063T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12085614 | |||||||
| chr1:12085729 | G | T | 1 | a0001c0001t0001g0173 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.151+1178G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12085729 | |||||||
| chr1:12086040 | G | A | 1 | a0001c0001t0001g0335 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.151+1489G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12086040 | |||||||
| chr1:12086146 | C | T | 10 | a0001c0001t0001g0257 a0001c0001t0008g0163 a0001c0001t0008g0362 others(7): Show |
10 | HG01243.hp2 HG01433.hp2 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.151+1595C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12086146 | |||||||
| chr1:12086148 | C | T | 1 | a0001c0003t0002g0213 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.151+1597C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12086148 | |||||||
| chr1:12086198 | G | A | 9 | a0001c0001t0001g0351 a0001c0001t0005g0355 a0001c0001t0006g0248 others(6): Show |
9 | HG01109.hp1 HG01884.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.151+1647G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12086198 | |||||||
| chr1:12086440 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.151+1889C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12086440 | |||||||
| chr1:12086490 | A | G | 1 | a0001c0002t0001g0309 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.151+1939A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12086490 | |||||||
| chr1:12086538 | A | G | 1 | a0001c0009t0001g0359 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.151+1987A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12086538 | |||||||
| chr1:12086672 | A | C | 1 | a0001c0003t0001g0091 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.151+2121A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12086672 | |||||||
| chr1:12087022 | G | A | 1 | a0001c0001t0002g0172 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.151+2471G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12087022 | |||||||
| chr1:12087074 | T | TATCC | 11 | a0001c0001t0001g0074 a0001c0001t0001g0246 a0001c0001t0001g0289 others(8): Show |
11 | NA18942.hp1 NA18942.hp2 NA18957.hp1 others(8): Show |
intron_variant | MODIFIER | c.151+2575_151+2578d others(6): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12087074 | ||||||
| chr1:12087074 | TATCC | T | 159 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(156): Show |
159 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.151+2575_151+2578d others(6): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12087074 | ||||||
| chr1:12087074 | TATCCATC others(1): Show |
T | 97 | a0001c0001t0001g0020 a0001c0001t0001g0034 a0001c0001t0001g0040 others(94): Show |
97 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.151+2571_151+2578d others(10): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12087074 | ||||||
| chr1:12087074 | TATCCATC others(5): Show |
T | 16 | a0001c0001t0001g0257 a0001c0001t0002g0172 a0001c0001t0008g0163 others(13): Show |
16 | HG01243.hp2 HG01433.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.151+2567_151+2578d others(14): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12087074 | ||||||
| chr1:12087074 | TATCCATC others(13): Show |
T | 24 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(21): Show |
24 | HG00280.hp2 HG00642.hp1 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.151+2559_151+2578d others(22): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12087074 | ||||||
| chr1:12087165 | C | CT | 67 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0020 others(64): Show |
67 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.151+2634dupT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12087165 | ||||||
| chr1:12087165 | C | CTT | 41 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(38): Show |
41 | HG00280.hp2 HG00642.hp1 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.151+2633_151+2634d others(4): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12087165 | ||||||
| chr1:12087165 | CT | C | 21 | a0001c0001t0001g0047 a0001c0001t0001g0124 a0001c0001t0001g0125 others(18): Show |
21 | HG00558.hp2 HG00738.hp1 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.151+2634delT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12087165 | ||||||
| chr1:12087165 | CTTTTTT | C | 9 | a0001c0001t0001g0151 a0001c0001t0006g0148 a0001c0001t0006g0150 others(6): Show |
9 | HG02622.hp1 HG02647.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.151+2629_151+2634d others(8): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12087165 | ||||||
| chr1:12087221 | A | T | 1 | a0001c0003t0012g0199 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.151+2670A>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12087221 | |||||||
| chr1:12087254 | G | A | 34 | a0001c0001t0001g0048 a0001c0001t0001g0138 a0001c0001t0001g0159 others(31): Show |
34 | HG00738.hp1 HG01081.hp1 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.151+2703G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12087254 | |||||||
| chr1:12087357 | G | T | 45 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(42): Show |
45 | HG00280.hp2 HG00642.hp1 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.151+2806G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12087357 | |||||||
| chr1:12087543 | G | A | 1 | a0001c0001t0002g0172 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.151+2992G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12087543 | |||||||
| chr1:12087647 | T | C | 1 | a0001c0002t0001g0053 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.151+3096T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12087647 | |||||||
| chr1:12087696 | G | A | 70 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0020 others(67): Show |
70 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.151+3145G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12087696 | |||||||
| chr1:12087867 | C | T | 3 | a0001c0001t0001g0138 a0001c0001t0009g0089 a0001c0003t0005g0092 |
3 | HG03139.hp1 HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.151+3316C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12087867 | |||||||
| chr1:12087960 | G | A | 1 | a0001c0001t0001g0245 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.151+3409G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12087960 | |||||||
| chr1:12088012 | C | T | 1 | a0001c0004t0001g0348 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.151+3461C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12088012 | |||||||
| chr1:12088014 | C | T | 2 | a0001c0001t0005g0355 a0002c0006t0001g0170 |
2 | HG02615.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.151+3463C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12088014 | |||||||
| chr1:12088015 | G | A | 1 | a0001c0004t0001g0088 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.151+3464G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12088015 | |||||||
| chr1:12088171 | T | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0144 a0001c0003t0001g0143 others(2): Show |
5 | HG02071.hp1 HG02523.hp1 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.151+3620T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12088171 | |||||||
| chr1:12088329 | TA | T | 32 | a0001c0001t0001g0201 a0001c0001t0001g0203 a0001c0001t0001g0257 others(29): Show |
32 | HG01109.hp1 HG01167.hp2 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.151+3780delA | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12088329 | ||||||
| chr1:12088331 | AG | A | 110 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0020 others(107): Show |
110 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.151+3781delG | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12088331 | |||||||
| chr1:12088410 | C | T | 10 | a0001c0001t0001g0257 a0001c0001t0008g0163 a0001c0001t0008g0362 others(7): Show |
10 | HG01243.hp2 HG01433.hp2 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.151+3859C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12088410 | |||||||
| chr1:12088544 | G | A | 10 | a0001c0001t0001g0096 a0001c0001t0008g0163 a0001c0001t0008g0362 others(7): Show |
10 | HG01243.hp2 HG01433.hp2 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.151+3993G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12088544 | |||||||
| chr1:12088604 | A | C | 9 | a0001c0001t0001g0201 a0001c0001t0007g0198 a0001c0003t0001g0091 others(6): Show |
9 | HG01167.hp2 HG01192.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.151+4053A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12088604 | |||||||
| chr1:12088665 | G | A | 2 | a0001c0001t0001g0054 a0001c0001t0001g0068 |
2 | HG00280.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.151+4114G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12088665 | |||||||
| chr1:12088795 | C | T | 1 | a0001c0003t0001g0336 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.151+4244C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12088795 | |||||||
| chr1:12088842 | C | T | 2 | a0001c0001t0001g0040 a0007c0020t0001g0019 |
2 | HG01255.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.151+4291C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12088842 | |||||||
| chr1:12088889 | C | T | 3 | a0001c0002t0001g0112 a0001c0002t0001g0140 a0001c0002t0018g0097 |
3 | HG00597.hp2 HG03704.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.151+4338C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12088889 | |||||||
| chr1:12088923 | G | A | 11 | a0001c0001t0001g0151 a0001c0001t0002g0218 a0001c0001t0006g0148 others(8): Show |
11 | HG02257.hp2 HG02280.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.151+4372G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12088923 | |||||||
| chr1:12088967 | C | G | 1 | a0001c0002t0001g0129 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.151+4416C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12088967 | |||||||
| chr1:12089052 | G | C | 2 | a0001c0003t0002g0213 a0002c0005t0002g0206 |
2 | HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.151+4501G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12089052 | |||||||
| chr1:12089146 | C | T | 9 | a0001c0001t0001g0096 a0001c0001t0008g0163 a0001c0002t0001g0255 others(6): Show |
9 | HG01243.hp2 HG01433.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.151+4595C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12089146 | |||||||
| chr1:12089234 | A | G | 8 | a0001c0001t0001g0173 a0001c0001t0002g0224 a0001c0004t0001g0088 others(5): Show |
8 | HG01891.hp2 HG02145.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.151+4683A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12089234 | |||||||
| chr1:12089238 | C | T | 1 | a0001c0001t0004g0177 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.151+4687C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12089238 | |||||||
| chr1:12089245 | A | G | 9 | a0001c0001t0001g0096 a0001c0001t0008g0163 a0001c0002t0001g0255 others(6): Show |
9 | HG01243.hp2 HG01433.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.151+4694A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12089245 | |||||||
| chr1:12089533 | A | T | 6 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0007g0193 others(3): Show |
6 | HG02615.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.151+4982A>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12089533 | |||||||
| chr1:12089600 | A | C | 2 | a0001c0004t0001g0165 a0001c0004t0001g0168 |
2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.151+5049A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12089600 | |||||||
| chr1:12089684 | G | A | 7 | a0001c0001t0001g0229 a0001c0002t0001g0166 a0001c0003t0002g0213 others(4): Show |
7 | HG01891.hp1 HG02257.hp2 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.151+5133G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12089684 | |||||||
| chr1:12089828 | C | T | 1 | a0001c0001t0001g0003 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.151+5277C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12089828 | |||||||
| chr1:12089829 | ACATCCAT others(102): Show |
A | 1 | a0001c0001t0001g0203 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.151+5313_151+5421d others(2): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12089829 | ||||||
| chr1:12090025 | C | G | 1 | a0001c0001t0001g0180 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.151+5474C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12090025 | |||||||
| chr1:12090030 | C | G | 6 | a0001c0002t0001g0166 a0001c0003t0002g0213 a0001c0004t0001g0196 others(3): Show |
6 | HG02257.hp2 HG03453.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.151+5479C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12090030 | |||||||
| chr1:12090056 | TACCCATC others(5): Show |
T | 10 | a0001c0001t0001g0201 a0001c0001t0002g0224 a0001c0001t0007g0198 others(7): Show |
10 | HG01167.hp2 HG01192.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.151+5507_151+5518d others(14): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12090056 | ||||||
| chr1:12090066 | TCCATCTA others(90): Show |
T | 11 | a0001c0001t0001g0229 a0001c0002t0001g0166 a0001c0003t0001g0219 others(8): Show |
11 | HG01891.hp1 HG02257.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.151+5665_151+5761d others(99): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12090066 | ||||||
| chr1:12090281 | T | C | 1 | a0001c0002t0001g0264 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.151+5730T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12090281 | |||||||
| chr1:12090321 | CCCAT | C | 38 | a0001c0001t0001g0096 a0001c0001t0001g0103 a0001c0001t0001g0229 others(35): Show |
38 | HG00558.hp2 HG01243.hp2 HG01433.hp2 others(35): Show |
intron_variant | MODIFIER | c.151+5790_151+5793d others(6): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12090321 | ||||||
| chr1:12090328 | A | G | 23 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(20): Show |
23 | HG00280.hp2 HG00738.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.151+5777A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12090328 | |||||||
| chr1:12090352 | G | A | 9 | a0001c0001t0001g0096 a0001c0001t0008g0163 a0001c0002t0001g0255 others(6): Show |
9 | HG01243.hp2 HG01433.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.151+5801G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12090352 | |||||||
| chr1:12090361 | TC | T | 3 | a0001c0001t0001g0229 a0001c0003t0001g0219 a0001c0003t0012g0236 |
3 | HG01891.hp1 HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.151+5812delC | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12090361 | ||||||
| chr1:12090431 | A | G | 3 | a0001c0001t0001g0103 a0001c0014t0001g0101 a0004c0028t0021g0113 |
3 | HG00558.hp2 NA18955.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.151+5880A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12090431 | |||||||
| chr1:12090536 | C | T | 1 | a0001c0002t0001g0166 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.151+5985C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12090536 | |||||||
| chr1:12090581 | C | T | 2 | a0001c0002t0001g0239 a0001c0002t0001g0243 |
2 | NA18999.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.151+6030C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12090581 | |||||||
| chr1:12090633 | C | A | 9 | a0001c0001t0001g0096 a0001c0001t0008g0163 a0001c0002t0001g0255 others(6): Show |
9 | HG01243.hp2 HG01433.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.151+6082C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12090633 | |||||||
| chr1:12090685 | A | G | 3 | a0001c0001t0001g0229 a0001c0003t0001g0219 a0001c0003t0012g0236 |
3 | HG01891.hp1 HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.151+6134A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12090685 | |||||||
| chr1:12090772 | C | T | 9 | a0001c0001t0001g0096 a0001c0001t0008g0163 a0001c0002t0001g0255 others(6): Show |
9 | HG01243.hp2 HG01433.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.151+6221C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12090772 | |||||||
| chr1:12090881 | C | A | 9 | a0001c0001t0001g0096 a0001c0001t0008g0163 a0001c0002t0001g0255 others(6): Show |
9 | HG01243.hp2 HG01433.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.152-6220C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12090881 | |||||||
| chr1:12090902 | C | T | 1 | a0001c0002t0001g0188 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.152-6199C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12090902 | |||||||
| chr1:12090909 | C | T | 1 | a0001c0004t0001g0348 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.152-6192C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12090909 | |||||||
| chr1:12091026 | C | T | 1 | a0001c0001t0001g0328 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.152-6075C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12091026 | |||||||
| chr1:12091041 | A | T | 1 | a0001c0004t0001g0348 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.152-6060A>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12091041 | |||||||
| chr1:12091146 | A | G | 1 | a0001c0001t0001g0203 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.152-5955A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12091146 | |||||||
| chr1:12091225 | G | A | 18 | a0001c0001t0001g0103 a0001c0001t0001g0246 a0001c0001t0001g0247 others(15): Show |
18 | HG00558.hp2 HG02040.hp2 HG02895.hp1 others(15): Show |
intron_variant | MODIFIER | c.152-5876G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12091225 | |||||||
| chr1:12091352 | G | A | 7 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0007g0193 others(4): Show |
7 | HG02257.hp1 HG02615.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.152-5749G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12091352 | |||||||
| chr1:12091361 | C | T | 1 | a0002c0005t0002g0206 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.152-5740C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12091361 | |||||||
| chr1:12091374 | T | C | 1 | a0001c0004t0001g0348 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.152-5727T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12091374 | |||||||
| chr1:12091457 | C | G | 1 | a0001c0002t0001g0166 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.152-5644C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12091457 | |||||||
| chr1:12091611 | G | C | 2 | a0001c0002t0001g0166 a0002c0005t0002g0206 |
2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.152-5490G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12091611 | |||||||
| chr1:12091826 | T | C | 1 | a0001c0002t0001g0055 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.152-5275T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12091826 | |||||||
| chr1:12091828 | A | G | 4 | a0001c0003t0002g0213 a0001c0004t0001g0196 a0002c0005t0005g0230 others(1): Show |
4 | HG02257.hp2 HG03453.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.152-5273A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12091828 | |||||||
| chr1:12091869 | A | G | 9 | a0001c0001t0001g0096 a0001c0001t0008g0163 a0001c0002t0001g0255 others(6): Show |
9 | HG01243.hp2 HG01433.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.152-5232A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12091869 | |||||||
| chr1:12092350 | A | G | 9 | a0001c0001t0001g0096 a0001c0001t0008g0163 a0001c0002t0001g0255 others(6): Show |
9 | HG01243.hp2 HG01433.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.152-4751A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12092350 | |||||||
| chr1:12092418 | C | T | 1 | a0001c0003t0001g0336 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.152-4683C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12092418 | |||||||
| chr1:12092509 | C | CT | 20 | a0001c0001t0001g0020 a0001c0001t0001g0086 a0001c0001t0001g0098 others(17): Show |
20 | HG00544.hp2 HG01069.hp2 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.152-4576dupT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12092509 | ||||||
| chr1:12092509 | CT | C | 56 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(53): Show |
56 | HG00280.hp2 HG00438.hp2 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.152-4576delT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12092509 | ||||||
| chr1:12092577 | T | C | 1 | a0001c0002t0001g0188 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.152-4524T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12092577 | |||||||
| chr1:12092757 | C | G | 3 | a0001c0002t0001g0015 a0001c0002t0001g0317 a0002c0006t0008g0162 |
3 | HG00544.hp2 HG02040.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.152-4344C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12092757 | |||||||
| chr1:12092798 | G | A | 19 | a0001c0001t0001g0103 a0001c0001t0001g0203 a0001c0001t0001g0246 others(16): Show |
19 | HG00558.hp2 HG02040.hp2 HG02647.hp2 others(16): Show |
intron_variant | MODIFIER | c.152-4303G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12092798 | |||||||
| chr1:12092808 | T | C | 1 | a0001c0003t0003g0152 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.152-4293T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12092808 | |||||||
| chr1:12092867 | G | A | 9 | a0001c0001t0001g0096 a0001c0001t0008g0163 a0001c0002t0001g0255 others(6): Show |
9 | HG01243.hp2 HG01433.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.152-4234G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12092867 | |||||||
| chr1:12092941 | G | A | 2 | a0001c0002t0001g0166 a0002c0005t0002g0206 |
2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.152-4160G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12092941 | |||||||
| chr1:12093086 | G | A | 4 | a0001c0001t0001g0201 a0001c0003t0001g0091 a0001c0003t0002g0197 others(1): Show |
4 | HG01192.hp1 HG02258.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.152-4015G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093086 | |||||||
| chr1:12093131 | G | A | 234 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(231): Show |
234 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.152-3970G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093131 | |||||||
| chr1:12093257 | T | C | 18 | a0001c0001t0001g0103 a0001c0001t0001g0246 a0001c0001t0001g0247 others(15): Show |
18 | HG00558.hp2 HG02040.hp2 HG02895.hp1 others(15): Show |
intron_variant | MODIFIER | c.152-3844T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093257 | |||||||
| chr1:12093341 | T | C | 1 | a0001c0004t0001g0348 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.152-3760T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093341 | |||||||
| chr1:12093356 | G | T | 20 | a0001c0001t0001g0103 a0001c0001t0001g0203 a0001c0001t0001g0246 others(17): Show |
20 | HG00558.hp2 HG02040.hp2 HG02647.hp2 others(17): Show |
intron_variant | MODIFIER | c.152-3745G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093356 | |||||||
| chr1:12093601 | C | T | 1 | a0001c0004t0001g0348 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.152-3500C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093601 | |||||||
| chr1:12093655 | C | T | 3 | a0001c0001t0001g0229 a0001c0003t0001g0219 a0001c0003t0012g0236 |
3 | HG01891.hp1 HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.152-3446C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093655 | |||||||
| chr1:12093658 | A | G | 10 | a0001c0001t0001g0229 a0001c0002t0001g0166 a0001c0003t0001g0219 others(7): Show |
10 | HG01891.hp1 HG02257.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.152-3443A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093658 | |||||||
| chr1:12093676 | T | G | 221 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(218): Show |
221 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.152-3425T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093676 | |||||||
| chr1:12093697 | C | T | 1 | a0001c0001t0001g0286 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.152-3404C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093697 | |||||||
| chr1:12093746 | G | A | 22 | a0001c0001t0001g0159 a0001c0001t0001g0173 a0001c0001t0002g0172 others(19): Show |
22 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.152-3355G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093746 | |||||||
| chr1:12093752 | G | A | 3 | a0001c0003t0002g0213 a0001c0004t0001g0196 a0002c0012t0023g0353 |
3 | HG02257.hp2 HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.152-3349G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093752 | |||||||
| chr1:12093809 | G | A | 10 | a0001c0001t0001g0201 a0001c0001t0002g0224 a0001c0001t0007g0198 others(7): Show |
10 | HG01167.hp2 HG01192.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.152-3292G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093809 | |||||||
| chr1:12093812 | T | A | 1 | a0002c0005t0001g0094 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.152-3289T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093812 | |||||||
| chr1:12093813 | G | C | 1 | a0002c0005t0001g0094 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.152-3288G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093813 | |||||||
| chr1:12093814 | T | C | 1 | a0002c0005t0001g0094 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.152-3287T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093814 | |||||||
| chr1:12093815 | A | G | 1 | a0002c0005t0001g0094 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.152-3286A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093815 | |||||||
| chr1:12093817 | T | A | 1 | a0002c0005t0001g0094 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.152-3284T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093817 | |||||||
| chr1:12093846 | C | T | 1 | a0001c0004t0010g0202 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.152-3255C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093846 | |||||||
| chr1:12093875 | T | G | 1 | a0002c0005t0001g0094 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.152-3226T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093875 | |||||||
| chr1:12093882 | T | C | 1 | a0002c0005t0001g0094 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.152-3219T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093882 | |||||||
| chr1:12093895 | C | A | 1 | a0001c0001t0002g0172 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.152-3206C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093895 | |||||||
| chr1:12093897 | C | T | 1 | a0002c0005t0001g0094 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.152-3204C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093897 | |||||||
| chr1:12093899 | G | C | 1 | a0002c0005t0001g0094 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.152-3202G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093899 | |||||||
| chr1:12093908 | A | G | 1 | a0002c0005t0001g0094 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.152-3193A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093908 | |||||||
| chr1:12093925 | A | G | 1 | a0002c0005t0001g0094 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.152-3176A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093925 | |||||||
| chr1:12093932 | A | G | 1 | a0002c0005t0001g0094 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.152-3169A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093932 | |||||||
| chr1:12093944 | G | A | 1 | a0002c0005t0001g0094 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.152-3157G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093944 | |||||||
| chr1:12093956 | A | AGTACTGG others(3): Show |
1 | a0002c0005t0001g0094 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.152-3144_152-3143i others(12): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12093956 | ||||||
| chr1:12093983 | T | A | 1 | a0002c0005t0001g0094 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.152-3118T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093983 | |||||||
| chr1:12093991 | G | A | 1 | a0002c0005t0001g0094 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.152-3110G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12093991 | |||||||
| chr1:12094005 | G | A | 1 | a0002c0005t0002g0206 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.152-3096G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12094005 | |||||||
| chr1:12094007 | T | G | 1 | a0002c0005t0001g0094 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.152-3094T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12094007 | |||||||
| chr1:12094013 | C | A | 1 | a0002c0005t0001g0094 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.152-3088C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12094013 | |||||||
| chr1:12094014 | C | G | 1 | a0002c0005t0001g0094 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.152-3087C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12094014 | |||||||
| chr1:12094015 | T | C | 1 | a0002c0005t0001g0094 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.152-3086T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12094015 | |||||||
| chr1:12094026 | T | C | 1 | a0002c0005t0001g0094 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.152-3075T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12094026 | |||||||
| chr1:12094027 | C | G | 1 | a0001c0001t0001g0203 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.152-3074C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12094027 | |||||||
| chr1:12094058 | C | CA | 64 | a0001c0001t0001g0034 a0001c0001t0001g0050 a0001c0001t0001g0058 others(61): Show |
64 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.152-3019dupA | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12094058 | ||||||
| chr1:12094058 | C | CAA | 22 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0014 others(19): Show |
22 | HG00280.hp2 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.152-3020_152-3019d others(4): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12094058 | ||||||
| chr1:12094058 | C | CAAA | 11 | a0001c0001t0006g0248 a0001c0002t0001g0053 a0001c0002t0001g0314 others(8): Show |
11 | HG00738.hp2 HG00741.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.152-3021_152-3019d others(5): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12094058 | ||||||
| chr1:12094058 | C | CAAAA | 11 | a0001c0001t0001g0012 a0001c0001t0001g0096 a0001c0001t0001g0229 others(8): Show |
11 | HG01891.hp1 HG01928.hp2 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.152-3022_152-3019d others(6): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12094058 | ||||||
| chr1:12094058 | CA | C | 105 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(102): Show |
105 | HG00438.hp2 HG00544.hp2 HG00609.hp1 others(102): Show |
intron_variant | MODIFIER | c.152-3019delA | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12094058 | ||||||
| chr1:12094058 | CAA | C | 6 | a0001c0001t0001g0138 a0001c0001t0001g0160 a0001c0001t0009g0089 others(3): Show |
6 | HG01515.hp1 HG03139.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.152-3020_152-3019d others(4): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12094058 | ||||||
| chr1:12094229 | G | T | 1 | a0002c0006t0001g0170 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.152-2872G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12094229 | |||||||
| chr1:12094342 | G | A | 1 | a0001c0017t0014g0265 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.152-2759G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12094342 | |||||||
| chr1:12094613 | G | GT | 28 | a0001c0001t0001g0012 a0001c0001t0001g0038 a0001c0001t0001g0075 others(25): Show |
28 | HG00140.hp2 HG00642.hp2 HG01358.hp2 others(25): Show |
intron_variant | MODIFIER | c.152-2471dupT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12094613 | ||||||
| chr1:12094613 | G | GTT | 23 | a0001c0001t0001g0096 a0001c0001t0001g0159 a0001c0001t0002g0218 others(20): Show |
23 | HG01243.hp2 HG01433.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.152-2472_152-2471d others(4): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12094613 | ||||||
| chr1:12094620 | TTTTTTTT others(5): Show |
T | 19 | a0001c0001t0001g0103 a0001c0001t0001g0246 a0001c0001t0001g0247 others(16): Show |
19 | HG00558.hp2 HG02040.hp2 HG02895.hp1 others(16): Show |
intron_variant | MODIFIER | c.152-2470_152-2459d others(14): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12094620 | ||||||
| chr1:12094689 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.152-2412G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12094689 | |||||||
| chr1:12094776 | C | T | 1 | a0009c0030t0001g0120 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.152-2325C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12094776 | |||||||
| chr1:12094921 | C | T | 11 | a0001c0001t0001g0096 a0001c0001t0008g0163 a0001c0001t0009g0234 others(8): Show |
11 | HG01243.hp2 HG01433.hp2 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.152-2180C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12094921 | |||||||
| chr1:12095014 | C | G | 23 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(20): Show |
23 | HG00280.hp2 HG00738.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.152-2087C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12095014 | |||||||
| chr1:12095200 | T | C | 1 | a0001c0002t0001g0032 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.152-1901T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12095200 | |||||||
| chr1:12095231 | G | A | 9 | a0001c0001t0001g0096 a0001c0001t0008g0163 a0001c0002t0001g0255 others(6): Show |
9 | HG01243.hp2 HG01433.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.152-1870G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12095231 | |||||||
| chr1:12095289 | CT | C | 24 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(21): Show |
24 | HG00280.hp2 HG00738.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.152-1797delT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12095289 | ||||||
| chr1:12095433 | G | A | 2 | a0001c0007t0001g0215 a0001c0007t0009g0357 |
2 | HG02622.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.152-1668G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12095433 | |||||||
| chr1:12095436 | T | C | 2 | a0001c0007t0001g0215 a0001c0007t0009g0357 |
2 | HG02622.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.152-1665T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12095436 | |||||||
| chr1:12095437 | G | A | 2 | a0001c0007t0001g0215 a0001c0007t0009g0357 |
2 | HG02622.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.152-1664G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12095437 | |||||||
| chr1:12095442 | G | C | 2 | a0001c0007t0001g0215 a0001c0007t0009g0357 |
2 | HG02622.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.152-1659G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12095442 | |||||||
| chr1:12095445 | A | T | 2 | a0001c0007t0001g0215 a0001c0007t0009g0357 |
2 | HG02622.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.152-1656A>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12095445 | |||||||
| chr1:12095588 | T | C | 2 | a0001c0001t0009g0234 a0001c0002t0001g0188 |
2 | HG02055.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.152-1513T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12095588 | |||||||
| chr1:12095640 | T | C | 1 | a0001c0001t0001g0330 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.152-1461T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12095640 | |||||||
| chr1:12095650 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.152-1451C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12095650 | |||||||
| chr1:12095654 | A | G | 1 | a0001c0003t0002g0213 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.152-1447A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12095654 | |||||||
| chr1:12095784 | A | G | 1 | a0001c0025t0001g0231 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.152-1317A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12095784 | |||||||
| chr1:12096175 | G | A | 1 | a0001c0001t0001g0258 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.152-926G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12096175 | |||||||
| chr1:12096179 | A | G | 24 | a0001c0001t0001g0038 a0001c0001t0001g0048 a0001c0001t0001g0138 others(21): Show |
24 | HG00738.hp1 HG01081.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.152-922A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12096179 | |||||||
| chr1:12096253 | C | T | 1 | a0001c0001t0002g0218 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.152-848C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12096253 | |||||||
| chr1:12096411 | A | G | 111 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(108): Show |
111 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.152-690A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12096411 | |||||||
| chr1:12096424 | T | TA | 55 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0014 others(52): Show |
55 | HG00280.hp2 HG00738.hp1 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.152-657dupA | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12096424 | ||||||
| chr1:12096424 | TA | T | 127 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(124): Show |
127 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.152-657delA | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12096424 | ||||||
| chr1:12096424 | TAA | T | 45 | a0001c0001t0001g0103 a0001c0001t0001g0159 a0001c0001t0001g0246 others(42): Show |
45 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.152-658_152-657del others(2): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12096424 | ||||||
| chr1:12096453 | A | G | 1 | a0001c0003t0001g0253 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.152-648A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12096453 | |||||||
| chr1:12096622 | A | G | 1 | a0002c0006t0001g0155 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.152-479A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12096622 | |||||||
| chr1:12096651 | G | C | 10 | a0001c0001t0001g0096 a0001c0001t0008g0163 a0001c0002t0001g0255 others(7): Show |
10 | HG01243.hp2 HG01433.hp2 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.152-450G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12096651 | |||||||
| chr1:12096715 | C | T | 16 | a0001c0001t0001g0159 a0001c0001t0002g0218 a0001c0001t0006g0248 others(13): Show |
16 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.152-386C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12096715 | |||||||
| chr1:12096789 | T | TCA | 17 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0203 others(14): Show |
17 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.152-295_152-294dup others(2): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12096789 | ||||||
| chr1:12096789 | TCA | T | 50 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(47): Show |
50 | HG00280.hp2 HG00738.hp1 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.152-295_152-294del others(2): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 12096789 | ||||||
| chr1:12096810 | T | C | 2 | a0001c0003t0002g0213 a0001c0004t0001g0196 |
2 | HG02257.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.152-291T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12096810 | |||||||
| chr1:12096913 | G | A | 1 | a0001c0002t0001g0334 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.152-188G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12096913 | |||||||
| chr1:12096980 | C | T | 4 | a0001c0001t0006g0148 a0001c0001t0006g0150 a0001c0002t0002g0147 others(1): Show |
4 | HG02622.hp1 HG02723.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.152-121C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12096980 | |||||||
| chr1:12097019 | A | C | 19 | a0001c0001t0001g0048 a0001c0001t0001g0151 a0001c0001t0001g0175 others(16): Show |
19 | HG00738.hp1 HG01081.hp1 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.152-82A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 2/14 | chr1 | 12097019 | |||||||
| chr1:12097231 | T | C | 21 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0014 others(18): Show |
21 | HG00280.hp2 HG00738.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.268+14T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12097231 | |||||||
| chr1:12097264 | G | C | 12 | a0001c0001t0001g0047 a0001c0001t0001g0096 a0001c0001t0008g0163 others(9): Show |
12 | HG01243.hp2 HG01433.hp2 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.268+47G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12097264 | |||||||
| chr1:12097683 | C | T | 2 | a0001c0001t0008g0163 a0001c0004t0001g0348 |
2 | HG03942.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.268+466C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12097683 | |||||||
| chr1:12097749 | G | C | 1 | a0001c0003t0012g0236 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.268+532G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12097749 | |||||||
| chr1:12097824 | G | A | 9 | a0001c0001t0001g0058 a0001c0002t0001g0043 a0001c0002t0001g0078 others(6): Show |
9 | HG00323.hp2 HG00741.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.268+607G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12097824 | |||||||
| chr1:12097869 | G | A | 1 | a0001c0002t0001g0266 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.268+652G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12097869 | |||||||
| chr1:12097870 | T | C | 2 | a0001c0003t0003g0225 a0001c0003t0003g0226 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.268+653T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12097870 | |||||||
| chr1:12098021 | G | C | 10 | a0001c0001t0001g0201 a0001c0001t0006g0358 a0001c0001t0007g0198 others(7): Show |
10 | HG01192.hp1 HG01884.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.268+804G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12098021 | |||||||
| chr1:12098237 | A | C | 1 | a0001c0001t0001g0318 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.268+1020A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12098237 | |||||||
| chr1:12098250 | T | C | 36 | a0001c0002t0001g0027 a0001c0002t0001g0031 a0001c0002t0001g0043 others(33): Show |
36 | HG00323.hp2 HG00741.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.268+1033T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12098250 | |||||||
| chr1:12098255 | A | G | 13 | a0001c0001t0001g0013 a0001c0001t0001g0034 a0001c0001t0001g0044 others(10): Show |
13 | HG02258.hp1 NA18953.hp1 NA18961.hp2 others(10): Show |
intron_variant | MODIFIER | c.268+1038A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12098255 | |||||||
| chr1:12098431 | A | G | 1 | a0001c0001t0004g0177 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.268+1214A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12098431 | |||||||
| chr1:12098510 | C | T | 22 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0034 others(19): Show |
22 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.268+1293C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12098510 | |||||||
| chr1:12098546 | T | C | 4 | a0001c0003t0001g0252 a0001c0003t0001g0253 a0001c0003t0003g0211 others(1): Show |
4 | HG01884.hp1 HG01884.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.268+1329T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12098546 | |||||||
| chr1:12098677 | TA | T | 80 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0233 others(77): Show |
80 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.268+1471delA | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 12098677 | ||||||
| chr1:12099014 | C | G | 3 | a0001c0001t0001g0346 a0001c0003t0001g0276 a0001c0013t0001g0251 |
3 | NA18967.hp2 NA18989.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.268+1797C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12099014 | |||||||
| chr1:12099214 | AAT | A | 4 | a0001c0001t0001g0233 a0001c0009t0001g0359 a0001c0009t0001g0360 others(1): Show |
4 | HG02145.hp1 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.268+1998_268+1999d others(4): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12099214 | |||||||
| chr1:12099301 | C | T | 79 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0233 others(76): Show |
79 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.268+2084C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12099301 | |||||||
| chr1:12099375 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.268+2158C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12099375 | |||||||
| chr1:12099763 | C | A | 22 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0034 others(19): Show |
22 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.268+2546C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12099763 | |||||||
| chr1:12099851 | C | G | 5 | a0001c0001t0001g0151 a0001c0001t0001g0351 a0001c0003t0002g0197 others(2): Show |
5 | HG01109.hp1 HG02647.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.268+2634C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12099851 | |||||||
| chr1:12099891 | G | A | 9 | a0001c0001t0001g0203 a0001c0001t0001g0229 a0001c0001t0016g0194 others(6): Show |
9 | HG02630.hp2 HG02647.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.268+2674G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12099891 | |||||||
| chr1:12100028 | G | A | 5 | a0001c0001t0001g0005 a0001c0003t0001g0143 a0001c0003t0001g0145 others(2): Show |
5 | HG00544.hp1 HG02071.hp1 NA18997.hp2 others(2): Show |
intron_variant | MODIFIER | c.268+2811G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12100028 | |||||||
| chr1:12100033 | G | T | 1 | a0001c0007t0001g0215 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.268+2816G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12100033 | |||||||
| chr1:12100050 | T | C | 6 | a0001c0001t0001g0233 a0001c0002t0001g0166 a0001c0004t0010g0202 others(3): Show |
6 | HG02145.hp1 HG02258.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.268+2833T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12100050 | |||||||
| chr1:12100124 | A | G | 110 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0013 others(107): Show |
110 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.268+2907A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12100124 | |||||||
| chr1:12100388 | A | G | 1 | a0001c0001t0001g0050 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.268+3171A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12100388 | |||||||
| chr1:12100449 | TG | T | 32 | a0001c0001t0001g0138 a0001c0001t0001g0159 a0001c0001t0001g0190 others(29): Show |
32 | HG01192.hp1 HG02109.hp2 HG02257.hp1 others(29): Show |
intron_variant | MODIFIER | c.268+3233delG | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12100449 | |||||||
| chr1:12100680 | C | T | 24 | a0001c0001t0001g0159 a0001c0001t0001g0201 a0001c0001t0001g0203 others(21): Show |
24 | HG01192.hp1 HG02109.hp2 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.268+3463C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12100680 | |||||||
| chr1:12100789 | T | G | 1 | a0001c0002t0001g0004 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.268+3572T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12100789 | |||||||
| chr1:12100849 | C | T | 1 | a0001c0003t0001g0139 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.269-3530C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12100849 | |||||||
| chr1:12100882 | G | A | 1 | a0001c0002t0001g0035 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.269-3497G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12100882 | |||||||
| chr1:12100889 | G | A | 80 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0233 others(77): Show |
80 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.269-3490G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12100889 | |||||||
| chr1:12100956 | CA | C | 25 | a0001c0001t0001g0173 a0001c0001t0002g0172 a0001c0001t0002g0218 others(22): Show |
25 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.269-3407delA | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 12100956 | ||||||
| chr1:12100956 | CAA | C | 137 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0013 others(134): Show |
137 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.269-3408_269-3407d others(4): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 12100956 | ||||||
| chr1:12101004 | C | T | 1 | a0001c0002t0001g0095 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.269-3375C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12101004 | |||||||
| chr1:12101186 | A | C | 2 | a0001c0009t0001g0359 a0001c0009t0001g0360 |
2 | HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.269-3193A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12101186 | |||||||
| chr1:12101416 | G | C | 1 | a0001c0002t0001g0314 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.269-2963G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12101416 | |||||||
| chr1:12101426 | C | CA | 25 | a0001c0001t0001g0030 a0001c0001t0001g0124 a0001c0001t0001g0160 others(22): Show |
25 | HG01256.hp2 HG01258.hp2 HG01515.hp1 others(22): Show |
intron_variant | MODIFIER | c.269-2941dupA | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 12101426 | ||||||
| chr1:12101426 | C | CAA | 121 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0013 others(118): Show |
121 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.269-2942_269-2941d others(4): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 12101426 | ||||||
| chr1:12101426 | C | CAAA | 8 | a0001c0001t0001g0203 a0001c0001t0001g0229 a0001c0001t0016g0194 others(5): Show |
8 | HG02630.hp2 HG02647.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.269-2943_269-2941d others(5): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 12101426 | ||||||
| chr1:12101561 | G | A | 2 | a0001c0001t0001g0138 a0001c0001t0009g0089 |
2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.269-2818G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12101561 | |||||||
| chr1:12101609 | A | G | 1 | a0001c0003t0003g0208 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.269-2770A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12101609 | |||||||
| chr1:12101686 | GT | G | 117 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0138 others(114): Show |
117 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.269-2685delT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 12101686 | ||||||
| chr1:12101695 | G | T | 22 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0034 others(19): Show |
22 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.269-2684G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12101695 | |||||||
| chr1:12101828 | T | G | 77 | a0001c0001t0006g0150 a0001c0002t0001g0004 a0001c0002t0001g0010 others(74): Show |
77 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.269-2551T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12101828 | |||||||
| chr1:12101863 | C | T | 7 | a0001c0001t0001g0093 a0001c0001t0001g0262 a0001c0001t0001g0271 others(4): Show |
7 | HG01257.hp1 HG02280.hp1 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.269-2516C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12101863 | |||||||
| chr1:12101964 | C | T | 23 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0034 others(20): Show |
23 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.269-2415C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12101964 | |||||||
| chr1:12102289 | G | A | 1 | a0001c0001t0001g0343 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.269-2090G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12102289 | |||||||
| chr1:12102290 | C | T | 1 | a0002c0016t0004g0228 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.269-2089C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12102290 | |||||||
| chr1:12102301 | G | A | 4 | a0001c0001t0006g0150 a0001c0009t0001g0359 a0001c0009t0001g0360 others(1): Show |
4 | HG02145.hp1 HG02622.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.269-2078G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12102301 | |||||||
| chr1:12102349 | T | C | 1 | a0002c0005t0005g0230 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.269-2030T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12102349 | |||||||
| chr1:12102422 | C | T | 1 | a0001c0003t0002g0214 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.269-1957C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12102422 | |||||||
| chr1:12102512 | CA | C | 6 | a0001c0001t0001g0201 a0001c0001t0007g0198 a0001c0003t0001g0091 others(3): Show |
6 | HG01192.hp1 HG02451.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.269-1866delA | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12102512 | |||||||
| chr1:12102535 | G | A | 3 | a0001c0001t0001g0138 a0001c0001t0009g0089 a0001c0003t0002g0214 |
3 | HG03041.hp1 HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.269-1844G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12102535 | |||||||
| chr1:12102610 | C | T | 1 | a0001c0003t0002g0213 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.269-1769C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12102610 | |||||||
| chr1:12102778 | G | A | 101 | a0001c0002t0001g0004 a0001c0002t0001g0010 a0001c0002t0001g0015 others(98): Show |
101 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.269-1601G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12102778 | |||||||
| chr1:12102977 | C | T | 7 | a0001c0001t0001g0229 a0001c0001t0016g0194 a0001c0003t0003g0208 others(4): Show |
7 | HG02630.hp2 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.269-1402C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12102977 | |||||||
| chr1:12102999 | G | T | 2 | a0001c0007t0001g0215 a0001c0007t0009g0357 |
2 | HG02622.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.269-1380G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12102999 | |||||||
| chr1:12103130 | G | A | 1 | a0001c0003t0002g0213 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.269-1249G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12103130 | |||||||
| chr1:12103224 | C | T | 22 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0034 others(19): Show |
22 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.269-1155C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12103224 | |||||||
| chr1:12103231 | G | T | 22 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0034 others(19): Show |
22 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.269-1148G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12103231 | |||||||
| chr1:12103303 | C | T | 1 | a0001c0004t0001g0196 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.269-1076C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12103303 | |||||||
| chr1:12103311 | C | T | 1 | a0001c0001t0006g0150 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.269-1068C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12103311 | |||||||
| chr1:12103354 | TA | T | 32 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0034 others(29): Show |
32 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(29): Show |
intron_variant | MODIFIER | c.269-1012delA | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 12103354 | ||||||
| chr1:12103496 | G | A | 4 | a0001c0001t0001g0159 a0001c0001t0005g0355 a0001c0003t0010g0259 others(1): Show |
4 | HG02615.hp2 HG02965.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.269-883G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12103496 | |||||||
| chr1:12103534 | A | G | 123 | a0001c0001t0001g0151 a0001c0001t0001g0159 a0001c0001t0001g0190 others(120): Show |
123 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.269-845A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12103534 | |||||||
| chr1:12103582 | G | A | 10 | a0001c0001t0001g0034 a0001c0001t0001g0190 a0001c0001t0001g0191 others(7): Show |
10 | HG02080.hp2 HG02257.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.269-797G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12103582 | |||||||
| chr1:12103626 | T | G | 22 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0034 others(19): Show |
22 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.269-753T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12103626 | |||||||
| chr1:12103644 | AT | A | 23 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0034 others(20): Show |
23 | HG00642.hp2 HG01168.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.269-725delT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 12103644 | ||||||
| chr1:12103662 | C | T | 106 | a0001c0002t0001g0004 a0001c0002t0001g0010 a0001c0002t0001g0015 others(103): Show |
106 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.269-717C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12103662 | |||||||
| chr1:12103717 | A | G | 1 | a0001c0003t0005g0092 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.269-662A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12103717 | |||||||
| chr1:12103773 | G | A | 4 | a0001c0001t0001g0159 a0001c0001t0005g0355 a0001c0003t0010g0259 others(1): Show |
4 | HG02615.hp2 HG02965.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.269-606G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12103773 | |||||||
| chr1:12103961 | A | G | 1 | a0001c0003t0002g0213 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.269-418A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12103961 | |||||||
| chr1:12104014 | T | C | 194 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0034 others(191): Show |
194 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(191): Show |
intron_variant | MODIFIER | c.269-365T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12104014 | |||||||
| chr1:12104021 | C | T | 143 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0034 others(140): Show |
143 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.269-358C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12104021 | |||||||
| chr1:12104022 | C | A | 22 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0034 others(19): Show |
22 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.269-357C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12104022 | |||||||
| chr1:12104033 | C | G | 1 | a0001c0002t0001g0133 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.269-346C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12104033 | |||||||
| chr1:12104033 | C | T | 51 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(48): Show |
51 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.269-346C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12104033 | |||||||
| chr1:12104080 | A | G | 143 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0034 others(140): Show |
143 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.269-299A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12104080 | |||||||
| chr1:12104153 | A | G | 5 | a0001c0001t0002g0218 a0001c0001t0007g0192 a0001c0001t0007g0193 others(2): Show |
5 | HG02055.hp1 HG02280.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.269-226A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12104153 | |||||||
| chr1:12104285 | G | A | 1 | a0001c0001t0007g0198 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.269-94G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12104285 | |||||||
| chr1:12104334 | G | C | 22 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0034 others(19): Show |
22 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.269-45G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 3/14 | chr1 | 12104334 | |||||||
| chr1:12104575 | T | C | 1 | a0001c0001t0008g0362 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.421+44T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12104575 | |||||||
| chr1:12104617 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.421+86C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12104617 | |||||||
| chr1:12104618 | G | A | 22 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0034 others(19): Show |
22 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.421+87G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12104618 | |||||||
| chr1:12104633 | G | T | 1 | a0001c0004t0025g0356 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.421+102G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12104633 | |||||||
| chr1:12104714 | C | A | 5 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0006g0150 others(2): Show |
5 | HG02257.hp1 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.421+183C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12104714 | |||||||
| chr1:12104751 | C | G | 1 | a0002c0016t0004g0228 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.421+220C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12104751 | |||||||
| chr1:12104818 | C | A | 5 | a0001c0001t0002g0218 a0001c0001t0007g0192 a0001c0001t0007g0193 others(2): Show |
5 | HG02055.hp1 HG02280.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.421+287C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12104818 | |||||||
| chr1:12104921 | G | A | 1 | a0001c0009t0001g0360 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.421+390G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12104921 | |||||||
| chr1:12104980 | T | C | 129 | a0001c0001t0001g0138 a0001c0001t0001g0201 a0001c0001t0001g0203 others(126): Show |
129 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.421+449T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12104980 | |||||||
| chr1:12104981 | C | T | 1 | a0001c0002t0001g0134 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.421+450C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12104981 | |||||||
| chr1:12105007 | C | T | 2 | a0002c0005t0001g0227 a0002c0005t0005g0232 |
2 | HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.421+476C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12105007 | |||||||
| chr1:12105034 | A | AC | 5 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0002g0172 others(2): Show |
5 | HG02257.hp1 HG02451.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.421+504dupC | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 12105034 | ||||||
| chr1:12105073 | G | A | 22 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0034 others(19): Show |
22 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.421+542G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12105073 | |||||||
| chr1:12105191 | C | G | 22 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0034 others(19): Show |
22 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.421+660C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12105191 | |||||||
| chr1:12105308 | G | A | 4 | a0001c0001t0001g0159 a0001c0001t0005g0355 a0001c0003t0010g0259 others(1): Show |
4 | HG02615.hp2 HG02965.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.421+777G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12105308 | |||||||
| chr1:12105316 | C | G | 3 | a0001c0003t0002g0197 a0001c0003t0005g0092 a0002c0006t0003g0149 |
3 | HG03130.hp1 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.421+785C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12105316 | |||||||
| chr1:12105426 | C | T | 3 | a0001c0003t0001g0237 a0001c0003t0002g0200 a0002c0006t0001g0222 |
3 | HG01243.hp1 HG02895.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.421+895C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12105426 | |||||||
| chr1:12105527 | C | CCT | 3 | a0001c0004t0002g0169 a0001c0013t0001g0280 a0002c0011t0004g0221 |
3 | HG02717.hp2 NA19082.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.421+1018_421+1019d others(4): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 12105527 | ||||||
| chr1:12105527 | C | CCTCT | 21 | a0001c0001t0001g0011 a0001c0001t0001g0034 a0001c0001t0001g0044 others(18): Show |
21 | HG00642.hp2 HG01109.hp1 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.421+1016_421+1019d others(6): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 12105527 | ||||||
| chr1:12105527 | C | CCTCTCT | 4 | a0001c0001t0001g0013 a0001c0001t0001g0342 a0002c0012t0001g0178 others(1): Show |
4 | HG03471.hp1 NA18990.hp2 NA19087.hp1 others(1): Show |
intron_variant | MODIFIER | c.421+1014_421+1019d others(8): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 12105527 | ||||||
| chr1:12105527 | CCTCT | C | 7 | a0001c0002t0001g0010 a0001c0002t0001g0045 a0001c0002t0001g0065 others(4): Show |
7 | HG00323.hp1 HG01261.hp1 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.421+1016_421+1019d others(6): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 12105527 | ||||||
| chr1:12105527 | CCTCTCTC others(1): Show |
C | 9 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0233 others(6): Show |
9 | HG02109.hp2 HG02257.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.421+1012_421+1019d others(10): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 12105527 | ||||||
| chr1:12105547 | T | A | 92 | a0001c0002t0001g0004 a0001c0002t0001g0015 a0001c0002t0001g0016 others(89): Show |
92 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.421+1016T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12105547 | |||||||
| chr1:12105558 | C | G | 1 | a0001c0001t0008g0362 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.421+1027C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12105558 | |||||||
| chr1:12105559 | A | T | 92 | a0001c0002t0001g0004 a0001c0002t0001g0015 a0001c0002t0001g0016 others(89): Show |
92 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.421+1028A>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12105559 | |||||||
| chr1:12105566 | C | G | 92 | a0001c0002t0001g0004 a0001c0002t0001g0015 a0001c0002t0001g0016 others(89): Show |
92 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.421+1035C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12105566 | |||||||
| chr1:12105570 | G | C | 92 | a0001c0002t0001g0004 a0001c0002t0001g0015 a0001c0002t0001g0016 others(89): Show |
92 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.421+1039G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12105570 | |||||||
| chr1:12105571 | T | A | 92 | a0001c0002t0001g0004 a0001c0002t0001g0015 a0001c0002t0001g0016 others(89): Show |
92 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.421+1040T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12105571 | |||||||
| chr1:12105573 | T | A | 92 | a0001c0002t0001g0004 a0001c0002t0001g0015 a0001c0002t0001g0016 others(89): Show |
92 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.421+1042T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12105573 | |||||||
| chr1:12105573 | T | TCA | 6 | a0001c0001t0001g0151 a0001c0001t0001g0351 a0001c0001t0002g0218 others(3): Show |
6 | HG01109.hp1 HG02055.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.421+1066_421+1067d others(4): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 12105573 | ||||||
| chr1:12105573 | T | TCACA | 177 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(174): Show |
177 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.421+1064_421+1067d others(6): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 12105573 | ||||||
| chr1:12105573 | T | TCACACA | 24 | a0001c0001t0001g0093 a0001c0001t0001g0125 a0001c0001t0001g0126 others(21): Show |
24 | HG00323.hp1 HG01168.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.421+1062_421+1067d others(8): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 12105573 | ||||||
| chr1:12105573 | TCA | T | 22 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0034 others(19): Show |
22 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.421+1066_421+1067d others(4): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 12105573 | ||||||
| chr1:12105939 | C | CA | 52 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0020 others(49): Show |
52 | HG00642.hp2 HG01106.hp2 HG01168.hp2 others(49): Show |
intron_variant | MODIFIER | c.421+1427dupA | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 12105939 | ||||||
| chr1:12105939 | CA | C | 8 | a0001c0002t0001g0078 a0001c0003t0001g0249 a0001c0003t0001g0253 others(5): Show |
8 | HG00323.hp2 HG01515.hp2 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.421+1427delA | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 12105939 | ||||||
| chr1:12105953 | A | G | 1 | a0002c0010t0001g0146 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.421+1422A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12105953 | |||||||
| chr1:12106040 | G | A | 2 | a0001c0007t0001g0215 a0001c0007t0009g0357 |
2 | HG02622.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.421+1509G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12106040 | |||||||
| chr1:12106097 | A | C | 1 | a0001c0003t0010g0259 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.421+1566A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12106097 | |||||||
| chr1:12106112 | C | T | 22 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0034 others(19): Show |
22 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.421+1581C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12106112 | |||||||
| chr1:12106149 | A | G | 8 | a0001c0002t0001g0166 a0001c0004t0001g0036 a0001c0004t0010g0202 others(5): Show |
8 | HG01106.hp2 HG02145.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.421+1618A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12106149 | |||||||
| chr1:12106309 | G | T | 10 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0233 others(7): Show |
10 | HG02109.hp2 HG02257.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.421+1778G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12106309 | |||||||
| chr1:12106442 | C | T | 6 | a0001c0001t0001g0096 a0001c0001t0001g0250 a0001c0001t0001g0272 others(3): Show |
6 | HG01099.hp2 HG01257.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.421+1911C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12106442 | |||||||
| chr1:12106798 | G | T | 129 | a0001c0001t0001g0138 a0001c0001t0001g0159 a0001c0001t0001g0201 others(126): Show |
129 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.421+2267G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12106798 | |||||||
| chr1:12106808 | G | A | 2 | a0001c0007t0001g0215 a0001c0007t0009g0357 |
2 | HG02622.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.421+2277G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12106808 | |||||||
| chr1:12106853 | C | T | 3 | a0001c0004t0001g0088 a0001c0004t0002g0169 a0002c0011t0004g0221 |
3 | HG02717.hp2 HG02809.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.421+2322C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12106853 | |||||||
| chr1:12107026 | C | A | 12 | a0001c0001t0001g0159 a0001c0001t0005g0355 a0001c0002t0001g0166 others(9): Show |
12 | HG01106.hp2 HG02145.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.421+2495C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12107026 | |||||||
| chr1:12107060 | A | G | 1 | a0001c0001t0001g0318 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.422-2506A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12107060 | |||||||
| chr1:12107084 | C | T | 12 | a0001c0001t0001g0159 a0001c0001t0005g0355 a0001c0002t0001g0166 others(9): Show |
12 | HG01106.hp2 HG02145.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.422-2482C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12107084 | |||||||
| chr1:12107091 | A | G | 1 | a0001c0002t0001g0016 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.422-2475A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12107091 | |||||||
| chr1:12107109 | TA | T | 3 | a0001c0002t0001g0166 a0001c0004t0001g0036 a0001c0004t0010g0202 |
3 | HG02258.hp2 HG02486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.422-2456delA | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12107109 | |||||||
| chr1:12107122 | C | T | 22 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0034 others(19): Show |
22 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.422-2444C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12107122 | |||||||
| chr1:12107169 | C | T | 1 | a0001c0002t0001g0130 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.422-2397C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12107169 | |||||||
| chr1:12107179 | G | A | 12 | a0001c0001t0001g0173 a0001c0003t0001g0167 a0001c0003t0001g0219 others(9): Show |
12 | HG01884.hp1 HG01884.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.422-2387G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12107179 | |||||||
| chr1:12107210 | T | C | 33 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0034 others(30): Show |
33 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.422-2356T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12107210 | |||||||
| chr1:12107322 | G | C | 4 | a0001c0001t0001g0030 a0001c0001t0001g0124 a0001c0001t0001g0160 others(1): Show |
4 | HG01256.hp2 HG01258.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.422-2244G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12107322 | |||||||
| chr1:12107335 | T | C | 193 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0034 others(190): Show |
193 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(190): Show |
intron_variant | MODIFIER | c.422-2231T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12107335 | |||||||
| chr1:12107359 | C | T | 12 | a0001c0001t0001g0173 a0001c0003t0001g0167 a0001c0003t0001g0219 others(9): Show |
12 | HG01884.hp1 HG01884.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.422-2207C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12107359 | |||||||
| chr1:12107374 | G | A | 6 | a0001c0002t0001g0043 a0001c0002t0001g0078 a0001c0002t0001g0128 others(3): Show |
6 | HG00323.hp2 HG00741.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.422-2192G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12107374 | |||||||
| chr1:12107394 | C | CA | 25 | a0001c0001t0001g0173 a0001c0001t0001g0190 a0001c0001t0001g0191 others(22): Show |
25 | HG01175.hp1 HG01884.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.422-2162dupA | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 12107394 | ||||||
| chr1:12107456 | G | A | 1 | a0001c0001t0006g0358 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.422-2110G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12107456 | |||||||
| chr1:12107569 | A | AAATATAC others(1): Show |
187 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0034 others(184): Show |
187 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(184): Show |
intron_variant | MODIFIER | c.422-1996_422-1995i others(10): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 12107569 | ||||||
| chr1:12107702 | AC | A | 128 | a0001c0001t0001g0138 a0001c0001t0001g0159 a0001c0001t0001g0201 others(125): Show |
128 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.422-1861delC | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 12107702 | ||||||
| chr1:12107802 | C | T | 2 | a0001c0002t0001g0166 a0001c0004t0001g0036 |
2 | HG02486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.422-1764C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12107802 | |||||||
| chr1:12107804 | C | G | 1 | a0001c0003t0001g0064 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.422-1762C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12107804 | |||||||
| chr1:12107822 | C | A | 1 | a0001c0001t0006g0150 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.422-1744C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12107822 | |||||||
| chr1:12107942 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.422-1624C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12107942 | |||||||
| chr1:12108020 | C | T | 1 | a0001c0003t0002g0213 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.422-1546C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12108020 | |||||||
| chr1:12108026 | C | A | 1 | a0001c0001t0001g0338 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.422-1540C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12108026 | |||||||
| chr1:12108034 | C | T | 33 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0034 others(30): Show |
33 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.422-1532C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12108034 | |||||||
| chr1:12108074 | A | ATT | 7 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0233 others(4): Show |
7 | HG02109.hp2 HG02257.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.422-1486_422-1485d others(4): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 12108074 | ||||||
| chr1:12108074 | A | ATTTTTTT others(4): Show |
1 | a0001c0001t0001g0244 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.422-1485_422-1484i others(13): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 12108074 | ||||||
| chr1:12108074 | A | ATTTTTTT others(5): Show |
9 | a0001c0001t0001g0011 a0001c0001t0001g0034 a0001c0001t0001g0106 others(6): Show |
9 | HG02258.hp1 HG02683.hp1 HG03834.hp2 others(6): Show |
intron_variant | MODIFIER | c.422-1485_422-1484i others(14): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 12108074 | ||||||
| chr1:12108074 | A | ATTTTTTT others(6): Show |
11 | a0001c0001t0001g0044 a0001c0001t0001g0136 a0001c0001t0001g0273 others(8): Show |
11 | HG00642.hp2 HG01255.hp2 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.422-1485_422-1484i others(15): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 12108074 | ||||||
| chr1:12108074 | A | ATTTTTTT others(7): Show |
1 | a0001c0001t0001g0013 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.422-1485_422-1484i others(16): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 12108074 | ||||||
| chr1:12108074 | A | ATTTTTTT others(15): Show |
1 | a0001c0003t0002g0213 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.422-1485_422-1484i others(24): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 12108074 | ||||||
| chr1:12108078 | T | A | 8 | a0001c0001t0001g0114 a0001c0001t0006g0148 a0001c0001t0006g0248 others(5): Show |
8 | HG00280.hp2 HG02895.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.422-1488T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12108078 | |||||||
| chr1:12108081 | T | A | 1 | a0001c0001t0001g0268 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.422-1485T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12108081 | |||||||
| chr1:12108082 | A | T | 33 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0034 others(30): Show |
33 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.422-1484A>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12108082 | |||||||
| chr1:12108088 | T | A | 13 | a0001c0001t0001g0068 a0001c0001t0001g0138 a0001c0001t0001g0201 others(10): Show |
13 | HG01192.hp1 HG01934.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.422-1478T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12108088 | |||||||
| chr1:12108089 | T | A | 9 | a0001c0001t0001g0173 a0001c0001t0001g0180 a0001c0001t0001g0242 others(6): Show |
9 | HG02145.hp2 HG02630.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.422-1477T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12108089 | |||||||
| chr1:12108269 | G | T | 33 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0034 others(30): Show |
33 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.422-1297G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12108269 | |||||||
| chr1:12108272 | GT | G | 22 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0034 others(19): Show |
22 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.422-1291delT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 12108272 | ||||||
| chr1:12108301 | A | T | 1 | a0001c0003t0002g0213 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.422-1265A>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12108301 | |||||||
| chr1:12108341 | G | C | 2 | a0001c0001t0001g0250 a0001c0001t0001g0296 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.422-1225G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12108341 | |||||||
| chr1:12108376 | C | T | 1 | a0001c0001t0001g0119 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.422-1190C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12108376 | |||||||
| chr1:12108401 | T | A | 173 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0034 others(170): Show |
173 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(170): Show |
intron_variant | MODIFIER | c.422-1165T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12108401 | |||||||
| chr1:12108466 | C | T | 22 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0034 others(19): Show |
22 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.422-1100C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12108466 | |||||||
| chr1:12108527 | G | A | 173 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0034 others(170): Show |
173 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(170): Show |
intron_variant | MODIFIER | c.422-1039G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12108527 | |||||||
| chr1:12108532 | T | C | 1 | a0001c0003t0005g0223 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.422-1034T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12108532 | |||||||
| chr1:12108669 | C | T | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.422-897C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12108669 | |||||||
| chr1:12108670 | G | A | 1 | a0001c0003t0002g0213 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.422-896G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12108670 | |||||||
| chr1:12108799 | T | C | 32 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0034 others(29): Show |
32 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(29): Show |
intron_variant | MODIFIER | c.422-767T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12108799 | |||||||
| chr1:12108873 | G | A | 1 | a0001c0003t0005g0223 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.422-693G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12108873 | |||||||
| chr1:12108897 | C | T | 10 | a0001c0001t0001g0138 a0001c0001t0001g0203 a0001c0001t0001g0229 others(7): Show |
10 | HG02647.hp2 HG02818.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.422-669C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12108897 | |||||||
| chr1:12108903 | G | C | 1 | a0002c0006t0001g0347 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.422-663G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12108903 | |||||||
| chr1:12108957 | T | C | 4 | a0001c0001t0001g0159 a0001c0001t0005g0355 a0001c0003t0010g0259 others(1): Show |
4 | HG02615.hp2 HG02965.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.422-609T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12108957 | |||||||
| chr1:12109037 | C | T | 3 | a0001c0001t0001g0005 a0002c0005t0001g0051 a0002c0005t0001g0084 |
3 | HG00544.hp1 HG02071.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.422-529C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12109037 | |||||||
| chr1:12109196 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.422-370A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12109196 | |||||||
| chr1:12109238 | G | A | 1 | a0001c0002t0001g0078 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.422-328G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12109238 | |||||||
| chr1:12109280 | G | A | 1 | a0001c0001t0002g0224 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.422-286G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12109280 | |||||||
| chr1:12109333 | G | A | 9 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0233 others(6): Show |
9 | HG02109.hp2 HG02257.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.422-233G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12109333 | |||||||
| chr1:12109343 | C | T | 129 | a0001c0001t0001g0138 a0001c0001t0001g0159 a0001c0001t0001g0201 others(126): Show |
129 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.422-223C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12109343 | |||||||
| chr1:12109559 | C | G | 1 | a0001c0001t0001g0305 | 1 | HG03239.hp1 | splice_region_variant&intron_variant | LOW | c.422-7C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 4/14 | chr1 | 12109559 | |||||||
| chr1:12109920 | C | G | 22 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0034 others(19): Show |
22 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.513-121C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 5/14 | chr1 | 12109920 | |||||||
| chr1:12109931 | G | A | 4 | a0001c0001t0001g0030 a0001c0001t0001g0124 a0001c0001t0001g0160 others(1): Show |
4 | HG01256.hp2 HG01258.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.513-110G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 5/14 | chr1 | 12109931 | |||||||
| chr1:12109938 | A | G | 10 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0233 others(7): Show |
10 | HG02109.hp2 HG02257.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.513-103A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 5/14 | chr1 | 12109938 | |||||||
| chr1:12109951 | C | T | 1 | a0001c0001t0007g0192 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.513-90C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 5/14 | chr1 | 12109951 | |||||||
| chr1:12110230 | C | T | 19 | a0001c0001t0001g0138 a0001c0001t0001g0201 a0001c0001t0001g0203 others(16): Show |
19 | HG01192.hp1 HG02451.hp2 HG02572.hp1 others(16): Show |
intron_variant | MODIFIER | c.676+26C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 6/14 | chr1 | 12110230 | |||||||
| chr1:12110231 | G | A | 32 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0034 others(29): Show |
32 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(29): Show |
intron_variant | MODIFIER | c.676+27G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 6/14 | chr1 | 12110231 | |||||||
| chr1:12110368 | G | A | 8 | a0001c0002t0001g0166 a0001c0004t0001g0036 a0001c0004t0010g0202 others(5): Show |
8 | HG01106.hp2 HG02145.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.676+164G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 6/14 | chr1 | 12110368 | |||||||
| chr1:12110368 | G | T | 32 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0034 others(29): Show |
32 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(29): Show |
intron_variant | MODIFIER | c.676+164G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 6/14 | chr1 | 12110368 | |||||||
| chr1:12110437 | C | G | 32 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0034 others(29): Show |
32 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(29): Show |
intron_variant | MODIFIER | c.676+233C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 6/14 | chr1 | 12110437 | |||||||
| chr1:12110519 | G | C | 22 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0034 others(19): Show |
22 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.676+315G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 6/14 | chr1 | 12110519 | |||||||
| chr1:12110629 | G | A | 1 | a0001c0004t0001g0036 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.676+425G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 6/14 | chr1 | 12110629 | |||||||
| chr1:12110678 | C | A | 32 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0034 others(29): Show |
32 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(29): Show |
intron_variant | MODIFIER | c.676+474C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 6/14 | chr1 | 12110678 | |||||||
| chr1:12110826 | G | A | 2 | a0002c0005t0002g0235 a0002c0006t0001g0222 |
2 | HG01243.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.676+622G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 6/14 | chr1 | 12110826 | |||||||
| chr1:12110866 | GGGA | G | 161 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0034 others(158): Show |
161 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.676+666_676+668del others(3): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr1 | 12110866 | ||||||
| chr1:12110917 | C | T | 22 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0034 others(19): Show |
22 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.676+713C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 6/14 | chr1 | 12110917 | |||||||
| chr1:12110935 | C | T | 7 | a0001c0001t0001g0151 a0001c0001t0001g0351 a0001c0001t0002g0218 others(4): Show |
7 | HG01109.hp1 HG02055.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.676+731C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 6/14 | chr1 | 12110935 | |||||||
| chr1:12110955 | T | C | 22 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0034 others(19): Show |
22 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.676+751T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 6/14 | chr1 | 12110955 | |||||||
| chr1:12111028 | G | A | 7 | a0001c0001t0001g0151 a0001c0001t0001g0351 a0001c0001t0002g0218 others(4): Show |
7 | HG01109.hp1 HG02055.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.676+824G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 6/14 | chr1 | 12111028 | |||||||
| chr1:12111135 | C | T | 2 | a0002c0012t0001g0178 a0002c0012t0023g0353 |
2 | HG03471.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.677-763C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 6/14 | chr1 | 12111135 | |||||||
| chr1:12111136 | G | T | 1 | a0001c0004t0010g0202 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.677-762G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 6/14 | chr1 | 12111136 | |||||||
| chr1:12111154 | T | A | 1 | a0001c0001t0004g0177 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.677-744T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 6/14 | chr1 | 12111154 | |||||||
| chr1:12111277 | G | A | 31 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0034 others(28): Show |
31 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(28): Show |
intron_variant | MODIFIER | c.677-621G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 6/14 | chr1 | 12111277 | |||||||
| chr1:12111300 | G | A | 1 | a0002c0006t0001g0021 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.677-598G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 6/14 | chr1 | 12111300 | |||||||
| chr1:12111328 | C | T | 5 | a0001c0003t0012g0236 a0001c0007t0015g0189 a0002c0005t0001g0059 others(2): Show |
5 | HG01891.hp1 HG02109.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.677-570C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 6/14 | chr1 | 12111328 | |||||||
| chr1:12111383 | T | C | 20 | a0001c0001t0001g0138 a0001c0001t0001g0201 a0001c0001t0001g0203 others(17): Show |
20 | HG01192.hp1 HG02451.hp2 HG02572.hp1 others(17): Show |
intron_variant | MODIFIER | c.677-515T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 6/14 | chr1 | 12111383 | |||||||
| chr1:12111461 | C | T | 24 | a0001c0002t0001g0016 a0001c0002t0001g0022 a0001c0002t0001g0027 others(21): Show |
24 | HG00438.hp2 HG00597.hp2 HG02074.hp1 others(21): Show |
intron_variant | MODIFIER | c.677-437C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 6/14 | chr1 | 12111461 | |||||||
| chr1:12111487 | C | G | 1 | a0001c0001t0001g0269 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.677-411C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 6/14 | chr1 | 12111487 | |||||||
| chr1:12111519 | A | C | 1 | a0001c0002t0001g0095 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.677-379A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 6/14 | chr1 | 12111519 | |||||||
| chr1:12111621 | A | G | 141 | a0001c0001t0001g0039 a0001c0001t0001g0151 a0001c0001t0001g0159 others(138): Show |
141 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.677-277A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 6/14 | chr1 | 12111621 | |||||||
| chr1:12111673 | G | T | 22 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0034 others(19): Show |
22 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.677-225G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 6/14 | chr1 | 12111673 | |||||||
| chr1:12111724 | C | T | 1 | a0001c0003t0001g0123 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.677-174C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 6/14 | chr1 | 12111724 | |||||||
| chr1:12112026 | G | A | 1 | a0003c0008t0017g0009 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.793+12G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12112026 | |||||||
| chr1:12112068 | C | T | 4 | a0001c0001t0001g0138 a0001c0001t0007g0198 a0001c0001t0009g0089 others(1): Show |
4 | HG02717.hp1 HG02818.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.793+54C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12112068 | |||||||
| chr1:12112091 | C | T | 3 | a0001c0002t0001g0166 a0001c0004t0001g0036 a0001c0004t0010g0202 |
3 | HG02258.hp2 HG02486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.793+77C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12112091 | |||||||
| chr1:12112337 | C | T | 8 | a0001c0001t0001g0203 a0001c0001t0001g0229 a0001c0001t0016g0194 others(5): Show |
8 | HG02647.hp2 HG02895.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.793+323C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12112337 | |||||||
| chr1:12112566 | A | T | 1 | a0001c0002t0001g0110 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.793+552A>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12112566 | |||||||
| chr1:12112567 | T | A | 22 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0034 others(19): Show |
22 | HG00642.hp2 HG01168.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.793+553T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12112567 | |||||||
| chr1:12112742 | G | A | 2 | a0001c0001t0001g0104 a0001c0001t0001g0144 |
2 | NA18966.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.793+728G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12112742 | |||||||
| chr1:12112790 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.793+776C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12112790 | |||||||
| chr1:12112810 | G | T | 32 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0034 others(29): Show |
32 | HG00642.hp2 HG01168.hp2 HG01175.hp1 others(29): Show |
intron_variant | MODIFIER | c.793+796G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12112810 | |||||||
| chr1:12112990 | T | C | 1 | a0001c0004t0001g0186 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.793+976T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12112990 | |||||||
| chr1:12113040 | A | C | 1 | a0001c0003t0005g0092 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.793+1026A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12113040 | |||||||
| chr1:12113267 | C | T | 1 | a0001c0003t0001g0064 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.793+1253C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12113267 | |||||||
| chr1:12113304 | A | G | 63 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0034 others(60): Show |
63 | HG00642.hp2 HG01255.hp2 HG01884.hp1 others(60): Show |
intron_variant | MODIFIER | c.793+1290A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12113304 | |||||||
| chr1:12113316 | C | T | 10 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0201 others(7): Show |
10 | HG01192.hp1 HG02257.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.793+1302C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12113316 | |||||||
| chr1:12113389 | G | A | 20 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0034 others(17): Show |
20 | HG00642.hp2 HG01255.hp2 HG01928.hp1 others(17): Show |
intron_variant | MODIFIER | c.793+1375G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12113389 | |||||||
| chr1:12113484 | T | TGA | 24 | a0001c0001t0001g0159 a0001c0001t0001g0173 a0001c0001t0001g0233 others(21): Show |
24 | HG01884.hp1 HG01884.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.793+1481_793+1482d others(4): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr1 | 12113484 | ||||||
| chr1:12113604 | T | C | 22 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0034 others(19): Show |
22 | HG00642.hp2 HG01255.hp2 HG01928.hp1 others(19): Show |
intron_variant | MODIFIER | c.793+1590T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12113604 | |||||||
| chr1:12113652 | A | G | 1 | a0001c0003t0001g0024 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.793+1638A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12113652 | |||||||
| chr1:12113663 | G | A | 2 | a0001c0001t0001g0151 a0001c0001t0001g0351 |
2 | HG01109.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.793+1649G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12113663 | |||||||
| chr1:12113685 | CAGAA | C | 149 | a0001c0001t0001g0005 a0001c0001t0001g0074 a0001c0001t0001g0079 others(146): Show |
149 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(146): Show |
intron_variant | MODIFIER | c.793+1675_793+1678d others(6): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr1 | 12113685 | ||||||
| chr1:12113731 | C | G | 22 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0034 others(19): Show |
22 | HG00642.hp2 HG01255.hp2 HG01928.hp1 others(19): Show |
intron_variant | MODIFIER | c.793+1717C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12113731 | |||||||
| chr1:12113781 | GAGAC | G | 20 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0034 others(17): Show |
20 | HG00642.hp2 HG01255.hp2 HG01928.hp1 others(17): Show |
intron_variant | MODIFIER | c.793+1775_793+1778d others(6): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr1 | 12113781 | ||||||
| chr1:12113807 | C | T | 1 | a0001c0001t0001g0028 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.794-1770C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12113807 | |||||||
| chr1:12113981 | A | C | 3 | a0001c0001t0001g0138 a0001c0001t0006g0150 a0001c0001t0009g0089 |
3 | HG02622.hp1 HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.794-1596A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12113981 | |||||||
| chr1:12114043 | G | A | 23 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0034 others(20): Show |
23 | HG00642.hp2 HG01255.hp2 HG01928.hp1 others(20): Show |
intron_variant | MODIFIER | c.794-1534G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12114043 | |||||||
| chr1:12114081 | C | G | 3 | a0001c0001t0006g0358 a0001c0002t0001g0188 a0002c0005t0001g0094 |
3 | HG02109.hp2 HG02559.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.794-1496C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12114081 | |||||||
| chr1:12114133 | C | T | 2 | a0001c0001t0006g0358 a0001c0002t0001g0188 |
2 | HG02109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.794-1444C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12114133 | |||||||
| chr1:12114173 | C | T | 1 | a0001c0002t0018g0097 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.794-1404C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12114173 | |||||||
| chr1:12114296 | G | A | 1 | a0001c0001t0001g0318 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.794-1281G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12114296 | |||||||
| chr1:12114336 | G | A | 2 | a0001c0001t0006g0358 a0001c0002t0001g0188 |
2 | HG02109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.794-1241G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12114336 | |||||||
| chr1:12114569 | C | T | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.794-1008C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12114569 | |||||||
| chr1:12114588 | A | G | 1 | a0001c0001t0001g0329 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.794-989A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12114588 | |||||||
| chr1:12114612 | G | A | 6 | a0001c0001t0001g0122 a0001c0001t0001g0187 a0001c0001t0001g0275 others(3): Show |
6 | NA18939.hp2 NA18953.hp2 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.794-965G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12114612 | |||||||
| chr1:12114636 | A | G | 5 | a0001c0002t0001g0010 a0001c0002t0001g0065 a0001c0002t0001g0130 others(2): Show |
5 | HG00323.hp1 HG01358.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-941A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12114636 | |||||||
| chr1:12114694 | C | CT | 104 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(101): Show |
104 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.794-854dupT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr1 | 12114694 | ||||||
| chr1:12114694 | C | CTT | 33 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0086 others(30): Show |
33 | HG00438.hp1 HG00741.hp1 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.794-855_794-854dup others(2): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr1 | 12114694 | ||||||
| chr1:12114694 | CT | C | 12 | a0001c0001t0001g0191 a0001c0001t0001g0201 a0001c0001t0001g0233 others(9): Show |
12 | HG01192.hp1 HG01884.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.794-854delT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr1 | 12114694 | ||||||
| chr1:12114694 | CTT | C | 19 | a0001c0001t0001g0159 a0001c0001t0001g0173 a0001c0001t0005g0355 others(16): Show |
19 | HG02145.hp2 HG02257.hp2 HG02615.hp2 others(16): Show |
intron_variant | MODIFIER | c.794-855_794-854del others(2): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr1 | 12114694 | ||||||
| chr1:12114694 | CTTTTTTT | C | 18 | a0001c0001t0001g0119 a0001c0001t0001g0127 a0001c0001t0001g0245 others(15): Show |
18 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(15): Show |
intron_variant | MODIFIER | c.794-860_794-854del others(7): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr1 | 12114694 | ||||||
| chr1:12114694 | CTTTTTTT others(1): Show |
C | 109 | a0001c0001t0001g0005 a0001c0001t0001g0074 a0001c0001t0001g0079 others(106): Show |
109 | HG00597.hp1 HG00597.hp2 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.794-861_794-854del others(8): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr1 | 12114694 | ||||||
| chr1:12114694 | CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0006g0358 a0001c0002t0001g0188 |
2 | HG02109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.794-863_794-854del others(10): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr1 | 12114694 | ||||||
| chr1:12114694 | CTTTTTTT others(4): Show |
C | 23 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0034 others(20): Show |
23 | HG00642.hp2 HG01255.hp2 HG01928.hp1 others(20): Show |
intron_variant | MODIFIER | c.794-864_794-854del others(11): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr1 | 12114694 | ||||||
| chr1:12114694 | CTTTTTTT others(7): Show |
C | 6 | a0001c0003t0002g0197 a0001c0009t0001g0359 a0001c0009t0001g0360 others(3): Show |
6 | HG01106.hp2 HG02145.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.794-867_794-854del others(14): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr1 | 12114694 | ||||||
| chr1:12114795 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.794-782G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12114795 | |||||||
| chr1:12114850 | A | C | 1 | a0001c0002t0001g0188 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.794-727A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12114850 | |||||||
| chr1:12114982 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.794-595C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12114982 | |||||||
| chr1:12115077 | T | TATCACCC others(2903): Show |
1 | a0001c0001t0001g0258 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.794-487_794-486ins others(2910): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr1 | 12115077 | ||||||
| chr1:12115094 | C | T | 1 | a0001c0001t0001g0289 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.794-483C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12115094 | |||||||
| chr1:12115348 | C | T | 1 | a0002c0006t0001g0170 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.794-229C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12115348 | |||||||
| chr1:12115400 | C | A | 1 | a0001c0001t0001g0346 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.794-177C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12115400 | |||||||
| chr1:12115403 | G | A | 1 | a0001c0001t0001g0346 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.794-174G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12115403 | |||||||
| chr1:12115404 | C | G | 1 | a0001c0001t0001g0346 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.794-173C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12115404 | |||||||
| chr1:12115406 | G | T | 1 | a0001c0001t0001g0346 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.794-171G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12115406 | |||||||
| chr1:12115407 | A | C | 1 | a0001c0001t0001g0346 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.794-170A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12115407 | |||||||
| chr1:12115408 | A | G | 1 | a0001c0001t0001g0346 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.794-169A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12115408 | |||||||
| chr1:12115409 | T | C | 1 | a0001c0001t0001g0346 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.794-168T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12115409 | |||||||
| chr1:12115410 | T | G | 1 | a0001c0001t0001g0346 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.794-167T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12115410 | |||||||
| chr1:12115411 | A | T | 1 | a0001c0001t0001g0346 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.794-166A>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12115411 | |||||||
| chr1:12115412 | T | G | 1 | a0001c0001t0001g0346 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.794-165T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 7/14 | chr1 | 12115412 | |||||||
| chr1:12115761 | A | G | 160 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0034 others(157): Show |
160 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(157): Show |
intron_variant | MODIFIER | c.946+32A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12115761 | |||||||
| chr1:12115828 | C | CTA | 8 | a0001c0001t0001g0159 a0001c0001t0001g0203 a0001c0001t0005g0355 others(5): Show |
8 | HG02615.hp2 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.946+100_946+101dup others(2): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr1 | 12115828 | ||||||
| chr1:12115974 | G | A | 5 | a0001c0002t0001g0015 a0001c0002t0001g0035 a0001c0002t0001g0045 others(2): Show |
5 | HG02040.hp1 HG02071.hp2 HG02080.hp2 others(2): Show |
intron_variant | MODIFIER | c.946+245G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12115974 | |||||||
| chr1:12116017 | T | C | 1 | a0001c0014t0001g0101 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.946+288T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12116017 | |||||||
| chr1:12116131 | G | A | 1 | a0001c0001t0007g0198 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.946+402G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12116131 | |||||||
| chr1:12116142 | C | T | 5 | a0001c0001t0001g0229 a0001c0001t0016g0194 a0001c0003t0003g0225 others(2): Show |
5 | HG01891.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.946+413C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12116142 | |||||||
| chr1:12116181 | A | G | 22 | a0001c0001t0001g0013 a0001c0001t0001g0034 a0001c0001t0001g0044 others(19): Show |
22 | HG00642.hp2 HG01255.hp2 HG01928.hp1 others(19): Show |
intron_variant | MODIFIER | c.946+452A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12116181 | |||||||
| chr1:12116200 | C | T | 22 | a0001c0001t0001g0013 a0001c0001t0001g0034 a0001c0001t0001g0044 others(19): Show |
22 | HG00642.hp2 HG01255.hp2 HG01928.hp1 others(19): Show |
intron_variant | MODIFIER | c.946+471C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12116200 | |||||||
| chr1:12116224 | A | G | 4 | a0001c0001t0001g0159 a0001c0001t0005g0355 a0001c0003t0010g0259 others(1): Show |
4 | HG02615.hp2 HG02965.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.946+495A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12116224 | |||||||
| chr1:12116263 | G | A | 7 | a0001c0001t0001g0028 a0001c0001t0001g0050 a0001c0001t0001g0286 others(4): Show |
7 | HG02056.hp2 NA18970.hp2 NA18994.hp1 others(4): Show |
intron_variant | MODIFIER | c.946+534G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12116263 | |||||||
| chr1:12116282 | C | T | 2 | a0001c0004t0001g0135 a0002c0010t0001g0146 |
2 | HG02074.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.946+553C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12116282 | |||||||
| chr1:12116372 | G | A | 2 | a0001c0001t0007g0192 a0001c0001t0007g0216 |
2 | HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.946+643G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12116372 | |||||||
| chr1:12116491 | G | C | 1 | a0002c0006t0001g0347 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.946+762G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12116491 | |||||||
| chr1:12116539 | G | A | 1 | a0001c0002t0001g0188 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.946+810G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12116539 | |||||||
| chr1:12116591 | A | G | 1 | a0001c0003t0001g0023 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.946+862A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12116591 | |||||||
| chr1:12116594 | A | T | 1 | a0001c0004t0002g0169 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.946+865A>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12116594 | |||||||
| chr1:12116613 | C | G | 2 | a0001c0025t0001g0231 a0002c0005t0005g0230 |
2 | HG03453.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.946+884C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12116613 | |||||||
| chr1:12116718 | T | G | 2 | a0001c0004t0001g0088 a0002c0011t0004g0221 |
2 | HG02809.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.946+989T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12116718 | |||||||
| chr1:12116759 | C | A | 1 | a0001c0003t0001g0185 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.946+1030C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12116759 | |||||||
| chr1:12116814 | C | A | 1 | a0001c0003t0001g0253 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.946+1085C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12116814 | |||||||
| chr1:12116857 | C | T | 1 | a0001c0003t0012g0199 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.946+1128C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12116857 | |||||||
| chr1:12116999 | C | T | 4 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0002t0001g0166 others(1): Show |
4 | HG02257.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.946+1270C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12116999 | |||||||
| chr1:12117038 | T | C | 11 | a0001c0001t0001g0151 a0001c0001t0001g0351 a0001c0001t0002g0218 others(8): Show |
11 | HG01109.hp1 HG02055.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.946+1309T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12117038 | |||||||
| chr1:12117232 | G | A | 1 | a0001c0003t0001g0288 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.946+1503G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12117232 | |||||||
| chr1:12117277 | T | C | 2 | a0001c0001t0001g0100 a0001c0002t0001g0055 |
2 | HG01069.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.946+1548T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12117277 | |||||||
| chr1:12117324 | C | T | 1 | a0001c0003t0005g0092 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.946+1595C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12117324 | |||||||
| chr1:12117423 | G | A | 1 | a0001c0004t0001g0088 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.946+1694G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12117423 | |||||||
| chr1:12117442 | A | G | 1 | a0001c0003t0001g0253 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.946+1713A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12117442 | |||||||
| chr1:12117475 | C | A | 1 | a0002c0005t0002g0206 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.946+1746C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12117475 | |||||||
| chr1:12117693 | T | C | 10 | a0001c0001t0002g0224 a0001c0007t0015g0189 a0001c0009t0001g0359 others(7): Show |
10 | HG01243.hp1 HG01891.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.946+1964T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12117693 | |||||||
| chr1:12117713 | G | A | 2 | a0001c0001t0011g0282 a0001c0004t0001g0267 |
2 | HG00609.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.946+1984G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12117713 | |||||||
| chr1:12117744 | C | T | 1 | a0001c0007t0009g0357 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.946+2015C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12117744 | |||||||
| chr1:12117777 | G | A | 9 | a0001c0001t0001g0058 a0001c0001t0001g0106 a0001c0003t0001g0102 others(6): Show |
9 | HG01071.hp2 HG01255.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.946+2048G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12117777 | |||||||
| chr1:12117843 | C | T | 1 | a0001c0002t0001g0004 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.946+2114C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12117843 | |||||||
| chr1:12118106 | T | TC | 47 | a0001c0001t0001g0063 a0001c0001t0001g0079 a0001c0001t0001g0103 others(44): Show |
47 | HG00438.hp2 HG00609.hp1 HG01167.hp2 others(44): Show |
intron_variant | MODIFIER | c.946+2385dupC | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr1 | 12118106 | ||||||
| chr1:12118111 | C | A | 1 | a0001c0001t0001g0173 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.946+2382C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12118111 | |||||||
| chr1:12118112 | C | A | 1 | a0001c0001t0001g0159 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.946+2383C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12118112 | |||||||
| chr1:12118113 | C | T | 1 | a0001c0001t0001g0263 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.946+2384C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12118113 | |||||||
| chr1:12118117 | C | A | 29 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0114 others(26): Show |
29 | HG00280.hp2 HG01106.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.946+2388C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12118117 | |||||||
| chr1:12118220 | T | TA | 30 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0114 others(27): Show |
30 | HG00280.hp2 HG01106.hp2 HG01516.hp2 others(27): Show |
intron_variant | MODIFIER | c.946+2491_946+2492i others(3): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12118220 | |||||||
| chr1:12118221 | G | A | 30 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0114 others(27): Show |
30 | HG00280.hp2 HG01106.hp2 HG01516.hp2 others(27): Show |
intron_variant | MODIFIER | c.946+2492G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12118221 | |||||||
| chr1:12118391 | G | A | 7 | a0001c0007t0015g0189 a0002c0005t0001g0059 a0002c0005t0002g0235 others(4): Show |
7 | HG01891.hp2 HG02559.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.946+2662G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12118391 | |||||||
| chr1:12118591 | G | C | 16 | a0001c0001t0001g0159 a0002c0005t0001g0059 a0002c0005t0001g0227 others(13): Show |
16 | HG01106.hp2 HG01243.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.946+2862G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12118591 | |||||||
| chr1:12118597 | A | G | 16 | a0001c0001t0001g0159 a0002c0005t0001g0059 a0002c0005t0001g0227 others(13): Show |
16 | HG01106.hp2 HG01243.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.946+2868A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12118597 | |||||||
| chr1:12118778 | A | C | 2 | a0001c0001t0006g0150 a0001c0003t0010g0195 |
2 | HG02622.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.946+3049A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12118778 | |||||||
| chr1:12118802 | G | A | 2 | a0001c0001t0001g0159 a0002c0006t0001g0222 |
2 | HG01243.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.946+3073G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12118802 | |||||||
| chr1:12118850 | T | G | 17 | a0001c0001t0001g0159 a0002c0005t0001g0059 a0002c0005t0001g0227 others(14): Show |
17 | HG01106.hp2 HG01243.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.946+3121T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12118850 | |||||||
| chr1:12118870 | C | G | 1 | a0001c0004t0025g0356 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.946+3141C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12118870 | |||||||
| chr1:12118876 | T | C | 1 | a0001c0002t0001g0018 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.946+3147T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12118876 | |||||||
| chr1:12119115 | G | A | 2 | a0002c0005t0002g0235 a0002c0006t0001g0155 |
2 | HG02976.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.946+3386G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12119115 | |||||||
| chr1:12119335 | G | A | 4 | a0002c0006t0003g0149 a0002c0012t0001g0178 a0002c0012t0023g0353 others(1): Show |
4 | HG01106.hp2 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.946+3606G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12119335 | |||||||
| chr1:12119346 | C | A | 1 | a0001c0001t0001g0047 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.946+3617C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12119346 | |||||||
| chr1:12119513 | T | G | 12 | a0002c0005t0001g0059 a0002c0005t0002g0206 a0002c0005t0002g0235 others(9): Show |
12 | HG01106.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.947-3771T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12119513 | |||||||
| chr1:12119555 | C | CT | 67 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0047 others(64): Show |
67 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.947-3716dupT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr1 | 12119555 | ||||||
| chr1:12119555 | C | CTT | 125 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(122): Show |
125 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(122): Show |
intron_variant | MODIFIER | c.947-3717_947-3716d others(4): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr1 | 12119555 | ||||||
| chr1:12119739 | T | C | 1 | a0001c0001t0001g0173 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.947-3545T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12119739 | |||||||
| chr1:12120041 | C | T | 2 | a0001c0003t0001g0091 a0001c0003t0001g0252 |
2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.947-3243C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12120041 | |||||||
| chr1:12120061 | A | T | 47 | a0001c0001t0001g0020 a0001c0001t0001g0063 a0001c0001t0001g0079 others(44): Show |
47 | HG00438.hp2 HG00558.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.947-3223A>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12120061 | |||||||
| chr1:12120067 | G | A | 233 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(230): Show |
233 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.947-3217G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12120067 | |||||||
| chr1:12120181 | G | A | 2 | a0001c0001t0001g0138 a0001c0001t0009g0089 |
2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.947-3103G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12120181 | |||||||
| chr1:12120320 | A | G | 5 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0002g0172 others(2): Show |
5 | HG02257.hp1 HG02451.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.947-2964A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12120320 | |||||||
| chr1:12120475 | C | T | 1 | a0001c0001t0001g0344 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.947-2809C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12120475 | |||||||
| chr1:12120748 | C | T | 231 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(228): Show |
231 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.947-2536C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12120748 | |||||||
| chr1:12120905 | C | A | 1 | a0002c0005t0006g0209 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.947-2379C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12120905 | |||||||
| chr1:12120906 | C | T | 2 | a0001c0001t0001g0151 a0001c0001t0001g0351 |
2 | HG01109.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.947-2378C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12120906 | |||||||
| chr1:12121344 | C | T | 43 | a0001c0001t0001g0020 a0001c0001t0001g0063 a0001c0001t0001g0079 others(40): Show |
43 | HG00438.hp2 HG00558.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.947-1940C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12121344 | |||||||
| chr1:12121395 | C | A | 1 | a0001c0002t0001g0243 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.947-1889C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12121395 | |||||||
| chr1:12121442 | T | G | 2 | a0001c0003t0001g0091 a0001c0003t0001g0252 |
2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.947-1842T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12121442 | |||||||
| chr1:12121615 | C | T | 5 | a0001c0001t0002g0218 a0001c0001t0006g0358 a0001c0001t0007g0192 others(2): Show |
5 | HG02109.hp2 HG02280.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.947-1669C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12121615 | |||||||
| chr1:12121695 | G | A | 1 | a0001c0001t0002g0224 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.947-1589G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12121695 | |||||||
| chr1:12121774 | A | G | 10 | a0001c0001t0001g0250 a0001c0001t0001g0272 a0001c0001t0001g0296 others(7): Show |
10 | HG01099.hp2 HG01257.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.947-1510A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12121774 | |||||||
| chr1:12121801 | G | A | 1 | a0001c0004t0001g0052 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.947-1483G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12121801 | |||||||
| chr1:12121934 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.947-1350A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12121934 | |||||||
| chr1:12121957 | C | T | 1 | a0002c0012t0023g0353 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.947-1327C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12121957 | |||||||
| chr1:12122048 | C | T | 1 | a0001c0003t0002g0213 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.947-1236C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12122048 | |||||||
| chr1:12122384 | C | T | 1 | a0001c0002t0011g0285 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.947-900C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12122384 | |||||||
| chr1:12122830 | C | T | 3 | a0002c0005t0001g0227 a0002c0005t0005g0230 a0002c0005t0005g0232 |
3 | HG03195.hp2 HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.947-454C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12122830 | |||||||
| chr1:12122890 | A | G | 1 | a0001c0001t0005g0355 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.947-394A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12122890 | |||||||
| chr1:12122921 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.947-363C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12122921 | |||||||
| chr1:12123117 | A | C | 260 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(257): Show |
260 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.947-167A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12123117 | |||||||
| chr1:12123181 | C | T | 1 | a0001c0002t0001g0045 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.947-103C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12123181 | |||||||
| chr1:12123188 | G | T | 45 | a0001c0001t0001g0058 a0001c0001t0001g0098 a0001c0001t0001g0099 others(42): Show |
45 | HG00280.hp2 HG01071.hp2 HG01255.hp2 others(42): Show |
intron_variant | MODIFIER | c.947-96G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 8/14 | chr1 | 12123188 | |||||||
| chr1:12123495 | C | T | 4 | a0001c0002t0002g0147 a0001c0003t0003g0211 a0001c0004t0001g0352 others(1): Show |
4 | HG01884.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1040+118C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 9/14 | chr1 | 12123495 | |||||||
| chr1:12123498 | T | C | 1 | a0001c0002t0001g0095 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1040+121T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 9/14 | chr1 | 12123498 | |||||||
| chr1:12123666 | C | T | 1 | a0001c0001t0002g0172 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1041-49C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 9/14 | chr1 | 12123666 | |||||||
| chr1:12123669 | C | G | 1 | a0001c0002t0001g0032 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1041-46C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 9/14 | chr1 | 12123669 | |||||||
| chr1:12123688 | A | G | 1 | a0002c0006t0001g0222 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1041-27A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 9/14 | chr1 | 12123688 | |||||||
| chr1:12123949 | G | A | 1 | a0001c0002t0001g0033 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1153+122G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12123949 | |||||||
| chr1:12124150 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1153+323G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12124150 | |||||||
| chr1:12124174 | T | C | 45 | a0001c0001t0001g0058 a0001c0001t0001g0098 a0001c0001t0001g0099 others(42): Show |
45 | HG00280.hp2 HG01071.hp2 HG01255.hp2 others(42): Show |
intron_variant | MODIFIER | c.1153+347T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12124174 | |||||||
| chr1:12124318 | T | C | 215 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(212): Show |
215 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(212): Show |
intron_variant | MODIFIER | c.1153+491T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12124318 | |||||||
| chr1:12124333 | G | A | 1 | a0001c0003t0001g0219 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1153+506G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12124333 | |||||||
| chr1:12124365 | C | T | 1 | a0001c0001t0001g0122 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1153+538C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12124365 | |||||||
| chr1:12124366 | G | A | 119 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(116): Show |
119 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.1153+539G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12124366 | |||||||
| chr1:12124462 | A | G | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(197): Show |
200 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(197): Show |
intron_variant | MODIFIER | c.1153+635A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12124462 | |||||||
| chr1:12124489 | A | G | 158 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(155): Show |
158 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(155): Show |
intron_variant | MODIFIER | c.1153+662A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12124489 | |||||||
| chr1:12124606 | G | A | 40 | a0001c0001t0001g0058 a0001c0001t0001g0098 a0001c0001t0001g0099 others(37): Show |
40 | HG00280.hp2 HG01071.hp2 HG01255.hp2 others(37): Show |
intron_variant | MODIFIER | c.1153+779G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12124606 | |||||||
| chr1:12124616 | G | A | 5 | a0001c0003t0003g0208 a0001c0007t0001g0215 a0001c0007t0009g0357 others(2): Show |
5 | HG02622.hp2 HG02630.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1153+789G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12124616 | |||||||
| chr1:12124653 | C | T | 1 | a0002c0006t0001g0155 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1153+826C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12124653 | |||||||
| chr1:12124657 | A | G | 1 | a0002c0006t0001g0222 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1153+830A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12124657 | |||||||
| chr1:12124667 | C | G | 120 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(117): Show |
120 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.1153+840C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12124667 | |||||||
| chr1:12124682 | C | G | 29 | a0001c0001t0001g0034 a0001c0001t0001g0047 a0001c0001t0001g0127 others(26): Show |
29 | HG00323.hp2 HG01358.hp1 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.1153+855C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12124682 | |||||||
| chr1:12124690 | C | T | 1 | a0001c0002t0001g0080 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1153+863C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12124690 | |||||||
| chr1:12124691 | G | A | 12 | a0002c0005t0001g0059 a0002c0005t0002g0206 a0002c0005t0002g0235 others(9): Show |
12 | HG01106.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1153+864G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12124691 | |||||||
| chr1:12124693 | G | A | 45 | a0001c0001t0001g0058 a0001c0001t0001g0098 a0001c0001t0001g0099 others(42): Show |
45 | HG00280.hp2 HG01071.hp2 HG01255.hp2 others(42): Show |
intron_variant | MODIFIER | c.1153+866G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12124693 | |||||||
| chr1:12124694 | C | T | 35 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0114 others(32): Show |
35 | HG00280.hp2 HG01516.hp2 HG01517.hp2 others(32): Show |
intron_variant | MODIFIER | c.1153+867C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12124694 | |||||||
| chr1:12124695 | G | A | 19 | a0002c0005t0001g0051 a0002c0005t0001g0084 a0002c0005t0001g0094 others(16): Show |
19 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(16): Show |
intron_variant | MODIFIER | c.1153+868G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12124695 | |||||||
| chr1:12124829 | C | CAAACA | 40 | a0001c0001t0001g0037 a0001c0001t0001g0047 a0001c0001t0001g0104 others(37): Show |
40 | HG00438.hp1 HG01074.hp1 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.1153+1050_1153+105 others(9): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 12124829 | ||||||
| chr1:12124829 | C | CAAACAAA others(3): Show |
10 | a0001c0001t0001g0114 a0001c0001t0001g0137 a0001c0001t0001g0151 others(7): Show |
10 | HG00280.hp2 HG02486.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1153+1045_1153+105 others(14): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 12124829 | ||||||
| chr1:12124829 | C | CAAACAAA others(15): Show |
1 | a0001c0003t0001g0315 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1153+1015_1153+101 others(26): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 12124829 | ||||||
| chr1:12124829 | C | CAAACAAA others(8): Show |
5 | a0001c0001t0001g0058 a0001c0003t0001g0102 a0001c0003t0001g0288 others(2): Show |
5 | HG01071.hp2 HG01255.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.1153+1040_1153+105 others(19): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 12124829 | ||||||
| chr1:12124829 | C | CAAACAAA others(13): Show |
3 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0003c0008t0001g0105 |
3 | HG01516.hp2 HG01517.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.1153+1035_1153+105 others(24): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 12124829 | ||||||
| chr1:12124829 | C | CAAACAAA others(18): Show |
2 | a0003c0008t0001g0087 a0003c0008t0017g0009 |
2 | NA19066.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1153+1030_1153+105 others(29): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 12124829 | ||||||
| chr1:12124829 | CAAACA | C | 26 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0030 others(23): Show |
26 | HG01168.hp1 HG01169.hp1 HG01256.hp2 others(23): Show |
intron_variant | MODIFIER | c.1153+1050_1153+105 others(9): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 12124829 | ||||||
| chr1:12124829 | CAAACAAA others(3): Show |
C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(109): Show |
112 | HG00140.hp2 HG00558.hp1 HG00738.hp2 others(109): Show |
intron_variant | MODIFIER | c.1153+1045_1153+105 others(14): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 12124829 | ||||||
| chr1:12124829 | CAAACAAA others(8): Show |
C | 3 | a0001c0003t0002g0213 a0001c0003t0010g0195 a0001c0017t0014g0265 |
3 | HG00140.hp1 HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1153+1040_1153+105 others(19): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 12124829 | ||||||
| chr1:12124874 | AAAAC | A | 16 | a0002c0005t0001g0051 a0002c0005t0001g0084 a0002c0005t0001g0094 others(13): Show |
16 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.1153+1055_1153+105 others(8): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 12124874 | ||||||
| chr1:12124878 | C | CA | 3 | a0002c0006t0001g0347 a0002c0016t0004g0228 a0004c0028t0021g0113 |
3 | HG03710.hp2 NA19009.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1153+1054dupA | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 12124878 | ||||||
| chr1:12124882 | C | A | 1 | a0001c0003t0001g0315 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1153+1055C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12124882 | |||||||
| chr1:12124883 | A | C | 1 | a0001c0003t0001g0315 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1153+1056A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12124883 | |||||||
| chr1:12124892 | A | G | 5 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0002g0172 others(2): Show |
5 | HG02257.hp1 HG02451.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1154-1059A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12124892 | |||||||
| chr1:12124894 | G | A | 20 | a0002c0005t0001g0051 a0002c0005t0001g0084 a0002c0005t0001g0094 others(17): Show |
20 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(17): Show |
intron_variant | MODIFIER | c.1154-1057G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12124894 | |||||||
| chr1:12124958 | A | T | 2 | a0002c0005t0001g0051 a0002c0005t0001g0084 |
2 | HG00544.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1154-993A>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12124958 | |||||||
| chr1:12124979 | G | A | 30 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0114 others(27): Show |
30 | HG00280.hp2 HG01516.hp2 HG01517.hp2 others(27): Show |
intron_variant | MODIFIER | c.1154-972G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12124979 | |||||||
| chr1:12125149 | G | A | 4 | a0002c0005t0001g0059 a0002c0005t0002g0235 a0002c0006t0001g0155 others(1): Show |
4 | HG01891.hp2 HG02559.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1154-802G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12125149 | |||||||
| chr1:12125278 | T | C | 258 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(255): Show |
258 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.1154-673T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12125278 | |||||||
| chr1:12125309 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1154-642C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12125309 | |||||||
| chr1:12125323 | C | T | 2 | a0001c0004t0001g0135 a0002c0010t0001g0146 |
2 | HG02074.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.1154-628C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12125323 | |||||||
| chr1:12125470 | C | T | 7 | a0001c0001t0001g0159 a0001c0003t0003g0208 a0001c0004t0001g0052 others(4): Show |
7 | HG02622.hp2 HG02630.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1154-481C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12125470 | |||||||
| chr1:12125476 | T | C | 61 | a0001c0001t0001g0020 a0001c0001t0001g0063 a0001c0001t0001g0079 others(58): Show |
61 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.1154-475T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12125476 | |||||||
| chr1:12125717 | A | G | 77 | a0001c0001t0001g0020 a0001c0001t0001g0063 a0001c0001t0001g0079 others(74): Show |
77 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.1154-234A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12125717 | |||||||
| chr1:12125726 | T | C | 77 | a0001c0001t0001g0020 a0001c0001t0001g0063 a0001c0001t0001g0079 others(74): Show |
77 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.1154-225T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12125726 | |||||||
| chr1:12125898 | TG | T | 3 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 |
3 | HG01099.hp1 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1154-52delG | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 10/14 | chr1 | 12125898 | |||||||
| chr1:12126148 | C | T | 1 | a0001c0001t0001g0180 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1256-35C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 11/14 | chr1 | 12126148 | |||||||
| chr1:12126251 | G | A | 5 | a0002c0005t0006g0209 a0002c0006t0003g0149 a0002c0012t0001g0178 others(2): Show |
5 | HG01106.hp2 HG02109.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1309+15G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12126251 | |||||||
| chr1:12126299 | C | T | 30 | a0001c0002t0001g0053 a0001c0003t0001g0145 a0002c0005t0001g0051 others(27): Show |
30 | HG00544.hp1 HG00597.hp1 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.1309+63C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12126299 | |||||||
| chr1:12126335 | G | A | 33 | a0001c0001t0002g0224 a0001c0002t0001g0053 a0001c0003t0001g0145 others(30): Show |
33 | HG00544.hp1 HG00544.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.1309+99G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12126335 | |||||||
| chr1:12126570 | G | T | 41 | a0001c0001t0001g0020 a0001c0001t0001g0050 a0001c0001t0001g0063 others(38): Show |
41 | HG00438.hp2 HG00558.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.1309+334G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12126570 | |||||||
| chr1:12126725 | C | T | 1 | a0001c0001t0001g0003 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1309+489C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12126725 | |||||||
| chr1:12126737 | C | A | 5 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0002g0172 others(2): Show |
5 | HG02257.hp1 HG02451.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1309+501C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12126737 | |||||||
| chr1:12126740 | T | C | 268 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(265): Show |
268 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.1309+504T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12126740 | |||||||
| chr1:12126857 | C | T | 8 | a0001c0001t0005g0355 a0001c0003t0001g0091 a0001c0003t0001g0167 others(5): Show |
8 | HG01243.hp1 HG01884.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1309+621C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12126857 | |||||||
| chr1:12126876 | A | G | 276 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(273): Show |
276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.1309+640A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12126876 | |||||||
| chr1:12126879 | G | A | 4 | a0001c0001t0005g0355 a0001c0003t0001g0167 a0001c0003t0010g0259 others(1): Show |
4 | HG02572.hp2 HG02615.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1309+643G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12126879 | |||||||
| chr1:12126994 | G | C | 48 | a0001c0001t0001g0020 a0001c0001t0001g0050 a0001c0001t0001g0063 others(45): Show |
48 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.1309+758G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12126994 | |||||||
| chr1:12127073 | C | T | 86 | a0001c0001t0001g0020 a0001c0001t0001g0038 a0001c0001t0001g0050 others(83): Show |
86 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.1309+837C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12127073 | |||||||
| chr1:12127084 | C | T | 1 | a0001c0017t0014g0265 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1309+848C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12127084 | |||||||
| chr1:12127107 | G | A | 2 | a0001c0003t0001g0091 a0001c0003t0001g0252 |
2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1309+871G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12127107 | |||||||
| chr1:12127175 | G | A | 35 | a0001c0001t0001g0034 a0001c0001t0001g0047 a0001c0001t0001g0096 others(32): Show |
35 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.1309+939G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12127175 | |||||||
| chr1:12127214 | G | T | 1 | a0001c0001t0001g0342 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1309+978G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12127214 | |||||||
| chr1:12127358 | G | A | 1 | a0002c0006t0001g0056 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1309+1122G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12127358 | |||||||
| chr1:12127365 | C | T | 1 | a0002c0010t0001g0345 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1309+1129C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12127365 | |||||||
| chr1:12127484 | T | C | 132 | a0001c0001t0001g0020 a0001c0001t0001g0034 a0001c0001t0001g0038 others(129): Show |
132 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(129): Show |
intron_variant | MODIFIER | c.1309+1248T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12127484 | |||||||
| chr1:12127536 | C | T | 11 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0233 others(8): Show |
11 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1309+1300C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12127536 | |||||||
| chr1:12127537 | G | A | 6 | a0001c0001t0001g0138 a0001c0001t0001g0173 a0001c0001t0001g0203 others(3): Show |
6 | HG02145.hp2 HG02647.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1309+1301G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12127537 | |||||||
| chr1:12127655 | A | G | 160 | a0001c0001t0001g0020 a0001c0001t0001g0034 a0001c0001t0001g0038 others(157): Show |
160 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(157): Show |
intron_variant | MODIFIER | c.1309+1419A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12127655 | |||||||
| chr1:12127724 | GCTGAGTG others(3): Show |
G | 7 | a0001c0001t0001g0229 a0001c0003t0001g0219 a0001c0003t0003g0225 others(4): Show |
7 | HG01167.hp2 HG01891.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1309+1490_1309+149 others(14): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 12127724 | ||||||
| chr1:12127748 | G | A | 3 | a0001c0003t0010g0195 a0002c0005t0001g0227 a0002c0005t0005g0232 |
3 | HG03195.hp2 HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1309+1512G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12127748 | |||||||
| chr1:12127971 | C | A | 133 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(130): Show |
133 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.1309+1735C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12127971 | |||||||
| chr1:12128037 | A | G | 266 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(263): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.1309+1801A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12128037 | |||||||
| chr1:12128066 | C | T | 2 | a0001c0001t0001g0037 a0001c0004t0001g0052 |
2 | HG01074.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.1309+1830C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12128066 | |||||||
| chr1:12128288 | G | A | 20 | a0001c0001t0001g0038 a0001c0001t0001g0093 a0001c0001t0001g0098 others(17): Show |
20 | HG01358.hp2 HG01516.hp2 HG01517.hp2 others(17): Show |
intron_variant | MODIFIER | c.1309+2052G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12128288 | |||||||
| chr1:12128332 | G | A | 1 | a0001c0002t0004g0260 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1309+2096G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12128332 | |||||||
| chr1:12128370 | T | C | 34 | a0001c0001t0001g0034 a0001c0001t0001g0047 a0001c0001t0001g0096 others(31): Show |
34 | HG00323.hp2 HG00597.hp1 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.1309+2134T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12128370 | |||||||
| chr1:12128413 | C | A | 11 | a0001c0004t0001g0196 a0001c0004t0003g0220 a0002c0005t0001g0059 others(8): Show |
11 | HG01106.hp2 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1309+2177C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12128413 | |||||||
| chr1:12128425 | G | A | 240 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(237): Show |
240 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.1309+2189G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12128425 | |||||||
| chr1:12128433 | C | T | 2 | a0001c0001t0001g0151 a0001c0001t0001g0351 |
2 | HG01109.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1309+2197C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12128433 | |||||||
| chr1:12128490 | T | G | 3 | a0003c0008t0001g0087 a0003c0008t0001g0105 a0003c0027t0001g0060 |
3 | NA18969.hp2 NA18970.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.1309+2254T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12128490 | |||||||
| chr1:12128556 | G | A | 32 | a0001c0001t0001g0034 a0001c0001t0001g0047 a0001c0001t0001g0096 others(29): Show |
32 | HG00323.hp2 HG00597.hp1 HG01358.hp1 others(29): Show |
intron_variant | MODIFIER | c.1309+2320G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12128556 | |||||||
| chr1:12128557 | G | A | 7 | a0001c0001t0001g0058 a0001c0003t0001g0288 a0001c0003t0001g0315 others(4): Show |
7 | HG01071.hp2 HG01928.hp1 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.1309+2321G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12128557 | |||||||
| chr1:12128569 | G | A | 1 | a0001c0004t0001g0320 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1309+2333G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12128569 | |||||||
| chr1:12128594 | C | G | 241 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(238): Show |
241 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.1309+2358C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12128594 | |||||||
| chr1:12128715 | G | C | 241 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(238): Show |
241 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.1309+2479G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12128715 | |||||||
| chr1:12128783 | A | G | 6 | a0001c0001t0001g0159 a0001c0003t0003g0208 a0001c0007t0001g0215 others(3): Show |
6 | HG02622.hp2 HG02630.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1309+2547A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12128783 | |||||||
| chr1:12128803 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1309+2567C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12128803 | |||||||
| chr1:12128823 | G | A | 1 | a0002c0006t0001g0222 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1309+2587G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12128823 | |||||||
| chr1:12128829 | A | C | 2 | a0001c0003t0002g0197 a0001c0003t0002g0213 |
2 | HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1309+2593A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12128829 | |||||||
| chr1:12128833 | C | CT | 25 | a0001c0001t0001g0013 a0001c0001t0001g0044 a0001c0001t0001g0086 others(22): Show |
25 | HG00558.hp1 HG02074.hp1 HG02165.hp2 others(22): Show |
intron_variant | MODIFIER | c.1309+2616dupT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 12128833 | ||||||
| chr1:12128833 | C | CTTT | 112 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(109): Show |
112 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.1309+2614_1309+261 others(7): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 12128833 | ||||||
| chr1:12128833 | C | CTTTT | 103 | a0001c0001t0001g0020 a0001c0001t0001g0039 a0001c0001t0001g0046 others(100): Show |
103 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.1309+2613_1309+261 others(8): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 12128833 | ||||||
| chr1:12128833 | C | CTTTTT | 21 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0047 others(18): Show |
21 | HG00323.hp2 HG00597.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.1309+2612_1309+261 others(9): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 12128833 | ||||||
| chr1:12128833 | CT | C | 8 | a0001c0001t0001g0058 a0001c0001t0001g0258 a0001c0003t0001g0288 others(5): Show |
8 | HG01071.hp2 HG01928.hp1 NA18969.hp2 others(5): Show |
intron_variant | MODIFIER | c.1309+2616delT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 12128833 | ||||||
| chr1:12128928 | G | A | 1 | a0002c0006t0001g0222 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1309+2692G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12128928 | |||||||
| chr1:12129176 | T | A | 240 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(237): Show |
240 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.1309+2940T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12129176 | |||||||
| chr1:12129204 | T | A | 9 | a0001c0001t0001g0229 a0001c0003t0001g0219 a0001c0003t0002g0197 others(6): Show |
9 | HG01167.hp2 HG01891.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1309+2968T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12129204 | |||||||
| chr1:12129238 | C | T | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1309+3002C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12129238 | |||||||
| chr1:12129432 | C | T | 108 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(105): Show |
108 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.1309+3196C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12129432 | |||||||
| chr1:12129504 | G | A | 167 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(164): Show |
167 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.1309+3268G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12129504 | |||||||
| chr1:12129552 | C | T | 1 | a0001c0004t0001g0168 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1309+3316C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12129552 | |||||||
| chr1:12129634 | G | A | 23 | a0001c0001t0001g0013 a0001c0001t0001g0044 a0001c0001t0001g0086 others(20): Show |
23 | HG00558.hp1 HG02165.hp2 HG02451.hp2 others(20): Show |
intron_variant | MODIFIER | c.1309+3398G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12129634 | |||||||
| chr1:12129790 | C | T | 1 | a0002c0005t0002g0235 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1309+3554C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12129790 | |||||||
| chr1:12129961 | G | A | 1 | a0001c0002t0001g0031 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1309+3725G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12129961 | |||||||
| chr1:12130078 | T | C | 6 | a0001c0001t0001g0138 a0001c0001t0001g0173 a0001c0001t0001g0203 others(3): Show |
6 | HG02145.hp2 HG02647.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1309+3842T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12130078 | |||||||
| chr1:12130155 | G | A | 5 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0002g0172 others(2): Show |
5 | HG02257.hp1 HG02451.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1309+3919G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12130155 | |||||||
| chr1:12130345 | A | T | 1 | a0001c0004t0010g0202 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1309+4109A>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12130345 | |||||||
| chr1:12130498 | C | T | 1 | a0003c0019t0004g0017 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1309+4262C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12130498 | |||||||
| chr1:12130624 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1309+4388C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12130624 | |||||||
| chr1:12130638 | A | T | 1 | a0002c0011t0004g0221 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1309+4402A>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12130638 | |||||||
| chr1:12130641 | G | A | 1 | a0001c0002t0001g0031 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1309+4405G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12130641 | |||||||
| chr1:12130651 | C | T | 9 | a0001c0001t0001g0138 a0001c0001t0001g0173 a0001c0001t0001g0203 others(6): Show |
9 | HG02145.hp2 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1309+4415C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12130651 | |||||||
| chr1:12130670 | C | T | 1 | a0001c0004t0001g0142 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1309+4434C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12130670 | |||||||
| chr1:12130671 | G | A | 2 | a0001c0003t0001g0091 a0001c0003t0001g0252 |
2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1309+4435G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12130671 | |||||||
| chr1:12130684 | G | A | 180 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(177): Show |
180 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.1309+4448G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12130684 | |||||||
| chr1:12130710 | C | T | 6 | a0001c0001t0001g0138 a0001c0001t0001g0173 a0001c0001t0001g0203 others(3): Show |
6 | HG02145.hp2 HG02647.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1309+4474C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12130710 | |||||||
| chr1:12131040 | C | T | 15 | a0001c0001t0001g0138 a0001c0001t0001g0159 a0001c0001t0001g0173 others(12): Show |
15 | HG01243.hp1 HG02145.hp2 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.1310-4548C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12131040 | |||||||
| chr1:12131143 | G | T | 243 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(240): Show |
243 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.1310-4445G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12131143 | |||||||
| chr1:12131310 | C | A | 9 | a0001c0001t0001g0138 a0001c0001t0001g0173 a0001c0001t0001g0203 others(6): Show |
9 | HG02145.hp2 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1310-4278C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12131310 | |||||||
| chr1:12131342 | C | T | 5 | a0001c0001t0001g0159 a0001c0007t0001g0215 a0001c0007t0009g0357 others(2): Show |
5 | HG02622.hp2 HG02965.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1310-4246C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12131342 | |||||||
| chr1:12131445 | G | A | 64 | a0001c0001t0001g0020 a0001c0001t0001g0046 a0001c0001t0001g0050 others(61): Show |
64 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1310-4143G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12131445 | |||||||
| chr1:12131474 | A | C | 1 | a0002c0005t0002g0206 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1310-4114A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12131474 | |||||||
| chr1:12131502 | AGTTTTTT | A | 271 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(268): Show |
271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.1310-4066_1310-406 others(11): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 12131502 | ||||||
| chr1:12131684 | A | G | 15 | a0001c0001t0001g0138 a0001c0001t0001g0159 a0001c0001t0001g0173 others(12): Show |
15 | HG01243.hp1 HG02145.hp2 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.1310-3904A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12131684 | |||||||
| chr1:12131714 | T | G | 15 | a0001c0001t0001g0138 a0001c0001t0001g0159 a0001c0001t0001g0173 others(12): Show |
15 | HG01243.hp1 HG02145.hp2 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.1310-3874T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12131714 | |||||||
| chr1:12131940 | C | T | 6 | a0001c0004t0001g0069 a0001c0004t0001g0070 a0001c0004t0001g0135 others(3): Show |
6 | HG02074.hp2 HG02523.hp1 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.1310-3648C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12131940 | |||||||
| chr1:12131943 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1310-3645G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12131943 | |||||||
| chr1:12132196 | A | G | 64 | a0001c0001t0001g0020 a0001c0001t0001g0046 a0001c0001t0001g0050 others(61): Show |
64 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1310-3392A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12132196 | |||||||
| chr1:12132213 | A | G | 272 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(269): Show |
272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.1310-3375A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12132213 | |||||||
| chr1:12132240 | G | T | 6 | a0001c0001t0001g0138 a0001c0001t0001g0173 a0001c0001t0001g0203 others(3): Show |
6 | HG02145.hp2 HG02647.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1310-3348G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12132240 | |||||||
| chr1:12132249 | C | T | 64 | a0001c0001t0001g0020 a0001c0001t0001g0046 a0001c0001t0001g0050 others(61): Show |
64 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1310-3339C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12132249 | |||||||
| chr1:12132269 | A | C | 1 | a0002c0006t0001g0222 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1310-3319A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12132269 | |||||||
| chr1:12132392 | A | G | 1 | a0002c0006t0001g0222 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1310-3196A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12132392 | |||||||
| chr1:12132446 | C | T | 1 | a0001c0002t0004g0260 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1310-3142C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12132446 | |||||||
| chr1:12132569 | A | G | 293 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(290): Show |
293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.1310-3019A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12132569 | |||||||
| chr1:12132837 | C | CA | 64 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0014 others(61): Show |
64 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.1310-2726dupA | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 12132837 | ||||||
| chr1:12132837 | C | CAA | 8 | a0001c0001t0001g0136 a0001c0002t0001g0033 a0001c0002t0001g0043 others(5): Show |
8 | HG00741.hp1 HG00741.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.1310-2727_1310-272 others(6): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 12132837 | ||||||
| chr1:12132837 | CA | C | 69 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0020 others(66): Show |
69 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.1310-2726delA | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 12132837 | ||||||
| chr1:12132837 | CAA | C | 67 | a0001c0001t0001g0038 a0001c0001t0001g0046 a0001c0001t0001g0047 others(64): Show |
67 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.1310-2727_1310-272 others(6): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 12132837 | ||||||
| chr1:12132837 | CAAA | C | 6 | a0001c0001t0005g0355 a0001c0002t0001g0027 a0001c0003t0010g0195 others(3): Show |
6 | HG02615.hp2 HG03195.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1310-2728_1310-272 others(7): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 12132837 | ||||||
| chr1:12132837 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0006g0358 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1310-2737_1310-272 others(16): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 12132837 | ||||||
| chr1:12132837 | CAAAAAAA others(6): Show |
C | 9 | a0001c0001t0001g0138 a0001c0001t0001g0173 a0001c0001t0001g0203 others(6): Show |
9 | HG02145.hp2 HG02647.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1310-2738_1310-272 others(17): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 12132837 | ||||||
| chr1:12132975 | C | T | 101 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(98): Show |
101 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.1310-2613C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12132975 | |||||||
| chr1:12132976 | G | A | 2 | a0001c0001t0001g0286 a0002c0005t0001g0094 |
2 | NA18942.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1310-2612G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12132976 | |||||||
| chr1:12133043 | G | A | 2 | a0001c0001t0002g0172 a0001c0004t0003g0220 |
2 | HG02451.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1310-2545G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12133043 | |||||||
| chr1:12133239 | G | A | 2 | a0001c0003t0002g0214 a0002c0005t0002g0235 |
2 | HG02976.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1310-2349G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12133239 | |||||||
| chr1:12133269 | C | T | 1 | a0001c0002t0001g0323 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1310-2319C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12133269 | |||||||
| chr1:12133326 | C | CT | 252 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0013 others(249): Show |
252 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.1310-2250dupT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 12133326 | ||||||
| chr1:12133470 | C | G | 252 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0013 others(249): Show |
252 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.1310-2118C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12133470 | |||||||
| chr1:12133523 | C | T | 1 | a0002c0005t0001g0121 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1310-2065C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12133523 | |||||||
| chr1:12133534 | G | T | 2 | a0001c0003t0002g0214 a0002c0005t0002g0235 |
2 | HG02976.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1310-2054G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12133534 | |||||||
| chr1:12133570 | T | C | 1 | a0002c0005t0005g0230 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1310-2018T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12133570 | |||||||
| chr1:12133672 | G | A | 3 | a0001c0003t0002g0214 a0002c0005t0002g0235 a0002c0011t0004g0221 |
3 | HG02976.hp2 HG03041.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1310-1916G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12133672 | |||||||
| chr1:12133688 | C | T | 1 | a0001c0004t0001g0088 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1310-1900C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12133688 | |||||||
| chr1:12133697 | G | A | 1 | a0001c0003t0001g0315 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1310-1891G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12133697 | |||||||
| chr1:12133738 | C | CA | 6 | a0001c0001t0001g0115 a0001c0001t0001g0159 a0001c0002t0001g0055 others(3): Show |
6 | HG01243.hp1 HG02080.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1310-1826dupA | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 12133738 | ||||||
| chr1:12133738 | CAA | C | 10 | a0001c0001t0001g0304 a0001c0001t0001g0329 a0001c0002t0001g0176 others(7): Show |
10 | HG01884.hp2 HG02922.hp1 HG03453.hp2 others(7): Show |
intron_variant | MODIFIER | c.1310-1827_1310-182 others(6): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 12133738 | ||||||
| chr1:12133738 | CAAA | C | 236 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(233): Show |
236 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.1310-1828_1310-182 others(7): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 12133738 | ||||||
| chr1:12133806 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1310-1782A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12133806 | |||||||
| chr1:12133868 | C | T | 34 | a0001c0001t0001g0034 a0001c0001t0001g0047 a0001c0001t0001g0096 others(31): Show |
34 | HG00323.hp2 HG00597.hp1 HG01358.hp1 others(31): Show |
intron_variant | MODIFIER | c.1310-1720C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12133868 | |||||||
| chr1:12133898 | C | T | 1 | a0001c0003t0001g0276 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1310-1690C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12133898 | |||||||
| chr1:12133913 | C | T | 14 | a0001c0001t0002g0218 a0001c0001t0007g0192 a0001c0001t0007g0216 others(11): Show |
14 | HG02280.hp2 HG02486.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1310-1675C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12133913 | |||||||
| chr1:12133922 | A | G | 2 | a0001c0003t0001g0091 a0001c0003t0001g0252 |
2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1310-1666A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12133922 | |||||||
| chr1:12134359 | G | T | 27 | a0001c0001t0001g0138 a0001c0001t0001g0173 a0001c0001t0001g0190 others(24): Show |
27 | HG01106.hp2 HG01243.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.1310-1229G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12134359 | |||||||
| chr1:12134394 | T | C | 286 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0013 others(283): Show |
286 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.1310-1194T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12134394 | |||||||
| chr1:12134409 | C | A | 7 | a0001c0001t0001g0138 a0001c0001t0001g0173 a0001c0001t0001g0203 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1310-1179C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12134409 | |||||||
| chr1:12134470 | T | C | 1 | a0001c0001t0016g0194 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1310-1118T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12134470 | |||||||
| chr1:12134555 | G | A | 145 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0014 others(142): Show |
145 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.1310-1033G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12134555 | |||||||
| chr1:12134688 | G | A | 32 | a0001c0001t0001g0034 a0001c0001t0001g0047 a0001c0001t0001g0096 others(29): Show |
32 | HG00323.hp2 HG00597.hp1 HG01358.hp1 others(29): Show |
intron_variant | MODIFIER | c.1310-900G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12134688 | |||||||
| chr1:12134732 | G | C | 34 | a0001c0001t0001g0034 a0001c0001t0001g0047 a0001c0001t0001g0096 others(31): Show |
34 | HG00323.hp2 HG00597.hp1 HG01358.hp1 others(31): Show |
intron_variant | MODIFIER | c.1310-856G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12134732 | |||||||
| chr1:12134945 | G | A | 1 | a0001c0001t0008g0163 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1310-643G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12134945 | |||||||
| chr1:12134952 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1310-636A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12134952 | |||||||
| chr1:12134969 | G | A | 11 | a0001c0001t0001g0138 a0001c0001t0001g0173 a0001c0001t0001g0203 others(8): Show |
11 | HG02109.hp2 HG02145.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1310-619G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12134969 | |||||||
| chr1:12134996 | G | T | 1 | a0001c0001t0001g0011 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1310-592G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12134996 | |||||||
| chr1:12135023 | A | T | 1 | a0001c0001t0001g0278 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1310-565A>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12135023 | |||||||
| chr1:12135054 | G | A | 6 | a0001c0001t0001g0229 a0001c0003t0001g0219 a0001c0003t0003g0225 others(3): Show |
6 | HG01167.hp2 HG01891.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1310-534G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12135054 | |||||||
| chr1:12135119 | G | C | 1 | a0001c0001t0011g0282 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1310-469G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12135119 | |||||||
| chr1:12135124 | G | A | 1 | a0001c0001t0001g0268 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1310-464G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12135124 | |||||||
| chr1:12135156 | A | G | 14 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0002t0001g0166 others(11): Show |
14 | HG01106.hp2 HG02055.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1310-432A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12135156 | |||||||
| chr1:12135167 | T | A | 251 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0013 others(248): Show |
251 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.1310-421T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12135167 | |||||||
| chr1:12135177 | T | A | 11 | a0001c0001t0001g0138 a0001c0001t0001g0173 a0001c0001t0001g0203 others(8): Show |
11 | HG02109.hp2 HG02145.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1310-411T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12135177 | |||||||
| chr1:12135294 | T | C | 250 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0013 others(247): Show |
250 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.1310-294T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12135294 | |||||||
| chr1:12135315 | C | CA | 52 | a0001c0001t0001g0034 a0001c0001t0001g0096 a0001c0001t0001g0106 others(49): Show |
52 | HG01106.hp2 HG01358.hp1 HG01884.hp1 others(49): Show |
intron_variant | MODIFIER | c.1310-255dupA | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 12135315 | ||||||
| chr1:12135315 | C | CAA | 67 | a0001c0001t0001g0020 a0001c0001t0001g0044 a0001c0001t0001g0046 others(64): Show |
67 | HG00558.hp2 HG00597.hp1 HG01884.hp2 others(64): Show |
intron_variant | MODIFIER | c.1310-256_1310-255d others(4): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 12135315 | ||||||
| chr1:12135315 | C | CAAA | 140 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(137): Show |
140 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.1310-257_1310-255d others(5): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 12135315 | ||||||
| chr1:12135315 | C | CAAAA | 14 | a0001c0001t0001g0005 a0001c0001t0001g0086 a0001c0001t0001g0136 others(11): Show |
14 | HG00597.hp2 HG01433.hp2 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.1310-258_1310-255d others(6): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 12135315 | ||||||
| chr1:12135446 | G | T | 1 | a0002c0010t0001g0146 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1310-142G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12135446 | |||||||
| chr1:12135537 | G | T | 1 | a0001c0002t0001g0254 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1310-51G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 12/14 | chr1 | 12135537 | |||||||
| chr1:12135672 | C | T | 11 | a0001c0001t0001g0138 a0001c0001t0001g0173 a0001c0001t0001g0203 others(8): Show |
11 | HG02109.hp2 HG02145.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1335+59C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12135672 | |||||||
| chr1:12135737 | C | G | 1 | a0002c0005t0005g0232 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1335+124C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12135737 | |||||||
| chr1:12135931 | C | T | 1 | a0001c0001t0007g0193 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1335+318C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12135931 | |||||||
| chr1:12136082 | T | C | 1 | a0001c0003t0003g0208 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1335+469T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12136082 | |||||||
| chr1:12136091 | G | A | 253 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0013 others(250): Show |
253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.1335+478G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12136091 | |||||||
| chr1:12136110 | TC | T | 59 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0044 others(56): Show |
59 | HG00438.hp2 HG00558.hp2 HG01109.hp1 others(56): Show |
intron_variant | MODIFIER | c.1335+498delC | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12136110 | |||||||
| chr1:12136208 | G | A | 1 | a0001c0003t0005g0223 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1335+595G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12136208 | |||||||
| chr1:12136265 | A | C | 1 | a0001c0001t0001g0093 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1335+652A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12136265 | |||||||
| chr1:12136284 | C | G | 50 | a0001c0001t0001g0020 a0001c0001t0001g0046 a0001c0001t0001g0050 others(47): Show |
50 | HG00438.hp2 HG00558.hp2 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.1335+671C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12136284 | |||||||
| chr1:12136447 | G | A | 1 | a0001c0004t0003g0220 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1335+834G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12136447 | |||||||
| chr1:12136469 | T | A | 222 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0013 others(219): Show |
222 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.1335+856T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12136469 | |||||||
| chr1:12136474 | C | G | 2 | a0001c0004t0025g0356 a0001c0025t0001g0231 |
2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1335+861C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12136474 | |||||||
| chr1:12136478 | G | A | 6 | a0001c0004t0001g0069 a0001c0004t0001g0070 a0001c0004t0001g0135 others(3): Show |
6 | HG02074.hp2 HG02523.hp1 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.1335+865G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12136478 | |||||||
| chr1:12136530 | T | G | 1 | a0001c0001t0001g0278 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1335+917T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12136530 | |||||||
| chr1:12136531 | C | T | 1 | a0001c0001t0001g0278 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1335+918C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12136531 | |||||||
| chr1:12136563 | C | T | 1 | a0002c0005t0001g0227 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1335+950C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12136563 | |||||||
| chr1:12136619 | C | A | 1 | a0001c0001t0001g0278 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1335+1006C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12136619 | |||||||
| chr1:12136620 | A | G | 1 | a0001c0001t0001g0278 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1335+1007A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12136620 | |||||||
| chr1:12136622 | C | T | 30 | a0001c0001t0001g0034 a0001c0001t0001g0096 a0001c0001t0001g0106 others(27): Show |
30 | HG00544.hp2 HG00597.hp1 HG01358.hp1 others(27): Show |
intron_variant | MODIFIER | c.1335+1009C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12136622 | |||||||
| chr1:12136649 | G | GA | 8 | a0001c0001t0001g0115 a0001c0001t0001g0159 a0001c0001t0001g0258 others(5): Show |
8 | HG02622.hp2 HG02965.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.1335+1054dupA | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr1 | 12136649 | ||||||
| chr1:12136649 | G | GAA | 9 | a0001c0001t0001g0058 a0001c0002t0001g0055 a0001c0003t0001g0288 others(6): Show |
9 | HG01071.hp2 HG01928.hp1 HG04199.hp1 others(6): Show |
intron_variant | MODIFIER | c.1335+1053_1335+105 others(6): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr1 | 12136649 | ||||||
| chr1:12136649 | GAA | G | 153 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0014 others(150): Show |
153 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.1335+1053_1335+105 others(6): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr1 | 12136649 | ||||||
| chr1:12136649 | GAAA | G | 69 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0044 others(66): Show |
69 | HG00438.hp2 HG00558.hp2 HG01106.hp2 others(66): Show |
intron_variant | MODIFIER | c.1335+1052_1335+105 others(7): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr1 | 12136649 | ||||||
| chr1:12136649 | GAAAA | G | 29 | a0001c0001t0001g0034 a0001c0001t0001g0096 a0001c0001t0001g0106 others(26): Show |
29 | HG00544.hp2 HG00597.hp1 HG01255.hp2 others(26): Show |
intron_variant | MODIFIER | c.1335+1051_1335+105 others(8): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr1 | 12136649 | ||||||
| chr1:12136673 | T | C | 6 | a0001c0004t0001g0069 a0001c0004t0001g0070 a0001c0004t0001g0135 others(3): Show |
6 | HG02074.hp2 HG02523.hp1 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.1335+1060T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12136673 | |||||||
| chr1:12136704 | A | G | 1 | a0001c0003t0001g0324 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1335+1091A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12136704 | |||||||
| chr1:12136712 | G | T | 253 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0013 others(250): Show |
253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.1335+1099G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12136712 | |||||||
| chr1:12136733 | A | G | 1 | a0001c0003t0001g0249 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1335+1120A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12136733 | |||||||
| chr1:12136779 | G | A | 4 | a0001c0001t0001g0233 a0001c0001t0007g0193 a0001c0001t0016g0194 others(1): Show |
4 | HG02258.hp2 HG02615.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1335+1166G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12136779 | |||||||
| chr1:12136870 | CT | C | 13 | a0001c0001t0001g0159 a0001c0001t0001g0180 a0001c0001t0001g0263 others(10): Show |
13 | HG01243.hp1 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1335+1282delT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr1 | 12136870 | ||||||
| chr1:12136870 | CTT | C | 21 | a0001c0001t0001g0058 a0001c0001t0001g0190 a0001c0001t0001g0191 others(18): Show |
21 | HG01071.hp2 HG01928.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.1335+1281_1335+128 others(6): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr1 | 12136870 | ||||||
| chr1:12136870 | CTTTTTTT | C | 137 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0014 others(134): Show |
137 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.1335+1276_1335+128 others(11): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr1 | 12136870 | ||||||
| chr1:12136870 | CTTTTTTT others(1): Show |
C | 45 | a0001c0001t0001g0034 a0001c0001t0001g0048 a0001c0001t0001g0096 others(42): Show |
45 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.1335+1275_1335+128 others(12): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr1 | 12136870 | ||||||
| chr1:12136870 | CTTTTTTT others(2): Show |
C | 64 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0044 others(61): Show |
64 | HG00438.hp2 HG00558.hp2 HG01106.hp2 others(61): Show |
intron_variant | MODIFIER | c.1335+1274_1335+128 others(13): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr1 | 12136870 | ||||||
| chr1:12136870 | CTTTTTTT others(3): Show |
C | 4 | a0001c0001t0001g0119 a0001c0001t0001g0286 a0001c0001t0001g0290 others(1): Show |
4 | HG02523.hp2 NA19012.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.1335+1273_1335+128 others(14): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr1 | 12136870 | ||||||
| chr1:12136877 | T | A | 1 | a0001c0001t0001g0278 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1335+1264T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12136877 | |||||||
| chr1:12136880 | T | C | 1 | a0001c0001t0001g0278 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1335+1267T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12136880 | |||||||
| chr1:12136898 | T | A | 1 | a0001c0001t0001g0247 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1335+1285T>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12136898 | |||||||
| chr1:12136921 | T | G | 1 | a0001c0001t0001g0278 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1335+1308T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12136921 | |||||||
| chr1:12136922 | C | T | 1 | a0001c0001t0001g0278 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1336-1307C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12136922 | |||||||
| chr1:12136923 | T | C | 1 | a0001c0001t0001g0278 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1336-1306T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12136923 | |||||||
| chr1:12137038 | C | T | 1 | a0002c0006t0001g0222 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1336-1191C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12137038 | |||||||
| chr1:12137045 | C | T | 260 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0013 others(257): Show |
260 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.1336-1184C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12137045 | |||||||
| chr1:12137283 | G | C | 1 | a0001c0003t0001g0219 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1336-946G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12137283 | |||||||
| chr1:12137316 | A | G | 1 | a0001c0002t0001g0045 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1336-913A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12137316 | |||||||
| chr1:12137327 | A | AATC | 161 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0014 others(158): Show |
161 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.1336-900_1336-899i others(5): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr1 | 12137327 | ||||||
| chr1:12137327 | A | C | 2 | a0001c0009t0001g0359 a0002c0011t0004g0221 |
2 | HG02976.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1336-902A>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12137327 | |||||||
| chr1:12137504 | C | A | 1 | a0001c0004t0003g0220 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1336-725C>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12137504 | |||||||
| chr1:12137540 | GTTTTTTT others(3): Show |
G | 7 | a0001c0001t0001g0138 a0001c0001t0001g0173 a0001c0001t0001g0203 others(4): Show |
7 | HG02109.hp2 HG02145.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1336-671_1336-662d others(12): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr1 | 12137540 | ||||||
| chr1:12137548 | GTTTTTTT others(4): Show |
G | 5 | a0001c0004t0001g0164 a0002c0005t0001g0059 a0002c0005t0005g0210 others(2): Show |
5 | HG02055.hp1 HG02559.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1336-660_1336-650d others(13): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr1 | 12137548 | ||||||
| chr1:12137558 | G | T | 33 | a0001c0001t0001g0034 a0001c0001t0001g0063 a0001c0001t0001g0096 others(30): Show |
33 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.1336-671G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12137558 | |||||||
| chr1:12137558 | GT | G | 160 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(157): Show |
160 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.1336-661delT | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr1 | 12137558 | ||||||
| chr1:12137559 | T | G | 3 | a0001c0001t0001g0063 a0001c0002t0001g0323 a0001c0003t0010g0195 |
3 | HG03471.hp2 NA18941.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.1336-670T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12137559 | |||||||
| chr1:12137559 | T | TG | 28 | a0001c0001t0001g0034 a0001c0001t0001g0106 a0001c0001t0001g0127 others(25): Show |
28 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.1336-670_1336-669i others(3): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12137559 | |||||||
| chr1:12137567 | TTG | T | 61 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0044 others(58): Show |
61 | HG00438.hp2 HG00558.hp2 HG01109.hp1 others(58): Show |
intron_variant | MODIFIER | c.1336-660_1336-659d others(4): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr1 | 12137567 | ||||||
| chr1:12137568 | T | G | 1 | a0002c0006t0001g0056 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1336-661T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12137568 | |||||||
| chr1:12137569 | G | T | 4 | a0001c0003t0001g0091 a0001c0003t0001g0252 a0002c0006t0001g0056 others(1): Show |
4 | HG01106.hp2 HG01884.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1336-660G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12137569 | |||||||
| chr1:12137570 | T | G | 64 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0044 others(61): Show |
64 | HG00438.hp2 HG00558.hp2 HG01106.hp2 others(61): Show |
intron_variant | MODIFIER | c.1336-659T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12137570 | |||||||
| chr1:12137878 | C | T | 1 | a0001c0002t0001g0302 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1336-351C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12137878 | |||||||
| chr1:12137879 | G | A | 4 | a0001c0001t0005g0355 a0002c0005t0001g0227 a0002c0005t0005g0230 others(1): Show |
4 | HG02615.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1336-350G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12137879 | |||||||
| chr1:12138089 | G | A | 4 | a0001c0001t0001g0229 a0001c0001t0005g0355 a0002c0005t0001g0227 others(1): Show |
4 | HG02615.hp2 HG03195.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1336-140G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12138089 | |||||||
| chr1:12138122 | G | A | 256 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(253): Show |
256 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(253): Show |
intron_variant | MODIFIER | c.1336-107G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | chr1 | 12138122 | |||||||
| chr1:12138146 | G | GA | 9 | a0001c0001t0007g0193 a0001c0002t0001g0340 a0001c0002t0004g0260 others(6): Show |
9 | HG01106.hp2 HG01884.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1336-73dupA | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr1 | 12138146 | ||||||
| chr1:12138535 | T | C | 10 | a0001c0001t0001g0233 a0001c0003t0001g0091 a0001c0003t0001g0252 others(7): Show |
10 | HG01106.hp2 HG01884.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1543+99T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12138535 | |||||||
| chr1:12138554 | A | G | 7 | a0001c0003t0001g0167 a0001c0003t0010g0259 a0001c0003t0026g0161 others(4): Show |
7 | HG02559.hp1 HG02572.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1543+118A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12138554 | |||||||
| chr1:12138578 | T | C | 255 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(252): Show |
255 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(252): Show |
intron_variant | MODIFIER | c.1543+142T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12138578 | |||||||
| chr1:12138586 | T | C | 2 | a0001c0001t0005g0355 a0002c0005t0005g0232 |
2 | HG02615.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1543+150T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12138586 | |||||||
| chr1:12138631 | G | A | 2 | a0001c0001t0001g0138 a0001c0001t0009g0089 |
2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1543+195G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12138631 | |||||||
| chr1:12138948 | G | GCCTTGAA others(59): Show |
44 | a0001c0001t0001g0020 a0001c0001t0001g0046 a0001c0001t0001g0074 others(41): Show |
44 | HG00438.hp2 HG00558.hp2 HG02015.hp1 others(41): Show |
intron_variant | MODIFIER | c.1543+515_1543+580d others(68): Show |
TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr1 | 12138948 | ||||||
| chr1:12139002 | G | A | 1 | a0001c0002t0001g0078 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1543+566G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12139002 | |||||||
| chr1:12139019 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1543+583A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12139019 | |||||||
| chr1:12139120 | G | C | 2 | a0002c0006t0003g0149 a0002c0010t0024g0354 |
2 | HG01891.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1543+684G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12139120 | |||||||
| chr1:12139138 | A | G | 5 | a0001c0001t0007g0198 a0001c0001t0009g0089 a0001c0001t0009g0234 others(2): Show |
5 | HG02055.hp2 HG02717.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1543+702A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12139138 | |||||||
| chr1:12139429 | G | A | 1 | a0001c0001t0001g0263 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1543+993G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12139429 | |||||||
| chr1:12139483 | T | G | 1 | a0001c0001t0001g0332 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1543+1047T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12139483 | |||||||
| chr1:12139505 | G | A | 3 | a0001c0001t0001g0233 a0001c0003t0010g0195 a0005c0015t0001g0350 |
3 | HG01106.hp2 HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1543+1069G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12139505 | |||||||
| chr1:12139694 | T | C | 3 | a0001c0001t0007g0193 a0001c0003t0007g0301 a0010c0024t0001g0238 |
3 | HG02257.hp1 HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1543+1258T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12139694 | |||||||
| chr1:12140093 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1543+1657C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12140093 | |||||||
| chr1:12140234 | C | T | 3 | a0001c0001t0001g0014 a0001c0001t0007g0192 a0001c0001t0007g0216 |
3 | HG01192.hp2 HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1543+1798C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12140234 | |||||||
| chr1:12140289 | C | T | 3 | a0001c0001t0001g0233 a0001c0003t0010g0195 a0005c0015t0001g0350 |
3 | HG01106.hp2 HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1543+1853C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12140289 | |||||||
| chr1:12140380 | A | G | 1 | a0001c0002t0001g0316 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1544-1907A>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12140380 | |||||||
| chr1:12140442 | C | T | 1 | a0001c0009t0001g0360 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1544-1845C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12140442 | |||||||
| chr1:12140572 | C | T | 4 | a0001c0001t0002g0172 a0001c0003t0002g0197 a0001c0004t0002g0169 others(1): Show |
4 | HG02451.hp1 HG02717.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1544-1715C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12140572 | |||||||
| chr1:12140656 | C | T | 1 | a0002c0006t0001g0222 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1544-1631C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12140656 | |||||||
| chr1:12140824 | C | T | 1 | a0001c0002t0001g0239 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1544-1463C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12140824 | |||||||
| chr1:12140973 | G | C | 1 | a0001c0002t0001g0078 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1544-1314G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12140973 | |||||||
| chr1:12140984 | C | G | 2 | a0001c0003t0001g0336 a0001c0003t0020g0073 |
2 | NA18942.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.1544-1303C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12140984 | |||||||
| chr1:12141026 | T | C | 26 | a0001c0001t0001g0138 a0001c0001t0001g0173 a0001c0001t0001g0190 others(23): Show |
26 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.1544-1261T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12141026 | |||||||
| chr1:12141183 | T | C | 42 | a0001c0001t0001g0138 a0001c0001t0001g0173 a0001c0001t0001g0190 others(39): Show |
42 | HG01167.hp2 HG01884.hp2 HG01891.hp1 others(39): Show |
intron_variant | MODIFIER | c.1544-1104T>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12141183 | |||||||
| chr1:12141191 | C | T | 10 | a0001c0002t0001g0015 a0001c0003t0001g0025 a0001c0003t0001g0057 others(7): Show |
10 | HG00558.hp1 HG00597.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.1544-1096C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12141191 | |||||||
| chr1:12141416 | C | T | 1 | a0001c0001t0001g0305 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1544-871C>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12141416 | |||||||
| chr1:12141519 | G | A | 1 | a0001c0003t0002g0214 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1544-768G>A | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12141519 | |||||||
| chr1:12141779 | G | T | 1 | a0001c0023t0001g0061 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1544-508G>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12141779 | |||||||
| chr1:12141788 | T | G | 89 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0030 others(86): Show |
89 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.1544-499T>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12141788 | |||||||
| chr1:12142018 | C | G | 3 | a0001c0003t0003g0225 a0001c0003t0003g0226 a0001c0007t0015g0189 |
3 | HG02895.hp2 HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1544-269C>G | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12142018 | |||||||
| chr1:12142038 | G | C | 155 | a0001c0001t0001g0011 a0001c0001t0001g0030 a0001c0001t0001g0037 others(152): Show |
155 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.1544-249G>C | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12142038 | |||||||
| chr1:12142063 | A | T | 3 | a0001c0003t0003g0225 a0001c0003t0003g0226 a0001c0007t0015g0189 |
3 | HG02895.hp2 HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1544-224A>T | TNFRSF8 | ENSG00000120949.15 | transcript | ENST00000263932.7 | protein_coding | 14/14 | chr1 | 12142063 |