| geneid | 7187 |
|---|---|
| ensemblid | ENSG00000131323.17 |
| hgncid | 12033 |
| symbol | TRAF3 |
| name | TNF receptor associated factor 3 |
| refseq_nuc | NM_145725.3 |
| refseq_prot | NP_663777.1 |
| ensembl_nuc | ENST00000392745.8 |
| ensembl_prot | ENSP00000376500.3 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 102777449 |
| end | 102911500 |
| strand | + |
| ver | v1.2 |
| region | chr14:102777449-102911500 |
| region5000 | chr14:102772449-102916500 |
| regionname0 | TRAF3_chr14_102777449_102911500 |
| regionname5000 | TRAF3_chr14_102772449_102916500 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 568 | 172 | 73 | 33 | 49 | 6 | 11 | 39 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0002 | 1/1 | 568 | 124 | 7 | 31 | 63 | 4 | 17 | 51 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 1707 | 167 | 69 | 32 | 49 | 6 | 11 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| c0002 | 1/1 | 1707 | 121 | 7 | 31 | 61 | 4 | 16 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| c0003 | 0/0 | 1707 | 4 | 4 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| c0004 | 0/0 | 1707 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| c0005 | 0/0 | 1707 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| c0006 | 0/0 | 1707 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| c0007 | 0/0 | 1707 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 6100 | 80 | 3 | 11 | 56 | 2 | 8 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0002 | 0/0 | 6100 | 42 | 2 | 13 | 23 | 1 | 3 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0003 | 0/1 | 6100 | 20 | 4 | 4 | 4 | 1 | 6 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0004 | 0/0 | 6100 | 14 | 0 | 4 | 10 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0005 | 0/0 | 6100 | 9 | 9 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0006 | 1/0 | 6100 | 9 | 1 | 7 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0007 | 0/0 | 6100 | 9 | 8 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0008 | 0/0 | 6100 | 8 | 7 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0009 | 0/0 | 6100 | 7 | 0 | 6 | 0 | 1 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0010 | 0/0 | 6100 | 6 | 5 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0011 | 0/0 | 6100 | 6 | 2 | 2 | 0 | 0 | 2 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0012 | 0/0 | 6100 | 6 | 5 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0013 | 0/0 | 6100 | 4 | 4 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0014 | 0/0 | 6100 | 4 | 0 | 0 | 4 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0015 | 0/0 | 6100 | 3 | 3 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0016 | 0/0 | 6100 | 3 | 0 | 0 | 0 | 3 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0017 | 0/0 | 6100 | 3 | 3 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0018 | 0/0 | 6100 | 3 | 1 | 2 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0019 | 0/0 | 6100 | 2 | 2 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0020 | 0/0 | 6100 | 2 | 2 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0021 | 0/0 | 6098 | 2 | 0 | 1 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0022 | 0/0 | 6100 | 2 | 2 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0023 | 0/0 | 6100 | 2 | 0 | 0 | 2 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0024 | 0/0 | 6100 | 2 | 1 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0025 | 0/0 | 6100 | 2 | 2 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0026 | 0/0 | 6100 | 2 | 0 | 0 | 0 | 0 | 2 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0027 | 0/0 | 6100 | 2 | 0 | 2 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0028 | 0/0 | 6100 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0029 | 0/0 | 6100 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0030 | 0/0 | 6100 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0031 | 0/0 | 6100 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0032 | 0/0 | 6100 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0033 | 0/0 | 6100 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0034 | 0/0 | 6100 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0035 | 0/0 | 6100 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0036 | 0/0 | 6100 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0037 | 0/0 | 6100 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0038 | 0/0 | 6100 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0039 | 0/0 | 6100 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0040 | 0/0 | 6100 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0041 | 0/0 | 6100 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0042 | 0/0 | 6100 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0043 | 0/0 | 6100 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0044 | 0/0 | 6100 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0045 | 0/0 | 6100 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0046 | 0/0 | 6100 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0047 | 0/0 | 6100 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0048 | 0/0 | 6100 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0049 | 0/0 | 6100 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0050 | 0/0 | 6100 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0051 | 0/0 | 6100 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0052 | 0/0 | 6100 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0053 | 0/0 | 6100 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0054 | 0/0 | 6100 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0055 | 0/0 | 6100 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0056 | 0/0 | 6100 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0057 | 0/0 | 6100 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0058 | 0/0 | 6100 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0059 | 0/0 | 6100 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0060 | 0/0 | 6100 | 1 | 0 | 0 | 0 | 1 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0061 | 0/0 | 6100 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0062 | 0/0 | 6100 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0063 | 0/0 | 6100 | 1 | 0 | 0 | 0 | 1 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0064 | 0/0 | 6100 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0065 | 0/0 | 6100 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0066 | 0/0 | 6100 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0067 | 0/0 | 6098 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0068 | 0/0 | 6098 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| t0069 | 0/0 | 6100 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0128 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0154 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1707 | 167 | 69 | 32 | 49 | 6 | 11 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0003 | 0/0 | 1707 | 4 | 4 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0004 | 0/0 | 1707 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0002c0002 | 1/1 | 1707 | 121 | 7 | 31 | 61 | 4 | 16 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0002c0005 | 0/0 | 1707 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0002c0006 | 0/0 | 1707 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0002c0007 | 0/0 | 1707 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 7806 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0001t0002 | 0/0 | 7806 | 42 | 2 | 13 | 23 | 1 | 3 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0001t0003 | 0/0 | 7806 | 2 | 1 | 0 | 0 | 1 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0001t0004 | 0/0 | 7806 | 14 | 0 | 4 | 10 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0001t0005 | 0/0 | 7806 | 8 | 8 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0001t0007 | 0/0 | 7806 | 9 | 8 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0001t0008 | 0/0 | 7806 | 8 | 7 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0001t0010 | 0/0 | 7806 | 6 | 5 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0001t0011 | 0/0 | 7806 | 6 | 2 | 2 | 0 | 0 | 2 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0001t0012 | 0/0 | 7806 | 6 | 5 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0001t0013 | 0/0 | 7806 | 4 | 4 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0001t0014 | 0/0 | 7806 | 4 | 0 | 0 | 4 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0001t0015 | 0/0 | 7806 | 3 | 3 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0001t0016 | 0/0 | 7806 | 3 | 0 | 0 | 0 | 3 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0001t0017 | 0/0 | 7806 | 3 | 3 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0001t0018 | 0/0 | 7806 | 3 | 1 | 2 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0001t0019 | 0/0 | 7806 | 2 | 2 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0001t0020 | 0/0 | 7806 | 2 | 2 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0001t0021 | 0/0 | 7804 | 2 | 0 | 1 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0001t0022 | 0/0 | 7806 | 2 | 2 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0001t0023 | 0/0 | 7806 | 2 | 0 | 0 | 2 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0001t0024 | 0/0 | 7806 | 2 | 1 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0001t0025 | 0/0 | 7806 | 2 | 2 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0001t0026 | 0/0 | 7806 | 2 | 0 | 0 | 0 | 0 | 2 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0001t0027 | 0/0 | 7806 | 2 | 0 | 2 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0001t0028 | 0/0 | 7806 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0001t0029 | 0/0 | 7806 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0001t0030 | 0/0 | 7806 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0001t0031 | 0/0 | 7806 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0001t0032 | 0/0 | 7806 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0001t0033 | 0/0 | 7806 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0001t0035 | 0/0 | 7806 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0001t0036 | 0/0 | 7806 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0001t0038 | 0/0 | 7806 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0001t0040 | 0/0 | 7806 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0001t0041 | 0/0 | 7806 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0001t0042 | 0/0 | 7806 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0001t0043 | 0/0 | 7806 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0001t0044 | 0/0 | 7806 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0001t0045 | 0/0 | 7806 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0001t0046 | 0/0 | 7806 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0001t0047 | 0/0 | 7806 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0001t0048 | 0/0 | 7806 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0001t0050 | 0/0 | 7806 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0001t0051 | 0/0 | 7806 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0001t0061 | 0/0 | 7806 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0001t0062 | 0/0 | 7806 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0001t0063 | 0/0 | 7806 | 1 | 0 | 0 | 0 | 1 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0001t0064 | 0/0 | 7806 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0001t0067 | 0/0 | 7804 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0001t0068 | 0/0 | 7804 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0001t0069 | 0/0 | 7806 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0003t0003 | 0/0 | 7806 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0003t0005 | 0/0 | 7806 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0003t0034 | 0/0 | 7806 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0003t0037 | 0/0 | 7806 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0001c0004t0039 | 0/0 | 7806 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0002c0002t0001 | 0/0 | 7806 | 76 | 3 | 11 | 53 | 2 | 7 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0002c0002t0003 | 0/1 | 7806 | 17 | 2 | 4 | 4 | 0 | 6 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0002c0002t0006 | 1/0 | 7806 | 9 | 1 | 7 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0002c0002t0009 | 0/0 | 7806 | 7 | 0 | 6 | 0 | 1 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0002c0002t0049 | 0/0 | 7806 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0002c0002t0052 | 0/0 | 7806 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0002c0002t0053 | 0/0 | 7806 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0002c0002t0054 | 0/0 | 7806 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0002c0002t0055 | 0/0 | 7806 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0002c0002t0056 | 0/0 | 7806 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0002c0002t0057 | 0/0 | 7806 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0002c0002t0058 | 0/0 | 7806 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0002c0002t0059 | 0/0 | 7806 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0002c0002t0060 | 0/0 | 7806 | 1 | 0 | 0 | 0 | 1 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0002c0002t0065 | 0/0 | 7806 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0002c0002t0066 | 0/0 | 7806 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0002c0005t0001 | 0/0 | 7806 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0002c0006t0001 | 0/0 | 7806 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| a0002c0007t0001 | 0/0 | 7806 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | copy fasta | chr14 | 102772449 | 102916500 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0004g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0004g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0004g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0004g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0004g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0004g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0004g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0004g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0005g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0005g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0005g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0005g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0005g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0005g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0005g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0005g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0007g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0007g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0007g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0007g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0007g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0007g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0007g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0007g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0007g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0008g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0008g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0008g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0008g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0008g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0008g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0008g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0008g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0010g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0010g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0010g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0010g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0010g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0010g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0011g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0011g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0011g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0011g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0011g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0011g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0012g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0012g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0012g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0012g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0012g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0012g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0013g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0013g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0013g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0013g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0014g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0014g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0014g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0014g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0015g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0015g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0015g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0016g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0016g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0016g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0017g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0017g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0017g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0018g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0018g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0018g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0019g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0019g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0020g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0020g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0021g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0021g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0022g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0022g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0023g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0023g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0024g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0024g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0025g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0025g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0026g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0026g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0027g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0027g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0028g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0029g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0030g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0031g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0032g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0033g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0035g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0036g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0038g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0040g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0041g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0042g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0043g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0044g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0045g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0046g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0047g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0048g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0050g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0051g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0061g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0062g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0063g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0064g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0067g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0068g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0001t0069g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0003t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0003t0005g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0003t0034g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0003t0037g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0001c0004t0039g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0003g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0003g0128 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0003g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0003g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0003g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0003g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0003g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0003g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0003g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0006g0154 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0006g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0006g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0006g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0006g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0006g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0006g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0006g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0006g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0009g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0009g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0009g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0009g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0009g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0009g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0009g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0049g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0052g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0053g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0054g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0055g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0056g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0057g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0058g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0059g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0060g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0065g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0002t0066g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0005t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0006t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| a0002c0007t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0255 | EUR | GBR | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0101 | EUR | GBR | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG00140 | hp1 | a0002 | c0002 | t0060 | g0213 | EUR | GBR | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0085 | EUR | GBR | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG00323 | hp1 | a0001 | c0001 | t0016 | g0103 | EUR | FIN | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG00323 | hp2 | a0002 | c0002 | t0009 | g0222 | EUR | FIN | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG00544 | hp1 | a0002 | c0002 | t0003 | g0151 | EAS | CHS | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | CHS | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG00558 | hp1 | a0001 | c0001 | t0064 | g0198 | EAS | CHS | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0190 | EAS | CHS | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG00609 | hp1 | a0001 | c0001 | t0023 | g0043 | EAS | CHS | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0225 | EAS | CHS | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0230 | EAS | CHS | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | CHS | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG00639 | hp1 | a0002 | c0002 | t0006 | g0156 | AMR | PUR | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG00639 | hp2 | a0001 | c0001 | t0010 | g0053 | AMR | PUR | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | CHS | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0209 | EAS | CHS | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG00733 | hp1 | a0002 | c0002 | t0055 | g0260 | AMR | PUR | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG00733 | hp2 | a0001 | c0001 | t0033 | g0123 | AMR | PUR | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG00735 | hp1 | a0001 | c0001 | t0044 | g0089 | AMR | PUR | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0238 | AMR | PUR | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0102 | AMR | PUR | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0081 | AMR | PUR | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG01069 | hp1 | a0001 | c0001 | t0027 | g0289 | AMR | PUR | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG01069 | hp2 | a0002 | c0002 | t0003 | g0131 | AMR | PUR | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG01071 | hp1 | a0002 | c0002 | t0052 | g0242 | AMR | PUR | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG01071 | hp2 | a0001 | c0001 | t0027 | g0288 | AMR | PUR | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0076 | AMR | PUR | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG01074 | hp2 | a0002 | c0002 | t0006 | g0159 | AMR | PUR | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG01081 | hp1 | a0002 | c0002 | t0009 | g0228 | AMR | PUR | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG01081 | hp2 | a0001 | c0001 | t0007 | g0096 | AMR | PUR | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG01099 | hp1 | a0002 | c0002 | t0003 | g0134 | AMR | PUR | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG01099 | hp2 | a0001 | c0001 | t0031 | g0183 | AMR | PUR | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG01109 | hp1 | a0002 | c0002 | t0006 | g0158 | AMR | PUR | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG01109 | hp2 | a0001 | c0001 | t0012 | g0098 | AMR | PUR | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG01167 | hp1 | a0001 | c0001 | t0018 | g0250 | AMR | PUR | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0079 | AMR | PUR | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG01169 | hp1 | a0002 | c0002 | t0009 | g0214 | AMR | PUR | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG01169 | hp2 | a0001 | c0001 | t0018 | g0186 | AMR | PUR | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG01175 | hp1 | a0002 | c0002 | t0009 | g0197 | AMR | PUR | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG01175 | hp2 | a0001 | c0001 | t0008 | g0064 | AMR | PUR | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG01192 | hp1 | a0002 | c0002 | t0006 | g0169 | AMR | PUR | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0067 | AMR | PUR | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG01243 | hp1 | a0002 | c0002 | t0001 | g0283 | AMR | PUR | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG01243 | hp2 | a0002 | c0002 | t0003 | g0153 | AMR | PUR | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG01256 | hp1 | a0002 | c0002 | t0003 | g0160 | AMR | CLM | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG01256 | hp2 | a0002 | c0002 | t0058 | g0192 | AMR | CLM | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0215 | AMR | CLM | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG01257 | hp2 | a0002 | c0002 | t0009 | g0185 | AMR | CLM | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0177 | AMR | CLM | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0280 | AMR | CLM | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0249 | AMR | CLM | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0111 | AMR | CLM | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0074 | AMR | CLM | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG01358 | hp2 | a0002 | c0002 | t0001 | g0261 | AMR | CLM | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0253 | AMR | CLM | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG01433 | hp2 | a0002 | c0002 | t0009 | g0216 | AMR | CLM | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG01496 | hp1 | a0001 | c0001 | t0011 | g0147 | AMR | CLM | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0257 | AMR | CLM | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0271 | EUR | IBS | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG01516 | hp2 | a0001 | c0001 | t0016 | g0105 | EUR | IBS | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG01517 | hp1 | a0001 | c0001 | t0063 | g0223 | EUR | IBS | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG01517 | hp2 | a0001 | c0001 | t0016 | g0104 | EUR | IBS | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG01884 | hp1 | a0001 | c0001 | t0022 | g0050 | AFR | ACB | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG01884 | hp2 | a0001 | c0001 | t0050 | g0180 | AFR | ACB | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG01928 | hp1 | a0001 | c0001 | t0030 | g0176 | AMR | PEL | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG01928 | hp2 | a0001 | c0001 | t0011 | g0148 | AMR | PEL | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG01934 | hp1 | a0002 | c0002 | t0009 | g0243 | AMR | PEL | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0077 | AMR | PEL | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0172 | AMR | PEL | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG01943 | hp2 | a0001 | c0001 | t0004 | g0040 | AMR | PEL | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0026 | AMR | PEL | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG01952 | hp2 | a0002 | c0002 | t0006 | g0161 | AMR | PEL | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0279 | AMR | PEL | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG01981 | hp2 | a0001 | c0001 | t0004 | g0173 | AMR | PEL | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG01993 | hp1 | a0001 | c0004 | t0039 | g0002 | AMR | PEL | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0072 | AMR | PEL | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0058 | AMR | PEL | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02004 | hp2 | a0002 | c0002 | t0006 | g0157 | AMR | PEL | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02055 | hp1 | a0001 | c0001 | t0015 | g0139 | AFR | ACB | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02055 | hp2 | a0001 | c0001 | t0005 | g0017 | AFR | ACB | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | KHV | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0227 | EAS | KHV | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0291 | EAS | KHV | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02135 | hp2 | a0002 | c0002 | t0066 | g0272 | EAS | KHV | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | CDX | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0246 | EAS | CDX | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | CDX | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0226 | EAS | CDX | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02257 | hp1 | a0001 | c0001 | t0015 | g0141 | AFR | ACB | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0278 | AFR | ACB | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02258 | hp1 | a0001 | c0001 | t0010 | g0019 | AFR | ACB | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02258 | hp2 | a0001 | c0001 | t0008 | g0038 | AFR | ACB | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02273 | hp1 | a0002 | c0002 | t0006 | g0162 | AMR | PEL | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0080 | AMR | PEL | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02300 | hp1 | a0001 | c0001 | t0004 | g0174 | AMR | PEL | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0202 | AMR | PEL | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02451 | hp1 | a0001 | c0001 | t0038 | g0015 | AFR | ACB | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02451 | hp2 | a0001 | c0001 | t0007 | g0008 | AFR | ACB | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0269 | EAS | KHV | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02523 | hp2 | a0001 | c0001 | t0014 | g0117 | EAS | KHV | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0282 | SAS | PJL | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0066 | SAS | PJL | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02615 | hp1 | a0001 | c0001 | t0012 | g0001 | AFR | GWD | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02615 | hp2 | a0001 | c0001 | t0013 | g0294 | AFR | GWD | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02622 | hp1 | a0001 | c0001 | t0013 | g0262 | AFR | GWD | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02622 | hp2 | a0001 | c0001 | t0020 | g0142 | AFR | GWD | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02630 | hp1 | a0001 | c0001 | t0040 | g0149 | AFR | GWD | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02630 | hp2 | a0001 | c0003 | t0037 | g0004 | AFR | GWD | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02683 | hp1 | a0002 | c0007 | t0001 | g0273 | SAS | PJL | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02683 | hp2 | a0002 | c0002 | t0003 | g0152 | SAS | PJL | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02698 | hp1 | a0002 | c0002 | t0049 | g0129 | SAS | PJL | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02698 | hp2 | a0001 | c0001 | t0026 | g0078 | SAS | PJL | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02717 | hp1 | a0002 | c0002 | t0003 | g0132 | AFR | GWD | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02717 | hp2 | a0001 | c0001 | t0007 | g0094 | AFR | GWD | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0100 | AFR | GWD | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02723 | hp2 | a0001 | c0001 | t0068 | g0029 | AFR | GWD | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02738 | hp1 | a0001 | c0001 | t0021 | g0099 | SAS | PJL | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02738 | hp2 | a0002 | c0002 | t0003 | g0135 | SAS | PJL | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02809 | hp1 | a0002 | c0002 | t0003 | g0133 | AFR | GWD | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0013 | AFR | GWD | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02818 | hp1 | a0001 | c0001 | t0020 | g0054 | AFR | GWD | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02818 | hp2 | a0001 | c0001 | t0007 | g0121 | AFR | GWD | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0009 | AFR | GWD | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02886 | hp2 | a0001 | c0001 | t0061 | g0264 | AFR | GWD | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02895 | hp1 | a0001 | c0001 | t0008 | g0039 | AFR | GWD | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02895 | hp2 | a0001 | c0001 | t0041 | g0051 | AFR | GWD | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02896 | hp1 | a0001 | c0001 | t0007 | g0045 | AFR | GWD | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02896 | hp2 | a0001 | c0001 | t0008 | g0063 | AFR | GWD | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02922 | hp1 | a0001 | c0001 | t0015 | g0140 | AFR | ESN | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02922 | hp2 | a0001 | c0001 | t0017 | g0144 | AFR | ESN | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02965 | hp1 | a0001 | c0001 | t0042 | g0005 | AFR | ESN | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02965 | hp2 | a0001 | c0001 | t0010 | g0022 | AFR | ESN | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02970 | hp1 | a0001 | c0001 | t0017 | g0145 | AFR | ESN | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02970 | hp2 | a0001 | c0001 | t0051 | g0284 | AFR | ESN | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02976 | hp1 | a0001 | c0003 | t0034 | g0003 | AFR | ESN | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02976 | hp2 | a0001 | c0001 | t0019 | g0055 | AFR | ESN | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG03017 | hp1 | a0002 | c0002 | t0057 | g0265 | SAS | PJL | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG03017 | hp2 | a0001 | c0001 | t0011 | g0165 | SAS | PJL | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG03041 | hp1 | a0001 | c0001 | t0007 | g0097 | AFR | GWD | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG03041 | hp2 | a0001 | c0001 | t0010 | g0018 | AFR | GWD | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG03098 | hp1 | a0001 | c0001 | t0012 | g0024 | AFR | MSL | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG03098 | hp2 | a0001 | c0001 | t0025 | g0052 | AFR | MSL | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG03130 | hp1 | a0001 | c0001 | t0010 | g0023 | AFR | ESN | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG03130 | hp2 | a0001 | c0001 | t0007 | g0163 | AFR | ESN | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG03195 | hp1 | a0001 | c0001 | t0005 | g0016 | AFR | ESN | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG03195 | hp2 | a0001 | c0001 | t0010 | g0020 | AFR | ESN | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG03209 | hp1 | a0001 | c0001 | t0024 | g0049 | AFR | MSL | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG03209 | hp2 | a0001 | c0003 | t0005 | g0181 | AFR | MSL | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG03225 | hp1 | a0001 | c0003 | t0003 | g0182 | AFR | MSL | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG03225 | hp2 | a0001 | c0001 | t0013 | g0263 | AFR | MSL | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0258 | SAS | PJL | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG03239 | hp2 | a0001 | c0001 | t0036 | g0146 | SAS | PJL | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG03453 | hp1 | a0001 | c0001 | t0008 | g0046 | AFR | MSL | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG03453 | hp2 | a0001 | c0001 | t0025 | g0122 | AFR | MSL | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG03486 | hp1 | a0001 | c0001 | t0007 | g0095 | AFR | MSL | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG03486 | hp2 | a0001 | c0001 | t0067 | g0125 | AFR | MSL | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG03516 | hp1 | a0001 | c0001 | t0012 | g0168 | AFR | ESN | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG03516 | hp2 | a0001 | c0001 | t0008 | g0037 | AFR | ESN | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG03540 | hp1 | a0002 | c0002 | t0001 | g0259 | AFR | GWD | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG03540 | hp2 | a0001 | c0001 | t0012 | g0179 | AFR | GWD | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG03579 | hp1 | a0001 | c0001 | t0018 | g0275 | AFR | MSL | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG03579 | hp2 | a0001 | c0001 | t0008 | g0030 | AFR | MSL | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0110 | SAS | STU | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0252 | SAS | STU | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0251 | SAS | PJL | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0106 | SAS | PJL | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG03710 | hp1 | a0001 | c0001 | t0011 | g0127 | SAS | PJL | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG03710 | hp2 | a0002 | c0002 | t0003 | g0136 | SAS | PJL | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0236 | SAS | BEB | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG03834 | hp2 | a0002 | c0002 | t0003 | g0006 | SAS | BEB | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG04115 | hp1 | a0002 | c0002 | t0003 | g0130 | SAS | STU | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG04115 | hp2 | a0001 | c0001 | t0028 | g0138 | SAS | STU | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0237 | SAS | BEB | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG04184 | hp2 | a0002 | c0002 | t0001 | g0281 | SAS | BEB | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG04204 | hp1 | a0002 | c0002 | t0003 | g0164 | SAS | STU | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG04204 | hp2 | a0002 | c0002 | t0053 | g0290 | SAS | STU | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0219 | EAS | CHB | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18747 | hp2 | a0001 | c0001 | t0014 | g0091 | EAS | CHB | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18906 | hp1 | a0001 | c0001 | t0011 | g0166 | AFR | YRI | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18906 | hp2 | a0001 | c0001 | t0019 | g0082 | AFR | YRI | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18940 | hp1 | a0002 | c0002 | t0001 | g0245 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18940 | hp2 | a0001 | c0001 | t0004 | g0175 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0241 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18943 | hp2 | a0002 | c0002 | t0001 | g0270 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18944 | hp1 | a0001 | c0001 | t0045 | g0047 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0188 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18948 | hp2 | a0001 | c0001 | t0029 | g0068 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18949 | hp1 | a0002 | c0002 | t0001 | g0234 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18949 | hp2 | a0002 | c0002 | t0003 | g0114 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18950 | hp1 | a0001 | c0001 | t0014 | g0092 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0229 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18951 | hp1 | a0002 | c0002 | t0003 | g0167 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18951 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0217 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18956 | hp1 | a0002 | c0002 | t0001 | g0235 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18956 | hp2 | a0001 | c0001 | t0048 | g0116 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18959 | hp1 | a0002 | c0002 | t0001 | g0268 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18959 | hp2 | a0002 | c0002 | t0001 | g0206 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0187 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18960 | hp2 | a0001 | c0001 | t0004 | g0034 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18962 | hp2 | a0002 | c0002 | t0001 | g0191 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18964 | hp1 | a0001 | c0001 | t0004 | g0035 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18964 | hp2 | a0002 | c0002 | t0001 | g0240 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0231 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18967 | hp1 | a0001 | c0001 | t0047 | g0028 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18967 | hp2 | a0002 | c0002 | t0001 | g0211 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0285 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0256 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18971 | hp2 | a0002 | c0006 | t0001 | g0204 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18973 | hp1 | a0002 | c0002 | t0001 | g0196 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0193 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18984 | hp2 | a0002 | c0002 | t0001 | g0233 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18986 | hp1 | a0002 | c0002 | t0054 | g0194 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0292 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18988 | hp1 | a0001 | c0001 | t0004 | g0061 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18988 | hp2 | a0002 | c0002 | t0001 | g0221 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18992 | hp1 | a0001 | c0001 | t0004 | g0171 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18992 | hp2 | a0002 | c0002 | t0001 | g0195 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18994 | hp1 | a0001 | c0001 | t0023 | g0075 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18994 | hp2 | a0002 | c0002 | t0001 | g0212 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0205 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18995 | hp2 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18999 | hp1 | a0002 | c0002 | t0059 | g0239 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18999 | hp2 | a0001 | c0001 | t0004 | g0126 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA19003 | hp2 | a0002 | c0002 | t0001 | g0267 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0207 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0232 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA19005 | hp2 | a0001 | c0001 | t0043 | g0031 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA19009 | hp1 | a0001 | c0001 | t0004 | g0170 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0200 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0248 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0210 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA19011 | hp1 | a0001 | c0001 | t0014 | g0090 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA19011 | hp2 | a0002 | c0005 | t0001 | g0203 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA19030 | hp1 | a0002 | c0002 | t0056 | g0244 | AFR | LWK | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | LWK | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA19043 | hp1 | a0001 | c0001 | t0013 | g0293 | AFR | LWK | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0011 | AFR | LWK | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA19054 | hp1 | a0002 | c0002 | t0001 | g0287 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA19054 | hp2 | a0001 | c0001 | t0024 | g0069 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0277 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA19057 | hp1 | a0002 | c0002 | t0003 | g0088 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA19057 | hp2 | a0002 | c0002 | t0065 | g0276 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA19060 | hp1 | a0002 | c0002 | t0001 | g0208 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA19062 | hp1 | a0001 | c0001 | t0004 | g0048 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA19062 | hp2 | a0002 | c0002 | t0001 | g0189 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0266 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0199 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA19074 | hp1 | a0001 | c0001 | t0046 | g0042 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0201 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA19077 | hp2 | a0002 | c0002 | t0001 | g0286 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA19079 | hp1 | a0002 | c0002 | t0001 | g0218 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA19080 | hp1 | a0001 | c0001 | t0069 | g0093 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA19080 | hp2 | a0002 | c0002 | t0001 | g0274 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA19089 | hp1 | a0002 | c0002 | t0001 | g0220 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA20129 | hp1 | a0001 | c0001 | t0022 | g0296 | AFR | ASW | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0014 | AFR | ASW | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA20905 | hp1 | a0001 | c0001 | t0026 | g0073 | SAS | GIH | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA20905 | hp2 | a0001 | c0001 | t0062 | g0247 | SAS | GIH | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG01123 | hp1 | a0001 | c0001 | t0021 | g0057 | AMR | CLM | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0254 | AMR | CLM | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02109 | hp1 | a0001 | c0001 | t0008 | g0062 | AFR | ACB | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02109 | hp2 | a0001 | c0001 | t0017 | g0143 | AFR | ACB | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02486 | hp1 | a0001 | c0001 | t0011 | g0150 | AFR | ACB | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02486 | hp2 | a0001 | c0001 | t0007 | g0119 | AFR | ACB | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02559 | hp1 | a0002 | c0002 | t0006 | g0155 | AFR | ACB | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG02559 | hp2 | a0001 | c0001 | t0012 | g0124 | AFR | ACB | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG03471 | hp1 | a0001 | c0001 | t0035 | g0012 | AFR | MSL | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0137 | AFR | MSL | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG06807 | hp1 | a0001 | c0001 | t0005 | g0010 | AFR | USA | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| HG06807 | hp2 | a0001 | c0001 | t0032 | g0021 | AFR | USA | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18955 | hp1 | a0002 | c0002 | t0001 | g0295 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0056 | AFR | LWK | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| NA21309 | hp2 | a0002 | c0002 | t0001 | g0224 | AFR | LWK | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0003 | g0128 | REF | REF | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| homoSapiens_grch38 | hp1 | a0002 | c0002 | t0006 | g0154 | REF | REF | TRAF3_chr14_102772449_102916500 | TRAF3 | chr14 | 102772449 | 102916500 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:102875712
|
T | C | 1 | a0001 | 172 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(169): Show |
missense_variant | MODERATE | c.386T>C | p.Met129Thr | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 5/12 | 769/7806 | 386/1707 | 129/568 | chr14 | 102875712 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:102870390
|
G | A | 1 | a0001c0004 | 1 | HG01993.hp1 | synonymous_variant | LOW | c.189G>A | p.Pro63Pro | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 3/12 | 572/7806 | 189/1707 | 63/568 | chr14 | 102870390 | ||
| chr14:102903386
|
G | A | 1 | a0002c0005 | 1 | NA19011.hp2 | synonymous_variant | LOW | c.1092G>A | p.Leu364Leu | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 11/12 | 1475/7806 | 1092/1707 | 364/568 | chr14 | 102903386 | ||
| chr14:102903404
|
C | T | 1 | a0001c0003 | 4 | HG02630.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
synonymous_variant | LOW | c.1110C>T | p.Ser370Ser | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 11/12 | 1493/7806 | 1110/1707 | 370/568 | chr14 | 102903404 | ||
| chr14:102905391
|
G | C | 1 | a0002c0006 | 1 | NA18971.hp2 | synonymous_variant | LOW | c.1314G>C | p.Leu438Leu | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 1697/7806 | 1314/1707 | 438/568 | chr14 | 102905391 | ||
| chr14:102905766
|
G | A | 1 | a0002c0007 | 1 | HG02683.hp1 | synonymous_variant | LOW | c.1689G>A | p.Ser563Ser | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 2072/7806 | 1689/1707 | 563/568 | chr14 | 102905766 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:102777549
|
A | C | 2 | a0001c0001t0014a0001c0001t0069 | 5 | HG02523.hp2 NA18747.hp2 NA18950.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-283A>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/12 | 92653 | chr14 | 102777549 | |||||
| chr14:102777558
|
G | T | 2 | a0001c0001t0014a0001c0001t0069 | 5 | HG02523.hp2 NA18747.hp2 NA18950.hp1 others(2): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-274G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/12 | chr14 | 102777558 | ||||||
| chr14:102777580
|
C | G | 2 | a0001c0001t0067a0001c0001t0068 | 2 | HG02723.hp2 HG03486.hp2 |
5_prime_UTR_variant | MODIFIER | c.-252C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/12 | 92622 | chr14 | 102777580 | |||||
| chr14:102777609
|
C | T | 25 | a0001c0001t0001a0001c0001t0013a0001c0001t0018others(22): Show | 112 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(109): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-223C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/12 | chr14 | 102777609 | ||||||
| chr14:102830348
|
G | A | 3 | a0001c0001t0015a0001c0001t0019a0001c0001t0051 | 6 | HG02055.hp1 HG02257.hp1 HG02922.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-142G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/12 | 39854 | chr14 | 102830348 | |||||
| chr14:102905797
|
G | A | 1 | a0001c0001t0028 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*13G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 13 | chr14 | 102905797 | |||||
| chr14:102905914
|
C | T | 1 | a0001c0001t0050 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*130C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 130 | chr14 | 102905914 | |||||
| chr14:102906003
|
C | T | 1 | a0002c0002t0049 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*219C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 219 | chr14 | 102906003 | |||||
| chr14:102906370
|
A | T | 1 | a0001c0001t0026 | 2 | HG02698.hp2 NA20905.hp1 |
3_prime_UTR_variant | MODIFIER | c.*586A>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 586 | chr14 | 102906370 | |||||
| chr14:102906437
|
C | T | 1 | a0002c0002t0066 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*653C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 653 | chr14 | 102906437 | |||||
| chr14:102906504
|
G | A | 1 | a0001c0001t0029 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*720G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 720 | chr14 | 102906504 | |||||
| chr14:102906507
|
A | G | 1 | a0001c0001t0029 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*723A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 723 | chr14 | 102906507 | |||||
| chr14:102906508
|
G | A | 1 | a0001c0001t0029 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*724G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 724 | chr14 | 102906508 | |||||
| chr14:102906777
|
G | A | 1 | a0002c0002t0052 | 1 | HG01071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*993G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 993 | chr14 | 102906777 | |||||
| chr14:102906847
|
G | A | 1 | a0001c0001t0030 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1063G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 1063 | chr14 | 102906847 | |||||
| chr14:102906851
|
A | G | 1 | a0002c0002t0065 | 1 | NA19057.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1067A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 1067 | chr14 | 102906851 | |||||
| chr14:102906853
|
G | A | 1 | a0001c0001t0015 | 3 | HG02055.hp1 HG02257.hp1 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1069G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 1069 | chr14 | 102906853 | |||||
| chr14:102907065
|
C | T | 1 | a0001c0001t0048 | 1 | NA18956.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1281C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 1281 | chr14 | 102907065 | |||||
| chr14:102907097
|
C | G | 30 | a0001c0001t0002a0001c0001t0004a0001c0001t0007others(27): Show | 119 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*1313C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 1313 | chr14 | 102907097 | |||||
| chr14:102907201
|
G | A | 1 | a0002c0002t0053 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1417G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 1417 | chr14 | 102907201 | |||||
| chr14:102907275
|
G | T | 1 | a0001c0001t0042 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1491G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 1491 | chr14 | 102907275 | |||||
| chr14:102907341
|
C | G | 1 | a0001c0001t0029 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1557C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 1557 | chr14 | 102907341 | |||||
| chr14:102907402
|
TCA | T | 3 | a0001c0001t0021a0001c0001t0067a0001c0001t0068 | 4 | HG01123.hp1 HG02723.hp2 HG02738.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1619_*1620delCA | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 1619 | chr14 | 102907402 | |||||
| chr14:102907537
|
G | A | 1 | a0002c0002t0054 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1753G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 1753 | chr14 | 102907537 | |||||
| chr14:102907570
|
C | T | 1 | a0001c0001t0041 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1786C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 1786 | chr14 | 102907570 | |||||
| chr14:102907571
|
G | A | 1 | a0002c0002t0055 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1787G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 1787 | chr14 | 102907571 | |||||
| chr14:102907708
|
C | T | 1 | a0001c0001t0040 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1924C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 1924 | chr14 | 102907708 | |||||
| chr14:102907789
|
G | C | 1 | a0001c0001t0043 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2005G>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 2005 | chr14 | 102907789 | |||||
| chr14:102907823
|
C | A | 4 | a0001c0001t0021a0001c0001t0044a0001c0001t0067others(1): Show | 5 | HG00735.hp1 HG01123.hp1 HG02723.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2039C>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 2039 | chr14 | 102907823 | |||||
| chr14:102907830
|
C | T | 4 | a0001c0001t0021a0001c0001t0044a0001c0001t0067others(1): Show | 5 | HG00735.hp1 HG01123.hp1 HG02723.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2046C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 2046 | chr14 | 102907830 | |||||
| chr14:102907983
|
A | C | 1 | a0001c0001t0041 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2199A>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 2199 | chr14 | 102907983 | |||||
| chr14:102908071
|
T | A | 1 | a0001c0001t0061 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2287T>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 2287 | chr14 | 102908071 | |||||
| chr14:102908105
|
C | T | 2 | a0001c0004t0039a0002c0002t0060 | 2 | HG00140.hp1 HG01993.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2321C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 2321 | chr14 | 102908105 | |||||
| chr14:102908132
|
T | C | 11 | a0001c0001t0010a0001c0001t0013a0001c0001t0018others(8): Show | 22 | HG00639.hp2 HG00733.hp2 HG01099.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2348T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 2348 | chr14 | 102908132 | |||||
| chr14:102908284
|
A | G | 1 | a0001c0001t0042 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2500A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 2500 | chr14 | 102908284 | |||||
| chr14:102908373
|
G | A | 6 | a0001c0001t0004a0001c0001t0023a0001c0001t0030others(3): Show | 20 | HG00609.hp1 HG01261.hp1 HG01928.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2589G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 2589 | chr14 | 102908373 | |||||
| chr14:102908441
|
C | T | 1 | a0002c0002t0059 | 1 | NA18999.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2657C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 2657 | chr14 | 102908441 | |||||
| chr14:102908547
|
T | C | 10 | a0001c0001t0005a0001c0001t0011a0001c0001t0027others(7): Show | 23 | HG01069.hp1 HG01071.hp2 HG01099.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2763T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 2763 | chr14 | 102908547 | |||||
| chr14:102908639
|
T | C | 1 | a0001c0001t0032 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2855T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 2855 | chr14 | 102908639 | |||||
| chr14:102908652
|
G | T | 1 | a0001c0001t0068 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2868G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 2868 | chr14 | 102908652 | |||||
| chr14:102908857
|
G | A | 1 | a0001c0001t0016 | 3 | HG00323.hp1 HG01516.hp2 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3073G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 3073 | chr14 | 102908857 | |||||
| chr14:102909057
|
G | T | 2 | a0001c0001t0035a0001c0001t0038 | 2 | HG02451.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3273G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 3273 | chr14 | 102909057 | |||||
| chr14:102909109
|
T | G | 1 | a0001c0001t0042 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3325T>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 3325 | chr14 | 102909109 | |||||
| chr14:102909137
|
G | T | 2 | a0001c0001t0005a0001c0003t0005 | 9 | HG02055.hp2 HG02809.hp2 HG02886.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3353G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 3353 | chr14 | 102909137 | |||||
| chr14:102909177
|
C | T | 2 | a0001c0003t0034a0001c0003t0037 | 2 | HG02630.hp2 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3393C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 3393 | chr14 | 102909177 | |||||
| chr14:102909203
|
A | G | 5 | a0001c0001t0011a0001c0001t0027a0001c0001t0028others(2): Show | 11 | HG01069.hp1 HG01071.hp2 HG01496.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3419A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 3419 | chr14 | 102909203 | |||||
| chr14:102909257
|
T | A | 74 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(71): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
3_prime_UTR_variant | MODIFIER | c.*3473T>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 3473 | chr14 | 102909257 | |||||
| chr14:102909357
|
A | C | 1 | a0001c0001t0036 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3573A>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 3573 | chr14 | 102909357 | |||||
| chr14:102909694
|
C | T | 30 | a0001c0001t0002a0001c0001t0004a0001c0001t0007others(27): Show | 124 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*3910C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 3910 | chr14 | 102909694 | |||||
| chr14:102909792
|
G | A | 1 | a0001c0004t0039 | 1 | HG01993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4008G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 4008 | chr14 | 102909792 | |||||
| chr14:102909815
|
C | T | 1 | a0001c0001t0046 | 1 | NA19074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4031C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 4031 | chr14 | 102909815 | |||||
| chr14:102909852
|
A | G | 1 | a0001c0004t0039 | 1 | HG01993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4068A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 4068 | chr14 | 102909852 | |||||
| chr14:102909857
|
G | A | 1 | a0001c0001t0061 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4073G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 4073 | chr14 | 102909857 | |||||
| chr14:102910057
|
T | C | 1 | a0001c0001t0047 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4273T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 4273 | chr14 | 102910057 | |||||
| chr14:102910121
|
G | A | 1 | a0001c0001t0023 | 2 | HG00609.hp1 NA18994.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4337G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 4337 | chr14 | 102910121 | |||||
| chr14:102910177
|
C | T | 1 | a0001c0001t0025 | 2 | HG03098.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4393C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 4393 | chr14 | 102910177 | |||||
| chr14:102910223
|
G | A | 1 | a0001c0001t0017 | 3 | HG02109.hp2 HG02922.hp2 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4439G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 4439 | chr14 | 102910223 | |||||
| chr14:102910491
|
G | A | 1 | a0002c0002t0009 | 7 | HG00323.hp2 HG01081.hp1 HG01169.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4707G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 4707 | chr14 | 102910491 | |||||
| chr14:102910919
|
A | G | 1 | a0001c0004t0039 | 1 | HG01993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5135A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 5135 | chr14 | 102910919 | |||||
| chr14:102910984
|
G | A | 31 | a0001c0001t0002a0001c0001t0004a0001c0001t0007others(28): Show | 124 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*5200G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 5200 | chr14 | 102910984 | |||||
| chr14:102911012
|
C | T | 1 | a0001c0001t0044 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5228C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 5228 | chr14 | 102911012 | |||||
| chr14:102911017
|
T | G | 17 | a0001c0001t0002a0001c0001t0004a0001c0001t0014others(14): Show | 78 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*5233T>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 5233 | chr14 | 102911017 | |||||
| chr14:102911125
|
A | G | 2 | a0001c0001t0020a0001c0001t0041 | 3 | HG02622.hp2 HG02818.hp1 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5341A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 5341 | chr14 | 102911125 | |||||
| chr14:102911140
|
A | G | 1 | a0002c0002t0057 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5356A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 5356 | chr14 | 102911140 | |||||
| chr14:102911146
|
C | T | 1 | a0001c0001t0018 | 3 | HG01167.hp1 HG01169.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5362C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 5362 | chr14 | 102911146 | |||||
| chr14:102911383
|
T | C | 2 | a0001c0001t0031a0001c0001t0042 | 2 | HG01099.hp2 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5599T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 5599 | chr14 | 102911383 | |||||
| chr14:102911396
|
G | A | 1 | a0001c0001t0045 | 1 | NA18944.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5612G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 5612 | chr14 | 102911396 | |||||
| chr14:102911405
|
A | T | 2 | a0001c0001t0008a0002c0002t0056 | 9 | HG01175.hp2 HG02109.hp1 HG02258.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*5621A>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 12/12 | 5621 | chr14 | 102911405 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:102777678
|
A | G | 1 | a0001c0001t0022g0296 | 1 | NA20129.hp1 | splice_region_variant&intron_variant | LOW | c.-157+3A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102777678 | ||||||
| chr14:102777733
|
C | G | 112 | a0001c0001t0001g0184a0001c0001t0013g0262a0001c0001t0013g0263others(109): Show | 112 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.-157+58C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102777733 | ||||||
| chr14:102777740
|
T | C | 1 | a0001c0001t0012g0001 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-157+65T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102777740 | ||||||
| chr14:102777783
|
TGCCCGGC others(4): Show |
T | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-157+120_-157+130d others(13): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102777783 | |||||
| chr14:102777913
|
T | C | 1 | a0001c0001t0001g0184 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-157+238T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102777913 | ||||||
| chr14:102777952
|
G | A | 114 | a0001c0001t0001g0184a0001c0001t0013g0262a0001c0001t0013g0263others(111): Show | 114 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.-157+277G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102777952 | ||||||
| chr14:102777995
|
C | T | 4 | a0001c0001t0022g0296a0001c0001t0031g0183a0001c0003t0003g0182others(1): Show | 4 | HG01099.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-157+320C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102777995 | ||||||
| chr14:102778005
|
C | T | 2 | a0001c0001t0012g0179a0001c0001t0050g0180 | 2 | HG01884.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-157+330C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102778005 | ||||||
| chr14:102778006
|
C | T | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-157+331C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102778006 | ||||||
| chr14:102778036
|
G | A | 1 | a0002c0002t0009g0185 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-157+361G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102778036 | ||||||
| chr14:102778077
|
C | T | 1 | a0002c0002t0001g0295 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-157+402C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102778077 | ||||||
| chr14:102778109
|
G | T | 1 | a0001c0001t0002g0178 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-157+434G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102778109 | ||||||
| chr14:102778189
|
C | G | 2 | a0001c0001t0012g0179a0001c0001t0050g0180 | 2 | HG01884.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-157+514C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102778189 | ||||||
| chr14:102778321
|
C | A | 1 | a0001c0001t0042g0005 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-157+646C>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102778321 | ||||||
| chr14:102778336
|
C | T | 2 | a0001c0001t0013g0293a0001c0001t0013g0294 | 2 | HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-157+661C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102778336 | ||||||
| chr14:102778426
|
G | A | 1 | a0002c0002t0003g0006 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-157+751G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102778426 | ||||||
| chr14:102778451
|
A | C | 2 | a0001c0003t0034g0003a0001c0003t0037g0004 | 2 | HG02630.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-157+776A>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102778451 | ||||||
| chr14:102778480
|
C | T | 8 | a0001c0001t0002g0172a0001c0001t0004g0170a0001c0001t0004g0171others(5): Show | 8 | HG01261.hp1 HG01928.hp1 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.-157+805C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102778480 | ||||||
| chr14:102778503
|
T | C | 253 | a0001c0001t0001g0184a0001c0001t0002g0025a0001c0001t0002g0026others(250): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.-157+828T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102778503 | ||||||
| chr14:102778597
|
C | CTGTG | 112 | a0001c0001t0001g0184a0001c0001t0013g0262a0001c0001t0013g0263others(109): Show | 112 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.-157+930_-157+933d others(6): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102778597 | |||||
| chr14:102778653
|
C | G | 2 | a0001c0003t0034g0003a0001c0003t0037g0004 | 2 | HG02630.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-157+978C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102778653 | ||||||
| chr14:102778823
|
C | T | 1 | a0001c0001t0004g0126 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-157+1148C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102778823 | ||||||
| chr14:102779101
|
C | T | 1 | a0002c0002t0001g0292 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-157+1426C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102779101 | ||||||
| chr14:102779222
|
A | G | 1 | a0001c0001t0067g0125 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-157+1547A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102779222 | ||||||
| chr14:102779269
|
C | CT | 12 | a0001c0001t0002g0032a0001c0001t0004g0033a0001c0001t0007g0163others(9): Show | 12 | HG01192.hp1 HG01884.hp2 HG03017.hp2 others(9): Show |
intron_variant | MODIFIER | c.-157+1623dupT | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102779269 | |||||
| chr14:102779269
|
C | CTT | 26 | a0001c0001t0002g0036a0001c0001t0002g0041a0001c0001t0002g0044others(23): Show | 26 | HG00609.hp1 HG00639.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.-157+1622_-157+162 others(6): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102779269 | |||||
| chr14:102779269
|
C | CTTT | 47 | a0001c0001t0002g0058a0001c0001t0002g0059a0001c0001t0002g0060others(44): Show | 47 | HG00140.hp2 HG00544.hp2 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.-157+1621_-157+162 others(7): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102779269 | |||||
| chr14:102779269
|
C | CTTTT | 27 | a0001c0001t0002g0101a0001c0001t0002g0102a0001c0001t0002g0106others(24): Show | 27 | HG00099.hp2 HG00323.hp1 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.-157+1620_-157+162 others(8): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102779269 | |||||
| chr14:102779269
|
CT | C | 8 | a0001c0001t0005g0137a0001c0001t0012g0179a0001c0001t0015g0139others(5): Show | 8 | HG02055.hp1 HG02965.hp1 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.-157+1623delT | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102779269 | |||||
| chr14:102779269
|
CTTTTTTT others(4): Show |
C | 18 | a0001c0001t0004g0007a0001c0001t0005g0009a0001c0001t0005g0010others(15): Show | 18 | HG02055.hp2 HG02258.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.-157+1613_-157+162 others(15): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102779269 | |||||
| chr14:102779269
|
CTTTTTTT others(7): Show |
C | 1 | a0002c0002t0001g0291 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-157+1610_-157+162 others(18): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102779269 | |||||
| chr14:102779269
|
CTTTTTTT others(8): Show |
C | 120 | a0001c0001t0001g0184a0001c0001t0011g0127a0001c0001t0013g0262others(117): Show | 120 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.-157+1609_-157+162 others(19): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102779269 | |||||
| chr14:102779269
|
CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0018g0186 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-157+1608_-157+162 others(20): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102779269 | |||||
| chr14:102779269
|
CTTTTTTT others(11): Show |
C | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-157+1606_-157+162 others(22): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102779269 | |||||
| chr14:102780013
|
T | G | 1 | a0001c0001t0003g0100 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-157+2338T>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102780013 | ||||||
| chr14:102780133
|
A | G | 124 | a0001c0001t0001g0184a0001c0001t0013g0262a0001c0001t0013g0263others(121): Show | 124 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.-157+2458A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102780133 | ||||||
| chr14:102780195
|
C | T | 1 | a0002c0002t0006g0162 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-157+2520C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102780195 | ||||||
| chr14:102780219
|
C | T | 1 | a0002c0002t0053g0290 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-157+2544C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102780219 | ||||||
| chr14:102780519
|
CT | C | 97 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(94): Show | 97 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.-157+2856delT | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102780519 | |||||
| chr14:102780536
|
C | T | 1 | a0001c0001t0015g0139 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-157+2861C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102780536 | ||||||
| chr14:102780717
|
A | G | 1 | a0001c0001t0007g0121 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-157+3042A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102780717 | ||||||
| chr14:102780729
|
T | C | 1 | a0001c0001t0002g0058 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-157+3054T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102780729 | ||||||
| chr14:102780906
|
G | C | 17 | a0001c0001t0005g0009a0001c0001t0005g0010a0001c0001t0005g0011others(14): Show | 17 | HG02055.hp2 HG02258.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.-157+3231G>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102780906 | ||||||
| chr14:102780946
|
C | T | 1 | a0001c0001t0003g0100 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-157+3271C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102780946 | ||||||
| chr14:102781013
|
G | C | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-157+3338G>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102781013 | ||||||
| chr14:102781175
|
AG | A | 121 | a0001c0001t0001g0184a0001c0001t0013g0262a0001c0001t0013g0263others(118): Show | 121 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.-157+3503delG | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102781175 | |||||
| chr14:102781507
|
C | A | 141 | a0001c0001t0001g0184a0001c0001t0003g0100a0001c0001t0010g0053others(138): Show | 141 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.-157+3832C>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102781507 | ||||||
| chr14:102781721
|
G | T | 5 | a0001c0001t0022g0296a0001c0001t0031g0183a0001c0001t0042g0005others(2): Show | 5 | HG01099.hp2 HG02965.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-157+4046G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102781721 | ||||||
| chr14:102781780
|
C | T | 2 | a0001c0001t0027g0288a0001c0001t0027g0289 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-157+4105C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102781780 | ||||||
| chr14:102781792
|
A | AT | 28 | a0001c0001t0002g0120a0001c0001t0007g0094a0001c0001t0007g0095others(25): Show | 28 | HG00621.hp2 HG00639.hp2 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.-157+4135dupT | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102781792 | |||||
| chr14:102782150
|
A | G | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-157+4475A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102782150 | ||||||
| chr14:102782196
|
A | G | 3 | a0002c0002t0001g0285a0002c0002t0001g0286a0002c0002t0001g0287 | 3 | NA18969.hp1 NA19054.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.-157+4521A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102782196 | ||||||
| chr14:102782393
|
C | A | 5 | a0001c0001t0005g0137a0001c0001t0015g0139a0001c0001t0015g0140others(2): Show | 5 | HG02055.hp1 HG02257.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-157+4718C>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102782393 | ||||||
| chr14:102782394
|
C | T | 7 | a0001c0001t0010g0018a0001c0001t0010g0019a0001c0001t0010g0020others(4): Show | 7 | HG02258.hp1 HG02965.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.-157+4719C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102782394 | ||||||
| chr14:102782561
|
T | C | 1 | a0001c0003t0005g0181 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-157+4886T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102782561 | ||||||
| chr14:102782590
|
T | C | 4 | a0002c0002t0001g0187a0002c0002t0001g0188a0002c0002t0001g0189others(1): Show | 4 | HG00558.hp2 NA18944.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.-157+4915T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102782590 | ||||||
| chr14:102782617
|
C | T | 44 | a0001c0001t0013g0262a0001c0001t0013g0263a0001c0001t0013g0293others(41): Show | 44 | HG00099.hp1 HG00733.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.-157+4942C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102782617 | ||||||
| chr14:102782622
|
A | T | 44 | a0001c0001t0013g0262a0001c0001t0013g0263a0001c0001t0013g0293others(41): Show | 44 | HG00099.hp1 HG00733.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.-157+4947A>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102782622 | ||||||
| chr14:102782642
|
A | G | 1 | a0002c0002t0001g0249 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-157+4967A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102782642 | ||||||
| chr14:102782701
|
T | TA | 9 | a0001c0001t0007g0163a0001c0001t0012g0001a0001c0001t0012g0179others(6): Show | 9 | HG01884.hp2 HG01993.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.-157+5041dupA | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102782701 | |||||
| chr14:102782701
|
TA | T | 125 | a0001c0001t0001g0184a0001c0001t0002g0027a0001c0001t0002g0118others(122): Show | 125 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.-157+5041delA | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102782701 | |||||
| chr14:102782721
|
A | T | 5 | a0001c0001t0014g0090a0001c0001t0014g0091a0001c0001t0014g0092others(2): Show | 5 | HG02523.hp2 NA18747.hp2 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.-157+5046A>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102782721 | ||||||
| chr14:102782790
|
G | C | 160 | a0001c0001t0001g0184a0001c0001t0003g0100a0001c0001t0005g0009others(157): Show | 160 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.-157+5115G>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102782790 | ||||||
| chr14:102782865
|
ATTTC | A | 3 | a0001c0001t0022g0050a0001c0001t0025g0052a0001c0001t0025g0122 | 3 | HG01884.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-157+5194_-157+519 others(8): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102782865 | |||||
| chr14:102783049
|
C | T | 3 | a0001c0001t0012g0001a0001c0001t0012g0179a0001c0001t0050g0180 | 3 | HG01884.hp2 HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-157+5374C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102783049 | ||||||
| chr14:102783081
|
C | T | 1 | a0001c0001t0044g0089 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-157+5406C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102783081 | ||||||
| chr14:102783147
|
G | A | 1 | a0001c0001t0042g0005 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-157+5472G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102783147 | ||||||
| chr14:102783212
|
C | G | 4 | a0001c0003t0003g0182a0001c0003t0005g0181a0001c0003t0034g0003others(1): Show | 4 | HG02630.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-157+5537C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102783212 | ||||||
| chr14:102783278
|
G | A | 2 | a0001c0001t0012g0098a0001c0001t0012g0124 | 2 | HG01109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-157+5603G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102783278 | ||||||
| chr14:102783339
|
T | C | 249 | a0001c0001t0001g0184a0001c0001t0002g0025a0001c0001t0002g0026others(246): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.-157+5664T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102783339 | ||||||
| chr14:102783438
|
A | G | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-157+5763A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102783438 | ||||||
| chr14:102783573
|
G | C | 1 | a0001c0001t0002g0101 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-157+5898G>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102783573 | ||||||
| chr14:102783598
|
T | C | 1 | a0002c0002t0001g0193 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-157+5923T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102783598 | ||||||
| chr14:102783603
|
C | T | 1 | a0001c0001t0004g0007 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-157+5928C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102783603 | ||||||
| chr14:102783875
|
T | A | 8 | a0001c0001t0010g0053a0001c0001t0012g0098a0001c0001t0012g0124others(5): Show | 8 | HG00639.hp2 HG01109.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.-157+6200T>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102783875 | ||||||
| chr14:102783880
|
C | G | 8 | a0001c0001t0010g0053a0001c0001t0012g0098a0001c0001t0012g0124others(5): Show | 8 | HG00639.hp2 HG01109.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.-157+6205C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102783880 | ||||||
| chr14:102783924
|
A | T | 8 | a0001c0001t0010g0053a0001c0001t0012g0098a0001c0001t0012g0124others(5): Show | 8 | HG00639.hp2 HG01109.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.-157+6249A>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102783924 | ||||||
| chr14:102784004
|
C | G | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-157+6329C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102784004 | ||||||
| chr14:102784150
|
C | T | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-157+6475C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102784150 | ||||||
| chr14:102784189
|
C | T | 11 | a0001c0001t0010g0053a0001c0001t0012g0098a0001c0001t0012g0124others(8): Show | 11 | HG00639.hp2 HG01099.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-157+6514C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102784189 | ||||||
| chr14:102784215
|
CT | C | 77 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0032others(74): Show | 77 | HG00140.hp2 HG00609.hp1 HG00673.hp1 others(74): Show |
intron_variant | MODIFIER | c.-157+6567delT | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102784215 | |||||
| chr14:102784215
|
CTT | C | 30 | a0001c0001t0002g0036a0001c0001t0002g0101a0001c0001t0002g0102others(27): Show | 30 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.-157+6566_-157+656 others(6): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102784215 | |||||
| chr14:102784215
|
CTTTTTTT others(4): Show |
C | 4 | a0001c0001t0004g0034a0001c0001t0004g0035a0001c0001t0004g0048others(1): Show | 4 | NA18960.hp2 NA18964.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.-157+6557_-157+656 others(15): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102784215 | |||||
| chr14:102784215
|
CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0002g0059a0001c0001t0002g0060 | 2 | HG00544.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.-157+6556_-157+656 others(16): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102784215 | |||||
| chr14:102784215
|
CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0184 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-157+6554_-157+656 others(18): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102784215 | |||||
| chr14:102784215
|
CTTTTTTT others(8): Show |
C | 123 | a0001c0001t0010g0018a0001c0001t0011g0127a0001c0001t0011g0165others(120): Show | 123 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.-157+6553_-157+656 others(19): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102784215 | |||||
| chr14:102784215
|
CTTTTTTT others(9): Show |
C | 1 | a0002c0002t0054g0194 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-157+6552_-157+656 others(20): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102784215 | |||||
| chr14:102784454
|
T | C | 3 | a0001c0001t0002g0120a0001c0001t0004g0033a0001c0001t0045g0047 | 3 | HG00621.hp2 NA18944.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.-157+6779T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102784454 | ||||||
| chr14:102784666
|
C | T | 98 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(95): Show | 98 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.-157+6991C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102784666 | ||||||
| chr14:102784789
|
G | A | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-157+7114G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102784789 | ||||||
| chr14:102784858
|
G | T | 2 | a0001c0001t0025g0052a0001c0001t0025g0122 | 2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-157+7183G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102784858 | ||||||
| chr14:102785115
|
T | G | 124 | a0001c0001t0001g0184a0001c0001t0010g0018a0001c0001t0011g0165others(121): Show | 124 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.-157+7440T>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102785115 | ||||||
| chr14:102785145
|
C | G | 1 | a0001c0001t0051g0284 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-157+7470C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102785145 | ||||||
| chr14:102785148
|
A | G | 1 | a0001c0001t0014g0092 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-157+7473A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102785148 | ||||||
| chr14:102785793
|
C | T | 2 | a0001c0001t0002g0112a0001c0001t0002g0178 | 2 | NA18952.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.-157+8118C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102785793 | ||||||
| chr14:102785807
|
C | G | 1 | a0001c0001t0038g0015 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-157+8132C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102785807 | ||||||
| chr14:102785893
|
G | C | 3 | a0001c0001t0033g0123a0001c0001t0067g0125a0001c0001t0068g0029 | 3 | HG00733.hp2 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-157+8218G>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102785893 | ||||||
| chr14:102785919
|
T | A | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-157+8244T>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102785919 | ||||||
| chr14:102785925
|
G | A | 76 | a0001c0001t0001g0184a0001c0001t0062g0247a0001c0001t0063g0223others(73): Show | 76 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.-157+8250G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102785925 | ||||||
| chr14:102785933
|
G | A | 97 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(94): Show | 97 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.-157+8258G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102785933 | ||||||
| chr14:102786030
|
G | A | 1 | a0001c0001t0002g0102 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-157+8355G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102786030 | ||||||
| chr14:102786151
|
A | G | 1 | a0002c0002t0001g0249 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-157+8476A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102786151 | ||||||
| chr14:102786228
|
G | A | 3 | a0001c0001t0008g0037a0001c0001t0008g0038a0001c0001t0008g0062 | 3 | HG02109.hp1 HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-157+8553G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102786228 | ||||||
| chr14:102786337
|
T | C | 3 | a0001c0001t0022g0050a0001c0001t0025g0052a0001c0001t0025g0122 | 3 | HG01884.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-157+8662T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102786337 | ||||||
| chr14:102786405
|
G | T | 7 | a0001c0001t0010g0018a0001c0001t0010g0019a0001c0001t0010g0020others(4): Show | 7 | HG02258.hp1 HG02965.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.-157+8730G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102786405 | ||||||
| chr14:102786690
|
A | T | 45 | a0001c0001t0013g0262a0001c0001t0013g0263a0001c0001t0013g0293others(42): Show | 45 | HG00099.hp1 HG00733.hp1 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.-157+9015A>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102786690 | ||||||
| chr14:102786791
|
C | G | 2 | a0001c0003t0003g0182a0001c0003t0005g0181 | 2 | HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-157+9116C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102786791 | ||||||
| chr14:102786926
|
C | G | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-157+9251C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102786926 | ||||||
| chr14:102786947
|
C | T | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-157+9272C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102786947 | ||||||
| chr14:102787108
|
G | A | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-157+9433G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102787108 | ||||||
| chr14:102787184
|
G | A | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-157+9509G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102787184 | ||||||
| chr14:102787229
|
G | A | 3 | a0002c0002t0001g0251a0002c0002t0001g0252a0002c0002t0001g0253 | 3 | HG01433.hp1 HG03688.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.-157+9554G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102787229 | ||||||
| chr14:102787261
|
T | G | 1 | a0001c0001t0022g0050 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-157+9586T>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102787261 | ||||||
| chr14:102787395
|
G | A | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-157+9720G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102787395 | ||||||
| chr14:102787519
|
C | CA | 6 | a0001c0001t0007g0008a0001c0001t0017g0143a0002c0002t0001g0195others(3): Show | 6 | HG01123.hp2 HG01175.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.-157+9862dupA | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102787519 | |||||
| chr14:102787680
|
C | T | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-157+10005C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102787680 | ||||||
| chr14:102787783
|
C | G | 3 | a0001c0001t0022g0296a0001c0001t0031g0183a0001c0001t0042g0005 | 3 | HG01099.hp2 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-157+10108C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102787783 | ||||||
| chr14:102787787
|
C | T | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-157+10112C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102787787 | ||||||
| chr14:102787836
|
A | G | 2 | a0001c0001t0012g0098a0001c0001t0012g0124 | 2 | HG01109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-157+10161A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102787836 | ||||||
| chr14:102787971
|
C | G | 1 | a0001c0001t0042g0005 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-157+10296C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102787971 | ||||||
| chr14:102788084
|
T | C | 267 | a0001c0001t0001g0184a0001c0001t0002g0025a0001c0001t0002g0026others(264): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.-157+10409T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102788084 | ||||||
| chr14:102788441
|
C | A | 1 | a0001c0001t0031g0183 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-157+10766C>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102788441 | ||||||
| chr14:102788531
|
G | A | 1 | a0001c0001t0064g0198 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-157+10856G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102788531 | ||||||
| chr14:102788672
|
C | T | 8 | a0001c0001t0010g0053a0001c0001t0012g0098a0001c0001t0012g0124others(5): Show | 8 | HG00639.hp2 HG01109.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.-157+10997C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102788672 | ||||||
| chr14:102788746
|
T | C | 2 | a0002c0002t0001g0199a0002c0002t0001g0200 | 2 | NA19009.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-157+11071T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102788746 | ||||||
| chr14:102788796
|
TCAAAA | T | 80 | a0001c0001t0001g0184a0001c0001t0017g0143a0001c0001t0017g0144others(77): Show | 80 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.-157+11143_-157+11 others(11): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102788796 | |||||
| chr14:102788885
|
C | T | 1 | a0002c0002t0058g0192 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-157+11210C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102788885 | ||||||
| chr14:102788927
|
C | T | 1 | a0001c0001t0008g0046 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-157+11252C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102788927 | ||||||
| chr14:102788966
|
A | G | 2 | a0001c0001t0048g0116a0002c0002t0003g0088 | 2 | NA18956.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.-157+11291A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102788966 | ||||||
| chr14:102789086
|
C | T | 1 | a0001c0001t0062g0247 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-157+11411C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102789086 | ||||||
| chr14:102789124
|
T | C | 128 | a0001c0001t0001g0184a0001c0001t0013g0262a0001c0001t0013g0263others(125): Show | 128 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.-157+11449T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102789124 | ||||||
| chr14:102789236
|
C | T | 1 | a0001c0001t0030g0176 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-157+11561C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102789236 | ||||||
| chr14:102789439
|
A | C | 4 | a0001c0003t0003g0182a0001c0003t0005g0181a0001c0003t0034g0003others(1): Show | 4 | HG02630.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-157+11764A>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102789439 | ||||||
| chr14:102789469
|
T | TG | 128 | a0001c0001t0001g0184a0001c0001t0013g0262a0001c0001t0013g0263others(125): Show | 128 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.-157+11794_-157+11 others(7): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102789469 | ||||||
| chr14:102789594
|
A | ATG | 8 | a0001c0001t0005g0137a0001c0001t0015g0139a0001c0001t0015g0140others(5): Show | 8 | HG02055.hp1 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-157+11948_-157+11 others(8): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102789594 | |||||
| chr14:102789594
|
A | ATGTG | 42 | a0001c0001t0003g0100a0001c0001t0013g0262a0001c0001t0013g0263others(39): Show | 42 | HG00099.hp1 HG00733.hp1 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.-157+11946_-157+11 others(10): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102789594 | |||||
| chr14:102789594
|
A | ATGTGTG | 3 | a0002c0002t0001g0280a0002c0002t0001g0281a0002c0002t0001g0282 | 3 | HG01261.hp2 HG02602.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-157+11944_-157+11 others(12): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102789594 | |||||
| chr14:102789594
|
A | G | 1 | a0002c0002t0001g0283 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-157+11919A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102789594 | ||||||
| chr14:102789594
|
ATG | A | 152 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(149): Show | 152 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.-157+11948_-157+11 others(8): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102789594 | |||||
| chr14:102789603
|
T | C | 1 | a0001c0001t0045g0047 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-157+11928T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102789603 | ||||||
| chr14:102789639
|
A | G | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-157+11964A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102789639 | ||||||
| chr14:102789742
|
C | T | 1 | a0001c0001t0011g0165 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-157+12067C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102789742 | ||||||
| chr14:102789768
|
G | T | 1 | a0001c0001t0033g0123 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-157+12093G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102789768 | ||||||
| chr14:102789777
|
ATGTT | A | 7 | a0001c0001t0008g0030a0001c0001t0008g0037a0001c0001t0008g0038others(4): Show | 7 | HG01175.hp2 HG02109.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-157+12107_-157+12 others(10): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102789777 | |||||
| chr14:102789834
|
T | C | 2 | a0001c0001t0016g0104a0001c0001t0016g0105 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-157+12159T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102789834 | ||||||
| chr14:102789862
|
C | G | 101 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(98): Show | 101 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.-157+12187C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102789862 | ||||||
| chr14:102789942
|
C | G | 4 | a0001c0003t0003g0182a0001c0003t0005g0181a0001c0003t0034g0003others(1): Show | 4 | HG02630.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-157+12267C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102789942 | ||||||
| chr14:102790113
|
C | T | 1 | a0001c0001t0002g0044 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-157+12438C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102790113 | ||||||
| chr14:102790228
|
G | A | 1 | a0001c0001t0007g0094 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-157+12553G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102790228 | ||||||
| chr14:102790291
|
C | T | 1 | a0002c0002t0001g0246 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-157+12616C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102790291 | ||||||
| chr14:102790540
|
G | A | 123 | a0001c0001t0001g0184a0001c0001t0013g0262a0001c0001t0013g0263others(120): Show | 123 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.-157+12865G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102790540 | ||||||
| chr14:102790624
|
A | G | 101 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(98): Show | 101 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.-157+12949A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102790624 | ||||||
| chr14:102790941
|
A | G | 1 | a0001c0001t0012g0168 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-157+13266A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102790941 | ||||||
| chr14:102790970
|
T | C | 2 | a0001c0001t0012g0098a0001c0001t0012g0124 | 2 | HG01109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-157+13295T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102790970 | ||||||
| chr14:102791074
|
T | C | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-157+13399T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102791074 | ||||||
| chr14:102791104
|
C | T | 5 | a0001c0001t0005g0137a0001c0001t0015g0139a0001c0001t0015g0140others(2): Show | 5 | HG02055.hp1 HG02257.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-157+13429C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102791104 | ||||||
| chr14:102791105
|
C | T | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-157+13430C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102791105 | ||||||
| chr14:102791166
|
C | T | 3 | a0001c0001t0033g0123a0001c0001t0067g0125a0001c0001t0068g0029 | 3 | HG00733.hp2 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-157+13491C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102791166 | ||||||
| chr14:102791787
|
G | A | 1 | a0001c0001t0002g0106 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-157+14112G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102791787 | ||||||
| chr14:102791813
|
C | CT | 104 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(101): Show | 104 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.-157+14149dupT | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102791813 | |||||
| chr14:102791903
|
C | A | 3 | a0001c0001t0012g0001a0001c0001t0012g0179a0001c0001t0050g0180 | 3 | HG01884.hp2 HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-157+14228C>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102791903 | ||||||
| chr14:102792090
|
A | G | 1 | a0002c0002t0006g0161 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-157+14415A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102792090 | ||||||
| chr14:102792109
|
T | C | 264 | a0001c0001t0001g0184a0001c0001t0002g0025a0001c0001t0002g0026others(261): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.-157+14434T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102792109 | ||||||
| chr14:102792113
|
C | CT | 193 | a0001c0001t0002g0025a0001c0001t0002g0027a0001c0001t0002g0036others(190): Show | 193 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.-157+14465dupT | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102792113 | |||||
| chr14:102792113
|
C | CTT | 32 | a0001c0001t0002g0026a0001c0001t0002g0083a0001c0001t0002g0084others(29): Show | 32 | HG00140.hp2 HG00558.hp2 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.-157+14464_-157+14 others(8): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102792113 | |||||
| chr14:102792113
|
C | CTTT | 6 | a0001c0001t0008g0064a0001c0001t0044g0089a0001c0001t0051g0284others(3): Show | 6 | HG00735.hp1 HG01175.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.-157+14463_-157+14 others(9): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102792113 | |||||
| chr14:102792113
|
CT | C | 8 | a0001c0001t0012g0098a0001c0001t0020g0054a0001c0001t0022g0050others(5): Show | 8 | HG01099.hp2 HG01109.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.-157+14465delT | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102792113 | |||||
| chr14:102792223
|
C | G | 5 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(2): Show | 5 | HG00738.hp2 HG01167.hp2 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.-157+14548C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102792223 | ||||||
| chr14:102792238
|
C | T | 5 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(2): Show | 5 | HG00738.hp2 HG01167.hp2 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.-157+14563C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102792238 | ||||||
| chr14:102792267
|
A | G | 1 | a0001c0001t0062g0247 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-157+14592A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102792267 | ||||||
| chr14:102792366
|
G | C | 3 | a0002c0002t0001g0215a0002c0002t0009g0197a0002c0002t0009g0216 | 3 | HG01175.hp1 HG01257.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.-157+14691G>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102792366 | ||||||
| chr14:102792432
|
A | AT | 15 | a0001c0001t0002g0086a0001c0001t0004g0007a0001c0001t0004g0048others(12): Show | 15 | HG00733.hp2 HG02109.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.-157+14779dupT | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102792432 | |||||
| chr14:102792432
|
AT | A | 138 | a0001c0001t0001g0184a0001c0001t0002g0036a0001c0001t0002g0066others(135): Show | 138 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(135): Show |
intron_variant | MODIFIER | c.-157+14779delT | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102792432 | |||||
| chr14:102792432
|
ATT | A | 12 | a0001c0003t0003g0182a0001c0003t0005g0181a0001c0003t0034g0003others(9): Show | 12 | HG00099.hp1 HG02630.hp2 HG02976.hp1 others(9): Show |
intron_variant | MODIFIER | c.-157+14778_-157+14 others(8): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102792432 | |||||
| chr14:102792450
|
T | C | 121 | a0001c0001t0001g0184a0001c0001t0011g0127a0001c0001t0013g0262others(118): Show | 121 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.-157+14775T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102792450 | ||||||
| chr14:102792569
|
G | A | 1 | a0002c0002t0058g0192 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-157+14894G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102792569 | ||||||
| chr14:102792655
|
A | G | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-157+14980A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102792655 | ||||||
| chr14:102792753
|
C | A | 1 | a0001c0001t0008g0062 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-157+15078C>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102792753 | ||||||
| chr14:102792866
|
A | G | 8 | a0001c0001t0010g0053a0001c0001t0012g0098a0001c0001t0012g0124others(5): Show | 8 | HG00639.hp2 HG01109.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.-157+15191A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102792866 | ||||||
| chr14:102792954
|
C | T | 1 | a0001c0001t0041g0051 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-157+15279C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102792954 | ||||||
| chr14:102793010
|
A | T | 17 | a0001c0001t0005g0009a0001c0001t0005g0010a0001c0001t0005g0011others(14): Show | 17 | HG02055.hp2 HG02258.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.-157+15335A>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102793010 | ||||||
| chr14:102793448
|
C | T | 3 | a0001c0001t0033g0123a0001c0001t0067g0125a0001c0001t0068g0029 | 3 | HG00733.hp2 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-157+15773C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102793448 | ||||||
| chr14:102793481
|
G | A | 1 | a0001c0001t0041g0051 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-157+15806G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102793481 | ||||||
| chr14:102793622
|
A | G | 1 | a0002c0002t0001g0277 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-157+15947A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102793622 | ||||||
| chr14:102793638
|
T | C | 1 | a0002c0002t0003g0153 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-157+15963T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102793638 | ||||||
| chr14:102793652
|
T | G | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-157+15977T>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102793652 | ||||||
| chr14:102793706
|
T | C | 3 | a0001c0001t0033g0123a0001c0001t0067g0125a0001c0001t0068g0029 | 3 | HG00733.hp2 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-157+16031T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102793706 | ||||||
| chr14:102793728
|
C | G | 1 | a0001c0001t0003g0100 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-157+16053C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102793728 | ||||||
| chr14:102793895
|
G | C | 4 | a0001c0003t0003g0182a0001c0003t0005g0181a0001c0003t0034g0003others(1): Show | 4 | HG02630.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-157+16220G>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102793895 | ||||||
| chr14:102794161
|
GTC | G | 120 | a0001c0001t0001g0184a0001c0001t0013g0262a0001c0001t0013g0263others(117): Show | 120 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.-157+16498_-157+16 others(8): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102794161 | |||||
| chr14:102794161
|
GTCTC | G | 3 | a0001c0001t0022g0296a0001c0001t0031g0183a0001c0001t0042g0005 | 3 | HG01099.hp2 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-157+16496_-157+16 others(10): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102794161 | |||||
| chr14:102794263
|
C | T | 1 | a0001c0001t0064g0198 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-157+16588C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102794263 | ||||||
| chr14:102794430
|
A | G | 1 | a0001c0001t0012g0124 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-157+16755A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102794430 | ||||||
| chr14:102794662
|
A | G | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-157+16987A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102794662 | ||||||
| chr14:102794663
|
G | C | 1 | a0001c0001t0002g0025 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-157+16988G>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102794663 | ||||||
| chr14:102794688
|
A | G | 1 | a0001c0001t0002g0115 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-157+17013A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102794688 | ||||||
| chr14:102794738
|
C | G | 2 | a0001c0001t0011g0165a0001c0001t0036g0146 | 2 | HG03017.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.-157+17063C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102794738 | ||||||
| chr14:102794787
|
A | G | 1 | a0001c0001t0007g0045 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-157+17112A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102794787 | ||||||
| chr14:102794945
|
T | A | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-157+17270T>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102794945 | ||||||
| chr14:102794963
|
T | C | 120 | a0001c0001t0001g0184a0001c0001t0013g0262a0001c0001t0013g0263others(117): Show | 120 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.-157+17288T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102794963 | ||||||
| chr14:102795398
|
A | G | 121 | a0001c0001t0001g0184a0001c0001t0011g0127a0001c0001t0013g0262others(118): Show | 121 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.-157+17723A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102795398 | ||||||
| chr14:102795584
|
CATG | C | 4 | a0001c0003t0003g0182a0001c0003t0005g0181a0001c0003t0034g0003others(1): Show | 4 | HG02630.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-157+17912_-157+17 others(9): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102795584 | |||||
| chr14:102795586
|
T | TATG | 117 | a0001c0001t0001g0184a0001c0001t0013g0262a0001c0001t0013g0263others(114): Show | 117 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.-157+17911_-157+17 others(9): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102795586 | ||||||
| chr14:102795587
|
G | T | 118 | a0001c0001t0001g0184a0001c0001t0013g0262a0001c0001t0013g0263others(115): Show | 118 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.-157+17912G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102795587 | ||||||
| chr14:102795588
|
A | G | 1 | a0002c0002t0054g0194 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-157+17913A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102795588 | ||||||
| chr14:102795590
|
A | ATGTG | 18 | a0001c0001t0018g0186a0001c0001t0018g0250a0001c0001t0027g0288others(15): Show | 18 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.-157+17918_-157+17 others(10): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102795590 | |||||
| chr14:102795590
|
A | ATGTGTG | 83 | a0001c0001t0001g0184a0001c0001t0013g0262a0001c0001t0013g0263others(80): Show | 83 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.-157+17918_-157+17 others(12): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102795590 | |||||
| chr14:102795590
|
A | ATGTGTGT others(1): Show |
16 | a0002c0002t0001g0195a0002c0002t0001g0196a0002c0002t0001g0201others(13): Show | 16 | HG00673.hp2 HG01071.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.-157+17918_-157+17 others(14): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102795590 | |||||
| chr14:102795590
|
A | G | 3 | a0001c0001t0013g0293a0001c0001t0013g0294a0002c0002t0054g0194 | 3 | HG02615.hp2 NA18986.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-157+17915A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102795590 | ||||||
| chr14:102795592
|
G | A | 2 | a0001c0001t0013g0293a0001c0001t0013g0294 | 2 | HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-157+17917G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102795592 | ||||||
| chr14:102795594
|
A | G | 119 | a0001c0001t0001g0184a0001c0001t0007g0163a0001c0001t0013g0262others(116): Show | 119 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.-157+17919A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102795594 | ||||||
| chr14:102795596
|
A | ATGTGTGT others(1): Show |
13 | a0001c0001t0005g0009a0001c0001t0005g0010a0001c0001t0005g0011others(10): Show | 13 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.-157+17922_-157+17 others(14): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102795596 | |||||
| chr14:102795596
|
A | ATGTGTGT others(3): Show |
4 | a0001c0001t0003g0100a0001c0001t0010g0053a0001c0001t0020g0054others(1): Show | 4 | HG00639.hp2 HG01993.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-157+17922_-157+17 others(16): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102795596 | |||||
| chr14:102795596
|
A | ATGTGTGT others(5): Show |
2 | a0001c0001t0035g0012a0001c0001t0038g0015 | 2 | HG02451.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-157+17922_-157+17 others(18): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102795596 | |||||
| chr14:102795596
|
A | G | 120 | a0001c0001t0001g0184a0001c0001t0013g0262a0001c0001t0013g0263others(117): Show | 120 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.-157+17921A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102795596 | ||||||
| chr14:102795598
|
A | ATGTGTGT others(3): Show |
86 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(83): Show | 86 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.-157+17936_-157+17 others(16): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102795598 | |||||
| chr14:102795598
|
A | ATGTGTGT others(5): Show |
20 | a0001c0001t0002g0083a0001c0001t0002g0084a0001c0001t0002g0086others(17): Show | 20 | HG00733.hp2 HG01496.hp1 HG01516.hp2 others(17): Show |
intron_variant | MODIFIER | c.-157+17934_-157+17 others(18): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102795598 | |||||
| chr14:102795598
|
A | ATGTGTGT others(7): Show |
6 | a0001c0001t0003g0085a0001c0001t0012g0168a0001c0001t0017g0143others(3): Show | 6 | HG00140.hp2 HG02109.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-157+17932_-157+17 others(20): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102795598 | |||||
| chr14:102795598
|
A | ATGTGTGT others(9): Show |
8 | a0001c0001t0002g0056a0001c0001t0011g0127a0001c0001t0011g0166others(5): Show | 8 | HG01123.hp1 HG02559.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.-157+17930_-157+17 others(22): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102795598 | |||||
| chr14:102795598
|
A | ATGTGTGT others(11): Show |
12 | a0001c0001t0011g0150a0001c0001t0011g0165a0001c0001t0036g0146others(9): Show | 12 | HG00544.hp1 HG00639.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.-157+17928_-157+17 others(24): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102795598 | |||||
| chr14:102795598
|
A | ATGTGTGT others(13): Show |
3 | a0002c0002t0003g0152a0002c0002t0003g0167a0002c0002t0006g0162 | 3 | HG02273.hp1 HG02683.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.-157+17926_-157+17 others(26): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102795598 | |||||
| chr14:102795598
|
A | G | 153 | a0001c0001t0001g0184a0001c0001t0003g0100a0001c0001t0005g0009others(150): Show | 153 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.-157+17923A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102795598 | ||||||
| chr14:102795613
|
T | TGTGTGTG others(4): Show |
1 | a0001c0001t0029g0068 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-157+17945_-157+17 others(17): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102795613 | |||||
| chr14:102795616
|
G | GTGTGTGT others(5): Show |
7 | a0001c0001t0010g0018a0001c0001t0010g0019a0001c0001t0010g0020others(4): Show | 7 | HG02258.hp1 HG02965.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.-157+17945_-157+17 others(18): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102795616 | |||||
| chr14:102795619
|
T | C | 4 | a0001c0003t0003g0182a0001c0003t0005g0181a0001c0003t0034g0003others(1): Show | 4 | HG02630.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-157+17944T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102795619 | ||||||
| chr14:102795938
|
C | T | 8 | a0001c0001t0010g0053a0001c0001t0012g0098a0001c0001t0012g0124others(5): Show | 8 | HG00639.hp2 HG01109.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.-157+18263C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102795938 | ||||||
| chr14:102796109
|
T | C | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-157+18434T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102796109 | ||||||
| chr14:102796169
|
T | G | 1 | a0001c0001t0007g0163 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-157+18494T>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102796169 | ||||||
| chr14:102796502
|
G | A | 1 | a0002c0002t0003g0152 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-157+18827G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102796502 | ||||||
| chr14:102796610
|
G | A | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-157+18935G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102796610 | ||||||
| chr14:102796683
|
G | A | 120 | a0001c0001t0001g0184a0001c0001t0013g0262a0001c0001t0013g0263others(117): Show | 120 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.-157+19008G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102796683 | ||||||
| chr14:102796686
|
A | G | 9 | a0001c0001t0003g0100a0001c0001t0010g0053a0001c0001t0012g0098others(6): Show | 9 | HG00639.hp2 HG01109.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.-157+19011A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102796686 | ||||||
| chr14:102796737
|
C | T | 3 | a0001c0001t0016g0103a0001c0001t0016g0104a0001c0001t0016g0105 | 3 | HG00323.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-157+19062C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102796737 | ||||||
| chr14:102796787
|
C | T | 1 | a0001c0001t0012g0168 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-157+19112C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102796787 | ||||||
| chr14:102796823
|
G | T | 1 | a0001c0001t0026g0078 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-157+19148G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102796823 | ||||||
| chr14:102797124
|
T | C | 18 | a0001c0001t0002g0027a0001c0001t0007g0045a0001c0001t0007g0094others(15): Show | 18 | HG01081.hp2 HG01175.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-157+19449T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102797124 | ||||||
| chr14:102797152
|
C | G | 100 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(97): Show | 100 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.-157+19477C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102797152 | ||||||
| chr14:102797223
|
T | A | 2 | a0002c0002t0001g0188a0002c0002t0001g0189 | 2 | NA18944.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.-157+19548T>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102797223 | ||||||
| chr14:102797380
|
G | A | 1 | a0001c0001t0042g0005 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-157+19705G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102797380 | ||||||
| chr14:102797451
|
A | G | 121 | a0001c0001t0001g0184a0001c0001t0011g0127a0001c0001t0013g0262others(118): Show | 121 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.-157+19776A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102797451 | ||||||
| chr14:102797469
|
A | AGAG | 3 | a0001c0001t0001g0184a0002c0002t0001g0240a0002c0002t0001g0241 | 3 | NA18943.hp1 NA18948.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.-157+19810_-157+19 others(9): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102797469 | |||||
| chr14:102797495
|
C | T | 1 | a0001c0001t0003g0100 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-157+19820C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102797495 | ||||||
| chr14:102797672
|
T | C | 264 | a0001c0001t0001g0184a0001c0001t0002g0025a0001c0001t0002g0026others(261): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.-157+19997T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102797672 | ||||||
| chr14:102797739
|
C | CT | 96 | a0001c0001t0001g0184a0001c0001t0005g0009a0001c0001t0005g0010others(93): Show | 96 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.-157+20078dupT | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102797739 | |||||
| chr14:102797836
|
C | G | 1 | a0001c0001t0040g0149 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-157+20161C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102797836 | ||||||
| chr14:102797873
|
G | A | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-157+20198G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102797873 | ||||||
| chr14:102797886
|
C | T | 1 | a0002c0002t0001g0283 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-157+20211C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102797886 | ||||||
| chr14:102797986
|
C | T | 99 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(96): Show | 99 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.-157+20311C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102797986 | ||||||
| chr14:102798200
|
C | G | 1 | a0002c0002t0001g0253 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-157+20525C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102798200 | ||||||
| chr14:102798225
|
C | G | 1 | a0002c0006t0001g0204 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-157+20550C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102798225 | ||||||
| chr14:102798253
|
G | A | 3 | a0001c0001t0033g0123a0001c0001t0067g0125a0001c0001t0068g0029 | 3 | HG00733.hp2 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-157+20578G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102798253 | ||||||
| chr14:102798285
|
G | A | 8 | a0001c0001t0007g0045a0001c0001t0007g0094a0001c0001t0007g0095others(5): Show | 8 | HG01081.hp2 HG02486.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.-157+20610G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102798285 | ||||||
| chr14:102798306
|
C | T | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-157+20631C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102798306 | ||||||
| chr14:102798372
|
G | A | 1 | a0001c0001t0019g0082 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-157+20697G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102798372 | ||||||
| chr14:102798628
|
A | G | 1 | a0002c0002t0001g0292 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-157+20953A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102798628 | ||||||
| chr14:102798637
|
C | G | 3 | a0001c0001t0033g0123a0001c0001t0067g0125a0001c0001t0068g0029 | 3 | HG00733.hp2 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-157+20962C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102798637 | ||||||
| chr14:102798649
|
A | T | 4 | a0001c0001t0010g0053a0001c0001t0012g0098a0001c0001t0012g0124others(1): Show | 4 | HG00639.hp2 HG01109.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.-157+20974A>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102798649 | ||||||
| chr14:102798650
|
T | A | 1 | a0001c0001t0012g0024 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-157+20975T>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102798650 | ||||||
| chr14:102798705
|
G | C | 4 | a0001c0003t0003g0182a0001c0003t0005g0181a0001c0003t0034g0003others(1): Show | 4 | HG02630.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-157+21030G>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102798705 | ||||||
| chr14:102798904
|
G | A | 1 | a0002c0002t0006g0161 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-157+21229G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102798904 | ||||||
| chr14:102798926
|
A | G | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-157+21251A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102798926 | ||||||
| chr14:102799029
|
T | C | 121 | a0001c0001t0001g0184a0001c0001t0011g0127a0001c0001t0013g0262others(118): Show | 121 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.-157+21354T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102799029 | ||||||
| chr14:102799169
|
T | C | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-157+21494T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102799169 | ||||||
| chr14:102799177
|
A | G | 1 | a0001c0001t0004g0171 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-157+21502A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102799177 | ||||||
| chr14:102799329
|
G | A | 75 | a0001c0001t0001g0184a0001c0001t0062g0247a0001c0001t0063g0223others(72): Show | 75 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.-157+21654G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102799329 | ||||||
| chr14:102799496
|
G | T | 1 | a0001c0001t0004g0171 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-157+21821G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102799496 | ||||||
| chr14:102799499
|
G | T | 1 | a0001c0001t0008g0030 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-157+21824G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102799499 | ||||||
| chr14:102799507
|
A | G | 120 | a0001c0001t0001g0184a0001c0001t0013g0262a0001c0001t0013g0263others(117): Show | 120 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.-157+21832A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102799507 | ||||||
| chr14:102799509
|
G | T | 1 | a0001c0001t0004g0171 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-157+21834G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102799509 | ||||||
| chr14:102799530
|
A | T | 100 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(97): Show | 100 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.-157+21855A>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102799530 | ||||||
| chr14:102799549
|
C | T | 2 | a0001c0001t0021g0057a0001c0001t0021g0099 | 2 | HG01123.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.-157+21874C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102799549 | ||||||
| chr14:102799740
|
C | T | 100 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(97): Show | 100 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.-157+22065C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102799740 | ||||||
| chr14:102800024
|
G | A | 1 | a0001c0001t0011g0147 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-157+22349G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102800024 | ||||||
| chr14:102800045
|
G | A | 140 | a0001c0001t0001g0184a0001c0001t0003g0100a0001c0001t0010g0053others(137): Show | 140 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.-157+22370G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102800045 | ||||||
| chr14:102800100
|
T | C | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-157+22425T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102800100 | ||||||
| chr14:102800372
|
G | A | 2 | a0001c0001t0035g0012a0001c0001t0038g0015 | 2 | HG02451.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-157+22697G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102800372 | ||||||
| chr14:102800465
|
C | T | 1 | a0001c0001t0004g0173 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-157+22790C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102800465 | ||||||
| chr14:102800610
|
G | T | 1 | a0001c0001t0022g0296 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-157+22935G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102800610 | ||||||
| chr14:102800695
|
CT | C | 10 | a0001c0001t0002g0032a0001c0001t0002g0036a0001c0001t0002g0056others(7): Show | 10 | HG00323.hp2 HG01517.hp1 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.-157+23040delT | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102800695 | |||||
| chr14:102800745
|
A | G | 17 | a0001c0001t0005g0009a0001c0001t0005g0010a0001c0001t0005g0011others(14): Show | 17 | HG02055.hp2 HG02258.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.-157+23070A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102800745 | ||||||
| chr14:102800826
|
G | A | 1 | a0001c0001t0051g0284 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-157+23151G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102800826 | ||||||
| chr14:102800848
|
G | A | 1 | a0001c0001t0024g0069 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-157+23173G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102800848 | ||||||
| chr14:102801058
|
C | T | 1 | a0001c0001t0007g0045 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-157+23383C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102801058 | ||||||
| chr14:102801066
|
T | C | 120 | a0001c0001t0001g0184a0001c0001t0013g0262a0001c0001t0013g0263others(117): Show | 120 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.-157+23391T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102801066 | ||||||
| chr14:102801121
|
G | A | 3 | a0001c0001t0012g0001a0001c0001t0012g0179a0001c0001t0050g0180 | 3 | HG01884.hp2 HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-157+23446G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102801121 | ||||||
| chr14:102801123
|
G | A | 2 | a0001c0001t0012g0001a0001c0001t0012g0179 | 2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-157+23448G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102801123 | ||||||
| chr14:102801127
|
C | T | 1 | a0001c0001t0002g0056 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-157+23452C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102801127 | ||||||
| chr14:102801145
|
G | T | 1 | a0002c0002t0001g0208 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-157+23470G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102801145 | ||||||
| chr14:102801163
|
G | C | 125 | a0001c0001t0001g0184a0001c0001t0013g0262a0001c0001t0013g0263others(122): Show | 125 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.-157+23488G>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102801163 | ||||||
| chr14:102801235
|
A | G | 5 | a0001c0001t0005g0137a0001c0001t0015g0139a0001c0001t0015g0140others(2): Show | 5 | HG02055.hp1 HG02257.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-157+23560A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102801235 | ||||||
| chr14:102801446
|
C | G | 5 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(2): Show | 5 | HG00738.hp2 HG01167.hp2 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.-157+23771C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102801446 | ||||||
| chr14:102801485
|
T | C | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-157+23810T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102801485 | ||||||
| chr14:102801633
|
C | G | 1 | a0001c0001t0019g0055 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-157+23958C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102801633 | ||||||
| chr14:102801771
|
C | T | 1 | a0002c0002t0001g0277 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-157+24096C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102801771 | ||||||
| chr14:102801772
|
G | A | 1 | a0001c0001t0041g0051 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-157+24097G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102801772 | ||||||
| chr14:102801868
|
T | A | 1 | a0001c0001t0003g0100 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-157+24193T>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102801868 | ||||||
| chr14:102801889
|
G | A | 1 | a0001c0001t0002g0027 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-157+24214G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102801889 | ||||||
| chr14:102801908
|
C | T | 1 | a0001c0001t0012g0168 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-157+24233C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102801908 | ||||||
| chr14:102802011
|
A | G | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-157+24336A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102802011 | ||||||
| chr14:102802015
|
C | CA | 100 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(97): Show | 100 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.-157+24355dupA | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102802015 | |||||
| chr14:102802015
|
CA | C | 8 | a0002c0002t0001g0236a0002c0002t0001g0237a0002c0002t0001g0238others(5): Show | 8 | HG00735.hp2 HG01069.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.-157+24355delA | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102802015 | |||||
| chr14:102802048
|
G | A | 124 | a0001c0001t0001g0184a0001c0001t0013g0262a0001c0001t0013g0263others(121): Show | 124 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.-157+24373G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102802048 | ||||||
| chr14:102802074
|
G | T | 120 | a0001c0001t0001g0184a0001c0001t0013g0262a0001c0001t0013g0263others(117): Show | 120 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.-157+24399G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102802074 | ||||||
| chr14:102802093
|
C | T | 1 | a0002c0002t0001g0277 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-157+24418C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102802093 | ||||||
| chr14:102802154
|
A | AT | 9 | a0001c0001t0007g0094a0001c0001t0007g0163a0001c0001t0021g0099others(6): Show | 9 | HG00609.hp1 HG01993.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.-157+24497dupT | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102802154 | |||||
| chr14:102802154
|
AT | A | 123 | a0001c0001t0001g0184a0001c0001t0002g0079a0001c0001t0013g0262others(120): Show | 123 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.-157+24497delT | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102802154 | |||||
| chr14:102802177
|
T | C | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-157+24502T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102802177 | ||||||
| chr14:102802194
|
G | A | 10 | a0001c0001t0002g0025a0001c0001t0002g0059a0001c0001t0002g0060others(7): Show | 10 | HG00544.hp2 HG00673.hp1 HG01993.hp2 others(7): Show |
intron_variant | MODIFIER | c.-157+24519G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102802194 | ||||||
| chr14:102802324
|
T | C | 1 | a0002c0002t0052g0242 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-157+24649T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102802324 | ||||||
| chr14:102802330
|
A | AT | 263 | a0001c0001t0001g0184a0001c0001t0002g0025a0001c0001t0002g0026others(260): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.-157+24660dupT | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102802330 | |||||
| chr14:102802430
|
A | T | 1 | a0001c0001t0022g0296 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-157+24755A>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102802430 | ||||||
| chr14:102802446
|
G | A | 1 | a0001c0001t0026g0073 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-157+24771G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102802446 | ||||||
| chr14:102802518
|
A | T | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-157+24843A>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102802518 | ||||||
| chr14:102802525
|
G | A | 3 | a0001c0001t0012g0001a0001c0001t0012g0179a0001c0001t0050g0180 | 3 | HG01884.hp2 HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-157+24850G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102802525 | ||||||
| chr14:102802608
|
C | T | 3 | a0002c0002t0003g0131a0002c0002t0003g0132a0002c0002t0003g0133 | 3 | HG01069.hp2 HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-157+24933C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102802608 | ||||||
| chr14:102802777
|
G | A | 4 | a0001c0003t0003g0182a0001c0003t0005g0181a0001c0003t0034g0003others(1): Show | 4 | HG02630.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-157+25102G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102802777 | ||||||
| chr14:102802844
|
C | G | 5 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(2): Show | 5 | HG00738.hp2 HG01167.hp2 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.-157+25169C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102802844 | ||||||
| chr14:102802914
|
G | A | 1 | a0002c0002t0003g0160 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-157+25239G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102802914 | ||||||
| chr14:102802930
|
A | G | 1 | a0001c0001t0031g0183 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-157+25255A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102802930 | ||||||
| chr14:102803012
|
T | A | 2 | a0001c0001t0021g0057a0001c0001t0021g0099 | 2 | HG01123.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.-157+25337T>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102803012 | ||||||
| chr14:102803326
|
T | A | 1 | a0001c0001t0004g0171 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-157+25651T>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102803326 | ||||||
| chr14:102803326
|
T | C | 6 | a0001c0001t0002g0058a0001c0001t0002g0067a0001c0001t0002g0074others(3): Show | 6 | HG01192.hp2 HG01358.hp1 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.-157+25651T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102803326 | ||||||
| chr14:102803418
|
C | A | 120 | a0001c0001t0001g0184a0001c0001t0013g0262a0001c0001t0013g0263others(117): Show | 120 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.-157+25743C>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102803418 | ||||||
| chr14:102803541
|
G | A | 1 | a0001c0001t0062g0247 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-157+25866G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102803541 | ||||||
| chr14:102803560
|
G | A | 1 | a0001c0001t0003g0100 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-157+25885G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102803560 | ||||||
| chr14:102803576
|
A | AT | 6 | a0001c0001t0023g0043a0001c0003t0003g0182a0001c0003t0005g0181others(3): Show | 6 | HG00609.hp1 HG01243.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.-157+25917dupT | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102803576 | |||||
| chr14:102803576
|
A | T | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-157+25901A>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102803576 | ||||||
| chr14:102803577
|
T | A | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-157+25902T>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102803577 | ||||||
| chr14:102803579
|
T | A | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-157+25904T>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102803579 | ||||||
| chr14:102803633
|
G | A | 2 | a0001c0001t0002g0172a0001c0001t0004g0174 | 2 | HG01943.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.-157+25958G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102803633 | ||||||
| chr14:102803755
|
T | A | 1 | a0001c0001t0019g0082 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-157+26080T>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102803755 | ||||||
| chr14:102803837
|
G | T | 4 | a0001c0003t0003g0182a0001c0003t0005g0181a0001c0003t0034g0003others(1): Show | 4 | HG02630.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-157+26162G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102803837 | ||||||
| chr14:102803940
|
G | A | 7 | a0001c0001t0005g0009a0001c0001t0005g0010a0001c0001t0005g0011others(4): Show | 7 | HG02055.hp2 HG02809.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-157+26265G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102803940 | ||||||
| chr14:102804463
|
A | G | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-156-25871A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102804463 | ||||||
| chr14:102804563
|
C | T | 2 | a0001c0001t0010g0022a0001c0001t0010g0023 | 2 | HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-156-25771C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102804563 | ||||||
| chr14:102804654
|
T | C | 1 | a0001c0001t0011g0147 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-156-25680T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102804654 | ||||||
| chr14:102804672
|
C | T | 3 | a0001c0001t0012g0001a0001c0001t0012g0179a0001c0001t0050g0180 | 3 | HG01884.hp2 HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-156-25662C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102804672 | ||||||
| chr14:102804729
|
A | G | 1 | a0001c0001t0002g0118 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-156-25605A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102804729 | ||||||
| chr14:102804821
|
T | A | 125 | a0001c0001t0001g0184a0001c0001t0013g0262a0001c0001t0013g0263others(122): Show | 125 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.-156-25513T>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102804821 | ||||||
| chr14:102804876
|
C | T | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-156-25458C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102804876 | ||||||
| chr14:102805090
|
G | C | 1 | a0002c0002t0001g0187 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-156-25244G>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102805090 | ||||||
| chr14:102805154
|
C | G | 8 | a0001c0001t0010g0053a0001c0001t0012g0098a0001c0001t0012g0124others(5): Show | 8 | HG00639.hp2 HG01109.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.-156-25180C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102805154 | ||||||
| chr14:102805204
|
C | G | 267 | a0001c0001t0001g0184a0001c0001t0002g0025a0001c0001t0002g0026others(264): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.-156-25130C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102805204 | ||||||
| chr14:102805218
|
G | A | 1 | a0001c0001t0007g0163 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-156-25116G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102805218 | ||||||
| chr14:102805263
|
G | A | 125 | a0001c0001t0001g0184a0001c0001t0013g0262a0001c0001t0013g0263others(122): Show | 125 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.-156-25071G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102805263 | ||||||
| chr14:102805541
|
C | T | 1 | a0001c0001t0012g0024 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-156-24793C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102805541 | ||||||
| chr14:102805551
|
G | A | 1 | a0001c0001t0002g0106 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-156-24783G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102805551 | ||||||
| chr14:102805581
|
C | T | 1 | a0002c0002t0001g0277 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-156-24753C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102805581 | ||||||
| chr14:102805688
|
G | A | 124 | a0001c0001t0001g0184a0001c0001t0013g0262a0001c0001t0013g0263others(121): Show | 124 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.-156-24646G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102805688 | ||||||
| chr14:102805840
|
G | A | 120 | a0001c0001t0001g0184a0001c0001t0013g0262a0001c0001t0013g0263others(117): Show | 120 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.-156-24494G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102805840 | ||||||
| chr14:102806119
|
G | A | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-156-24215G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102806119 | ||||||
| chr14:102806196
|
G | A | 1 | a0001c0001t0003g0100 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-156-24138G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102806196 | ||||||
| chr14:102806441
|
G | C | 3 | a0001c0001t0022g0296a0001c0001t0031g0183a0001c0001t0042g0005 | 3 | HG01099.hp2 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-156-23893G>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102806441 | ||||||
| chr14:102806467
|
T | C | 1 | a0001c0001t0002g0080 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-156-23867T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102806467 | ||||||
| chr14:102806641
|
A | C | 4 | a0001c0003t0003g0182a0001c0003t0005g0181a0001c0003t0034g0003others(1): Show | 4 | HG02630.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-156-23693A>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102806641 | ||||||
| chr14:102806652
|
C | G | 1 | a0001c0001t0004g0033 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-156-23682C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102806652 | ||||||
| chr14:102806659
|
T | C | 2 | a0001c0001t0002g0101a0001c0001t0002g0102 | 2 | HG00099.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.-156-23675T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102806659 | ||||||
| chr14:102806804
|
C | T | 1 | a0002c0002t0059g0239 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-156-23530C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102806804 | ||||||
| chr14:102806817
|
C | G | 1 | a0002c0002t0001g0256 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-156-23517C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102806817 | ||||||
| chr14:102806862
|
C | T | 1 | a0002c0002t0003g0114 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-156-23472C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102806862 | ||||||
| chr14:102806994
|
A | G | 1 | a0001c0001t0050g0180 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-156-23340A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102806994 | ||||||
| chr14:102807108
|
TTTTCTCC others(5): Show |
T | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-156-23217_-156-23 others(18): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102807108 | |||||
| chr14:102807118
|
G | A | 118 | a0001c0001t0001g0184a0001c0001t0013g0262a0001c0001t0013g0263others(115): Show | 118 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.-156-23216G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102807118 | ||||||
| chr14:102807131
|
C | A | 2 | a0001c0001t0021g0057a0001c0001t0021g0099 | 2 | HG01123.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.-156-23203C>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102807131 | ||||||
| chr14:102807339
|
C | T | 1 | a0001c0001t0051g0284 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-156-22995C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102807339 | ||||||
| chr14:102807478
|
A | G | 3 | a0002c0002t0003g0128a0002c0002t0003g0134a0002c0002t0049g0129 | 3 | HG01099.hp1 HG02698.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-156-22856A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102807478 | ||||||
| chr14:102807506
|
C | T | 1 | a0001c0001t0002g0074 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-156-22828C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102807506 | ||||||
| chr14:102807507
|
G | A | 4 | a0001c0001t0017g0143a0001c0001t0017g0144a0001c0001t0017g0145others(1): Show | 4 | HG02109.hp2 HG02922.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-156-22827G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102807507 | ||||||
| chr14:102807623
|
C | A | 1 | a0001c0003t0034g0003 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-156-22711C>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102807623 | ||||||
| chr14:102807626
|
C | T | 1 | a0002c0002t0001g0283 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-156-22708C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102807626 | ||||||
| chr14:102807821
|
G | A | 1 | a0001c0001t0041g0051 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-156-22513G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102807821 | ||||||
| chr14:102808152
|
G | A | 1 | a0001c0001t0019g0055 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-156-22182G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102808152 | ||||||
| chr14:102808210
|
A | G | 120 | a0001c0001t0001g0184a0001c0001t0013g0262a0001c0001t0013g0263others(117): Show | 120 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.-156-22124A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102808210 | ||||||
| chr14:102808428
|
G | C | 3 | a0001c0001t0033g0123a0001c0001t0067g0125a0001c0001t0068g0029 | 3 | HG00733.hp2 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-156-21906G>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102808428 | ||||||
| chr14:102808512
|
CA | C | 257 | a0001c0001t0001g0184a0001c0001t0002g0025a0001c0001t0002g0026others(254): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.-156-21807delA | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102808512 | |||||
| chr14:102808531
|
A | G | 1 | a0001c0001t0002g0066 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-156-21803A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102808531 | ||||||
| chr14:102808639
|
A | G | 1 | a0002c0002t0001g0256 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-156-21695A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102808639 | ||||||
| chr14:102808701
|
A | G | 5 | a0001c0001t0005g0137a0001c0001t0015g0139a0001c0001t0015g0140others(2): Show | 5 | HG02055.hp1 HG02257.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-156-21633A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102808701 | ||||||
| chr14:102808931
|
T | C | 2 | a0001c0001t0031g0183a0001c0001t0042g0005 | 2 | HG01099.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-156-21403T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102808931 | ||||||
| chr14:102808959
|
G | C | 1 | a0001c0001t0002g0026 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-156-21375G>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102808959 | ||||||
| chr14:102808966
|
C | T | 1 | a0001c0001t0044g0089 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-156-21368C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102808966 | ||||||
| chr14:102809085
|
C | T | 17 | a0001c0001t0005g0009a0001c0001t0005g0010a0001c0001t0005g0011others(14): Show | 17 | HG02055.hp2 HG02258.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.-156-21249C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102809085 | ||||||
| chr14:102809285
|
C | T | 1 | a0001c0001t0005g0014 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-156-21049C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102809285 | ||||||
| chr14:102809291
|
C | T | 1 | a0002c0002t0001g0207 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-156-21043C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102809291 | ||||||
| chr14:102809413
|
A | C | 1 | a0001c0001t0003g0100 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-156-20921A>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102809413 | ||||||
| chr14:102809529
|
C | CT | 7 | a0001c0001t0007g0163a0001c0001t0012g0168a0002c0002t0001g0200others(4): Show | 7 | HG02155.hp2 HG03130.hp2 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.-156-20784dupT | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102809529 | |||||
| chr14:102809529
|
CT | C | 102 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(99): Show | 102 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.-156-20784delT | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102809529 | |||||
| chr14:102809529
|
CTT | C | 33 | a0001c0001t0002g0107a0001c0001t0005g0009a0001c0001t0005g0010others(30): Show | 33 | HG00639.hp2 HG01109.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.-156-20785_-156-20 others(8): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102809529 | |||||
| chr14:102809572
|
G | T | 1 | a0002c0002t0001g0283 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-156-20762G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102809572 | ||||||
| chr14:102809593
|
C | T | 1 | a0001c0001t0003g0100 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-156-20741C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102809593 | ||||||
| chr14:102809633
|
T | C | 125 | a0001c0001t0001g0184a0001c0001t0013g0262a0001c0001t0013g0263others(122): Show | 125 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.-156-20701T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102809633 | ||||||
| chr14:102809766
|
G | A | 2 | a0001c0001t0016g0104a0001c0001t0016g0105 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-156-20568G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102809766 | ||||||
| chr14:102809821
|
C | G | 1 | a0001c0001t0002g0120 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-156-20513C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102809821 | ||||||
| chr14:102809864
|
A | G | 1 | a0001c0001t0004g0126 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-156-20470A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102809864 | ||||||
| chr14:102809868
|
G | A | 3 | a0001c0001t0033g0123a0001c0001t0067g0125a0001c0001t0068g0029 | 3 | HG00733.hp2 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-156-20466G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102809868 | ||||||
| chr14:102809946
|
A | C | 8 | a0001c0001t0005g0009a0001c0001t0005g0010a0001c0001t0005g0011others(5): Show | 8 | HG02055.hp2 HG02451.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-156-20388A>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102809946 | ||||||
| chr14:102810088
|
A | G | 1 | a0001c0001t0012g0098 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-156-20246A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102810088 | ||||||
| chr14:102810101
|
G | C | 8 | a0001c0001t0010g0053a0001c0001t0012g0098a0001c0001t0012g0124others(5): Show | 8 | HG00639.hp2 HG01109.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.-156-20233G>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102810101 | ||||||
| chr14:102810225
|
G | T | 9 | a0001c0001t0005g0137a0001c0001t0012g0168a0001c0001t0015g0139others(6): Show | 9 | HG02055.hp1 HG02109.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-156-20109G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102810225 | ||||||
| chr14:102810241
|
G | A | 2 | a0001c0001t0021g0057a0001c0001t0021g0099 | 2 | HG01123.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.-156-20093G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102810241 | ||||||
| chr14:102810351
|
T | G | 4 | a0001c0003t0003g0182a0001c0003t0005g0181a0001c0003t0034g0003others(1): Show | 4 | HG02630.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-156-19983T>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102810351 | ||||||
| chr14:102810518
|
A | G | 120 | a0001c0001t0001g0184a0001c0001t0013g0262a0001c0001t0013g0263others(117): Show | 120 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.-156-19816A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102810518 | ||||||
| chr14:102810551
|
C | G | 8 | a0001c0001t0010g0053a0001c0001t0012g0098a0001c0001t0012g0124others(5): Show | 8 | HG00639.hp2 HG01109.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.-156-19783C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102810551 | ||||||
| chr14:102810719
|
C | G | 8 | a0001c0001t0010g0053a0001c0001t0012g0098a0001c0001t0012g0124others(5): Show | 8 | HG00639.hp2 HG01109.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.-156-19615C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102810719 | ||||||
| chr14:102810883
|
C | T | 1 | a0001c0001t0018g0275 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-156-19451C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102810883 | ||||||
| chr14:102810897
|
C | T | 1 | a0002c0002t0001g0206 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-156-19437C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102810897 | ||||||
| chr14:102811059
|
A | G | 2 | a0001c0001t0021g0057a0001c0001t0021g0099 | 2 | HG01123.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.-156-19275A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102811059 | ||||||
| chr14:102811088
|
C | G | 8 | a0001c0001t0010g0053a0001c0001t0012g0098a0001c0001t0012g0124others(5): Show | 8 | HG00639.hp2 HG01109.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.-156-19246C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102811088 | ||||||
| chr14:102811131
|
A | G | 9 | a0001c0001t0005g0137a0001c0001t0012g0168a0001c0001t0015g0139others(6): Show | 9 | HG02055.hp1 HG02109.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-156-19203A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102811131 | ||||||
| chr14:102811298
|
CT | C | 19 | a0001c0001t0005g0009a0001c0001t0005g0010a0001c0001t0005g0011others(16): Show | 19 | HG01993.hp1 HG02055.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.-156-19021delT | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102811298 | |||||
| chr14:102811470
|
C | T | 4 | a0001c0003t0003g0182a0001c0003t0005g0181a0001c0003t0034g0003others(1): Show | 4 | HG02630.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-156-18864C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102811470 | ||||||
| chr14:102811548
|
C | CG | 7 | a0001c0001t0013g0262a0001c0001t0013g0263a0001c0001t0013g0293others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-156-18784dupG | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102811548 | |||||
| chr14:102811550
|
G | GT | 108 | a0001c0001t0002g0025a0001c0001t0002g0027a0001c0001t0002g0059others(105): Show | 108 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.-156-18760dupT | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102811550 | |||||
| chr14:102811550
|
G | GTT | 33 | a0001c0001t0001g0184a0001c0001t0008g0039a0001c0001t0012g0179others(30): Show | 33 | HG00099.hp1 HG01123.hp2 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.-156-18761_-156-18 others(8): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102811550 | |||||
| chr14:102811550
|
GT | G | 34 | a0001c0001t0010g0019a0001c0001t0010g0053a0001c0001t0011g0127others(31): Show | 34 | HG00544.hp1 HG00639.hp1 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.-156-18760delT | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102811550 | |||||
| chr14:102811551
|
T | G | 1 | a0001c0001t0043g0031 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-156-18783T>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102811551 | ||||||
| chr14:102811604
|
G | T | 4 | a0001c0003t0003g0182a0001c0003t0005g0181a0001c0003t0034g0003others(1): Show | 4 | HG02630.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-156-18730G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102811604 | ||||||
| chr14:102811676
|
C | T | 4 | a0001c0003t0003g0182a0001c0003t0005g0181a0001c0003t0034g0003others(1): Show | 4 | HG02630.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-156-18658C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102811676 | ||||||
| chr14:102811677
|
G | A | 120 | a0001c0001t0001g0184a0001c0001t0013g0262a0001c0001t0013g0263others(117): Show | 120 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.-156-18657G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102811677 | ||||||
| chr14:102811728
|
AGT | A | 94 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(91): Show | 94 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.-156-18573_-156-18 others(8): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102811728 | |||||
| chr14:102811728
|
AGTGT | A | 52 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0003g0100others(49): Show | 52 | HG00544.hp1 HG00544.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.-156-18575_-156-18 others(10): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102811728 | |||||
| chr14:102811728
|
AGTGTGT | A | 8 | a0001c0001t0011g0147a0001c0001t0011g0148a0001c0001t0011g0166others(5): Show | 8 | HG01123.hp2 HG01496.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.-156-18577_-156-18 others(12): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102811728 | |||||
| chr14:102811728
|
AGTGTGTG others(1): Show |
A | 118 | a0001c0001t0001g0184a0001c0001t0012g0001a0001c0001t0013g0262others(115): Show | 118 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.-156-18579_-156-18 others(14): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102811728 | |||||
| chr14:102811788
|
C | A | 3 | a0001c0001t0033g0123a0001c0001t0067g0125a0001c0001t0068g0029 | 3 | HG00733.hp2 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-156-18546C>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102811788 | ||||||
| chr14:102811913
|
C | CT | 10 | a0001c0001t0011g0150a0001c0001t0012g0001a0001c0001t0012g0168others(7): Show | 10 | HG01884.hp2 HG02486.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.-156-18391dupT | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102811913 | |||||
| chr14:102811913
|
C | CTTTT | 14 | a0001c0001t0013g0262a0001c0001t0013g0293a0001c0001t0018g0186others(11): Show | 14 | HG00099.hp1 HG00733.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.-156-18394_-156-18 others(10): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102811913 | |||||
| chr14:102811913
|
C | CTTTTT | 54 | a0001c0001t0012g0098a0001c0001t0012g0124a0001c0001t0013g0263others(51): Show | 54 | HG00140.hp1 HG00609.hp2 HG01099.hp1 others(51): Show |
intron_variant | MODIFIER | c.-156-18395_-156-18 others(11): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102811913 | |||||
| chr14:102811913
|
C | CTTTTTT | 35 | a0001c0001t0010g0053a0001c0001t0022g0050a0001c0001t0063g0223others(32): Show | 35 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.-156-18396_-156-18 others(12): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102811913 | |||||
| chr14:102811913
|
C | CTTTTTTT | 18 | a0001c0001t0007g0163a0001c0001t0008g0063a0001c0001t0020g0054others(15): Show | 18 | HG01071.hp1 HG01123.hp2 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.-156-18397_-156-18 others(13): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102811913 | |||||
| chr14:102811913
|
C | CTTTTTTT others(1): Show |
14 | a0001c0001t0002g0041a0001c0001t0002g0056a0001c0001t0002g0110others(11): Show | 14 | HG00609.hp1 HG00735.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.-156-18398_-156-18 others(14): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102811913 | |||||
| chr14:102811913
|
C | CTTTTTTT others(2): Show |
36 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0032others(33): Show | 36 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.-156-18399_-156-18 others(15): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102811913 | |||||
| chr14:102811913
|
C | CTTTTTTT others(3): Show |
23 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0059others(20): Show | 23 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.-156-18400_-156-18 others(16): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102811913 | |||||
| chr14:102811913
|
C | CTTTTTTT others(4): Show |
5 | a0001c0001t0002g0036a0001c0001t0002g0109a0001c0001t0003g0085others(2): Show | 5 | HG00140.hp2 HG02698.hp2 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.-156-18401_-156-18 others(17): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102811913 | |||||
| chr14:102811913
|
C | CTTTTTTT others(5): Show |
5 | a0001c0001t0002g0086a0001c0001t0021g0057a0001c0001t0021g0099others(2): Show | 5 | HG01123.hp1 HG02738.hp1 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.-156-18402_-156-18 others(18): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102811913 | |||||
| chr14:102811913
|
C | CTTTTTTT others(6): Show |
2 | a0001c0001t0016g0103a0001c0001t0051g0284 | 2 | HG00323.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-156-18403_-156-18 others(19): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102811913 | |||||
| chr14:102811913
|
C | CTTTTTTT others(8): Show |
3 | a0001c0001t0002g0076a0001c0001t0002g0115a0001c0001t0008g0046 | 3 | HG01074.hp1 HG03453.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.-156-18405_-156-18 others(21): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102811913 | |||||
| chr14:102811913
|
C | CTTTTTTT others(9): Show |
1 | a0001c0001t0002g0087 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-156-18406_-156-18 others(22): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102811913 | |||||
| chr14:102811913
|
C | CTTTTTTT others(10): Show |
1 | a0001c0001t0002g0072 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-156-18407_-156-18 others(23): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102811913 | |||||
| chr14:102811913
|
C | CTTTTTTT others(12): Show |
1 | a0001c0001t0030g0176 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-156-18409_-156-18 others(25): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102811913 | |||||
| chr14:102811913
|
C | CTTTTTTT others(14): Show |
1 | a0001c0001t0069g0093 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-156-18411_-156-18 others(27): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102811913 | |||||
| chr14:102811913
|
C | CTTTTTTT others(20): Show |
1 | a0001c0001t0024g0069 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-156-18417_-156-18 others(33): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102811913 | |||||
| chr14:102811913
|
CT | C | 6 | a0001c0001t0005g0137a0001c0001t0015g0139a0001c0001t0017g0143others(3): Show | 6 | HG01099.hp2 HG02055.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.-156-18391delT | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102811913 | |||||
| chr14:102811913
|
CTTTTT | C | 16 | a0001c0001t0005g0009a0001c0001t0005g0010a0001c0001t0005g0011others(13): Show | 16 | HG02258.hp1 HG02451.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.-156-18395_-156-18 others(11): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102811913 | |||||
| chr14:102811913
|
CTTTTTTT | C | 6 | a0001c0001t0007g0094a0001c0001t0007g0095a0001c0001t0007g0096others(3): Show | 6 | HG01081.hp2 HG02486.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-156-18397_-156-18 others(13): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102811913 | |||||
| chr14:102811913
|
CTTTTTTT others(4): Show |
C | 4 | a0001c0003t0003g0182a0001c0003t0005g0181a0001c0003t0034g0003others(1): Show | 4 | HG02630.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-156-18401_-156-18 others(17): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102811913 | |||||
| chr14:102811913
|
CTTTTTTT others(6): Show |
C | 2 | a0001c0001t0022g0296a0002c0002t0001g0283 | 2 | HG01243.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-156-18403_-156-18 others(19): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102811913 | |||||
| chr14:102811913
|
CTTTTTTT others(7): Show |
C | 1 | a0002c0002t0001g0232 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-156-18404_-156-18 others(20): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102811913 | |||||
| chr14:102811988
|
C | A | 1 | a0001c0001t0041g0051 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-156-18346C>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102811988 | ||||||
| chr14:102812647
|
T | C | 1 | a0001c0001t0011g0165 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-156-17687T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102812647 | ||||||
| chr14:102812658
|
G | A | 1 | a0002c0002t0001g0234 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-156-17676G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102812658 | ||||||
| chr14:102812701
|
CGAGGTCA others(120): Show |
C | 4 | a0001c0003t0003g0182a0001c0003t0005g0181a0001c0003t0034g0003others(1): Show | 4 | HG02630.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-156-17630_-156-17 others(6): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102812701 | |||||
| chr14:102812751
|
T | C | 120 | a0001c0001t0001g0184a0001c0001t0013g0262a0001c0001t0013g0263others(117): Show | 120 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.-156-17583T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102812751 | ||||||
| chr14:102812787
|
C | T | 1 | a0001c0001t0022g0296 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-156-17547C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102812787 | ||||||
| chr14:102812792
|
G | A | 1 | a0001c0001t0028g0138 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-156-17542G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102812792 | ||||||
| chr14:102812914
|
G | A | 3 | a0001c0001t0015g0139a0001c0001t0015g0140a0001c0001t0015g0141 | 3 | HG02055.hp1 HG02257.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-156-17420G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102812914 | ||||||
| chr14:102812915
|
T | C | 44 | a0001c0001t0013g0262a0001c0001t0013g0263a0001c0001t0013g0293others(41): Show | 44 | HG00099.hp1 HG00733.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.-156-17419T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102812915 | ||||||
| chr14:102812921
|
A | C | 3 | a0001c0001t0033g0123a0001c0001t0067g0125a0001c0001t0068g0029 | 3 | HG00733.hp2 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-156-17413A>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102812921 | ||||||
| chr14:102812966
|
A | G | 100 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(97): Show | 100 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.-156-17368A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102812966 | ||||||
| chr14:102813044
|
C | G | 1 | a0001c0001t0003g0100 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-156-17290C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102813044 | ||||||
| chr14:102813080
|
A | G | 1 | a0002c0002t0006g0158 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-156-17254A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102813080 | ||||||
| chr14:102813162
|
ACGGGGTT others(47): Show |
A | 120 | a0001c0001t0001g0184a0001c0001t0013g0262a0001c0001t0013g0263others(117): Show | 120 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.-156-17169_-156-17 others(60): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102813162 | |||||
| chr14:102813453
|
C | CT | 3 | a0002c0002t0001g0251a0002c0002t0001g0252a0002c0002t0001g0253 | 3 | HG01433.hp1 HG03688.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.-156-16877dupT | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102813453 | |||||
| chr14:102813457
|
TC | T | 7 | a0001c0001t0013g0263a0001c0003t0003g0182a0001c0003t0005g0181others(4): Show | 7 | HG01069.hp2 HG01993.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-156-16876delC | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102813457 | ||||||
| chr14:102813458
|
C | T | 118 | a0001c0001t0001g0184a0001c0001t0013g0262a0001c0001t0013g0293others(115): Show | 118 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.-156-16876C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102813458 | ||||||
| chr14:102813607
|
C | T | 1 | a0002c0002t0001g0193 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-156-16727C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102813607 | ||||||
| chr14:102813641
|
G | A | 1 | a0001c0001t0014g0091 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-156-16693G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102813641 | ||||||
| chr14:102813702
|
C | T | 2 | a0002c0002t0001g0295a0002c0002t0065g0276 | 2 | NA18955.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.-156-16632C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102813702 | ||||||
| chr14:102813730
|
C | A | 120 | a0001c0001t0001g0184a0001c0001t0013g0262a0001c0001t0013g0263others(117): Show | 120 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.-156-16604C>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102813730 | ||||||
| chr14:102813840
|
G | C | 4 | a0001c0003t0003g0182a0001c0003t0005g0181a0001c0003t0034g0003others(1): Show | 4 | HG02630.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-156-16494G>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102813840 | ||||||
| chr14:102814185
|
G | A | 1 | a0001c0001t0019g0082 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-156-16149G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102814185 | ||||||
| chr14:102814320
|
G | A | 125 | a0001c0001t0001g0184a0001c0001t0013g0262a0001c0001t0013g0263others(122): Show | 125 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.-156-16014G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102814320 | ||||||
| chr14:102814338
|
C | T | 2 | a0001c0001t0015g0139a0001c0001t0015g0140 | 2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-156-15996C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102814338 | ||||||
| chr14:102814414
|
T | G | 17 | a0001c0001t0005g0009a0001c0001t0005g0010a0001c0001t0005g0011others(14): Show | 17 | HG02055.hp2 HG02258.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.-156-15920T>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102814414 | ||||||
| chr14:102814469
|
T | G | 1 | a0001c0001t0011g0150 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-156-15865T>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102814469 | ||||||
| chr14:102814475
|
A | C | 17 | a0001c0001t0005g0009a0001c0001t0005g0010a0001c0001t0005g0011others(14): Show | 17 | HG02055.hp2 HG02258.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.-156-15859A>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102814475 | ||||||
| chr14:102814513
|
A | T | 9 | a0001c0001t0005g0137a0001c0001t0012g0168a0001c0001t0015g0139others(6): Show | 9 | HG02055.hp1 HG02109.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-156-15821A>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102814513 | ||||||
| chr14:102814551
|
A | G | 8 | a0001c0001t0013g0262a0001c0001t0013g0263a0001c0001t0013g0293others(5): Show | 8 | HG01167.hp1 HG01169.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-156-15783A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102814551 | ||||||
| chr14:102814556
|
G | A | 1 | a0002c0002t0001g0280 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-156-15778G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102814556 | ||||||
| chr14:102814620
|
G | A | 1 | a0001c0001t0041g0051 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-156-15714G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102814620 | ||||||
| chr14:102814653
|
G | A | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-156-15681G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102814653 | ||||||
| chr14:102814654
|
G | A | 1 | a0001c0001t0038g0015 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-156-15680G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102814654 | ||||||
| chr14:102814869
|
A | C | 1 | a0001c0001t0007g0008 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-156-15465A>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102814869 | ||||||
| chr14:102814886
|
G | C | 4 | a0001c0003t0003g0182a0001c0003t0005g0181a0001c0003t0034g0003others(1): Show | 4 | HG02630.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-156-15448G>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102814886 | ||||||
| chr14:102815000
|
A | G | 4 | a0001c0001t0010g0053a0001c0001t0012g0098a0001c0001t0012g0124others(1): Show | 4 | HG00639.hp2 HG01109.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.-156-15334A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102815000 | ||||||
| chr14:102815003
|
A | G | 269 | a0001c0001t0001g0184a0001c0001t0002g0025a0001c0001t0002g0026others(266): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.-156-15331A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102815003 | ||||||
| chr14:102815108
|
A | T | 1 | a0002c0002t0001g0209 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-156-15226A>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102815108 | ||||||
| chr14:102815147
|
C | T | 1 | a0002c0002t0001g0292 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-156-15187C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102815147 | ||||||
| chr14:102815344
|
G | T | 3 | a0001c0001t0012g0001a0001c0001t0012g0179a0001c0001t0050g0180 | 3 | HG01884.hp2 HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-156-14990G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102815344 | ||||||
| chr14:102815470
|
G | C | 3 | a0001c0001t0017g0143a0001c0001t0017g0144a0001c0001t0017g0145 | 3 | HG02109.hp2 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-156-14864G>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102815470 | ||||||
| chr14:102815552
|
T | A | 4 | a0001c0001t0013g0262a0001c0001t0013g0263a0001c0001t0013g0293others(1): Show | 4 | HG02615.hp2 HG02622.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-156-14782T>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102815552 | ||||||
| chr14:102815667
|
A | G | 1 | a0001c0001t0002g0101 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-156-14667A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102815667 | ||||||
| chr14:102815835
|
A | G | 1 | a0001c0001t0002g0067 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-156-14499A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102815835 | ||||||
| chr14:102816105
|
A | AT | 11 | a0001c0001t0010g0053a0001c0001t0012g0098a0001c0001t0012g0124others(8): Show | 11 | HG00639.hp2 HG01099.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-156-14216dupT | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102816105 | |||||
| chr14:102816105
|
AT | A | 7 | a0001c0001t0002g0056a0001c0001t0004g0048a0001c0001t0007g0097others(4): Show | 7 | HG03041.hp1 HG03239.hp2 NA18971.hp1 others(4): Show |
intron_variant | MODIFIER | c.-156-14216delT | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102816105 | |||||
| chr14:102816265
|
C | G | 121 | a0001c0001t0001g0184a0001c0001t0013g0262a0001c0001t0013g0263others(118): Show | 121 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.-156-14069C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102816265 | ||||||
| chr14:102816377
|
A | G | 1 | a0001c0001t0002g0079 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-156-13957A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102816377 | ||||||
| chr14:102816380
|
T | C | 1 | a0001c0001t0033g0123 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-156-13954T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102816380 | ||||||
| chr14:102816402
|
T | C | 1 | a0002c0006t0001g0204 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-156-13932T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102816402 | ||||||
| chr14:102816682
|
G | A | 263 | a0001c0001t0001g0184a0001c0001t0002g0025a0001c0001t0002g0026others(260): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.-156-13652G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102816682 | ||||||
| chr14:102816936
|
C | T | 124 | a0001c0001t0001g0184a0001c0001t0013g0262a0001c0001t0013g0263others(121): Show | 124 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.-156-13398C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102816936 | ||||||
| chr14:102816949
|
C | T | 1 | a0002c0002t0001g0270 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-156-13385C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102816949 | ||||||
| chr14:102816982
|
T | C | 1 | a0001c0001t0007g0119 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-156-13352T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102816982 | ||||||
| chr14:102817092
|
A | G | 4 | a0001c0001t0010g0053a0001c0001t0012g0098a0001c0001t0012g0124others(1): Show | 4 | HG00639.hp2 HG01109.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.-156-13242A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102817092 | ||||||
| chr14:102817367
|
G | A | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-156-12967G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102817367 | ||||||
| chr14:102817372
|
T | C | 2 | a0001c0001t0002g0101a0001c0001t0002g0102 | 2 | HG00099.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.-156-12962T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102817372 | ||||||
| chr14:102817414
|
G | C | 9 | a0001c0001t0005g0137a0001c0001t0012g0168a0001c0001t0015g0139others(6): Show | 9 | HG02055.hp1 HG02109.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-156-12920G>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102817414 | ||||||
| chr14:102817439
|
C | T | 3 | a0001c0001t0012g0001a0001c0001t0012g0179a0001c0001t0050g0180 | 3 | HG01884.hp2 HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-156-12895C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102817439 | ||||||
| chr14:102817524
|
C | G | 1 | a0001c0001t0002g0115 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-156-12810C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102817524 | ||||||
| chr14:102817663
|
A | G | 8 | a0001c0001t0010g0053a0001c0001t0012g0098a0001c0001t0012g0124others(5): Show | 8 | HG00639.hp2 HG01109.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.-156-12671A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102817663 | ||||||
| chr14:102817711
|
A | G | 13 | a0001c0001t0005g0137a0001c0001t0012g0168a0001c0001t0015g0139others(10): Show | 13 | HG02055.hp1 HG02109.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.-156-12623A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102817711 | ||||||
| chr14:102817770
|
T | C | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-156-12564T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102817770 | ||||||
| chr14:102817833
|
T | C | 1 | a0001c0001t0003g0100 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-156-12501T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102817833 | ||||||
| chr14:102817939
|
A | G | 101 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(98): Show | 101 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.-156-12395A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102817939 | ||||||
| chr14:102818070
|
T | C | 1 | a0001c0001t0002g0058 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-156-12264T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102818070 | ||||||
| chr14:102818275
|
G | A | 85 | a0001c0001t0001g0184a0001c0001t0004g0007a0001c0001t0005g0137others(82): Show | 85 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.-156-12059G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102818275 | ||||||
| chr14:102818341
|
C | G | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-156-11993C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102818341 | ||||||
| chr14:102818344
|
C | G | 1 | a0001c0001t0046g0042 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-156-11990C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102818344 | ||||||
| chr14:102818457
|
G | A | 1 | a0001c0001t0021g0099 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-156-11877G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102818457 | ||||||
| chr14:102818473
|
G | A | 1 | a0001c0001t0007g0163 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-156-11861G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102818473 | ||||||
| chr14:102818506
|
G | A | 1 | a0001c0001t0035g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-156-11828G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102818506 | ||||||
| chr14:102818542
|
A | G | 153 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.-156-11792A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102818542 | ||||||
| chr14:102818604
|
T | C | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-156-11730T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102818604 | ||||||
| chr14:102818613
|
T | C | 3 | a0001c0001t0017g0143a0001c0001t0017g0144a0001c0001t0017g0145 | 3 | HG02109.hp2 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-156-11721T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102818613 | ||||||
| chr14:102818655
|
A | C | 1 | a0001c0001t0043g0031 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-156-11679A>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102818655 | ||||||
| chr14:102818732
|
C | G | 3 | a0001c0001t0022g0296a0001c0001t0031g0183a0001c0001t0042g0005 | 3 | HG01099.hp2 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-156-11602C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102818732 | ||||||
| chr14:102818804
|
A | G | 1 | a0002c0002t0059g0239 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-156-11530A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102818804 | ||||||
| chr14:102818949
|
T | G | 2 | a0001c0001t0003g0100a0001c0004t0039g0002 | 2 | HG01993.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-156-11385T>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102818949 | ||||||
| chr14:102818954
|
A | G | 1 | a0002c0006t0001g0204 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-156-11380A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102818954 | ||||||
| chr14:102819055
|
T | TA | 99 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(96): Show | 99 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.-156-11266dupA | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102819055 | |||||
| chr14:102819092
|
T | A | 4 | a0001c0003t0003g0182a0001c0003t0005g0181a0001c0003t0034g0003others(1): Show | 4 | HG02630.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-156-11242T>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102819092 | ||||||
| chr14:102819289
|
C | T | 9 | a0001c0001t0005g0137a0001c0001t0012g0168a0001c0001t0015g0139others(6): Show | 9 | HG02055.hp1 HG02109.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-156-11045C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102819289 | ||||||
| chr14:102819838
|
A | G | 1 | a0002c0002t0065g0276 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-156-10496A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102819838 | ||||||
| chr14:102819845
|
G | A | 1 | a0002c0002t0001g0252 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-156-10489G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102819845 | ||||||
| chr14:102819871
|
C | A | 2 | a0002c0002t0001g0278a0002c0002t0001g0279 | 2 | HG01981.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.-156-10463C>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102819871 | ||||||
| chr14:102820057
|
G | A | 1 | a0001c0001t0047g0028 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-156-10277G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102820057 | ||||||
| chr14:102820133
|
G | C | 2 | a0001c0001t0002g0059a0001c0001t0002g0060 | 2 | HG00544.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.-156-10201G>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102820133 | ||||||
| chr14:102820203
|
C | T | 2 | a0001c0001t0012g0098a0001c0001t0012g0124 | 2 | HG01109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-156-10131C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102820203 | ||||||
| chr14:102820265
|
T | C | 4 | a0001c0001t0002g0076a0001c0001t0016g0103a0001c0001t0016g0104others(1): Show | 4 | HG00323.hp1 HG01074.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-156-10069T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102820265 | ||||||
| chr14:102820522
|
G | A | 1 | a0001c0001t0040g0149 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-156-9812G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102820522 | ||||||
| chr14:102820573
|
C | CATATATA others(1): Show |
3 | a0001c0001t0002g0106a0001c0001t0002g0113a0001c0001t0007g0163 | 3 | HG03130.hp2 HG03704.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.-156-9726_-156-971 others(12): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820573 | |||||
| chr14:102820573
|
C | CATATATA others(3): Show |
1 | a0001c0001t0002g0058 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-156-9728_-156-971 others(14): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820573 | |||||
| chr14:102820573
|
C | CATATATA others(5): Show |
3 | a0001c0001t0003g0085a0001c0001t0008g0062a0001c0001t0014g0092 | 3 | HG00140.hp2 HG02109.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.-156-9730_-156-971 others(16): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820573 | |||||
| chr14:102820573
|
C | CATATATA others(7): Show |
3 | a0001c0001t0002g0056a0001c0001t0002g0074a0001c0001t0011g0148 | 3 | HG01358.hp1 HG01928.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-156-9732_-156-971 others(18): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820573 | |||||
| chr14:102820573
|
C | CATATATA others(9): Show |
1 | a0001c0001t0008g0030 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-156-9734_-156-971 others(20): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820573 | |||||
| chr14:102820573
|
C | CATATATA others(17): Show |
2 | a0001c0001t0002g0072a0001c0001t0002g0083 | 2 | HG01993.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.-156-9742_-156-971 others(28): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820573 | |||||
| chr14:102820573
|
C | CATATATA others(21): Show |
2 | a0001c0001t0002g0108a0001c0001t0002g0118 | 2 | NA18984.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.-156-9746_-156-971 others(32): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820573 | |||||
| chr14:102820573
|
CATAT | C | 5 | a0001c0001t0013g0294a0001c0001t0026g0073a0001c0001t0026g0078others(2): Show | 5 | HG02615.hp2 HG02698.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-156-9722_-156-971 others(8): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820573 | |||||
| chr14:102820573
|
CATATATA others(3): Show |
C | 1 | a0001c0001t0069g0093 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-156-9728_-156-971 others(14): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820573 | |||||
| chr14:102820573
|
CATATATA others(5): Show |
C | 1 | a0001c0001t0013g0293 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-156-9730_-156-971 others(16): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820573 | |||||
| chr14:102820573
|
CATATATA others(7): Show |
C | 5 | a0001c0001t0002g0087a0001c0001t0027g0288a0001c0001t0027g0289others(2): Show | 5 | HG00099.hp1 HG01069.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.-156-9732_-156-971 others(18): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820573 | |||||
| chr14:102820573
|
CATATATA others(9): Show |
C | 11 | a0001c0001t0061g0264a0002c0002t0001g0248a0002c0002t0001g0251others(8): Show | 11 | HG01123.hp2 HG01257.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.-156-9734_-156-971 others(20): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820573 | |||||
| chr14:102820573
|
CATATATA others(11): Show |
C | 5 | a0001c0001t0004g0035a0001c0001t0015g0139a0001c0001t0015g0140others(2): Show | 5 | HG02055.hp1 HG02257.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-156-9736_-156-971 others(22): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820573 | |||||
| chr14:102820573
|
CATATATA others(13): Show |
C | 1 | a0001c0001t0029g0068 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-156-9738_-156-971 others(24): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820573 | |||||
| chr14:102820590
|
ATATATAT others(22): Show |
A | 1 | a0001c0001t0035g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-156-9742_-156-971 others(33): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820590 | |||||
| chr14:102820592
|
ATATATAT others(18): Show |
A | 1 | a0001c0001t0043g0031 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-156-9740_-156-971 others(29): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820592 | |||||
| chr14:102820592
|
ATATATAT others(23): Show |
A | 1 | a0001c0001t0005g0011 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-156-9740_-156-971 others(34): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820592 | |||||
| chr14:102820593
|
TATATATA others(12): Show |
T | 2 | a0001c0001t0004g0048a0001c0001t0004g0170 | 2 | NA19009.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.-156-9740_-156-972 others(23): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102820593 | ||||||
| chr14:102820594
|
ATATATAT others(16): Show |
A | 1 | a0001c0001t0020g0054 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-156-9738_-156-971 others(27): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820594 | |||||
| chr14:102820594
|
ATATATAT others(18): Show |
A | 1 | a0001c0001t0002g0065 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-156-9738_-156-971 others(29): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820594 | |||||
| chr14:102820594
|
ATATATAT others(21): Show |
A | 1 | a0001c0001t0012g0024 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-156-9738_-156-971 others(32): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820594 | |||||
| chr14:102820594
|
ATATATAT others(22): Show |
A | 2 | a0001c0001t0010g0019a0001c0001t0010g0020 | 2 | HG02258.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-156-9738_-156-971 others(33): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820594 | |||||
| chr14:102820594
|
ATATATAT others(23): Show |
A | 7 | a0001c0001t0005g0009a0001c0001t0005g0010a0001c0001t0005g0013others(4): Show | 7 | HG02055.hp2 HG02809.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-156-9738_-156-970 others(34): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820594 | |||||
| chr14:102820594
|
ATATATAT others(24): Show |
A | 1 | a0001c0001t0010g0022 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-156-9738_-156-970 others(35): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820594 | |||||
| chr14:102820594
|
ATATATAT others(25): Show |
A | 1 | a0001c0001t0010g0018 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-156-9738_-156-970 others(36): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820594 | |||||
| chr14:102820595
|
TATATATA others(8): Show |
T | 2 | a0001c0001t0017g0144a0001c0001t0021g0099 | 2 | HG02738.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-156-9738_-156-972 others(19): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102820595 | ||||||
| chr14:102820595
|
TATATATA others(10): Show |
T | 2 | a0002c0002t0001g0259a0002c0002t0001g0280 | 2 | HG01261.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-156-9738_-156-972 others(21): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102820595 | ||||||
| chr14:102820595
|
TATATATA others(12): Show |
T | 2 | a0001c0001t0002g0036a0001c0001t0004g0034 | 2 | NA18960.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.-156-9738_-156-972 others(23): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102820595 | ||||||
| chr14:102820596
|
ATATATAT others(12): Show |
A | 4 | a0001c0001t0004g0061a0002c0002t0003g0133a0002c0002t0003g0134others(1): Show | 4 | HG01099.hp1 HG02698.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-156-9736_-156-971 others(23): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820596 | |||||
| chr14:102820596
|
ATATATAT others(13): Show |
A | 1 | a0002c0002t0054g0194 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-156-9736_-156-971 others(24): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820596 | |||||
| chr14:102820596
|
ATATATAT others(16): Show |
A | 1 | a0001c0001t0010g0053 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-156-9736_-156-971 others(27): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820596 | |||||
| chr14:102820596
|
ATATATAT others(17): Show |
A | 1 | a0001c0001t0004g0040 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-156-9736_-156-971 others(28): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820596 | |||||
| chr14:102820596
|
ATATATAT others(23): Show |
A | 1 | a0001c0001t0007g0008 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-156-9736_-156-970 others(34): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820596 | |||||
| chr14:102820596
|
ATATATAT others(24): Show |
A | 1 | a0001c0003t0037g0004 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-156-9736_-156-970 others(35): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820596 | |||||
| chr14:102820596
|
ATATATAT others(25): Show |
A | 2 | a0001c0003t0003g0182a0001c0003t0005g0181 | 2 | HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-156-9736_-156-970 others(36): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820596 | |||||
| chr14:102820597
|
TATATATA others(8): Show |
T | 4 | a0001c0001t0018g0186a0001c0001t0018g0250a0001c0001t0018g0275others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-156-9736_-156-972 others(19): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102820597 | ||||||
| chr14:102820597
|
TATATATA others(10): Show |
T | 2 | a0002c0002t0001g0220a0002c0002t0001g0266 | 2 | NA19065.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.-156-9736_-156-972 others(21): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102820597 | ||||||
| chr14:102820598
|
ATATATAT others(10): Show |
A | 8 | a0002c0002t0001g0257a0002c0002t0001g0267a0002c0002t0001g0268others(5): Show | 8 | HG01243.hp1 HG01496.hp2 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.-156-9734_-156-971 others(21): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820598 | |||||
| chr14:102820598
|
ATATATAT others(11): Show |
A | 5 | a0002c0002t0001g0205a0002c0002t0001g0206a0002c0002t0001g0256others(2): Show | 5 | HG01516.hp1 HG02717.hp1 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.-156-9734_-156-971 others(22): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820598 | |||||
| chr14:102820598
|
ATATATAT others(12): Show |
A | 8 | a0001c0001t0001g0184a0001c0001t0062g0247a0001c0001t0064g0198others(5): Show | 8 | HG00558.hp1 HG02300.hp2 NA18948.hp1 others(5): Show |
intron_variant | MODIFIER | c.-156-9734_-156-971 others(23): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820598 | |||||
| chr14:102820598
|
ATATATAT others(13): Show |
A | 6 | a0002c0002t0001g0226a0002c0002t0001g0227a0002c0002t0001g0230others(3): Show | 6 | HG00621.hp1 HG01071.hp1 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.-156-9734_-156-971 others(24): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820598 | |||||
| chr14:102820598
|
ATATATAT others(15): Show |
A | 1 | a0001c0001t0012g0098 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-156-9734_-156-971 others(26): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820598 | |||||
| chr14:102820598
|
ATATATAT others(17): Show |
A | 1 | a0001c0001t0012g0124 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-156-9734_-156-971 others(28): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820598 | |||||
| chr14:102820598
|
ATATATAT others(22): Show |
A | 2 | a0001c0001t0032g0021a0001c0001t0038g0015 | 2 | HG02451.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-156-9734_-156-970 others(33): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820598 | |||||
| chr14:102820598
|
ATATATAT others(24): Show |
A | 1 | a0001c0003t0034g0003 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-156-9734_-156-970 others(35): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820598 | |||||
| chr14:102820599
|
TATATATA others(8): Show |
T | 5 | a0001c0001t0002g0107a0001c0001t0002g0109a0001c0001t0002g0112others(2): Show | 5 | NA18952.hp1 NA18962.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.-156-9734_-156-972 others(19): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102820599 | ||||||
| chr14:102820600
|
A | T | 1 | a0001c0001t0024g0049 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-156-9734A>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102820600 | ||||||
| chr14:102820600
|
ATATATAT others(8): Show |
A | 2 | a0001c0001t0013g0263a0002c0002t0053g0290 | 2 | HG03225.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-156-9732_-156-971 others(19): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820600 | |||||
| chr14:102820600
|
ATATATAT others(9): Show |
A | 1 | a0002c0002t0001g0277 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-156-9732_-156-971 others(20): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820600 | |||||
| chr14:102820600
|
ATATATAT others(10): Show |
A | 5 | a0001c0001t0003g0100a0002c0002t0001g0209a0002c0002t0001g0237others(2): Show | 5 | HG00673.hp2 HG02257.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-156-9732_-156-971 others(21): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820600 | |||||
| chr14:102820600
|
ATATATAT others(11): Show |
A | 7 | a0002c0002t0001g0207a0002c0002t0001g0208a0002c0002t0001g0211others(4): Show | 7 | HG03834.hp1 NA18949.hp1 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.-156-9732_-156-971 others(22): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820600 | |||||
| chr14:102820600
|
ATATATAT others(12): Show |
A | 19 | a0002c0002t0001g0191a0002c0002t0001g0199a0002c0002t0001g0200others(16): Show | 19 | HG00609.hp2 HG00735.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.-156-9732_-156-971 others(23): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820600 | |||||
| chr14:102820600
|
ATATATAT others(13): Show |
A | 1 | a0002c0002t0001g0240 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-156-9732_-156-971 others(24): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820600 | |||||
| chr14:102820600
|
ATATATAT others(14): Show |
A | 1 | a0002c0002t0001g0224 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-156-9732_-156-971 others(25): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820600 | |||||
| chr14:102820601
|
TATATATA others(6): Show |
T | 1 | a0002c0002t0001g0282 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-156-9732_-156-972 others(17): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102820601 | ||||||
| chr14:102820602
|
A | T | 1 | a0001c0001t0024g0049 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-156-9732A>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102820602 | ||||||
| chr14:102820602
|
ATATATAT others(6): Show |
A | 1 | a0001c0001t0013g0262 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-156-9730_-156-971 others(17): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820602 | |||||
| chr14:102820602
|
ATATATAT others(7): Show |
A | 1 | a0002c0002t0001g0261 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-156-9730_-156-971 others(18): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820602 | |||||
| chr14:102820602
|
ATATATAT others(8): Show |
A | 1 | a0001c0001t0047g0028 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-156-9730_-156-971 others(19): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820602 | |||||
| chr14:102820602
|
ATATATAT others(9): Show |
A | 1 | a0002c0002t0060g0213 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-156-9730_-156-971 others(20): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820602 | |||||
| chr14:102820602
|
ATATATAT others(10): Show |
A | 2 | a0002c0002t0001g0195a0002c0002t0056g0244 | 2 | NA18992.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-156-9730_-156-971 others(21): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820602 | |||||
| chr14:102820602
|
ATATATAT others(11): Show |
A | 2 | a0002c0002t0001g0245a0002c0002t0003g0088 | 2 | NA18940.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.-156-9730_-156-971 others(22): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820602 | |||||
| chr14:102820602
|
ATATATAT others(12): Show |
A | 10 | a0001c0001t0063g0223a0002c0002t0001g0188a0002c0002t0001g0190others(7): Show | 10 | HG00323.hp2 HG00558.hp2 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.-156-9730_-156-971 others(23): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820602 | |||||
| chr14:102820602
|
ATATATAT others(14): Show |
A | 1 | a0001c0001t0022g0296 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-156-9730_-156-971 others(25): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820602 | |||||
| chr14:102820604
|
A | T | 1 | a0001c0001t0024g0049 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-156-9730A>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102820604 | ||||||
| chr14:102820604
|
ATATATAT others(6): Show |
A | 1 | a0001c0001t0024g0069 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-156-9728_-156-971 others(17): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820604 | |||||
| chr14:102820604
|
ATATATAT others(8): Show |
A | 1 | a0002c0002t0055g0260 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-156-9728_-156-971 others(19): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820604 | |||||
| chr14:102820604
|
ATATATAT others(9): Show |
A | 2 | a0002c0002t0003g0151a0002c0002t0003g0167 | 2 | HG00544.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.-156-9728_-156-971 others(20): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820604 | |||||
| chr14:102820604
|
ATATATAT others(10): Show |
A | 2 | a0002c0002t0001g0193a0002c0002t0001g0246 | 2 | HG02155.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.-156-9728_-156-971 others(21): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820604 | |||||
| chr14:102820604
|
ATATATAT others(12): Show |
A | 3 | a0002c0002t0001g0189a0002c0002t0009g0197a0002c0002t0009g0216 | 3 | HG01175.hp1 HG01433.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.-156-9728_-156-971 others(23): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820604 | |||||
| chr14:102820604
|
ATATATAT others(13): Show |
A | 2 | a0002c0002t0001g0187a0002c0002t0001g0215 | 2 | HG01257.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.-156-9728_-156-970 others(24): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820604 | |||||
| chr14:102820606
|
A | T | 1 | a0001c0001t0024g0049 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-156-9728A>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102820606 | ||||||
| chr14:102820606
|
ATATATAT others(3): Show |
A | 3 | a0001c0001t0016g0104a0001c0001t0016g0105a0001c0001t0020g0142 | 3 | HG01516.hp2 HG01517.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-156-9726_-156-971 others(14): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820606 | |||||
| chr14:102820606
|
ATATATAT others(6): Show |
A | 1 | a0002c0002t0001g0249 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-156-9726_-156-971 others(17): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820606 | |||||
| chr14:102820606
|
ATATATAT others(12): Show |
A | 1 | a0002c0002t0001g0235 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-156-9726_-156-970 others(23): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820606 | |||||
| chr14:102820608
|
A | T | 3 | a0001c0001t0002g0066a0001c0001t0007g0119a0001c0001t0024g0049 | 3 | HG02486.hp2 HG02602.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-156-9726A>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102820608 | ||||||
| chr14:102820610
|
A | T | 5 | a0001c0001t0002g0066a0001c0001t0007g0119a0001c0001t0024g0049others(2): Show | 5 | HG02135.hp2 HG02486.hp2 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.-156-9724A>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102820610 | ||||||
| chr14:102820610
|
ATATATTT others(4): Show |
A | 1 | a0001c0001t0016g0103 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-156-9722_-156-971 others(15): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820610 | |||||
| chr14:102820612
|
A | T | 10 | a0001c0001t0002g0066a0001c0001t0007g0119a0001c0001t0013g0294others(7): Show | 10 | HG02135.hp2 HG02486.hp2 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.-156-9722A>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102820612 | ||||||
| chr14:102820614
|
A | ATATATAT others(10): Show |
1 | a0001c0001t0008g0038 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-156-9719_-156-971 others(21): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820614 | |||||
| chr14:102820614
|
A | ATATATAT others(18): Show |
1 | a0001c0001t0002g0025 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-156-9719_-156-971 others(29): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820614 | |||||
| chr14:102820614
|
A | ATATATAT others(28): Show |
1 | a0001c0001t0002g0044 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-156-9719_-156-971 others(39): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820614 | |||||
| chr14:102820614
|
A | ATATATAT others(30): Show |
1 | a0001c0001t0004g0173 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-156-9719_-156-971 others(41): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820614 | |||||
| chr14:102820614
|
A | ATATATAT others(19): Show |
1 | a0001c0001t0002g0071 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-156-9719_-156-971 others(30): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820614 | |||||
| chr14:102820614
|
A | ATATATAT others(23): Show |
1 | a0001c0001t0002g0070 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-156-9719_-156-971 others(34): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820614 | |||||
| chr14:102820614
|
A | ATATATAT others(17): Show |
2 | a0001c0001t0002g0101a0001c0001t0002g0115 | 2 | HG00099.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.-156-9719_-156-971 others(28): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820614 | |||||
| chr14:102820614
|
A | ATATATAT others(18): Show |
1 | a0001c0001t0045g0047 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-156-9719_-156-971 others(29): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820614 | |||||
| chr14:102820614
|
A | ATATATAT others(15): Show |
1 | a0001c0001t0046g0042 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-156-9719_-156-971 others(26): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820614 | |||||
| chr14:102820614
|
A | ATATATAT others(13): Show |
3 | a0001c0001t0004g0126a0001c0001t0008g0064a0001c0001t0011g0147 | 3 | HG01175.hp2 HG01496.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.-156-9719_-156-971 others(24): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820614 | |||||
| chr14:102820614
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0008g0037 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-156-9719_-156-971 others(25): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820614 | |||||
| chr14:102820614
|
A | ATATATAT others(15): Show |
1 | a0001c0001t0014g0117 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-156-9719_-156-971 others(26): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820614 | |||||
| chr14:102820614
|
A | ATATATAT others(16): Show |
1 | a0001c0001t0004g0007 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-156-9719_-156-971 others(27): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820614 | |||||
| chr14:102820614
|
A | ATATATAT others(19): Show |
1 | a0001c0001t0031g0183 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-156-9719_-156-971 others(30): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820614 | |||||
| chr14:102820614
|
A | ATATATAT others(12): Show |
1 | a0001c0001t0002g0076 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-156-9719_-156-971 others(23): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820614 | |||||
| chr14:102820614
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0017g0145 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-156-9719_-156-971 others(25): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820614 | |||||
| chr14:102820614
|
A | ATATATAT others(17): Show |
1 | a0001c0001t0004g0175 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-156-9719_-156-971 others(28): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820614 | |||||
| chr14:102820614
|
A | ATATATAT others(10): Show |
1 | a0001c0001t0025g0052 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-156-9719_-156-971 others(21): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820614 | |||||
| chr14:102820614
|
A | ATATATAT others(11): Show |
1 | a0001c0001t0002g0102 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-156-9719_-156-971 others(22): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820614 | |||||
| chr14:102820614
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0025g0122 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-156-9719_-156-971 others(19): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820614 | |||||
| chr14:102820614
|
A | ATATATAT others(9): Show |
1 | a0001c0001t0011g0166 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-156-9719_-156-971 others(20): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820614 | |||||
| chr14:102820614
|
A | ATATATAT others(13): Show |
1 | a0001c0001t0051g0284 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-156-9719_-156-971 others(24): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820614 | |||||
| chr14:102820614
|
A | ATATATAT others(6): Show |
4 | a0001c0001t0002g0041a0001c0001t0002g0172a0001c0001t0008g0039others(1): Show | 4 | HG01943.hp1 HG02895.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-156-9719_-156-971 others(17): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820614 | |||||
| chr14:102820614
|
A | ATATATAT others(7): Show |
1 | a0001c0001t0002g0032 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-156-9719_-156-971 others(18): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820614 | |||||
| chr14:102820614
|
A | ATATATAT others(13): Show |
1 | a0001c0001t0007g0096 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-156-9719_-156-971 others(24): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820614 | |||||
| chr14:102820614
|
A | ATATATAT others(3): Show |
1 | a0001c0001t0011g0150 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-156-9719_-156-971 others(14): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820614 | |||||
| chr14:102820614
|
A | ATATATAT others(6): Show |
3 | a0001c0001t0004g0174a0001c0001t0019g0082a0001c0001t0022g0050 | 3 | HG01884.hp1 HG02300.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-156-9719_-156-971 others(17): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820614 | |||||
| chr14:102820614
|
A | ATATATAT others(7): Show |
1 | a0001c0001t0007g0045 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-156-9719_-156-971 others(18): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820614 | |||||
| chr14:102820614
|
A | ATATATAT others(11): Show |
1 | a0001c0001t0007g0097 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-156-9719_-156-971 others(22): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820614 | |||||
| chr14:102820614
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0007g0121 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-156-9719_-156-971 others(25): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820614 | |||||
| chr14:102820614
|
A | ATATATAT others(24): Show |
1 | a0001c0001t0040g0149 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-156-9719_-156-971 others(35): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820614 | |||||
| chr14:102820614
|
A | ATTTTTTT others(3): Show |
1 | a0001c0001t0012g0168 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-156-9698_-156-968 others(14): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820614 | |||||
| chr14:102820614
|
A | ATTTTTTT others(8): Show |
1 | a0001c0001t0007g0094 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-156-9703_-156-968 others(19): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102820614 | |||||
| chr14:102820614
|
A | T | 32 | a0001c0001t0002g0066a0001c0001t0002g0120a0001c0001t0004g0048others(29): Show | 32 | HG00099.hp1 HG00621.hp2 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.-156-9720A>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102820614 | ||||||
| chr14:102820615
|
T | TA | 4 | a0001c0004t0039g0002a0002c0002t0003g0160a0002c0002t0006g0156others(1): Show | 4 | HG00639.hp1 HG01256.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.-156-9719_-156-971 others(5): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102820615 | ||||||
| chr14:102820615
|
T | TATATATA others(6): Show |
4 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0084others(1): Show | 4 | HG01167.hp2 HG01346.hp2 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.-156-9719_-156-971 others(17): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102820615 | ||||||
| chr14:102820615
|
T | TATATATA others(8): Show |
3 | a0001c0001t0002g0081a0001c0001t0002g0086a0001c0001t0007g0095 | 3 | HG00738.hp2 HG03486.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.-156-9719_-156-971 others(19): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102820615 | ||||||
| chr14:102820615
|
T | TATATATA others(10): Show |
1 | a0001c0001t0014g0091 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-156-9719_-156-971 others(21): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102820615 | ||||||
| chr14:102820615
|
T | TATATATA others(18): Show |
1 | a0001c0001t0048g0116 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-156-9719_-156-971 others(29): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102820615 | ||||||
| chr14:102820615
|
T | TATATATA others(24): Show |
1 | a0001c0001t0012g0179 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-156-9719_-156-971 others(35): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102820615 | ||||||
| chr14:102820616
|
T | A | 14 | a0001c0001t0002g0058a0001c0001t0002g0067a0001c0001t0002g0074others(11): Show | 14 | HG00140.hp2 HG01074.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.-156-9718T>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102820616 | ||||||
| chr14:102820617
|
T | A | 12 | a0001c0001t0002g0026a0001c0001t0002g0077a0001c0001t0002g0079others(9): Show | 12 | HG00738.hp2 HG01167.hp2 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.-156-9717T>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102820617 | ||||||
| chr14:102820618
|
T | A | 12 | a0001c0001t0002g0058a0001c0001t0002g0067a0001c0001t0002g0074others(9): Show | 12 | HG00140.hp2 HG01192.hp2 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.-156-9716T>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102820618 | ||||||
| chr14:102820619
|
T | A | 10 | a0001c0001t0002g0026a0001c0001t0002g0077a0001c0001t0002g0080others(7): Show | 10 | HG01934.hp2 HG01952.hp1 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.-156-9715T>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102820619 | ||||||
| chr14:102820620
|
T | A | 6 | a0001c0001t0002g0074a0001c0001t0002g0083a0001c0001t0002g0113others(3): Show | 6 | HG01243.hp2 HG01358.hp1 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.-156-9714T>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102820620 | ||||||
| chr14:102820621
|
T | A | 4 | a0001c0001t0002g0026a0001c0001t0002g0077a0001c0001t0050g0180others(1): Show | 4 | HG01884.hp2 HG01934.hp2 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.-156-9713T>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102820621 | ||||||
| chr14:102820622
|
T | A | 3 | a0001c0001t0002g0113a0001c0001t0011g0127a0001c0001t0028g0138 | 3 | HG03710.hp1 HG04115.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.-156-9712T>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102820622 | ||||||
| chr14:102820623
|
T | A | 2 | a0001c0001t0002g0026a0001c0001t0050g0180 | 2 | HG01884.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.-156-9711T>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102820623 | ||||||
| chr14:102820624
|
T | A | 1 | a0001c0001t0028g0138 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-156-9710T>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102820624 | ||||||
| chr14:102820625
|
T | A | 1 | a0001c0001t0002g0026 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-156-9709T>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102820625 | ||||||
| chr14:102820646
|
G | T | 1 | a0001c0001t0032g0021 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-156-9688G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102820646 | ||||||
| chr14:102820684
|
G | C | 3 | a0001c0001t0018g0186a0001c0001t0018g0250a0001c0001t0018g0275 | 3 | HG01167.hp1 HG01169.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-156-9650G>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102820684 | ||||||
| chr14:102820734
|
G | A | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-156-9600G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102820734 | ||||||
| chr14:102820738
|
C | T | 8 | a0001c0001t0010g0053a0001c0001t0012g0098a0001c0001t0012g0124others(5): Show | 8 | HG00639.hp2 HG01109.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.-156-9596C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102820738 | ||||||
| chr14:102820910
|
C | T | 1 | a0001c0001t0003g0100 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-156-9424C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102820910 | ||||||
| chr14:102821022
|
A | G | 1 | a0002c0002t0009g0197 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-156-9312A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102821022 | ||||||
| chr14:102821038
|
T | C | 2 | a0002c0002t0001g0238a0002c0002t0001g0249 | 2 | HG00735.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.-156-9296T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102821038 | ||||||
| chr14:102821445
|
C | T | 1 | a0002c0002t0001g0240 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-156-8889C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102821445 | ||||||
| chr14:102821772
|
G | A | 1 | a0002c0002t0003g0088 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-156-8562G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102821772 | ||||||
| chr14:102821796
|
C | T | 4 | a0001c0003t0003g0182a0001c0003t0005g0181a0001c0003t0034g0003others(1): Show | 4 | HG02630.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-156-8538C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102821796 | ||||||
| chr14:102821832
|
G | A | 100 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(97): Show | 100 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.-156-8502G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102821832 | ||||||
| chr14:102821931
|
A | C | 3 | a0001c0001t0015g0139a0001c0001t0015g0140a0001c0001t0015g0141 | 3 | HG02055.hp1 HG02257.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-156-8403A>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102821931 | ||||||
| chr14:102822035
|
C | T | 2 | a0001c0001t0027g0288a0001c0001t0027g0289 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-156-8299C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102822035 | ||||||
| chr14:102822515
|
C | T | 2 | a0001c0001t0002g0065a0001c0001t0043g0031 | 2 | HG02165.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.-156-7819C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102822515 | ||||||
| chr14:102822543
|
T | G | 1 | a0002c0007t0001g0273 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-156-7791T>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102822543 | ||||||
| chr14:102822754
|
C | T | 8 | a0001c0001t0013g0262a0001c0001t0013g0263a0001c0001t0013g0293others(5): Show | 8 | HG01167.hp1 HG01169.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-156-7580C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102822754 | ||||||
| chr14:102822862
|
C | T | 1 | a0001c0001t0019g0055 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-156-7472C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102822862 | ||||||
| chr14:102823006
|
C | A | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-156-7328C>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102823006 | ||||||
| chr14:102823006
|
C | CA | 104 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(101): Show | 104 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.-156-7314dupA | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102823006 | |||||
| chr14:102823300
|
T | C | 76 | a0001c0001t0001g0184a0001c0001t0062g0247a0001c0001t0063g0223others(73): Show | 76 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.-156-7034T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102823300 | ||||||
| chr14:102823448
|
T | C | 1 | a0001c0001t0002g0083 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-156-6886T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102823448 | ||||||
| chr14:102823465
|
A | G | 1 | a0001c0001t0002g0107 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-156-6869A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102823465 | ||||||
| chr14:102823660
|
G | A | 1 | a0001c0001t0019g0082 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-156-6674G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102823660 | ||||||
| chr14:102823769
|
C | A | 1 | a0001c0001t0012g0124 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-156-6565C>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102823769 | ||||||
| chr14:102823851
|
A | G | 1 | a0001c0001t0007g0008 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-156-6483A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102823851 | ||||||
| chr14:102823880
|
G | GCAGCCT | 126 | a0001c0001t0001g0184a0001c0001t0003g0100a0001c0001t0013g0262others(123): Show | 126 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.-156-6451_-156-645 others(10): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102823880 | |||||
| chr14:102823884
|
T | C | 127 | a0001c0001t0001g0184a0001c0001t0003g0100a0001c0001t0013g0262others(124): Show | 127 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.-156-6450T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102823884 | ||||||
| chr14:102823924
|
T | C | 1 | a0001c0001t0019g0055 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-156-6410T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102823924 | ||||||
| chr14:102823925
|
G | C | 12 | a0001c0001t0062g0247a0002c0002t0001g0225a0002c0002t0001g0236others(9): Show | 12 | HG00140.hp1 HG00609.hp2 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.-156-6409G>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102823925 | ||||||
| chr14:102824331
|
C | T | 1 | a0002c0002t0001g0232 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-156-6003C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102824331 | ||||||
| chr14:102824340
|
G | C | 6 | a0001c0001t0003g0100a0001c0001t0005g0009a0001c0003t0003g0182others(3): Show | 6 | HG02630.hp2 HG02723.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-156-5994G>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102824340 | ||||||
| chr14:102824388
|
A | G | 5 | a0001c0001t0007g0119a0001c0001t0012g0124a0001c0001t0013g0263others(2): Show | 5 | HG02486.hp2 HG02559.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-156-5946A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102824388 | ||||||
| chr14:102824427
|
T | A | 1 | a0001c0001t0031g0183 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-156-5907T>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102824427 | ||||||
| chr14:102824601
|
G | T | 31 | a0001c0003t0003g0182a0001c0003t0005g0181a0001c0003t0034g0003others(28): Show | 31 | HG00099.hp1 HG00733.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.-156-5733G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102824601 | ||||||
| chr14:102824694
|
G | A | 43 | a0001c0001t0010g0018a0001c0001t0010g0019a0001c0001t0010g0020others(40): Show | 43 | HG00099.hp1 HG00639.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.-156-5640G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102824694 | ||||||
| chr14:102824951
|
C | T | 1 | a0002c0002t0003g0151 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-156-5383C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102824951 | ||||||
| chr14:102824984
|
G | A | 1 | a0001c0001t0019g0055 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-156-5350G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102824984 | ||||||
| chr14:102825148
|
C | T | 1 | a0002c0002t0059g0239 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-156-5186C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102825148 | ||||||
| chr14:102825187
|
G | A | 1 | a0001c0001t0022g0050 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-156-5147G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102825187 | ||||||
| chr14:102825194
|
C | T | 1 | a0001c0001t0031g0183 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-156-5140C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102825194 | ||||||
| chr14:102825229
|
T | G | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-156-5105T>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102825229 | ||||||
| chr14:102825245
|
T | C | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-156-5089T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102825245 | ||||||
| chr14:102825361
|
A | G | 171 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(168): Show | 171 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.-156-4973A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102825361 | ||||||
| chr14:102825523
|
G | A | 1 | a0002c0002t0001g0193 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-156-4811G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102825523 | ||||||
| chr14:102825551
|
T | C | 1 | a0001c0001t0022g0050 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-156-4783T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102825551 | ||||||
| chr14:102825624
|
G | A | 1 | a0002c0002t0006g0156 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-156-4710G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102825624 | ||||||
| chr14:102825772
|
G | A | 11 | a0001c0001t0005g0009a0001c0001t0005g0010a0001c0001t0005g0011others(8): Show | 11 | HG01884.hp2 HG02055.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.-156-4562G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102825772 | ||||||
| chr14:102825773
|
T | C | 169 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(166): Show | 169 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.-156-4561T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102825773 | ||||||
| chr14:102825774
|
G | A | 2 | a0001c0003t0003g0182a0001c0003t0005g0181 | 2 | HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-156-4560G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102825774 | ||||||
| chr14:102825810
|
A | G | 2 | a0002c0002t0001g0261a0002c0002t0055g0260 | 2 | HG00733.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.-156-4524A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102825810 | ||||||
| chr14:102825813
|
G | A | 112 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(109): Show | 112 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.-156-4521G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102825813 | ||||||
| chr14:102825854
|
G | A | 112 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(109): Show | 112 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.-156-4480G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102825854 | ||||||
| chr14:102825942
|
C | T | 5 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(2): Show | 5 | HG00738.hp2 HG01167.hp2 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.-156-4392C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102825942 | ||||||
| chr14:102826018
|
C | T | 1 | a0001c0001t0050g0180 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-156-4316C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102826018 | ||||||
| chr14:102826151
|
C | G | 4 | a0001c0003t0003g0182a0001c0003t0005g0181a0001c0003t0034g0003others(1): Show | 4 | HG02630.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-156-4183C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102826151 | ||||||
| chr14:102826460
|
C | T | 1 | a0001c0001t0036g0146 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-156-3874C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102826460 | ||||||
| chr14:102826490
|
C | A | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-156-3844C>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102826490 | ||||||
| chr14:102826509
|
A | G | 1 | a0002c0002t0003g0153 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-156-3825A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102826509 | ||||||
| chr14:102826597
|
C | T | 1 | a0001c0003t0034g0003 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-156-3737C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102826597 | ||||||
| chr14:102826622
|
A | G | 162 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(159): Show | 162 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.-156-3712A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102826622 | ||||||
| chr14:102826633
|
A | G | 3 | a0002c0002t0001g0285a0002c0002t0001g0286a0002c0002t0001g0287 | 3 | NA18969.hp1 NA19054.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.-156-3701A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102826633 | ||||||
| chr14:102826718
|
C | T | 1 | a0001c0001t0007g0119 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-156-3616C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102826718 | ||||||
| chr14:102826844
|
C | T | 1 | a0001c0001t0020g0054 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-156-3490C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102826844 | ||||||
| chr14:102826906
|
G | A | 1 | a0002c0002t0059g0239 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-156-3428G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102826906 | ||||||
| chr14:102826975
|
C | G | 18 | a0001c0001t0005g0009a0001c0001t0005g0010a0001c0001t0005g0011others(15): Show | 18 | HG01109.hp2 HG01884.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.-156-3359C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102826975 | ||||||
| chr14:102827043
|
C | G | 3 | a0001c0001t0017g0143a0001c0001t0017g0144a0001c0001t0017g0145 | 3 | HG02109.hp2 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-156-3291C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102827043 | ||||||
| chr14:102827233
|
T | C | 1 | a0002c0002t0003g0164 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-156-3101T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102827233 | ||||||
| chr14:102827277
|
T | C | 1 | a0001c0001t0042g0005 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-156-3057T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102827277 | ||||||
| chr14:102827281
|
G | A | 1 | a0001c0001t0002g0032 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-156-3053G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102827281 | ||||||
| chr14:102827379
|
C | T | 168 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(165): Show | 168 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.-156-2955C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102827379 | ||||||
| chr14:102827508
|
T | C | 163 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(160): Show | 163 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.-156-2826T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102827508 | ||||||
| chr14:102827740
|
C | T | 2 | a0001c0001t0011g0127a0001c0001t0028g0138 | 2 | HG03710.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-156-2594C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102827740 | ||||||
| chr14:102827938
|
G | A | 1 | a0002c0002t0003g0128 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-156-2396G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102827938 | ||||||
| chr14:102828063
|
C | T | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-156-2271C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102828063 | ||||||
| chr14:102828064
|
G | A | 1 | a0001c0001t0003g0100 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-156-2270G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102828064 | ||||||
| chr14:102828380
|
A | G | 1 | a0002c0002t0001g0241 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-156-1954A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102828380 | ||||||
| chr14:102828446
|
A | C | 1 | a0001c0001t0003g0100 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-156-1888A>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102828446 | ||||||
| chr14:102828602
|
G | A | 2 | a0001c0001t0067g0125a0001c0001t0068g0029 | 2 | HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-156-1732G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102828602 | ||||||
| chr14:102828737
|
G | A | 1 | a0002c0002t0001g0278 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-156-1597G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102828737 | ||||||
| chr14:102828864
|
G | A | 1 | a0001c0001t0002g0071 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-156-1470G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102828864 | ||||||
| chr14:102828952
|
G | C | 1 | a0001c0001t0010g0020 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-156-1382G>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102828952 | ||||||
| chr14:102828985
|
C | A | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-156-1349C>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102828985 | ||||||
| chr14:102829029
|
G | T | 1 | a0002c0002t0001g0249 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-156-1305G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102829029 | ||||||
| chr14:102829061
|
T | A | 1 | a0002c0002t0006g0156 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-156-1273T>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102829061 | ||||||
| chr14:102829125
|
A | G | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-156-1209A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102829125 | ||||||
| chr14:102829250
|
G | A | 1 | a0001c0001t0003g0085 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-156-1084G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102829250 | ||||||
| chr14:102829473
|
C | G | 3 | a0001c0001t0015g0139a0001c0001t0015g0140a0001c0001t0015g0141 | 3 | HG02055.hp1 HG02257.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-156-861C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102829473 | ||||||
| chr14:102829980
|
A | AAAATAAA others(9): Show |
1 | a0001c0001t0002g0110 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-156-350_-156-335d others(18): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 102829980 | |||||
| chr14:102830117
|
G | A | 1 | a0002c0002t0001g0199 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-156-217G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102830117 | ||||||
| chr14:102830121
|
C | T | 1 | a0001c0001t0042g0005 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-156-213C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102830121 | ||||||
| chr14:102830236
|
A | G | 1 | a0001c0001t0010g0053 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-156-98A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 1/11 | chr14 | 102830236 | ||||||
| chr14:102830488
|
A | ATTG | 163 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(160): Show | 163 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.-18+17_-18+19dupTT others(1): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102830488 | |||||
| chr14:102830495
|
T | A | 2 | a0001c0001t0031g0183a0001c0001t0042g0005 | 2 | HG01099.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-18+23T>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102830495 | ||||||
| chr14:102830778
|
T | C | 2 | a0001c0001t0031g0183a0001c0001t0042g0005 | 2 | HG01099.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-18+306T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102830778 | ||||||
| chr14:102831236
|
A | C | 1 | a0001c0001t0002g0113 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-18+764A>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102831236 | ||||||
| chr14:102831282
|
A | G | 1 | a0001c0001t0008g0046 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-18+810A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102831282 | ||||||
| chr14:102831345
|
C | G | 1 | a0001c0001t0026g0078 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-18+873C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102831345 | ||||||
| chr14:102831510
|
G | C | 113 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(110): Show | 113 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.-18+1038G>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102831510 | ||||||
| chr14:102831531
|
C | T | 1 | a0002c0002t0003g0006 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-18+1059C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102831531 | ||||||
| chr14:102831730
|
C | T | 1 | a0001c0001t0003g0100 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-18+1258C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102831730 | ||||||
| chr14:102831820
|
A | G | 1 | a0002c0002t0001g0287 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-18+1348A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102831820 | ||||||
| chr14:102831993
|
G | C | 2 | a0001c0001t0019g0082a0001c0001t0051g0284 | 2 | HG02970.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-18+1521G>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102831993 | ||||||
| chr14:102832139
|
CATG | C | 9 | a0001c0001t0011g0127a0001c0001t0011g0147a0001c0001t0011g0148others(6): Show | 9 | HG01496.hp1 HG01928.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-18+1670_-18+1672d others(5): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102832139 | |||||
| chr14:102832155
|
A | G | 11 | a0001c0001t0005g0009a0001c0001t0005g0010a0001c0001t0005g0011others(8): Show | 11 | HG02055.hp2 HG02109.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.-18+1683A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102832155 | ||||||
| chr14:102832359
|
C | T | 9 | a0001c0001t0011g0127a0001c0001t0011g0147a0001c0001t0011g0148others(6): Show | 9 | HG01496.hp1 HG01928.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-18+1887C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102832359 | ||||||
| chr14:102832363
|
C | T | 2 | a0001c0001t0050g0180a0002c0002t0001g0240 | 2 | HG01884.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.-18+1891C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102832363 | ||||||
| chr14:102832400
|
G | A | 3 | a0001c0001t0012g0001a0001c0001t0012g0179a0001c0001t0050g0180 | 3 | HG01884.hp2 HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-18+1928G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102832400 | ||||||
| chr14:102832439
|
C | T | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-18+1967C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102832439 | ||||||
| chr14:102832503
|
G | A | 1 | a0002c0002t0001g0234 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-18+2031G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102832503 | ||||||
| chr14:102832545
|
G | A | 2 | a0001c0001t0031g0183a0001c0001t0042g0005 | 2 | HG01099.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-18+2073G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102832545 | ||||||
| chr14:102832717
|
A | C | 1 | a0001c0001t0062g0247 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-18+2245A>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102832717 | ||||||
| chr14:102832889
|
G | A | 1 | a0002c0002t0006g0159 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-18+2417G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102832889 | ||||||
| chr14:102832956
|
C | A | 1 | a0001c0001t0002g0106 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-18+2484C>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102832956 | ||||||
| chr14:102833012
|
G | A | 4 | a0002c0002t0001g0196a0002c0002t0001g0201a0002c0002t0001g0210others(1): Show | 4 | NA18967.hp2 NA18973.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+2540G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102833012 | ||||||
| chr14:102833043
|
C | A | 3 | a0001c0001t0012g0001a0001c0001t0012g0179a0001c0001t0050g0180 | 3 | HG01884.hp2 HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-18+2571C>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102833043 | ||||||
| chr14:102833157
|
T | C | 1 | a0001c0001t0033g0123 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-18+2685T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102833157 | ||||||
| chr14:102833379
|
T | C | 171 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(168): Show | 171 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.-18+2907T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102833379 | ||||||
| chr14:102833547
|
G | T | 2 | a0002c0002t0001g0285a0002c0002t0001g0286 | 2 | NA18969.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.-18+3075G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102833547 | ||||||
| chr14:102833629
|
G | A | 1 | a0001c0001t0003g0100 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-18+3157G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102833629 | ||||||
| chr14:102833632
|
A | G | 8 | a0001c0001t0002g0026a0001c0001t0002g0058a0001c0001t0002g0067others(5): Show | 8 | HG01192.hp2 HG01358.hp1 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.-18+3160A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102833632 | ||||||
| chr14:102833994
|
G | GA | 129 | a0001c0001t0001g0184a0001c0001t0002g0056a0001c0001t0003g0100others(126): Show | 129 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.-18+3530dupA | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102833994 | |||||
| chr14:102833994
|
G | GAA | 137 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(134): Show | 137 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.-18+3529_-18+3530d others(4): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102833994 | |||||
| chr14:102833994
|
G | GGA | 19 | a0001c0001t0011g0127a0001c0001t0011g0147a0001c0001t0011g0148others(16): Show | 19 | HG01496.hp1 HG01928.hp2 HG01993.hp1 others(16): Show |
intron_variant | MODIFIER | c.-18+3522_-18+3523i others(4): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102833994 | ||||||
| chr14:102834187
|
C | T | 1 | a0001c0001t0003g0100 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-18+3715C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102834187 | ||||||
| chr14:102834265
|
A | G | 9 | a0001c0001t0015g0139a0001c0001t0015g0140a0001c0001t0015g0141others(6): Show | 9 | HG02055.hp1 HG02109.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-18+3793A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102834265 | ||||||
| chr14:102834293
|
C | T | 1 | a0001c0001t0048g0116 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-18+3821C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102834293 | ||||||
| chr14:102834309
|
A | T | 4 | a0001c0001t0012g0098a0001c0001t0012g0124a0001c0001t0020g0054others(1): Show | 4 | HG01109.hp2 HG02559.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+3837A>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102834309 | ||||||
| chr14:102834553
|
G | T | 5 | a0001c0001t0017g0143a0001c0001t0017g0144a0001c0001t0017g0145others(2): Show | 5 | HG02109.hp2 HG02922.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18+4081G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102834553 | ||||||
| chr14:102834687
|
C | CA | 8 | a0001c0001t0031g0183a0001c0001t0042g0005a0001c0004t0039g0002others(5): Show | 8 | HG01099.hp2 HG01123.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.-18+4235dupA | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102834687 | |||||
| chr14:102834687
|
C | CAAAA | 46 | a0001c0001t0002g0041a0001c0001t0002g0065a0001c0001t0002g0106others(43): Show | 46 | HG00639.hp2 HG00733.hp2 HG01109.hp2 others(43): Show |
intron_variant | MODIFIER | c.-18+4232_-18+4235d others(6): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102834687 | |||||
| chr14:102834687
|
C | CAAAAA | 98 | a0001c0001t0002g0025a0001c0001t0002g0027a0001c0001t0002g0032others(95): Show | 98 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.-18+4231_-18+4235d others(7): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102834687 | |||||
| chr14:102834687
|
C | CAAAAAA | 8 | a0001c0001t0002g0026a0001c0001t0002g0109a0001c0001t0002g0120others(5): Show | 8 | HG00621.hp2 HG01952.hp1 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-18+4230_-18+4235d others(8): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102834687 | |||||
| chr14:102834719
|
C | T | 18 | a0001c0001t0011g0127a0001c0001t0011g0147a0001c0001t0011g0148others(15): Show | 18 | HG01496.hp1 HG01928.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.-18+4247C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102834719 | ||||||
| chr14:102834735
|
C | T | 171 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(168): Show | 171 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.-18+4263C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102834735 | ||||||
| chr14:102834863
|
A | C | 171 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(168): Show | 171 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.-18+4391A>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102834863 | ||||||
| chr14:102834869
|
CAATTGCA others(11): Show |
C | 2 | a0001c0001t0031g0183a0001c0001t0042g0005 | 2 | HG01099.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-18+4403_-18+4420d others(20): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102834869 | |||||
| chr14:102834925
|
T | A | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-18+4453T>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102834925 | ||||||
| chr14:102835053
|
C | G | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-18+4581C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102835053 | ||||||
| chr14:102835181
|
G | A | 5 | a0001c0001t0017g0143a0001c0001t0017g0144a0001c0001t0017g0145others(2): Show | 5 | HG02109.hp2 HG02922.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18+4709G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102835181 | ||||||
| chr14:102835237
|
A | G | 155 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(152): Show | 155 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.-18+4765A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102835237 | ||||||
| chr14:102835250
|
A | G | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-18+4778A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102835250 | ||||||
| chr14:102835351
|
C | T | 4 | a0001c0003t0003g0182a0001c0003t0005g0181a0001c0003t0034g0003others(1): Show | 4 | HG02630.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+4879C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102835351 | ||||||
| chr14:102835586
|
C | T | 3 | a0002c0002t0001g0215a0002c0002t0009g0197a0002c0002t0009g0216 | 3 | HG01175.hp1 HG01257.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.-18+5114C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102835586 | ||||||
| chr14:102835650
|
G | A | 1 | a0001c0001t0033g0123 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-18+5178G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102835650 | ||||||
| chr14:102835713
|
T | C | 1 | a0001c0003t0037g0004 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-18+5241T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102835713 | ||||||
| chr14:102835960
|
T | G | 2 | a0002c0002t0001g0210a0002c0002t0001g0211 | 2 | NA18967.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.-18+5488T>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102835960 | ||||||
| chr14:102836220
|
C | G | 5 | a0001c0001t0005g0011a0001c0001t0005g0013a0001c0001t0005g0014others(2): Show | 5 | HG02055.hp2 HG02809.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18+5748C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102836220 | ||||||
| chr14:102836281
|
A | T | 1 | a0001c0001t0003g0100 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-18+5809A>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102836281 | ||||||
| chr14:102836463
|
C | T | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-18+5991C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102836463 | ||||||
| chr14:102836616
|
G | A | 19 | a0001c0001t0010g0018a0001c0001t0010g0019a0001c0001t0010g0020others(16): Show | 19 | HG00639.hp2 HG01109.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.-18+6144G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102836616 | ||||||
| chr14:102836974
|
A | T | 171 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(168): Show | 171 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.-18+6502A>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102836974 | ||||||
| chr14:102836982
|
G | A | 1 | a0002c0002t0001g0207 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-18+6510G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102836982 | ||||||
| chr14:102836984
|
A | G | 4 | a0002c0002t0001g0187a0002c0002t0001g0188a0002c0002t0001g0189others(1): Show | 4 | HG00558.hp2 NA18944.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+6512A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102836984 | ||||||
| chr14:102837111
|
A | C | 1 | a0002c0002t0001g0281 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-18+6639A>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102837111 | ||||||
| chr14:102837118
|
TTG | T | 135 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0032others(132): Show | 135 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.-18+6670_-18+6671d others(4): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102837118 | |||||
| chr14:102837118
|
TTGTGTG | T | 17 | a0001c0001t0010g0018a0001c0001t0010g0019a0001c0001t0010g0020others(14): Show | 17 | HG00639.hp2 HG01109.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-18+6666_-18+6671d others(8): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102837118 | |||||
| chr14:102837120
|
G | T | 6 | a0001c0001t0002g0025a0001c0001t0002g0059a0001c0001t0004g0035others(3): Show | 6 | HG02615.hp1 HG03540.hp2 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18+6648G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102837120 | ||||||
| chr14:102837122
|
G | T | 124 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0032others(121): Show | 124 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.-18+6650G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102837122 | ||||||
| chr14:102837126
|
G | T | 17 | a0001c0001t0010g0018a0001c0001t0010g0019a0001c0001t0010g0020others(14): Show | 17 | HG00639.hp2 HG01109.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-18+6654G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102837126 | ||||||
| chr14:102837139
|
TG | T | 3 | a0001c0001t0002g0025a0001c0001t0004g0035a0001c0001t0004g0061 | 3 | NA18964.hp1 NA18966.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.-18+6668delG | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102837139 | ||||||
| chr14:102837142
|
G | T | 146 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(143): Show | 146 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.-18+6670G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102837142 | ||||||
| chr14:102837143
|
T | TG | 5 | a0001c0001t0021g0057a0001c0001t0021g0099a0001c0001t0033g0123others(2): Show | 5 | HG00733.hp2 HG01123.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18+6671_-18+6672i others(3): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102837143 | ||||||
| chr14:102837144
|
T | G | 2 | a0001c0001t0003g0100a0001c0001t0068g0029 | 2 | HG02723.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-18+6672T>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102837144 | ||||||
| chr14:102837146
|
T | G | 1 | a0001c0001t0003g0100 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-18+6674T>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102837146 | ||||||
| chr14:102837150
|
T | G | 7 | a0001c0001t0012g0001a0001c0001t0012g0179a0001c0001t0021g0057others(4): Show | 7 | HG00733.hp2 HG01123.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18+6678T>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102837150 | ||||||
| chr14:102837150
|
T | TG | 36 | a0001c0001t0027g0288a0002c0002t0001g0206a0002c0002t0001g0248others(33): Show | 36 | HG00099.hp1 HG00733.hp1 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.-18+6687dupG | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102837150 | |||||
| chr14:102837153
|
G | C | 1 | a0001c0001t0019g0055 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-18+6681G>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102837153 | ||||||
| chr14:102837177
|
T | C | 131 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(128): Show | 131 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.-18+6705T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102837177 | ||||||
| chr14:102837264
|
G | A | 1 | a0002c0002t0001g0292 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-18+6792G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102837264 | ||||||
| chr14:102837434
|
C | T | 2 | a0001c0001t0021g0057a0001c0001t0021g0099 | 2 | HG01123.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.-18+6962C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102837434 | ||||||
| chr14:102837641
|
TA | T | 20 | a0001c0001t0003g0100a0001c0001t0005g0009a0001c0001t0005g0010others(17): Show | 20 | HG00733.hp2 HG01099.hp2 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.-18+7181delA | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102837641 | |||||
| chr14:102837757
|
G | A | 1 | a0002c0002t0001g0278 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-18+7285G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102837757 | ||||||
| chr14:102838087
|
C | T | 1 | a0001c0001t0061g0264 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-18+7615C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102838087 | ||||||
| chr14:102838088
|
C | T | 141 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(138): Show | 141 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.-18+7616C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102838088 | ||||||
| chr14:102838107
|
G | A | 10 | a0001c0001t0013g0262a0001c0001t0013g0263a0001c0001t0013g0293others(7): Show | 10 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.-18+7635G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102838107 | ||||||
| chr14:102838597
|
G | A | 1 | a0001c0001t0025g0052 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-18+8125G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102838597 | ||||||
| chr14:102838740
|
G | T | 141 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(138): Show | 141 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.-18+8268G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102838740 | ||||||
| chr14:102838895
|
A | T | 1 | a0002c0002t0001g0249 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-18+8423A>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102838895 | ||||||
| chr14:102838949
|
C | A | 1 | a0002c0002t0001g0188 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-18+8477C>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102838949 | ||||||
| chr14:102838984
|
T | C | 3 | a0001c0001t0002g0083a0001c0001t0002g0084a0001c0001t0002g0086 | 3 | HG02129.hp1 NA19070.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.-18+8512T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102838984 | ||||||
| chr14:102838986
|
C | T | 3 | a0001c0001t0015g0139a0001c0001t0015g0140a0001c0001t0015g0141 | 3 | HG02055.hp1 HG02257.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-18+8514C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102838986 | ||||||
| chr14:102839072
|
C | G | 8 | a0001c0001t0005g0009a0001c0001t0005g0010a0001c0001t0005g0011others(5): Show | 8 | HG02055.hp2 HG02809.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-18+8600C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102839072 | ||||||
| chr14:102839210
|
C | CCT | 41 | a0001c0001t0002g0027a0001c0001t0002g0041a0001c0001t0002g0044others(38): Show | 41 | HG00544.hp2 HG00609.hp1 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.-18+8738_-18+8739i others(4): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102839210 | ||||||
| chr14:102839210
|
C | CCTT | 16 | a0001c0001t0002g0025a0001c0001t0002g0071a0001c0001t0002g0072others(13): Show | 16 | HG01993.hp2 HG02896.hp1 HG02896.hp2 others(13): Show |
intron_variant | MODIFIER | c.-18+8738_-18+8739i others(5): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102839210 | ||||||
| chr14:102839210
|
C | CCTTT | 9 | a0001c0001t0004g0126a0001c0001t0007g0008a0001c0001t0007g0094others(6): Show | 9 | HG01081.hp2 HG02451.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-18+8738_-18+8739i others(6): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102839210 | ||||||
| chr14:102839210
|
C | CT | 53 | a0001c0001t0003g0100a0001c0001t0010g0018a0001c0001t0010g0019others(50): Show | 53 | HG00639.hp2 HG00733.hp2 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.-18+8766dupT | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102839210 | |||||
| chr14:102839210
|
C | CTT | 21 | a0001c0001t0011g0127a0001c0001t0011g0150a0001c0001t0011g0165others(18): Show | 21 | HG00733.hp1 HG01123.hp1 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.-18+8765_-18+8766d others(4): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102839210 | |||||
| chr14:102839210
|
C | CTTTTTTT others(7): Show |
1 | a0001c0001t0005g0137 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-18+8753_-18+8766d others(16): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102839210 | |||||
| chr14:102839210
|
CTTTTTTT others(1): Show |
C | 43 | a0001c0001t0002g0026a0001c0001t0002g0032a0001c0001t0002g0036others(40): Show | 43 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.-18+8759_-18+8766d others(10): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102839210 | |||||
| chr14:102839210
|
CTTTTTTT others(4): Show |
C | 5 | a0001c0003t0003g0182a0001c0003t0005g0181a0001c0003t0034g0003others(2): Show | 5 | HG00099.hp1 HG02630.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18+8756_-18+8766d others(13): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102839210 | |||||
| chr14:102839210
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0012g0024 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-18+8754_-18+8766d others(15): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102839210 | |||||
| chr14:102839210
|
CTTTTTTT others(7): Show |
C | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-18+8753_-18+8766d others(16): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102839210 | |||||
| chr14:102839218
|
T | C | 2 | a0001c0001t0002g0067a0001c0001t0047g0028 | 2 | HG01192.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.-18+8746T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102839218 | ||||||
| chr14:102839219
|
T | C | 42 | a0001c0001t0002g0026a0001c0001t0002g0032a0001c0001t0002g0036others(39): Show | 42 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.-18+8747T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102839219 | ||||||
| chr14:102839220
|
T | C | 1 | a0001c0001t0016g0103 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-18+8748T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102839220 | ||||||
| chr14:102839279
|
C | T | 1 | a0001c0001t0004g0040 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-18+8807C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102839279 | ||||||
| chr14:102839762
|
A | C | 3 | a0001c0001t0012g0001a0001c0001t0012g0179a0001c0001t0050g0180 | 3 | HG01884.hp2 HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-18+9290A>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102839762 | ||||||
| chr14:102839769
|
A | T | 171 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(168): Show | 171 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.-18+9297A>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102839769 | ||||||
| chr14:102839822
|
G | A | 1 | a0002c0002t0001g0282 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-18+9350G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102839822 | ||||||
| chr14:102839878
|
G | A | 163 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(160): Show | 163 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.-18+9406G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102839878 | ||||||
| chr14:102839894
|
T | G | 1 | a0002c0002t0001g0234 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-18+9422T>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102839894 | ||||||
| chr14:102840318
|
A | G | 1 | a0002c0002t0001g0267 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-18+9846A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102840318 | ||||||
| chr14:102840404
|
A | T | 12 | a0001c0001t0005g0009a0001c0001t0005g0010a0001c0001t0005g0011others(9): Show | 12 | HG02055.hp2 HG02630.hp2 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.-18+9932A>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102840404 | ||||||
| chr14:102840422
|
G | T | 1 | a0001c0001t0002g0118 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-18+9950G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102840422 | ||||||
| chr14:102840458
|
T | A | 1 | a0001c0001t0035g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-18+9986T>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102840458 | ||||||
| chr14:102840622
|
A | G | 4 | a0001c0001t0002g0025a0001c0001t0002g0071a0001c0001t0002g0072others(1): Show | 4 | HG01993.hp2 NA18966.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+10150A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102840622 | ||||||
| chr14:102840681
|
A | C | 3 | a0001c0001t0012g0001a0001c0001t0012g0179a0001c0001t0050g0180 | 3 | HG01884.hp2 HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-18+10209A>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102840681 | ||||||
| chr14:102840773
|
A | C | 131 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(128): Show | 131 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.-18+10301A>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102840773 | ||||||
| chr14:102841175
|
G | C | 1 | a0001c0001t0042g0005 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-18+10703G>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102841175 | ||||||
| chr14:102841318
|
G | C | 159 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(156): Show | 159 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.-18+10846G>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102841318 | ||||||
| chr14:102841333
|
C | A | 1 | a0001c0001t0003g0100 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-18+10861C>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102841333 | ||||||
| chr14:102841347
|
G | C | 1 | a0001c0001t0067g0125 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-18+10875G>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102841347 | ||||||
| chr14:102841441
|
A | G | 9 | a0001c0001t0011g0127a0001c0001t0011g0147a0001c0001t0011g0148others(6): Show | 9 | HG01496.hp1 HG01928.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-18+10969A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102841441 | ||||||
| chr14:102841482
|
G | A | 1 | a0002c0002t0001g0240 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-18+11010G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102841482 | ||||||
| chr14:102841520
|
C | T | 1 | a0002c0002t0001g0241 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-18+11048C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102841520 | ||||||
| chr14:102841668
|
C | T | 3 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0002g0087 | 3 | HG01993.hp2 NA18969.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.-18+11196C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102841668 | ||||||
| chr14:102841696
|
G | T | 9 | a0001c0001t0010g0018a0001c0001t0010g0019a0001c0001t0010g0020others(6): Show | 9 | HG00639.hp2 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-18+11224G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102841696 | ||||||
| chr14:102841697
|
T | C | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-18+11225T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102841697 | ||||||
| chr14:102841765
|
A | G | 3 | a0002c0002t0001g0199a0002c0002t0001g0200a0002c0002t0001g0217 | 3 | NA18952.hp2 NA19009.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-18+11293A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102841765 | ||||||
| chr14:102841864
|
G | A | 1 | a0001c0001t0004g0126 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-18+11392G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102841864 | ||||||
| chr14:102842040
|
TTGAAGAG | T | 3 | a0002c0002t0001g0191a0002c0002t0001g0229a0002c0002t0001g0233 | 3 | NA18950.hp2 NA18962.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.-18+11570_-18+1157 others(11): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102842040 | |||||
| chr14:102842148
|
G | A | 3 | a0001c0001t0017g0143a0001c0001t0017g0144a0001c0001t0017g0145 | 3 | HG02109.hp2 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-18+11676G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102842148 | ||||||
| chr14:102842295
|
A | G | 1 | a0001c0001t0050g0180 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-18+11823A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102842295 | ||||||
| chr14:102842386
|
G | A | 1 | a0002c0002t0001g0234 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-18+11914G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102842386 | ||||||
| chr14:102842391
|
A | G | 1 | a0001c0001t0011g0150 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-18+11919A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102842391 | ||||||
| chr14:102842762
|
A | C | 24 | a0001c0001t0010g0018a0001c0001t0010g0019a0001c0001t0010g0020others(21): Show | 24 | HG00639.hp2 HG00733.hp2 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.-18+12290A>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102842762 | ||||||
| chr14:102842858
|
T | A | 1 | a0001c0001t0005g0013 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-18+12386T>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102842858 | ||||||
| chr14:102842875
|
T | C | 1 | a0001c0001t0002g0083 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-18+12403T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102842875 | ||||||
| chr14:102843054
|
T | C | 23 | a0001c0001t0005g0009a0001c0001t0005g0010a0001c0001t0005g0011others(20): Show | 23 | HG01069.hp1 HG01071.hp2 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.-18+12582T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102843054 | ||||||
| chr14:102843151
|
C | T | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-18+12679C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102843151 | ||||||
| chr14:102843285
|
G | A | 173 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(170): Show | 173 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.-18+12813G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102843285 | ||||||
| chr14:102843304
|
TAGAA | T | 9 | a0001c0001t0015g0139a0001c0001t0015g0140a0001c0001t0015g0141others(6): Show | 9 | HG02055.hp1 HG02109.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-18+12838_-18+1284 others(8): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102843304 | |||||
| chr14:102843309
|
A | G | 1 | a0001c0001t0005g0016 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-18+12837A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102843309 | ||||||
| chr14:102843406
|
C | T | 113 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(110): Show | 113 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.-18+12934C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102843406 | ||||||
| chr14:102843521
|
A | G | 2 | a0001c0001t0011g0147a0001c0001t0011g0148 | 2 | HG01496.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.-18+13049A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102843521 | ||||||
| chr14:102843671
|
G | A | 1 | a0001c0001t0050g0180 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-18+13199G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102843671 | ||||||
| chr14:102844421
|
A | T | 172 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(169): Show | 172 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.-18+13949A>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102844421 | ||||||
| chr14:102844508
|
G | C | 1 | a0002c0002t0001g0267 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-18+14036G>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102844508 | ||||||
| chr14:102844755
|
A | G | 1 | a0001c0001t0038g0015 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-18+14283A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102844755 | ||||||
| chr14:102845132
|
G | A | 1 | a0001c0001t0069g0093 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-18+14660G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102845132 | ||||||
| chr14:102845155
|
C | G | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-18+14683C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102845155 | ||||||
| chr14:102845221
|
G | A | 2 | a0001c0001t0019g0082a0001c0001t0051g0284 | 2 | HG02970.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-18+14749G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102845221 | ||||||
| chr14:102845317
|
C | G | 1 | a0001c0001t0050g0180 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-18+14845C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102845317 | ||||||
| chr14:102845328
|
G | A | 1 | a0001c0001t0004g0171 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-18+14856G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102845328 | ||||||
| chr14:102845518
|
A | AT | 168 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(165): Show | 168 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.-18+15060dupT | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102845518 | |||||
| chr14:102845518
|
A | G | 1 | a0002c0002t0049g0129 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-18+15046A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102845518 | ||||||
| chr14:102845518
|
A | T | 2 | a0001c0001t0031g0183a0002c0002t0001g0188 | 2 | HG01099.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.-18+15046A>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102845518 | ||||||
| chr14:102845519
|
T | A | 1 | a0002c0002t0001g0282 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-18+15047T>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102845519 | ||||||
| chr14:102845808
|
G | T | 112 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(109): Show | 112 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.-18+15336G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102845808 | ||||||
| chr14:102845980
|
C | CA | 8 | a0002c0002t0001g0225a0002c0002t0001g0238a0002c0002t0001g0249others(5): Show | 8 | HG00140.hp1 HG00609.hp2 HG00735.hp2 others(5): Show |
intron_variant | MODIFIER | c.-18+15537dupA | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102845980 | |||||
| chr14:102845980
|
CA | C | 71 | a0001c0001t0003g0100a0001c0003t0034g0003a0002c0002t0001g0191others(68): Show | 71 | HG00099.hp1 HG00544.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.-18+15537delA | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102845980 | |||||
| chr14:102845980
|
CAAAA | C | 7 | a0001c0001t0012g0001a0001c0001t0012g0179a0001c0001t0021g0057others(4): Show | 7 | HG00733.hp2 HG01099.hp2 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18+15534_-18+1553 others(8): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102845980 | |||||
| chr14:102845980
|
CAAAAA | C | 19 | a0001c0001t0005g0137a0001c0001t0010g0018a0001c0001t0010g0019others(16): Show | 19 | HG00639.hp2 HG01109.hp2 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.-18+15533_-18+1553 others(9): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102845980 | |||||
| chr14:102845980
|
CAAAAAA | C | 16 | a0001c0001t0005g0009a0001c0001t0005g0010a0001c0001t0005g0011others(13): Show | 16 | HG01496.hp1 HG02055.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.-18+15532_-18+1553 others(10): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102845980 | |||||
| chr14:102845980
|
CAAAAAAA others(1): Show |
C | 7 | a0001c0001t0015g0139a0001c0001t0015g0140a0001c0001t0015g0141others(4): Show | 7 | HG02055.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18+15530_-18+1553 others(12): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102845980 | |||||
| chr14:102845980
|
CAAAAAAA others(14): Show |
C | 1 | a0001c0001t0050g0180 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-18+15517_-18+1553 others(25): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102845980 | |||||
| chr14:102846003
|
A | G | 18 | a0001c0001t0010g0018a0001c0001t0010g0019a0001c0001t0010g0020others(15): Show | 18 | HG00639.hp2 HG01109.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.-18+15531A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102846003 | ||||||
| chr14:102846004
|
AAAAAAT | A | 89 | a0001c0001t0002g0025a0001c0001t0002g0036a0001c0001t0002g0041others(86): Show | 89 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.-18+15534_-18+1553 others(10): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102846004 | |||||
| chr14:102846005
|
AAAAAT | A | 21 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0032others(18): Show | 21 | HG00544.hp2 HG00609.hp1 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.-18+15535_-18+1553 others(9): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102846005 | |||||
| chr14:102846010
|
T | C | 4 | a0001c0003t0003g0182a0001c0003t0005g0181a0001c0003t0034g0003others(1): Show | 4 | HG02630.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+15538T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102846010 | ||||||
| chr14:102846097
|
C | T | 2 | a0001c0001t0011g0127a0001c0001t0028g0138 | 2 | HG03710.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-18+15625C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102846097 | ||||||
| chr14:102846103
|
G | A | 12 | a0001c0001t0005g0009a0001c0001t0005g0010a0001c0001t0005g0011others(9): Show | 12 | HG02055.hp2 HG02630.hp2 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.-18+15631G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102846103 | ||||||
| chr14:102846274
|
C | T | 1 | a0001c0001t0012g0024 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-18+15802C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102846274 | ||||||
| chr14:102846396
|
A | T | 7 | a0001c0001t0012g0024a0001c0001t0012g0098a0001c0001t0012g0124others(4): Show | 7 | HG01109.hp2 HG02559.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-18+15924A>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102846396 | ||||||
| chr14:102846557
|
C | G | 2 | a0002c0002t0003g0152a0002c0002t0003g0164 | 2 | HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-18+16085C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102846557 | ||||||
| chr14:102846628
|
T | G | 66 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0032others(63): Show | 66 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.-18+16156T>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102846628 | ||||||
| chr14:102846638
|
T | TA | 28 | a0001c0001t0002g0041a0001c0001t0002g0084a0001c0001t0002g0106others(25): Show | 28 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.-18+16194dupA | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102846638 | |||||
| chr14:102846638
|
T | TAA | 89 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0036others(86): Show | 89 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.-18+16193_-18+1619 others(6): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102846638 | |||||
| chr14:102846638
|
T | TAAA | 17 | a0001c0001t0002g0025a0001c0001t0002g0032a0001c0001t0002g0056others(14): Show | 17 | HG01175.hp2 HG01358.hp1 HG02300.hp1 others(14): Show |
intron_variant | MODIFIER | c.-18+16192_-18+1619 others(7): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102846638 | |||||
| chr14:102846638
|
T | TAAAAAA | 11 | a0001c0001t0005g0009a0001c0001t0005g0010a0001c0001t0005g0011others(8): Show | 11 | HG01069.hp1 HG01071.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.-18+16189_-18+1619 others(10): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102846638 | |||||
| chr14:102846638
|
T | TAAAAAAA | 6 | a0001c0001t0005g0017a0001c0001t0005g0137a0001c0001t0011g0127others(3): Show | 6 | HG01928.hp2 HG02055.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18+16188_-18+1619 others(11): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102846638 | |||||
| chr14:102846638
|
T | TAAAAAAA others(3): Show |
2 | a0001c0003t0003g0182a0001c0003t0005g0181 | 2 | HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-18+16185_-18+1619 others(14): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102846638 | |||||
| chr14:102846638
|
T | TAAAAAAA others(25): Show |
1 | a0001c0003t0037g0004 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-18+16194_-18+1619 others(36): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102846638 | |||||
| chr14:102846638
|
T | TAAAAAAA others(29): Show |
1 | a0001c0003t0034g0003 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-18+16194_-18+1619 others(40): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102846638 | |||||
| chr14:102846638
|
TA | T | 15 | a0001c0001t0010g0018a0001c0001t0012g0001a0001c0001t0012g0179others(12): Show | 15 | HG00099.hp1 HG00323.hp2 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.-18+16194delA | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102846638 | |||||
| chr14:102846667
|
T | A | 1 | a0002c0002t0060g0213 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-18+16195T>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102846667 | ||||||
| chr14:102846672
|
C | T | 5 | a0001c0001t0017g0143a0001c0001t0017g0144a0001c0001t0017g0145others(2): Show | 5 | HG02109.hp2 HG02922.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18+16200C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102846672 | ||||||
| chr14:102846890
|
T | C | 1 | a0002c0002t0001g0258 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-18+16418T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102846890 | ||||||
| chr14:102847033
|
G | A | 4 | a0001c0003t0003g0182a0001c0003t0005g0181a0001c0003t0034g0003others(1): Show | 4 | HG02630.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+16561G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102847033 | ||||||
| chr14:102847231
|
T | C | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-18+16759T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102847231 | ||||||
| chr14:102847315
|
C | T | 4 | a0001c0003t0003g0182a0001c0003t0005g0181a0001c0003t0034g0003others(1): Show | 4 | HG02630.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18+16843C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102847315 | ||||||
| chr14:102847359
|
G | A | 1 | a0001c0001t0011g0148 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-18+16887G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102847359 | ||||||
| chr14:102847406
|
C | G | 1 | a0002c0002t0001g0259 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-18+16934C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102847406 | ||||||
| chr14:102847442
|
T | G | 5 | a0001c0001t0017g0143a0001c0001t0017g0144a0001c0001t0017g0145others(2): Show | 5 | HG02109.hp2 HG02922.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18+16970T>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102847442 | ||||||
| chr14:102847567
|
T | G | 2 | a0002c0002t0009g0214a0002c0002t0009g0228 | 2 | HG01081.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-18+17095T>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102847567 | ||||||
| chr14:102847881
|
T | G | 1 | a0002c0002t0052g0242 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-18+17409T>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102847881 | ||||||
| chr14:102847914
|
C | T | 1 | a0002c0002t0055g0260 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-18+17442C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102847914 | ||||||
| chr14:102848064
|
G | C | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-18+17592G>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102848064 | ||||||
| chr14:102848189
|
T | G | 1 | a0002c0002t0001g0267 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-18+17717T>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102848189 | ||||||
| chr14:102848230
|
G | A | 3 | a0001c0001t0002g0120a0001c0001t0004g0033a0001c0001t0045g0047 | 3 | HG00621.hp2 NA18944.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.-18+17758G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102848230 | ||||||
| chr14:102848620
|
G | A | 1 | a0001c0001t0035g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-18+18148G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102848620 | ||||||
| chr14:102848651
|
C | T | 1 | a0002c0002t0003g0131 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-18+18179C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102848651 | ||||||
| chr14:102848894
|
C | T | 1 | a0002c0002t0001g0248 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-18+18422C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102848894 | ||||||
| chr14:102848929
|
G | C | 2 | a0001c0001t0031g0183a0001c0001t0042g0005 | 2 | HG01099.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-18+18457G>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102848929 | ||||||
| chr14:102849256
|
T | C | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-18+18784T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102849256 | ||||||
| chr14:102849266
|
C | T | 1 | a0001c0001t0002g0083 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-18+18794C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102849266 | ||||||
| chr14:102849322
|
G | A | 6 | a0001c0001t0011g0147a0001c0001t0011g0148a0001c0001t0011g0150others(3): Show | 6 | HG01069.hp1 HG01071.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18+18850G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102849322 | ||||||
| chr14:102849915
|
T | C | 1 | a0001c0001t0005g0137 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-18+19443T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102849915 | ||||||
| chr14:102850329
|
A | G | 1 | a0001c0001t0017g0145 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-17-19856A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102850329 | ||||||
| chr14:102850685
|
G | A | 7 | a0001c0001t0011g0127a0001c0001t0021g0057a0001c0001t0021g0099others(4): Show | 7 | HG00733.hp2 HG01123.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-17-19500G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102850685 | ||||||
| chr14:102850688
|
T | TA | 25 | a0001c0001t0005g0009a0001c0001t0005g0010a0001c0001t0005g0011others(22): Show | 25 | HG00733.hp2 HG01074.hp2 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.-17-19473dupA | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102850688 | |||||
| chr14:102850688
|
T | TAA | 9 | a0001c0001t0005g0017a0001c0001t0011g0127a0001c0001t0012g0001others(6): Show | 9 | HG01109.hp2 HG02055.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-17-19474_-17-1947 others(6): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102850688 | |||||
| chr14:102850688
|
T | TAAA | 34 | a0001c0001t0002g0041a0001c0001t0002g0113a0001c0001t0002g0115others(31): Show | 34 | HG00639.hp2 HG01069.hp1 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.-17-19475_-17-1947 others(7): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102850688 | |||||
| chr14:102850688
|
T | TAAAA | 89 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(86): Show | 89 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.-17-19476_-17-1947 others(8): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102850688 | |||||
| chr14:102850688
|
T | TAAAAA | 19 | a0001c0001t0002g0036a0001c0001t0002g0058a0001c0001t0002g0083others(16): Show | 19 | HG00140.hp2 HG00609.hp1 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.-17-19477_-17-1947 others(9): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102850688 | |||||
| chr14:102850688
|
TA | T | 6 | a0001c0001t0050g0180a0002c0002t0001g0255a0002c0002t0003g0114others(3): Show | 6 | HG00099.hp1 HG00544.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.-17-19473delA | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102850688 | |||||
| chr14:102851014
|
G | A | 5 | a0001c0001t0017g0143a0001c0001t0017g0144a0001c0001t0017g0145others(2): Show | 5 | HG02109.hp2 HG02922.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17-19171G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102851014 | ||||||
| chr14:102851520
|
G | A | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-17-18665G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102851520 | ||||||
| chr14:102851731
|
A | C | 1 | a0001c0001t0002g0060 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-17-18454A>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102851731 | ||||||
| chr14:102851741
|
C | A | 1 | a0001c0001t0003g0100 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-17-18444C>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102851741 | ||||||
| chr14:102851837
|
T | C | 294 | a0001c0001t0001g0184a0001c0001t0002g0025a0001c0001t0002g0026others(291): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.-17-18348T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102851837 | ||||||
| chr14:102851859
|
T | C | 5 | a0001c0001t0002g0107a0001c0001t0002g0109a0001c0001t0002g0112others(2): Show | 5 | NA18952.hp1 NA18962.hp1 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17-18326T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102851859 | ||||||
| chr14:102851930
|
C | T | 1 | a0001c0003t0034g0003 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-17-18255C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102851930 | ||||||
| chr14:102851937
|
C | T | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-17-18248C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102851937 | ||||||
| chr14:102852143
|
TA | T | 4 | a0001c0003t0003g0182a0001c0003t0005g0181a0001c0003t0034g0003others(1): Show | 4 | HG02630.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-18041delA | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102852143 | ||||||
| chr14:102852418
|
C | CT | 3 | a0002c0002t0001g0285a0002c0002t0001g0286a0002c0002t0001g0287 | 3 | NA18969.hp1 NA19054.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.-17-17766dupT | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102852418 | |||||
| chr14:102852441
|
C | G | 4 | a0001c0001t0021g0057a0001c0001t0021g0099a0001c0001t0067g0125others(1): Show | 4 | HG01123.hp1 HG02723.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17-17744C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102852441 | ||||||
| chr14:102852812
|
C | T | 1 | a0002c0002t0001g0238 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-17-17373C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102852812 | ||||||
| chr14:102852813
|
G | A | 1 | a0002c0002t0001g0240 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-17-17372G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102852813 | ||||||
| chr14:102852874
|
A | C | 1 | a0002c0002t0060g0213 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-17-17311A>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102852874 | ||||||
| chr14:102852885
|
A | G | 3 | a0001c0001t0015g0139a0001c0001t0015g0140a0001c0001t0015g0141 | 3 | HG02055.hp1 HG02257.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-17-17300A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102852885 | ||||||
| chr14:102852932
|
C | T | 4 | a0002c0002t0001g0227a0002c0002t0001g0230a0002c0002t0001g0234others(1): Show | 4 | HG00621.hp1 HG02129.hp2 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17-17253C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102852932 | ||||||
| chr14:102852933
|
G | A | 1 | a0002c0002t0001g0212 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-17-17252G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102852933 | ||||||
| chr14:102853329
|
G | A | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-17-16856G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102853329 | ||||||
| chr14:102853498
|
C | T | 155 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(152): Show | 155 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.-17-16687C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102853498 | ||||||
| chr14:102853592
|
T | C | 4 | a0001c0001t0004g0034a0001c0001t0004g0035a0001c0001t0004g0048others(1): Show | 4 | NA18960.hp2 NA18964.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17-16593T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102853592 | ||||||
| chr14:102853644
|
C | T | 170 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(167): Show | 170 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.-17-16541C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102853644 | ||||||
| chr14:102853645
|
G | A | 1 | a0001c0001t0003g0100 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-17-16540G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102853645 | ||||||
| chr14:102853711
|
T | A | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-17-16474T>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102853711 | ||||||
| chr14:102853711
|
T | G | 161 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(158): Show | 161 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.-17-16474T>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102853711 | ||||||
| chr14:102853729
|
T | C | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-17-16456T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102853729 | ||||||
| chr14:102853763
|
G | C | 111 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(108): Show | 111 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.-17-16422G>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102853763 | ||||||
| chr14:102853769
|
C | T | 1 | a0001c0001t0007g0097 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-17-16416C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102853769 | ||||||
| chr14:102853833
|
C | T | 1 | a0001c0001t0005g0137 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-17-16352C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102853833 | ||||||
| chr14:102853837
|
T | TA | 154 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(151): Show | 154 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.-17-16332dupA | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102853837 | |||||
| chr14:102853837
|
T | TAA | 8 | a0001c0001t0010g0019a0001c0001t0010g0020a0001c0001t0012g0098others(5): Show | 8 | HG01109.hp2 HG02258.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-17-16333_-17-1633 others(6): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102853837 | |||||
| chr14:102854110
|
A | G | 1 | a0001c0001t0002g0067 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-17-16075A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102854110 | ||||||
| chr14:102854171
|
G | A | 1 | a0002c0002t0001g0225 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-17-16014G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102854171 | ||||||
| chr14:102854219
|
T | C | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-17-15966T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102854219 | ||||||
| chr14:102854248
|
G | A | 1 | a0001c0001t0004g0175 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-17-15937G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102854248 | ||||||
| chr14:102854268
|
G | A | 5 | a0001c0003t0003g0182a0001c0003t0005g0181a0001c0003t0034g0003others(2): Show | 5 | HG02559.hp1 HG02630.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17-15917G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102854268 | ||||||
| chr14:102854297
|
A | G | 1 | a0002c0002t0003g0152 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-17-15888A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102854297 | ||||||
| chr14:102854456
|
T | C | 1 | a0002c0002t0001g0282 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-17-15729T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102854456 | ||||||
| chr14:102854554
|
G | A | 1 | a0001c0001t0050g0180 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-17-15631G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102854554 | ||||||
| chr14:102854614
|
C | T | 18 | a0001c0001t0010g0018a0001c0001t0010g0019a0001c0001t0010g0020others(15): Show | 18 | HG00639.hp2 HG01109.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.-17-15571C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102854614 | ||||||
| chr14:102854624
|
G | A | 162 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(159): Show | 162 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.-17-15561G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102854624 | ||||||
| chr14:102854651
|
C | T | 149 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(146): Show | 149 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.-17-15534C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102854651 | ||||||
| chr14:102854670
|
G | GT | 3 | a0001c0001t0015g0139a0001c0001t0015g0140a0001c0001t0015g0141 | 3 | HG02055.hp1 HG02257.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-17-15514dupT | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102854670 | |||||
| chr14:102854672
|
A | T | 3 | a0001c0001t0015g0139a0001c0001t0015g0140a0001c0001t0015g0141 | 3 | HG02055.hp1 HG02257.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-17-15513A>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102854672 | ||||||
| chr14:102854801
|
G | A | 1 | a0002c0002t0003g0153 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-17-15384G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102854801 | ||||||
| chr14:102854801
|
GT | G | 167 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(164): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.-17-15365delT | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102854801 | |||||
| chr14:102854801
|
GTT | G | 21 | a0001c0001t0005g0011a0001c0001t0005g0014a0001c0001t0005g0016others(18): Show | 21 | HG01069.hp1 HG01071.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-15366_-17-1536 others(6): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102854801 | |||||
| chr14:102854820
|
T | A | 9 | a0001c0001t0012g0024a0001c0001t0012g0098a0001c0001t0012g0124others(6): Show | 9 | HG01099.hp2 HG01109.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-17-15365T>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102854820 | ||||||
| chr14:102854825
|
A | G | 1 | a0001c0001t0002g0083 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-17-15360A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102854825 | ||||||
| chr14:102854856
|
A | AGG | 3 | a0001c0001t0015g0139a0001c0001t0015g0140a0001c0001t0015g0141 | 3 | HG02055.hp1 HG02257.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-17-15329_-17-1532 others(6): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102854856 | ||||||
| chr14:102854857
|
T | G | 3 | a0001c0001t0015g0139a0001c0001t0015g0140a0001c0001t0015g0141 | 3 | HG02055.hp1 HG02257.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-17-15328T>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102854857 | ||||||
| chr14:102854911
|
G | A | 1 | a0001c0001t0047g0028 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-17-15274G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102854911 | ||||||
| chr14:102854954
|
G | T | 1 | a0002c0002t0003g0136 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-17-15231G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102854954 | ||||||
| chr14:102854977
|
CCAT | C | 5 | a0002c0002t0001g0199a0002c0002t0001g0200a0002c0002t0001g0217others(2): Show | 5 | NA18747.hp1 NA18952.hp2 NA19009.hp2 others(2): Show |
intron_variant | MODIFIER | c.-17-15207_-17-1520 others(7): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102854977 | ||||||
| chr14:102855121
|
G | A | 1 | a0001c0001t0050g0180 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-17-15064G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102855121 | ||||||
| chr14:102855266
|
G | A | 171 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(168): Show | 171 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.-17-14919G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102855266 | ||||||
| chr14:102855615
|
G | A | 2 | a0001c0001t0025g0052a0001c0001t0025g0122 | 2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-17-14570G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102855615 | ||||||
| chr14:102855657
|
G | A | 1 | a0001c0001t0003g0100 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-17-14528G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102855657 | ||||||
| chr14:102855694
|
C | G | 171 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(168): Show | 171 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.-17-14491C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102855694 | ||||||
| chr14:102855794
|
TA | T | 146 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(143): Show | 146 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(143): Show |
intron_variant | MODIFIER | c.-17-14376delA | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102855794 | |||||
| chr14:102855921
|
G | T | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-17-14264G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102855921 | ||||||
| chr14:102855985
|
G | A | 5 | a0001c0001t0021g0057a0001c0001t0021g0099a0001c0001t0033g0123others(2): Show | 5 | HG00733.hp2 HG01123.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-17-14200G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102855985 | ||||||
| chr14:102856042
|
C | T | 1 | a0001c0001t0004g0170 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-17-14143C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102856042 | ||||||
| chr14:102856097
|
C | CA | 68 | a0001c0001t0001g0184a0001c0001t0002g0026a0001c0001t0002g0027others(65): Show | 68 | HG00558.hp2 HG00621.hp1 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.-17-14064dupA | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102856097 | |||||
| chr14:102856097
|
C | CAA | 11 | a0001c0001t0004g0033a0001c0001t0005g0009a0001c0001t0005g0010others(8): Show | 11 | HG00609.hp1 HG02055.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.-17-14065_-17-1406 others(6): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102856097 | |||||
| chr14:102856097
|
CA | C | 22 | a0001c0001t0002g0044a0001c0001t0002g0115a0001c0001t0004g0175others(19): Show | 22 | HG00639.hp2 HG01069.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.-17-14064delA | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102856097 | |||||
| chr14:102856097
|
CAAAAAAA others(4): Show |
C | 1 | a0002c0002t0052g0242 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-17-14074_-17-1406 others(15): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102856097 | |||||
| chr14:102856134
|
C | T | 171 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(168): Show | 171 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.-17-14051C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102856134 | ||||||
| chr14:102856365
|
T | C | 6 | a0001c0001t0021g0057a0001c0001t0021g0099a0001c0001t0033g0123others(3): Show | 6 | HG00733.hp2 HG01123.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.-17-13820T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102856365 | ||||||
| chr14:102856457
|
C | A | 2 | a0001c0001t0031g0183a0001c0001t0042g0005 | 2 | HG01099.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-17-13728C>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102856457 | ||||||
| chr14:102856494
|
A | G | 1 | a0001c0001t0033g0123 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-17-13691A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102856494 | ||||||
| chr14:102856542
|
T | C | 1 | a0002c0002t0060g0213 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-17-13643T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102856542 | ||||||
| chr14:102856798
|
T | G | 10 | a0001c0001t0005g0009a0001c0001t0005g0010a0001c0001t0005g0011others(7): Show | 10 | HG02055.hp2 HG02615.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.-17-13387T>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102856798 | ||||||
| chr14:102856929
|
G | A | 1 | a0001c0001t0036g0146 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-17-13256G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102856929 | ||||||
| chr14:102857111
|
A | G | 131 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(128): Show | 131 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.-17-13074A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102857111 | ||||||
| chr14:102857120
|
G | T | 4 | a0001c0001t0021g0057a0001c0001t0021g0099a0001c0001t0067g0125others(1): Show | 4 | HG01123.hp1 HG02723.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17-13065G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102857120 | ||||||
| chr14:102857129
|
C | T | 9 | a0001c0001t0007g0008a0001c0001t0007g0045a0001c0001t0007g0094others(6): Show | 9 | HG01081.hp2 HG02451.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-17-13056C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102857129 | ||||||
| chr14:102857130
|
G | A | 1 | a0001c0001t0003g0100 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-17-13055G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102857130 | ||||||
| chr14:102857156
|
A | T | 3 | a0001c0001t0016g0104a0001c0001t0016g0105a0001c0001t0063g0223 | 3 | HG01516.hp2 HG01517.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-17-13029A>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102857156 | ||||||
| chr14:102857263
|
A | G | 2 | a0002c0002t0001g0199a0002c0002t0001g0200 | 2 | NA19009.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-17-12922A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102857263 | ||||||
| chr14:102857329
|
T | G | 1 | a0001c0001t0020g0054 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-17-12856T>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102857329 | ||||||
| chr14:102857348
|
G | A | 1 | a0001c0001t0031g0183 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-17-12837G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102857348 | ||||||
| chr14:102857402
|
A | C | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-17-12783A>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102857402 | ||||||
| chr14:102857488
|
C | A | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-17-12697C>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102857488 | ||||||
| chr14:102857578
|
C | T | 120 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(117): Show | 120 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.-17-12607C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102857578 | ||||||
| chr14:102857610
|
T | C | 170 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(167): Show | 170 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.-17-12575T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102857610 | ||||||
| chr14:102857618
|
C | T | 1 | a0002c0002t0001g0241 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-17-12567C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102857618 | ||||||
| chr14:102857623
|
C | T | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-17-12562C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102857623 | ||||||
| chr14:102857814
|
C | T | 1 | a0001c0001t0050g0180 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-17-12371C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102857814 | ||||||
| chr14:102857870
|
A | G | 2 | a0001c0001t0027g0288a0001c0001t0027g0289 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-17-12315A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102857870 | ||||||
| chr14:102858103
|
T | A | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-17-12082T>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102858103 | ||||||
| chr14:102858154
|
CT | C | 120 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(117): Show | 120 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.-17-12017delT | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102858154 | |||||
| chr14:102858176
|
C | T | 4 | a0001c0003t0003g0182a0001c0003t0005g0181a0001c0003t0034g0003others(1): Show | 4 | HG02630.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-12009C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102858176 | ||||||
| chr14:102858254
|
C | T | 1 | a0001c0001t0002g0115 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-17-11931C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102858254 | ||||||
| chr14:102858256
|
A | G | 2 | a0001c0001t0031g0183a0001c0001t0042g0005 | 2 | HG01099.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-17-11929A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102858256 | ||||||
| chr14:102858341
|
C | T | 1 | a0002c0002t0059g0239 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-17-11844C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102858341 | ||||||
| chr14:102858373
|
G | A | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-17-11812G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102858373 | ||||||
| chr14:102858527
|
TATA | T | 139 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(136): Show | 139 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.-17-11654_-17-1165 others(7): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102858527 | |||||
| chr14:102858850
|
A | G | 6 | a0001c0001t0002g0060a0001c0001t0014g0090a0001c0001t0014g0091others(3): Show | 6 | HG00544.hp2 HG02523.hp2 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.-17-11335A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102858850 | ||||||
| chr14:102859193
|
C | CA | 21 | a0001c0001t0005g0009a0001c0001t0005g0010a0001c0001t0005g0011others(18): Show | 21 | HG00639.hp2 HG02109.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.-17-10978dupA | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102859193 | |||||
| chr14:102859193
|
CA | C | 113 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(110): Show | 113 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.-17-10978delA | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102859193 | |||||
| chr14:102859395
|
A | G | 1 | a0002c0002t0001g0277 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-17-10790A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102859395 | ||||||
| chr14:102859420
|
T | G | 19 | a0001c0001t0005g0009a0001c0001t0005g0010a0001c0001t0005g0011others(16): Show | 19 | HG01069.hp1 HG01071.hp2 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.-17-10765T>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102859420 | ||||||
| chr14:102859808
|
C | T | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-17-10377C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102859808 | ||||||
| chr14:102859833
|
T | G | 5 | a0001c0001t0017g0143a0001c0001t0017g0144a0001c0001t0017g0145others(2): Show | 5 | HG02109.hp2 HG02922.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17-10352T>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102859833 | ||||||
| chr14:102860135
|
G | A | 9 | a0001c0001t0015g0139a0001c0001t0015g0140a0001c0001t0015g0141others(6): Show | 9 | HG02055.hp1 HG02109.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-17-10050G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102860135 | ||||||
| chr14:102860344
|
C | T | 3 | a0001c0001t0002g0083a0001c0001t0002g0084a0001c0001t0002g0086 | 3 | HG02129.hp1 NA19070.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.-17-9841C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102860344 | ||||||
| chr14:102860443
|
T | C | 143 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(140): Show | 143 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.-17-9742T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102860443 | ||||||
| chr14:102860461
|
G | C | 204 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(201): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.-17-9724G>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102860461 | ||||||
| chr14:102860487
|
C | G | 1 | a0001c0001t0007g0096 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-17-9698C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102860487 | ||||||
| chr14:102860508
|
G | A | 3 | a0002c0002t0001g0187a0002c0002t0001g0188a0002c0002t0001g0189 | 3 | NA18944.hp2 NA18960.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.-17-9677G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102860508 | ||||||
| chr14:102860599
|
G | C | 204 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(201): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.-17-9586G>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102860599 | ||||||
| chr14:102860645
|
A | G | 7 | a0001c0001t0012g0024a0001c0001t0012g0098a0001c0001t0012g0124others(4): Show | 7 | HG01109.hp2 HG02559.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-17-9540A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102860645 | ||||||
| chr14:102860769
|
G | T | 2 | a0001c0001t0002g0101a0001c0001t0002g0102 | 2 | HG00099.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.-17-9416G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102860769 | ||||||
| chr14:102860876
|
T | C | 1 | a0002c0002t0001g0225 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-17-9309T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102860876 | ||||||
| chr14:102861004
|
G | A | 1 | a0001c0001t0003g0100 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-17-9181G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102861004 | ||||||
| chr14:102861588
|
G | A | 1 | a0001c0001t0050g0180 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-17-8597G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102861588 | ||||||
| chr14:102861821
|
C | T | 120 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(117): Show | 120 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.-17-8364C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102861821 | ||||||
| chr14:102861865
|
C | T | 2 | a0001c0001t0002g0084a0001c0001t0002g0086 | 2 | NA19070.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.-17-8320C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102861865 | ||||||
| chr14:102862011
|
T | G | 2 | a0002c0002t0001g0261a0002c0002t0055g0260 | 2 | HG00733.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.-17-8174T>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102862011 | ||||||
| chr14:102862200
|
A | T | 9 | a0001c0001t0010g0018a0001c0001t0010g0019a0001c0001t0010g0020others(6): Show | 9 | HG00639.hp2 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-17-7985A>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102862200 | ||||||
| chr14:102862401
|
CA | C | 166 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.-17-7764delA | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102862401 | |||||
| chr14:102862569
|
G | C | 2 | a0001c0001t0012g0001a0001c0001t0012g0179 | 2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-17-7616G>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102862569 | ||||||
| chr14:102863035
|
G | A | 1 | a0002c0002t0009g0243 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-17-7150G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102863035 | ||||||
| chr14:102863093
|
C | A | 171 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(168): Show | 171 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.-17-7092C>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102863093 | ||||||
| chr14:102863119
|
A | T | 1 | a0002c0002t0001g0280 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-17-7066A>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102863119 | ||||||
| chr14:102863205
|
G | A | 13 | a0002c0002t0001g0206a0002c0002t0001g0248a0002c0002t0001g0256others(10): Show | 13 | HG02135.hp2 HG02523.hp1 NA18943.hp2 others(10): Show |
intron_variant | MODIFIER | c.-17-6980G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102863205 | ||||||
| chr14:102863411
|
C | T | 5 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(2): Show | 5 | HG00738.hp2 HG01167.hp2 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.-17-6774C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102863411 | ||||||
| chr14:102863499
|
A | G | 3 | a0002c0002t0001g0279a0002c0002t0003g0134a0002c0002t0003g0160 | 3 | HG01099.hp1 HG01256.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.-17-6686A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102863499 | ||||||
| chr14:102863519
|
G | A | 1 | a0001c0001t0002g0067 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-17-6666G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102863519 | ||||||
| chr14:102863681
|
C | T | 18 | a0001c0001t0010g0018a0001c0001t0010g0019a0001c0001t0010g0020others(15): Show | 18 | HG00639.hp2 HG01109.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.-17-6504C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102863681 | ||||||
| chr14:102863807
|
C | G | 33 | a0002c0002t0001g0206a0002c0002t0001g0248a0002c0002t0001g0251others(30): Show | 33 | HG00099.hp1 HG00733.hp1 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.-17-6378C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102863807 | ||||||
| chr14:102863980
|
T | A | 1 | a0002c0002t0003g0135 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-17-6205T>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102863980 | ||||||
| chr14:102864026
|
T | G | 2 | a0001c0001t0012g0024a0001c0001t0041g0051 | 2 | HG02895.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-17-6159T>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102864026 | ||||||
| chr14:102864147
|
C | CT | 13 | a0001c0001t0003g0100a0001c0001t0005g0017a0001c0001t0015g0139others(10): Show | 13 | HG01069.hp2 HG01261.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.-17-6020dupT | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102864147 | |||||
| chr14:102864171
|
C | T | 7 | a0001c0001t0010g0018a0001c0001t0010g0019a0001c0001t0010g0020others(4): Show | 7 | HG00639.hp2 HG02258.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-17-6014C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102864171 | ||||||
| chr14:102864272
|
T | C | 172 | a0001c0001t0001g0184a0001c0001t0002g0025a0001c0001t0002g0026others(169): Show | 172 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.-17-5913T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102864272 | ||||||
| chr14:102864296
|
C | G | 5 | a0001c0001t0021g0057a0001c0001t0021g0099a0001c0001t0033g0123others(2): Show | 5 | HG00733.hp2 HG01123.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-17-5889C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102864296 | ||||||
| chr14:102864400
|
G | A | 2 | a0001c0003t0003g0182a0001c0003t0005g0181 | 2 | HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-17-5785G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102864400 | ||||||
| chr14:102864405
|
C | T | 1 | a0001c0001t0050g0180 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-17-5780C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102864405 | ||||||
| chr14:102864423
|
C | T | 1 | a0001c0001t0005g0137 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-17-5762C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102864423 | ||||||
| chr14:102864440
|
G | A | 3 | a0001c0001t0008g0064a0001c0001t0031g0183a0001c0001t0042g0005 | 3 | HG01099.hp2 HG01175.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-17-5745G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102864440 | ||||||
| chr14:102864536
|
C | T | 109 | a0001c0001t0001g0184a0001c0001t0002g0025a0001c0001t0002g0026others(106): Show | 109 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.-17-5649C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102864536 | ||||||
| chr14:102864561
|
A | T | 9 | a0001c0001t0003g0100a0001c0001t0021g0057a0001c0001t0021g0099others(6): Show | 9 | HG00733.hp2 HG01099.hp2 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.-17-5624A>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102864561 | ||||||
| chr14:102864584
|
C | T | 4 | a0001c0003t0003g0182a0001c0003t0005g0181a0001c0003t0034g0003others(1): Show | 4 | HG02630.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-5601C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102864584 | ||||||
| chr14:102864643
|
C | T | 7 | a0001c0001t0003g0100a0001c0001t0021g0057a0001c0001t0021g0099others(4): Show | 7 | HG00733.hp2 HG01123.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.-17-5542C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102864643 | ||||||
| chr14:102864760
|
A | G | 1 | a0002c0002t0001g0287 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-17-5425A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102864760 | ||||||
| chr14:102864812
|
T | C | 1 | a0001c0001t0020g0142 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-17-5373T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102864812 | ||||||
| chr14:102864938
|
G | A | 2 | a0002c0002t0001g0283a0002c0002t0057g0265 | 2 | HG01243.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.-17-5247G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102864938 | ||||||
| chr14:102865253
|
A | T | 143 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(140): Show | 143 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.-17-4932A>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102865253 | ||||||
| chr14:102865271
|
C | T | 62 | a0002c0002t0001g0187a0002c0002t0001g0188a0002c0002t0001g0189others(59): Show | 62 | HG00323.hp2 HG00558.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.-17-4914C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102865271 | ||||||
| chr14:102865497
|
A | AT | 23 | a0001c0001t0004g0177a0001c0001t0005g0009a0001c0001t0005g0010others(20): Show | 23 | HG00140.hp1 HG01069.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.-17-4668dupT | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102865497 | |||||
| chr14:102865497
|
AT | A | 15 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0002g0172others(12): Show | 15 | HG00323.hp1 HG01109.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.-17-4668delT | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102865497 | |||||
| chr14:102865720
|
G | C | 10 | a0001c0001t0013g0262a0001c0001t0013g0263a0001c0001t0013g0293others(7): Show | 10 | HG01167.hp1 HG01169.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.-17-4465G>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102865720 | ||||||
| chr14:102866071
|
A | G | 7 | a0001c0001t0011g0147a0001c0001t0011g0148a0001c0001t0011g0150others(4): Show | 7 | HG01069.hp1 HG01071.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.-17-4114A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102866071 | ||||||
| chr14:102866080
|
G | A | 5 | a0001c0001t0021g0057a0001c0001t0021g0099a0001c0001t0033g0123others(2): Show | 5 | HG00733.hp2 HG01123.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-17-4105G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102866080 | ||||||
| chr14:102866189
|
A | G | 1 | a0001c0001t0035g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-17-3996A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102866189 | ||||||
| chr14:102866277
|
G | A | 1 | a0001c0001t0050g0180 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-17-3908G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102866277 | ||||||
| chr14:102866420
|
A | T | 11 | a0001c0001t0012g0024a0001c0001t0012g0098a0001c0001t0012g0124others(8): Show | 11 | HG01109.hp2 HG02559.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.-17-3765A>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102866420 | ||||||
| chr14:102866697
|
T | C | 1 | a0002c0002t0001g0230 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-17-3488T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102866697 | ||||||
| chr14:102866804
|
C | T | 1 | a0002c0002t0003g0164 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-17-3381C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102866804 | ||||||
| chr14:102866808
|
A | G | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-17-3377A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102866808 | ||||||
| chr14:102866820
|
G | A | 1 | a0001c0001t0050g0180 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-17-3365G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102866820 | ||||||
| chr14:102866850
|
A | AAC | 60 | a0002c0002t0001g0191a0002c0002t0001g0195a0002c0002t0001g0196others(57): Show | 60 | HG00099.hp1 HG00621.hp1 HG00673.hp2 others(57): Show |
intron_variant | MODIFIER | c.-17-3293_-17-3292d others(4): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102866850 | |||||
| chr14:102866850
|
A | AACAC | 14 | a0002c0002t0001g0224a0002c0002t0001g0237a0002c0002t0001g0238others(11): Show | 14 | HG00140.hp1 HG00735.hp2 HG01123.hp2 others(11): Show |
intron_variant | MODIFIER | c.-17-3295_-17-3292d others(6): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102866850 | |||||
| chr14:102866850
|
A | AACACAC | 4 | a0002c0002t0001g0236a0002c0002t0001g0280a0002c0002t0054g0194others(1): Show | 4 | HG01261.hp2 HG03834.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17-3297_-17-3292d others(8): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102866850 | |||||
| chr14:102866850
|
A | AACACACA others(3): Show |
1 | a0002c0002t0001g0225 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-17-3301_-17-3292d others(12): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102866850 | |||||
| chr14:102866850
|
AAC | A | 93 | a0001c0001t0001g0184a0001c0001t0002g0025a0001c0001t0002g0026others(90): Show | 93 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.-17-3293_-17-3292d others(4): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102866850 | |||||
| chr14:102866850
|
AACAC | A | 14 | a0001c0001t0004g0033a0001c0001t0007g0095a0001c0001t0007g0119others(11): Show | 14 | HG00733.hp2 HG01123.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.-17-3295_-17-3292d others(6): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102866850 | |||||
| chr14:102866850
|
AACACAC | A | 3 | a0001c0001t0002g0058a0001c0003t0003g0182a0001c0003t0005g0181 | 3 | HG02004.hp1 HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-17-3297_-17-3292d others(8): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102866850 | |||||
| chr14:102866850
|
AACACACA others(5): Show |
A | 1 | a0001c0001t0017g0143 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-17-3303_-17-3292d others(14): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102866850 | |||||
| chr14:102866850
|
AACACACA others(7): Show |
A | 4 | a0001c0001t0017g0144a0001c0001t0017g0145a0001c0001t0019g0082others(1): Show | 4 | HG02922.hp2 HG02970.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-3305_-17-3292d others(16): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102866850 | |||||
| chr14:102866850
|
AACACACA others(19): Show |
A | 1 | a0002c0002t0009g0185 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-17-3317_-17-3292d others(28): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102866850 | |||||
| chr14:102866892
|
C | CACACACA others(5): Show |
1 | a0001c0001t0003g0100 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-17-3292_-17-3291i others(14): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102866892 | |||||
| chr14:102866892
|
C | CACACACA others(3): Show |
9 | a0001c0001t0010g0019a0001c0001t0010g0020a0001c0001t0012g0168others(6): Show | 9 | HG01884.hp2 HG02055.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-17-3292_-17-3291i others(12): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102866892 | |||||
| chr14:102866892
|
C | CACACAG | 11 | a0001c0001t0011g0147a0001c0001t0011g0148a0001c0001t0012g0024others(8): Show | 11 | HG01099.hp2 HG01496.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.-17-3292_-17-3291i others(8): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102866892 | |||||
| chr14:102866892
|
C | CACAG | 8 | a0001c0001t0005g0011a0001c0001t0010g0018a0001c0001t0010g0022others(5): Show | 8 | HG00639.hp2 HG02486.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-17-3292_-17-3291i others(6): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102866892 | |||||
| chr14:102866892
|
C | CAG | 14 | a0001c0001t0005g0010a0001c0001t0005g0137a0001c0001t0007g0094others(11): Show | 14 | HG01069.hp1 HG01071.hp2 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.-17-3292_-17-3291i others(4): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102866892 | |||||
| chr14:102866892
|
C | G | 129 | a0001c0001t0001g0184a0001c0001t0002g0025a0001c0001t0002g0026others(126): Show | 129 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.-17-3293C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102866892 | ||||||
| chr14:102866918
|
T | A | 9 | a0002c0002t0001g0215a0002c0002t0001g0279a0002c0002t0003g0160others(6): Show | 9 | HG00323.hp2 HG01081.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.-17-3267T>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102866918 | ||||||
| chr14:102866928
|
C | T | 3 | a0001c0001t0069g0093a0002c0002t0001g0227a0002c0002t0001g0291 | 3 | HG02129.hp2 HG02135.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.-17-3257C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102866928 | ||||||
| chr14:102866952
|
C | A | 1 | a0001c0001t0010g0018 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-17-3233C>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102866952 | ||||||
| chr14:102867031
|
G | A | 9 | a0001c0001t0010g0018a0001c0001t0010g0019a0001c0001t0010g0020others(6): Show | 9 | HG00639.hp2 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-17-3154G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102867031 | ||||||
| chr14:102867061
|
G | T | 1 | a0002c0002t0001g0225 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-17-3124G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102867061 | ||||||
| chr14:102867101
|
T | A | 7 | a0001c0001t0005g0009a0001c0001t0005g0010a0001c0001t0005g0011others(4): Show | 7 | HG02055.hp2 HG02809.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-17-3084T>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102867101 | ||||||
| chr14:102867114
|
C | T | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-17-3071C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102867114 | ||||||
| chr14:102867158
|
T | C | 1 | a0001c0001t0003g0100 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-17-3027T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102867158 | ||||||
| chr14:102867352
|
A | G | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-17-2833A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102867352 | ||||||
| chr14:102867592
|
C | T | 1 | a0002c0002t0001g0246 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-17-2593C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102867592 | ||||||
| chr14:102867764
|
C | G | 4 | a0001c0003t0003g0182a0001c0003t0005g0181a0001c0003t0034g0003others(1): Show | 4 | HG02630.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-2421C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102867764 | ||||||
| chr14:102867938
|
C | T | 1 | a0001c0001t0050g0180 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-17-2247C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102867938 | ||||||
| chr14:102867960
|
C | T | 1 | a0002c0002t0001g0246 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-17-2225C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102867960 | ||||||
| chr14:102868170
|
T | C | 1 | a0001c0001t0012g0168 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-17-2015T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102868170 | ||||||
| chr14:102868235
|
A | C | 19 | a0001c0001t0005g0009a0001c0001t0005g0010a0001c0001t0005g0011others(16): Show | 19 | HG01069.hp1 HG01071.hp2 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.-17-1950A>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102868235 | ||||||
| chr14:102868267
|
C | G | 2 | a0001c0001t0012g0001a0001c0001t0012g0179 | 2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-17-1918C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102868267 | ||||||
| chr14:102868412
|
A | C | 2 | a0001c0001t0012g0001a0001c0001t0012g0179 | 2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-17-1773A>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102868412 | ||||||
| chr14:102868564
|
A | G | 1 | a0001c0001t0002g0072 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-17-1621A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102868564 | ||||||
| chr14:102868802
|
C | T | 1 | a0001c0001t0002g0070 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-17-1383C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102868802 | ||||||
| chr14:102868891
|
G | A | 8 | a0001c0001t0004g0040a0001c0001t0004g0170a0001c0001t0004g0171others(5): Show | 8 | HG01261.hp1 HG01928.hp1 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.-17-1294G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102868891 | ||||||
| chr14:102868905
|
T | C | 172 | a0001c0001t0001g0184a0001c0001t0002g0025a0001c0001t0002g0026others(169): Show | 172 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.-17-1280T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102868905 | ||||||
| chr14:102869003
|
C | A | 11 | a0002c0002t0001g0206a0002c0002t0001g0248a0002c0002t0001g0256others(8): Show | 11 | HG02135.hp2 HG02523.hp1 NA18943.hp2 others(8): Show |
intron_variant | MODIFIER | c.-17-1182C>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102869003 | ||||||
| chr14:102869004
|
C | T | 1 | a0002c0002t0001g0286 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-17-1181C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102869004 | ||||||
| chr14:102869005
|
G | A | 37 | a0001c0001t0005g0009a0001c0001t0005g0010a0001c0001t0005g0011others(34): Show | 37 | HG00639.hp2 HG01069.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.-17-1180G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102869005 | ||||||
| chr14:102869157
|
G | A | 2 | a0002c0002t0003g0152a0002c0002t0003g0164 | 2 | HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-17-1028G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102869157 | ||||||
| chr14:102869308
|
C | G | 1 | a0001c0001t0003g0100 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-17-877C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102869308 | ||||||
| chr14:102869418
|
T | C | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-17-767T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102869418 | ||||||
| chr14:102869542
|
C | G | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-17-643C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102869542 | ||||||
| chr14:102869592
|
G | T | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-17-593G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102869592 | ||||||
| chr14:102869613
|
C | T | 24 | a0001c0001t0005g0009a0001c0001t0005g0010a0001c0001t0005g0011others(21): Show | 24 | HG01069.hp1 HG01071.hp2 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.-17-572C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102869613 | ||||||
| chr14:102869704
|
G | T | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-17-481G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102869704 | ||||||
| chr14:102869737
|
C | T | 2 | a0001c0001t0019g0082a0001c0001t0051g0284 | 2 | HG02970.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-17-448C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102869737 | ||||||
| chr14:102869804
|
T | TA | 25 | a0001c0001t0007g0095a0001c0001t0010g0018a0001c0001t0010g0019others(22): Show | 25 | HG00733.hp2 HG01109.hp2 HG01123.hp1 others(22): Show |
intron_variant | MODIFIER | c.-17-363dupA | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | 102869804 | |||||
| chr14:102869822
|
A | T | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-17-363A>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102869822 | ||||||
| chr14:102869914
|
A | G | 4 | a0001c0003t0003g0182a0001c0003t0005g0181a0001c0003t0034g0003others(1): Show | 4 | HG02630.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-271A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102869914 | ||||||
| chr14:102870087
|
G | T | 1 | a0001c0001t0002g0027 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-17-98G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102870087 | ||||||
| chr14:102870181
|
A | G | 5 | a0001c0001t0018g0186a0001c0001t0018g0250a0001c0001t0018g0275others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG02886.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.-17-4A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 2/11 | chr14 | 102870181 | ||||||
| chr14:102870453
|
GCCCTCGC others(5): Show |
G | 2 | a0001c0001t0007g0096a0001c0001t0007g0121 | 2 | HG01081.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.245+10_245+21delCT others(10): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 102870453 | |||||
| chr14:102870467
|
C | T | 26 | a0001c0001t0002g0066a0001c0001t0005g0009a0001c0001t0005g0010others(23): Show | 26 | HG01069.hp1 HG01071.hp2 HG01496.hp1 others(23): Show |
intron_variant | MODIFIER | c.245+21C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 3/11 | chr14 | 102870467 | ||||||
| chr14:102870490
|
C | T | 2 | a0001c0001t0012g0001a0001c0001t0012g0179 | 2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.245+44C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 3/11 | chr14 | 102870490 | ||||||
| chr14:102870625
|
G | A | 1 | a0001c0001t0041g0051 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.245+179G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 3/11 | chr14 | 102870625 | ||||||
| chr14:102870666
|
G | A | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.245+220G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 3/11 | chr14 | 102870666 | ||||||
| chr14:102870700
|
C | T | 7 | a0001c0001t0012g0024a0001c0001t0012g0098a0001c0001t0012g0124others(4): Show | 7 | HG01109.hp2 HG02559.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.245+254C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 3/11 | chr14 | 102870700 | ||||||
| chr14:102870791
|
C | T | 1 | a0001c0001t0069g0093 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.245+345C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 3/11 | chr14 | 102870791 | ||||||
| chr14:102870916
|
T | C | 163 | a0001c0001t0001g0184a0001c0001t0002g0025a0001c0001t0002g0026others(160): Show | 163 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.245+470T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 3/11 | chr14 | 102870916 | ||||||
| chr14:102870921
|
C | T | 5 | a0001c0001t0021g0057a0001c0001t0021g0099a0001c0001t0033g0123others(2): Show | 5 | HG00733.hp2 HG01123.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.245+475C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 3/11 | chr14 | 102870921 | ||||||
| chr14:102871014
|
G | A | 2 | a0002c0002t0001g0236a0002c0002t0001g0237 | 2 | HG03834.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.245+568G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 3/11 | chr14 | 102871014 | ||||||
| chr14:102871148
|
C | G | 1 | a0002c0002t0003g0133 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.245+702C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 3/11 | chr14 | 102871148 | ||||||
| chr14:102871202
|
G | T | 1 | a0001c0001t0024g0049 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.246-715G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 3/11 | chr14 | 102871202 | ||||||
| chr14:102871298
|
C | T | 1 | a0002c0002t0001g0278 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.246-619C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 3/11 | chr14 | 102871298 | ||||||
| chr14:102871447
|
G | A | 1 | a0001c0001t0003g0100 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.246-470G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 3/11 | chr14 | 102871447 | ||||||
| chr14:102871561
|
GCAAGGCT others(3): Show |
G | 7 | a0001c0001t0010g0018a0001c0001t0010g0019a0001c0001t0010g0020others(4): Show | 7 | HG00639.hp2 HG02258.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.246-351_246-342del others(10): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 102871561 | |||||
| chr14:102871731
|
A | G | 2 | a0002c0002t0001g0255a0002c0002t0053g0290 | 2 | HG00099.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.246-186A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 3/11 | chr14 | 102871731 | ||||||
| chr14:102871771
|
G | A | 1 | a0001c0001t0040g0149 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.246-146G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 3/11 | chr14 | 102871771 | ||||||
| chr14:102871980
|
T | G | 2 | a0001c0001t0031g0183a0001c0001t0042g0005 | 2 | HG01099.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.297+12T>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 4/11 | chr14 | 102871980 | ||||||
| chr14:102871987
|
T | A | 146 | a0001c0001t0001g0184a0001c0001t0002g0025a0001c0001t0002g0026others(143): Show | 146 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.297+19T>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 4/11 | chr14 | 102871987 | ||||||
| chr14:102872086
|
C | T | 1 | a0001c0001t0003g0100 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.297+118C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 4/11 | chr14 | 102872086 | ||||||
| chr14:102872231
|
G | A | 2 | a0002c0002t0001g0261a0002c0002t0055g0260 | 2 | HG00733.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.297+263G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 4/11 | chr14 | 102872231 | ||||||
| chr14:102872432
|
C | G | 1 | a0002c0002t0003g0160 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.297+464C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 4/11 | chr14 | 102872432 | ||||||
| chr14:102872517
|
C | T | 2 | a0001c0001t0023g0043a0001c0001t0023g0075 | 2 | HG00609.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.297+549C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 4/11 | chr14 | 102872517 | ||||||
| chr14:102872697
|
T | C | 4 | a0001c0001t0021g0057a0001c0001t0021g0099a0001c0001t0067g0125others(1): Show | 4 | HG01123.hp1 HG02723.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.297+729T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 4/11 | chr14 | 102872697 | ||||||
| chr14:102872699
|
C | CT | 153 | a0001c0001t0001g0184a0001c0001t0002g0025a0001c0001t0002g0026others(150): Show | 153 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.297+741dupT | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 102872699 | |||||
| chr14:102872699
|
C | CTT | 12 | a0001c0001t0011g0127a0001c0001t0011g0147a0001c0001t0011g0148others(9): Show | 12 | HG01069.hp1 HG01071.hp2 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.297+740_297+741dup others(2): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 102872699 | |||||
| chr14:102872849
|
G | A | 1 | a0002c0002t0059g0239 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.297+881G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 4/11 | chr14 | 102872849 | ||||||
| chr14:102873251
|
G | C | 2 | a0001c0001t0031g0183a0001c0001t0042g0005 | 2 | HG01099.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.297+1283G>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 4/11 | chr14 | 102873251 | ||||||
| chr14:102873286
|
T | C | 1 | a0001c0001t0002g0070 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.297+1318T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 4/11 | chr14 | 102873286 | ||||||
| chr14:102873509
|
A | G | 11 | a0001c0001t0011g0127a0001c0001t0011g0147a0001c0001t0011g0148others(8): Show | 11 | HG01069.hp1 HG01071.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.297+1541A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 4/11 | chr14 | 102873509 | ||||||
| chr14:102873589
|
G | A | 5 | a0001c0003t0003g0182a0001c0003t0005g0181a0001c0003t0034g0003others(2): Show | 5 | HG01993.hp1 HG02630.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.297+1621G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 4/11 | chr14 | 102873589 | ||||||
| chr14:102873639
|
A | G | 1 | a0001c0001t0025g0052 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.297+1671A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 4/11 | chr14 | 102873639 | ||||||
| chr14:102873762
|
C | CT | 111 | a0001c0001t0001g0184a0001c0001t0002g0025a0001c0001t0002g0026others(108): Show | 111 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.297+1804dupT | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 102873762 | |||||
| chr14:102873785
|
G | A | 1 | a0001c0001t0050g0180 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.297+1817G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 4/11 | chr14 | 102873785 | ||||||
| chr14:102874054
|
G | A | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.298-1570G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 4/11 | chr14 | 102874054 | ||||||
| chr14:102874216
|
TGATTGCA others(11): Show |
T | 3 | a0001c0001t0016g0104a0001c0001t0016g0105a0001c0001t0063g0223 | 3 | HG01516.hp2 HG01517.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.298-1407_298-1390d others(20): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 4/11 | chr14 | 102874216 | ||||||
| chr14:102874231
|
G | T | 1 | a0001c0001t0028g0138 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.298-1393G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 4/11 | chr14 | 102874231 | ||||||
| chr14:102874293
|
C | G | 1 | a0002c0002t0001g0268 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.298-1331C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 4/11 | chr14 | 102874293 | ||||||
| chr14:102874417
|
C | T | 4 | a0001c0003t0003g0182a0001c0003t0005g0181a0001c0003t0034g0003others(1): Show | 4 | HG02630.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.298-1207C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 4/11 | chr14 | 102874417 | ||||||
| chr14:102874450
|
G | T | 1 | a0001c0001t0050g0180 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.298-1174G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 4/11 | chr14 | 102874450 | ||||||
| chr14:102874650
|
C | CT | 154 | a0001c0001t0001g0184a0001c0001t0002g0025a0001c0001t0002g0026others(151): Show | 154 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.298-960dupT | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 102874650 | |||||
| chr14:102874719
|
T | C | 172 | a0001c0001t0001g0184a0001c0001t0002g0025a0001c0001t0002g0026others(169): Show | 172 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.298-905T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 4/11 | chr14 | 102874719 | ||||||
| chr14:102875130
|
A | G | 9 | a0001c0001t0010g0018a0001c0001t0010g0019a0001c0001t0010g0020others(6): Show | 9 | HG00639.hp2 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.298-494A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 4/11 | chr14 | 102875130 | ||||||
| chr14:102875141
|
T | G | 5 | a0001c0001t0021g0057a0001c0001t0021g0099a0001c0001t0033g0123others(2): Show | 5 | HG00733.hp2 HG01123.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.298-483T>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 4/11 | chr14 | 102875141 | ||||||
| chr14:102875214
|
C | G | 1 | a0001c0003t0034g0003 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.298-410C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 4/11 | chr14 | 102875214 | ||||||
| chr14:102875220
|
T | C | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.298-404T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 4/11 | chr14 | 102875220 | ||||||
| chr14:102875270
|
C | A | 1 | a0001c0001t0033g0123 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.298-354C>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 4/11 | chr14 | 102875270 | ||||||
| chr14:102875465
|
C | T | 4 | a0001c0001t0002g0107a0001c0001t0002g0109a0001c0001t0002g0112others(1): Show | 4 | NA18952.hp1 NA18962.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.298-159C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 4/11 | chr14 | 102875465 | ||||||
| chr14:102875528
|
G | GT | 192 | a0001c0001t0001g0184a0001c0001t0002g0025a0001c0001t0002g0026others(189): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.298-84dupT | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 102875528 | |||||
| chr14:102875528
|
G | GTT | 12 | a0001c0001t0002g0032a0001c0001t0002g0036a0001c0001t0002g0079others(9): Show | 12 | HG00738.hp2 HG01099.hp2 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.298-85_298-84dupTT | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr14 | 102875528 | |||||
| chr14:102875762
|
T | G | 1 | a0002c0002t0001g0240 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.402+34T>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 5/11 | chr14 | 102875762 | ||||||
| chr14:102875943
|
C | T | 1 | a0002c0002t0001g0267 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.402+215C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 5/11 | chr14 | 102875943 | ||||||
| chr14:102875952
|
CT | C | 4 | a0001c0003t0003g0182a0001c0003t0005g0181a0001c0003t0034g0003others(1): Show | 4 | HG02630.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.402+225delT | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 5/11 | chr14 | 102875952 | ||||||
| chr14:102876545
|
A | G | 4 | a0001c0003t0003g0182a0001c0003t0005g0181a0001c0003t0034g0003others(1): Show | 4 | HG02630.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.570+20A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102876545 | ||||||
| chr14:102876586
|
C | A | 2 | a0001c0001t0004g0040a0001c0001t0004g0174 | 2 | HG01943.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.570+61C>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102876586 | ||||||
| chr14:102876679
|
T | C | 4 | a0001c0001t0012g0098a0001c0001t0012g0124a0001c0001t0020g0054others(1): Show | 4 | HG01109.hp2 HG02559.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.570+154T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102876679 | ||||||
| chr14:102876718
|
C | T | 1 | a0001c0001t0011g0150 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.570+193C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102876718 | ||||||
| chr14:102876769
|
C | T | 1 | a0001c0001t0003g0100 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.570+244C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102876769 | ||||||
| chr14:102876770
|
G | A | 3 | a0002c0002t0003g0131a0002c0002t0003g0132a0002c0002t0003g0133 | 3 | HG01069.hp2 HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.570+245G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102876770 | ||||||
| chr14:102876814
|
C | T | 1 | a0001c0001t0015g0141 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.570+289C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102876814 | ||||||
| chr14:102876858
|
A | T | 1 | a0001c0001t0010g0023 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.570+333A>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102876858 | ||||||
| chr14:102876872
|
A | G | 1 | a0001c0001t0042g0005 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.570+347A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102876872 | ||||||
| chr14:102876962
|
A | T | 1 | a0001c0001t0007g0094 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.570+437A>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102876962 | ||||||
| chr14:102876984
|
C | T | 5 | a0001c0001t0021g0057a0001c0001t0021g0099a0001c0001t0033g0123others(2): Show | 5 | HG00733.hp2 HG01123.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.570+459C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102876984 | ||||||
| chr14:102877003
|
C | T | 7 | a0001c0001t0012g0024a0001c0001t0012g0098a0001c0001t0012g0124others(4): Show | 7 | HG01109.hp2 HG02559.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.570+478C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102877003 | ||||||
| chr14:102877004
|
A | G | 7 | a0001c0001t0012g0024a0001c0001t0012g0098a0001c0001t0012g0124others(4): Show | 7 | HG01109.hp2 HG02559.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.570+479A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102877004 | ||||||
| chr14:102877013
|
G | T | 7 | a0001c0001t0012g0024a0001c0001t0012g0098a0001c0001t0012g0124others(4): Show | 7 | HG01109.hp2 HG02559.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.570+488G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102877013 | ||||||
| chr14:102877020
|
A | G | 7 | a0001c0001t0012g0024a0001c0001t0012g0098a0001c0001t0012g0124others(4): Show | 7 | HG01109.hp2 HG02559.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.570+495A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102877020 | ||||||
| chr14:102877040
|
GTTCCACA others(495): Show |
G | 7 | a0001c0001t0012g0024a0001c0001t0012g0098a0001c0001t0012g0124others(4): Show | 7 | HG01109.hp2 HG02559.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.570+525_570+1026de others(1): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 102877040 | |||||
| chr14:102877076
|
G | A | 1 | a0002c0002t0001g0259 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.570+551G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102877076 | ||||||
| chr14:102877137
|
T | A | 7 | a0001c0001t0003g0100a0001c0001t0021g0057a0001c0001t0021g0099others(4): Show | 7 | HG00733.hp2 HG01123.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.570+612T>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102877137 | ||||||
| chr14:102877147
|
G | A | 1 | a0001c0001t0050g0180 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.570+622G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102877147 | ||||||
| chr14:102877163
|
G | A | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.570+638G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102877163 | ||||||
| chr14:102877183
|
GTTCCACA others(64): Show |
G | 1 | a0001c0001t0002g0059 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.570+694_570+764del others(71): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 102877183 | |||||
| chr14:102877265
|
C | G | 1 | a0002c0002t0001g0205 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.570+740C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102877265 | ||||||
| chr14:102877298
|
G | C | 2 | a0001c0001t0002g0108a0001c0001t0024g0069 | 2 | NA19004.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.570+773G>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102877298 | ||||||
| chr14:102877306
|
G | A | 2 | a0001c0001t0031g0183a0001c0001t0042g0005 | 2 | HG01099.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.570+781G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102877306 | ||||||
| chr14:102877306
|
G | GCTCAGCT others(29): Show |
5 | a0001c0001t0021g0057a0001c0001t0021g0099a0001c0001t0033g0123others(2): Show | 5 | HG00733.hp2 HG01123.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.570+799_570+800ins others(36): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 102877306 | |||||
| chr14:102877326
|
GTTCCACA others(29): Show |
G | 4 | a0001c0003t0003g0182a0001c0003t0005g0181a0001c0003t0034g0003others(1): Show | 4 | HG02630.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.570+816_570+851del others(36): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 102877326 | |||||
| chr14:102877342
|
G | T | 1 | a0002c0002t0001g0278 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.570+817G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102877342 | ||||||
| chr14:102877381
|
C | G | 4 | a0002c0002t0006g0156a0002c0002t0006g0157a0002c0002t0006g0161others(1): Show | 4 | HG00639.hp1 HG01192.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.570+856C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102877381 | ||||||
| chr14:102877397
|
C | T | 3 | a0002c0002t0003g0131a0002c0002t0003g0132a0002c0002t0003g0133 | 3 | HG01069.hp2 HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.570+872C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102877397 | ||||||
| chr14:102877398
|
G | A | 1 | a0001c0001t0011g0165 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.570+873G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102877398 | ||||||
| chr14:102877414
|
G | A | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.570+889G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102877414 | ||||||
| chr14:102877453
|
TAGCTCAT others(101): Show |
T | 5 | a0001c0001t0002g0058a0001c0001t0002g0067a0001c0001t0002g0074others(2): Show | 5 | HG01192.hp2 HG01358.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.570+966_570+1073de others(1): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 102877453 | |||||
| chr14:102877491
|
A | ACTCATAG others(29): Show |
1 | a0001c0001t0003g0100 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.570+981_570+1016du others(37): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 102877491 | |||||
| chr14:102877615
|
A | G | 7 | a0001c0001t0012g0024a0001c0001t0012g0098a0001c0001t0012g0124others(4): Show | 7 | HG01109.hp2 HG02559.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.570+1090A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102877615 | ||||||
| chr14:102877638
|
G | A | 1 | a0002c0002t0001g0281 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.570+1113G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102877638 | ||||||
| chr14:102877665
|
C | T | 9 | a0001c0001t0015g0139a0001c0001t0015g0140a0001c0001t0015g0141others(6): Show | 9 | HG02055.hp1 HG02109.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.570+1140C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102877665 | ||||||
| chr14:102877671
|
A | G | 5 | a0001c0001t0021g0057a0001c0001t0021g0099a0001c0001t0033g0123others(2): Show | 5 | HG00733.hp2 HG01123.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.570+1146A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102877671 | ||||||
| chr14:102877793
|
C | T | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.570+1268C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102877793 | ||||||
| chr14:102877970
|
C | A | 172 | a0001c0001t0001g0184a0001c0001t0002g0025a0001c0001t0002g0026others(169): Show | 172 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.570+1445C>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102877970 | ||||||
| chr14:102878004
|
T | C | 1 | a0001c0003t0005g0181 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.570+1479T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102878004 | ||||||
| chr14:102878177
|
G | T | 4 | a0001c0001t0021g0057a0001c0001t0021g0099a0001c0001t0067g0125others(1): Show | 4 | HG01123.hp1 HG02723.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.570+1652G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102878177 | ||||||
| chr14:102878351
|
AGTGTGTG others(9): Show |
A | 2 | a0002c0002t0001g0209a0002c0002t0001g0226 | 2 | HG00673.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.570+1839_570+1854d others(18): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 102878351 | |||||
| chr14:102878381
|
AGTGTGAA others(21): Show |
A | 1 | a0001c0001t0031g0183 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.570+1872_570+1899d others(30): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 102878381 | |||||
| chr14:102878411
|
T | G | 1 | a0002c0002t0049g0129 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.570+1886T>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102878411 | ||||||
| chr14:102878538
|
G | T | 4 | a0001c0003t0003g0182a0001c0003t0005g0181a0001c0003t0034g0003others(1): Show | 4 | HG02630.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.570+2013G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102878538 | ||||||
| chr14:102878579
|
G | A | 2 | a0001c0001t0012g0001a0001c0001t0012g0179 | 2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.570+2054G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102878579 | ||||||
| chr14:102878689
|
G | C | 172 | a0001c0001t0001g0184a0001c0001t0002g0025a0001c0001t0002g0026others(169): Show | 172 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.570+2164G>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102878689 | ||||||
| chr14:102878863
|
C | T | 2 | a0002c0002t0001g0209a0002c0002t0001g0252 | 2 | HG00673.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.570+2338C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102878863 | ||||||
| chr14:102878948
|
G | A | 5 | a0001c0001t0017g0143a0001c0001t0017g0144a0001c0001t0017g0145others(2): Show | 5 | HG02109.hp2 HG02922.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.570+2423G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102878948 | ||||||
| chr14:102878968
|
C | T | 3 | a0002c0002t0001g0285a0002c0002t0001g0286a0002c0002t0001g0287 | 3 | NA18969.hp1 NA19054.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.570+2443C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102878968 | ||||||
| chr14:102879002
|
C | T | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.570+2477C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102879002 | ||||||
| chr14:102879130
|
G | A | 163 | a0001c0001t0001g0184a0001c0001t0002g0025a0001c0001t0002g0026others(160): Show | 163 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.570+2605G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102879130 | ||||||
| chr14:102879140
|
G | A | 1 | a0001c0001t0004g0061 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.570+2615G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102879140 | ||||||
| chr14:102879366
|
A | G | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.570+2841A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102879366 | ||||||
| chr14:102879487
|
G | C | 3 | a0001c0001t0015g0139a0001c0001t0015g0140a0001c0001t0015g0141 | 3 | HG02055.hp1 HG02257.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.570+2962G>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102879487 | ||||||
| chr14:102879559
|
G | A | 4 | a0001c0003t0003g0182a0001c0003t0005g0181a0001c0003t0034g0003others(1): Show | 4 | HG02630.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.570+3034G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102879559 | ||||||
| chr14:102879572
|
G | A | 1 | a0001c0001t0003g0100 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.570+3047G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102879572 | ||||||
| chr14:102879623
|
G | A | 2 | a0001c0001t0031g0183a0001c0001t0042g0005 | 2 | HG01099.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.570+3098G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102879623 | ||||||
| chr14:102879694
|
A | G | 7 | a0001c0001t0010g0018a0001c0001t0010g0019a0001c0001t0010g0020others(4): Show | 7 | HG00639.hp2 HG02258.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.570+3169A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102879694 | ||||||
| chr14:102879700
|
G | A | 1 | a0001c0001t0002g0056 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.570+3175G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102879700 | ||||||
| chr14:102879867
|
A | G | 1 | a0001c0001t0050g0180 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.570+3342A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102879867 | ||||||
| chr14:102879879
|
G | A | 1 | a0001c0001t0025g0122 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.570+3354G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102879879 | ||||||
| chr14:102879953
|
C | T | 3 | a0002c0002t0001g0256a0002c0002t0001g0269a0002c0002t0001g0270 | 3 | HG02523.hp1 NA18943.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.570+3428C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102879953 | ||||||
| chr14:102879963
|
A | G | 5 | a0001c0001t0021g0057a0001c0001t0021g0099a0001c0001t0033g0123others(2): Show | 5 | HG00733.hp2 HG01123.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.570+3438A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102879963 | ||||||
| chr14:102880073
|
C | T | 1 | a0002c0002t0001g0225 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.570+3548C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102880073 | ||||||
| chr14:102880159
|
T | C | 1 | a0001c0001t0002g0066 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.570+3634T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102880159 | ||||||
| chr14:102880185
|
G | A | 1 | a0001c0001t0051g0284 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.570+3660G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102880185 | ||||||
| chr14:102880279
|
A | G | 168 | a0001c0001t0001g0184a0001c0001t0002g0025a0001c0001t0002g0026others(165): Show | 168 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.570+3754A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102880279 | ||||||
| chr14:102880451
|
A | G | 1 | a0001c0001t0041g0051 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.570+3926A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102880451 | ||||||
| chr14:102880477
|
C | T | 1 | a0002c0002t0001g0234 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.570+3952C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102880477 | ||||||
| chr14:102880491
|
T | C | 172 | a0001c0001t0001g0184a0001c0001t0002g0025a0001c0001t0002g0026others(169): Show | 172 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.570+3966T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102880491 | ||||||
| chr14:102880502
|
T | A | 23 | a0001c0001t0005g0009a0001c0001t0005g0010a0001c0001t0005g0011others(20): Show | 23 | HG01069.hp1 HG01071.hp2 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.570+3977T>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102880502 | ||||||
| chr14:102880510
|
G | A | 1 | a0001c0001t0011g0127 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.570+3985G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102880510 | ||||||
| chr14:102880625
|
T | C | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.570+4100T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102880625 | ||||||
| chr14:102880678
|
A | G | 2 | a0001c0003t0034g0003a0001c0003t0037g0004 | 2 | HG02630.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.570+4153A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102880678 | ||||||
| chr14:102880804
|
G | A | 1 | a0002c0002t0001g0282 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.570+4279G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102880804 | ||||||
| chr14:102880816
|
G | A | 1 | a0001c0001t0046g0042 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.570+4291G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102880816 | ||||||
| chr14:102880825
|
C | G | 2 | a0002c0002t0001g0196a0002c0002t0001g0201 | 2 | NA18973.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.570+4300C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102880825 | ||||||
| chr14:102881008
|
G | A | 4 | a0001c0001t0018g0186a0001c0001t0018g0250a0001c0001t0018g0275others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.570+4483G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102881008 | ||||||
| chr14:102881261
|
G | A | 1 | a0001c0003t0037g0004 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.570+4736G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102881261 | ||||||
| chr14:102881378
|
C | A | 2 | a0001c0001t0031g0183a0001c0001t0042g0005 | 2 | HG01099.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.571-4811C>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102881378 | ||||||
| chr14:102881395
|
CA | C | 165 | a0001c0001t0001g0184a0001c0001t0002g0025a0001c0001t0002g0026others(162): Show | 165 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.571-4779delA | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 102881395 | |||||
| chr14:102881395
|
CAA | C | 7 | a0001c0001t0017g0143a0001c0001t0017g0144a0001c0001t0017g0145others(4): Show | 7 | HG02109.hp2 HG02630.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.571-4780_571-4779d others(4): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 102881395 | |||||
| chr14:102881402
|
A | C | 21 | a0001c0001t0005g0009a0001c0001t0005g0010a0001c0001t0005g0011others(18): Show | 21 | HG01069.hp1 HG01071.hp2 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.571-4787A>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102881402 | ||||||
| chr14:102881408
|
A | G | 5 | a0001c0001t0021g0057a0001c0001t0021g0099a0001c0001t0033g0123others(2): Show | 5 | HG00733.hp2 HG01123.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.571-4781A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102881408 | ||||||
| chr14:102881414
|
A | G | 1 | a0002c0002t0001g0251 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.571-4775A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102881414 | ||||||
| chr14:102881475
|
A | G | 1 | a0001c0001t0042g0005 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.571-4714A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102881475 | ||||||
| chr14:102881653
|
G | A | 1 | a0001c0001t0035g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.571-4536G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102881653 | ||||||
| chr14:102881700
|
T | C | 2 | a0001c0001t0010g0022a0001c0001t0010g0023 | 2 | HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.571-4489T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102881700 | ||||||
| chr14:102881711
|
C | T | 1 | a0002c0002t0001g0224 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.571-4478C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102881711 | ||||||
| chr14:102881758
|
C | T | 1 | a0001c0001t0050g0180 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.571-4431C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102881758 | ||||||
| chr14:102881818
|
C | T | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.571-4371C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102881818 | ||||||
| chr14:102881824
|
A | G | 2 | a0001c0001t0003g0100a0001c0001t0050g0180 | 2 | HG01884.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.571-4365A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102881824 | ||||||
| chr14:102881858
|
G | A | 2 | a0001c0001t0042g0005a0001c0004t0039g0002 | 2 | HG01993.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.571-4331G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102881858 | ||||||
| chr14:102881935
|
A | G | 2 | a0001c0001t0023g0043a0001c0001t0023g0075 | 2 | HG00609.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.571-4254A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102881935 | ||||||
| chr14:102882218
|
A | G | 2 | a0001c0001t0012g0001a0001c0001t0012g0179 | 2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.571-3971A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102882218 | ||||||
| chr14:102882365
|
G | T | 9 | a0001c0001t0010g0018a0001c0001t0010g0019a0001c0001t0010g0020others(6): Show | 9 | HG00639.hp2 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.571-3824G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102882365 | ||||||
| chr14:102882406
|
C | G | 172 | a0001c0001t0001g0184a0001c0001t0002g0025a0001c0001t0002g0026others(169): Show | 172 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.571-3783C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102882406 | ||||||
| chr14:102882409
|
G | T | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.571-3780G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102882409 | ||||||
| chr14:102882416
|
G | A | 5 | a0001c0001t0017g0143a0001c0001t0017g0144a0001c0001t0017g0145others(2): Show | 5 | HG02109.hp2 HG02922.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.571-3773G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102882416 | ||||||
| chr14:102882567
|
G | GT | 155 | a0001c0001t0001g0184a0001c0001t0002g0025a0001c0001t0002g0026others(152): Show | 155 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.571-3608dupT | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 102882567 | |||||
| chr14:102882567
|
G | T | 5 | a0002c0002t0001g0279a0002c0002t0001g0285a0002c0002t0001g0286others(2): Show | 5 | HG01256.hp1 HG01981.hp1 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.571-3622G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102882567 | ||||||
| chr14:102882572
|
T | TG | 9 | a0001c0001t0007g0008a0001c0001t0007g0045a0001c0001t0007g0094others(6): Show | 9 | HG01081.hp2 HG02451.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.571-3617_571-3616i others(3): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102882572 | ||||||
| chr14:102882584
|
A | G | 2 | a0001c0001t0012g0001a0001c0001t0012g0179 | 2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.571-3605A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102882584 | ||||||
| chr14:102882621
|
T | C | 1 | a0002c0002t0001g0266 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.571-3568T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102882621 | ||||||
| chr14:102882680
|
C | T | 1 | a0001c0001t0004g0007 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.571-3509C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102882680 | ||||||
| chr14:102882710
|
G | T | 1 | a0001c0001t0008g0064 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.571-3479G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102882710 | ||||||
| chr14:102882839
|
G | A | 168 | a0001c0001t0001g0184a0001c0001t0002g0025a0001c0001t0002g0026others(165): Show | 168 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.571-3350G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102882839 | ||||||
| chr14:102882868
|
G | A | 1 | a0001c0001t0003g0100 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.571-3321G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102882868 | ||||||
| chr14:102883103
|
G | A | 1 | a0001c0001t0012g0179 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.571-3086G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102883103 | ||||||
| chr14:102883201
|
T | C | 1 | a0001c0001t0050g0180 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.571-2988T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102883201 | ||||||
| chr14:102883290
|
T | G | 1 | a0001c0001t0024g0049 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.571-2899T>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102883290 | ||||||
| chr14:102883397
|
A | G | 1 | a0001c0001t0064g0198 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.571-2792A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102883397 | ||||||
| chr14:102883675
|
T | A | 1 | a0001c0001t0002g0112 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.571-2514T>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102883675 | ||||||
| chr14:102883860
|
C | G | 112 | a0001c0001t0001g0184a0001c0001t0002g0025a0001c0001t0002g0026others(109): Show | 112 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.571-2329C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102883860 | ||||||
| chr14:102884157
|
G | T | 4 | a0001c0003t0003g0182a0001c0003t0005g0181a0001c0003t0034g0003others(1): Show | 4 | HG02630.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.571-2032G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102884157 | ||||||
| chr14:102884164
|
TCA | T | 4 | a0001c0003t0003g0182a0001c0003t0005g0181a0001c0003t0034g0003others(1): Show | 4 | HG02630.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.571-2024_571-2023d others(4): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102884164 | ||||||
| chr14:102884251
|
G | A | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.571-1938G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102884251 | ||||||
| chr14:102884287
|
G | A | 1 | a0001c0001t0003g0100 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.571-1902G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102884287 | ||||||
| chr14:102884316
|
C | A | 1 | a0001c0001t0004g0171 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.571-1873C>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102884316 | ||||||
| chr14:102884475
|
A | G | 1 | a0001c0001t0004g0007 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.571-1714A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102884475 | ||||||
| chr14:102884476
|
T | C | 163 | a0001c0001t0001g0184a0001c0001t0002g0025a0001c0001t0002g0026others(160): Show | 163 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.571-1713T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102884476 | ||||||
| chr14:102884488
|
A | T | 4 | a0001c0003t0003g0182a0001c0003t0005g0181a0001c0003t0034g0003others(1): Show | 4 | HG02630.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.571-1701A>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102884488 | ||||||
| chr14:102884674
|
G | A | 6 | a0001c0001t0002g0026a0001c0001t0002g0058a0001c0001t0002g0067others(3): Show | 6 | HG01192.hp2 HG01358.hp1 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.571-1515G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102884674 | ||||||
| chr14:102884706
|
G | A | 1 | a0002c0002t0055g0260 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.571-1483G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102884706 | ||||||
| chr14:102885192
|
C | T | 33 | a0002c0002t0001g0206a0002c0002t0001g0248a0002c0002t0001g0251others(30): Show | 33 | HG00099.hp1 HG00733.hp1 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.571-997C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102885192 | ||||||
| chr14:102885210
|
G | A | 1 | a0001c0001t0002g0066 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.571-979G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102885210 | ||||||
| chr14:102885218
|
C | T | 1 | a0001c0001t0002g0059 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.571-971C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102885218 | ||||||
| chr14:102885278
|
C | G | 1 | a0001c0001t0019g0055 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.571-911C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102885278 | ||||||
| chr14:102885377
|
C | T | 1 | a0002c0002t0001g0270 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.571-812C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102885377 | ||||||
| chr14:102885446
|
C | A | 3 | a0001c0001t0002g0032a0001c0001t0002g0036a0001c0001t0029g0068 | 3 | NA18948.hp2 NA18955.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.571-743C>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102885446 | ||||||
| chr14:102885493
|
C | T | 139 | a0001c0001t0001g0184a0001c0001t0002g0025a0001c0001t0002g0026others(136): Show | 139 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.571-696C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102885493 | ||||||
| chr14:102885514
|
G | C | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.571-675G>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102885514 | ||||||
| chr14:102885541
|
G | T | 2 | a0002c0002t0001g0215a0002c0002t0009g0216 | 2 | HG01257.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.571-648G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102885541 | ||||||
| chr14:102885589
|
A | G | 1 | a0001c0001t0012g0168 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.571-600A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102885589 | ||||||
| chr14:102885594
|
G | A | 9 | a0001c0001t0015g0139a0001c0001t0015g0140a0001c0001t0015g0141others(6): Show | 9 | HG02055.hp1 HG02109.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.571-595G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102885594 | ||||||
| chr14:102885738
|
A | T | 1 | a0002c0002t0065g0276 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.571-451A>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102885738 | ||||||
| chr14:102885746
|
G | T | 8 | a0001c0001t0002g0032a0001c0001t0002g0036a0001c0001t0002g0079others(5): Show | 8 | HG00738.hp2 HG01167.hp2 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.571-443G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102885746 | ||||||
| chr14:102885749
|
A | T | 4 | a0001c0001t0011g0127a0001c0001t0011g0165a0001c0001t0028g0138others(1): Show | 4 | HG03017.hp2 HG03239.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.571-440A>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102885749 | ||||||
| chr14:102885756
|
C | T | 1 | a0001c0001t0035g0012 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.571-433C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102885756 | ||||||
| chr14:102885827
|
G | T | 11 | a0001c0001t0011g0127a0001c0001t0011g0147a0001c0001t0011g0148others(8): Show | 11 | HG01069.hp1 HG01071.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.571-362G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102885827 | ||||||
| chr14:102885829
|
G | C | 19 | a0001c0001t0005g0009a0001c0001t0005g0010a0001c0001t0005g0011others(16): Show | 19 | HG01069.hp1 HG01071.hp2 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.571-360G>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102885829 | ||||||
| chr14:102885929
|
G | A | 1 | a0001c0001t0021g0099 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.571-260G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102885929 | ||||||
| chr14:102886005
|
G | T | 1 | a0001c0001t0002g0106 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.571-184G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 6/11 | chr14 | 102886005 | ||||||
| chr14:102886338
|
T | G | 1 | a0001c0001t0004g0171 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.651+69T>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 7/11 | chr14 | 102886338 | ||||||
| chr14:102886346
|
C | T | 23 | a0001c0001t0005g0009a0001c0001t0005g0010a0001c0001t0005g0011others(20): Show | 23 | HG01069.hp1 HG01071.hp2 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.651+77C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 7/11 | chr14 | 102886346 | ||||||
| chr14:102886356
|
C | T | 1 | a0001c0001t0002g0025 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.651+87C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 7/11 | chr14 | 102886356 | ||||||
| chr14:102886429
|
T | A | 1 | a0001c0001t0033g0123 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.651+160T>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 7/11 | chr14 | 102886429 | ||||||
| chr14:102886612
|
C | T | 5 | a0001c0001t0021g0057a0001c0001t0021g0099a0001c0001t0033g0123others(2): Show | 5 | HG00733.hp2 HG01123.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.651+343C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 7/11 | chr14 | 102886612 | ||||||
| chr14:102886625
|
G | A | 4 | a0001c0003t0003g0182a0001c0003t0005g0181a0001c0003t0034g0003others(1): Show | 4 | HG02630.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.651+356G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 7/11 | chr14 | 102886625 | ||||||
| chr14:102886657
|
G | A | 1 | a0001c0001t0007g0163 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.651+388G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 7/11 | chr14 | 102886657 | ||||||
| chr14:102886679
|
C | T | 5 | a0001c0001t0021g0057a0001c0001t0021g0099a0001c0001t0033g0123others(2): Show | 5 | HG00733.hp2 HG01123.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.651+410C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 7/11 | chr14 | 102886679 | ||||||
| chr14:102886720
|
C | T | 1 | a0001c0001t0022g0296 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.651+451C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 7/11 | chr14 | 102886720 | ||||||
| chr14:102886735
|
A | C | 4 | a0001c0001t0021g0057a0001c0001t0021g0099a0001c0001t0067g0125others(1): Show | 4 | HG01123.hp1 HG02723.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.651+466A>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 7/11 | chr14 | 102886735 | ||||||
| chr14:102886752
|
G | A | 1 | a0002c0002t0001g0227 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.651+483G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 7/11 | chr14 | 102886752 | ||||||
| chr14:102886754
|
C | T | 1 | a0001c0001t0041g0051 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.651+485C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 7/11 | chr14 | 102886754 | ||||||
| chr14:102886764
|
A | G | 121 | a0001c0001t0001g0184a0001c0001t0002g0025a0001c0001t0002g0026others(118): Show | 121 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.651+495A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 7/11 | chr14 | 102886764 | ||||||
| chr14:102886943
|
CT | C | 7 | a0001c0001t0004g0040a0001c0001t0004g0170a0001c0001t0004g0171others(4): Show | 7 | HG01261.hp1 HG01928.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.651+676delT | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 102886943 | |||||
| chr14:102886972
|
G | T | 1 | a0001c0001t0003g0085 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.651+703G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 7/11 | chr14 | 102886972 | ||||||
| chr14:102887039
|
C | A | 5 | a0001c0001t0021g0057a0001c0001t0021g0099a0001c0001t0033g0123others(2): Show | 5 | HG00733.hp2 HG01123.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.651+770C>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 7/11 | chr14 | 102887039 | ||||||
| chr14:102887041
|
C | T | 1 | a0001c0001t0028g0138 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.651+772C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 7/11 | chr14 | 102887041 | ||||||
| chr14:102887146
|
G | A | 1 | a0001c0001t0038g0015 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.651+877G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 7/11 | chr14 | 102887146 | ||||||
| chr14:102887166
|
G | A | 1 | a0001c0001t0004g0175 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.651+897G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 7/11 | chr14 | 102887166 | ||||||
| chr14:102887215
|
G | T | 1 | a0001c0001t0002g0076 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.651+946G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 7/11 | chr14 | 102887215 | ||||||
| chr14:102887369
|
A | T | 2 | a0001c0001t0010g0019a0001c0001t0010g0020 | 2 | HG02258.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.651+1100A>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 7/11 | chr14 | 102887369 | ||||||
| chr14:102887585
|
T | C | 1 | a0002c0002t0001g0261 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.651+1316T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 7/11 | chr14 | 102887585 | ||||||
| chr14:102887847
|
G | A | 171 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(168): Show | 171 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.651+1578G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 7/11 | chr14 | 102887847 | ||||||
| chr14:102888136
|
A | G | 1 | a0001c0001t0021g0099 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.652-1424A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 7/11 | chr14 | 102888136 | ||||||
| chr14:102888324
|
G | A | 1 | a0001c0001t0019g0055 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.652-1236G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 7/11 | chr14 | 102888324 | ||||||
| chr14:102888709
|
G | T | 1 | a0001c0001t0008g0064 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.652-851G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 7/11 | chr14 | 102888709 | ||||||
| chr14:102889050
|
T | C | 1 | a0002c0002t0003g0135 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.652-510T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 7/11 | chr14 | 102889050 | ||||||
| chr14:102889217
|
T | G | 1 | a0001c0001t0014g0117 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.652-343T>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 7/11 | chr14 | 102889217 | ||||||
| chr14:102889468
|
T | C | 2 | a0001c0001t0027g0288a0001c0001t0027g0289 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.652-92T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 7/11 | chr14 | 102889468 | ||||||
| chr14:102889748
|
T | C | 4 | a0001c0003t0003g0182a0001c0003t0005g0181a0001c0003t0034g0003others(1): Show | 4 | HG02630.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.726+114T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 8/11 | chr14 | 102889748 | ||||||
| chr14:102890068
|
A | G | 1 | a0002c0002t0052g0242 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.726+434A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 8/11 | chr14 | 102890068 | ||||||
| chr14:102890402
|
TTC | T | 4 | a0001c0003t0003g0182a0001c0003t0005g0181a0001c0003t0034g0003others(1): Show | 4 | HG02630.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.726+770_726+771del others(2): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 102890402 | |||||
| chr14:102890912
|
C | T | 119 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(116): Show | 119 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.727-413C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 8/11 | chr14 | 102890912 | ||||||
| chr14:102890913
|
G | A | 4 | a0001c0001t0003g0100a0001c0001t0031g0183a0001c0001t0042g0005others(1): Show | 4 | HG01099.hp2 HG01884.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.727-412G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 8/11 | chr14 | 102890913 | ||||||
| chr14:102890973
|
C | T | 171 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(168): Show | 171 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.727-352C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 8/11 | chr14 | 102890973 | ||||||
| chr14:102890979
|
A | G | 1 | a0002c0002t0053g0290 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.727-346A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 8/11 | chr14 | 102890979 | ||||||
| chr14:102891149
|
A | G | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.727-176A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 8/11 | chr14 | 102891149 | ||||||
| chr14:102891266
|
G | T | 162 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(159): Show | 162 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.727-59G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 8/11 | chr14 | 102891266 | ||||||
| chr14:102891309
|
A | G | 1 | a0002c0002t0003g0006 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.727-16A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 8/11 | chr14 | 102891309 | ||||||
| chr14:102891449
|
T | C | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.819+32T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 9/11 | chr14 | 102891449 | ||||||
| chr14:102891733
|
A | C | 111 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(108): Show | 111 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.819+316A>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 9/11 | chr14 | 102891733 | ||||||
| chr14:102891987
|
A | T | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.819+570A>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 9/11 | chr14 | 102891987 | ||||||
| chr14:102892047
|
C | CT | 11 | a0001c0001t0002g0115a0001c0001t0003g0100a0001c0001t0004g0035others(8): Show | 11 | HG01175.hp1 HG01175.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.819+651dupT | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr14 | 102892047 | |||||
| chr14:102892047
|
CT | C | 22 | a0001c0001t0002g0113a0001c0001t0010g0018a0001c0001t0010g0019others(19): Show | 22 | HG00323.hp1 HG00639.hp2 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.819+651delT | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr14 | 102892047 | |||||
| chr14:102892194
|
A | G | 2 | a0001c0003t0003g0182a0001c0003t0005g0181 | 2 | HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.819+777A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 9/11 | chr14 | 102892194 | ||||||
| chr14:102892210
|
A | G | 1 | a0002c0002t0001g0268 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.819+793A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 9/11 | chr14 | 102892210 | ||||||
| chr14:102892245
|
A | G | 1 | a0002c0002t0001g0277 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.819+828A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 9/11 | chr14 | 102892245 | ||||||
| chr14:102892663
|
G | A | 1 | a0001c0001t0012g0098 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.819+1246G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 9/11 | chr14 | 102892663 | ||||||
| chr14:102893035
|
C | G | 1 | a0001c0001t0022g0296 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.819+1618C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 9/11 | chr14 | 102893035 | ||||||
| chr14:102893128
|
C | T | 1 | a0001c0001t0012g0001 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.819+1711C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 9/11 | chr14 | 102893128 | ||||||
| chr14:102893155
|
G | A | 157 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(154): Show | 157 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.819+1738G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 9/11 | chr14 | 102893155 | ||||||
| chr14:102893208
|
C | G | 2 | a0002c0002t0003g0128a0002c0002t0049g0129 | 2 | HG02698.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.819+1791C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 9/11 | chr14 | 102893208 | ||||||
| chr14:102893220
|
C | A | 1 | a0002c0002t0001g0245 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.819+1803C>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 9/11 | chr14 | 102893220 | ||||||
| chr14:102893220
|
C | CA | 7 | a0001c0001t0002g0032a0001c0001t0002g0113a0001c0003t0003g0182others(4): Show | 7 | HG02630.hp2 HG02976.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.819+1815dupA | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr14 | 102893220 | |||||
| chr14:102893257
|
G | T | 1 | a0001c0001t0002g0060 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.819+1840G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 9/11 | chr14 | 102893257 | ||||||
| chr14:102893308
|
T | G | 9 | a0001c0001t0010g0018a0001c0001t0010g0019a0001c0001t0010g0020others(6): Show | 9 | HG00639.hp2 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.819+1891T>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 9/11 | chr14 | 102893308 | ||||||
| chr14:102893368
|
C | T | 1 | a0001c0001t0007g0008 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.819+1951C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 9/11 | chr14 | 102893368 | ||||||
| chr14:102893387
|
C | CA | 21 | a0001c0001t0002g0032a0001c0001t0003g0100a0001c0001t0004g0035others(18): Show | 21 | HG00639.hp2 HG01069.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.819+1987dupA | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr14 | 102893387 | |||||
| chr14:102893514
|
C | T | 2 | a0001c0001t0012g0001a0001c0001t0012g0179 | 2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.819+2097C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 9/11 | chr14 | 102893514 | ||||||
| chr14:102893663
|
A | G | 65 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0032others(62): Show | 65 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.819+2246A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 9/11 | chr14 | 102893663 | ||||||
| chr14:102893735
|
G | A | 1 | a0001c0001t0019g0082 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.819+2318G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 9/11 | chr14 | 102893735 | ||||||
| chr14:102894103
|
G | A | 120 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(117): Show | 120 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.819+2686G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 9/11 | chr14 | 102894103 | ||||||
| chr14:102894320
|
C | T | 1 | a0002c0002t0003g0134 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.819+2903C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 9/11 | chr14 | 102894320 | ||||||
| chr14:102894379
|
A | G | 1 | a0001c0001t0004g0040 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.820-2882A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 9/11 | chr14 | 102894379 | ||||||
| chr14:102894533
|
C | A | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.820-2728C>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 9/11 | chr14 | 102894533 | ||||||
| chr14:102894736
|
C | T | 1 | a0002c0002t0001g0235 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.820-2525C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 9/11 | chr14 | 102894736 | ||||||
| chr14:102894786
|
C | T | 14 | a0001c0001t0002g0110a0001c0001t0002g0120a0001c0001t0004g0007others(11): Show | 14 | HG00609.hp1 HG00621.hp2 HG03688.hp1 others(11): Show |
intron_variant | MODIFIER | c.820-2475C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 9/11 | chr14 | 102894786 | ||||||
| chr14:102894898
|
A | G | 1 | a0001c0001t0002g0115 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.820-2363A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 9/11 | chr14 | 102894898 | ||||||
| chr14:102895255
|
T | C | 1 | a0001c0001t0005g0016 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.820-2006T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 9/11 | chr14 | 102895255 | ||||||
| chr14:102895354
|
C | T | 4 | a0001c0001t0021g0057a0001c0001t0021g0099a0001c0001t0067g0125others(1): Show | 4 | HG01123.hp1 HG02723.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.820-1907C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 9/11 | chr14 | 102895354 | ||||||
| chr14:102895399
|
G | A | 162 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(159): Show | 162 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.820-1862G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 9/11 | chr14 | 102895399 | ||||||
| chr14:102895555
|
A | G | 1 | a0001c0001t0050g0180 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.820-1706A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 9/11 | chr14 | 102895555 | ||||||
| chr14:102895584
|
C | T | 1 | a0002c0002t0001g0255 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.820-1677C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 9/11 | chr14 | 102895584 | ||||||
| chr14:102895600
|
T | C | 162 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(159): Show | 162 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.820-1661T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 9/11 | chr14 | 102895600 | ||||||
| chr14:102895645
|
G | A | 1 | a0001c0001t0002g0067 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.820-1616G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 9/11 | chr14 | 102895645 | ||||||
| chr14:102895680
|
A | C | 120 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(117): Show | 120 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.820-1581A>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 9/11 | chr14 | 102895680 | ||||||
| chr14:102895693
|
A | G | 4 | a0001c0001t0003g0100a0001c0001t0031g0183a0001c0001t0042g0005others(1): Show | 4 | HG01099.hp2 HG01884.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.820-1568A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 9/11 | chr14 | 102895693 | ||||||
| chr14:102895747
|
A | G | 1 | a0001c0001t0002g0106 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.820-1514A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 9/11 | chr14 | 102895747 | ||||||
| chr14:102895766
|
T | G | 3 | a0001c0001t0002g0041a0001c0001t0002g0065a0001c0001t0043g0031 | 3 | HG02165.hp1 NA19005.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.820-1495T>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 9/11 | chr14 | 102895766 | ||||||
| chr14:102895867
|
G | A | 1 | a0002c0002t0001g0238 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.820-1394G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 9/11 | chr14 | 102895867 | ||||||
| chr14:102895900
|
C | T | 1 | a0002c0002t0001g0278 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.820-1361C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 9/11 | chr14 | 102895900 | ||||||
| chr14:102895912
|
G | A | 1 | a0001c0001t0003g0100 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.820-1349G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 9/11 | chr14 | 102895912 | ||||||
| chr14:102895970
|
C | T | 1 | a0002c0002t0001g0224 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.820-1291C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 9/11 | chr14 | 102895970 | ||||||
| chr14:102895983
|
T | C | 1 | a0001c0001t0050g0180 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.820-1278T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 9/11 | chr14 | 102895983 | ||||||
| chr14:102896011
|
G | A | 7 | a0001c0001t0012g0024a0001c0001t0012g0098a0001c0001t0012g0124others(4): Show | 7 | HG01109.hp2 HG02559.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.820-1250G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 9/11 | chr14 | 102896011 | ||||||
| chr14:102896074
|
A | G | 2 | a0001c0003t0003g0182a0001c0003t0005g0181 | 2 | HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.820-1187A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 9/11 | chr14 | 102896074 | ||||||
| chr14:102896260
|
C | G | 1 | a0002c0007t0001g0273 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.820-1001C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 9/11 | chr14 | 102896260 | ||||||
| chr14:102896387
|
A | G | 5 | a0001c0001t0021g0057a0001c0001t0021g0099a0001c0001t0033g0123others(2): Show | 5 | HG00733.hp2 HG01123.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.820-874A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 9/11 | chr14 | 102896387 | ||||||
| chr14:102896443
|
T | A | 1 | a0001c0001t0021g0057 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.820-818T>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 9/11 | chr14 | 102896443 | ||||||
| chr14:102896451
|
G | A | 1 | a0002c0005t0001g0203 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.820-810G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 9/11 | chr14 | 102896451 | ||||||
| chr14:102896466
|
TAAATG | T | 4 | a0001c0003t0003g0182a0001c0003t0005g0181a0001c0003t0034g0003others(1): Show | 4 | HG02630.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.820-789_820-785del others(5): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr14 | 102896466 | |||||
| chr14:102896557
|
A | G | 2 | a0001c0001t0019g0082a0001c0001t0051g0284 | 2 | HG02970.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.820-704A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 9/11 | chr14 | 102896557 | ||||||
| chr14:102897077
|
G | A | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.820-184G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 9/11 | chr14 | 102897077 | ||||||
| chr14:102897246
|
G | T | 1 | a0002c0002t0003g0160 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.820-15G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 9/11 | chr14 | 102897246 | ||||||
| chr14:102897721
|
A | G | 1 | a0001c0001t0068g0029 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.960+320A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102897721 | ||||||
| chr14:102897860
|
C | T | 1 | a0001c0001t0004g0126 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.960+459C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102897860 | ||||||
| chr14:102898235
|
G | A | 1 | a0001c0001t0003g0100 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.960+834G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102898235 | ||||||
| chr14:102898400
|
G | T | 156 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(153): Show | 156 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(153): Show |
intron_variant | MODIFIER | c.960+999G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102898400 | ||||||
| chr14:102898549
|
A | G | 1 | a0002c0002t0001g0245 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.960+1148A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102898549 | ||||||
| chr14:102898738
|
T | G | 1 | a0002c0002t0001g0190 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.960+1337T>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102898738 | ||||||
| chr14:102899007
|
C | T | 1 | a0002c0002t0001g0292 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.960+1606C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102899007 | ||||||
| chr14:102899074
|
A | G | 1 | a0001c0001t0023g0075 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.960+1673A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102899074 | ||||||
| chr14:102899185
|
A | G | 1 | a0002c0002t0001g0190 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.960+1784A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102899185 | ||||||
| chr14:102899190
|
G | A | 1 | a0002c0002t0001g0281 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.960+1789G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102899190 | ||||||
| chr14:102899232
|
A | G | 9 | a0001c0001t0010g0018a0001c0001t0010g0019a0001c0001t0010g0020others(6): Show | 9 | HG00639.hp2 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.960+1831A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102899232 | ||||||
| chr14:102899303
|
G | A | 1 | a0001c0001t0003g0100 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.960+1902G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102899303 | ||||||
| chr14:102899352
|
G | A | 2 | a0001c0001t0010g0022a0001c0001t0010g0023 | 2 | HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.960+1951G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102899352 | ||||||
| chr14:102899359
|
C | T | 1 | a0002c0002t0001g0259 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.960+1958C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102899359 | ||||||
| chr14:102899491
|
C | G | 14 | a0001c0001t0002g0110a0001c0001t0002g0120a0001c0001t0004g0007others(11): Show | 14 | HG00609.hp1 HG00621.hp2 HG03688.hp1 others(11): Show |
intron_variant | MODIFIER | c.960+2090C>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102899491 | ||||||
| chr14:102899637
|
G | A | 2 | a0001c0001t0012g0001a0001c0001t0012g0179 | 2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.960+2236G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102899637 | ||||||
| chr14:102899653
|
A | G | 11 | a0001c0001t0011g0127a0001c0001t0011g0147a0001c0001t0011g0148others(8): Show | 11 | HG01069.hp1 HG01071.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.960+2252A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102899653 | ||||||
| chr14:102899656
|
C | T | 7 | a0001c0001t0010g0018a0001c0001t0010g0019a0001c0001t0010g0020others(4): Show | 7 | HG00639.hp2 HG02258.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.960+2255C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102899656 | ||||||
| chr14:102899670
|
T | G | 1 | a0001c0001t0003g0100 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.960+2269T>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102899670 | ||||||
| chr14:102899901
|
C | T | 1 | a0001c0001t0011g0166 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.960+2500C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102899901 | ||||||
| chr14:102900152
|
G | A | 4 | a0001c0003t0003g0182a0001c0003t0005g0181a0001c0003t0034g0003others(1): Show | 4 | HG02630.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.960+2751G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102900152 | ||||||
| chr14:102900173
|
C | T | 8 | a0001c0001t0002g0032a0001c0001t0002g0036a0001c0001t0002g0079others(5): Show | 8 | HG00738.hp2 HG01167.hp2 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.960+2772C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102900173 | ||||||
| chr14:102900179
|
G | GAAAA | 53 | a0001c0001t0002g0027a0001c0001t0002g0110a0001c0001t0004g0007others(50): Show | 53 | HG00639.hp2 HG01081.hp2 HG01167.hp1 others(50): Show |
intron_variant | MODIFIER | c.960+2778_960+2779i others(6): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102900179 | ||||||
| chr14:102900179
|
G | GAAAAA | 28 | a0001c0001t0002g0056a0001c0001t0002g0120a0001c0001t0004g0034others(25): Show | 28 | HG00609.hp1 HG00621.hp2 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.960+2778_960+2779i others(7): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102900179 | ||||||
| chr14:102900179
|
G | GAAAAAA | 4 | a0001c0001t0004g0048a0001c0001t0011g0148a0001c0001t0025g0052others(1): Show | 4 | HG01928.hp2 HG02630.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.960+2778_960+2779i others(8): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102900179 | ||||||
| chr14:102900180
|
G | A | 95 | a0001c0001t0002g0027a0001c0001t0002g0056a0001c0001t0002g0110others(92): Show | 95 | HG00609.hp1 HG00621.hp2 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.960+2779G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102900180 | ||||||
| chr14:102900180
|
G | GA | 13 | a0001c0001t0001g0184a0002c0002t0001g0205a0002c0002t0001g0211others(10): Show | 13 | HG01123.hp2 HG01346.hp1 HG01952.hp2 others(10): Show |
intron_variant | MODIFIER | c.960+2802dupA | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr14 | 102900180 | |||||
| chr14:102900180
|
G | GAAAA | 47 | a0001c0001t0002g0026a0001c0001t0002g0032a0001c0001t0002g0036others(44): Show | 47 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.960+2799_960+2802d others(6): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr14 | 102900180 | |||||
| chr14:102900180
|
G | GAAAAA | 18 | a0001c0001t0002g0025a0001c0001t0002g0066a0001c0001t0002g0077others(15): Show | 18 | HG01346.hp2 HG01934.hp2 HG01981.hp2 others(15): Show |
intron_variant | MODIFIER | c.960+2798_960+2802d others(7): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr14 | 102900180 | |||||
| chr14:102900180
|
GAAAAAAA others(3): Show |
G | 1 | a0002c0002t0006g0156 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.960+2793_960+2802d others(12): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr14 | 102900180 | |||||
| chr14:102900205
|
A | C | 161 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(158): Show | 161 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(158): Show |
intron_variant | MODIFIER | c.960+2804A>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102900205 | ||||||
| chr14:102900273
|
C | T | 7 | a0001c0001t0007g0045a0001c0001t0007g0095a0001c0001t0007g0096others(4): Show | 7 | HG01081.hp2 HG02486.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.960+2872C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102900273 | ||||||
| chr14:102900361
|
C | T | 118 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(115): Show | 118 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.961-2894C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102900361 | ||||||
| chr14:102900381
|
A | G | 2 | a0002c0002t0001g0283a0002c0002t0057g0265 | 2 | HG01243.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.961-2874A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102900381 | ||||||
| chr14:102900429
|
C | T | 2 | a0002c0002t0001g0261a0002c0002t0055g0260 | 2 | HG00733.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.961-2826C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102900429 | ||||||
| chr14:102900457
|
C | T | 10 | a0001c0001t0005g0009a0001c0001t0005g0010a0001c0001t0005g0011others(7): Show | 10 | HG02055.hp2 HG02615.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.961-2798C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102900457 | ||||||
| chr14:102900491
|
A | G | 2 | a0002c0002t0001g0261a0002c0002t0055g0260 | 2 | HG00733.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.961-2764A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102900491 | ||||||
| chr14:102900528
|
G | A | 1 | a0002c0002t0059g0239 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.961-2727G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102900528 | ||||||
| chr14:102900681
|
G | A | 7 | a0001c0001t0012g0024a0001c0001t0012g0098a0001c0001t0012g0124others(4): Show | 7 | HG01109.hp2 HG02559.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.961-2574G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102900681 | ||||||
| chr14:102900690
|
A | G | 1 | a0001c0001t0017g0143 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.961-2565A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102900690 | ||||||
| chr14:102900754
|
C | T | 1 | a0002c0002t0006g0155 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.961-2501C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102900754 | ||||||
| chr14:102900869
|
C | T | 2 | a0001c0001t0012g0001a0001c0001t0012g0179 | 2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.961-2386C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102900869 | ||||||
| chr14:102900922
|
A | G | 1 | a0001c0003t0034g0003 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.961-2333A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102900922 | ||||||
| chr14:102901268
|
TC | T | 3 | a0001c0001t0017g0143a0001c0001t0017g0144a0001c0001t0017g0145 | 3 | HG02109.hp2 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.961-1986delC | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102901268 | ||||||
| chr14:102901296
|
G | T | 11 | a0001c0001t0011g0127a0001c0001t0011g0147a0001c0001t0011g0148others(8): Show | 11 | HG01069.hp1 HG01071.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.961-1959G>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102901296 | ||||||
| chr14:102901330
|
G | A | 153 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(150): Show | 153 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(150): Show |
intron_variant | MODIFIER | c.961-1925G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102901330 | ||||||
| chr14:102901365
|
A | G | 1 | a0001c0001t0003g0100 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.961-1890A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102901365 | ||||||
| chr14:102901371
|
C | T | 153 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(150): Show | 153 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(150): Show |
intron_variant | MODIFIER | c.961-1884C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102901371 | ||||||
| chr14:102901499
|
C | T | 1 | a0002c0002t0001g0225 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.961-1756C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102901499 | ||||||
| chr14:102901559
|
G | A | 1 | a0001c0001t0033g0123 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.961-1696G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102901559 | ||||||
| chr14:102901581
|
C | T | 18 | a0001c0001t0010g0018a0001c0001t0010g0019a0001c0001t0010g0020others(15): Show | 18 | HG00639.hp2 HG01109.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.961-1674C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102901581 | ||||||
| chr14:102901591
|
T | G | 1 | a0002c0002t0003g0131 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.961-1664T>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102901591 | ||||||
| chr14:102901610
|
G | A | 7 | a0001c0001t0012g0024a0001c0001t0012g0098a0001c0001t0012g0124others(4): Show | 7 | HG01109.hp2 HG02559.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.961-1645G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102901610 | ||||||
| chr14:102901766
|
T | G | 19 | a0001c0001t0005g0009a0001c0001t0005g0010a0001c0001t0005g0011others(16): Show | 19 | HG01069.hp1 HG01071.hp2 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.961-1489T>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102901766 | ||||||
| chr14:102901796
|
G | A | 1 | a0002c0002t0001g0268 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.961-1459G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102901796 | ||||||
| chr14:102901807
|
G | A | 1 | a0002c0002t0001g0218 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.961-1448G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102901807 | ||||||
| chr14:102901877
|
C | T | 2 | a0001c0001t0010g0022a0001c0001t0010g0023 | 2 | HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.961-1378C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102901877 | ||||||
| chr14:102901933
|
T | C | 6 | a0001c0001t0017g0143a0001c0001t0017g0144a0001c0001t0017g0145others(3): Show | 6 | HG02109.hp2 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.961-1322T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102901933 | ||||||
| chr14:102902251
|
G | C | 4 | a0001c0003t0003g0182a0001c0003t0005g0181a0001c0003t0034g0003others(1): Show | 4 | HG02630.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.961-1004G>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102902251 | ||||||
| chr14:102902465
|
C | CAGGGTAG others(3): Show |
1 | a0001c0001t0029g0068 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.961-789_961-780dup others(10): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr14 | 102902465 | |||||
| chr14:102902537
|
G | GAGACC | 4 | a0001c0001t0017g0143a0001c0001t0017g0144a0001c0001t0017g0145others(1): Show | 4 | HG02109.hp2 HG02922.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.961-717_961-713dup others(5): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr14 | 102902537 | |||||
| chr14:102902740
|
G | A | 1 | a0002c0002t0003g0006 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.961-515G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102902740 | ||||||
| chr14:102903109
|
C | T | 1 | a0001c0001t0002g0118 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.961-146C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102903109 | ||||||
| chr14:102903150
|
G | A | 1 | a0001c0001t0050g0180 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.961-105G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 10/11 | chr14 | 102903150 | ||||||
| chr14:102903491
|
C | T | 1 | a0001c0001t0038g0015 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1135+62C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 11/11 | chr14 | 102903491 | ||||||
| chr14:102903619
|
G | A | 1 | a0001c0001t0012g0024 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1135+190G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 11/11 | chr14 | 102903619 | ||||||
| chr14:102903782
|
C | T | 137 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(134): Show | 137 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(134): Show |
intron_variant | MODIFIER | c.1135+353C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 11/11 | chr14 | 102903782 | ||||||
| chr14:102903826
|
C | T | 170 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(167): Show | 170 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(167): Show |
intron_variant | MODIFIER | c.1135+397C>T | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 11/11 | chr14 | 102903826 | ||||||
| chr14:102904011
|
G | A | 8 | a0001c0001t0005g0009a0001c0001t0005g0010a0001c0001t0005g0011others(5): Show | 8 | HG02055.hp2 HG02809.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1135+582G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 11/11 | chr14 | 102904011 | ||||||
| chr14:102904374
|
T | A | 1 | a0002c0002t0056g0244 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1136-839T>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 11/11 | chr14 | 102904374 | ||||||
| chr14:102904542
|
G | A | 1 | a0001c0001t0002g0066 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1136-671G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 11/11 | chr14 | 102904542 | ||||||
| chr14:102904753
|
T | C | 121 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(118): Show | 121 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.1136-460T>C | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 11/11 | chr14 | 102904753 | ||||||
| chr14:102904797
|
G | A | 1 | a0001c0001t0002g0041 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1136-416G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 11/11 | chr14 | 102904797 | ||||||
| chr14:102904809
|
C | CA | 28 | a0001c0001t0005g0009a0001c0001t0005g0010a0001c0001t0005g0011others(25): Show | 28 | HG01069.hp1 HG01071.hp2 HG01358.hp2 others(25): Show |
intron_variant | MODIFIER | c.1136-385dupA | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 102904809 | |||||
| chr14:102904809
|
CA | C | 31 | a0001c0001t0003g0100a0001c0001t0010g0018a0001c0001t0010g0019others(28): Show | 31 | HG00639.hp2 HG00733.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.1136-385delA | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 102904809 | |||||
| chr14:102904809
|
CAA | C | 116 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0027others(113): Show | 116 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.1136-386_1136-385d others(4): Show |
TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 102904809 | |||||
| chr14:102904910
|
G | A | 63 | a0001c0001t0001g0184a0002c0002t0001g0187a0002c0002t0001g0188others(60): Show | 63 | HG00323.hp2 HG00558.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.1136-303G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 11/11 | chr14 | 102904910 | ||||||
| chr14:102904956
|
A | G | 1 | a0001c0004t0039g0002 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1136-257A>G | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 11/11 | chr14 | 102904956 | ||||||
| chr14:102905075
|
G | A | 4 | a0002c0002t0009g0214a0002c0002t0009g0222a0002c0002t0009g0228others(1): Show | 4 | HG00323.hp2 HG01081.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.1136-138G>A | TRAF3 | ENSG00000131323.17 | transcript | ENST00000392745.8 | protein_coding | 11/11 | chr14 | 102905075 |