Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 84231 |
| ensemblid | ENSG00000131653.14 |
| hgncid | 20456 |
| symbol | TRAF7 |
| name | TNF receptor associated factor 7 |
| refseq_nuc | NM_032271.3 |
| refseq_prot | NP_115647.2 |
| ensembl_nuc | ENST00000326181.11 |
| ensembl_prot | ENSP00000318944.6 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 2155782 |
| end | 2178129 |
| strand | + |
| ver | v1.2 |
| region | chr16:2155782-2178129 |
| region5000 | chr16:2150782-2183129 |
| regionname0 | TRAF7_chr16_2155782_2178129 |
| regionname5000 | TRAF7_chr16_2150782_2183129 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 670 | 315 | 94 | 63 | 100 | 14 | 42 | 62 | TRAF7_chr16_2150782_2183129 | TRAF7 | MSSGK others(665): Show |
chr16 | 2150782 | 2183129 |
| a0002 | 0/0 | 670 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | TRAF7_chr16_2150782_2183129 | TRAF7 | MSSGK others(665): Show |
chr16 | 2150782 | 2183129 |
| a0003 | 0/0 | 670 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | MSSGK others(665): Show |
chr16 | 2150782 | 2183129 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2010 | 296 | 87 | 58 | 94 | 13 | 42 | TRAF7_chr16_2150782_2183129 | TRAF7 | ATGAG others(2005): Show |
chr16 | 2150782 | 2183129 | ||
| a0001c0002 | 0/0 | 2010 | 7 | 6 | 1 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | ATGAG others(2005): Show |
chr16 | 2150782 | 2183129 | ||
| a0001c0003 | 0/0 | 2010 | 5 | 0 | 0 | 4 | 1 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | ATGAG others(2005): Show |
chr16 | 2150782 | 2183129 | ||
| a0001c0005 | 0/0 | 2010 | 3 | 0 | 3 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | ATGAG others(2005): Show |
chr16 | 2150782 | 2183129 | ||
| a0001c0006 | 0/0 | 2010 | 2 | 0 | 0 | 2 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | ATGAG others(2005): Show |
chr16 | 2150782 | 2183129 | ||
| a0001c0007 | 0/0 | 2010 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | ATGAG others(2005): Show |
chr16 | 2150782 | 2183129 | ||
| a0001c0008 | 0/0 | 2010 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | ATGAG others(2005): Show |
chr16 | 2150782 | 2183129 | ||
| a0002c0004 | 0/0 | 2010 | 4 | 0 | 0 | 4 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | ATGAG others(2005): Show |
chr16 | 2150782 | 2183129 | ||
| a0003c0009 | 0/0 | 2010 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | ATGAG others(2005): Show |
chr16 | 2150782 | 2183129 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3683 | 224 | 42 | 48 | 86 | 10 | 36 | TRAF7_chr16_2150782_2183129 | TRAF7 | CCCTT others(3678): Show |
chr16 | 2150782 | 2183129 |
| a0001c0001t0002 | 0/0 | 3683 | 33 | 30 | 2 | 0 | 1 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | CCCTT others(3678): Show |
chr16 | 2150782 | 2183129 |
| a0001c0001t0003 | 0/0 | 3683 | 11 | 0 | 5 | 0 | 2 | 4 | TRAF7_chr16_2150782_2183129 | TRAF7 | CCCTT others(3678): Show |
chr16 | 2150782 | 2183129 |
| a0001c0001t0004 | 0/0 | 3683 | 3 | 1 | 0 | 2 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | CCCTT others(3678): Show |
chr16 | 2150782 | 2183129 |
| a0001c0001t0005 | 0/0 | 3683 | 2 | 2 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | CCCTT others(3678): Show |
chr16 | 2150782 | 2183129 |
| a0001c0001t0006 | 0/0 | 3683 | 2 | 2 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | CCCTT others(3678): Show |
chr16 | 2150782 | 2183129 |
| a0001c0001t0007 | 0/0 | 3683 | 2 | 0 | 0 | 0 | 0 | 2 | TRAF7_chr16_2150782_2183129 | TRAF7 | CCCTT others(3678): Show |
chr16 | 2150782 | 2183129 |
| a0001c0001t0008 | 0/0 | 3683 | 2 | 2 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | CCCTT others(3678): Show |
chr16 | 2150782 | 2183129 |
| a0001c0001t0009 | 0/0 | 3683 | 2 | 0 | 0 | 2 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | CCCTT others(3678): Show |
chr16 | 2150782 | 2183129 |
| a0001c0001t0010 | 0/0 | 3683 | 2 | 0 | 0 | 2 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | CCCTT others(3678): Show |
chr16 | 2150782 | 2183129 |
| a0001c0001t0011 | 0/0 | 3683 | 2 | 2 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | CCCTT others(3678): Show |
chr16 | 2150782 | 2183129 |
| a0001c0001t0012 | 0/0 | 3683 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | CCCTT others(3678): Show |
chr16 | 2150782 | 2183129 |
| a0001c0001t0013 | 0/0 | 3683 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | CCCTT others(3678): Show |
chr16 | 2150782 | 2183129 |
| a0001c0001t0014 | 0/0 | 3683 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | CCCTT others(3678): Show |
chr16 | 2150782 | 2183129 |
| a0001c0001t0015 | 0/0 | 3683 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | CCCTT others(3678): Show |
chr16 | 2150782 | 2183129 |
| a0001c0001t0016 | 0/0 | 3670 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | CCCTT others(3665): Show |
chr16 | 2150782 | 2183129 |
| a0001c0001t0017 | 0/0 | 3683 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | CCCTT others(3678): Show |
chr16 | 2150782 | 2183129 |
| a0001c0001t0018 | 0/0 | 3683 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | CCCTT others(3678): Show |
chr16 | 2150782 | 2183129 |
| a0001c0001t0019 | 0/0 | 3683 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | CCCTT others(3678): Show |
chr16 | 2150782 | 2183129 |
| a0001c0001t0021 | 0/0 | 3683 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | CCCTT others(3678): Show |
chr16 | 2150782 | 2183129 |
| a0001c0001t0022 | 0/0 | 3683 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | CCCTT others(3678): Show |
chr16 | 2150782 | 2183129 |
| a0001c0001t0023 | 0/0 | 3683 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | CCCTT others(3678): Show |
chr16 | 2150782 | 2183129 |
| a0001c0002t0001 | 0/0 | 3683 | 7 | 6 | 1 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | CCCTT others(3678): Show |
chr16 | 2150782 | 2183129 |
| a0001c0003t0001 | 0/0 | 3683 | 5 | 0 | 0 | 4 | 1 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | CCCTT others(3678): Show |
chr16 | 2150782 | 2183129 |
| a0001c0005t0001 | 0/0 | 3683 | 3 | 0 | 3 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | CCCTT others(3678): Show |
chr16 | 2150782 | 2183129 |
| a0001c0006t0001 | 0/0 | 3683 | 2 | 0 | 0 | 2 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | CCCTT others(3678): Show |
chr16 | 2150782 | 2183129 |
| a0001c0007t0020 | 0/0 | 3683 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | CCCTT others(3678): Show |
chr16 | 2150782 | 2183129 |
| a0001c0008t0001 | 0/0 | 3683 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | CCCTT others(3678): Show |
chr16 | 2150782 | 2183129 |
| a0002c0004t0001 | 0/0 | 3683 | 4 | 0 | 0 | 4 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | CCCTT others(3678): Show |
chr16 | 2150782 | 2183129 |
| a0003c0009t0001 | 0/0 | 3683 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | CCCTT others(3678): Show |
chr16 | 2150782 | 2183129 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 25 | 2 | 6 | 9 | 1 | 7 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0002 | 0/0 | 21 | 0 | 9 | 6 | 2 | 4 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0003 | 0/0 | 23 | 0 | 4 | 13 | 0 | 6 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0004 | 0/0 | 15 | 14 | 1 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0005 | 0/0 | 6 | 1 | 3 | 0 | 0 | 2 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0006 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0007 | 0/0 | 4 | 2 | 1 | 0 | 1 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0049 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0064 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0002g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0002g0010 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0002g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0002g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0002g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0002g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0002g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0002g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0003g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0004g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0004g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0005g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0005g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0006g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0006g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0007g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0007g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0008g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0008g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0009g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0010g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0011g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0012g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0013g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0014g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0015g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0016g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0017g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0018g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0019g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0021g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0022g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0001t0023g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0002t0001g0001 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0003t0001g0004 | 0/0 | 4 | 0 | 0 | 3 | 1 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0005t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0005t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0005t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0006t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0006t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0007t0020g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0001c0008t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0002c0004t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0002c0004t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| a0003c0009t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0129 | EUR | GBR | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0073 | EUR | GBR | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | GBR | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | GBR | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG00280 | hp1 | a0001 | c0003 | t0001 | g0004 | EUR | FIN | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | FIN | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0055 | EUR | FIN | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG00423 | hp2 | a0001 | c0001 | t0009 | g0003 | EAS | CHS | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | CHS | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | CHS | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG00639 | hp2 | a0001 | c0008 | t0001 | g0062 | AMR | PUR | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG00735 | hp1 | a0003 | c0009 | t0001 | g0002 | AMR | PUR | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG00735 | hp2 | a0001 | c0001 | t0015 | g0104 | AMR | PUR | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG01074 | hp2 | a0001 | c0005 | t0001 | g0072 | AMR | PUR | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0066 | AMR | PUR | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0028 | AMR | CLM | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0028 | AMR | CLM | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG01261 | hp2 | a0001 | c0001 | t0017 | g0001 | AMR | CLM | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0148 | AMR | CLM | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG01433 | hp1 | a0001 | c0005 | t0001 | g0039 | AMR | CLM | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0047 | EUR | IBS | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | ACB | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0044 | AFR | ACB | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0065 | AMR | PEL | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | ACB | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02083 | hp1 | a0001 | c0001 | t0018 | g0105 | EAS | KHV | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02258 | hp1 | a0001 | c0001 | t0008 | g0071 | AFR | ACB | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | ACB | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02280 | hp2 | a0001 | c0001 | t0011 | g0023 | AFR | ACB | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02300 | hp2 | a0001 | c0001 | t0016 | g0145 | AMR | PEL | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | GWD | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | GWD | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0043 | AFR | GWD | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02630 | hp2 | a0001 | c0001 | t0013 | g0058 | AFR | GWD | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02647 | hp2 | a0001 | c0001 | t0012 | g0037 | AFR | GWD | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02698 | hp1 | a0001 | c0001 | t0007 | g0134 | SAS | PJL | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0123 | SAS | PJL | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0042 | AFR | GWD | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02717 | hp2 | a0001 | c0001 | t0008 | g0139 | AFR | GWD | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0142 | AFR | GWD | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | GWD | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02809 | hp2 | a0001 | c0001 | t0019 | g0167 | AFR | GWD | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02895 | hp1 | a0001 | c0001 | t0006 | g0157 | AFR | GWD | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0060 | AFR | ESN | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | ESN | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | ESN | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG03041 | hp1 | a0001 | c0001 | t0022 | g0163 | AFR | GWD | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | GWD | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG03098 | hp2 | a0001 | c0007 | t0020 | g0158 | AFR | MSL | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | ESN | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | ESN | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | ESN | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG03195 | hp1 | a0001 | c0001 | t0011 | g0023 | AFR | ESN | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | MSL | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0050 | AFR | MSL | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0153 | AFR | MSL | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | MSL | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | MSL | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ESN | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | GWD | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | GWD | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | MSL | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | MSL | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | STU | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0076 | SAS | PJL | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | BEB | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | BEB | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | BEB | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG04115 | hp1 | a0001 | c0001 | t0007 | g0002 | SAS | STU | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0063 | SAS | STU | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0124 | SAS | BEB | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | BEB | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | STU | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | STU | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0054 | AFR | YRI | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | YRI | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | CHB | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | CHB | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA18906 | hp2 | a0001 | c0001 | t0014 | g0017 | AFR | YRI | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA18943 | hp1 | a0001 | c0001 | t0021 | g0006 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA18944 | hp1 | a0001 | c0006 | t0001 | g0096 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA18944 | hp2 | a0002 | c0004 | t0001 | g0002 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA18950 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA18951 | hp1 | a0002 | c0004 | t0001 | g0002 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA18969 | hp2 | a0001 | c0001 | t0009 | g0003 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA18981 | hp2 | a0002 | c0004 | t0001 | g0131 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA18986 | hp1 | a0001 | c0006 | t0001 | g0001 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA18990 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA19002 | hp1 | a0001 | c0001 | t0004 | g0015 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA19004 | hp2 | a0001 | c0003 | t0001 | g0080 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA19005 | hp1 | a0001 | c0001 | t0010 | g0011 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA19007 | hp1 | a0002 | c0004 | t0001 | g0002 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0048 | AFR | LWK | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0057 | AFR | LWK | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA19043 | hp1 | a0001 | c0001 | t0005 | g0152 | AFR | LWK | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0059 | AFR | LWK | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA19077 | hp2 | a0001 | c0001 | t0010 | g0011 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA19078 | hp1 | a0001 | c0001 | t0004 | g0125 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA19080 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | YRI | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | YRI | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ASW | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0045 | AFR | ASW | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0061 | EUR | TSI | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0119 | EUR | TSI | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | GIH | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | GIH | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG01123 | hp1 | a0001 | c0005 | t0001 | g0029 | AMR | CLM | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | ACB | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | ACB | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ACB | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0046 | AFR | ACB | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | ACB | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG03471 | hp1 | a0001 | c0001 | t0006 | g0156 | AFR | MSL | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | MSL | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | USA | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | USA | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA20300 | hp1 | a0001 | c0001 | t0023 | g0038 | AFR | USA | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | USA | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | LWK | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | LWK | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0049 | REF | REF | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0064 | REF | REF | TRAF7_chr16_2150782_2183129 | TRAF7 | chr16 | 2150782 | 2183129 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:2163948 | A | G | 1 | a0003 | 1 | HG00735.hp1 | missense_variant | MODERATE | c.28A>G | p.Asn10Asp | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/21 | 143/3683 | 28/2013 | 10/670 | chr16 | 2163948 | |||
| chr16:2165882 | A | G | 1 | a0002 | 4 | NA18944.hp2 NA18951.hp1 NA18981.hp2 others(1): Show |
missense_variant | MODERATE | c.85A>G | p.Arg29Gly | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 3/21 | 200/3683 | 85/2013 | 29/670 | chr16 | 2165882 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:2170640 | C | T | 1 | a0002c0004 | 4 | NA18944.hp2 NA18951.hp1 NA18981.hp2 others(1): Show |
synonymous_variant | LOW | c.258C>T | p.Ser86Ser | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 5/21 | 373/3683 | 258/2013 | 86/670 | chr16 | 2170640 | |||
| chr16:2170646 | C | T | 1 | a0001c0006 | 2 | NA18944.hp1 NA18986.hp1 |
synonymous_variant | LOW | c.264C>T | p.Ser88Ser | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 5/21 | 379/3683 | 264/2013 | 88/670 | chr16 | 2170646 | |||
| chr16:2171592 | C | T | 1 | a0001c0002 | 7 | HG01243.hp1 HG02109.hp2 HG02280.hp1 others(4): Show |
synonymous_variant | LOW | c.462C>T | p.Cys154Cys | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 7/21 | 577/3683 | 462/2013 | 154/670 | chr16 | 2171592 | |||
| chr16:2172285 | C | T | 1 | a0001c0005 | 3 | HG01074.hp2 HG01123.hp1 HG01433.hp1 |
synonymous_variant | LOW | c.570C>T | p.His190His | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 8/21 | 685/3683 | 570/2013 | 190/670 | chr16 | 2172285 | |||
| chr16:2172597 | C | T | 1 | a0001c0008 | 1 | HG00639.hp2 | splice_region_variant&synonymous_variant | LOW | c.792C>T | p.Tyr264Tyr | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 9/21 | 907/3683 | 792/2013 | 264/670 | chr16 | 2172597 | |||
| chr16:2176174 | C | T | 1 | a0001c0007 | 1 | HG03098.hp2 | synonymous_variant | LOW | c.1872C>T | p.Ser624Ser | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 19/21 | 1987/3683 | 1872/2013 | 624/670 | chr16 | 2176174 | |||
| chr16:2176327 | C | T | 1 | a0001c0003 | 5 | HG00280.hp1 NA18950.hp1 NA18990.hp2 others(2): Show |
synonymous_variant | LOW | c.1941C>T | p.Thr647Thr | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 20/21 | 2056/3683 | 1941/2013 | 647/670 | chr16 | 2176327 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:2155797 | C | T | 1 | a0001c0001t0023 | 1 | NA20300.hp1 | 5_prime_UTR_variant | MODIFIER | c.-100C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/21 | 8124 | chr16 | 2155797 | ||||||
| chr16:2155798 | G | T | 1 | a0001c0001t0011 | 2 | HG02280.hp2 HG03195.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-99G>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/21 | chr16 | 2155798 | |||||||
| chr16:2155820 | G | A | 6 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0011 others(3): Show |
40 | HG01069.hp1 HG01071.hp2 HG01515.hp1 others(37): Show |
5_prime_UTR_variant | MODIFIER | c.-77G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/21 | 8101 | chr16 | 2155820 | ||||||
| chr16:2176703 | G | A | 1 | a0001c0001t0005 | 2 | HG03453.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*129G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 21/21 | 129 | chr16 | 2176703 | ||||||
| chr16:2176705 | G | C | 1 | a0001c0001t0015 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*131G>C | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 21/21 | 131 | chr16 | 2176705 | ||||||
| chr16:2176781 | G | A | 1 | a0001c0001t0006 | 2 | HG02895.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*207G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 21/21 | 207 | chr16 | 2176781 | ||||||
| chr16:2176805 | GCCCACCC others(6): Show |
G | 1 | a0001c0001t0016 | 1 | HG02300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*253_*265delCCATCC others(7): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 21/21 | 253 | INFO_REALIGN_3_PRIME | chr16 | 2176805 | |||||
| chr16:2177086 | C | T | 1 | a0001c0001t0016 | 1 | HG02300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*512C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 21/21 | 512 | chr16 | 2177086 | ||||||
| chr16:2177206 | C | T | 1 | a0001c0001t0010 | 2 | NA19005.hp1 NA19077.hp2 |
3_prime_UTR_variant | MODIFIER | c.*632C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 21/21 | 632 | chr16 | 2177206 | ||||||
| chr16:2177212 | C | T | 1 | a0001c0001t0014 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*638C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 21/21 | 638 | chr16 | 2177212 | ||||||
| chr16:2177215 | C | T | 2 | a0001c0001t0004 a0001c0001t0013 |
4 | HG02630.hp2 HG02723.hp1 NA19002.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*641C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 21/21 | 641 | chr16 | 2177215 | ||||||
| chr16:2177288 | G | A | 1 | a0001c0001t0017 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*714G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 21/21 | 714 | chr16 | 2177288 | ||||||
| chr16:2177367 | C | T | 1 | a0001c0001t0003 | 11 | HG00323.hp2 HG01081.hp2 HG01256.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*793C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 21/21 | 793 | chr16 | 2177367 | ||||||
| chr16:2177384 | C | T | 1 | a0001c0001t0009 | 2 | HG00423.hp2 NA18969.hp2 |
3_prime_UTR_variant | MODIFIER | c.*810C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 21/21 | 810 | chr16 | 2177384 | ||||||
| chr16:2177428 | T | C | 1 | a0001c0001t0018 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*854T>C | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 21/21 | 854 | chr16 | 2177428 | ||||||
| chr16:2177492 | G | A | 1 | a0001c0001t0019 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*918G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 21/21 | 918 | chr16 | 2177492 | ||||||
| chr16:2177584 | C | G | 1 | a0001c0001t0022 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1010C>G | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 21/21 | 1010 | chr16 | 2177584 | ||||||
| chr16:2177665 | G | T | 1 | a0001c0001t0012 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1091G>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 21/21 | 1091 | chr16 | 2177665 | ||||||
| chr16:2177817 | C | A | 1 | a0001c0007t0020 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1243C>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 21/21 | 1243 | chr16 | 2177817 | ||||||
| chr16:2177818 | G | A | 1 | a0001c0001t0007 | 2 | HG02698.hp1 HG04115.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1244G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 21/21 | 1244 | chr16 | 2177818 | ||||||
| chr16:2177871 | C | G | 2 | a0001c0001t0008 a0001c0001t0019 |
3 | HG02258.hp1 HG02717.hp2 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1297C>G | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 21/21 | 1297 | chr16 | 2177871 | ||||||
| chr16:2178010 | T | C | 1 | a0001c0001t0021 | 1 | NA18943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1436T>C | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 21/21 | 1436 | chr16 | 2178010 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:2155919 | G | C | 1 | a0001c0001t0012g0037 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-39+61G>C | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2155919 | |||||||
| chr16:2155929 | G | T | 1 | a0001c0001t0001g0168 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-39+71G>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2155929 | |||||||
| chr16:2155930 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-39+72C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2155930 | |||||||
| chr16:2155938 | TCGAGGCG others(3): Show |
T | 1 | a0001c0001t0019g0167 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-39+96_-39+105delC others(9): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr16 | 2155938 | ||||||
| chr16:2156002 | C | CGGTCGGG others(5): Show |
2 | a0001c0001t0005g0152 a0001c0001t0005g0153 |
2 | HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-39+149_-39+160dup others(12): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr16 | 2156002 | ||||||
| chr16:2156019 | A | G | 14 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0159 others(11): Show |
17 | HG00423.hp1 HG00673.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.-39+161A>G | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2156019 | |||||||
| chr16:2156043 | C | G | 4 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0150 others(1): Show |
6 | HG00408.hp1 HG00609.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.-39+185C>G | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2156043 | |||||||
| chr16:2156482 | T | A | 22 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0002g0009 others(19): Show |
31 | HG01069.hp1 HG01071.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.-39+624T>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2156482 | |||||||
| chr16:2156538 | G | A | 5 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0051 others(2): Show |
7 | HG02071.hp2 HG02074.hp2 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.-39+680G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2156538 | |||||||
| chr16:2156590 | A | G | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(138): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.-39+732A>G | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2156590 | |||||||
| chr16:2156729 | T | TG | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(167): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.-39+875dupG | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr16 | 2156729 | ||||||
| chr16:2156742 | G | A | 6 | a0001c0001t0001g0053 a0001c0001t0001g0154 a0001c0001t0001g0155 others(3): Show |
6 | HG02257.hp1 HG02895.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-39+884G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2156742 | |||||||
| chr16:2156792 | G | A | 1 | a0001c0001t0003g0148 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-39+934G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2156792 | |||||||
| chr16:2156795 | G | T | 1 | a0001c0001t0001g0147 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-39+937G>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2156795 | |||||||
| chr16:2156890 | C | G | 1 | a0001c0001t0001g0146 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-39+1032C>G | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2156890 | |||||||
| chr16:2157093 | ACCCCTTC others(45): Show |
A | 4 | a0001c0001t0006g0156 a0001c0001t0006g0157 a0001c0001t0016g0145 others(1): Show |
4 | HG02300.hp2 HG02895.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-39+1238_-39+1289d others(54): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr16 | 2157093 | ||||||
| chr16:2157097 | C | T | 2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | HG02257.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-39+1239C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2157097 | |||||||
| chr16:2157244 | A | G | 1 | a0001c0001t0001g0144 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-39+1386A>G | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2157244 | |||||||
| chr16:2157248 | T | A | 1 | a0001c0001t0002g0009 | 4 | HG02055.hp1 HG03130.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-39+1390T>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2157248 | |||||||
| chr16:2157260 | G | A | 1 | a0001c0001t0012g0037 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-39+1402G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2157260 | |||||||
| chr16:2157285 | G | C | 1 | a0001c0001t0003g0066 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-39+1427G>C | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2157285 | |||||||
| chr16:2157350 | G | A | 1 | a0001c0001t0002g0054 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-39+1492G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2157350 | |||||||
| chr16:2157474 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-39+1616G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2157474 | |||||||
| chr16:2157513 | G | A | 1 | a0001c0001t0003g0055 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-39+1655G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2157513 | |||||||
| chr16:2157561 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-39+1703C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2157561 | |||||||
| chr16:2157745 | C | A | 1 | a0001c0001t0001g0067 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-39+1887C>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2157745 | |||||||
| chr16:2157804 | G | A | 1 | a0001c0001t0023g0038 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-39+1946G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2157804 | |||||||
| chr16:2157845 | G | C | 1 | a0001c0001t0001g0068 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-39+1987G>C | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2157845 | |||||||
| chr16:2158012 | G | T | 1 | a0001c0001t0001g0053 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-39+2154G>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2158012 | |||||||
| chr16:2158077 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-39+2219G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2158077 | |||||||
| chr16:2158123 | A | G | 1 | a0001c0001t0016g0145 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-39+2265A>G | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2158123 | |||||||
| chr16:2158175 | G | T | 1 | a0001c0001t0003g0065 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-39+2317G>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2158175 | |||||||
| chr16:2158276 | C | T | 1 | a0001c0001t0001g0166 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-39+2418C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2158276 | |||||||
| chr16:2158403 | C | T | 3 | a0001c0001t0001g0141 a0001c0001t0001g0143 a0001c0001t0004g0142 |
3 | HG02723.hp1 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-39+2545C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2158403 | |||||||
| chr16:2158756 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-39+2898G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2158756 | |||||||
| chr16:2158765 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-39+2907C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2158765 | |||||||
| chr16:2158766 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-39+2908G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2158766 | |||||||
| chr16:2158767 | GC | G | 5 | a0001c0001t0002g0019 a0001c0001t0004g0142 a0001c0001t0008g0139 others(2): Show |
6 | HG02717.hp2 HG02723.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-39+2910delC | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2158767 | |||||||
| chr16:2158768 | C | CG | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(103): Show |
179 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.-39+2923dupG | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr16 | 2158768 | ||||||
| chr16:2158768 | C | CGG | 46 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(43): Show |
69 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.-39+2922_-39+2923d others(4): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr16 | 2158768 | ||||||
| chr16:2158768 | C | G | 3 | a0001c0001t0001g0141 a0001c0001t0001g0143 a0001c0001t0008g0071 |
3 | HG02258.hp1 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-39+2910C>G | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2158768 | |||||||
| chr16:2158770 | G | C | 1 | a0001c0001t0008g0071 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-39+2912G>C | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2158770 | |||||||
| chr16:2158771 | G | C | 3 | a0001c0001t0002g0019 a0001c0001t0008g0139 a0001c0001t0019g0167 |
4 | HG02717.hp2 HG02809.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-39+2913G>C | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2158771 | |||||||
| chr16:2158888 | G | A | 13 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0029 others(10): Show |
21 | HG00099.hp2 HG00140.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.-39+3030G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2158888 | |||||||
| chr16:2159297 | T | G | 117 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(114): Show |
221 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.-39+3439T>G | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2159297 | |||||||
| chr16:2159313 | G | A | 1 | a0001c0001t0016g0145 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-39+3455G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2159313 | |||||||
| chr16:2159376 | A | G | 1 | a0001c0001t0016g0145 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-39+3518A>G | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2159376 | |||||||
| chr16:2159447 | G | A | 3 | a0001c0001t0002g0021 a0001c0001t0002g0044 a0001c0001t0002g0050 |
4 | HG01891.hp1 HG01891.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-39+3589G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2159447 | |||||||
| chr16:2159475 | G | A | 1 | a0001c0001t0001g0122 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-39+3617G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2159475 | |||||||
| chr16:2159557 | C | T | 1 | a0001c0001t0002g0059 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-39+3699C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2159557 | |||||||
| chr16:2159575 | G | A | 1 | a0001c0001t0001g0079 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-39+3717G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2159575 | |||||||
| chr16:2159638 | C | T | 1 | a0001c0001t0019g0167 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-39+3780C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2159638 | |||||||
| chr16:2160089 | C | T | 1 | a0001c0001t0013g0058 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-38-3794C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2160089 | |||||||
| chr16:2160155 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-38-3728C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2160155 | |||||||
| chr16:2160264 | T | A | 2 | a0001c0001t0005g0152 a0001c0001t0005g0153 |
2 | HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-38-3619T>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2160264 | |||||||
| chr16:2160406 | G | A | 25 | a0001c0001t0001g0053 a0001c0001t0001g0141 a0001c0001t0001g0143 others(22): Show |
27 | HG00323.hp2 HG00639.hp2 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.-38-3477G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2160406 | |||||||
| chr16:2160434 | GGGCAGGT others(10): Show |
G | 2 | a0001c0001t0002g0045 a0001c0001t0006g0156 |
2 | HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-38-3442_-38-3426d others(19): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr16 | 2160434 | ||||||
| chr16:2160441 | T | C | 1 | a0001c0001t0006g0157 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-38-3442T>C | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2160441 | |||||||
| chr16:2160450 | C | T | 1 | a0001c0001t0006g0157 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-38-3433C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2160450 | |||||||
| chr16:2160451 | A | G | 29 | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0001g0141 others(26): Show |
32 | HG00323.hp2 HG00639.hp2 HG01256.hp1 others(29): Show |
intron_variant | MODIFIER | c.-38-3432A>G | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2160451 | |||||||
| chr16:2160455 | A | G | 1 | a0001c0001t0006g0157 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-38-3428A>G | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2160455 | |||||||
| chr16:2160467 | T | C | 1 | a0001c0001t0006g0157 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-38-3416T>C | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2160467 | |||||||
| chr16:2160502 | C | CGGCGGGC others(42): Show |
1 | a0001c0001t0019g0167 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-38-3357_-38-3309d others(51): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr16 | 2160502 | ||||||
| chr16:2160502 | CGGCGGGC others(42): Show |
C | 1 | a0001c0001t0001g0120 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-38-3357_-38-3309d others(51): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr16 | 2160502 | ||||||
| chr16:2160526 | AGGTGCTC others(42): Show |
A | 5 | a0001c0001t0001g0141 a0001c0001t0001g0143 a0001c0001t0004g0142 others(2): Show |
5 | HG02723.hp1 HG02970.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-38-3340_-38-3292d others(51): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr16 | 2160526 | ||||||
| chr16:2160538 | A | AGGCGGTG others(293): Show |
1 | a0001c0001t0001g0004 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-38-3304_-38-3303i others(302): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr16 | 2160538 | ||||||
| chr16:2160538 | AGGCGGTG others(10): Show |
A | 2 | a0001c0001t0001g0053 a0001c0001t0001g0116 |
2 | HG03209.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.-38-3334_-38-3318d others(19): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr16 | 2160538 | ||||||
| chr16:2160549 | ATGGGCGG others(10): Show |
A | 7 | a0001c0001t0002g0021 a0001c0001t0002g0044 a0001c0001t0002g0046 others(4): Show |
8 | HG01891.hp1 HG01891.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-38-3320_-38-3304d others(19): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr16 | 2160549 | ||||||
| chr16:2160555 | G | GGGCGGTG others(59): Show |
1 | a0001c0001t0002g0045 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-38-3318_-38-3317i others(68): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr16 | 2160555 | ||||||
| chr16:2160566 | G | A | 1 | a0001c0001t0002g0045 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-38-3317G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2160566 | |||||||
| chr16:2160575 | C | A | 17 | a0001c0001t0002g0019 a0001c0001t0003g0028 a0001c0001t0003g0055 others(14): Show |
19 | HG00323.hp2 HG00639.hp2 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.-38-3308C>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2160575 | |||||||
| chr16:2160623 | G | A | 1 | a0001c0003t0001g0080 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-38-3260G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2160623 | |||||||
| chr16:2160805 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-38-3078C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2160805 | |||||||
| chr16:2161062 | C | T | 2 | a0001c0001t0001g0034 a0001c0001t0002g0009 |
6 | HG01884.hp2 HG02055.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.-38-2821C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2161062 | |||||||
| chr16:2161157 | T | C | 2 | a0001c0001t0003g0028 a0001c0001t0003g0148 |
3 | HG01256.hp1 HG01258.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.-38-2726T>C | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2161157 | |||||||
| chr16:2161168 | C | CCCCTCCT others(5): Show |
1 | a0001c0001t0001g0030 | 2 | HG00438.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.-38-2704_-38-2693d others(14): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr16 | 2161168 | ||||||
| chr16:2161208 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-38-2675C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2161208 | |||||||
| chr16:2161241 | T | C | 1 | a0001c0001t0004g0125 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-38-2642T>C | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2161241 | |||||||
| chr16:2161243 | C | T | 3 | a0001c0001t0002g0026 a0001c0001t0002g0046 a0001c0001t0013g0058 |
4 | HG02486.hp2 HG02559.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38-2640C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2161243 | |||||||
| chr16:2161261 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-38-2622G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2161261 | |||||||
| chr16:2161464 | G | C | 2 | a0001c0001t0001g0081 a0001c0001t0001g0159 |
2 | NA18971.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.-38-2419G>C | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2161464 | |||||||
| chr16:2161537 | G | C | 1 | a0001c0001t0001g0012 | 3 | HG01109.hp2 HG01261.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-38-2346G>C | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2161537 | |||||||
| chr16:2161538 | C | A | 1 | a0001c0001t0001g0012 | 3 | HG01109.hp2 HG01261.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-38-2345C>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2161538 | |||||||
| chr16:2161718 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-38-2165C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2161718 | |||||||
| chr16:2161740 | C | G | 1 | a0001c0001t0001g0119 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-38-2143C>G | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2161740 | |||||||
| chr16:2162131 | A | G | 1 | a0001c0001t0001g0068 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-38-1752A>G | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2162131 | |||||||
| chr16:2162226 | GGGCCTGG others(807): Show |
G | 1 | a0001c0001t0003g0055 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-38-1653_-38-840de others(1): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr16 | 2162226 | ||||||
| chr16:2162275 | C | T | 8 | a0001c0001t0001g0141 a0001c0001t0001g0143 a0001c0001t0002g0019 others(5): Show |
9 | HG02258.hp1 HG02717.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.-38-1608C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2162275 | |||||||
| chr16:2162294 | C | T | 4 | a0001c0001t0002g0019 a0001c0001t0008g0071 a0001c0001t0008g0139 others(1): Show |
5 | HG02258.hp1 HG02717.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-38-1589C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2162294 | |||||||
| chr16:2162315 | G | A | 2 | a0001c0001t0001g0002 a0001c0001t0001g0015 |
3 | HG02080.hp1 HG03927.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-38-1568G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2162315 | |||||||
| chr16:2162703 | G | T | 1 | a0001c0001t0012g0037 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-38-1180G>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2162703 | |||||||
| chr16:2162767 | G | A | 4 | a0001c0001t0001g0001 a0001c0001t0001g0089 a0001c0001t0001g0119 others(1): Show |
8 | HG01081.hp1 HG01123.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.-38-1116G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2162767 | |||||||
| chr16:2162888 | C | T | 1 | a0001c0001t0003g0066 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-38-995C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2162888 | |||||||
| chr16:2162960 | C | G | 1 | a0001c0001t0001g0014 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-38-923C>G | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2162960 | |||||||
| chr16:2162979 | G | T | 1 | a0001c0001t0001g0003 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-38-904G>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2162979 | |||||||
| chr16:2162987 | G | A | 4 | a0001c0001t0002g0019 a0001c0001t0008g0071 a0001c0001t0008g0139 others(1): Show |
5 | HG02258.hp1 HG02717.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-38-896G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2162987 | |||||||
| chr16:2163089 | C | T | 4 | a0001c0001t0002g0021 a0001c0001t0002g0044 a0001c0001t0002g0048 others(1): Show |
5 | HG01891.hp1 HG01891.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.-38-794C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2163089 | |||||||
| chr16:2163119 | C | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0078 |
5 | HG00140.hp1 HG00738.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.-38-764C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2163119 | |||||||
| chr16:2163178 | C | T | 1 | a0001c0001t0002g0009 | 4 | HG02055.hp1 HG03130.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-38-705C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2163178 | |||||||
| chr16:2163256 | G | A | 1 | a0001c0001t0002g0044 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-38-627G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2163256 | |||||||
| chr16:2163258 | G | A | 3 | a0001c0001t0002g0021 a0001c0001t0002g0044 a0001c0001t0002g0050 |
4 | HG01891.hp1 HG01891.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-38-625G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2163258 | |||||||
| chr16:2163277 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-38-606C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2163277 | |||||||
| chr16:2163329 | G | C | 1 | a0001c0001t0002g0048 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-38-554G>C | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2163329 | |||||||
| chr16:2163523 | C | T | 1 | a0001c0001t0002g0019 | 2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-38-360C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2163523 | |||||||
| chr16:2163759 | G | GT | 33 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0030 others(30): Show |
63 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.-38-123dupT | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr16 | 2163759 | ||||||
| chr16:2163774 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-38-109G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2163774 | |||||||
| chr16:2163799 | G | C | 1 | a0001c0001t0003g0066 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-38-84G>C | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2163799 | |||||||
| chr16:2163819 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-38-64C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 1/20 | chr16 | 2163819 | |||||||
| chr16:2164096 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.81+95G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164096 | |||||||
| chr16:2164127 | G | C | 1 | a0001c0001t0001g0103 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.81+126G>C | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164127 | |||||||
| chr16:2164128 | G | T | 5 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0002g0047 others(2): Show |
5 | HG01109.hp1 HG01515.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.81+127G>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164128 | |||||||
| chr16:2164134 | G | GGGTGGTG others(12): Show |
1 | a0001c0001t0003g0123 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.81+134_81+135insGT others(17): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2164134 | ||||||
| chr16:2164134 | G | GGGTGTGG others(11): Show |
1 | a0001c0001t0003g0055 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.81+134_81+135insGT others(16): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2164134 | ||||||
| chr16:2164139 | G | GGT | 15 | a0001c0001t0001g0015 a0001c0001t0001g0029 a0001c0001t0001g0040 others(12): Show |
17 | HG01123.hp1 HG01243.hp2 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.81+158_81+159dupTG | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2164139 | ||||||
| chr16:2164139 | G | GGTGTGT | 5 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0002g0010 others(2): Show |
8 | HG01069.hp1 HG01071.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.81+154_81+159dupTG others(4): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2164139 | ||||||
| chr16:2164139 | G | GGTGTGTG others(1): Show |
4 | a0001c0001t0001g0053 a0001c0001t0002g0017 a0001c0001t0002g0020 others(1): Show |
5 | HG02109.hp1 HG02897.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.81+152_81+159dupTG others(6): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2164139 | ||||||
| chr16:2164139 | G | GGTGTGTG others(3): Show |
2 | a0001c0001t0002g0018 a0001c0001t0002g0042 |
3 | HG02717.hp1 HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.81+150_81+159dupTG others(8): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2164139 | ||||||
| chr16:2164139 | G | GGTGTGTG others(5): Show |
1 | a0001c0001t0002g0043 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.81+148_81+159dupTG others(10): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2164139 | ||||||
| chr16:2164139 | G | GGTGTGTG others(9): Show |
2 | a0001c0001t0003g0061 a0001c0008t0001g0062 |
2 | HG00639.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.81+144_81+159dupTG others(14): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2164139 | ||||||
| chr16:2164139 | G | GGTGTGTG others(11): Show |
3 | a0001c0001t0003g0065 a0001c0001t0003g0076 a0001c0001t0003g0124 |
3 | HG01978.hp2 HG03710.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.81+142_81+159dupTG others(16): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2164139 | ||||||
| chr16:2164139 | G | GGTGTGTG others(13): Show |
1 | a0001c0001t0003g0148 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.81+140_81+159dupTG others(18): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2164139 | ||||||
| chr16:2164139 | G | GGTGTGTG others(15): Show |
1 | a0001c0001t0003g0063 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.81+159_81+160insTG others(20): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2164139 | ||||||
| chr16:2164139 | G | GT | 3 | a0001c0001t0003g0055 a0001c0001t0003g0123 a0001c0001t0007g0134 |
3 | HG00323.hp2 HG02698.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.81+138_81+139insT | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164139 | |||||||
| chr16:2164145 | TGTGTGTG others(31): Show |
T | 2 | a0001c0001t0001g0032 a0001c0001t0015g0104 |
3 | HG00735.hp2 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.81+146_81+183delTG others(36): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2164145 | ||||||
| chr16:2164147 | TGTGTGTG others(31): Show |
T | 1 | a0001c0001t0001g0094 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.81+150_81+187delTG others(36): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2164147 | ||||||
| chr16:2164149 | TGTGTGTG others(29): Show |
T | 1 | a0001c0001t0001g0003 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.81+152_81+187delTG others(34): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2164149 | ||||||
| chr16:2164153 | TGTGTGTG others(3): Show |
T | 2 | a0001c0001t0001g0133 a0001c0001t0001g0151 |
2 | HG00408.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.81+154_81+163delTG others(8): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2164153 | ||||||
| chr16:2164155 | TGTGTGCG others(5): Show |
T | 1 | a0001c0001t0001g0083 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.81+156_81+167delTG others(10): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2164155 | ||||||
| chr16:2164155 | TGTGTGCG others(23): Show |
T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0056 |
3 | HG01884.hp2 HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.81+158_81+187delTG others(28): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2164155 | ||||||
| chr16:2164155 | TGTGTGCG others(27): Show |
T | 1 | a0001c0001t0001g0001 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.81+160_81+193delCG others(32): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2164155 | ||||||
| chr16:2164157 | T | C | 2 | a0001c0001t0001g0003 a0001c0001t0001g0004 |
2 | HG02451.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.81+156T>C | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164157 | |||||||
| chr16:2164157 | T | TGC | 7 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(4): Show |
9 | HG00423.hp2 HG00642.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.81+157_81+158insCG | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2164157 | ||||||
| chr16:2164157 | TGTGCGCG others(3): Show |
T | 3 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0035 |
8 | HG00609.hp1 HG01256.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.81+158_81+167delTG others(8): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2164157 | ||||||
| chr16:2164157 | TGTGCGCG others(21): Show |
T | 2 | a0001c0001t0001g0002 a0001c0001t0001g0005 |
2 | HG01515.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.81+162_81+189delCG others(26): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2164157 | ||||||
| chr16:2164157 | TGTGCGCG others(25): Show |
T | 1 | a0001c0001t0001g0001 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.81+160_81+191delCG others(30): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2164157 | ||||||
| chr16:2164159 | T | C | 13 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(10): Show |
19 | HG00423.hp2 HG00642.hp2 HG01516.hp2 others(16): Show |
intron_variant | MODIFIER | c.81+158T>C | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164159 | |||||||
| chr16:2164159 | T | TGC | 52 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(49): Show |
84 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.81+179_81+180dupGC | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2164159 | ||||||
| chr16:2164159 | T | TGCGC | 6 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(3): Show |
10 | HG00140.hp1 HG01978.hp1 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.81+177_81+180dupGC others(2): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2164159 | ||||||
| chr16:2164159 | T | TGTGC | 13 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(10): Show |
20 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(17): Show |
intron_variant | MODIFIER | c.81+159_81+160insTG others(2): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2164159 | ||||||
| chr16:2164159 | T | TGTGCGCG others(3): Show |
1 | a0001c0001t0002g0009 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.81+159_81+160insTG others(8): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2164159 | ||||||
| chr16:2164159 | T | TGTGCGCG others(5): Show |
1 | a0001c0001t0002g0009 | 2 | HG02055.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.81+159_81+160insTG others(10): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2164159 | ||||||
| chr16:2164159 | T | TGTGTGTG others(5): Show |
1 | a0001c0001t0002g0048 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.81+159_81+160insTG others(10): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2164159 | ||||||
| chr16:2164159 | TGC | T | 4 | a0001c0001t0001g0101 a0001c0001t0001g0137 a0001c0001t0002g0009 others(1): Show |
4 | HG02027.hp1 HG02129.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.81+179_81+180delGC | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2164159 | ||||||
| chr16:2164159 | TGCGC | T | 4 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0003g0066 others(1): Show |
5 | HG00140.hp2 HG01081.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.81+177_81+180delGC others(2): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2164159 | ||||||
| chr16:2164159 | TGCGCGC | T | 11 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0012 others(8): Show |
16 | HG00738.hp2 HG01081.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.81+175_81+180delGC others(4): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2164159 | ||||||
| chr16:2164159 | TGCGCGCG others(1): Show |
T | 7 | a0001c0001t0001g0001 a0001c0001t0001g0088 a0001c0001t0001g0097 others(4): Show |
9 | HG00673.hp2 HG01952.hp2 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.81+173_81+180delGC others(6): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2164159 | ||||||
| chr16:2164159 | TGCGCGCG others(3): Show |
T | 11 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0036 others(8): Show |
21 | HG00280.hp1 HG00741.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.81+171_81+180delGC others(8): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2164159 | ||||||
| chr16:2164159 | TGCGCGCG others(5): Show |
T | 1 | a0001c0001t0001g0013 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.81+169_81+180delGC others(10): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2164159 | ||||||
| chr16:2164159 | TGCGCGCG others(7): Show |
T | 3 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0070 |
4 | HG00597.hp1 HG02145.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.81+167_81+180delGC others(12): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2164159 | ||||||
| chr16:2164159 | TGCGCGCG others(19): Show |
T | 2 | a0001c0001t0001g0108 a0001c0001t0016g0145 |
2 | HG02300.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.81+160_81+185delCG others(24): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2164159 | ||||||
| chr16:2164161 | C | T | 39 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0053 others(36): Show |
46 | HG00323.hp2 HG00423.hp1 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.81+160C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164161 | |||||||
| chr16:2164163 | C | T | 32 | a0001c0001t0001g0053 a0001c0001t0001g0141 a0001c0001t0001g0143 others(29): Show |
39 | HG00323.hp2 HG01069.hp1 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.81+162C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164163 | |||||||
| chr16:2164165 | C | T | 26 | a0001c0001t0001g0053 a0001c0001t0001g0117 a0001c0001t0001g0141 others(23): Show |
33 | HG01069.hp1 HG01071.hp2 HG01256.hp1 others(30): Show |
intron_variant | MODIFIER | c.81+164C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164165 | |||||||
| chr16:2164165 | CGCGCGCG others(21): Show |
C | 1 | a0001c0001t0001g0030 | 2 | HG00438.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.81+166_81+193delCG others(26): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2164165 | ||||||
| chr16:2164166 | GCGCGCGC others(9): Show |
G | 2 | a0001c0001t0006g0156 a0001c0001t0006g0157 |
2 | HG02895.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.81+170_81+185delCG others(14): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2164166 | ||||||
| chr16:2164167 | C | T | 22 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0117 others(19): Show |
28 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.81+166C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164167 | |||||||
| chr16:2164167 | CGCGCGCG others(13): Show |
C | 1 | a0001c0001t0001g0016 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.81+170_81+189delCG others(18): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2164167 | ||||||
| chr16:2164168 | GCGCGCGC others(7): Show |
G | 6 | a0001c0001t0001g0112 a0001c0001t0001g0141 a0001c0001t0001g0143 others(3): Show |
6 | HG02723.hp1 HG02735.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+172_81+185delCG others(12): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2164168 | ||||||
| chr16:2164169 | C | T | 15 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0140 others(12): Show |
20 | HG00673.hp2 HG00738.hp2 HG01069.hp1 others(17): Show |
intron_variant | MODIFIER | c.81+168C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164169 | |||||||
| chr16:2164169 | CGCGCGCG others(11): Show |
C | 1 | a0001c0001t0001g0003 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.81+172_81+189delCG others(16): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2164169 | ||||||
| chr16:2164170 | G | C | 1 | a0001c0001t0001g0025 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.81+169G>C | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164170 | |||||||
| chr16:2164171 | C | T | 9 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0002g0010 others(6): Show |
13 | HG01069.hp1 HG01071.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.81+170C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164171 | |||||||
| chr16:2164172 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0010g0011 |
2 | NA18966.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.81+171G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164172 | |||||||
| chr16:2164173 | C | T | 11 | a0001c0001t0001g0004 a0001c0001t0001g0117 a0001c0001t0001g0154 others(8): Show |
15 | HG00639.hp1 HG01069.hp1 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.81+172C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164173 | |||||||
| chr16:2164173 | CGCGCGCG others(11): Show |
C | 1 | a0001c0001t0012g0037 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.81+174_81+191delCG others(16): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2164173 | ||||||
| chr16:2164174 | G | T | 1 | a0001c0001t0001g0117 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.81+173G>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164174 | |||||||
| chr16:2164175 | C | G | 1 | a0001c0001t0001g0117 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.81+174C>G | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164175 | |||||||
| chr16:2164175 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.81+174C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164175 | |||||||
| chr16:2164176 | G | A | 1 | a0001c0001t0001g0002 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.81+175G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164176 | |||||||
| chr16:2164177 | C | G | 1 | a0001c0001t0001g0117 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.81+176C>G | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164177 | |||||||
| chr16:2164181 | C | T | 2 | a0001c0001t0001g0117 a0001c0001t0010g0011 |
2 | NA19077.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.81+180C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164181 | |||||||
| chr16:2164183 | C | T | 10 | a0001c0001t0001g0117 a0001c0001t0001g0141 a0001c0001t0001g0143 others(7): Show |
10 | HG02723.hp1 HG02895.hp1 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.81+182C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164183 | |||||||
| chr16:2164184 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.81+183G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164184 | |||||||
| chr16:2164184 | G | T | 1 | a0001c0001t0001g0117 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.81+183G>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164184 | |||||||
| chr16:2164185 | C | A | 1 | a0001c0001t0001g0117 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.81+184C>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164185 | |||||||
| chr16:2164185 | C | T | 7 | a0001c0001t0001g0141 a0001c0001t0001g0143 a0001c0001t0004g0142 others(4): Show |
7 | HG02723.hp1 HG02895.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.81+184C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164185 | |||||||
| chr16:2164187 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.81+186T>C | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164187 | |||||||
| chr16:2164191 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.81+190T>C | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164191 | |||||||
| chr16:2164198 | T | C | 1 | a0001c0001t0001g0117 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.81+197T>C | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164198 | |||||||
| chr16:2164199 | T | G | 1 | a0001c0001t0001g0117 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.81+198T>G | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164199 | |||||||
| chr16:2164200 | G | C | 1 | a0001c0001t0001g0117 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.81+199G>C | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164200 | |||||||
| chr16:2164202 | G | GCCTGGTT others(420): Show |
1 | a0001c0001t0001g0117 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.81+201_81+202insCC others(425): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164202 | |||||||
| chr16:2164209 | T | G | 1 | a0001c0001t0001g0117 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.81+208T>G | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164209 | |||||||
| chr16:2164209 | T | TAGTGCTG others(444): Show |
1 | a0001c0005t0001g0072 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.81+302_81+752dupAC others(449): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2164209 | ||||||
| chr16:2164247 | T | C | 1 | a0001c0001t0001g0083 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.81+246T>C | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164247 | |||||||
| chr16:2164323 | A | T | 10 | a0001c0001t0003g0028 a0001c0001t0003g0055 a0001c0001t0003g0061 others(7): Show |
11 | HG00323.hp2 HG00639.hp2 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.81+322A>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164323 | |||||||
| chr16:2164332 | T | G | 9 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0002g0010 others(6): Show |
13 | HG01069.hp1 HG01071.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.81+331T>G | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164332 | |||||||
| chr16:2164347 | C | T | 1 | a0001c0001t0002g0045 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.81+346C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164347 | |||||||
| chr16:2164385 | G | C | 9 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0002g0010 others(6): Show |
13 | HG01069.hp1 HG01071.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.81+384G>C | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164385 | |||||||
| chr16:2164387 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.81+386G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164387 | |||||||
| chr16:2164444 | G | C | 1 | a0001c0001t0018g0105 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.81+443G>C | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164444 | |||||||
| chr16:2164446 | T | G | 1 | a0001c0001t0018g0105 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.81+445T>G | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164446 | |||||||
| chr16:2164455 | T | G | 1 | a0001c0001t0018g0105 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.81+454T>G | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164455 | |||||||
| chr16:2164492 | G | A | 1 | a0001c0001t0001g0079 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.81+491G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164492 | |||||||
| chr16:2164523 | A | G | 2 | a0001c0001t0002g0021 a0001c0001t0002g0050 |
3 | HG01891.hp1 HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.81+522A>G | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164523 | |||||||
| chr16:2164533 | G | A | 1 | a0001c0001t0001g0035 | 2 | HG00609.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.81+532G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164533 | |||||||
| chr16:2164574 | A | G | 30 | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0001g0154 others(27): Show |
36 | HG00323.hp2 HG00639.hp2 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.81+573A>G | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164574 | |||||||
| chr16:2164592 | G | A | 2 | a0001c0001t0001g0084 a0001c0001t0001g0085 |
2 | HG00609.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.81+591G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164592 | |||||||
| chr16:2164627 | CGTGGCGC others(34): Show |
C | 3 | a0001c0001t0001g0141 a0001c0001t0001g0143 a0001c0001t0004g0142 |
3 | HG02723.hp1 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.81+642_81+682delCG others(39): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2164627 | ||||||
| chr16:2164633 | G | A | 1 | a0001c0001t0001g0159 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.81+632G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164633 | |||||||
| chr16:2164684 | T | C | 1 | a0001c0001t0002g0047 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.81+683T>C | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164684 | |||||||
| chr16:2164684 | T | TGCATGGT others(75): Show |
1 | a0001c0001t0001g0128 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.81+700_81+781dupGA others(80): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2164684 | ||||||
| chr16:2164684 | T | TGCATGGT others(34): Show |
1 | a0001c0001t0023g0038 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.81+707_81+708insTG others(39): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2164684 | ||||||
| chr16:2164717 | GGCCTGGT others(116): Show |
G | 1 | a0001c0001t0001g0067 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.81+905_82-851del | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2164717 | ||||||
| chr16:2164742 | GAGTGCTG others(34): Show |
G | 2 | a0001c0001t0001g0002 a0001c0001t0001g0129 |
2 | HG00099.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.81+782_81+822delTA others(39): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2164742 | ||||||
| chr16:2164778 | C | T | 1 | a0001c0001t0001g0006 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.81+777C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164778 | |||||||
| chr16:2164779 | G | A | 4 | a0001c0001t0001g0122 a0001c0001t0002g0021 a0001c0001t0002g0044 others(1): Show |
5 | HG01891.hp1 HG01891.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.81+778G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164779 | |||||||
| chr16:2164783 | T | G | 1 | a0001c0001t0001g0002 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.81+782T>G | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164783 | |||||||
| chr16:2164790 | G | A | 5 | a0001c0001t0001g0141 a0001c0001t0001g0143 a0001c0001t0004g0142 others(2): Show |
5 | HG02723.hp1 HG02970.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.81+789G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164790 | |||||||
| chr16:2164799 | G | GGCCTGGT others(34): Show |
1 | a0001c0001t0001g0013 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.81+831_81+871dupTG others(39): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2164799 | ||||||
| chr16:2164832 | T | C | 1 | a0001c0001t0001g0002 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.81+831T>C | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164832 | |||||||
| chr16:2164837 | C | T | 1 | a0003c0009t0001g0002 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.81+836C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164837 | |||||||
| chr16:2164865 | GAGTGCTG others(34): Show |
G | 1 | a0001c0001t0001g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.81+905_82-933delTA others(39): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2164865 | ||||||
| chr16:2164874 | GTGGCCTG others(198): Show |
G | 1 | a0001c0001t0001g0079 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.81+905_82-769del | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2164874 | ||||||
| chr16:2164906 | T | G | 2 | a0001c0001t0001g0001 a0001c0001t0001g0121 |
2 | HG01346.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.81+905T>G | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164906 | |||||||
| chr16:2164942 | C | T | 1 | a0001c0001t0003g0065 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.82-937C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164942 | |||||||
| chr16:2164963 | A | AGCCTGGT others(34): Show |
2 | a0001c0001t0001g0025 a0001c0001t0002g0025 |
2 | HG02257.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.82-882_82-842dupGT others(39): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2164963 | ||||||
| chr16:2164963 | A | G | 4 | a0001c0001t0002g0019 a0001c0001t0008g0071 a0001c0001t0008g0139 others(1): Show |
5 | HG02258.hp1 HG02717.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.82-916A>G | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164963 | |||||||
| chr16:2164984 | G | A | 2 | a0001c0001t0001g0030 a0001c0001t0001g0160 |
3 | HG00438.hp2 NA18747.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.82-895G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164984 | |||||||
| chr16:2164997 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.82-882G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2164997 | |||||||
| chr16:2164997 | GTGGCCTG others(34): Show |
G | 1 | a0001c0001t0004g0125 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.82-861_82-821delGT others(39): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2164997 | ||||||
| chr16:2165018 | G | C | 49 | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0001g0135 others(46): Show |
59 | HG00323.hp2 HG00639.hp2 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.82-861G>C | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2165018 | |||||||
| chr16:2165020 | T | G | 49 | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0001g0135 others(46): Show |
59 | HG00323.hp2 HG00639.hp2 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.82-859T>G | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2165020 | |||||||
| chr16:2165025 | G | A | 36 | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0001g0087 others(33): Show |
44 | HG01069.hp1 HG01071.hp2 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.82-854G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2165025 | |||||||
| chr16:2165025 | G | C | 10 | a0001c0001t0003g0028 a0001c0001t0003g0055 a0001c0001t0003g0061 others(7): Show |
11 | HG00323.hp2 HG00639.hp2 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.82-854G>C | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2165025 | |||||||
| chr16:2165038 | A | G | 2 | a0001c0001t0001g0101 a0001c0001t0002g0024 |
3 | HG02027.hp1 HG02615.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.82-841A>G | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2165038 | |||||||
| chr16:2165059 | C | G | 49 | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0001g0135 others(46): Show |
59 | HG00323.hp2 HG00639.hp2 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.82-820C>G | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2165059 | |||||||
| chr16:2165061 | G | T | 49 | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0001g0135 others(46): Show |
59 | HG00323.hp2 HG00639.hp2 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.82-818G>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2165061 | |||||||
| chr16:2165078 | C | T | 49 | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0001g0135 others(46): Show |
59 | HG00323.hp2 HG00639.hp2 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.82-801C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2165078 | |||||||
| chr16:2165079 | A | G | 50 | a0001c0001t0001g0022 a0001c0001t0001g0053 a0001c0001t0001g0056 others(47): Show |
61 | HG00323.hp2 HG00639.hp2 HG01069.hp1 others(58): Show |
intron_variant | MODIFIER | c.82-800A>G | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2165079 | |||||||
| chr16:2165084 | C | G | 49 | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0001g0135 others(46): Show |
59 | HG00323.hp2 HG00639.hp2 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.82-795C>G | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2165084 | |||||||
| chr16:2165085 | T | C | 49 | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0001g0135 others(46): Show |
59 | HG00323.hp2 HG00639.hp2 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.82-794T>C | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2165085 | |||||||
| chr16:2165086 | G | A | 49 | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0001g0135 others(46): Show |
59 | HG00323.hp2 HG00639.hp2 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.82-793G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2165086 | |||||||
| chr16:2165099 | G | A | 1 | a0001c0001t0001g0088 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.82-780G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2165099 | |||||||
| chr16:2165100 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.82-779G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2165100 | |||||||
| chr16:2165102 | T | TAAGCGTG others(34): Show |
1 | a0001c0001t0001g0035 | 2 | HG00609.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.82-738_82-698dupCT others(39): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2165102 | ||||||
| chr16:2165141 | C | G | 1 | a0001c0001t0001g0100 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.82-738C>G | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2165141 | |||||||
| chr16:2165143 | G | T | 1 | a0001c0001t0001g0100 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.82-736G>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2165143 | |||||||
| chr16:2165148 | G | A | 48 | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0001g0135 others(45): Show |
58 | HG00323.hp2 HG00639.hp2 HG01069.hp1 others(55): Show |
intron_variant | MODIFIER | c.82-731G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2165148 | |||||||
| chr16:2165160 | C | T | 3 | a0001c0001t0001g0053 a0001c0001t0002g0045 a0001c0001t0002g0046 |
3 | HG02486.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.82-719C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2165160 | |||||||
| chr16:2165182 | G | C | 2 | a0001c0001t0001g0089 a0001c0001t0001g0100 |
2 | HG01123.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.82-697G>C | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2165182 | |||||||
| chr16:2165184 | T | G | 2 | a0001c0001t0001g0089 a0001c0001t0001g0100 |
2 | HG01123.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.82-695T>G | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2165184 | |||||||
| chr16:2165202 | A | G | 10 | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0001g0089 others(7): Show |
11 | HG01123.hp2 HG02258.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.82-677A>G | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2165202 | |||||||
| chr16:2165230 | G | A | 1 | a0001c0001t0001g0051 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.82-649G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2165230 | |||||||
| chr16:2165242 | CGTGGCGC others(75): Show |
C | 1 | a0001c0001t0001g0084 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.82-604_82-523delTA others(80): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2165242 | ||||||
| chr16:2165247 | C | T | 1 | a0001c0001t0001g0027 | 2 | HG01106.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.82-632C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2165247 | |||||||
| chr16:2165291 | G | A | 1 | a0001c0001t0001g0035 | 2 | HG00609.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.82-588G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2165291 | |||||||
| chr16:2165311 | T | C | 37 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0053 others(34): Show |
43 | HG00323.hp2 HG00639.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.82-568T>C | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2165311 | |||||||
| chr16:2165312 | G | T | 2 | a0001c0001t0001g0133 a0001c0001t0001g0151 |
2 | HG00408.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.82-567G>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2165312 | |||||||
| chr16:2165324 | T | C | 3 | a0001c0001t0001g0008 a0001c0001t0001g0146 a0001c0001t0008g0071 |
3 | HG02258.hp1 NA19068.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.82-555T>C | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2165324 | |||||||
| chr16:2165332 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.82-547G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2165332 | |||||||
| chr16:2165364 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.82-515G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2165364 | |||||||
| chr16:2165393 | C | CGTGTGAG others(362): Show |
1 | a0001c0001t0001g0106 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.82-454_82-86dupATG others(366): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2165393 | ||||||
| chr16:2165398 | GAGTGCTG others(34): Show |
G | 2 | a0001c0001t0003g0061 a0001c0001t0003g0123 |
2 | HG02698.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.82-440_82-400delTA others(39): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2165398 | ||||||
| chr16:2165439 | T | G | 1 | a0001c0001t0001g0056 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.82-440T>G | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2165439 | |||||||
| chr16:2165453 | C | G | 1 | a0001c0001t0003g0055 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.82-426C>G | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2165453 | |||||||
| chr16:2165465 | C | T | 2 | a0001c0001t0006g0156 a0001c0001t0006g0157 |
2 | HG02895.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.82-414C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2165465 | |||||||
| chr16:2165468 | G | A | 1 | a0001c0001t0001g0014 | 3 | HG00280.hp2 HG01496.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.82-411G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2165468 | |||||||
| chr16:2165480 | G | T | 1 | a0001c0001t0001g0056 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.82-399G>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2165480 | |||||||
| chr16:2165499 | C | T | 1 | a0001c0001t0001g0115 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.82-380C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2165499 | |||||||
| chr16:2165500 | T | C | 1 | a0001c0001t0001g0115 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.82-379T>C | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2165500 | |||||||
| chr16:2165505 | G | A | 3 | a0001c0001t0001g0056 a0001c0001t0003g0061 a0001c0001t0003g0123 |
3 | HG02698.hp2 HG03516.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.82-374G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2165505 | |||||||
| chr16:2165515 | A | G | 34 | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0001g0141 others(31): Show |
40 | HG00323.hp2 HG00639.hp2 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.82-364A>G | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2165515 | |||||||
| chr16:2165537 | GGCCTGGT others(75): Show |
G | 1 | a0001c0001t0003g0061 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.82-325_82-244delTA others(80): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2165537 | ||||||
| chr16:2165545 | C | T | 1 | a0001c0001t0001g0002 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.82-334C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2165545 | |||||||
| chr16:2165551 | G | C | 1 | a0001c0001t0003g0123 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.82-328G>C | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2165551 | |||||||
| chr16:2165553 | T | G | 1 | a0001c0001t0003g0123 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.82-326T>G | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2165553 | |||||||
| chr16:2165554 | T | A | 18 | a0001c0001t0001g0141 a0001c0001t0001g0143 a0001c0001t0002g0019 others(15): Show |
20 | HG00323.hp2 HG00639.hp2 HG01256.hp1 others(17): Show |
intron_variant | MODIFIER | c.82-325T>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2165554 | |||||||
| chr16:2165558 | G | A | 1 | a0001c0001t0003g0123 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.82-321G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2165558 | |||||||
| chr16:2165562 | TAGTGCTG others(75): Show |
G | 1 | a0001c0001t0003g0123 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.82-317_82-236delTA others(80): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2165562 | |||||||
| chr16:2165598 | C | T | 4 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0094 others(1): Show |
8 | HG01884.hp2 HG02451.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.82-281C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2165598 | |||||||
| chr16:2165619 | A | AGCCTGGT others(34): Show |
1 | a0001c0001t0001g0120 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.82-235_82-195dupGA others(39): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2165619 | ||||||
| chr16:2165628 | G | A | 7 | a0001c0001t0003g0028 a0001c0001t0003g0055 a0001c0001t0003g0063 others(4): Show |
8 | HG00323.hp2 HG00639.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.82-251G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2165628 | |||||||
| chr16:2165633 | G | C | 1 | a0001c0001t0003g0061 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.82-246G>C | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2165633 | |||||||
| chr16:2165635 | T | G | 1 | a0001c0001t0003g0061 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.82-244T>G | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2165635 | |||||||
| chr16:2165640 | G | A | 1 | a0001c0001t0003g0061 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.82-239G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2165640 | |||||||
| chr16:2165640 | G | GTGTGAGT others(34): Show |
32 | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0001g0141 others(29): Show |
38 | HG00323.hp2 HG00639.hp2 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.82-206_82-205insCT others(39): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr16 | 2165640 | ||||||
| chr16:2165688 | C | T | 1 | a0001c0001t0002g0019 | 2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.82-191C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2165688 | |||||||
| chr16:2165710 | G | A | 2 | a0001c0001t0016g0145 a0001c0007t0020g0158 |
2 | HG02300.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.82-169G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2165710 | |||||||
| chr16:2165735 | G | A | 1 | a0001c0001t0001g0164 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.82-144G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2165735 | |||||||
| chr16:2165751 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.82-128G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 2/20 | chr16 | 2165751 | |||||||
| chr16:2165969 | G | A | 1 | a0001c0007t0020g0158 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.139+33G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 3/20 | chr16 | 2165969 | |||||||
| chr16:2166009 | TGAGG | T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0090 a0001c0001t0021g0006 |
6 | HG01074.hp1 HG02004.hp2 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.139+76_139+79delGG others(2): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr16 | 2166009 | ||||||
| chr16:2166023 | C | T | 2 | a0001c0001t0001g0087 a0001c0001t0001g0099 |
2 | HG02132.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.139+87C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 3/20 | chr16 | 2166023 | |||||||
| chr16:2166072 | G | C | 100 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0013 others(97): Show |
158 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.139+136G>C | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 3/20 | chr16 | 2166072 | |||||||
| chr16:2166149 | C | T | 1 | a0001c0001t0001g0114 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.139+213C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 3/20 | chr16 | 2166149 | |||||||
| chr16:2166255 | T | C | 4 | a0001c0001t0002g0019 a0001c0001t0008g0071 a0001c0001t0008g0139 others(1): Show |
5 | HG02258.hp1 HG02717.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.139+319T>C | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 3/20 | chr16 | 2166255 | |||||||
| chr16:2166296 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.139+360G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 3/20 | chr16 | 2166296 | |||||||
| chr16:2166325 | C | G | 5 | a0001c0001t0001g0141 a0001c0001t0001g0143 a0001c0001t0004g0142 others(2): Show |
5 | HG02723.hp1 HG02970.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.139+389C>G | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 3/20 | chr16 | 2166325 | |||||||
| chr16:2166432 | C | T | 2 | a0001c0001t0001g0031 a0001c0001t0001g0069 |
3 | HG01106.hp2 HG01433.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.139+496C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 3/20 | chr16 | 2166432 | |||||||
| chr16:2166629 | T | C | 1 | a0002c0004t0001g0131 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.139+693T>C | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 3/20 | chr16 | 2166629 | |||||||
| chr16:2166638 | G | A | 3 | a0001c0001t0001g0053 a0001c0001t0002g0045 a0001c0001t0002g0046 |
3 | HG02486.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.139+702G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 3/20 | chr16 | 2166638 | |||||||
| chr16:2166674 | T | A | 1 | a0002c0004t0001g0131 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.139+738T>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 3/20 | chr16 | 2166674 | |||||||
| chr16:2166741 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.139+805C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 3/20 | chr16 | 2166741 | |||||||
| chr16:2166821 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.139+885G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 3/20 | chr16 | 2166821 | |||||||
| chr16:2166824 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.139+888G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 3/20 | chr16 | 2166824 | |||||||
| chr16:2166915 | T | A | 1 | a0002c0004t0001g0131 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.139+979T>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 3/20 | chr16 | 2166915 | |||||||
| chr16:2166960 | C | T | 4 | a0001c0001t0002g0019 a0001c0001t0008g0071 a0001c0001t0008g0139 others(1): Show |
5 | HG02258.hp1 HG02717.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.139+1024C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 3/20 | chr16 | 2166960 | |||||||
| chr16:2166970 | A | C | 1 | a0001c0001t0001g0115 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.139+1034A>C | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 3/20 | chr16 | 2166970 | |||||||
| chr16:2166975 | CT | C | 8 | a0001c0001t0001g0154 a0001c0001t0002g0010 a0001c0001t0002g0017 others(5): Show |
12 | HG01069.hp1 HG01071.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.139+1044delT | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr16 | 2166975 | ||||||
| chr16:2166999 | G | A | 1 | a0001c0008t0001g0062 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.139+1063G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 3/20 | chr16 | 2166999 | |||||||
| chr16:2167012 | T | C | 5 | a0001c0001t0001g0141 a0001c0001t0001g0143 a0001c0001t0004g0142 others(2): Show |
5 | HG02723.hp1 HG02970.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.140-1065T>C | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 3/20 | chr16 | 2167012 | |||||||
| chr16:2167239 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.140-838G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 3/20 | chr16 | 2167239 | |||||||
| chr16:2167254 | G | A | 2 | a0001c0001t0001g0031 a0001c0001t0001g0069 |
3 | HG01106.hp2 HG01433.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.140-823G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 3/20 | chr16 | 2167254 | |||||||
| chr16:2167304 | C | T | 1 | a0001c0001t0002g0042 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.140-773C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 3/20 | chr16 | 2167304 | |||||||
| chr16:2167320 | CTCTCGAG others(7): Show |
C | 8 | a0001c0001t0003g0028 a0001c0001t0003g0055 a0001c0001t0003g0061 others(5): Show |
9 | HG00323.hp2 HG00639.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.140-749_140-736del others(14): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr16 | 2167320 | ||||||
| chr16:2167572 | C | T | 2 | a0001c0001t0001g0053 a0001c0001t0002g0046 |
2 | HG02486.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.140-505C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 3/20 | chr16 | 2167572 | |||||||
| chr16:2167597 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.140-480C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 3/20 | chr16 | 2167597 | |||||||
| chr16:2167608 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.140-469C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 3/20 | chr16 | 2167608 | |||||||
| chr16:2167931 | TC | T | 5 | a0001c0001t0001g0141 a0001c0001t0001g0143 a0001c0001t0004g0142 others(2): Show |
5 | HG02723.hp1 HG02970.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.140-143delC | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr16 | 2167931 | ||||||
| chr16:2168063 | C | A | 1 | a0001c0001t0001g0117 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.140-14C>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 3/20 | chr16 | 2168063 | |||||||
| chr16:2168373 | C | A | 1 | a0001c0001t0001g0115 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.231+205C>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 4/20 | chr16 | 2168373 | |||||||
| chr16:2168502 | G | A | 1 | a0001c0001t0008g0071 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.231+334G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 4/20 | chr16 | 2168502 | |||||||
| chr16:2168530 | A | T | 1 | a0001c0001t0001g0115 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.231+362A>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 4/20 | chr16 | 2168530 | |||||||
| chr16:2168612 | G | C | 1 | a0001c0001t0001g0115 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.231+444G>C | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 4/20 | chr16 | 2168612 | |||||||
| chr16:2168613 | C | G | 1 | a0001c0001t0001g0115 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.231+445C>G | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 4/20 | chr16 | 2168613 | |||||||
| chr16:2168649 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.231+481G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 4/20 | chr16 | 2168649 | |||||||
| chr16:2168736 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.231+568G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 4/20 | chr16 | 2168736 | |||||||
| chr16:2168760 | G | T | 1 | a0001c0001t0001g0085 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.231+592G>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 4/20 | chr16 | 2168760 | |||||||
| chr16:2168821 | G | A | 1 | a0001c0001t0002g0046 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.231+653G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 4/20 | chr16 | 2168821 | |||||||
| chr16:2169007 | C | T | 4 | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0002g0045 others(1): Show |
4 | HG02486.hp2 HG03209.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.231+839C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 4/20 | chr16 | 2169007 | |||||||
| chr16:2169131 | G | A | 2 | a0001c0001t0001g0084 a0001c0001t0001g0127 |
2 | HG00621.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.231+963G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 4/20 | chr16 | 2169131 | |||||||
| chr16:2169209 | C | G | 1 | a0001c0001t0001g0090 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.231+1041C>G | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 4/20 | chr16 | 2169209 | |||||||
| chr16:2169297 | T | A | 1 | a0001c0001t0001g0115 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.231+1129T>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 4/20 | chr16 | 2169297 | |||||||
| chr16:2169331 | C | G | 6 | a0001c0001t0001g0013 a0001c0001t0001g0086 a0001c0001t0001g0121 others(3): Show |
8 | HG02258.hp2 HG02622.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.231+1163C>G | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 4/20 | chr16 | 2169331 | |||||||
| chr16:2169354 | T | C | 2 | a0001c0001t0003g0028 a0001c0001t0003g0148 |
3 | HG01256.hp1 HG01258.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.231+1186T>C | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 4/20 | chr16 | 2169354 | |||||||
| chr16:2169373 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.231+1205G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 4/20 | chr16 | 2169373 | |||||||
| chr16:2169396 | C | T | 2 | a0001c0001t0001g0133 a0001c0001t0001g0151 |
2 | HG00408.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.232-1218C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 4/20 | chr16 | 2169396 | |||||||
| chr16:2169549 | C | T | 1 | a0001c0001t0003g0065 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.232-1065C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 4/20 | chr16 | 2169549 | |||||||
| chr16:2169582 | G | A | 1 | a0001c0001t0002g0048 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.232-1032G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 4/20 | chr16 | 2169582 | |||||||
| chr16:2169623 | C | G | 1 | a0001c0001t0001g0161 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.232-991C>G | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 4/20 | chr16 | 2169623 | |||||||
| chr16:2169662 | C | T | 2 | a0001c0001t0001g0144 a0001c0001t0002g0057 |
2 | HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.232-952C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 4/20 | chr16 | 2169662 | |||||||
| chr16:2169750 | A | T | 15 | a0001c0001t0001g0141 a0001c0001t0001g0143 a0001c0001t0003g0028 others(12): Show |
16 | HG00323.hp2 HG00639.hp2 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.232-864A>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 4/20 | chr16 | 2169750 | |||||||
| chr16:2169934 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.232-680C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 4/20 | chr16 | 2169934 | |||||||
| chr16:2170056 | C | T | 3 | a0001c0001t0001g0146 a0001c0001t0001g0164 a0001c0001t0001g0165 |
3 | NA19011.hp1 NA19068.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.232-558C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 4/20 | chr16 | 2170056 | |||||||
| chr16:2170391 | C | T | 1 | a0001c0001t0001g0111 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.232-223C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 4/20 | chr16 | 2170391 | |||||||
| chr16:2170504 | T | C | 1 | a0001c0001t0001g0036 | 2 | HG01943.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.232-110T>C | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 4/20 | chr16 | 2170504 | |||||||
| chr16:2170574 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.232-40C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 4/20 | chr16 | 2170574 | |||||||
| chr16:2170595 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.232-19C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 4/20 | chr16 | 2170595 | |||||||
| chr16:2170803 | C | G | 1 | a0001c0006t0001g0096 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.348+73C>G | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 5/20 | chr16 | 2170803 | |||||||
| chr16:2170882 | G | A | 1 | a0001c0001t0001g0117 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.348+152G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 5/20 | chr16 | 2170882 | |||||||
| chr16:2170932 | C | G | 2 | a0001c0001t0001g0122 a0001c0001t0001g0132 |
2 | NA18973.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.348+202C>G | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 5/20 | chr16 | 2170932 | |||||||
| chr16:2171101 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.349-163C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 5/20 | chr16 | 2171101 | |||||||
| chr16:2171156 | T | C | 41 | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0001g0141 others(38): Show |
50 | HG00323.hp2 HG00639.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.349-108T>C | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 5/20 | chr16 | 2171156 | |||||||
| chr16:2171368 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.441+12G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 6/20 | chr16 | 2171368 | |||||||
| chr16:2171439 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.441+83G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 6/20 | chr16 | 2171439 | |||||||
| chr16:2171474 | T | C | 1 | a0001c0001t0001g0122 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.442-98T>C | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 6/20 | chr16 | 2171474 | |||||||
| chr16:2171554 | C | T | 5 | a0001c0001t0001g0141 a0001c0001t0001g0143 a0001c0001t0004g0142 others(2): Show |
5 | HG02723.hp1 HG02970.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-18C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 6/20 | chr16 | 2171554 | |||||||
| chr16:2171635 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.475+30G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 7/20 | chr16 | 2171635 | |||||||
| chr16:2171646 | C | T | 1 | a0001c0001t0008g0071 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.475+41C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 7/20 | chr16 | 2171646 | |||||||
| chr16:2171770 | C | T | 1 | a0001c0001t0002g0048 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.475+165C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 7/20 | chr16 | 2171770 | |||||||
| chr16:2171909 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.476-282C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 7/20 | chr16 | 2171909 | |||||||
| chr16:2172427 | C | A | 1 | a0001c0001t0015g0104 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.660-38C>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 8/20 | chr16 | 2172427 | |||||||
| chr16:2172452 | C | T | 2 | a0001c0001t0001g0041 a0001c0001t0001g0053 |
2 | HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.660-13C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 8/20 | chr16 | 2172452 | |||||||
| chr16:2172768 | G | A | 6 | a0001c0001t0003g0028 a0001c0001t0003g0055 a0001c0001t0003g0065 others(3): Show |
7 | HG00323.hp2 HG00639.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.794+169G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 9/20 | chr16 | 2172768 | |||||||
| chr16:2172801 | C | T | 1 | a0001c0001t0001g0016 | 3 | HG00140.hp2 HG01516.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.794+202C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 9/20 | chr16 | 2172801 | |||||||
| chr16:2172894 | T | G | 1 | a0001c0001t0008g0071 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.795-288T>G | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 9/20 | chr16 | 2172894 | |||||||
| chr16:2172915 | G | A | 1 | a0001c0001t0016g0145 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.795-267G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 9/20 | chr16 | 2172915 | |||||||
| chr16:2172935 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.795-247C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 9/20 | chr16 | 2172935 | |||||||
| chr16:2172999 | T | C | 42 | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0001g0074 others(39): Show |
51 | HG00323.hp2 HG00639.hp2 HG01069.hp1 others(48): Show |
intron_variant | MODIFIER | c.795-183T>C | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 9/20 | chr16 | 2172999 | |||||||
| chr16:2173443 | C | T | 3 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0002g0060 |
3 | HG01109.hp1 HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1013-38C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 10/20 | chr16 | 2173443 | |||||||
| chr16:2173651 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1086+97G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 11/20 | chr16 | 2173651 | |||||||
| chr16:2173683 | G | A | 1 | a0001c0001t0005g0153 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1087-105G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 11/20 | chr16 | 2173683 | |||||||
| chr16:2173687 | CCCCTGCC others(53): Show |
C | 1 | a0001c0001t0001g0117 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1087-89_1087-30del others(60): Show |
TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr16 | 2173687 | ||||||
| chr16:2173851 | G | A | 1 | a0001c0001t0001g0092 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1135+15G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 12/20 | chr16 | 2173851 | |||||||
| chr16:2173876 | C | A | 1 | a0001c0001t0008g0071 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1135+40C>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 12/20 | chr16 | 2173876 | |||||||
| chr16:2174196 | C | A | 1 | a0001c0001t0019g0167 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1264-55C>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 13/20 | chr16 | 2174196 | |||||||
| chr16:2174379 | C | T | 2 | a0001c0001t0001g0078 a0001c0001t0001g0090 |
2 | HG00738.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.1346+46C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 14/20 | chr16 | 2174379 | |||||||
| chr16:2174392 | C | A | 1 | a0001c0007t0020g0158 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1346+59C>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 14/20 | chr16 | 2174392 | |||||||
| chr16:2174439 | T | A | 1 | a0001c0001t0001g0115 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1346+106T>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 14/20 | chr16 | 2174439 | |||||||
| chr16:2174446 | C | A | 1 | a0001c0001t0007g0134 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1346+113C>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 14/20 | chr16 | 2174446 | |||||||
| chr16:2174466 | C | T | 3 | a0001c0001t0003g0061 a0001c0001t0003g0063 a0001c0001t0003g0123 |
3 | HG02698.hp2 HG04115.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1346+133C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 14/20 | chr16 | 2174466 | |||||||
| chr16:2174602 | C | T | 4 | a0001c0001t0001g0141 a0001c0001t0001g0143 a0001c0001t0022g0163 others(1): Show |
4 | HG02970.hp1 HG03041.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1346+269C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 14/20 | chr16 | 2174602 | |||||||
| chr16:2174628 | G | C | 1 | a0001c0001t0001g0093 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1346+295G>C | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 14/20 | chr16 | 2174628 | |||||||
| chr16:2174690 | C | T | 1 | a0001c0001t0001g0094 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1346+357C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 14/20 | chr16 | 2174690 | |||||||
| chr16:2174802 | G | A | 1 | a0001c0001t0002g0048 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1347-309G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 14/20 | chr16 | 2174802 | |||||||
| chr16:2175181 | A | G | 1 | a0001c0001t0003g0076 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1386+31A>G | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 15/20 | chr16 | 2175181 | |||||||
| chr16:2175182 | G | A | 1 | a0001c0001t0003g0076 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1386+32G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 15/20 | chr16 | 2175182 | |||||||
| chr16:2175435 | G | A | 1 | a0001c0001t0016g0145 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1503+18G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 16/20 | chr16 | 2175435 | |||||||
| chr16:2175469 | G | A | 1 | a0001c0001t0006g0157 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1504-31G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 16/20 | chr16 | 2175469 | |||||||
| chr16:2175707 | G | C | 2 | a0001c0001t0001g0108 a0001c0001t0001g0115 |
2 | NA18977.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1626+85G>C | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 17/20 | chr16 | 2175707 | |||||||
| chr16:2175775 | C | T | 1 | a0001c0001t0003g0124 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1627-59C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 17/20 | chr16 | 2175775 | |||||||
| chr16:2175822 | G | A | 10 | a0001c0001t0003g0028 a0001c0001t0003g0055 a0001c0001t0003g0061 others(7): Show |
11 | HG00323.hp2 HG00639.hp2 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.1627-12G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 17/20 | chr16 | 2175822 | |||||||
| chr16:2175970 | T | C | 1 | a0001c0001t0002g0047 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1746+17T>C | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 18/20 | chr16 | 2175970 | |||||||
| chr16:2176242 | C | G | 1 | a0001c0001t0001g0075 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1879-23C>G | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 19/20 | chr16 | 2176242 | |||||||
| chr16:2176435 | G | A | 4 | a0001c0001t0001g0141 a0001c0001t0001g0143 a0001c0001t0022g0163 others(1): Show |
4 | HG02970.hp1 HG03041.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1998+51G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 20/20 | chr16 | 2176435 | |||||||
| chr16:2176488 | C | T | 1 | a0001c0001t0002g0045 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1999-72C>T | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 20/20 | chr16 | 2176488 | |||||||
| chr16:2176556 | G | A | 1 | a0001c0001t0019g0167 | 1 | HG02809.hp2 | splice_region_variant&intron_variant | LOW | c.1999-4G>A | TRAF7 | ENSG00000131653.14 | transcript | ENST00000326181.11 | protein_coding | 20/20 | chr16 | 2176556 |