Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 10188 |
|---|---|
| ensemblid | ENSG00000061938.21 |
| hgncid | 19297 |
| symbol | TNK2 |
| name | tyrosine kinase non receptor 2 |
| refseq_nuc | NM_001382273.1 |
| refseq_prot | NP_001369202.1 |
| ensembl_nuc | ENST00000672887.2 |
| ensembl_prot | ENSP00000499899.1 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 195863364 |
| end | 195908551 |
| strand | - |
| ver | v1.2 |
| region | chr3:195863364-195908551 |
| region5000 | chr3:195858364-195913551 |
| regionname0 | TNK2_chr3_195863364_195908551 |
| regionname5000 | TNK2_chr3_195858364_195913551 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1055 | 254 | 76 | 35 | 108 | 11 | 22 | 78 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0002 | 0/0 | 650 | 48 | 10 | 16 | 14 | 0 | 8 | 9 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0003 | 0/0 | 1055 | 22 | 0 | 13 | 2 | 3 | 4 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0004 | 0/0 | 1055 | 12 | 0 | 0 | 12 | 0 | 0 | 10 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0005 | 0/0 | 1055 | 6 | 0 | 0 | 6 | 0 | 0 | 5 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0006 | 0/0 | 892 | 3 | 1 | 1 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0007 | 0/0 | 1055 | 3 | 1 | 2 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0008 | 0/0 | 1055 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0009 | 0/0 | 1055 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0010 | 0/0 | 1055 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0011 | 0/0 | 1055 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0012 | 0/0 | 1055 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0013 | 0/0 | 650 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0014 | 0/0 | 892 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0015 | 0/0 | 1055 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0016 | 0/0 | 650 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0017 | 0/0 | 650 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0018 | 0/0 | 1055 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0019 | 0/0 | 892 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0020 | 0/0 | 1055 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0021 | 0/0 | 1055 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0022 | 0/0 | 1055 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0023 | 0/0 | 1055 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0024 | 0/0 | 1055 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0025 | 0/0 | 1055 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0026 | 0/0 | 650 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0027 | 0/0 | 1055 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0028 | 0/0 | 650 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 3168 | 103 | 21 | 24 | 40 | 4 | 13 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0002 | 0/0 | 3168 | 48 | 29 | 6 | 10 | 2 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0003 | 0/0 | 3168 | 37 | 0 | 2 | 32 | 0 | 3 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0004 | 0/0 | 3169 | 15 | 1 | 5 | 6 | 0 | 3 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0005 | 0/0 | 3168 | 13 | 0 | 7 | 0 | 3 | 3 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0006 | 0/1 | 3168 | 13 | 5 | 0 | 4 | 1 | 2 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0007 | 0/0 | 3168 | 10 | 0 | 0 | 10 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0008 | 0/0 | 3169 | 7 | 2 | 2 | 2 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0009 | 0/0 | 3168 | 7 | 0 | 0 | 7 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0010 | 0/0 | 3169 | 6 | 0 | 4 | 1 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0011 | 0/0 | 3168 | 6 | 4 | 0 | 2 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0012 | 0/0 | 3168 | 6 | 0 | 1 | 2 | 0 | 3 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0013 | 0/0 | 3168 | 5 | 3 | 0 | 2 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0014 | 0/0 | 3168 | 4 | 4 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0015 | 0/0 | 3168 | 4 | 0 | 4 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0016 | 0/0 | 3168 | 3 | 3 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0017 | 0/0 | 3168 | 3 | 3 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0018 | 0/0 | 3169 | 3 | 0 | 0 | 3 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0019 | 0/0 | 3168 | 3 | 0 | 0 | 3 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0020 | 0/0 | 3168 | 3 | 0 | 0 | 0 | 3 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0021 | 0/0 | 3168 | 3 | 1 | 2 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0022 | 0/0 | 3168 | 3 | 0 | 0 | 3 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0023 | 0/0 | 3169 | 2 | 1 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0024 | 0/0 | 3168 | 2 | 0 | 1 | 0 | 1 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0025 | 0/0 | 3169 | 2 | 1 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0026 | 0/0 | 3169 | 2 | 2 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0027 | 0/0 | 3169 | 2 | 1 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0028 | 0/0 | 3168 | 2 | 0 | 0 | 0 | 0 | 2 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0029 | 0/0 | 3168 | 2 | 0 | 0 | 2 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0030 | 0/0 | 3168 | 2 | 0 | 2 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0031 | 0/0 | 3168 | 2 | 0 | 0 | 2 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0032 | 0/0 | 3168 | 2 | 0 | 0 | 2 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0033 | 0/0 | 3168 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0034 | 0/0 | 3168 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0035 | 0/0 | 3170 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0036 | 0/0 | 3168 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0037 | 0/0 | 3168 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0038 | 0/0 | 3169 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0039 | 0/0 | 3168 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0040 | 0/0 | 3168 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0041 | 0/0 | 3169 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0042 | 0/0 | 3168 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0043 | 0/0 | 3168 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0044 | 0/0 | 3169 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0045 | 0/0 | 3168 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0046 | 0/0 | 3168 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0047 | 0/0 | 3168 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0048 | 0/0 | 3169 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0049 | 0/0 | 3168 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0050 | 0/0 | 3168 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0051 | 0/0 | 3169 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0052 | 0/0 | 3168 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0053 | 0/0 | 3168 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0054 | 0/0 | 3168 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0055 | 0/0 | 3168 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0056 | 0/0 | 3168 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0057 | 0/0 | 3169 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0058 | 0/0 | 3168 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0059 | 0/0 | 3168 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0060 | 0/0 | 3169 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0061 | 0/0 | 3168 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0062 | 0/0 | 3168 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0063 | 0/0 | 3169 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0064 | 0/0 | 3168 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0065 | 0/0 | 3169 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0066 | 0/0 | 3169 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0067 | 0/0 | 3170 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0068 | 0/0 | 3169 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0069 | 0/0 | 3169 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0070 | 0/0 | 3168 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0071 | 0/0 | 3168 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0072 | 0/0 | 3170 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0073 | 0/0 | 3169 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0074 | 0/0 | 3169 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0075 | 0/0 | 3168 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0076 | 0/0 | 3169 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0077 | 0/0 | 3168 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0078 | 0/0 | 3168 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| c0079 | 0/0 | 3169 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 903 | 264 | 77 | 63 | 84 | 9 | 30 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| t0002 | 1/0 | 903 | 66 | 2 | 7 | 43 | 5 | 8 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| t0003 | 0/0 | 903 | 15 | 0 | 2 | 13 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| t0004 | 0/0 | 903 | 8 | 8 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| t0005 | 0/0 | 903 | 7 | 0 | 0 | 7 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| t0006 | 0/0 | 903 | 5 | 5 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| t0007 | 0/0 | 903 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| t0008 | 0/0 | 903 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| t0009 | 0/0 | 903 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| t0010 | 0/0 | 903 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| t0011 | 0/0 | 903 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| t0012 | 0/0 | 903 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| t0013 | 0/0 | 903 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0087 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0243 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 3168 | 103 | 21 | 24 | 40 | 4 | 13 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0002 | 0/0 | 3168 | 48 | 29 | 6 | 10 | 2 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0003 | 0/0 | 3168 | 37 | 0 | 2 | 32 | 0 | 3 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0006 | 0/1 | 3168 | 13 | 5 | 0 | 4 | 1 | 2 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0009 | 0/0 | 3168 | 7 | 0 | 0 | 7 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0011 | 0/0 | 3168 | 6 | 4 | 0 | 2 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0012 | 0/0 | 3168 | 6 | 0 | 1 | 2 | 0 | 3 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0013 | 0/0 | 3168 | 5 | 3 | 0 | 2 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0014 | 0/0 | 3168 | 4 | 4 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0017 | 0/0 | 3168 | 3 | 3 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0019 | 0/0 | 3168 | 3 | 0 | 0 | 3 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0020 | 0/0 | 3168 | 3 | 0 | 0 | 0 | 3 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0024 | 0/0 | 3168 | 2 | 0 | 1 | 0 | 1 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0031 | 0/0 | 3168 | 2 | 0 | 0 | 2 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0033 | 0/0 | 3168 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0034 | 0/0 | 3168 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0036 | 0/0 | 3168 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0037 | 0/0 | 3168 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0040 | 0/0 | 3168 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0042 | 0/0 | 3168 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0050 | 0/0 | 3168 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0053 | 0/0 | 3168 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0058 | 0/0 | 3168 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0061 | 0/0 | 3168 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0062 | 0/0 | 3168 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0070 | 0/0 | 3168 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0002c0004 | 0/0 | 3169 | 15 | 1 | 5 | 6 | 0 | 3 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0002c0008 | 0/0 | 3169 | 7 | 2 | 2 | 2 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0002c0010 | 0/0 | 3169 | 6 | 0 | 4 | 1 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0002c0018 | 0/0 | 3169 | 3 | 0 | 0 | 3 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0002c0023 | 0/0 | 3169 | 2 | 1 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0002c0026 | 0/0 | 3169 | 2 | 2 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0002c0027 | 0/0 | 3169 | 2 | 1 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0002c0041 | 0/0 | 3169 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0002c0044 | 0/0 | 3169 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0002c0057 | 0/0 | 3169 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0002c0060 | 0/0 | 3169 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0002c0065 | 0/0 | 3169 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0002c0066 | 0/0 | 3169 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0002c0067 | 0/0 | 3170 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0002c0068 | 0/0 | 3169 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0002c0072 | 0/0 | 3170 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0002c0073 | 0/0 | 3169 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0002c0074 | 0/0 | 3169 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0003c0005 | 0/0 | 3168 | 13 | 0 | 7 | 0 | 3 | 3 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0003c0015 | 0/0 | 3168 | 4 | 0 | 4 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0003c0030 | 0/0 | 3168 | 2 | 0 | 2 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0003c0043 | 0/0 | 3168 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0003c0046 | 0/0 | 3168 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0003c0054 | 0/0 | 3168 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0004c0007 | 0/0 | 3168 | 10 | 0 | 0 | 10 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0004c0032 | 0/0 | 3168 | 2 | 0 | 0 | 2 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0005c0022 | 0/0 | 3168 | 3 | 0 | 0 | 3 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0005c0029 | 0/0 | 3168 | 2 | 0 | 0 | 2 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0005c0056 | 0/0 | 3168 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0006c0025 | 0/0 | 3169 | 2 | 1 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0006c0069 | 0/0 | 3169 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0007c0021 | 0/0 | 3168 | 3 | 1 | 2 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0008c0016 | 0/0 | 3168 | 3 | 3 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0009c0028 | 0/0 | 3168 | 2 | 0 | 0 | 0 | 0 | 2 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0010c0059 | 0/0 | 3168 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0011c0078 | 0/0 | 3168 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0012c0045 | 0/0 | 3168 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0013c0076 | 0/0 | 3169 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0014c0063 | 0/0 | 3169 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0015c0064 | 0/0 | 3168 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0016c0051 | 0/0 | 3169 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0017c0035 | 0/0 | 3170 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0018c0039 | 0/0 | 3168 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0019c0038 | 0/0 | 3169 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0020c0071 | 0/0 | 3168 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0021c0075 | 0/0 | 3168 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0022c0055 | 0/0 | 3168 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0023c0052 | 0/0 | 3168 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0024c0077 | 0/0 | 3168 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0025c0047 | 0/0 | 3168 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0026c0048 | 0/0 | 3169 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0027c0049 | 0/0 | 3168 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0028c0079 | 0/0 | 3169 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4070 | 71 | 18 | 19 | 22 | 2 | 10 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0001t0002 | 1/0 | 4070 | 30 | 2 | 5 | 17 | 2 | 3 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0001t0007 | 0/0 | 4070 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0001t0008 | 0/0 | 4070 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0002t0001 | 0/0 | 4070 | 48 | 29 | 6 | 10 | 2 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0003t0001 | 0/0 | 4070 | 15 | 0 | 0 | 13 | 0 | 2 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0003t0002 | 0/0 | 4070 | 6 | 0 | 0 | 5 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0003t0003 | 0/0 | 4070 | 9 | 0 | 2 | 7 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0003t0005 | 0/0 | 4070 | 6 | 0 | 0 | 6 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0003t0013 | 0/0 | 4070 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0006t0001 | 0/1 | 4070 | 12 | 5 | 0 | 4 | 1 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0006t0012 | 0/0 | 4070 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0009t0002 | 0/0 | 4070 | 7 | 0 | 0 | 7 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0011t0001 | 0/0 | 4070 | 6 | 4 | 0 | 2 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0012t0001 | 0/0 | 4070 | 5 | 0 | 1 | 2 | 0 | 2 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0012t0011 | 0/0 | 4070 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0013t0001 | 0/0 | 4070 | 5 | 3 | 0 | 2 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0014t0004 | 0/0 | 4070 | 4 | 4 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0017t0006 | 0/0 | 4070 | 3 | 3 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0019t0003 | 0/0 | 4070 | 3 | 0 | 0 | 3 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0020t0002 | 0/0 | 4070 | 3 | 0 | 0 | 0 | 3 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0024t0001 | 0/0 | 4070 | 2 | 0 | 1 | 0 | 1 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0031t0001 | 0/0 | 4070 | 2 | 0 | 0 | 2 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0033t0001 | 0/0 | 4070 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0034t0006 | 0/0 | 4070 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0036t0001 | 0/0 | 4070 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0037t0004 | 0/0 | 4070 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0040t0001 | 0/0 | 4070 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0042t0001 | 0/0 | 4070 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0050t0001 | 0/0 | 4070 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0053t0003 | 0/0 | 4070 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0058t0004 | 0/0 | 4070 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0061t0001 | 0/0 | 4070 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0062t0001 | 0/0 | 4070 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0001c0070t0001 | 0/0 | 4070 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0002c0004t0001 | 0/0 | 4071 | 8 | 1 | 4 | 1 | 0 | 2 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0002c0004t0002 | 0/0 | 4071 | 7 | 0 | 1 | 5 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0002c0008t0001 | 0/0 | 4071 | 4 | 2 | 1 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0002c0008t0002 | 0/0 | 4071 | 3 | 0 | 1 | 1 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0002c0010t0001 | 0/0 | 4071 | 6 | 0 | 4 | 1 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0002c0018t0001 | 0/0 | 4071 | 2 | 0 | 0 | 2 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0002c0018t0003 | 0/0 | 4071 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0002c0023t0001 | 0/0 | 4071 | 2 | 1 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0002c0026t0001 | 0/0 | 4071 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0002c0026t0009 | 0/0 | 4071 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0002c0027t0001 | 0/0 | 4071 | 2 | 1 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0002c0041t0001 | 0/0 | 4071 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0002c0044t0006 | 0/0 | 4071 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0002c0057t0004 | 0/0 | 4071 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0002c0060t0001 | 0/0 | 4071 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0002c0065t0002 | 0/0 | 4071 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0002c0066t0002 | 0/0 | 4071 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0002c0067t0001 | 0/0 | 4072 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0002c0068t0001 | 0/0 | 4071 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0002c0072t0001 | 0/0 | 4072 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0002c0073t0001 | 0/0 | 4071 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0002c0074t0001 | 0/0 | 4071 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0003c0005t0001 | 0/0 | 4070 | 13 | 0 | 7 | 0 | 3 | 3 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0003c0015t0001 | 0/0 | 4070 | 4 | 0 | 4 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0003c0030t0001 | 0/0 | 4070 | 2 | 0 | 2 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0003c0043t0001 | 0/0 | 4070 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0003c0046t0001 | 0/0 | 4070 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0003c0054t0001 | 0/0 | 4070 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0004c0007t0001 | 0/0 | 4070 | 10 | 0 | 0 | 10 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0004c0032t0001 | 0/0 | 4070 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0004c0032t0002 | 0/0 | 4070 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0005c0022t0002 | 0/0 | 4070 | 3 | 0 | 0 | 3 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0005c0029t0002 | 0/0 | 4070 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0005c0029t0010 | 0/0 | 4070 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0005c0056t0002 | 0/0 | 4070 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0006c0025t0001 | 0/0 | 4071 | 2 | 1 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0006c0069t0001 | 0/0 | 4071 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0007c0021t0001 | 0/0 | 4070 | 3 | 1 | 2 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0008c0016t0001 | 0/0 | 4070 | 3 | 3 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0009c0028t0001 | 0/0 | 4070 | 2 | 0 | 0 | 0 | 0 | 2 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0010c0059t0001 | 0/0 | 4070 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0011c0078t0001 | 0/0 | 4070 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0012c0045t0001 | 0/0 | 4070 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0013c0076t0001 | 0/0 | 4071 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0014c0063t0002 | 0/0 | 4071 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0015c0064t0001 | 0/0 | 4070 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0016c0051t0001 | 0/0 | 4071 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0017c0035t0004 | 0/0 | 4072 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0018c0039t0001 | 0/0 | 4070 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0019c0038t0001 | 0/0 | 4071 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0020c0071t0002 | 0/0 | 4070 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0021c0075t0001 | 0/0 | 4070 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0022c0055t0003 | 0/0 | 4070 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0023c0052t0005 | 0/0 | 4070 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0024c0077t0001 | 0/0 | 4070 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0025c0047t0001 | 0/0 | 4070 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0026c0048t0001 | 0/0 | 4071 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0027c0049t0001 | 0/0 | 4070 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| a0028c0079t0001 | 0/0 | 4071 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | copy fasta | chr3 | 195858364 | 195913551 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0001g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0002g0243 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0002g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0007g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0001t0008g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0002t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0002t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0002t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0002t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0002t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0002t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0002t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0002t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0002t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0002t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0002t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0002t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0002t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0002t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0002t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0002t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0002t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0002t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0002t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0002t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0003t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0003t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0003t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0003t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0003t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0003t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0003t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0003t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0003t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0003t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0003t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0003t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0003t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0003t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0003t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0003t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0003t0003g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0003t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0003t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0003t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0003t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0003t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0003t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0003t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0003t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0003t0005g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0003t0005g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0003t0005g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0003t0005g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0003t0005g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0003t0005g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0003t0013g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0006t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0006t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0006t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0006t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0006t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0006t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0006t0001g0087 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0006t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0006t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0006t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0006t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0006t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0006t0012g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0009t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0009t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0009t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0009t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0009t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0009t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0009t0002g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0011t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0011t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0011t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0011t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0011t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0011t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0012t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0012t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0012t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0012t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0012t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0012t0011g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0013t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0013t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0013t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0013t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0013t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0014t0004g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0014t0004g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0014t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0017t0006g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0017t0006g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0017t0006g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0019t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0019t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0019t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0020t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0020t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0020t0002g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0024t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0024t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0031t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0031t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0033t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0034t0006g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0036t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0037t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0040t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0042t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0050t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0053t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0058t0004g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0061t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0062t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0001c0070t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0002c0004t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0002c0004t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0002c0004t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0002c0004t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0002c0004t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0002c0004t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0002c0004t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0002c0004t0001g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0002c0004t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0002c0004t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0002c0004t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0002c0004t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0002c0004t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0002c0004t0002g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0002c0004t0002g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0002c0008t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0002c0008t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0002c0008t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0002c0008t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0002c0008t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0002c0008t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0002c0008t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0002c0010t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0002c0010t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0002c0010t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0002c0010t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0002c0010t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0002c0010t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0002c0018t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0002c0018t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0002c0018t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0002c0023t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0002c0023t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0002c0026t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0002c0026t0009g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0002c0027t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0002c0027t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0002c0041t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0002c0044t0006g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0002c0057t0004g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0002c0060t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0002c0065t0002g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0002c0066t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0002c0067t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0002c0068t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0002c0072t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0002c0073t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0002c0074t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0003c0005t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0003c0005t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0003c0005t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0003c0005t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0003c0005t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0003c0005t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0003c0005t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0003c0005t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0003c0005t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0003c0005t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0003c0005t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0003c0005t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0003c0005t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0003c0015t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0003c0015t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0003c0015t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0003c0015t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0003c0030t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0003c0030t0001g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0003c0043t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0003c0046t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0003c0054t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0004c0007t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0004c0007t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0004c0007t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0004c0007t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0004c0007t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0004c0007t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0004c0007t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0004c0007t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0004c0007t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0004c0007t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0004c0032t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0004c0032t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0005c0022t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0005c0022t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0005c0022t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0005c0029t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0005c0029t0010g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0005c0056t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0006c0025t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0006c0025t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0006c0069t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0007c0021t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0007c0021t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0007c0021t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0008c0016t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0008c0016t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0009c0028t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0009c0028t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0010c0059t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0011c0078t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0012c0045t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0013c0076t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0014c0063t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0015c0064t0001g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0016c0051t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0017c0035t0004g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0018c0039t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0019c0038t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0020c0071t0002g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0021c0075t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0022c0055t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0023c0052t0005g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0024c0077t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0025c0047t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0026c0048t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0027c0049t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| a0028c0079t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0290 | EUR | GBR | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG00099 | hp2 | a0001 | c0020 | t0002 | g0335 | EUR | GBR | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG00140 | hp1 | a0001 | c0006 | t0001 | g0061 | EUR | GBR | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG00140 | hp2 | a0003 | c0005 | t0001 | g0245 | EUR | GBR | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0048 | EUR | FIN | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG00280 | hp2 | a0001 | c0020 | t0002 | g0252 | EUR | FIN | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0031 | EUR | FIN | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0116 | EUR | FIN | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | CHS | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG00408 | hp2 | a0005 | c0022 | t0002 | g0057 | EAS | CHS | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG00423 | hp1 | a0004 | c0007 | t0001 | g0260 | EAS | CHS | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG00423 | hp2 | a0001 | c0003 | t0001 | g0138 | EAS | CHS | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG00558 | hp1 | a0004 | c0032 | t0001 | g0303 | EAS | CHS | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG00558 | hp2 | a0001 | c0003 | t0005 | g0201 | EAS | CHS | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG00597 | hp1 | a0028 | c0079 | t0001 | g0044 | EAS | CHS | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | CHS | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG00609 | hp1 | a0001 | c0003 | t0002 | g0158 | EAS | CHS | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG00609 | hp2 | a0001 | c0003 | t0001 | g0150 | EAS | CHS | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG00621 | hp1 | a0002 | c0004 | t0002 | g0146 | EAS | CHS | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0045 | EAS | CHS | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG00639 | hp1 | a0013 | c0076 | t0001 | g0078 | AMR | PUR | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | PUR | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG00642 | hp2 | a0027 | c0049 | t0001 | g0022 | AMR | PUR | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | CHS | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG00673 | hp2 | a0001 | c0040 | t0001 | g0019 | EAS | CHS | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0306 | AMR | PUR | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0029 | AMR | PUR | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG00735 | hp2 | a0002 | c0073 | t0001 | g0068 | AMR | PUR | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0316 | AMR | PUR | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG00741 | hp2 | a0002 | c0067 | t0001 | g0082 | AMR | PUR | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01069 | hp2 | a0003 | c0005 | t0001 | g0054 | AMR | PUR | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0342 | AMR | PUR | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01071 | hp1 | a0002 | c0010 | t0001 | g0053 | AMR | PUR | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01071 | hp2 | a0002 | c0004 | t0001 | g0341 | AMR | PUR | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01074 | hp1 | a0003 | c0030 | t0001 | g0360 | AMR | PUR | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01074 | hp2 | a0002 | c0010 | t0001 | g0035 | AMR | PUR | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | PUR | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01081 | hp2 | a0003 | c0005 | t0001 | g0042 | AMR | PUR | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01099 | hp1 | a0001 | c0024 | t0001 | g0189 | AMR | PUR | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01099 | hp2 | a0003 | c0005 | t0001 | g0037 | AMR | PUR | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01109 | hp1 | a0010 | c0059 | t0001 | g0021 | AMR | PUR | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01109 | hp2 | a0002 | c0008 | t0002 | g0172 | AMR | PUR | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01167 | hp1 | a0003 | c0015 | t0001 | g0080 | AMR | PUR | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0329 | AMR | PUR | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01175 | hp1 | a0002 | c0023 | t0001 | g0207 | AMR | PUR | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01175 | hp2 | a0002 | c0072 | t0001 | g0091 | AMR | PUR | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01192 | hp1 | a0002 | c0008 | t0001 | g0219 | AMR | PUR | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0178 | AMR | PUR | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01243 | hp1 | a0003 | c0015 | t0001 | g0064 | AMR | PUR | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0179 | AMR | PUR | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0052 | AMR | CLM | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01255 | hp2 | a0002 | c0004 | t0002 | g0332 | AMR | CLM | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01256 | hp1 | a0001 | c0012 | t0001 | g0067 | AMR | CLM | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0358 | AMR | CLM | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01258 | hp1 | a0002 | c0004 | t0001 | g0357 | AMR | CLM | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0333 | AMR | CLM | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | CLM | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01261 | hp2 | a0002 | c0068 | t0001 | g0063 | AMR | CLM | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | CLM | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01346 | hp2 | a0003 | c0030 | t0001 | g0072 | AMR | CLM | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | CLM | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01358 | hp2 | a0003 | c0015 | t0001 | g0084 | AMR | CLM | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | CLM | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0047 | AMR | CLM | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01433 | hp2 | a0003 | c0015 | t0001 | g0020 | AMR | CLM | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01496 | hp1 | a0002 | c0010 | t0001 | g0030 | AMR | CLM | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01496 | hp2 | a0001 | c0003 | t0003 | g0126 | AMR | CLM | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01516 | hp1 | a0003 | c0005 | t0001 | g0041 | EUR | IBS | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0328 | EUR | IBS | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01884 | hp1 | a0001 | c0014 | t0004 | g0002 | AFR | ACB | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01884 | hp2 | a0001 | c0011 | t0001 | g0108 | AFR | ACB | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01891 | hp1 | a0007 | c0021 | t0001 | g0118 | AFR | ACB | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01891 | hp2 | a0001 | c0014 | t0004 | g0002 | AFR | ACB | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01934 | hp1 | a0006 | c0025 | t0001 | g0216 | AMR | PEL | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01934 | hp2 | a0002 | c0004 | t0001 | g0279 | AMR | PEL | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01943 | hp2 | a0003 | c0005 | t0001 | g0034 | AMR | PEL | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01952 | hp1 | a0007 | c0021 | t0001 | g0113 | AMR | PEL | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01952 | hp2 | a0002 | c0004 | t0001 | g0282 | AMR | PEL | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01975 | hp1 | a0018 | c0039 | t0001 | g0038 | AMR | PEL | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01978 | hp1 | a0003 | c0005 | t0001 | g0039 | AMR | PEL | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01978 | hp2 | a0003 | c0005 | t0001 | g0046 | AMR | PEL | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01993 | hp1 | a0002 | c0010 | t0001 | g0043 | AMR | PEL | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0297 | AMR | PEL | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PEL | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02004 | hp2 | a0001 | c0036 | t0001 | g0023 | AMR | PEL | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0177 | EAS | KHV | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0136 | EAS | KHV | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | KHV | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | KHV | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0192 | AFR | ACB | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02055 | hp2 | a0002 | c0004 | t0001 | g0350 | AFR | ACB | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | KHV | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02056 | hp2 | a0002 | c0018 | t0001 | g0147 | EAS | KHV | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02071 | hp2 | a0002 | c0010 | t0001 | g0024 | EAS | KHV | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02074 | hp1 | a0001 | c0009 | t0002 | g0354 | EAS | KHV | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02074 | hp2 | a0001 | c0033 | t0001 | g0176 | EAS | KHV | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02080 | hp1 | a0002 | c0008 | t0002 | g0253 | EAS | KHV | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | KHV | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | KHV | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02083 | hp2 | a0002 | c0004 | t0002 | g0241 | EAS | KHV | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0338 | EAS | KHV | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02129 | hp2 | a0001 | c0003 | t0003 | g0170 | EAS | KHV | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02132 | hp1 | a0001 | c0003 | t0005 | g0197 | EAS | KHV | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02135 | hp1 | a0001 | c0003 | t0002 | g0206 | EAS | KHV | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | KHV | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0248 | AFR | ACB | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0212 | AFR | ACB | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02148 | hp1 | a0019 | c0038 | t0001 | g0032 | AMR | PEL | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02148 | hp2 | a0001 | c0003 | t0003 | g0124 | AMR | PEL | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02155 | hp1 | a0021 | c0075 | t0001 | g0079 | EAS | CDX | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02155 | hp2 | a0003 | c0046 | t0001 | g0027 | EAS | CDX | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02165 | hp1 | a0001 | c0003 | t0001 | g0200 | EAS | CDX | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02165 | hp2 | a0001 | c0003 | t0005 | g0199 | EAS | CDX | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0235 | AFR | ACB | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0326 | AFR | ACB | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0223 | AFR | ACB | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | ACB | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02273 | hp1 | a0003 | c0005 | t0001 | g0033 | AMR | PEL | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0036 | AMR | PEL | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02280 | hp1 | a0001 | c0014 | t0004 | g0093 | AFR | ACB | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0220 | AFR | ACB | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PEL | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02300 | hp2 | a0007 | c0021 | t0001 | g0115 | AMR | PEL | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0221 | AFR | ACB | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02451 | hp2 | a0001 | c0011 | t0001 | g0107 | AFR | ACB | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02523 | hp1 | a0006 | c0069 | t0001 | g0280 | EAS | KHV | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02523 | hp2 | a0001 | c0003 | t0001 | g0122 | EAS | KHV | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0363 | AFR | GWD | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02572 | hp2 | a0008 | c0016 | t0001 | g0004 | AFR | GWD | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02602 | hp1 | a0002 | c0010 | t0001 | g0028 | SAS | PJL | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02602 | hp2 | a0024 | c0077 | t0001 | g0086 | SAS | PJL | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02615 | hp1 | a0017 | c0035 | t0004 | g0233 | AFR | GWD | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02615 | hp2 | a0001 | c0006 | t0001 | g0092 | AFR | GWD | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02622 | hp1 | a0001 | c0011 | t0001 | g0231 | AFR | GWD | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02622 | hp2 | a0002 | c0026 | t0009 | g0099 | AFR | GWD | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02630 | hp2 | a0002 | c0044 | t0006 | g0015 | AFR | GWD | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02647 | hp1 | a0002 | c0008 | t0001 | g0010 | AFR | GWD | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0130 | AFR | GWD | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02683 | hp1 | a0001 | c0006 | t0001 | g0066 | SAS | PJL | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02683 | hp2 | a0009 | c0028 | t0001 | g0295 | SAS | PJL | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0049 | SAS | PJL | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02698 | hp2 | a0009 | c0028 | t0001 | g0344 | SAS | PJL | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0186 | AFR | GWD | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02717 | hp2 | a0008 | c0016 | t0001 | g0224 | AFR | GWD | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02723 | hp1 | a0012 | c0045 | t0001 | g0009 | AFR | GWD | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02723 | hp2 | a0008 | c0016 | t0001 | g0004 | AFR | GWD | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02735 | hp1 | a0001 | c0012 | t0001 | g0088 | SAS | PJL | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0293 | SAS | PJL | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02809 | hp1 | a0002 | c0027 | t0001 | g0114 | AFR | GWD | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02809 | hp2 | a0002 | c0023 | t0001 | g0017 | AFR | GWD | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02818 | hp1 | a0001 | c0006 | t0001 | g0100 | AFR | GWD | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02818 | hp2 | a0001 | c0013 | t0001 | g0119 | AFR | GWD | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02886 | hp1 | a0025 | c0047 | t0001 | g0008 | AFR | GWD | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | GWD | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0211 | AFR | GWD | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0018 | AFR | GWD | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0348 | AFR | GWD | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | GWD | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0226 | AFR | ESN | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02922 | hp2 | a0001 | c0062 | t0001 | g0239 | AFR | ESN | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02970 | hp1 | a0001 | c0013 | t0001 | g0120 | AFR | ESN | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02970 | hp2 | a0001 | c0017 | t0006 | g0013 | AFR | ESN | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02976 | hp1 | a0001 | c0050 | t0001 | g0213 | AFR | ESN | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ESN | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG03017 | hp1 | a0001 | c0003 | t0001 | g0171 | SAS | PJL | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0364 | AFR | GWD | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0181 | AFR | ESN | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG03130 | hp2 | a0001 | c0061 | t0001 | g0238 | AFR | ESN | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG03139 | hp1 | a0001 | c0017 | t0006 | g0012 | AFR | ESN | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0214 | AFR | ESN | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG03195 | hp1 | a0001 | c0058 | t0004 | g0237 | AFR | ESN | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG03195 | hp2 | a0002 | c0060 | t0001 | g0240 | AFR | ESN | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG03209 | hp1 | a0002 | c0008 | t0001 | g0182 | AFR | MSL | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0336 | AFR | MSL | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0353 | AFR | MSL | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG03225 | hp2 | a0001 | c0011 | t0001 | g0230 | AFR | MSL | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | MSL | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG03453 | hp2 | a0001 | c0001 | t0007 | g0232 | AFR | MSL | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0222 | AFR | MSL | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | MSL | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG03490 | hp1 | a0003 | c0005 | t0001 | g0059 | SAS | PJL | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG03490 | hp2 | a0001 | c0012 | t0001 | g0085 | SAS | PJL | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0356 | SAS | PJL | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG03492 | hp2 | a0003 | c0005 | t0001 | g0058 | SAS | PJL | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0217 | AFR | ESN | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ESN | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG03540 | hp1 | a0001 | c0034 | t0006 | g0016 | AFR | GWD | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG03540 | hp2 | a0001 | c0006 | t0001 | g0229 | AFR | GWD | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0225 | AFR | MSL | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0184 | AFR | MSL | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0313 | SAS | PJL | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG03654 | hp2 | a0002 | c0027 | t0001 | g0117 | SAS | PJL | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG03688 | hp1 | a0001 | c0003 | t0001 | g0149 | SAS | STU | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG03688 | hp2 | a0002 | c0074 | t0001 | g0073 | SAS | STU | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0355 | SAS | PJL | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0270 | SAS | BEB | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG03831 | hp2 | a0002 | c0065 | t0002 | g0318 | SAS | BEB | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG03834 | hp1 | a0003 | c0005 | t0001 | g0055 | SAS | BEB | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG03834 | hp2 | a0001 | c0006 | t0012 | g0065 | SAS | BEB | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | BEB | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG03942 | hp2 | a0002 | c0004 | t0001 | g0283 | SAS | BEB | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG04115 | hp1 | a0011 | c0078 | t0001 | g0272 | SAS | STU | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG04115 | hp2 | a0003 | c0054 | t0001 | g0134 | SAS | STU | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0315 | SAS | BEB | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG04184 | hp2 | a0002 | c0008 | t0002 | g0267 | SAS | BEB | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG04199 | hp1 | a0015 | c0064 | t0001 | g0347 | SAS | STU | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG04199 | hp2 | a0002 | c0004 | t0001 | g0131 | SAS | STU | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0062 | SAS | STU | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG04204 | hp2 | a0002 | c0004 | t0002 | g0258 | SAS | STU | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG04228 | hp1 | a0014 | c0063 | t0002 | g0247 | SAS | STU | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0325 | SAS | STU | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | CHB | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0175 | EAS | CHB | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0227 | AFR | YRI | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0193 | AFR | YRI | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18939 | hp1 | a0005 | c0029 | t0002 | g0320 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18940 | hp1 | a0001 | c0031 | t0001 | g0089 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18940 | hp2 | a0002 | c0008 | t0001 | g0204 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18941 | hp1 | a0002 | c0018 | t0001 | g0159 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18941 | hp2 | a0001 | c0003 | t0001 | g0168 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18942 | hp1 | a0001 | c0003 | t0003 | g0140 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18942 | hp2 | a0005 | c0022 | t0002 | g0309 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0202 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18949 | hp1 | a0016 | c0051 | t0001 | g0208 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18949 | hp2 | a0001 | c0006 | t0001 | g0097 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18951 | hp2 | a0003 | c0043 | t0001 | g0025 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18952 | hp1 | a0001 | c0003 | t0003 | g0154 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18952 | hp2 | a0001 | c0013 | t0001 | g0277 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18954 | hp1 | a0022 | c0055 | t0003 | g0153 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18954 | hp2 | a0004 | c0007 | t0001 | g0310 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18956 | hp1 | a0020 | c0071 | t0002 | g0346 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18956 | hp2 | a0001 | c0003 | t0003 | g0135 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18957 | hp1 | a0001 | c0011 | t0001 | g0060 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18959 | hp1 | a0001 | c0003 | t0001 | g0155 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0187 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18960 | hp1 | a0002 | c0004 | t0002 | g0362 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18960 | hp2 | a0004 | c0007 | t0001 | g0289 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18961 | hp1 | a0001 | c0011 | t0001 | g0081 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18963 | hp2 | a0001 | c0006 | t0001 | g0083 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18964 | hp1 | a0001 | c0019 | t0003 | g0133 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18964 | hp2 | a0023 | c0052 | t0005 | g0198 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18969 | hp1 | a0004 | c0007 | t0001 | g0300 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18969 | hp2 | a0005 | c0029 | t0010 | g0345 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18971 | hp1 | a0001 | c0003 | t0001 | g0169 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18973 | hp1 | a0001 | c0003 | t0005 | g0196 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18973 | hp2 | a0001 | c0003 | t0003 | g0137 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18975 | hp2 | a0005 | c0056 | t0002 | g0040 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18978 | hp1 | a0001 | c0070 | t0001 | g0352 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18978 | hp2 | a0002 | c0041 | t0001 | g0026 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18979 | hp1 | a0026 | c0048 | t0001 | g0123 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18979 | hp2 | a0001 | c0003 | t0001 | g0148 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0174 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18980 | hp2 | a0002 | c0004 | t0002 | g0327 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0361 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18984 | hp1 | a0001 | c0009 | t0002 | g0324 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18984 | hp2 | a0001 | c0003 | t0002 | g0157 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18986 | hp1 | a0001 | c0019 | t0003 | g0132 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18986 | hp2 | a0001 | c0012 | t0001 | g0075 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18989 | hp1 | a0004 | c0007 | t0001 | g0307 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18989 | hp2 | a0001 | c0009 | t0002 | g0266 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18990 | hp1 | a0001 | c0001 | t0008 | g0269 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18990 | hp2 | a0001 | c0003 | t0003 | g0125 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18992 | hp2 | a0002 | c0004 | t0002 | g0143 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18993 | hp1 | a0001 | c0013 | t0001 | g0145 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18993 | hp2 | a0002 | c0066 | t0002 | g0242 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18994 | hp1 | a0001 | c0053 | t0003 | g0129 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18994 | hp2 | a0004 | c0007 | t0001 | g0271 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18995 | hp1 | a0001 | c0003 | t0001 | g0276 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18999 | hp1 | a0001 | c0003 | t0001 | g0156 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA19002 | hp2 | a0001 | c0003 | t0003 | g0142 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA19004 | hp1 | a0001 | c0003 | t0002 | g0151 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0203 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA19010 | hp1 | a0004 | c0007 | t0001 | g0299 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0322 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | LWK | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA19030 | hp2 | a0002 | c0026 | t0001 | g0074 | AFR | LWK | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0218 | AFR | LWK | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA19043 | hp2 | a0001 | c0006 | t0001 | g0077 | AFR | LWK | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA19054 | hp1 | a0004 | c0007 | t0001 | g0302 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA19054 | hp2 | a0002 | c0018 | t0003 | g0152 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA19056 | hp2 | a0001 | c0003 | t0001 | g0160 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA19058 | hp1 | a0001 | c0009 | t0002 | g0263 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA19058 | hp2 | a0001 | c0006 | t0001 | g0070 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0180 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA19060 | hp2 | a0001 | c0009 | t0002 | g0255 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA19066 | hp1 | a0001 | c0006 | t0001 | g0069 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA19066 | hp2 | a0004 | c0007 | t0001 | g0262 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA19068 | hp2 | a0001 | c0003 | t0001 | g0166 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA19070 | hp1 | a0001 | c0031 | t0001 | g0090 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA19074 | hp1 | a0001 | c0012 | t0001 | g0071 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA19074 | hp2 | a0004 | c0007 | t0001 | g0312 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA19077 | hp1 | a0001 | c0003 | t0002 | g0127 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0340 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA19079 | hp1 | a0005 | c0022 | t0002 | g0319 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA19079 | hp2 | a0001 | c0009 | t0002 | g0330 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA19080 | hp1 | a0001 | c0009 | t0002 | g0331 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA19080 | hp2 | a0004 | c0032 | t0002 | g0301 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0321 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA19081 | hp2 | a0001 | c0003 | t0005 | g0257 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA19083 | hp1 | a0002 | c0004 | t0001 | g0256 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA19083 | hp2 | a0001 | c0003 | t0013 | g0365 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA19090 | hp1 | a0001 | c0003 | t0005 | g0139 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA19090 | hp2 | a0001 | c0003 | t0001 | g0195 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA19091 | hp1 | a0001 | c0019 | t0003 | g0194 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0191 | AFR | YRI | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0003 | AFR | YRI | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0101 | AFR | ASW | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA20129 | hp2 | a0001 | c0013 | t0001 | g0121 | AFR | ASW | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA20752 | hp1 | a0001 | c0024 | t0001 | g0190 | EUR | TSI | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA20752 | hp2 | a0001 | c0020 | t0002 | g0251 | EUR | TSI | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA20805 | hp1 | a0003 | c0005 | t0001 | g0051 | EUR | TSI | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0334 | EUR | TSI | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA20905 | hp1 | a0001 | c0003 | t0002 | g0141 | SAS | GIH | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA20905 | hp2 | a0001 | c0012 | t0011 | g0102 | SAS | GIH | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0359 | AMR | CLM | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | CLM | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02109 | hp1 | a0006 | c0025 | t0001 | g0096 | AFR | ACB | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0185 | AFR | ACB | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0228 | AFR | ACB | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02486 | hp2 | a0001 | c0017 | t0006 | g0014 | AFR | ACB | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02559 | hp1 | a0001 | c0014 | t0004 | g0109 | AFR | ACB | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0011 | AFR | MSL | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG03471 | hp2 | a0002 | c0057 | t0004 | g0236 | AFR | MSL | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0205 | AFR | USA | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| HG06807 | hp2 | a0001 | c0006 | t0001 | g0098 | AFR | USA | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0351 | AFR | USA | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA20300 | hp2 | a0001 | c0037 | t0004 | g0110 | AFR | USA | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0183 | AFR | LWK | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| NA21309 | hp2 | a0001 | c0042 | t0001 | g0234 | AFR | LWK | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0006 | t0001 | g0087 | REF | REF | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0243 | REF | REF | TNK2_chr3_195858364_195913551 | TNK2 | chr3 | 195858364 | 195913551 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:195864185
|
C | T | 2 | a0002a0007 | 5 | HG01891.hp1 HG01952.hp1 HG02300.hp2 others(2): Show |
missense_variant&splice_region_variant | MODERATE | c.3164G>A | p.Arg1055His | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 16/16 | 3249/4070 | 3164/3168 | 1055/1055 | chr3 | 195864185 | ||
| chr3:195867585
|
C | T | 1 | a0002 | 1 | HG00735.hp2 | missense_variant | MODERATE | c.2713G>A | p.Val905Met | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 13/16 | 2798/4070 | 2713/3168 | 905/1055 | chr3 | 195867585 | ||
| chr3:195867623
|
C | T | 1 | a0005 | 6 | HG00408.hp2 NA18939.hp1 NA18942.hp2 others(3): Show |
missense_variant | MODERATE | c.2675G>A | p.Arg892His | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 13/16 | 2760/4070 | 2675/3168 | 892/1055 | chr3 | 195867623 | ||
| chr3:195867659
|
C | T | 1 | a0021 | 1 | HG02155.hp1 | missense_variant | MODERATE | c.2639G>A | p.Arg880Gln | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 13/16 | 2724/4070 | 2639/3168 | 880/1055 | chr3 | 195867659 | ||
| chr3:195867836
|
C | CG | 5 | a0002a0006a0014others(2): Show | 8 | HG00741.hp2 HG01175.hp2 HG01934.hp1 others(5): Show |
frameshift_variant | HIGH | c.2461dupC | p.Arg821fs | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 13/16 | 2546/4070 | 2461/3168 | 821/1055 | chr3 | 195867836 | ||
| chr3:195867848
|
G | A | 1 | a0002 | 1 | NA18993.hp2 | missense_variant | MODERATE | c.2450C>T | p.Pro817Leu | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 13/16 | 2535/4070 | 2450/3168 | 817/1055 | chr3 | 195867848 | ||
| chr3:195867983
|
G | A | 1 | a0018 | 1 | HG01975.hp1 | missense_variant | MODERATE | c.2315C>T | p.Ser772Phe | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 13/16 | 2400/4070 | 2315/3168 | 772/1055 | chr3 | 195867983 | ||
| chr3:195868010
|
C | T | 1 | a0020 | 1 | NA18956.hp1 | missense_variant | MODERATE | c.2288G>A | p.Arg763Gln | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 13/16 | 2373/4070 | 2288/3168 | 763/1055 | chr3 | 195868010 | ||
| chr3:195868011
|
G | A | 1 | a0026 | 1 | NA18979.hp1 | missense_variant | MODERATE | c.2287C>T | p.Arg763Trp | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 13/16 | 2372/4070 | 2287/3168 | 763/1055 | chr3 | 195868011 | ||
| chr3:195868026
|
C | T | 1 | a0002 | 1 | HG03831.hp2 | missense_variant | MODERATE | c.2272G>A | p.Val758Ile | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 13/16 | 2357/4070 | 2272/3168 | 758/1055 | chr3 | 195868026 | ||
| chr3:195868079
|
G | A | 6 | a0002a0003a0013others(3): Show | 34 | HG00140.hp2 HG00639.hp1 HG00642.hp2 others(31): Show |
missense_variant | MODERATE | c.2219C>T | p.Pro740Leu | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 13/16 | 2304/4070 | 2219/3168 | 740/1055 | chr3 | 195868079 | ||
| chr3:195868173
|
C | A | 1 | a0022 | 1 | NA18954.hp1 | missense_variant | MODERATE | c.2125G>T | p.Gly709Trp | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 13/16 | 2210/4070 | 2125/3168 | 709/1055 | chr3 | 195868173 | ||
| chr3:195868341
|
C | T | 1 | a0009 | 2 | HG02683.hp2 HG02698.hp2 |
missense_variant | MODERATE | c.1957G>A | p.Val653Met | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 13/16 | 2042/4070 | 1957/3168 | 653/1055 | chr3 | 195868341 | ||
| chr3:195868357
|
C | CG | 6 | a0002a0013a0016others(3): Show | 53 | HG00597.hp1 HG00621.hp1 HG00639.hp1 others(50): Show |
frameshift_variant | HIGH | c.1940dupC | p.Pro648fs | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 13/16 | 2025/4070 | 1940/3168 | 647/1055 | chr3 | 195868357 | ||
| chr3:195868412
|
C | G | 1 | a0017 | 1 | HG02615.hp1 | missense_variant | MODERATE | c.1886G>C | p.Arg629Pro | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 13/16 | 1971/4070 | 1886/3168 | 629/1055 | chr3 | 195868412 | ||
| chr3:195868487
|
A | T | 1 | a0023 | 1 | NA18964.hp2 | missense_variant | MODERATE | c.1811T>A | p.Leu604Gln | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 13/16 | 1896/4070 | 1811/3168 | 604/1055 | chr3 | 195868487 | ||
| chr3:195868503
|
G | A | 1 | a0008 | 3 | HG02572.hp2 HG02717.hp2 HG02723.hp2 |
missense_variant | MODERATE | c.1795C>T | p.Pro599Ser | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 13/16 | 1880/4070 | 1795/3168 | 599/1055 | chr3 | 195868503 | ||
| chr3:195868622
|
C | T | 1 | a0016 | 1 | NA18949.hp1 | missense_variant | MODERATE | c.1676G>A | p.Arg559Gln | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 13/16 | 1761/4070 | 1676/3168 | 559/1055 | chr3 | 195868622 | ||
| chr3:195868631
|
C | T | 2 | a0014a0015 | 2 | HG04199.hp1 HG04228.hp1 |
missense_variant | MODERATE | c.1667G>A | p.Gly556Asp | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 13/16 | 1752/4070 | 1667/3168 | 556/1055 | chr3 | 195868631 | ||
| chr3:195868688
|
C | A | 1 | a0013 | 1 | HG00639.hp1 | missense_variant | MODERATE | c.1610G>T | p.Ser537Ile | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 13/16 | 1695/4070 | 1610/3168 | 537/1055 | chr3 | 195868688 | ||
| chr3:195869515
|
G | C | 1 | a0012 | 1 | HG02723.hp1 | missense_variant | MODERATE | c.1570C>G | p.Pro524Ala | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 12/16 | 1655/4070 | 1570/3168 | 524/1055 | chr3 | 195869515 | ||
| chr3:195870129
|
G | C | 1 | a0024 | 1 | HG02602.hp2 | missense_variant | MODERATE | c.1528C>G | p.Leu510Val | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 11/16 | 1613/4070 | 1528/3168 | 510/1055 | chr3 | 195870129 | ||
| chr3:195870141
|
G | A | 1 | a0025 | 1 | HG02886.hp1 | missense_variant | MODERATE | c.1516C>T | p.Pro506Ser | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 11/16 | 1601/4070 | 1516/3168 | 506/1055 | chr3 | 195870141 | ||
| chr3:195872310
|
G | A | 1 | a0011 | 1 | HG04115.hp1 | missense_variant | MODERATE | c.1417C>T | p.Arg473Cys | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/16 | 1502/4070 | 1417/3168 | 473/1055 | chr3 | 195872310 | ||
| chr3:195878463
|
G | A | 1 | a0026 | 1 | NA18979.hp1 | missense_variant | MODERATE | c.1144C>T | p.Arg382Trp | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 8/16 | 1229/4070 | 1144/3168 | 382/1055 | chr3 | 195878463 | ||
| chr3:195878482
|
T | G | 1 | a0027 | 1 | HG00642.hp2 | missense_variant | MODERATE | c.1125A>C | p.Arg375Ser | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 8/16 | 1210/4070 | 1125/3168 | 375/1055 | chr3 | 195878482 | ||
| chr3:195884963
|
G | A | 1 | a0010 | 1 | HG01109.hp1 | missense_variant | MODERATE | c.305C>T | p.Ser102Leu | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 4/16 | 390/4070 | 305/3168 | 102/1055 | chr3 | 195884963 | ||
| chr3:195884973
|
G | A | 2 | a0004a0028 | 13 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(10): Show |
missense_variant | MODERATE | c.295C>T | p.Arg99Trp | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 4/16 | 380/4070 | 295/3168 | 99/1055 | chr3 | 195884973 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:195867724
|
G | A | 1 | a0001c0053 | 1 | NA18994.hp1 | synonymous_variant | LOW | c.2574C>T | p.Cys858Cys | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 13/16 | 2659/4070 | 2574/3168 | 858/1055 | chr3 | 195867724 | ||
| chr3:195867934
|
A | G | 21 | a0001c0006a0001c0011a0001c0012others(18): Show | 52 | HG00140.hp1 HG00639.hp1 HG00735.hp2 others(49): Show |
synonymous_variant | LOW | c.2364T>C | p.Ala788Ala | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 13/16 | 2449/4070 | 2364/3168 | 788/1055 | chr3 | 195867934 | ||
| chr3:195867987
|
G | A | 2 | a0001c0040a0001c0070 | 2 | HG00673.hp2 NA18978.hp1 |
synonymous_variant | LOW | c.2311C>T | p.Leu771Leu | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 13/16 | 2396/4070 | 2311/3168 | 771/1055 | chr3 | 195867987 | ||
| chr3:195868114
|
C | T | 1 | a0001c0024 | 2 | HG01099.hp1 NA20752.hp1 |
synonymous_variant | LOW | c.2184G>A | p.Glu728Glu | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 13/16 | 2269/4070 | 2184/3168 | 728/1055 | chr3 | 195868114 | ||
| chr3:195868183
|
C | T | 12 | a0001c0006a0001c0012a0001c0036others(9): Show | 30 | HG00140.hp1 HG00735.hp2 HG01109.hp1 others(27): Show |
synonymous_variant | LOW | c.2115G>A | p.Pro705Pro | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 13/16 | 2200/4070 | 2115/3168 | 705/1055 | chr3 | 195868183 | ||
| chr3:195868219
|
C | G | 1 | a0017c0035 | 1 | HG02615.hp1 | synonymous_variant | LOW | c.2079G>C | p.Arg693Arg | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 13/16 | 2164/4070 | 2079/3168 | 693/1055 | chr3 | 195868219 | ||
| chr3:195868426
|
C | T | 1 | a0001c0040 | 1 | HG00673.hp2 | synonymous_variant | LOW | c.1872G>A | p.Thr624Thr | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 13/16 | 1957/4070 | 1872/3168 | 624/1055 | chr3 | 195868426 | ||
| chr3:195868489
|
G | C | 1 | a0020c0071 | 1 | NA18956.hp1 | synonymous_variant | LOW | c.1809C>G | p.Ser603Ser | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 13/16 | 1894/4070 | 1809/3168 | 603/1055 | chr3 | 195868489 | ||
| chr3:195868498
|
G | A | 1 | a0020c0071 | 1 | NA18956.hp1 | synonymous_variant | LOW | c.1800C>T | p.Cys600Cys | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 13/16 | 1885/4070 | 1800/3168 | 600/1055 | chr3 | 195868498 | ||
| chr3:195868534
|
G | A | 19 | a0001c0012a0001c0013a0001c0014others(16): Show | 37 | HG00408.hp2 HG00558.hp1 HG00673.hp2 others(34): Show |
synonymous_variant | LOW | c.1764C>T | p.Phe588Phe | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 13/16 | 1849/4070 | 1764/3168 | 588/1055 | chr3 | 195868534 | ||
| chr3:195868594
|
C | T | 1 | a0001c0034 | 1 | HG03540.hp1 | synonymous_variant | LOW | c.1704G>A | p.Ala568Ala | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 13/16 | 1789/4070 | 1704/3168 | 568/1055 | chr3 | 195868594 | ||
| chr3:195868606
|
C | T | 1 | a0001c0033 | 1 | HG02074.hp2 | synonymous_variant | LOW | c.1692G>A | p.Ala564Ala | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 13/16 | 1777/4070 | 1692/3168 | 564/1055 | chr3 | 195868606 | ||
| chr3:195868630
|
G | A | 2 | a0014c0063a0015c0064 | 2 | HG04199.hp1 HG04228.hp1 |
synonymous_variant | LOW | c.1668C>T | p.Gly556Gly | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 13/16 | 1753/4070 | 1668/3168 | 556/1055 | chr3 | 195868630 | ||
| chr3:195868642
|
C | T | 1 | a0001c0020 | 3 | HG00099.hp2 HG00280.hp2 NA20752.hp2 |
synonymous_variant | LOW | c.1656G>A | p.Leu552Leu | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 13/16 | 1741/4070 | 1656/3168 | 552/1055 | chr3 | 195868642 | ||
| chr3:195868663
|
G | A | 2 | a0001c0017a0002c0044 | 4 | HG02486.hp2 HG02630.hp2 HG02970.hp2 others(1): Show |
synonymous_variant | LOW | c.1635C>T | p.Ser545Ser | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 13/16 | 1720/4070 | 1635/3168 | 545/1055 | chr3 | 195868663 | ||
| chr3:195870136
|
G | C | 1 | a0003c0046 | 1 | HG02155.hp2 | synonymous_variant | LOW | c.1521C>G | p.Pro507Pro | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 11/16 | 1606/4070 | 1521/3168 | 507/1055 | chr3 | 195870136 | ||
| chr3:195879058
|
G | A | 1 | a0001c0009 | 7 | HG02074.hp1 NA18984.hp1 NA18989.hp2 others(4): Show |
synonymous_variant | LOW | c.1005C>T | p.Asn335Asn | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 7/16 | 1090/4070 | 1005/3168 | 335/1055 | chr3 | 195879058 | ||
| chr3:195879130
|
G | A | 1 | a0001c0050 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.933C>T | p.Ser311Ser | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 7/16 | 1018/4070 | 933/3168 | 311/1055 | chr3 | 195879130 | ||
| chr3:195879148
|
G | A | 9 | a0001c0003a0001c0019a0001c0053others(6): Show | 49 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(46): Show |
synonymous_variant | LOW | c.915C>T | p.Arg305Arg | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 7/16 | 1000/4070 | 915/3168 | 305/1055 | chr3 | 195879148 | ||
| chr3:195884917
|
G | A | 5 | a0001c0058a0001c0061a0001c0062others(2): Show | 5 | HG02922.hp2 HG03130.hp2 HG03195.hp1 others(2): Show |
synonymous_variant | LOW | c.351C>T | p.Leu117Leu | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 4/16 | 436/4070 | 351/3168 | 117/1055 | chr3 | 195884917 | ||
| chr3:195888496
|
G | A | 3 | a0001c0061a0001c0062a0002c0060 | 3 | HG02922.hp2 HG03130.hp2 HG03195.hp2 |
synonymous_variant | LOW | c.93C>T | p.Asn31Asn | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/16 | 178/4070 | 93/3168 | 31/1055 | chr3 | 195888496 | ||
| chr3:195888505
|
A | G | 43 | a0001c0002a0001c0003a0001c0014others(40): Show | 163 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(160): Show |
synonymous_variant | LOW | c.84T>C | p.Asp28Asp | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/16 | 169/4070 | 84/3168 | 28/1055 | chr3 | 195888505 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:195863557
|
C | T | 1 | a0005c0029t0010 | 1 | NA18969.hp2 | 3_prime_UTR_variant | MODIFIER | c.*624G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 16/16 | 624 | chr3 | 195863557 | |||||
| chr3:195863755
|
G | A | 1 | a0001c0001t0008 | 1 | NA18990.hp1 | 3_prime_UTR_variant | MODIFIER | c.*426C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 16/16 | 426 | chr3 | 195863755 | |||||
| chr3:195863786
|
G | A | 5 | a0001c0014t0004a0001c0037t0004a0001c0058t0004others(2): Show | 8 | HG01884.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*395C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 16/16 | 395 | chr3 | 195863786 | |||||
| chr3:195863994
|
G | A | 1 | a0002c0026t0009 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*187C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 16/16 | 187 | chr3 | 195863994 | |||||
| chr3:195864004
|
A | G | 79 | a0001c0001t0001a0001c0001t0007a0001c0001t0008others(76): Show | 305 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(302): Show |
3_prime_UTR_variant | MODIFIER | c.*177T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 16/16 | 177 | chr3 | 195864004 | |||||
| chr3:195864008
|
G | A | 2 | a0001c0003t0005a0023c0052t0005 | 7 | HG00558.hp2 HG02132.hp1 HG02165.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*173C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 16/16 | 173 | chr3 | 195864008 | |||||
| chr3:195864010
|
G | T | 5 | a0001c0003t0003a0001c0019t0003a0001c0053t0003others(2): Show | 15 | HG01496.hp2 HG02129.hp2 HG02148.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*171C>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 16/16 | 171 | chr3 | 195864010 | |||||
| chr3:195864051
|
T | C | 1 | a0001c0012t0011 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*130A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 16/16 | 130 | chr3 | 195864051 | |||||
| chr3:195864053
|
G | C | 3 | a0001c0017t0006a0001c0034t0006a0002c0044t0006 | 5 | HG02486.hp2 HG02630.hp2 HG02970.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*128C>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 16/16 | 128 | chr3 | 195864053 | |||||
| chr3:195864068
|
G | A | 1 | a0001c0006t0012 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*113C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 16/16 | 113 | chr3 | 195864068 | |||||
| chr3:195864135
|
C | G | 1 | a0001c0001t0007 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*46G>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 16/16 | 46 | chr3 | 195864135 | |||||
| chr3:195908536
|
T | A | 1 | a0001c0003t0013 | 1 | NA19083.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-70A>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/16 | chr3 | 195908536 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:195864250
|
C | G | 2 | a0001c0040t0001g0019a0001c0070t0001g0352 | 2 | HG00673.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.3162-63G>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 15/15 | chr3 | 195864250 | ||||||
| chr3:195864462
|
G | A | 1 | a0002c0004t0001g0131 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3162-275C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 15/15 | chr3 | 195864462 | ||||||
| chr3:195864462
|
GAGACAGC others(58): Show |
G | 12 | a0001c0002t0001g0174a0001c0002t0001g0187a0004c0007t0001g0260others(9): Show | 12 | HG00423.hp1 NA18954.hp2 NA18959.hp2 others(9): Show |
intron_variant | MODIFIER | c.3162-340_3162-276d others(67): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 15/15 | chr3 | 195864462 | ||||||
| chr3:195864469
|
C | T | 1 | a0001c0001t0001g0304 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.3162-282G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 15/15 | chr3 | 195864469 | ||||||
| chr3:195864527
|
C | G | 18 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0007g0232others(15): Show | 18 | HG00673.hp2 HG01109.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.3162-340G>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 15/15 | chr3 | 195864527 | ||||||
| chr3:195864535
|
G | A | 6 | a0001c0001t0002g0264a0001c0001t0002g0273a0001c0001t0002g0305others(3): Show | 6 | NA18948.hp1 NA18993.hp2 NA19004.hp1 others(3): Show |
intron_variant | MODIFIER | c.3162-348C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 15/15 | chr3 | 195864535 | ||||||
| chr3:195864566
|
T | C | 2 | a0001c0040t0001g0019a0001c0070t0001g0352 | 2 | HG00673.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.3162-379A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 15/15 | chr3 | 195864566 | ||||||
| chr3:195864627
|
A | G | 1 | a0001c0003t0005g0257 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.3162-440T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 15/15 | chr3 | 195864627 | ||||||
| chr3:195864656
|
T | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0076a0001c0001t0001g0103others(198): Show | 205 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.3162-469A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 15/15 | chr3 | 195864656 | ||||||
| chr3:195864692
|
G | A | 32 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0002t0001g0045others(29): Show | 32 | HG00140.hp2 HG00621.hp2 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.3162-505C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 15/15 | chr3 | 195864692 | ||||||
| chr3:195864821
|
C | T | 8 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(5): Show | 8 | HG01975.hp2 HG02109.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.3162-634G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 15/15 | chr3 | 195864821 | ||||||
| chr3:195864846
|
A | C | 32 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0002t0001g0045others(29): Show | 32 | HG00140.hp2 HG00621.hp2 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.3162-659T>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 15/15 | chr3 | 195864846 | ||||||
| chr3:195864851
|
C | T | 6 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(3): Show | 6 | HG01975.hp2 HG02572.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.3162-664G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 15/15 | chr3 | 195864851 | ||||||
| chr3:195864852
|
G | A | 4 | a0001c0001t0002g0333a0001c0001t0002g0334a0002c0004t0002g0332others(1): Show | 4 | HG01109.hp2 HG01255.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.3162-665C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 15/15 | chr3 | 195864852 | ||||||
| chr3:195864886
|
C | T | 2 | a0001c0001t0001g0278a0001c0001t0001g0353 | 2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3162-699G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 15/15 | chr3 | 195864886 | ||||||
| chr3:195864893
|
G | T | 1 | a0019c0038t0001g0032 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.3162-706C>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 15/15 | chr3 | 195864893 | ||||||
| chr3:195864924
|
C | T | 100 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0209others(97): Show | 101 | HG00140.hp1 HG00140.hp2 HG00621.hp2 others(98): Show |
intron_variant | MODIFIER | c.3162-737G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 15/15 | chr3 | 195864924 | ||||||
| chr3:195864959
|
A | ATGCAAAT others(383): Show |
7 | a0001c0014t0004g0002a0001c0014t0004g0093a0001c0014t0004g0109others(4): Show | 8 | HG01884.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.3162-773_3162-772i others(392): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 15/15 | chr3 | 195864959 | ||||||
| chr3:195864989
|
C | T | 100 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0209others(97): Show | 101 | HG00140.hp1 HG00140.hp2 HG00621.hp2 others(98): Show |
intron_variant | MODIFIER | c.3162-802G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 15/15 | chr3 | 195864989 | ||||||
| chr3:195865070
|
C | G | 1 | a0001c0002t0001g0175 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3162-883G>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 15/15 | chr3 | 195865070 | ||||||
| chr3:195865071
|
G | C | 1 | a0001c0002t0001g0175 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3162-884C>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 15/15 | chr3 | 195865071 | ||||||
| chr3:195865087
|
A | AGGTGCAA others(383): Show |
2 | a0001c0006t0001g0066a0003c0015t0001g0084 | 2 | HG01358.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.3162-901_3162-900i others(392): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 15/15 | chr3 | 195865087 | ||||||
| chr3:195865089
|
G | A | 1 | a0001c0002t0001g0175 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3162-902C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 15/15 | chr3 | 195865089 | ||||||
| chr3:195865089
|
G | GTGCAAAT others(448): Show |
3 | a0001c0006t0001g0069a0001c0006t0001g0070a0001c0006t0001g0083 | 3 | NA18963.hp2 NA19058.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.3162-903_3162-902i others(457): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 15/15 | chr3 | 195865089 | ||||||
| chr3:195865089
|
G | GTGCAAAT others(448): Show |
22 | a0001c0006t0001g0087a0001c0006t0001g0092a0001c0006t0001g0097others(19): Show | 22 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.3162-903_3162-902i others(457): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 15/15 | chr3 | 195865089 | ||||||
| chr3:195865089
|
G | GTGCAAAT others(448): Show |
1 | a0001c0011t0001g0107 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3162-903_3162-902i others(457): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 15/15 | chr3 | 195865089 | ||||||
| chr3:195865089
|
GTGCAAAT others(58): Show |
G | 1 | a0001c0002t0001g0178 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3162-967_3162-903d others(67): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 15/15 | chr3 | 195865089 | ||||||
| chr3:195865111
|
C | T | 1 | a0003c0043t0001g0025 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.3162-924G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 15/15 | chr3 | 195865111 | ||||||
| chr3:195865162
|
C | CAGTAAGA others(448): Show |
2 | a0001c0006t0001g0077a0002c0026t0001g0074 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3162-976_3162-975i others(457): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 15/15 | chr3 | 195865162 | ||||||
| chr3:195865202
|
G | A | 2 | a0001c0001t0001g0281a0001c0001t0001g0348 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.3162-1015C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 15/15 | chr3 | 195865202 | ||||||
| chr3:195865205
|
T | G | 8 | a0002c0010t0001g0035a0002c0010t0001g0043a0003c0005t0001g0034others(5): Show | 8 | HG01074.hp1 HG01074.hp2 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.3162-1018A>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 15/15 | chr3 | 195865205 | ||||||
| chr3:195865241
|
C | CGAGACAG others(448): Show |
13 | a0001c0006t0001g0061a0001c0006t0001g0229a0001c0011t0001g0060others(10): Show | 13 | HG00140.hp1 HG02155.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.3162-1055_3162-105 others(459): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 15/15 | chr3 | 195865241 | ||||||
| chr3:195865241
|
C | CGAGACAG others(448): Show |
1 | a0001c0012t0001g0071 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.3162-1055_3162-105 others(459): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 15/15 | chr3 | 195865241 | ||||||
| chr3:195865241
|
C | T | 32 | a0001c0006t0001g0077a0001c0006t0001g0087a0001c0006t0001g0092others(29): Show | 33 | HG00639.hp1 HG00673.hp2 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.3162-1054G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 15/15 | chr3 | 195865241 | ||||||
| chr3:195865411
|
C | T | 31 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0002t0001g0045others(28): Show | 31 | HG00140.hp2 HG00621.hp2 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.3162-1224G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 15/15 | chr3 | 195865411 | ||||||
| chr3:195865466
|
CGAGTGCC others(58): Show |
C | 1 | a0001c0003t0001g0122 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.3162-1344_3162-128 others(69): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 15/15 | chr3 | 195865466 | ||||||
| chr3:195865507
|
G | A | 1 | a0002c0008t0002g0172 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3162-1320C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 15/15 | chr3 | 195865507 | ||||||
| chr3:195865697
|
C | T | 1 | a0001c0012t0001g0071 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.3161+1192G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 15/15 | chr3 | 195865697 | ||||||
| chr3:195865699
|
A | AC | 13 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0007g0232others(10): Show | 13 | HG01891.hp1 HG01952.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.3161+1189dupG | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 15/15 | chr3 | 195865699 | ||||||
| chr3:195865702
|
C | T | 1 | a0001c0042t0001g0234 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3161+1187G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 15/15 | chr3 | 195865702 | ||||||
| chr3:195865720
|
A | T | 7 | a0002c0010t0001g0035a0002c0010t0001g0043a0003c0005t0001g0034others(4): Show | 7 | HG01074.hp1 HG01074.hp2 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.3161+1169T>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 15/15 | chr3 | 195865720 | ||||||
| chr3:195865730
|
GGGAGTGC others(62): Show |
G | 2 | a0001c0001t0001g0246a0001c0001t0001g0339 | 2 | NA18961.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.3161+1090_3161+115 others(73): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 15/15 | chr3 | 195865730 | ||||||
| chr3:195865815
|
T | TGGCGCCA others(18): Show |
2 | a0001c0040t0001g0019a0001c0070t0001g0352 | 2 | HG00673.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.3161+1049_3161+107 others(29): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 15/15 | chr3 | 195865815 | ||||||
| chr3:195865947
|
C | G | 54 | a0001c0002t0001g0130a0001c0002t0001g0186a0001c0006t0001g0061others(51): Show | 55 | HG00140.hp1 HG00639.hp1 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.3161+942G>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 15/15 | chr3 | 195865947 | ||||||
| chr3:195866002
|
T | TC | 11 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0006t0001g0100others(8): Show | 11 | HG01891.hp1 HG01952.hp1 HG02300.hp2 others(8): Show |
intron_variant | MODIFIER | c.3161+886dupG | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 15/15 | chr3 | 195866002 | ||||||
| chr3:195866096
|
A | G | 2 | a0001c0040t0001g0019a0001c0070t0001g0352 | 2 | HG00673.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.3161+793T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 15/15 | chr3 | 195866096 | ||||||
| chr3:195866380
|
T | C | 1 | a0001c0006t0012g0065 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.3161+509A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 15/15 | chr3 | 195866380 | ||||||
| chr3:195866419
|
T | G | 24 | a0001c0001t0001g0001a0001c0001t0001g0076a0001c0001t0002g0062others(21): Show | 27 | HG01192.hp1 HG01255.hp1 HG01934.hp1 others(24): Show |
intron_variant | MODIFIER | c.3161+470A>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 15/15 | chr3 | 195866419 | ||||||
| chr3:195866527
|
T | G | 100 | a0001c0001t0001g0001a0001c0001t0001g0076a0001c0001t0001g0103others(97): Show | 104 | HG00140.hp1 HG00639.hp1 HG00735.hp2 others(101): Show |
intron_variant | MODIFIER | c.3161+362A>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 15/15 | chr3 | 195866527 | ||||||
| chr3:195866579
|
G | C | 1 | a0010c0059t0001g0021 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3161+310C>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 15/15 | chr3 | 195866579 | ||||||
| chr3:195866671
|
T | C | 1 | a0001c0042t0001g0234 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3161+218A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 15/15 | chr3 | 195866671 | ||||||
| chr3:195866802
|
C | A | 1 | a0001c0001t0001g0336 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3161+87G>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 15/15 | chr3 | 195866802 | ||||||
| chr3:195866806
|
G | C | 44 | a0001c0006t0001g0061a0001c0006t0001g0066a0001c0006t0001g0069others(41): Show | 44 | HG00140.hp1 HG00639.hp1 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.3161+83C>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 15/15 | chr3 | 195866806 | ||||||
| chr3:195866851
|
T | C | 2 | a0001c0001t0001g0308a0002c0023t0001g0207 | 2 | HG01175.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3161+38A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 15/15 | chr3 | 195866851 | ||||||
| chr3:195867280
|
CCT | C | 32 | a0001c0001t0001g0364a0001c0002t0001g0045a0002c0004t0002g0327others(29): Show | 32 | HG00140.hp2 HG00621.hp2 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.2938-18_2938-17del others(2): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 13/15 | chr3 | 195867280 | ||||||
| chr3:195867355
|
G | T | 1 | a0022c0055t0003g0153 | 1 | NA18954.hp1 | splice_region_variant&intron_variant | LOW | c.2937+6C>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 13/15 | chr3 | 195867355 | ||||||
| chr3:195868716
|
T | C | 1 | a0001c0014t0004g0002 | 2 | HG01884.hp1 HG01891.hp2 |
splice_region_variant&intron_variant | LOW | c.1589-7A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 12/15 | chr3 | 195868716 | ||||||
| chr3:195868761
|
A | G | 318 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0056others(315): Show | 323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.1589-52T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 12/15 | chr3 | 195868761 | ||||||
| chr3:195868779
|
C | T | 1 | a0001c0002t0001g0047 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1589-70G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 12/15 | chr3 | 195868779 | ||||||
| chr3:195868786
|
G | A | 83 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0144others(80): Show | 84 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.1589-77C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 12/15 | chr3 | 195868786 | ||||||
| chr3:195868830
|
C | T | 22 | a0001c0001t0001g0001a0001c0001t0001g0076a0001c0001t0001g0116others(19): Show | 23 | HG00280.hp1 HG00323.hp2 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.1589-121G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 12/15 | chr3 | 195868830 | ||||||
| chr3:195868852
|
C | T | 3 | a0001c0001t0001g0274a0001c0001t0008g0269a0002c0004t0001g0256 | 3 | NA18990.hp1 NA19056.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1589-143G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 12/15 | chr3 | 195868852 | ||||||
| chr3:195868914
|
C | T | 1 | a0001c0002t0001g0180 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1589-205G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 12/15 | chr3 | 195868914 | ||||||
| chr3:195868944
|
C | T | 5 | a0001c0001t0001g0001a0001c0001t0001g0076a0001c0001t0002g0062others(2): Show | 6 | HG01255.hp1 HG03017.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1589-235G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 12/15 | chr3 | 195868944 | ||||||
| chr3:195868946
|
T | C | 8 | a0001c0001t0001g0103a0001c0006t0001g0229a0001c0011t0001g0230others(5): Show | 8 | HG02622.hp1 HG02647.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.1589-237A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 12/15 | chr3 | 195868946 | ||||||
| chr3:195869060
|
C | T | 1 | a0001c0001t0001g0270 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1589-351G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 12/15 | chr3 | 195869060 | ||||||
| chr3:195869096
|
G | A | 12 | a0001c0001t0001g0336a0001c0006t0001g0098a0001c0006t0001g0100others(9): Show | 13 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.1589-387C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 12/15 | chr3 | 195869096 | ||||||
| chr3:195869190
|
G | A | 1 | a0001c0001t0007g0232 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1588+307C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 12/15 | chr3 | 195869190 | ||||||
| chr3:195869215
|
A | AGAAGCCA others(58): Show |
1 | a0001c0053t0003g0129 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1588+217_1588+281d others(67): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 12/15 | chr3 | 195869215 | ||||||
| chr3:195869245
|
G | A | 1 | a0001c0002t0001g0181 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1588+252C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 12/15 | chr3 | 195869245 | ||||||
| chr3:195869274
|
C | T | 1 | a0002c0010t0001g0024 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1588+223G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 12/15 | chr3 | 195869274 | ||||||
| chr3:195869336
|
G | A | 1 | a0001c0001t0001g0343 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1588+161C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 12/15 | chr3 | 195869336 | ||||||
| chr3:195869336
|
G | T | 2 | a0001c0002t0001g0184a0002c0008t0001g0182 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1588+161C>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 12/15 | chr3 | 195869336 | ||||||
| chr3:195869337
|
G | C | 8 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0343others(5): Show | 9 | HG01109.hp1 HG01361.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.1588+160C>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 12/15 | chr3 | 195869337 | ||||||
| chr3:195869338
|
G | A | 4 | a0001c0014t0004g0002a0001c0058t0004g0237a0002c0057t0004g0236others(1): Show | 5 | HG01884.hp1 HG01891.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1588+159C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 12/15 | chr3 | 195869338 | ||||||
| chr3:195869366
|
G | A | 36 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0287others(33): Show | 36 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.1588+131C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 12/15 | chr3 | 195869366 | ||||||
| chr3:195869368
|
G | A | 1 | a0001c0003t0005g0139 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1588+129C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 12/15 | chr3 | 195869368 | ||||||
| chr3:195869463
|
C | G | 1 | a0001c0002t0001g0036 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1588+34G>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 12/15 | chr3 | 195869463 | ||||||
| chr3:195869578
|
G | A | 1 | a0008c0016t0001g0224 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1544-37C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 11/15 | chr3 | 195869578 | ||||||
| chr3:195869608
|
G | A | 1 | a0001c0003t0001g0155 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1544-67C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 11/15 | chr3 | 195869608 | ||||||
| chr3:195869630
|
T | TAG | 95 | a0001c0001t0001g0095a0001c0001t0001g0103a0001c0001t0001g0104others(92): Show | 96 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.1544-91_1544-90dup others(2): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 11/15 | chr3 | 195869630 | ||||||
| chr3:195869662
|
C | T | 1 | a0001c0001t0001g0343 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1544-121G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 11/15 | chr3 | 195869662 | ||||||
| chr3:195869674
|
C | T | 2 | a0001c0001t0001g0292a0002c0004t0001g0341 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1544-133G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 11/15 | chr3 | 195869674 | ||||||
| chr3:195869678
|
C | G | 1 | a0001c0002t0001g0186 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1544-137G>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 11/15 | chr3 | 195869678 | ||||||
| chr3:195869721
|
G | A | 1 | a0001c0002t0001g0215 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1544-180C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 11/15 | chr3 | 195869721 | ||||||
| chr3:195869765
|
C | T | 202 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0076others(199): Show | 207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.1544-224G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 11/15 | chr3 | 195869765 | ||||||
| chr3:195869854
|
G | T | 2 | a0001c0002t0001g0130a0001c0002t0001g0186 | 2 | HG02647.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1543+260C>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 11/15 | chr3 | 195869854 | ||||||
| chr3:195870036
|
T | C | 115 | a0001c0001t0001g0006a0001c0001t0001g0104a0001c0001t0001g0105others(112): Show | 116 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.1543+78A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 11/15 | chr3 | 195870036 | ||||||
| chr3:195870039
|
G | A | 1 | a0001c0002t0001g0180 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1543+75C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 11/15 | chr3 | 195870039 | ||||||
| chr3:195870259
|
C | T | 4 | a0004c0032t0002g0301a0005c0022t0002g0057a0005c0022t0002g0309others(1): Show | 4 | HG00408.hp2 NA18942.hp2 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.1452-54G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195870259 | ||||||
| chr3:195870355
|
C | T | 1 | a0006c0025t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1452-150G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195870355 | ||||||
| chr3:195870360
|
G | A | 1 | a0001c0001t0001g0285 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1452-155C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195870360 | ||||||
| chr3:195870374
|
G | A | 1 | a0001c0020t0002g0335 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1452-169C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195870374 | ||||||
| chr3:195870374
|
G | C | 4 | a0001c0003t0005g0197a0001c0003t0005g0199a0001c0040t0001g0019others(1): Show | 4 | HG00597.hp1 HG00673.hp2 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.1452-169C>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195870374 | ||||||
| chr3:195870417
|
T | C | 69 | a0001c0001t0001g0076a0001c0001t0001g0103a0001c0001t0001g0104others(66): Show | 70 | HG00140.hp2 HG00280.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.1452-212A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195870417 | ||||||
| chr3:195870449
|
C | T | 5 | a0001c0001t0001g0246a0001c0001t0001g0339a0001c0002t0001g0175others(2): Show | 5 | HG02015.hp1 HG02074.hp2 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.1452-244G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195870449 | ||||||
| chr3:195870564
|
C | T | 2 | a0014c0063t0002g0247a0015c0064t0001g0347 | 2 | HG04199.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1452-359G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195870564 | ||||||
| chr3:195870565
|
G | A | 1 | a0001c0003t0003g0124 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1452-360C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195870565 | ||||||
| chr3:195870634
|
G | A | 1 | a0002c0060t0001g0240 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1452-429C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195870634 | ||||||
| chr3:195870678
|
G | A | 307 | a0001c0001t0001g0006a0001c0001t0001g0056a0001c0001t0001g0095others(304): Show | 310 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(307): Show |
intron_variant | MODIFIER | c.1452-473C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195870678 | ||||||
| chr3:195870739
|
A | C | 1 | a0001c0011t0001g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1452-534T>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195870739 | ||||||
| chr3:195870770
|
A | G | 7 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(4): Show | 7 | HG01975.hp2 HG02109.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1452-565T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195870770 | ||||||
| chr3:195870893
|
A | AGTGTGTG others(81): Show |
9 | a0001c0001t0001g0323a0001c0001t0002g0321a0001c0001t0002g0322others(6): Show | 9 | HG00408.hp2 NA18939.hp1 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.1452-776_1452-689d others(90): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195870893 | ||||||
| chr3:195870901
|
T | TGGGCCCG others(81): Show |
32 | a0001c0001t0001g0001a0001c0001t0001g0076a0001c0001t0001g0095others(29): Show | 35 | HG01192.hp1 HG01361.hp2 HG01934.hp1 others(32): Show |
intron_variant | MODIFIER | c.1452-697_1452-696i others(90): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195870901 | ||||||
| chr3:195870908
|
G | GCTGTGTG others(81): Show |
4 | a0002c0027t0001g0117a0007c0021t0001g0113a0007c0021t0001g0115others(1): Show | 4 | HG01891.hp1 HG01952.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.1452-704_1452-703i others(90): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195870908 | ||||||
| chr3:195870933
|
G | A | 1 | a0027c0049t0001g0022 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1452-728C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195870933 | ||||||
| chr3:195870935
|
C | T | 1 | a0027c0049t0001g0022 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1452-730G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195870935 | ||||||
| chr3:195870943
|
TGGGTTCT others(23): Show |
T | 1 | a0002c0026t0001g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1452-768_1452-739d others(32): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195870943 | ||||||
| chr3:195870957
|
G | T | 234 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0056others(231): Show | 239 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.1452-752C>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195870957 | ||||||
| chr3:195870962
|
A | G | 2 | a0001c0014t0004g0093a0027c0049t0001g0022 | 2 | HG00642.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1452-757T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195870962 | ||||||
| chr3:195870964
|
T | C | 2 | a0001c0014t0004g0093a0027c0049t0001g0022 | 2 | HG00642.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1452-759A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195870964 | ||||||
| chr3:195870973
|
G | GGGGTTCT others(22): Show |
37 | a0001c0002t0001g0029a0001c0002t0001g0031a0001c0002t0001g0036others(34): Show | 37 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.1452-797_1452-769d others(31): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195870973 | ||||||
| chr3:195870973
|
GGGGTTCT others(22): Show |
G | 97 | a0001c0001t0001g0006a0001c0001t0001g0056a0001c0001t0001g0116others(94): Show | 98 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.1452-797_1452-769d others(31): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195870973 | ||||||
| chr3:195870992
|
G | A | 1 | a0001c0014t0004g0093 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1452-787C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195870992 | ||||||
| chr3:195870994
|
C | T | 1 | a0001c0014t0004g0093 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1452-789G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195870994 | ||||||
| chr3:195871014
|
T | C | 4 | a0001c0001t0001g0056a0001c0001t0001g0291a0001c0001t0001g0294others(1): Show | 4 | HG02071.hp1 HG02135.hp2 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.1452-809A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195871014 | ||||||
| chr3:195871021
|
GCCCGCTG others(23): Show |
G | 1 | a0002c0010t0001g0028 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1452-846_1452-817d others(32): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195871021 | ||||||
| chr3:195871157
|
G | A | 1 | a0001c0001t0002g0163 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1452-952C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195871157 | ||||||
| chr3:195871197
|
G | A | 1 | a0001c0006t0001g0092 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1452-992C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195871197 | ||||||
| chr3:195871352
|
C | A | 1 | a0001c0002t0001g0130 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1451+924G>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195871352 | ||||||
| chr3:195871358
|
G | A | 1 | a0001c0001t0002g0326 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1451+918C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195871358 | ||||||
| chr3:195871434
|
T | C | 7 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(4): Show | 7 | HG01975.hp2 HG02109.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1451+842A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195871434 | ||||||
| chr3:195871506
|
C | A | 1 | a0002c0004t0001g0350 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1451+770G>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195871506 | ||||||
| chr3:195871516
|
G | T | 1 | a0002c0004t0001g0131 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1451+760C>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195871516 | ||||||
| chr3:195871556
|
G | A | 1 | a0010c0059t0001g0021 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1451+720C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195871556 | ||||||
| chr3:195871562
|
T | G | 2 | a0001c0001t0001g0308a0002c0004t0001g0350 | 2 | HG02055.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1451+714A>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195871562 | ||||||
| chr3:195871661
|
G | A | 2 | a0001c0002t0001g0202a0001c0002t0001g0203 | 2 | NA18948.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1451+615C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195871661 | ||||||
| chr3:195871735
|
G | A | 1 | a0001c0002t0001g0235 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1451+541C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195871735 | ||||||
| chr3:195871751
|
C | T | 1 | a0001c0040t0001g0019 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1451+525G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195871751 | ||||||
| chr3:195871810
|
G | A | 2 | a0001c0003t0005g0139a0001c0003t0005g0196 | 2 | NA18973.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1451+466C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195871810 | ||||||
| chr3:195871917
|
C | G | 1 | a0001c0002t0001g0235 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1451+359G>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195871917 | ||||||
| chr3:195871933
|
C | CTCCCCTG others(82): Show |
25 | a0001c0001t0001g0001a0001c0001t0001g0076a0001c0001t0002g0062others(22): Show | 28 | HG01192.hp1 HG01934.hp1 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.1451+342_1451+343i others(91): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195871933 | ||||||
| chr3:195871947
|
A | C | 1 | a0001c0042t0001g0234 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1451+329T>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195871947 | ||||||
| chr3:195871948
|
T | C | 1 | a0001c0042t0001g0234 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1451+328A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195871948 | ||||||
| chr3:195871948
|
TTCCCCTG others(8): Show |
T | 96 | a0001c0001t0001g0006a0001c0001t0001g0056a0001c0001t0001g0244others(93): Show | 97 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.1451+313_1451+327d others(17): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195871948 | ||||||
| chr3:195871954
|
T | C | 1 | a0001c0002t0001g0235 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1451+322A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195871954 | ||||||
| chr3:195871954
|
T | TGGAGAAC others(52): Show |
1 | a0002c0072t0001g0091 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1451+321_1451+322i others(61): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195871954 | ||||||
| chr3:195871954
|
T | TGGAGAAC others(22): Show |
80 | a0001c0002t0001g0029a0001c0002t0001g0031a0001c0002t0001g0036others(77): Show | 81 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.1451+293_1451+321d others(31): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195871954 | ||||||
| chr3:195871963
|
C | CTCCCCTG others(67): Show |
14 | a0001c0001t0001g0095a0001c0001t0001g0111a0001c0001t0001g0112others(11): Show | 14 | HG00323.hp2 HG01361.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.1451+312_1451+313i others(76): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195871963 | ||||||
| chr3:195871969
|
T | TGGAGAAC others(7): Show |
6 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(3): Show | 6 | HG01975.hp2 HG02572.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1451+293_1451+306d others(16): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195871969 | ||||||
| chr3:195871978
|
C | CTCCCCGG others(37): Show |
7 | a0001c0006t0001g0077a0001c0006t0001g0092a0001c0006t0001g0098others(4): Show | 7 | HG00673.hp2 HG02615.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1451+297_1451+298i others(46): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195871978 | ||||||
| chr3:195871992
|
C | A | 120 | a0001c0001t0001g0001a0001c0001t0001g0076a0001c0001t0002g0062others(117): Show | 124 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.1451+284G>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195871992 | ||||||
| chr3:195871993
|
C | CTCCCCTG others(8): Show |
2 | a0001c0002t0001g0130a0001c0002t0001g0186 | 2 | HG02647.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1451+268_1451+282d others(17): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195871993 | ||||||
| chr3:195871993
|
C | T | 120 | a0001c0001t0001g0001a0001c0001t0001g0076a0001c0001t0002g0062others(117): Show | 124 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.1451+283G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195871993 | ||||||
| chr3:195872007
|
A | C | 6 | a0001c0006t0001g0077a0001c0006t0001g0092a0001c0006t0001g0098others(3): Show | 6 | HG02615.hp2 HG02622.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1451+269T>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195872007 | ||||||
| chr3:195872008
|
T | C | 6 | a0001c0006t0001g0077a0001c0006t0001g0092a0001c0006t0001g0098others(3): Show | 6 | HG02615.hp2 HG02622.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1451+268A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195872008 | ||||||
| chr3:195872022
|
C | A | 116 | a0001c0001t0001g0006a0001c0001t0001g0056a0001c0001t0001g0095others(113): Show | 117 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.1451+254G>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195872022 | ||||||
| chr3:195872023
|
C | T | 116 | a0001c0001t0001g0006a0001c0001t0001g0056a0001c0001t0001g0095others(113): Show | 117 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.1451+253G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195872023 | ||||||
| chr3:195872052
|
A | C | 41 | a0001c0001t0001g0001a0001c0001t0001g0076a0001c0001t0001g0095others(38): Show | 44 | HG00323.hp2 HG01192.hp1 HG01361.hp2 others(41): Show |
intron_variant | MODIFIER | c.1451+224T>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195872052 | ||||||
| chr3:195872053
|
C | T | 2 | a0001c0006t0001g0077a0002c0026t0001g0074 | 2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1451+223G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195872053 | ||||||
| chr3:195872074
|
T | C | 2 | a0001c0003t0001g0150a0001c0003t0001g0195 | 2 | HG00609.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1451+202A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195872074 | ||||||
| chr3:195872074
|
T | TC | 49 | a0001c0006t0001g0061a0001c0006t0001g0066a0001c0006t0001g0069others(46): Show | 50 | HG00140.hp1 HG00639.hp1 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.1451+201_1451+202i others(3): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195872074 | ||||||
| chr3:195872077
|
A | AGAACATT others(9): Show |
2 | a0001c0011t0001g0107a0001c0011t0001g0108 | 2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1451+198_1451+199i others(18): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195872077 | ||||||
| chr3:195872077
|
A | G | 49 | a0001c0006t0001g0061a0001c0006t0001g0066a0001c0006t0001g0069others(46): Show | 50 | HG00140.hp1 HG00639.hp1 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.1451+199T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195872077 | ||||||
| chr3:195872080
|
A | G | 1 | a0001c0006t0001g0098 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1451+196T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195872080 | ||||||
| chr3:195872104
|
G | C | 1 | a0001c0003t0002g0157 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1451+172C>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195872104 | ||||||
| chr3:195872121
|
G | A | 1 | a0012c0045t0001g0009 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1451+155C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195872121 | ||||||
| chr3:195872134
|
G | C | 1 | a0001c0003t0002g0206 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1451+142C>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195872134 | ||||||
| chr3:195872213
|
G | A | 1 | a0001c0006t0001g0061 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1451+63C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195872213 | ||||||
| chr3:195872214
|
T | C | 135 | a0001c0001t0001g0006a0001c0001t0001g0056a0001c0001t0001g0244others(132): Show | 136 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.1451+62A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195872214 | ||||||
| chr3:195872263
|
G | C | 1 | a0001c0002t0001g0203 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1451+13C>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 10/15 | chr3 | 195872263 | ||||||
| chr3:195872590
|
G | A | 1 | a0001c0001t0002g0163 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1257-120C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195872590 | ||||||
| chr3:195872805
|
G | C | 1 | a0001c0012t0011g0102 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1257-335C>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195872805 | ||||||
| chr3:195872941
|
A | G | 1 | a0001c0014t0004g0002 | 2 | HG01884.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.1257-471T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195872941 | ||||||
| chr3:195872947
|
G | A | 1 | a0006c0025t0001g0216 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1257-477C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195872947 | ||||||
| chr3:195872956
|
G | A | 1 | a0001c0014t0004g0002 | 2 | HG01884.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.1257-486C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195872956 | ||||||
| chr3:195873154
|
C | T | 28 | a0001c0001t0001g0001a0001c0001t0001g0076a0001c0001t0002g0062others(25): Show | 31 | HG01192.hp1 HG01255.hp1 HG01934.hp1 others(28): Show |
intron_variant | MODIFIER | c.1257-684G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195873154 | ||||||
| chr3:195873212
|
C | A | 2 | a0001c0003t0005g0139a0001c0003t0005g0196 | 2 | NA18973.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1257-742G>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195873212 | ||||||
| chr3:195873265
|
TGGGCAGG others(5): Show |
T | 3 | a0001c0003t0001g0171a0001c0058t0004g0237a0002c0057t0004g0236 | 3 | HG03017.hp1 HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1257-807_1257-796d others(14): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195873265 | ||||||
| chr3:195873355
|
G | A | 4 | a0001c0011t0001g0060a0001c0011t0001g0081a0001c0031t0001g0089others(1): Show | 4 | NA18940.hp1 NA18957.hp1 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.1257-885C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195873355 | ||||||
| chr3:195873356
|
T | C | 188 | a0001c0001t0001g0006a0001c0001t0001g0056a0001c0001t0001g0103others(185): Show | 189 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.1257-886A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195873356 | ||||||
| chr3:195873410
|
AGTCTGGG others(32): Show |
A | 95 | a0001c0001t0001g0006a0001c0001t0001g0056a0001c0001t0001g0244others(92): Show | 96 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.1257-979_1257-941d others(41): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195873410 | ||||||
| chr3:195873462
|
GGGGGCGG others(31): Show |
G | 1 | a0002c0004t0001g0256 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1257-1030_1257-993 others(41): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195873462 | ||||||
| chr3:195873467
|
C | T | 1 | a0002c0008t0002g0267 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1257-997G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195873467 | ||||||
| chr3:195873500
|
C | CG | 6 | a0001c0002t0001g0178a0001c0002t0001g0202a0001c0003t0005g0139others(3): Show | 6 | HG00642.hp2 HG01192.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.1257-1031dupC | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195873500 | ||||||
| chr3:195873518
|
C | G | 1 | a0001c0001t0001g0095 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1257-1048G>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195873518 | ||||||
| chr3:195873537
|
C | G | 1 | a0001c0001t0002g0248 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1257-1067G>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195873537 | ||||||
| chr3:195873539
|
C | CG | 9 | a0001c0001t0002g0188a0001c0001t0002g0265a0001c0070t0001g0352others(6): Show | 9 | HG00597.hp1 HG02056.hp1 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.1257-1070dupC | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195873539 | ||||||
| chr3:195873547
|
G | A | 1 | a0001c0014t0004g0093 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1257-1077C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195873547 | ||||||
| chr3:195873677
|
G | A | 2 | a0001c0002t0001g0045a0002c0041t0001g0026 | 2 | HG00621.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.1257-1207C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195873677 | ||||||
| chr3:195873714
|
A | G | 1 | a0001c0003t0013g0365 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1257-1244T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195873714 | ||||||
| chr3:195873724
|
C | T | 1 | a0002c0044t0006g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1257-1254G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195873724 | ||||||
| chr3:195873735
|
G | A | 1 | a0002c0026t0001g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1257-1265C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195873735 | ||||||
| chr3:195873769
|
C | A | 1 | a0001c0002t0001g0178 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1257-1299G>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195873769 | ||||||
| chr3:195873840
|
C | T | 13 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0116others(10): Show | 13 | HG00323.hp2 HG01361.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.1257-1370G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195873840 | ||||||
| chr3:195873981
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1257-1511C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195873981 | ||||||
| chr3:195874153
|
G | A | 1 | a0009c0028t0001g0344 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1257-1683C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874153 | ||||||
| chr3:195874200
|
T | C | 6 | a0001c0002t0001g0018a0001c0017t0006g0012a0001c0017t0006g0013others(3): Show | 6 | HG02486.hp2 HG02630.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1257-1730A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874200 | ||||||
| chr3:195874254
|
G | T | 1 | a0001c0001t0001g0314 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1257-1784C>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874254 | ||||||
| chr3:195874284
|
C | T | 5 | a0001c0002t0001g0011a0002c0008t0001g0010a0002c0023t0001g0017others(2): Show | 5 | HG02647.hp1 HG02723.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1257-1814G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874284 | ||||||
| chr3:195874290
|
C | T | 1 | a0005c0029t0002g0320 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1257-1820G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874290 | ||||||
| chr3:195874435
|
C | T | 1 | a0002c0004t0002g0332 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1257-1965G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874435 | ||||||
| chr3:195874450
|
G | A | 49 | a0001c0001t0001g0144a0001c0003t0001g0122a0001c0003t0001g0138others(46): Show | 49 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.1257-1980C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874450 | ||||||
| chr3:195874515
|
A | G | 1 | a0001c0040t0001g0019 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1257-2045T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874515 | ||||||
| chr3:195874532
|
A | G | 1 | a0001c0040t0001g0019 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1257-2062T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874532 | ||||||
| chr3:195874542
|
G | A | 1 | a0027c0049t0001g0022 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1257-2072C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874542 | ||||||
| chr3:195874573
|
AGAAGCTC others(481): Show |
A | 61 | a0001c0001t0001g0006a0001c0001t0001g0244a0001c0001t0001g0249others(58): Show | 62 | HG00408.hp1 HG00639.hp2 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.1257-2591_1257-210 others(4): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874573 | ||||||
| chr3:195874577
|
G | A | 39 | a0001c0001t0001g0001a0001c0001t0001g0076a0001c0001t0001g0095others(36): Show | 42 | HG00323.hp2 HG00673.hp2 HG01361.hp2 others(39): Show |
intron_variant | MODIFIER | c.1257-2107C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874577 | ||||||
| chr3:195874579
|
TCCCCCTC others(748): Show |
T | 1 | a0023c0052t0005g0198 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1257-2864_1257-211 others(4): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874579 | ||||||
| chr3:195874580
|
C | CCCCCTCG others(37): Show |
1 | a0001c0001t0002g0326 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1257-2154_1257-211 others(48): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874580 | ||||||
| chr3:195874580
|
CCCCCTCG others(170): Show |
C | 3 | a0001c0011t0001g0230a0001c0014t0004g0109a0001c0037t0004g0110 | 3 | HG02559.hp1 HG03225.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1257-2287_1257-211 others(4): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874580 | ||||||
| chr3:195874580
|
CCCCCTCG others(258): Show |
C | 1 | a0001c0002t0001g0235 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1257-2375_1257-211 others(4): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874580 | ||||||
| chr3:195874580
|
CCCCCTCG others(702): Show |
C | 1 | a0001c0040t0001g0019 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1257-2819_1257-211 others(4): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874580 | ||||||
| chr3:195874605
|
A | G | 123 | a0001c0001t0001g0001a0001c0001t0001g0076a0001c0001t0001g0095others(120): Show | 127 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.1257-2135T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874605 | ||||||
| chr3:195874649
|
A | G | 50 | a0001c0001t0001g0076a0001c0001t0001g0095a0001c0006t0001g0061others(47): Show | 50 | HG00140.hp1 HG00639.hp1 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.1257-2179T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874649 | ||||||
| chr3:195874662
|
AGAAGCTC others(126): Show |
A | 1 | a0001c0014t0004g0093 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1257-2325_1257-219 others(4): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874662 | ||||||
| chr3:195874662
|
AGAAGCTC others(614): Show |
A | 1 | a0001c0001t0001g0304 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1257-2813_1257-219 others(4): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874662 | ||||||
| chr3:195874668
|
TCCCCTCG others(659): Show |
T | 2 | a0001c0001t0001g0095a0010c0059t0001g0021 | 2 | HG01109.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1257-2864_1257-219 others(4): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874668 | ||||||
| chr3:195874710
|
ACTCTCCC others(348): Show |
A | 21 | a0001c0001t0001g0076a0001c0001t0001g0104a0001c0001t0001g0105others(18): Show | 21 | HG00621.hp2 HG01099.hp2 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.1257-2595_1257-224 others(4): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874710 | ||||||
| chr3:195874712
|
TCTCCCTC others(40): Show |
T | 32 | a0001c0003t0001g0122a0001c0003t0001g0138a0001c0003t0001g0149others(29): Show | 32 | HG00423.hp2 HG00558.hp2 HG01496.hp2 others(29): Show |
intron_variant | MODIFIER | c.1257-2289_1257-224 others(51): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874712 | ||||||
| chr3:195874712
|
TCTCCCTC others(351): Show |
T | 14 | a0001c0001t0001g0144a0001c0003t0001g0148a0001c0003t0001g0150others(11): Show | 14 | HG00609.hp1 HG00609.hp2 HG02056.hp2 others(11): Show |
intron_variant | MODIFIER | c.1257-2600_1257-224 others(4): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874712 | ||||||
| chr3:195874713
|
CTCCCTCG others(37): Show |
C | 52 | a0001c0001t0001g0290a0001c0002t0001g0052a0001c0006t0001g0061others(49): Show | 53 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.1257-2287_1257-224 others(48): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874713 | ||||||
| chr3:195874713
|
CTCCCTCG others(525): Show |
C | 27 | a0001c0001t0001g0056a0001c0001t0001g0274a0001c0001t0001g0275others(24): Show | 27 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(24): Show |
intron_variant | MODIFIER | c.1257-2775_1257-224 others(4): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874713 | ||||||
| chr3:195874714
|
T | C | 142 | a0001c0001t0001g0001a0001c0001t0001g0103a0001c0001t0001g0111others(139): Show | 146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.1257-2244A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874714 | ||||||
| chr3:195874724
|
T | G | 1 | a0001c0001t0001g0103 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1257-2254A>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874724 | ||||||
| chr3:195874751
|
G | A | 67 | a0001c0001t0001g0001a0001c0001t0001g0103a0001c0001t0001g0111others(64): Show | 70 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.1257-2281C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874751 | ||||||
| chr3:195874755
|
G | A | 1 | a0002c0008t0001g0010 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1257-2285C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874755 | ||||||
| chr3:195874757
|
TCCCCTCG others(615): Show |
T | 1 | a0001c0002t0001g0185 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1256+2874_1257-228 others(4): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874757 | ||||||
| chr3:195874782
|
GCTCCGAG others(37): Show |
G | 1 | a0001c0001t0001g0103 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1257-2356_1257-231 others(48): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874782 | ||||||
| chr3:195874782
|
GCTCCGAG others(304): Show |
G | 1 | a0001c0001t0002g0062 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1257-2623_1257-231 others(4): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874782 | ||||||
| chr3:195874795
|
G | A | 151 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(148): Show | 155 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.1257-2325C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874795 | ||||||
| chr3:195874795
|
GGAAGCTC others(37): Show |
G | 2 | a0001c0002t0001g0205a0002c0023t0001g0207 | 2 | HG01175.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1257-2369_1257-232 others(48): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874795 | ||||||
| chr3:195874798
|
AGCTCCCC others(261): Show |
A | 1 | a0001c0042t0001g0234 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1257-2596_1257-232 others(4): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874798 | ||||||
| chr3:195874801
|
TCCCCTCG others(526): Show |
T | 33 | a0001c0001t0001g0001a0001c0001t0001g0111a0001c0001t0001g0112others(30): Show | 36 | HG00323.hp2 HG01361.hp2 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.1257-2864_1257-233 others(4): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874801 | ||||||
| chr3:195874801
|
TCCCCTCG others(571): Show |
T | 2 | a0001c0001t0001g0281a0001c0001t0001g0348 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1256+2874_1257-233 others(4): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874801 | ||||||
| chr3:195874826
|
A | G | 53 | a0001c0001t0001g0246a0001c0001t0001g0270a0001c0001t0001g0290others(50): Show | 53 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(50): Show |
intron_variant | MODIFIER | c.1257-2356T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874826 | ||||||
| chr3:195874839
|
A | G | 5 | a0001c0001t0002g0163a0001c0001t0002g0333a0001c0001t0002g0334others(2): Show | 5 | HG01255.hp2 HG01258.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.1257-2369T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874839 | ||||||
| chr3:195874839
|
AGAAGCTC others(215): Show |
A | 17 | a0001c0002t0001g0029a0001c0002t0001g0031a0001c0002t0001g0048others(14): Show | 17 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(14): Show |
intron_variant | MODIFIER | c.1257-2591_1257-237 others(4): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874839 | ||||||
| chr3:195874843
|
G | A | 4 | a0001c0001t0001g0270a0001c0001t0001g0314a0001c0050t0001g0213others(1): Show | 4 | HG02602.hp2 HG02976.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.1257-2373C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874843 | ||||||
| chr3:195874845
|
T | TCCCCCTC others(484): Show |
1 | a0001c0001t0001g0314 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1257-2376_1257-237 others(495): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874845 | ||||||
| chr3:195874845
|
TCCCCTCG others(482): Show |
T | 5 | a0001c0017t0006g0012a0001c0017t0006g0013a0001c0017t0006g0014others(2): Show | 5 | HG02486.hp2 HG02630.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1257-2864_1257-237 others(4): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874845 | ||||||
| chr3:195874846
|
CCCCTCGG others(303): Show |
C | 1 | a0001c0050t0001g0213 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1257-2686_1257-237 others(4): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874846 | ||||||
| chr3:195874846
|
CCCCTCGG others(392): Show |
C | 1 | a0024c0077t0001g0086 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1257-2775_1257-237 others(4): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874846 | ||||||
| chr3:195874846
|
CCCCTCGG others(436): Show |
C | 1 | a0001c0001t0001g0270 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1257-2819_1257-237 others(4): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874846 | ||||||
| chr3:195874928
|
AGAAGCTC others(527): Show |
A | 1 | a0001c0002t0001g0177 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1256+2791_1257-245 others(4): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874928 | ||||||
| chr3:195874932
|
G | A | 1 | a0001c0001t0001g0290 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1257-2462C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874932 | ||||||
| chr3:195874934
|
TCCCCTCG others(393): Show |
T | 2 | a0001c0001t0001g0103a0001c0002t0001g0218 | 2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1257-2864_1257-246 others(4): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874934 | ||||||
| chr3:195874934
|
TCCCCTCG others(438): Show |
T | 1 | a0001c0002t0001g0178 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1256+2874_1257-246 others(4): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874934 | ||||||
| chr3:195874935
|
CCCCTCGG others(214): Show |
C | 1 | a0001c0001t0001g0290 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1257-2686_1257-246 others(4): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874935 | ||||||
| chr3:195874959
|
A | G | 89 | a0001c0002t0001g0052a0001c0003t0001g0122a0001c0003t0001g0138others(86): Show | 90 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.1257-2489T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874959 | ||||||
| chr3:195874976
|
G | A | 48 | a0001c0006t0001g0061a0001c0006t0001g0066a0001c0006t0001g0069others(45): Show | 49 | HG00140.hp1 HG00639.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.1257-2506C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874976 | ||||||
| chr3:195874978
|
T | TC | 46 | a0001c0006t0001g0061a0001c0006t0001g0066a0001c0006t0001g0069others(43): Show | 47 | HG00140.hp1 HG00639.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.1257-2509dupG | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874978 | ||||||
| chr3:195874978
|
TCCCCTCG others(349): Show |
T | 4 | a0001c0002t0001g0052a0002c0010t0001g0053a0003c0005t0001g0051others(1): Show | 4 | HG01069.hp2 HG01071.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.1257-2864_1257-250 others(4): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874978 | ||||||
| chr3:195874978
|
TCCCCTCG others(394): Show |
T | 30 | a0001c0003t0001g0122a0001c0003t0001g0149a0001c0003t0001g0168others(27): Show | 30 | HG00558.hp2 HG01496.hp2 HG02129.hp2 others(27): Show |
intron_variant | MODIFIER | c.1256+2874_1257-250 others(4): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874978 | ||||||
| chr3:195874979
|
CCCCTCGG others(126): Show |
C | 1 | a0002c0008t0001g0010 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1257-2642_1257-251 others(4): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874979 | ||||||
| chr3:195874979
|
CCCCTCGG others(303): Show |
C | 1 | a0001c0006t0001g0087 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1257-2819_1257-251 others(4): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195874979 | ||||||
| chr3:195875020
|
A | G | 50 | a0001c0001t0001g0314a0001c0003t0001g0138a0001c0003t0013g0365others(47): Show | 51 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.1257-2550T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875020 | ||||||
| chr3:195875020
|
ACTCCCCC others(394): Show |
A | 21 | a0001c0001t0001g0246a0001c0001t0001g0339a0001c0002t0001g0130others(18): Show | 21 | HG01175.hp1 HG01243.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.1256+2832_1257-255 others(4): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875020 | ||||||
| chr3:195875023
|
CCCCCTCG others(126): Show |
C | 1 | a0001c0014t0004g0093 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1257-2686_1257-255 others(4): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875023 | ||||||
| chr3:195875023
|
CCCCCTCG others(215): Show |
C | 3 | a0001c0002t0001g0235a0001c0014t0004g0109a0001c0037t0004g0110 | 3 | HG02257.hp1 HG02559.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1257-2775_1257-255 others(4): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875023 | ||||||
| chr3:195875048
|
GCTCGGAG others(82): Show |
G | 1 | a0001c0011t0001g0230 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1257-2667_1257-257 others(93): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875048 | ||||||
| chr3:195875052
|
G | C | 47 | a0001c0001t0001g0314a0001c0006t0001g0061a0001c0006t0001g0066others(44): Show | 48 | HG00140.hp1 HG00639.hp1 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.1257-2582C>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875052 | ||||||
| chr3:195875061
|
G | A | 1 | a0001c0001t0001g0314 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1257-2591C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875061 | ||||||
| chr3:195875065
|
G | A | 4 | a0002c0008t0001g0219a0003c0005t0001g0034a0003c0005t0001g0245others(1): Show | 4 | HG00140.hp2 HG00642.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1257-2595C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875065 | ||||||
| chr3:195875065
|
GCTCCCCC others(126): Show |
G | 14 | a0001c0002t0001g0029a0001c0002t0001g0031a0001c0002t0001g0048others(11): Show | 14 | HG00280.hp1 HG00323.hp1 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.1257-2728_1257-259 others(4): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875065 | ||||||
| chr3:195875065
|
GCTCCCCC others(259): Show |
G | 47 | a0001c0003t0001g0138a0001c0006t0001g0061a0001c0006t0001g0066others(44): Show | 48 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.1257-2861_1257-259 others(4): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875065 | ||||||
| chr3:195875067
|
T | A | 1 | a0001c0042t0001g0234 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1257-2597A>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875067 | ||||||
| chr3:195875068
|
C | CCCCCTCG others(37): Show |
1 | a0001c0009t0002g0263 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1257-2642_1257-259 others(48): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875068 | ||||||
| chr3:195875068
|
CCCCCTCG others(303): Show |
C | 1 | a0001c0003t0013g0365 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1256+2875_1257-259 others(4): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875068 | ||||||
| chr3:195875075
|
G | A | 1 | a0001c0001t0001g0287 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1257-2605C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875075 | ||||||
| chr3:195875093
|
A | G | 48 | a0001c0001t0001g0076a0001c0001t0001g0104a0001c0001t0001g0105others(45): Show | 48 | HG00140.hp2 HG00609.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.1257-2623T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875093 | ||||||
| chr3:195875106
|
A | G | 4 | a0001c0001t0001g0165a0001c0001t0002g0094a0001c0003t0002g0141others(1): Show | 4 | NA18939.hp2 NA18993.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.1257-2636T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875106 | ||||||
| chr3:195875137
|
A | G | 29 | a0001c0001t0001g0076a0001c0001t0001g0104a0001c0001t0001g0105others(26): Show | 29 | HG00140.hp2 HG00621.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1257-2667T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875137 | ||||||
| chr3:195875198
|
A | G | 1 | a0001c0001t0001g0290 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1257-2728T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875198 | ||||||
| chr3:195875201
|
CCCCCTCG others(81): Show |
C | 4 | a0001c0001t0001g0076a0003c0005t0001g0034a0003c0005t0001g0245others(1): Show | 4 | HG00140.hp2 HG00642.hp2 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.1257-2819_1257-273 others(92): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875201 | ||||||
| chr3:195875230
|
C | G | 1 | a0001c0001t0001g0290 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1257-2760G>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875230 | ||||||
| chr3:195875239
|
G | A | 114 | a0001c0001t0001g0006a0001c0001t0001g0104a0001c0001t0001g0105others(111): Show | 115 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.1257-2769C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875239 | ||||||
| chr3:195875243
|
G | A | 1 | a0001c0014t0004g0093 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1257-2773C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875243 | ||||||
| chr3:195875243
|
GCTCCCCT others(81): Show |
G | 1 | a0001c0011t0001g0230 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1257-2861_1257-277 others(92): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875243 | ||||||
| chr3:195875283
|
C | A | 146 | a0001c0001t0001g0006a0001c0001t0001g0056a0001c0001t0001g0104others(143): Show | 147 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.1257-2813G>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875283 | ||||||
| chr3:195875287
|
G | A | 3 | a0001c0001t0001g0290a0001c0014t0004g0093a0002c0008t0001g0010 | 3 | HG00099.hp1 HG02280.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1257-2817C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875287 | ||||||
| chr3:195875289
|
T | TC | 4 | a0001c0001t0001g0290a0001c0009t0002g0255a0001c0014t0004g0093others(1): Show | 4 | HG00099.hp1 HG02280.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1257-2820dupG | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875289 | ||||||
| chr3:195875289
|
TCCCCTCG others(38): Show |
T | 2 | a0001c0001t0001g0164a0001c0050t0001g0213 | 2 | HG02976.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.1257-2864_1257-282 others(49): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875289 | ||||||
| chr3:195875318
|
C | G | 1 | a0001c0001t0001g0290 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1257-2848G>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875318 | ||||||
| chr3:195875327
|
A | G | 1 | a0001c0001t0001g0290 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1257-2857T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875327 | ||||||
| chr3:195875331
|
A | ACTCCCCC others(38): Show |
4 | a0001c0009t0002g0263a0001c0009t0002g0266a0001c0009t0002g0330others(1): Show | 4 | NA18989.hp2 NA19058.hp1 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.1257-2862_1257-286 others(49): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875331 | ||||||
| chr3:195875331
|
A | G | 24 | a0001c0001t0001g0076a0001c0001t0001g0144a0001c0001t0001g0290others(21): Show | 24 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.1257-2861T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875331 | ||||||
| chr3:195875331
|
ACTCCCCC others(83): Show |
A | 1 | a0001c0042t0001g0234 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1256+2832_1257-286 others(94): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875331 | ||||||
| chr3:195875335
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1257-2865G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875335 | ||||||
| chr3:195875363
|
C | G | 66 | a0001c0001t0001g0144a0001c0001t0001g0290a0001c0003t0001g0138others(63): Show | 67 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(64): Show |
intron_variant | MODIFIER | c.1256+2890G>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875363 | ||||||
| chr3:195875372
|
A | G | 68 | a0001c0001t0001g0144a0001c0001t0001g0290a0001c0003t0001g0138others(65): Show | 69 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(66): Show |
intron_variant | MODIFIER | c.1256+2881T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875372 | ||||||
| chr3:195875372
|
AGAAACTC others(83): Show |
A | 1 | a0001c0001t0002g0062 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1256+2791_1256+288 others(94): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875372 | ||||||
| chr3:195875373
|
G | T | 50 | a0001c0006t0001g0061a0001c0006t0001g0066a0001c0006t0001g0069others(47): Show | 51 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.1256+2880C>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875373 | ||||||
| chr3:195875376
|
A | G | 63 | a0001c0001t0001g0076a0001c0001t0001g0103a0001c0001t0001g0104others(60): Show | 63 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.1256+2877T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875376 | ||||||
| chr3:195875376
|
ACTCCCCC others(38): Show |
A | 3 | a0003c0005t0001g0034a0003c0005t0001g0245a0027c0049t0001g0022 | 3 | HG00140.hp2 HG00642.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.1256+2832_1256+287 others(49): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875376 | ||||||
| chr3:195875379
|
C | CCCCCTCG others(82): Show |
1 | a0002c0066t0002g0242 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1256+2873_1256+287 others(93): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875379 | ||||||
| chr3:195875404
|
G | A | 1 | a0001c0002t0001g0185 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1256+2849C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875404 | ||||||
| chr3:195875408
|
C | G | 106 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(103): Show | 107 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.1256+2845G>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875408 | ||||||
| chr3:195875417
|
A | G | 111 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(108): Show | 112 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.1256+2836T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875417 | ||||||
| chr3:195875418
|
G | T | 35 | a0001c0002t0001g0018a0001c0002t0001g0029a0001c0002t0001g0031others(32): Show | 35 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.1256+2835C>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875418 | ||||||
| chr3:195875421
|
G | A | 39 | a0001c0001t0001g0281a0001c0001t0001g0348a0001c0002t0001g0018others(36): Show | 39 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.1256+2832C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875421 | ||||||
| chr3:195875463
|
G | T | 1 | a0001c0040t0001g0019 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1256+2790C>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875463 | ||||||
| chr3:195875466
|
G | A | 2 | a0001c0002t0001g0177a0001c0040t0001g0019 | 2 | HG00673.hp2 HG02015.hp1 |
intron_variant | MODIFIER | c.1256+2787C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875466 | ||||||
| chr3:195875493
|
C | T | 1 | a0001c0014t0004g0093 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1256+2760G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875493 | ||||||
| chr3:195875494
|
A | G | 1 | a0002c0008t0002g0267 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1256+2759T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875494 | ||||||
| chr3:195875498
|
C | G | 1 | a0002c0008t0002g0267 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1256+2755G>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875498 | ||||||
| chr3:195875499
|
A | G | 1 | a0002c0008t0002g0267 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1256+2754T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875499 | ||||||
| chr3:195875540
|
G | A | 5 | a0001c0014t0004g0002a0001c0037t0004g0110a0001c0040t0001g0019others(2): Show | 6 | HG00673.hp2 HG01884.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.1256+2713C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875540 | ||||||
| chr3:195875548
|
C | T | 1 | a0001c0001t0002g0326 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1256+2705G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875548 | ||||||
| chr3:195875571
|
C | T | 1 | a0003c0015t0001g0064 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1256+2682G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875571 | ||||||
| chr3:195875654
|
C | T | 1 | a0002c0008t0001g0204 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1256+2599G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875654 | ||||||
| chr3:195875657
|
CCT | C | 218 | a0001c0001t0001g0001a0001c0001t0001g0076a0001c0001t0001g0095others(215): Show | 222 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.1256+2594_1256+259 others(6): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875657 | ||||||
| chr3:195875660
|
C | G | 1 | a0001c0002t0001g0235 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1256+2593G>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875660 | ||||||
| chr3:195875660
|
C | T | 20 | a0001c0002t0001g0029a0001c0002t0001g0031a0001c0002t0001g0036others(17): Show | 20 | HG00140.hp2 HG00323.hp1 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.1256+2593G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875660 | ||||||
| chr3:195875691
|
C | T | 1 | a0003c0005t0001g0245 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1256+2562G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875691 | ||||||
| chr3:195875693
|
T | C | 10 | a0001c0006t0001g0229a0001c0011t0001g0230a0001c0011t0001g0231others(7): Show | 11 | HG01884.hp1 HG01891.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1256+2560A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875693 | ||||||
| chr3:195875722
|
G | C | 2 | a0001c0024t0001g0189a0001c0024t0001g0190 | 2 | HG01099.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1256+2531C>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875722 | ||||||
| chr3:195875916
|
C | T | 114 | a0001c0001t0001g0001a0001c0001t0001g0076a0001c0001t0001g0095others(111): Show | 118 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.1256+2337G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195875916 | ||||||
| chr3:195876004
|
G | A | 1 | a0001c0011t0001g0108 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1256+2249C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195876004 | ||||||
| chr3:195876056
|
C | T | 1 | a0001c0001t0002g0062 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1256+2197G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195876056 | ||||||
| chr3:195876119
|
C | A | 1 | a0001c0001t0001g0323 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1256+2134G>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195876119 | ||||||
| chr3:195876131
|
C | T | 1 | a0001c0002t0001g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1256+2122G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195876131 | ||||||
| chr3:195876234
|
G | C | 1 | a0019c0038t0001g0032 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1256+2019C>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195876234 | ||||||
| chr3:195876458
|
C | T | 2 | a0001c0002t0001g0130a0001c0002t0001g0186 | 2 | HG02647.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1256+1795G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195876458 | ||||||
| chr3:195876493
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1256+1760A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195876493 | ||||||
| chr3:195876548
|
C | T | 2 | a0001c0001t0001g0209a0001c0001t0001g0210 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1256+1705G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195876548 | ||||||
| chr3:195876610
|
C | T | 1 | a0003c0005t0001g0034 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1256+1643G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195876610 | ||||||
| chr3:195876696
|
C | T | 1 | a0001c0001t0002g0273 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1256+1557G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195876696 | ||||||
| chr3:195876729
|
G | A | 1 | a0001c0003t0001g0200 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1256+1524C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195876729 | ||||||
| chr3:195876738
|
G | A | 1 | a0001c0001t0001g0291 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1256+1515C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195876738 | ||||||
| chr3:195876763
|
G | A | 199 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0076others(196): Show | 201 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.1256+1490C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195876763 | ||||||
| chr3:195876781
|
T | G | 301 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0056others(298): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.1256+1472A>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195876781 | ||||||
| chr3:195876795
|
G | A | 155 | a0001c0001t0001g0006a0001c0001t0001g0056a0001c0001t0001g0103others(152): Show | 159 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.1256+1458C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195876795 | ||||||
| chr3:195876981
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1256+1272C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195876981 | ||||||
| chr3:195877006
|
G | A | 1 | a0010c0059t0001g0021 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1256+1247C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195877006 | ||||||
| chr3:195877122
|
G | A | 2 | a0001c0001t0001g0281a0001c0001t0001g0348 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1256+1131C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195877122 | ||||||
| chr3:195877173
|
C | T | 1 | a0001c0001t0007g0232 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1256+1080G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195877173 | ||||||
| chr3:195877196
|
C | G | 1 | a0010c0059t0001g0021 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1256+1057G>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195877196 | ||||||
| chr3:195877511
|
G | C | 1 | a0001c0012t0011g0102 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1256+742C>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195877511 | ||||||
| chr3:195877550
|
T | C | 41 | a0001c0001t0001g0076a0001c0006t0001g0061a0001c0006t0001g0066others(38): Show | 41 | HG00140.hp1 HG00639.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.1256+703A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195877550 | ||||||
| chr3:195877666
|
G | A | 1 | a0001c0002t0001g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1256+587C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195877666 | ||||||
| chr3:195877676
|
C | T | 1 | a0002c0004t0002g0146 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1256+577G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195877676 | ||||||
| chr3:195877724
|
G | A | 2 | a0001c0002t0001g0205a0002c0023t0001g0207 | 2 | HG01175.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1256+529C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195877724 | ||||||
| chr3:195877794
|
G | A | 1 | a0004c0007t0001g0289 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1256+459C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195877794 | ||||||
| chr3:195877795
|
A | G | 1 | a0004c0007t0001g0289 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1256+458T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195877795 | ||||||
| chr3:195877797
|
G | C | 2 | a0001c0001t0001g0261a0001c0001t0001g0297 | 2 | HG01993.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.1256+456C>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195877797 | ||||||
| chr3:195877805
|
G | A | 4 | a0001c0003t0001g0200a0001c0003t0005g0197a0001c0003t0005g0199others(1): Show | 4 | HG00558.hp2 HG02132.hp1 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.1256+448C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195877805 | ||||||
| chr3:195877909
|
AGGGAGAG others(5): Show |
A | 5 | a0001c0058t0004g0237a0001c0061t0001g0238a0001c0062t0001g0239others(2): Show | 5 | HG02922.hp2 HG03130.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1256+332_1256+343d others(14): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195877909 | ||||||
| chr3:195877989
|
C | G | 1 | a0001c0014t0004g0093 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1256+264G>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195877989 | ||||||
| chr3:195878229
|
G | A | 57 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(54): Show | 57 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.1256+24C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | 195878229 | ||||||
| chr3:195878398
|
C | A | 1 | a0001c0001t0001g0095 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1161+48G>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 8/15 | chr3 | 195878398 | ||||||
| chr3:195878419
|
GC | G | 4 | a0001c0006t0001g0098a0001c0006t0001g0100a0002c0026t0001g0074others(1): Show | 4 | HG02622.hp2 HG02818.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1161+26delG | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 8/15 | chr3 | 195878419 | ||||||
| chr3:195878617
|
T | C | 1 | a0001c0040t0001g0019 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1015-25A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 7/15 | chr3 | 195878617 | ||||||
| chr3:195878730
|
A | G | 1 | a0004c0007t0001g0289 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1015-138T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 7/15 | chr3 | 195878730 | ||||||
| chr3:195878779
|
G | A | 10 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(7): Show | 10 | HG01975.hp2 HG02109.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1015-187C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 7/15 | chr3 | 195878779 | ||||||
| chr3:195878839
|
G | A | 1 | a0010c0059t0001g0021 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1014+210C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 7/15 | chr3 | 195878839 | ||||||
| chr3:195878847
|
G | A | 1 | a0002c0004t0002g0241 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1014+202C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 7/15 | chr3 | 195878847 | ||||||
| chr3:195878905
|
TGGGAGGC others(12): Show |
T | 1 | a0001c0040t0001g0019 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1014+125_1014+143d others(21): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 7/15 | chr3 | 195878905 | ||||||
| chr3:195878908
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1014+141C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 7/15 | chr3 | 195878908 | ||||||
| chr3:195878918
|
A | G | 59 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(56): Show | 59 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.1014+131T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 7/15 | chr3 | 195878918 | ||||||
| chr3:195878919
|
A | C | 59 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(56): Show | 59 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.1014+130T>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 7/15 | chr3 | 195878919 | ||||||
| chr3:195879037
|
C | T | 1 | a0010c0059t0001g0021 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1014+12G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 7/15 | chr3 | 195879037 | ||||||
| chr3:195879282
|
C | G | 1 | a0006c0025t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.888-107G>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195879282 | ||||||
| chr3:195879321
|
G | A | 1 | a0001c0002t0001g0235 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.888-146C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195879321 | ||||||
| chr3:195879405
|
G | T | 1 | a0010c0059t0001g0021 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.888-230C>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195879405 | ||||||
| chr3:195879520
|
T | C | 1 | a0018c0039t0001g0038 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.888-345A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195879520 | ||||||
| chr3:195879725
|
C | T | 1 | a0001c0002t0001g0214 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.888-550G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195879725 | ||||||
| chr3:195879805
|
G | GGGAAAGT others(7): Show |
1 | a0003c0015t0001g0084 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.888-644_888-631dup others(14): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195879805 | ||||||
| chr3:195879899
|
A | G | 168 | a0001c0001t0001g0001a0001c0001t0001g0076a0001c0001t0001g0095others(165): Show | 172 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.888-724T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195879899 | ||||||
| chr3:195880041
|
T | A | 1 | a0001c0040t0001g0019 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.888-866A>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880041 | ||||||
| chr3:195880369
|
A | AAATGCCC others(362): Show |
1 | a0001c0020t0002g0335 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.888-1195_888-1194i others(371): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880369 | ||||||
| chr3:195880409
|
A | ACCCCCCC others(99): Show |
1 | a0001c0001t0001g0349 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.888-1340_888-1235d others(108): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880409 | ||||||
| chr3:195880472
|
G | A | 226 | a0001c0001t0001g0001a0001c0001t0001g0076a0001c0001t0001g0095others(223): Show | 230 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.888-1297C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880472 | ||||||
| chr3:195880480
|
C | CGAGAGGA others(263): Show |
1 | a0001c0009t0002g0331 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.888-1306_888-1305i others(272): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880480 | ||||||
| chr3:195880480
|
C | CGGAGAGG others(317): Show |
1 | a0001c0009t0002g0324 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.888-1306_888-1305i others(326): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880480 | ||||||
| chr3:195880480
|
C | CGGAGAGG others(102): Show |
1 | a0002c0004t0002g0143 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.888-1306_888-1305i others(111): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880480 | ||||||
| chr3:195880480
|
C | CGGAGAGG others(264): Show |
3 | a0001c0009t0002g0255a0001c0009t0002g0266a0001c0009t0002g0330 | 3 | NA18989.hp2 NA19060.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.888-1306_888-1305i others(273): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880480 | ||||||
| chr3:195880510
|
A | AC | 41 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(38): Show | 41 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.888-1336dupG | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880510 | ||||||
| chr3:195880510
|
A | ACCCCCCC others(322): Show |
1 | a0001c0009t0002g0354 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.888-1336_888-1335i others(331): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880510 | ||||||
| chr3:195880510
|
AC | A | 37 | a0001c0001t0001g0246a0001c0001t0001g0339a0001c0002t0001g0018others(34): Show | 37 | HG01175.hp1 HG01192.hp2 HG01496.hp2 others(34): Show |
intron_variant | MODIFIER | c.888-1336delG | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880510 | ||||||
| chr3:195880510
|
ACC | A | 144 | a0001c0001t0001g0001a0001c0001t0001g0076a0001c0001t0001g0095others(141): Show | 148 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.888-1337_888-1336d others(4): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880510 | ||||||
| chr3:195880511
|
CCCCCCCC others(50): Show |
C | 1 | a0013c0076t0001g0078 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.888-1393_888-1337d others(59): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880511 | ||||||
| chr3:195880511
|
CCCCCCCC others(301): Show |
C | 1 | a0001c0012t0011g0102 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.887+1232_888-1337d others(2): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880511 | ||||||
| chr3:195880514
|
C | CCCCCCCC others(348): Show |
2 | a0001c0001t0001g0298a0001c0001t0001g0311 | 2 | NA18971.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.888-1340_888-1339i others(357): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880514 | ||||||
| chr3:195880516
|
C | G | 4 | a0001c0001t0001g0306a0001c0001t0001g0358a0002c0004t0001g0357others(1): Show | 4 | HG00733.hp2 HG01256.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.888-1341G>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880516 | ||||||
| chr3:195880519
|
C | A | 9 | a0001c0014t0004g0002a0001c0014t0004g0109a0001c0037t0004g0110others(6): Show | 10 | HG01884.hp1 HG01891.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.888-1344G>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880519 | ||||||
| chr3:195880547
|
G | T | 2 | a0001c0058t0004g0237a0002c0057t0004g0236 | 2 | HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.888-1372C>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880547 | ||||||
| chr3:195880550
|
T | A | 1 | a0002c0074t0001g0073 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.888-1375A>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880550 | ||||||
| chr3:195880554
|
A | T | 3 | a0001c0003t0001g0166a0001c0009t0002g0263a0002c0004t0002g0327 | 3 | NA18980.hp2 NA19058.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.888-1379T>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880554 | ||||||
| chr3:195880568
|
G | C | 2 | a0001c0009t0002g0263a0002c0004t0002g0327 | 2 | NA18980.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.888-1393C>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880568 | ||||||
| chr3:195880568
|
GCCCCCCA others(43): Show |
G | 1 | a0001c0003t0001g0155 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.887+1433_888-1394d others(52): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880568 | ||||||
| chr3:195880568
|
GCCCCCCA others(144): Show |
G | 1 | a0010c0059t0001g0021 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.887+1332_888-1394d others(2): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880568 | ||||||
| chr3:195880568
|
GCCCCCCA others(503): Show |
G | 1 | a0001c0002t0001g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.887+973_888-1394de others(1): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880568 | ||||||
| chr3:195880574
|
CAGCAATG others(93): Show |
C | 1 | a0002c0004t0002g0327 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.887+1377_888-1400d others(102): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880574 | ||||||
| chr3:195880579
|
A | G | 4 | a0001c0002t0001g0217a0001c0003t0005g0197a0001c0003t0005g0199others(1): Show | 4 | HG02132.hp1 HG02165.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.888-1404T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880579 | ||||||
| chr3:195880587
|
C | T | 223 | a0001c0001t0001g0001a0001c0001t0001g0076a0001c0001t0001g0095others(220): Show | 227 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.888-1412G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880587 | ||||||
| chr3:195880618
|
CCCCCCCA others(143): Show |
C | 3 | a0001c0003t0005g0197a0001c0003t0005g0199a0003c0054t0001g0134 | 3 | HG02132.hp1 HG02165.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.887+1283_887+1432d others(2): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880618 | ||||||
| chr3:195880624
|
C | A | 41 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0002t0001g0029others(38): Show | 41 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(38): Show |
intron_variant | MODIFIER | c.887+1427G>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880624 | ||||||
| chr3:195880624
|
CAGCAATG others(40): Show |
C | 1 | a0001c0009t0002g0263 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.887+1380_887+1426d others(49): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880624 | ||||||
| chr3:195880637
|
TGAAGAGG others(44): Show |
T | 1 | a0001c0003t0001g0276 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.887+1363_887+1413d others(53): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880637 | ||||||
| chr3:195880654
|
A | C | 4 | a0001c0001t0007g0232a0001c0014t0004g0002a0001c0014t0004g0109others(1): Show | 5 | HG01884.hp1 HG01891.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.887+1397T>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880654 | ||||||
| chr3:195880672
|
A | C | 1 | a0001c0009t0002g0263 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.887+1379T>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880672 | ||||||
| chr3:195880674
|
T | C | 1 | a0001c0009t0002g0263 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.887+1377A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880674 | ||||||
| chr3:195880683
|
A | C | 2 | a0001c0009t0002g0263a0002c0004t0002g0327 | 2 | NA18980.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.887+1368T>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880683 | ||||||
| chr3:195880688
|
C | CGGAGAGG others(94): Show |
1 | a0001c0001t0002g0265 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.887+1262_887+1362d others(103): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880688 | ||||||
| chr3:195880688
|
C | T | 2 | a0001c0009t0002g0263a0002c0004t0002g0327 | 2 | NA18980.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.887+1363G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880688 | ||||||
| chr3:195880688
|
CGGAGAGG others(43): Show |
C | 1 | a0003c0005t0001g0033 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.887+1313_887+1362d others(52): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880688 | ||||||
| chr3:195880708
|
T | A | 1 | a0001c0003t0001g0276 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.887+1343A>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880708 | ||||||
| chr3:195880718
|
A | ACCCCCCC others(44): Show |
1 | a0002c0004t0002g0332 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.887+1282_887+1332d others(53): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880718 | ||||||
| chr3:195880718
|
ACCCCCCC others(44): Show |
A | 34 | a0001c0001t0001g0076a0001c0001t0001g0336a0001c0006t0001g0061others(31): Show | 34 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.887+1282_887+1332d others(53): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880718 | ||||||
| chr3:195880718
|
ACCCCCCC others(95): Show |
A | 2 | a0001c0011t0001g0107a0001c0011t0001g0108 | 2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.887+1231_887+1332d others(2): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880718 | ||||||
| chr3:195880719
|
C | CCCCCCCC others(252): Show |
3 | a0001c0019t0003g0132a0001c0019t0003g0133a0001c0019t0003g0194 | 3 | NA18964.hp1 NA18986.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.887+1331_887+1332i others(261): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880719 | ||||||
| chr3:195880719
|
CCCCCCCA others(93): Show |
C | 1 | a0001c0014t0004g0109 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.887+1232_887+1331d others(102): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880719 | ||||||
| chr3:195880730
|
A | ATGCCCCT others(46): Show |
1 | a0001c0002t0001g0211 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.887+1320_887+1321i others(55): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880730 | ||||||
| chr3:195880730
|
A | ATGCCCCT others(149): Show |
9 | a0001c0002t0001g0036a0002c0008t0002g0267a0002c0010t0001g0035others(6): Show | 9 | HG01074.hp1 HG01074.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.887+1320_887+1321i others(158): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880730 | ||||||
| chr3:195880730
|
A | ATGCCCCT others(46): Show |
1 | a0002c0027t0001g0114 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.887+1320_887+1321i others(55): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880730 | ||||||
| chr3:195880730
|
A | G | 5 | a0001c0003t0001g0276a0001c0019t0003g0132a0001c0019t0003g0133others(2): Show | 5 | HG01109.hp1 NA18964.hp1 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.887+1321T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880730 | ||||||
| chr3:195880740
|
G | A | 1 | a0001c0001t0002g0333 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.887+1311C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880740 | ||||||
| chr3:195880753
|
A | G | 1 | a0003c0043t0001g0025 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.887+1298T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880753 | ||||||
| chr3:195880755
|
C | A | 1 | a0001c0001t0002g0333 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.887+1296G>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880755 | ||||||
| chr3:195880758
|
T | A | 161 | a0001c0001t0001g0001a0001c0001t0001g0095a0001c0001t0001g0103others(158): Show | 165 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.887+1293A>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880758 | ||||||
| chr3:195880766
|
A | T | 1 | a0001c0001t0002g0333 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.887+1285T>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880766 | ||||||
| chr3:195880768
|
A | ACCCGCCC others(47): Show |
3 | a0001c0003t0001g0169a0001c0003t0002g0141a0002c0018t0001g0159 | 3 | NA18941.hp1 NA18971.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.887+1282_887+1283i others(56): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880768 | ||||||
| chr3:195880769
|
C | CCCCCCCC others(707): Show |
1 | a0001c0001t0001g0308 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.887+1281_887+1282i others(716): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880769 | ||||||
| chr3:195880770
|
C | CCCCCCAG others(44): Show |
1 | a0001c0009t0002g0331 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.887+1280_887+1281i others(53): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880770 | ||||||
| chr3:195880770
|
C | CCG | 157 | a0001c0001t0001g0001a0001c0001t0001g0095a0001c0001t0001g0103others(154): Show | 161 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.887+1280_887+1281i others(4): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880770 | ||||||
| chr3:195880771
|
C | T | 1 | a0001c0001t0002g0333 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.887+1280G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880771 | ||||||
| chr3:195880772
|
C | A | 1 | a0001c0001t0002g0333 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.887+1279G>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880772 | ||||||
| chr3:195880773
|
C | A | 1 | a0001c0001t0002g0333 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.887+1278G>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880773 | ||||||
| chr3:195880775
|
C | T | 1 | a0001c0001t0002g0333 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.887+1276G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880775 | ||||||
| chr3:195880781
|
A | G | 108 | a0001c0001t0001g0001a0001c0001t0001g0095a0001c0001t0001g0103others(105): Show | 112 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.887+1270T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880781 | ||||||
| chr3:195880784
|
C | A | 1 | a0001c0001t0002g0333 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.887+1267G>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880784 | ||||||
| chr3:195880789
|
T | C | 2 | a0001c0001t0002g0333a0002c0004t0002g0327 | 2 | HG01258.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.887+1262A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880789 | ||||||
| chr3:195880809
|
T | A | 2 | a0001c0002t0001g0217a0001c0011t0001g0060 | 2 | HG03516.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.887+1242A>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880809 | ||||||
| chr3:195880809
|
TCCCTGTA others(44): Show |
T | 1 | a0002c0072t0001g0091 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.887+1191_887+1241d others(53): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880809 | ||||||
| chr3:195880819
|
A | AC | 32 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(29): Show | 32 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.887+1231dupG | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880819 | ||||||
| chr3:195880819
|
AC | A | 49 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0353others(46): Show | 49 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.887+1231delG | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880819 | ||||||
| chr3:195880821
|
C | CCCCCCAG others(146): Show |
1 | a0001c0003t0003g0124 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.887+1229_887+1230i others(155): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880821 | ||||||
| chr3:195880825
|
C | A | 1 | a0001c0014t0004g0109 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.887+1226G>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880825 | ||||||
| chr3:195880826
|
C | CAGCAATG others(43): Show |
3 | a0001c0003t0003g0125a0001c0003t0003g0126a0005c0056t0002g0040 | 3 | HG01496.hp2 NA18975.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.887+1224_887+1225i others(52): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880826 | ||||||
| chr3:195880832
|
A | G | 2 | a0001c0001t0001g0317a0001c0003t0003g0124 | 2 | HG02148.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.887+1219T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880832 | ||||||
| chr3:195880832
|
ATGCCCCT others(250): Show |
A | 3 | a0001c0001t0001g0165a0001c0002t0001g0225a0001c0013t0001g0145 | 3 | HG03579.hp1 NA18939.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.887+962_887+1218de others(1): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880832 | ||||||
| chr3:195880835
|
C | A | 3 | a0001c0003t0003g0125a0001c0003t0003g0126a0005c0056t0002g0040 | 3 | HG01496.hp2 NA18975.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.887+1216G>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880835 | ||||||
| chr3:195880840
|
T | C | 3 | a0001c0003t0003g0125a0001c0003t0003g0126a0005c0056t0002g0040 | 3 | HG01496.hp2 NA18975.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.887+1211A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880840 | ||||||
| chr3:195880841
|
G | A | 12 | a0001c0003t0001g0169a0001c0003t0001g0276a0001c0003t0002g0141others(9): Show | 12 | HG00609.hp1 HG02132.hp1 HG02165.hp2 others(9): Show |
intron_variant | MODIFIER | c.887+1210C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880841 | ||||||
| chr3:195880842
|
G | A | 12 | a0001c0003t0001g0148a0001c0003t0002g0127a0001c0003t0003g0135others(9): Show | 12 | NA18942.hp1 NA18949.hp1 NA18952.hp1 others(9): Show |
intron_variant | MODIFIER | c.887+1209C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880842 | ||||||
| chr3:195880847
|
G | A | 1 | a0010c0059t0001g0021 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.887+1204C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880847 | ||||||
| chr3:195880857
|
C | A | 13 | a0001c0002t0001g0181a0001c0003t0001g0148a0001c0003t0002g0127others(10): Show | 13 | HG03130.hp1 NA18942.hp1 NA18949.hp1 others(10): Show |
intron_variant | MODIFIER | c.887+1194G>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880857 | ||||||
| chr3:195880860
|
A | T | 128 | a0001c0001t0001g0001a0001c0001t0001g0095a0001c0001t0001g0103others(125): Show | 132 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.887+1191T>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880860 | ||||||
| chr3:195880868
|
A | T | 13 | a0001c0003t0001g0148a0001c0003t0002g0127a0001c0003t0003g0135others(10): Show | 13 | HG00280.hp2 NA18942.hp1 NA18949.hp1 others(10): Show |
intron_variant | MODIFIER | c.887+1183T>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880868 | ||||||
| chr3:195880870
|
A | AC | 7 | a0001c0003t0001g0122a0001c0003t0001g0200a0001c0003t0005g0196others(4): Show | 7 | HG00558.hp2 HG02056.hp2 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.887+1180dupG | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880870 | ||||||
| chr3:195880871
|
CCCG | C | 7 | a0001c0002t0001g0217a0001c0003t0003g0125a0001c0003t0003g0126others(4): Show | 7 | HG01433.hp2 HG01496.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.887+1177_887+1179d others(5): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880871 | ||||||
| chr3:195880871
|
CCCGCCCC others(199): Show |
C | 36 | a0001c0001t0001g0095a0001c0001t0001g0116a0001c0001t0007g0232others(33): Show | 37 | HG00323.hp2 HG01175.hp1 HG01884.hp1 others(34): Show |
intron_variant | MODIFIER | c.887+974_887+1179de others(1): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880871 | ||||||
| chr3:195880871
|
CCCGCCCC others(299): Show |
C | 1 | a0001c0011t0001g0060 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.887+874_887+1179de others(1): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880871 | ||||||
| chr3:195880872
|
CCG | C | 61 | a0001c0001t0001g0001a0001c0001t0001g0103a0001c0001t0001g0104others(58): Show | 64 | HG00280.hp2 HG01192.hp1 HG01192.hp2 others(61): Show |
intron_variant | MODIFIER | c.887+1177_887+1178d others(4): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880872 | ||||||
| chr3:195880872
|
CCGCCCCC others(198): Show |
C | 2 | a0001c0002t0001g0192a0001c0040t0001g0019 | 2 | HG00673.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.887+974_887+1178de others(1): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880872 | ||||||
| chr3:195880873
|
CGCCCCCC others(197): Show |
C | 4 | a0001c0003t0001g0155a0001c0003t0001g0156a0001c0003t0001g0160others(1): Show | 4 | NA18959.hp1 NA18999.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.887+974_887+1177de others(1): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880873 | ||||||
| chr3:195880874
|
G | A | 4 | a0001c0001t0001g0111a0001c0001t0001g0112a0002c0027t0001g0114others(1): Show | 4 | HG01109.hp1 HG01361.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.887+1177C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880874 | ||||||
| chr3:195880874
|
G | C | 16 | a0001c0003t0001g0122a0001c0003t0001g0138a0001c0003t0001g0149others(13): Show | 16 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(13): Show |
intron_variant | MODIFIER | c.887+1177C>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880874 | ||||||
| chr3:195880874
|
G | GCCCCCCA others(43): Show |
2 | a0001c0001t0001g0290a0001c0001t0002g0326 | 2 | HG00099.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.887+1127_887+1176d others(52): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880874 | ||||||
| chr3:195880874
|
G | GCCCCCCA others(94): Show |
2 | a0001c0009t0002g0266a0001c0009t0002g0330 | 2 | NA18989.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.887+1176_887+1177i others(103): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880874 | ||||||
| chr3:195880874
|
GCCCCCCA others(247): Show |
G | 1 | a0001c0001t0001g0286 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.887+923_887+1176de others(1): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880874 | ||||||
| chr3:195880875
|
C | T | 13 | a0001c0003t0001g0148a0001c0003t0002g0127a0001c0003t0003g0135others(10): Show | 13 | HG00280.hp2 NA18942.hp1 NA18949.hp1 others(10): Show |
intron_variant | MODIFIER | c.887+1176G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880875 | ||||||
| chr3:195880876
|
C | A | 13 | a0001c0003t0001g0148a0001c0003t0002g0127a0001c0003t0003g0135others(10): Show | 13 | HG00280.hp2 NA18942.hp1 NA18949.hp1 others(10): Show |
intron_variant | MODIFIER | c.887+1175G>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880876 | ||||||
| chr3:195880877
|
C | A | 13 | a0001c0003t0001g0148a0001c0003t0002g0127a0001c0003t0003g0135others(10): Show | 13 | HG00280.hp2 NA18942.hp1 NA18949.hp1 others(10): Show |
intron_variant | MODIFIER | c.887+1174G>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880877 | ||||||
| chr3:195880879
|
C | T | 13 | a0001c0003t0001g0148a0001c0003t0002g0127a0001c0003t0003g0135others(10): Show | 13 | HG00280.hp2 NA18942.hp1 NA18949.hp1 others(10): Show |
intron_variant | MODIFIER | c.887+1172G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880879 | ||||||
| chr3:195880885
|
A | G | 36 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0002t0001g0029others(33): Show | 36 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.887+1166T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880885 | ||||||
| chr3:195880885
|
ATGCCCCT others(247): Show |
A | 47 | a0001c0001t0001g0076a0001c0001t0001g0111a0001c0001t0001g0112others(44): Show | 47 | HG00140.hp1 HG00735.hp2 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.887+912_887+1165de others(1): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880885 | ||||||
| chr3:195880886
|
T | C | 1 | a0001c0050t0001g0213 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.887+1165A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880886 | ||||||
| chr3:195880888
|
C | A | 13 | a0001c0003t0001g0148a0001c0003t0002g0127a0001c0003t0003g0135others(10): Show | 13 | HG00280.hp2 NA18942.hp1 NA18949.hp1 others(10): Show |
intron_variant | MODIFIER | c.887+1163G>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880888 | ||||||
| chr3:195880893
|
T | C | 14 | a0001c0003t0001g0148a0001c0003t0002g0127a0001c0003t0003g0135others(11): Show | 14 | HG00280.hp2 NA18942.hp1 NA18949.hp1 others(11): Show |
intron_variant | MODIFIER | c.887+1158A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880893 | ||||||
| chr3:195880894
|
G | A | 16 | a0001c0003t0001g0122a0001c0003t0001g0138a0001c0003t0001g0149others(13): Show | 16 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(13): Show |
intron_variant | MODIFIER | c.887+1157C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880894 | ||||||
| chr3:195880908
|
A | ATCTATCC others(43): Show |
1 | a0001c0001t0001g0314 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.887+1093_887+1142d others(52): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880908 | ||||||
| chr3:195880913
|
T | A | 55 | a0001c0001t0001g0001a0001c0001t0001g0103a0001c0001t0001g0104others(52): Show | 58 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.887+1138A>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880913 | ||||||
| chr3:195880921
|
A | T | 1 | a0001c0001t0001g0306 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.887+1130T>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880921 | ||||||
| chr3:195880923
|
A | AC | 44 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0246others(41): Show | 44 | HG00140.hp2 HG00280.hp1 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.887+1127dupG | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880923 | ||||||
| chr3:195880923
|
A | ACCCCCCC others(96): Show |
1 | a0001c0009t0002g0354 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.887+1127_887+1128i others(105): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880923 | ||||||
| chr3:195880923
|
A | ACCCCCCC others(45): Show |
1 | a0002c0004t0001g0279 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.887+1127_887+1128i others(54): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880923 | ||||||
| chr3:195880924
|
C | CCCG | 25 | a0001c0001t0001g0001a0001c0001t0002g0062a0001c0002t0001g0181others(22): Show | 26 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.887+1126_887+1127i others(5): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880924 | ||||||
| chr3:195880924
|
CCCCCCCA others(146): Show |
C | 2 | a0001c0050t0001g0213a0003c0005t0001g0059 | 2 | HG02976.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.887+974_887+1126de others(1): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880924 | ||||||
| chr3:195880926
|
CCCCCAGC others(144): Show |
C | 17 | a0001c0002t0001g0003a0001c0002t0001g0183a0001c0002t0001g0212others(14): Show | 19 | HG01192.hp1 HG01934.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.887+974_887+1124de others(1): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880926 | ||||||
| chr3:195880926
|
CCCCCAGC others(194): Show |
C | 13 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(10): Show | 13 | HG01258.hp2 HG01975.hp2 HG02129.hp2 others(10): Show |
intron_variant | MODIFIER | c.887+924_887+1124de others(1): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880926 | ||||||
| chr3:195880934
|
AATGCCCC others(45): Show |
A | 1 | a0002c0004t0002g0327 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.887+1065_887+1116d others(54): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880934 | ||||||
| chr3:195880935
|
A | G | 5 | a0001c0003t0003g0125a0001c0003t0003g0126a0001c0017t0006g0012others(2): Show | 5 | HG01433.hp2 HG01496.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.887+1116T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880935 | ||||||
| chr3:195880945
|
G | A | 1 | a0001c0009t0002g0263 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.887+1106C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880945 | ||||||
| chr3:195880958
|
G | A | 87 | a0001c0001t0001g0001a0001c0001t0001g0209a0001c0001t0001g0210others(84): Show | 88 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.887+1093C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880958 | ||||||
| chr3:195880960
|
C | A | 1 | a0001c0009t0002g0263 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.887+1091G>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880960 | ||||||
| chr3:195880963
|
T | A | 26 | a0001c0001t0001g0246a0001c0001t0001g0339a0001c0002t0001g0174others(23): Show | 26 | HG01192.hp2 HG01243.hp2 HG02015.hp1 others(23): Show |
intron_variant | MODIFIER | c.887+1088A>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880963 | ||||||
| chr3:195880968
|
GTAACACC others(97): Show |
G | 1 | a0001c0002t0001g0215 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.887+979_887+1082de others(1): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880968 | ||||||
| chr3:195880971
|
A | T | 1 | a0001c0009t0002g0263 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.887+1080T>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880971 | ||||||
| chr3:195880974
|
CCCGCCCC others(47): Show |
C | 2 | a0001c0001t0001g0001a0001c0001t0002g0062 | 3 | HG03017.hp2 HG03704.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.887+1023_887+1076d others(56): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880974 | ||||||
| chr3:195880974
|
CCCGCCCC others(96): Show |
C | 25 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0002t0001g0045others(22): Show | 25 | HG00280.hp1 HG00621.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.887+974_887+1076de others(1): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880974 | ||||||
| chr3:195880974
|
CCCGCCCC others(344): Show |
C | 1 | a0001c0009t0002g0263 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.887+726_887+1076de others(1): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880974 | ||||||
| chr3:195880975
|
CCG | C | 12 | a0001c0002t0001g0235a0001c0003t0001g0122a0001c0003t0001g0138others(9): Show | 12 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(9): Show |
intron_variant | MODIFIER | c.887+1074_887+1075d others(4): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880975 | ||||||
| chr3:195880975
|
CCGCCCCC others(95): Show |
C | 2 | a0002c0010t0001g0053a0003c0005t0001g0054 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.887+974_887+1075de others(1): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880975 | ||||||
| chr3:195880975
|
CCGCCCCC others(145): Show |
C | 1 | a0003c0005t0001g0058 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.887+924_887+1075de others(1): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880975 | ||||||
| chr3:195880976
|
CG | C | 12 | a0001c0002t0001g0029a0001c0002t0001g0031a0001c0002t0001g0181others(9): Show | 12 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(9): Show |
intron_variant | MODIFIER | c.887+1074delC | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880976 | ||||||
| chr3:195880977
|
G | C | 3 | a0001c0003t0003g0125a0001c0003t0003g0126a0005c0056t0002g0040 | 3 | HG01496.hp2 NA18975.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.887+1074C>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880977 | ||||||
| chr3:195880977
|
G | GC | 10 | a0001c0003t0001g0148a0001c0003t0002g0127a0001c0003t0003g0135others(7): Show | 10 | NA18942.hp1 NA18952.hp1 NA18954.hp1 others(7): Show |
intron_variant | MODIFIER | c.887+1073dupG | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880977 | ||||||
| chr3:195880977
|
GCCCCCAG others(144): Show |
G | 15 | a0001c0001t0001g0246a0001c0001t0001g0339a0001c0002t0001g0174others(12): Show | 15 | HG01192.hp2 HG01243.hp2 HG02015.hp1 others(12): Show |
intron_variant | MODIFIER | c.887+923_887+1073de others(1): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880977 | ||||||
| chr3:195880977
|
GCCCCCAG others(248): Show |
G | 1 | a0001c0003t0001g0168 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.887+819_887+1073de others(1): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880977 | ||||||
| chr3:195880981
|
CCAGCGAT others(44): Show |
C | 1 | a0001c0012t0001g0071 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.887+1019_887+1069d others(53): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880981 | ||||||
| chr3:195880986
|
G | A | 39 | a0001c0002t0001g0029a0001c0002t0001g0031a0001c0002t0001g0181others(36): Show | 39 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.887+1065C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880986 | ||||||
| chr3:195880987
|
A | G | 11 | a0001c0003t0001g0148a0001c0003t0002g0127a0001c0003t0003g0135others(8): Show | 11 | NA18942.hp1 NA18949.hp1 NA18952.hp1 others(8): Show |
intron_variant | MODIFIER | c.887+1064T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880987 | ||||||
| chr3:195880987
|
ATGCCCCT others(95): Show |
A | 1 | a0006c0025t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.887+962_887+1063de others(1): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195880987 | ||||||
| chr3:195881009
|
T | C | 39 | a0001c0002t0001g0029a0001c0002t0001g0031a0001c0002t0001g0181others(36): Show | 39 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.887+1042A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881009 | ||||||
| chr3:195881010
|
G | A | 27 | a0001c0002t0001g0029a0001c0002t0001g0031a0001c0002t0001g0181others(24): Show | 27 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.887+1041C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881010 | ||||||
| chr3:195881015
|
T | A | 3 | a0003c0005t0001g0039a0003c0005t0001g0041a0003c0005t0001g0245 | 3 | HG00140.hp2 HG01516.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.887+1036A>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881015 | ||||||
| chr3:195881020
|
C | G | 39 | a0001c0002t0001g0029a0001c0002t0001g0031a0001c0002t0001g0181others(36): Show | 39 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.887+1031G>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881020 | ||||||
| chr3:195881025
|
A | AC | 4 | a0001c0003t0003g0124a0003c0005t0001g0039a0003c0005t0001g0041others(1): Show | 4 | HG00140.hp2 HG01516.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.887+1025dupG | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881025 | ||||||
| chr3:195881026
|
CCACCCGC others(42): Show |
C | 1 | a0001c0003t0001g0171 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.887+976_887+1024de others(50): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881026 | ||||||
| chr3:195881026
|
CCACCCGC others(44): Show |
C | 7 | a0001c0002t0001g0029a0001c0002t0001g0031a0001c0002t0001g0181others(4): Show | 7 | HG00280.hp2 HG00323.hp1 HG00735.hp1 others(4): Show |
intron_variant | MODIFIER | c.887+974_887+1024de others(52): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881026 | ||||||
| chr3:195881027
|
CA | C | 4 | a0001c0003t0003g0125a0001c0003t0003g0126a0003c0005t0001g0042others(1): Show | 4 | HG01081.hp2 HG01496.hp2 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.887+1023delT | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881027 | ||||||
| chr3:195881028
|
A | C | 23 | a0001c0002t0001g0235a0001c0003t0001g0122a0001c0003t0001g0138others(20): Show | 23 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.887+1023T>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881028 | ||||||
| chr3:195881028
|
A | G | 4 | a0001c0003t0003g0124a0003c0005t0001g0039a0003c0005t0001g0041others(1): Show | 4 | HG00140.hp2 HG01516.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.887+1023T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881028 | ||||||
| chr3:195881029
|
C | G | 12 | a0001c0002t0001g0235a0001c0003t0001g0122a0001c0003t0001g0138others(9): Show | 12 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(9): Show |
intron_variant | MODIFIER | c.887+1022G>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881029 | ||||||
| chr3:195881032
|
G | C | 33 | a0001c0001t0001g0001a0001c0001t0002g0062a0001c0002t0001g0235others(30): Show | 34 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.887+1019C>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881032 | ||||||
| chr3:195881038
|
A | G | 12 | a0001c0002t0001g0235a0001c0003t0001g0122a0001c0003t0001g0138others(9): Show | 12 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(9): Show |
intron_variant | MODIFIER | c.887+1013T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881038 | ||||||
| chr3:195881049
|
A | G | 34 | a0001c0001t0001g0001a0001c0001t0002g0062a0001c0002t0001g0235others(31): Show | 35 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.887+1002T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881049 | ||||||
| chr3:195881061
|
G | C | 22 | a0001c0001t0001g0001a0001c0001t0002g0062a0001c0003t0001g0148others(19): Show | 23 | HG00140.hp2 HG01081.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.887+990C>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881061 | ||||||
| chr3:195881061
|
G | T | 12 | a0001c0002t0001g0235a0001c0003t0001g0122a0001c0003t0001g0138others(9): Show | 12 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(9): Show |
intron_variant | MODIFIER | c.887+990C>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881061 | ||||||
| chr3:195881062
|
A | G | 12 | a0001c0002t0001g0235a0001c0003t0001g0122a0001c0003t0001g0138others(9): Show | 12 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(9): Show |
intron_variant | MODIFIER | c.887+989T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881062 | ||||||
| chr3:195881066
|
G | A | 34 | a0001c0001t0001g0001a0001c0001t0002g0062a0001c0002t0001g0235others(31): Show | 35 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.887+985C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881066 | ||||||
| chr3:195881072
|
C | CTAACACC others(43): Show |
1 | a0001c0001t0001g0287 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.887+929_887+978dup others(50): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881072 | ||||||
| chr3:195881072
|
C | G | 22 | a0001c0001t0001g0001a0001c0001t0002g0062a0001c0003t0001g0148others(19): Show | 23 | HG00140.hp2 HG01081.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.887+979G>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881072 | ||||||
| chr3:195881072
|
CTAACACC others(43): Show |
C | 1 | a0011c0078t0001g0272 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.887+929_887+978del others(50): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881072 | ||||||
| chr3:195881072
|
CTAACACC others(297): Show |
C | 4 | a0001c0006t0012g0065a0001c0014t0004g0109a0004c0032t0001g0303others(1): Show | 4 | HG00558.hp1 HG02559.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.887+675_887+978del | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881072 | ||||||
| chr3:195881077
|
A | C | 1 | a0001c0003t0001g0171 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.887+974T>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881077 | ||||||
| chr3:195881078
|
C | CCA | 12 | a0001c0002t0001g0235a0001c0003t0001g0122a0001c0003t0001g0138others(9): Show | 12 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(9): Show |
intron_variant | MODIFIER | c.887+972_887+973ins others(2): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881078 | ||||||
| chr3:195881078
|
C | G | 17 | a0001c0002t0001g0003a0001c0002t0001g0183a0001c0002t0001g0212others(14): Show | 19 | HG01192.hp1 HG01934.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.887+973G>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881078 | ||||||
| chr3:195881082
|
C | G | 12 | a0001c0002t0001g0235a0001c0003t0001g0122a0001c0003t0001g0138others(9): Show | 12 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(9): Show |
intron_variant | MODIFIER | c.887+969G>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881082 | ||||||
| chr3:195881089
|
G | A | 129 | a0001c0001t0001g0001a0001c0001t0001g0095a0001c0001t0001g0116others(126): Show | 133 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.887+962C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881089 | ||||||
| chr3:195881098
|
G | A | 14 | a0001c0003t0001g0148a0001c0003t0001g0155a0001c0003t0001g0156others(11): Show | 14 | HG03017.hp1 NA18942.hp1 NA18949.hp1 others(11): Show |
intron_variant | MODIFIER | c.887+953C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881098 | ||||||
| chr3:195881099
|
G | A | 12 | a0001c0002t0001g0235a0001c0003t0001g0122a0001c0003t0001g0138others(9): Show | 12 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(9): Show |
intron_variant | MODIFIER | c.887+952C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881099 | ||||||
| chr3:195881111
|
C | G | 12 | a0001c0002t0001g0235a0001c0003t0001g0122a0001c0003t0001g0138others(9): Show | 12 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(9): Show |
intron_variant | MODIFIER | c.887+940G>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881111 | ||||||
| chr3:195881112
|
A | G | 3 | a0003c0005t0001g0039a0003c0005t0001g0041a0003c0005t0001g0245 | 3 | HG00140.hp2 HG01516.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.887+939T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881112 | ||||||
| chr3:195881116
|
A | G | 12 | a0001c0002t0001g0235a0001c0003t0001g0122a0001c0003t0001g0138others(9): Show | 12 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(9): Show |
intron_variant | MODIFIER | c.887+935T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881116 | ||||||
| chr3:195881117
|
T | A | 93 | a0001c0001t0001g0001a0001c0001t0001g0095a0001c0001t0001g0116others(90): Show | 95 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.887+934A>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881117 | ||||||
| chr3:195881122
|
G | C | 12 | a0001c0002t0001g0235a0001c0003t0001g0122a0001c0003t0001g0138others(9): Show | 12 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(9): Show |
intron_variant | MODIFIER | c.887+929C>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881122 | ||||||
| chr3:195881122
|
G | GTAACACC others(147): Show |
1 | a0001c0001t0002g0305 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.887+928_887+929ins others(154): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881122 | ||||||
| chr3:195881128
|
C | CCCA | 8 | a0001c0001t0001g0116a0001c0013t0001g0119a0001c0013t0001g0120others(5): Show | 8 | HG00323.hp2 HG01891.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.887+922_887+923ins others(3): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881128 | ||||||
| chr3:195881128
|
C | CCCG | 88 | a0001c0001t0001g0001a0001c0001t0001g0095a0001c0001t0001g0209others(85): Show | 90 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.887+922_887+923ins others(3): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881128 | ||||||
| chr3:195881128
|
C | CCCGCCCC others(47): Show |
2 | a0003c0005t0001g0039a0003c0005t0001g0245 | 2 | HG00140.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.887+922_887+923ins others(54): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881128 | ||||||
| chr3:195881128
|
C | CCCGCCCC others(99): Show |
1 | a0003c0005t0001g0041 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.887+922_887+923ins others(106): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881128 | ||||||
| chr3:195881128
|
C | G | 14 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(11): Show | 14 | HG01258.hp2 HG01975.hp2 HG02129.hp2 others(11): Show |
intron_variant | MODIFIER | c.887+923G>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881128 | ||||||
| chr3:195881131
|
C | G | 1 | a0010c0059t0001g0021 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.887+920G>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881131 | ||||||
| chr3:195881132
|
C | G | 3 | a0003c0005t0001g0039a0003c0005t0001g0041a0003c0005t0001g0245 | 3 | HG00140.hp2 HG01516.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.887+919G>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881132 | ||||||
| chr3:195881134
|
CAGCAGTG others(145): Show |
C | 1 | a0010c0059t0001g0021 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.887+765_887+916del | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881134 | ||||||
| chr3:195881139
|
G | A | 153 | a0001c0001t0001g0001a0001c0001t0001g0095a0001c0001t0001g0103others(150): Show | 157 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.887+912C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881139 | ||||||
| chr3:195881139
|
G | GTGCCCCT others(299): Show |
1 | a0001c0001t0001g0314 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.887+606_887+911dup others(306): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881139 | ||||||
| chr3:195881139
|
G | GTGCCCCT others(709): Show |
1 | a0001c0020t0002g0251 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.887+911_887+912ins others(716): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881139 | ||||||
| chr3:195881139
|
G | GTGCCCCT others(202): Show |
2 | a0001c0019t0003g0133a0001c0019t0003g0194 | 2 | NA18964.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.887+911_887+912ins others(209): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881139 | ||||||
| chr3:195881139
|
G | GTGCCCCT others(201): Show |
1 | a0001c0019t0003g0132 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.887+911_887+912ins others(208): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881139 | ||||||
| chr3:195881139
|
G | GTGCCCCT others(512): Show |
1 | a0001c0003t0001g0169 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.887+911_887+912ins others(519): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881139 | ||||||
| chr3:195881139
|
G | GTGCCCCT others(203): Show |
1 | a0023c0052t0005g0198 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.887+911_887+912ins others(210): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881139 | ||||||
| chr3:195881149
|
G | A | 2 | a0003c0005t0001g0039a0003c0005t0001g0245 | 2 | HG00140.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.887+902C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881149 | ||||||
| chr3:195881161
|
C | G | 3 | a0003c0005t0001g0039a0003c0005t0001g0041a0003c0005t0001g0245 | 3 | HG00140.hp2 HG01516.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.887+890G>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881161 | ||||||
| chr3:195881162
|
A | G | 3 | a0001c0001t0002g0334a0002c0057t0004g0236a0006c0025t0001g0096 | 3 | HG02109.hp1 HG03471.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.887+889T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881162 | ||||||
| chr3:195881166
|
A | G | 3 | a0003c0005t0001g0039a0003c0005t0001g0041a0003c0005t0001g0245 | 3 | HG00140.hp2 HG01516.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.887+885T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881166 | ||||||
| chr3:195881167
|
T | A | 1 | a0003c0005t0001g0042 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.887+884A>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881167 | ||||||
| chr3:195881172
|
G | C | 9 | a0001c0002t0001g0018a0001c0017t0006g0012a0001c0017t0006g0013others(6): Show | 9 | HG00140.hp2 HG01516.hp1 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.887+879C>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881172 | ||||||
| chr3:195881177
|
A | ACCCGCCC others(97): Show |
1 | a0001c0003t0002g0158 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.887+873_887+874ins others(104): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881177 | ||||||
| chr3:195881177
|
A | ACCCGCCC others(97): Show |
4 | a0002c0010t0001g0035a0002c0010t0001g0043a0003c0005t0001g0034others(1): Show | 4 | HG01074.hp1 HG01074.hp2 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.887+873_887+874ins others(104): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881177 | ||||||
| chr3:195881177
|
A | ACCCGCCC others(97): Show |
1 | a0001c0003t0002g0141 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.887+873_887+874ins others(104): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881177 | ||||||
| chr3:195881179
|
C | CCG | 11 | a0001c0001t0002g0334a0001c0002t0001g0036a0001c0002t0001g0217others(8): Show | 11 | HG01099.hp2 HG01975.hp1 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.887+871_887+872ins others(2): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881179 | ||||||
| chr3:195881181
|
C | G | 2 | a0003c0015t0001g0084a0003c0054t0001g0134 | 2 | HG01358.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.887+870G>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881181 | ||||||
| chr3:195881184
|
CAGCAATG others(95): Show |
C | 2 | a0003c0015t0001g0084a0003c0054t0001g0134 | 2 | HG01358.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.887+765_887+866del | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881184 | ||||||
| chr3:195881188
|
A | G | 13 | a0001c0001t0002g0334a0001c0002t0001g0036a0001c0002t0001g0217others(10): Show | 13 | HG00609.hp1 HG01099.hp2 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.887+863T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881188 | ||||||
| chr3:195881189
|
A | G | 14 | a0001c0003t0001g0122a0001c0003t0001g0138a0001c0003t0001g0150others(11): Show | 14 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(11): Show |
intron_variant | MODIFIER | c.887+862T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881189 | ||||||
| chr3:195881199
|
G | A | 5 | a0001c0003t0002g0141a0002c0010t0001g0035a0002c0010t0001g0043others(2): Show | 5 | HG01074.hp1 HG01074.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.887+852C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881199 | ||||||
| chr3:195881209
|
A | AGGATCTG others(44): Show |
2 | a0001c0003t0005g0197a0002c0018t0001g0159 | 2 | HG02132.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.887+841_887+842ins others(51): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881209 | ||||||
| chr3:195881211
|
C | G | 6 | a0001c0002t0001g0036a0001c0002t0001g0217a0002c0008t0002g0267others(3): Show | 6 | HG01099.hp2 HG01975.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.887+840G>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881211 | ||||||
| chr3:195881211
|
C | T | 2 | a0002c0057t0004g0236a0006c0025t0001g0096 | 2 | HG02109.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.887+840G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881211 | ||||||
| chr3:195881212
|
G | A | 28 | a0001c0002t0001g0036a0001c0002t0001g0217a0001c0003t0001g0122others(25): Show | 28 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(25): Show |
intron_variant | MODIFIER | c.887+839C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881212 | ||||||
| chr3:195881216
|
A | G | 6 | a0001c0002t0001g0036a0001c0002t0001g0217a0002c0008t0002g0267others(3): Show | 6 | HG01099.hp2 HG01975.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.887+835T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881216 | ||||||
| chr3:195881220
|
C | T | 2 | a0001c0003t0002g0141a0001c0003t0002g0158 | 2 | HG00609.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.887+831G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881220 | ||||||
| chr3:195881222
|
G | C | 8 | a0001c0002t0001g0036a0001c0002t0001g0217a0002c0008t0002g0267others(5): Show | 8 | HG01099.hp2 HG01975.hp1 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.887+829C>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881222 | ||||||
| chr3:195881229
|
CCGCCCCC others(145): Show |
C | 1 | a0001c0002t0001g0217 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.887+670_887+821del | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881229 | ||||||
| chr3:195881230
|
C | A | 2 | a0002c0057t0004g0236a0006c0025t0001g0096 | 2 | HG02109.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.887+821G>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881230 | ||||||
| chr3:195881230
|
CG | C | 8 | a0001c0002t0001g0036a0001c0003t0002g0141a0001c0003t0005g0197others(5): Show | 8 | HG01099.hp2 HG01975.hp1 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.887+820delC | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881230 | ||||||
| chr3:195881231
|
G | C | 3 | a0001c0003t0002g0158a0002c0057t0004g0236a0006c0025t0001g0096 | 3 | HG00609.hp1 HG02109.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.887+820C>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881231 | ||||||
| chr3:195881234
|
C | G | 2 | a0002c0057t0004g0236a0006c0025t0001g0096 | 2 | HG02109.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.887+817G>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881234 | ||||||
| chr3:195881240
|
G | A | 11 | a0001c0002t0001g0036a0001c0003t0002g0141a0001c0003t0002g0158others(8): Show | 11 | HG00140.hp2 HG00609.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.887+811C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881240 | ||||||
| chr3:195881241
|
A | G | 2 | a0003c0005t0001g0041a0003c0005t0001g0245 | 2 | HG00140.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.887+810T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881241 | ||||||
| chr3:195881242
|
T | C | 5 | a0001c0002t0001g0036a0002c0008t0002g0267a0003c0005t0001g0037others(2): Show | 5 | HG01099.hp2 HG01975.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.887+809A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881242 | ||||||
| chr3:195881251
|
G | A | 2 | a0002c0057t0004g0236a0006c0025t0001g0096 | 2 | HG02109.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.887+800C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881251 | ||||||
| chr3:195881251
|
GAGAGGAC others(45): Show |
G | 3 | a0001c0003t0001g0150a0001c0003t0005g0201a0002c0008t0002g0172 | 3 | HG00558.hp2 HG00609.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.887+748_887+799del others(52): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881251 | ||||||
| chr3:195881251
|
GAGAGGAC others(197): Show |
G | 8 | a0001c0003t0001g0122a0001c0003t0001g0138a0001c0003t0001g0195others(5): Show | 8 | HG00423.hp2 HG02056.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.887+596_887+799del | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881251 | ||||||
| chr3:195881261
|
A | G | 5 | a0001c0002t0001g0036a0002c0008t0002g0267a0003c0005t0001g0037others(2): Show | 5 | HG01099.hp2 HG01975.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.887+790T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881261 | ||||||
| chr3:195881263
|
T | C | 9 | a0001c0002t0001g0036a0001c0003t0005g0197a0002c0008t0002g0267others(6): Show | 9 | HG00140.hp2 HG01099.hp2 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.887+788A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881263 | ||||||
| chr3:195881263
|
T | G | 7 | a0002c0010t0001g0035a0002c0010t0001g0043a0002c0057t0004g0236others(4): Show | 7 | HG01074.hp1 HG01074.hp2 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.887+788A>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881263 | ||||||
| chr3:195881264
|
G | A | 16 | a0001c0002t0001g0036a0001c0003t0005g0197a0002c0008t0002g0267others(13): Show | 16 | HG00140.hp2 HG01074.hp1 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.887+787C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881264 | ||||||
| chr3:195881268
|
A | G | 7 | a0002c0010t0001g0035a0002c0010t0001g0043a0002c0057t0004g0236others(4): Show | 7 | HG01074.hp1 HG01074.hp2 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.887+783T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881268 | ||||||
| chr3:195881274
|
C | G | 9 | a0001c0002t0001g0036a0001c0003t0005g0197a0002c0008t0002g0267others(6): Show | 9 | HG00140.hp2 HG01099.hp2 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.887+777G>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881274 | ||||||
| chr3:195881281
|
CA | C | 10 | a0001c0002t0001g0036a0002c0008t0002g0267a0002c0010t0001g0035others(7): Show | 10 | HG01074.hp1 HG01074.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.887+769delT | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881281 | ||||||
| chr3:195881282
|
A | C | 3 | a0002c0018t0001g0159a0003c0005t0001g0041a0003c0005t0001g0245 | 3 | HG00140.hp2 HG01516.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.887+769T>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881282 | ||||||
| chr3:195881283
|
C | G | 2 | a0003c0005t0001g0041a0003c0005t0001g0245 | 2 | HG00140.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.887+768G>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881283 | ||||||
| chr3:195881286
|
G | C | 16 | a0001c0002t0001g0036a0001c0003t0005g0197a0002c0008t0002g0267others(13): Show | 16 | HG00140.hp2 HG01074.hp1 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.887+765C>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881286 | ||||||
| chr3:195881286
|
GCCAGCAA others(196): Show |
G | 1 | a0002c0004t0002g0332 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.887+562_887+764del | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881286 | ||||||
| chr3:195881292
|
A | G | 6 | a0001c0003t0005g0197a0003c0005t0001g0041a0003c0005t0001g0245others(3): Show | 6 | HG00140.hp2 HG01109.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.887+759T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881292 | ||||||
| chr3:195881293
|
A | G | 2 | a0002c0057t0004g0236a0006c0025t0001g0096 | 2 | HG02109.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.887+758T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881293 | ||||||
| chr3:195881294
|
T | C | 5 | a0002c0010t0001g0035a0002c0010t0001g0043a0003c0005t0001g0034others(2): Show | 5 | HG01074.hp1 HG01074.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.887+757A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881294 | ||||||
| chr3:195881303
|
A | G | 12 | a0002c0010t0001g0035a0002c0010t0001g0043a0002c0057t0004g0236others(9): Show | 12 | HG00140.hp2 HG01074.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.887+748T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881303 | ||||||
| chr3:195881313
|
A | G | 4 | a0001c0003t0002g0141a0001c0003t0005g0197a0002c0018t0001g0159others(1): Show | 4 | HG01978.hp1 HG02132.hp1 NA18941.hp1 others(1): Show |
intron_variant | MODIFIER | c.887+738T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881313 | ||||||
| chr3:195881315
|
G | C | 15 | a0001c0002t0001g0036a0001c0003t0002g0141a0001c0003t0005g0197others(12): Show | 15 | HG01074.hp1 HG01074.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.887+736C>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881315 | ||||||
| chr3:195881320
|
G | A | 15 | a0001c0002t0001g0036a0001c0003t0002g0141a0001c0003t0005g0197others(12): Show | 15 | HG01074.hp1 HG01074.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.887+731C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881320 | ||||||
| chr3:195881326
|
C | CTAACACC others(43): Show |
1 | a0001c0001t0002g0162 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.887+675_887+724dup others(50): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881326 | ||||||
| chr3:195881326
|
C | CTAACACC others(195): Show |
1 | a0001c0001t0001g0304 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.887+724_887+725ins others(202): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881326 | ||||||
| chr3:195881326
|
C | G | 15 | a0001c0002t0001g0036a0001c0003t0002g0141a0001c0003t0005g0197others(12): Show | 15 | HG01074.hp1 HG01074.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.887+725G>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881326 | ||||||
| chr3:195881326
|
CTAACACC others(43): Show |
C | 12 | a0001c0014t0004g0002a0001c0037t0004g0110a0004c0007t0001g0262others(9): Show | 13 | HG00597.hp1 HG01884.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.887+675_887+724del others(50): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881326 | ||||||
| chr3:195881331
|
A | AC | 15 | a0001c0003t0001g0150a0001c0003t0002g0141a0001c0003t0005g0201others(12): Show | 15 | HG00140.hp2 HG00558.hp2 HG00609.hp2 others(12): Show |
intron_variant | MODIFIER | c.887+719dupG | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881331 | ||||||
| chr3:195881331
|
A | ACCCGCCC others(97): Show |
5 | a0001c0002t0001g0036a0002c0008t0002g0267a0003c0005t0001g0037others(2): Show | 5 | HG01099.hp2 HG01975.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.887+719_887+720ins others(104): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881331 | ||||||
| chr3:195881337
|
C | T | 1 | a0001c0009t0002g0263 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.887+714G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881337 | ||||||
| chr3:195881342
|
A | G | 3 | a0001c0003t0002g0141a0001c0003t0005g0197a0002c0018t0001g0159 | 3 | HG02132.hp1 NA18941.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.887+709T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881342 | ||||||
| chr3:195881343
|
G | A | 14 | a0001c0003t0001g0150a0001c0003t0002g0141a0001c0003t0005g0197others(11): Show | 14 | HG00140.hp2 HG00558.hp2 HG00609.hp2 others(11): Show |
intron_variant | MODIFIER | c.887+708C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881343 | ||||||
| chr3:195881344
|
T | C | 8 | a0001c0003t0001g0150a0001c0003t0005g0201a0002c0008t0002g0172others(5): Show | 8 | HG00140.hp2 HG00558.hp2 HG00609.hp2 others(5): Show |
intron_variant | MODIFIER | c.887+707A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881344 | ||||||
| chr3:195881346
|
C | A | 1 | a0001c0009t0002g0263 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.887+705G>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881346 | ||||||
| chr3:195881351
|
T | C | 1 | a0001c0009t0002g0263 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.887+700A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881351 | ||||||
| chr3:195881353
|
G | A | 6 | a0001c0003t0001g0150a0001c0003t0002g0141a0001c0003t0005g0201others(3): Show | 6 | HG00558.hp2 HG00609.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.887+698C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881353 | ||||||
| chr3:195881363
|
A | G | 9 | a0001c0003t0001g0150a0001c0003t0005g0201a0002c0008t0002g0172others(6): Show | 9 | HG00140.hp2 HG00558.hp2 HG00609.hp2 others(6): Show |
intron_variant | MODIFIER | c.887+688T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881363 | ||||||
| chr3:195881366
|
A | G | 1 | a0006c0025t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.887+685T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881366 | ||||||
| chr3:195881374
|
C | T | 3 | a0001c0003t0002g0141a0001c0003t0002g0158a0001c0003t0005g0197 | 3 | HG00609.hp1 HG02132.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.887+677G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881374 | ||||||
| chr3:195881376
|
GTAACACC others(95): Show |
G | 1 | a0003c0015t0001g0084 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.887+573_887+674del | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881376 | ||||||
| chr3:195881381
|
A | AC | 17 | a0001c0002t0001g0036a0001c0003t0001g0150a0001c0003t0002g0141others(14): Show | 17 | HG00558.hp2 HG00609.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.887+669dupG | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881381 | ||||||
| chr3:195881383
|
C | A | 1 | a0002c0026t0001g0074 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.887+668G>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881383 | ||||||
| chr3:195881392
|
A | G | 9 | a0001c0003t0001g0150a0001c0003t0001g0171a0001c0003t0003g0126others(6): Show | 9 | HG00423.hp1 HG00558.hp2 HG00609.hp2 others(6): Show |
intron_variant | MODIFIER | c.887+659T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881392 | ||||||
| chr3:195881393
|
G | A | 26 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(23): Show | 26 | HG00140.hp2 HG00423.hp1 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.887+658C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881393 | ||||||
| chr3:195881393
|
G | GTGCCCCT others(95): Show |
1 | a0004c0007t0001g0302 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.887+657_887+658ins others(102): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881393 | ||||||
| chr3:195881393
|
G | GTGCCCCT others(146): Show |
1 | a0003c0005t0001g0042 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.887+657_887+658ins others(153): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881393 | ||||||
| chr3:195881393
|
GTGCCCCT others(45): Show |
G | 1 | a0001c0001t0001g0343 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.887+606_887+657del others(52): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881393 | ||||||
| chr3:195881394
|
T | C | 1 | a0001c0002t0001g0217 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.887+657A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881394 | ||||||
| chr3:195881403
|
G | A | 3 | a0001c0003t0005g0197a0002c0008t0002g0172a0010c0059t0001g0021 | 3 | HG01109.hp1 HG01109.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.887+648C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881403 | ||||||
| chr3:195881413
|
A | AGGATCTG others(44): Show |
1 | a0001c0003t0003g0126 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.887+637_887+638ins others(51): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881413 | ||||||
| chr3:195881413
|
A | G | 3 | a0001c0002t0001g0217a0001c0003t0005g0197a0006c0025t0001g0096 | 3 | HG02109.hp1 HG02132.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.887+638T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881413 | ||||||
| chr3:195881415
|
C | G | 1 | a0004c0007t0001g0260 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.887+636G>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881415 | ||||||
| chr3:195881415
|
C | T | 3 | a0001c0003t0001g0171a0001c0003t0002g0141a0001c0003t0002g0158 | 3 | HG00609.hp1 HG03017.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.887+636G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881415 | ||||||
| chr3:195881416
|
A | G | 12 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(9): Show | 12 | HG00609.hp1 HG01975.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.887+635T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881416 | ||||||
| chr3:195881418
|
C | T | 1 | a0002c0018t0001g0159 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.887+633G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881418 | ||||||
| chr3:195881420
|
A | G | 1 | a0004c0007t0001g0260 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.887+631T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881420 | ||||||
| chr3:195881426
|
G | A | 1 | a0002c0018t0001g0159 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.887+625C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881426 | ||||||
| chr3:195881426
|
G | C | 3 | a0001c0003t0002g0141a0001c0003t0002g0158a0004c0007t0001g0260 | 3 | HG00423.hp1 HG00609.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.887+625C>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881426 | ||||||
| chr3:195881431
|
ACCCGCCC others(97): Show |
A | 1 | a0003c0054t0001g0134 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.887+516_887+619del | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881431 | ||||||
| chr3:195881434
|
C | A | 1 | a0001c0003t0002g0158 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.887+617G>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881434 | ||||||
| chr3:195881434
|
CG | C | 8 | a0001c0002t0001g0217a0001c0003t0001g0171a0001c0003t0002g0141others(5): Show | 8 | HG00423.hp1 HG01496.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.887+616delC | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881434 | ||||||
| chr3:195881435
|
G | C | 5 | a0001c0003t0002g0158a0001c0019t0003g0132a0001c0019t0003g0133others(2): Show | 5 | HG00609.hp1 NA18941.hp1 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.887+616C>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881435 | ||||||
| chr3:195881438
|
C | G | 1 | a0001c0003t0002g0158 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.887+613G>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881438 | ||||||
| chr3:195881444
|
G | A | 8 | a0001c0002t0001g0217a0001c0003t0001g0171a0001c0003t0002g0141others(5): Show | 8 | HG00423.hp1 HG00609.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.887+607C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881444 | ||||||
| chr3:195881446
|
T | C | 3 | a0001c0003t0001g0171a0001c0040t0001g0019a0004c0007t0001g0260 | 3 | HG00423.hp1 HG00673.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.887+605A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881446 | ||||||
| chr3:195881455
|
G | A | 8 | a0001c0002t0001g0217a0001c0003t0001g0150a0001c0003t0002g0141others(5): Show | 8 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(5): Show |
intron_variant | MODIFIER | c.887+596C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881455 | ||||||
| chr3:195881455
|
GAGAGGAC others(95): Show |
G | 9 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(6): Show | 9 | HG01975.hp2 HG02572.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.887+494_887+595del | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881455 | ||||||
| chr3:195881465
|
A | G | 6 | a0001c0003t0001g0150a0001c0003t0001g0171a0001c0003t0002g0141others(3): Show | 6 | HG00423.hp1 HG00558.hp2 HG00609.hp2 others(3): Show |
intron_variant | MODIFIER | c.887+586T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881465 | ||||||
| chr3:195881465
|
AGGATCTG others(44): Show |
A | 1 | a0002c0008t0002g0172 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.887+535_887+585del others(51): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881465 | ||||||
| chr3:195881467
|
G | C | 12 | a0001c0002t0001g0217a0001c0003t0001g0150a0001c0003t0001g0171others(9): Show | 12 | HG00423.hp1 HG00558.hp2 HG00609.hp2 others(9): Show |
intron_variant | MODIFIER | c.887+584C>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881467 | ||||||
| chr3:195881472
|
G | A | 12 | a0001c0002t0001g0217a0001c0003t0001g0150a0001c0003t0001g0171others(9): Show | 12 | HG00423.hp1 HG00558.hp2 HG00609.hp2 others(9): Show |
intron_variant | MODIFIER | c.887+579C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881472 | ||||||
| chr3:195881476
|
C | T | 3 | a0001c0002t0001g0217a0006c0025t0001g0096a0010c0059t0001g0021 | 3 | HG01109.hp1 HG02109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.887+575G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881476 | ||||||
| chr3:195881478
|
C | CTAACACC others(95): Show |
1 | a0001c0001t0002g0305 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.887+572_887+573ins others(102): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881478 | ||||||
| chr3:195881478
|
C | G | 12 | a0001c0002t0001g0217a0001c0003t0001g0150a0001c0003t0001g0171others(9): Show | 12 | HG00423.hp1 HG00558.hp2 HG00609.hp2 others(9): Show |
intron_variant | MODIFIER | c.887+573G>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881478 | ||||||
| chr3:195881495
|
A | G | 7 | a0001c0003t0001g0150a0001c0003t0001g0171a0001c0003t0003g0126others(4): Show | 7 | HG00558.hp2 HG00609.hp2 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.887+556T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881495 | ||||||
| chr3:195881496
|
A | G | 1 | a0001c0003t0002g0158 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.887+555T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881496 | ||||||
| chr3:195881497
|
C | CGCCCCTT others(44): Show |
2 | a0001c0003t0001g0148a0005c0056t0002g0040 | 2 | NA18975.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.887+553_887+554ins others(51): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881497 | ||||||
| chr3:195881497
|
C | T | 11 | a0001c0003t0001g0150a0001c0003t0001g0171a0001c0003t0002g0158others(8): Show | 11 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(8): Show |
intron_variant | MODIFIER | c.887+554G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881497 | ||||||
| chr3:195881502
|
C | T | 2 | a0001c0002t0001g0217a0006c0025t0001g0096 | 2 | HG02109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.887+549G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881502 | ||||||
| chr3:195881506
|
G | A | 43 | a0001c0003t0001g0122a0001c0003t0001g0138a0001c0003t0001g0149others(40): Show | 43 | HG00423.hp1 HG00423.hp2 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.887+545C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881506 | ||||||
| chr3:195881506
|
GAGAGGAC others(44): Show |
G | 1 | a0004c0032t0001g0303 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.887+494_887+544del others(51): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881506 | ||||||
| chr3:195881516
|
G | A | 20 | a0001c0002t0001g0036a0001c0002t0001g0217a0001c0003t0001g0148others(17): Show | 20 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(17): Show |
intron_variant | MODIFIER | c.887+535C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881516 | ||||||
| chr3:195881516
|
GGCATCTA others(44): Show |
G | 4 | a0001c0009t0002g0266a0001c0009t0002g0330a0001c0009t0002g0331others(1): Show | 4 | HG01109.hp1 NA18989.hp2 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.887+484_887+534del others(51): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881516 | ||||||
| chr3:195881521
|
C | T | 1 | a0002c0018t0001g0159 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.887+530G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881521 | ||||||
| chr3:195881524
|
T | A | 1 | a0001c0009t0002g0263 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.887+527A>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881524 | ||||||
| chr3:195881527
|
C | T | 1 | a0001c0003t0001g0150 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.887+524G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881527 | ||||||
| chr3:195881529
|
G | A | 1 | a0002c0018t0001g0159 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.887+522C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881529 | ||||||
| chr3:195881534
|
AC | A | 10 | a0001c0003t0001g0148a0001c0003t0001g0171a0001c0003t0002g0158others(7): Show | 10 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(7): Show |
intron_variant | MODIFIER | c.887+516delG | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881534 | ||||||
| chr3:195881535
|
C | CCCCCCCC others(43): Show |
1 | a0001c0003t0001g0149 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.887+515_887+516ins others(50): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881535 | ||||||
| chr3:195881535
|
CCCCCCCC others(43): Show |
C | 4 | a0001c0006t0001g0098a0001c0006t0001g0100a0002c0026t0001g0074others(1): Show | 4 | HG02622.hp2 HG02818.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.887+466_887+515del others(50): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881535 | ||||||
| chr3:195881546
|
A | AATGCCCC others(43): Show |
1 | a0001c0001t0001g0254 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.887+455_887+504dup others(50): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881546 | ||||||
| chr3:195881546
|
A | G | 46 | a0001c0003t0001g0122a0001c0003t0001g0138a0001c0003t0001g0148others(43): Show | 46 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.887+505T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881546 | ||||||
| chr3:195881547
|
A | G | 1 | a0001c0003t0002g0158 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.887+504T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881547 | ||||||
| chr3:195881552
|
CCTTGAAG others(97): Show |
C | 1 | a0001c0003t0001g0168 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.887+395_887+498del | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881552 | ||||||
| chr3:195881553
|
C | T | 1 | a0006c0025t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.887+498G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881553 | ||||||
| chr3:195881557
|
A | G | 40 | a0001c0003t0001g0122a0001c0003t0001g0138a0001c0003t0001g0148others(37): Show | 40 | HG00423.hp2 HG00609.hp1 HG02056.hp2 others(37): Show |
intron_variant | MODIFIER | c.887+494T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881557 | ||||||
| chr3:195881567
|
A | G | 12 | a0001c0001t0002g0264a0001c0001t0002g0340a0001c0003t0001g0149others(9): Show | 12 | HG00558.hp2 HG00609.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.887+484T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881567 | ||||||
| chr3:195881578
|
C | T | 6 | a0001c0003t0001g0155a0001c0003t0001g0156a0001c0003t0001g0160others(3): Show | 6 | HG00423.hp1 HG02132.hp1 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.887+473G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881578 | ||||||
| chr3:195881580
|
GTAACACC others(96): Show |
G | 4 | a0001c0003t0001g0155a0001c0003t0001g0156a0001c0003t0001g0160others(1): Show | 4 | NA18959.hp1 NA18984.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.887+368_887+470del | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881580 | ||||||
| chr3:195881585
|
A | AC | 54 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(51): Show | 54 | HG00558.hp2 HG00609.hp2 HG01175.hp1 others(51): Show |
intron_variant | MODIFIER | c.887+465dupG | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881585 | ||||||
| chr3:195881585
|
A | ACCCCCCC others(44): Show |
1 | a0001c0002t0001g0221 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.887+465_887+466ins others(51): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881585 | ||||||
| chr3:195881585
|
A | ACCCGCCC others(302): Show |
1 | a0022c0055t0003g0153 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.887+465_887+466ins others(309): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881585 | ||||||
| chr3:195881590
|
C | CCCCAGCG others(46): Show |
1 | a0001c0002t0001g0180 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.887+460_887+461ins others(53): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881590 | ||||||
| chr3:195881596
|
G | A | 3 | a0001c0002t0001g0180a0001c0009t0002g0263a0004c0007t0001g0260 | 3 | HG00423.hp1 NA19058.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.887+455C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881596 | ||||||
| chr3:195881598
|
T | C | 1 | a0004c0007t0001g0260 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.887+453A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881598 | ||||||
| chr3:195881598
|
T | TGCCCCTT others(44): Show |
1 | a0001c0003t0002g0158 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.887+452_887+453ins others(51): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881598 | ||||||
| chr3:195881601
|
C | A | 1 | a0001c0002t0001g0217 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.887+450G>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881601 | ||||||
| chr3:195881603
|
C | T | 1 | a0004c0007t0001g0260 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.887+448G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881603 | ||||||
| chr3:195881603
|
CTTGAAGA others(46): Show |
C | 1 | a0001c0003t0001g0150 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.887+395_887+447del others(53): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881603 | ||||||
| chr3:195881607
|
A | G | 13 | a0001c0003t0001g0148a0001c0003t0001g0149a0001c0003t0001g0171others(10): Show | 13 | HG00423.hp1 HG00558.hp2 HG03017.hp1 others(10): Show |
intron_variant | MODIFIER | c.887+444T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881607 | ||||||
| chr3:195881617
|
A | G | 29 | a0001c0003t0001g0122a0001c0003t0001g0138a0001c0003t0001g0166others(26): Show | 29 | HG00423.hp2 HG01496.hp2 HG02056.hp2 others(26): Show |
intron_variant | MODIFIER | c.887+434T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881617 | ||||||
| chr3:195881628
|
T | C | 37 | a0001c0003t0001g0122a0001c0003t0001g0138a0001c0003t0001g0148others(34): Show | 37 | HG00423.hp1 HG00423.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.887+423A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881628 | ||||||
| chr3:195881630
|
GTAACACC others(46): Show |
G | 4 | a0001c0003t0001g0171a0001c0003t0001g0200a0001c0003t0002g0151others(1): Show | 4 | HG00558.hp2 HG02165.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.887+368_887+420del others(53): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881630 | ||||||
| chr3:195881635
|
AC | A | 136 | a0001c0001t0001g0001a0001c0001t0001g0076a0001c0001t0001g0095others(133): Show | 140 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(137): Show |
intron_variant | MODIFIER | c.887+415delG | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881635 | ||||||
| chr3:195881635
|
ACC | A | 31 | a0001c0002t0001g0178a0001c0002t0001g0235a0001c0003t0001g0122others(28): Show | 31 | HG00423.hp2 HG00609.hp1 HG01192.hp2 others(28): Show |
intron_variant | MODIFIER | c.887+414_887+415del others(2): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881635 | ||||||
| chr3:195881637
|
C | CCCCCCCA others(144): Show |
1 | a0001c0003t0003g0125 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.887+413_887+414ins others(151): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881637 | ||||||
| chr3:195881637
|
C | CCCCCCCA others(195): Show |
1 | a0001c0003t0003g0124 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.887+413_887+414ins others(202): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881637 | ||||||
| chr3:195881638
|
CCCCCCCC others(99): Show |
C | 1 | a0001c0009t0002g0263 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.887+307_887+412del | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881638 | ||||||
| chr3:195881640
|
C | A | 1 | a0001c0002t0001g0011 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.887+411G>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881640 | ||||||
| chr3:195881641
|
CCCCCAGC others(48): Show |
C | 1 | a0001c0053t0003g0129 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.887+355_887+409del others(55): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881641 | ||||||
| chr3:195881643
|
C | A | 1 | a0001c0002t0001g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.887+408G>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881643 | ||||||
| chr3:195881643
|
C | G | 2 | a0001c0002t0001g0180a0005c0056t0002g0040 | 2 | NA18975.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.887+408G>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881643 | ||||||
| chr3:195881649
|
A | G | 31 | a0001c0003t0001g0122a0001c0003t0001g0138a0001c0003t0001g0148others(28): Show | 31 | HG00423.hp2 HG00609.hp1 HG01496.hp2 others(28): Show |
intron_variant | MODIFIER | c.887+402T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881649 | ||||||
| chr3:195881651
|
C | T | 33 | a0001c0003t0001g0122a0001c0003t0001g0138a0001c0003t0001g0148others(30): Show | 33 | HG00423.hp2 HG00609.hp1 HG01496.hp2 others(30): Show |
intron_variant | MODIFIER | c.887+400G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881651 | ||||||
| chr3:195881656
|
T | C | 33 | a0001c0003t0001g0122a0001c0003t0001g0138a0001c0003t0001g0148others(30): Show | 33 | HG00423.hp2 HG00609.hp1 HG01496.hp2 others(30): Show |
intron_variant | MODIFIER | c.887+395A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881656 | ||||||
| chr3:195881656
|
T | TTTGGAGA others(97): Show |
1 | a0027c0049t0001g0022 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.887+291_887+394dup others(104): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881656 | ||||||
| chr3:195881659
|
G | A | 1 | a0016c0051t0001g0208 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.887+392C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881659 | ||||||
| chr3:195881660
|
G | A | 1 | a0022c0055t0003g0153 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.887+391C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881660 | ||||||
| chr3:195881670
|
A | G | 1 | a0022c0055t0003g0153 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.887+381T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881670 | ||||||
| chr3:195881672
|
C | G | 2 | a0001c0003t0003g0137a0002c0018t0003g0152 | 2 | NA18973.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.887+379G>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881672 | ||||||
| chr3:195881675
|
T | C | 43 | a0001c0002t0001g0183a0001c0002t0001g0184a0001c0002t0001g0186others(40): Show | 43 | HG00423.hp2 HG00609.hp1 HG01496.hp2 others(40): Show |
intron_variant | MODIFIER | c.887+376A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881675 | ||||||
| chr3:195881681
|
C | T | 36 | a0001c0003t0001g0122a0001c0003t0001g0138a0001c0003t0001g0148others(33): Show | 36 | HG00423.hp2 HG00609.hp1 HG01496.hp2 others(33): Show |
intron_variant | MODIFIER | c.887+370G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881681 | ||||||
| chr3:195881683
|
A | G | 36 | a0001c0003t0001g0122a0001c0003t0001g0138a0001c0003t0001g0148others(33): Show | 36 | HG00423.hp2 HG00609.hp1 HG01496.hp2 others(33): Show |
intron_variant | MODIFIER | c.887+368T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881683 | ||||||
| chr3:195881712
|
G | A | 1 | a0001c0053t0003g0129 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.887+339C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881712 | ||||||
| chr3:195881723
|
A | G | 1 | a0001c0001t0001g0290 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.887+328T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881723 | ||||||
| chr3:195881725
|
G | C | 1 | a0001c0003t0001g0160 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.887+326C>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881725 | ||||||
| chr3:195881787
|
G | C | 1 | a0001c0001t0001g0112 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.887+264C>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195881787 | ||||||
| chr3:195882031
|
T | C | 2 | a0001c0002t0001g0045a0002c0041t0001g0026 | 2 | HG00621.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.887+20A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 6/15 | chr3 | 195882031 | ||||||
| chr3:195882511
|
A | G | 1 | a0002c0008t0001g0204 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.610-183T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 5/15 | chr3 | 195882511 | ||||||
| chr3:195882686
|
C | T | 1 | a0023c0052t0005g0198 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.610-358G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 5/15 | chr3 | 195882686 | ||||||
| chr3:195882773
|
G | A | 1 | a0003c0015t0001g0020 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.609+384C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 5/15 | chr3 | 195882773 | ||||||
| chr3:195882851
|
C | T | 2 | a0001c0001t0001g0355a0001c0001t0001g0356 | 2 | HG03491.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.609+306G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 5/15 | chr3 | 195882851 | ||||||
| chr3:195882867
|
A | G | 1 | a0001c0009t0002g0266 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.609+290T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 5/15 | chr3 | 195882867 | ||||||
| chr3:195882868
|
G | A | 1 | a0001c0009t0002g0266 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.609+289C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 5/15 | chr3 | 195882868 | ||||||
| chr3:195882937
|
A | G | 39 | a0001c0001t0001g0246a0001c0001t0001g0339a0001c0002t0001g0011others(36): Show | 39 | HG01175.hp1 HG01192.hp2 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.609+220T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 5/15 | chr3 | 195882937 | ||||||
| chr3:195882960
|
G | A | 5 | a0001c0058t0004g0237a0001c0061t0001g0238a0001c0062t0001g0239others(2): Show | 5 | HG02922.hp2 HG03130.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.609+197C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 5/15 | chr3 | 195882960 | ||||||
| chr3:195882971
|
G | A | 1 | a0001c0003t0005g0201 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.609+186C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 5/15 | chr3 | 195882971 | ||||||
| chr3:195883041
|
G | A | 1 | a0001c0001t0001g0337 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.609+116C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 5/15 | chr3 | 195883041 | ||||||
| chr3:195883550
|
G | A | 1 | a0001c0002t0001g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.457-241C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 4/15 | chr3 | 195883550 | ||||||
| chr3:195883592
|
T | C | 3 | a0001c0003t0001g0122a0001c0006t0001g0097a0001c0040t0001g0019 | 3 | HG00673.hp2 HG02523.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.457-283A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 4/15 | chr3 | 195883592 | ||||||
| chr3:195883622
|
AT | A | 10 | a0001c0001t0001g0106a0001c0001t0001g0356a0001c0001t0002g0329others(7): Show | 10 | HG01167.hp2 HG01255.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.457-314delA | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 4/15 | chr3 | 195883622 | ||||||
| chr3:195883675
|
C | T | 5 | a0001c0002t0001g0011a0002c0008t0001g0010a0002c0023t0001g0017others(2): Show | 5 | HG02647.hp1 HG02723.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.457-366G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 4/15 | chr3 | 195883675 | ||||||
| chr3:195883707
|
C | T | 3 | a0001c0002t0001g0049a0001c0024t0001g0189a0001c0024t0001g0190 | 3 | HG01099.hp1 HG02698.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.457-398G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 4/15 | chr3 | 195883707 | ||||||
| chr3:195883862
|
G | A | 12 | a0001c0002t0001g0011a0001c0002t0001g0018a0001c0014t0004g0093others(9): Show | 12 | HG02280.hp1 HG02486.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.457-553C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 4/15 | chr3 | 195883862 | ||||||
| chr3:195883872
|
A | G | 59 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(56): Show | 59 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.457-563T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 4/15 | chr3 | 195883872 | ||||||
| chr3:195883921
|
CACAGCGG others(28): Show |
C | 1 | a0002c0060t0001g0240 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.457-647_457-613del others(35): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 4/15 | chr3 | 195883921 | ||||||
| chr3:195883971
|
G | A | 1 | a0007c0021t0001g0118 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.457-662C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 4/15 | chr3 | 195883971 | ||||||
| chr3:195883984
|
A | G | 1 | a0007c0021t0001g0115 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.457-675T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 4/15 | chr3 | 195883984 | ||||||
| chr3:195884001
|
T | C | 2 | a0001c0006t0001g0097a0001c0040t0001g0019 | 2 | HG00673.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.457-692A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 4/15 | chr3 | 195884001 | ||||||
| chr3:195884036
|
C | T | 1 | a0001c0001t0001g0336 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.457-727G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 4/15 | chr3 | 195884036 | ||||||
| chr3:195884144
|
G | A | 1 | a0001c0001t0002g0334 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.456+668C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 4/15 | chr3 | 195884144 | ||||||
| chr3:195884369
|
G | A | 47 | a0001c0002t0001g0029a0001c0002t0001g0031a0001c0002t0001g0036others(44): Show | 48 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.456+443C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 4/15 | chr3 | 195884369 | ||||||
| chr3:195884423
|
A | G | 1 | a0001c0001t0002g0007 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.456+389T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 4/15 | chr3 | 195884423 | ||||||
| chr3:195884767
|
C | T | 1 | a0001c0001t0001g0288 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.456+45G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 4/15 | chr3 | 195884767 | ||||||
| chr3:195885163
|
T | C | 227 | a0001c0001t0001g0001a0001c0001t0001g0076a0001c0001t0001g0095others(224): Show | 231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.235-130A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 3/15 | chr3 | 195885163 | ||||||
| chr3:195885177
|
T | A | 1 | a0001c0001t0001g0076 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.235-144A>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 3/15 | chr3 | 195885177 | ||||||
| chr3:195885213
|
C | T | 1 | a0002c0074t0001g0073 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.235-180G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 3/15 | chr3 | 195885213 | ||||||
| chr3:195885390
|
A | AC | 23 | a0001c0001t0001g0103a0001c0001t0001g0288a0001c0001t0001g0304others(20): Show | 23 | HG00621.hp2 HG00673.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.235-358dupG | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 3/15 | chr3 | 195885390 | ||||||
| chr3:195885493
|
A | C | 1 | a0001c0001t0001g0103 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.235-460T>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 3/15 | chr3 | 195885493 | ||||||
| chr3:195885589
|
T | C | 2 | a0001c0006t0001g0087a0024c0077t0001g0086 | 2 | HG02602.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.235-556A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 3/15 | chr3 | 195885589 | ||||||
| chr3:195885862
|
C | T | 1 | a0010c0059t0001g0021 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.235-829G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 3/15 | chr3 | 195885862 | ||||||
| chr3:195885897
|
C | A | 1 | a0016c0051t0001g0208 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.235-864G>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 3/15 | chr3 | 195885897 | ||||||
| chr3:195886067
|
A | G | 6 | a0001c0002t0001g0018a0001c0017t0006g0012a0001c0017t0006g0013others(3): Show | 6 | HG02486.hp2 HG02630.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.234+910T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 3/15 | chr3 | 195886067 | ||||||
| chr3:195886149
|
C | G | 24 | a0001c0001t0001g0001a0001c0001t0002g0062a0001c0002t0001g0003others(21): Show | 27 | HG01192.hp1 HG01934.hp1 HG02145.hp2 others(24): Show |
intron_variant | MODIFIER | c.234+828G>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 3/15 | chr3 | 195886149 | ||||||
| chr3:195886201
|
G | A | 1 | a0001c0002t0001g0228 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.234+776C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 3/15 | chr3 | 195886201 | ||||||
| chr3:195886227
|
C | T | 1 | a0010c0059t0001g0021 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.234+750G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 3/15 | chr3 | 195886227 | ||||||
| chr3:195886397
|
C | A | 10 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(7): Show | 10 | HG01975.hp2 HG02109.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.234+580G>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 3/15 | chr3 | 195886397 | ||||||
| chr3:195886397
|
C | T | 2 | a0001c0001t0001g0268a0002c0004t0001g0279 | 2 | HG01358.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.234+580G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 3/15 | chr3 | 195886397 | ||||||
| chr3:195886740
|
G | C | 3 | a0001c0002t0001g0202a0001c0002t0001g0203a0002c0008t0001g0204 | 3 | NA18940.hp2 NA18948.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.234+237C>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 3/15 | chr3 | 195886740 | ||||||
| chr3:195886869
|
G | A | 2 | a0001c0061t0001g0238a0001c0062t0001g0239 | 2 | HG02922.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.234+108C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 3/15 | chr3 | 195886869 | ||||||
| chr3:195886946
|
C | T | 2 | a0001c0001t0002g0264a0001c0001t0002g0340 | 2 | NA19007.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.234+31G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 3/15 | chr3 | 195886946 | ||||||
| chr3:195887107
|
T | C | 18 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(15): Show | 19 | HG01884.hp1 HG01891.hp2 HG01975.hp2 others(16): Show |
intron_variant | MODIFIER | c.164-60A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/15 | chr3 | 195887107 | ||||||
| chr3:195887205
|
G | A | 1 | a0001c0001t0002g0162 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.164-158C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/15 | chr3 | 195887205 | ||||||
| chr3:195887278
|
G | A | 1 | a0001c0003t0001g0148 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.164-231C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/15 | chr3 | 195887278 | ||||||
| chr3:195887439
|
C | CTACCTAT others(91): Show |
4 | a0001c0001t0001g0317a0001c0001t0001g0337a0001c0013t0001g0277others(1): Show | 4 | NA18951.hp1 NA18952.hp2 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-490_164-393dup others(98): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/15 | chr3 | 195887439 | ||||||
| chr3:195887484
|
G | A | 1 | a0001c0002t0001g0184 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.164-437C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/15 | chr3 | 195887484 | ||||||
| chr3:195887484
|
G | GTTATTAC others(42): Show |
17 | a0001c0002t0001g0130a0001c0002t0001g0179a0001c0002t0001g0181others(14): Show | 17 | HG01175.hp1 HG01243.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.164-486_164-438dup others(49): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/15 | chr3 | 195887484 | ||||||
| chr3:195887484
|
GTTATTAC others(42): Show |
G | 1 | a0010c0059t0001g0021 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.164-486_164-438del others(49): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/15 | chr3 | 195887484 | ||||||
| chr3:195887496
|
T | C | 1 | a0001c0014t0004g0093 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.164-449A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/15 | chr3 | 195887496 | ||||||
| chr3:195887582
|
A | G | 7 | a0001c0001t0001g0095a0001c0006t0001g0077a0001c0011t0001g0107others(4): Show | 7 | HG01884.hp2 HG02451.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.164-535T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/15 | chr3 | 195887582 | ||||||
| chr3:195887615
|
C | A | 1 | a0011c0078t0001g0272 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.164-568G>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/15 | chr3 | 195887615 | ||||||
| chr3:195887657
|
T | C | 72 | a0001c0001t0001g0006a0001c0001t0001g0056a0001c0001t0001g0244others(69): Show | 73 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.164-610A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/15 | chr3 | 195887657 | ||||||
| chr3:195887738
|
CGT | C | 16 | a0001c0002t0001g0011a0001c0002t0001g0018a0001c0002t0001g0049others(13): Show | 16 | HG01099.hp1 HG01109.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.163+686_163+687del others(2): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/15 | chr3 | 195887738 | ||||||
| chr3:195887746
|
T | C | 1 | a0001c0014t0004g0093 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.163+680A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/15 | chr3 | 195887746 | ||||||
| chr3:195887747
|
G | T | 4 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0351others(1): Show | 4 | HG00639.hp2 HG02258.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.163+679C>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/15 | chr3 | 195887747 | ||||||
| chr3:195887754
|
C | T | 1 | a0001c0001t0007g0232 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.163+672G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/15 | chr3 | 195887754 | ||||||
| chr3:195887762
|
CACGTGTG others(5): Show |
C | 2 | a0001c0024t0001g0189a0001c0024t0001g0190 | 2 | HG01099.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.163+652_163+663del others(12): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/15 | chr3 | 195887762 | ||||||
| chr3:195887766
|
T | C | 26 | a0001c0002t0001g0130a0001c0002t0001g0174a0001c0002t0001g0175others(23): Show | 26 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.163+660A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/15 | chr3 | 195887766 | ||||||
| chr3:195887776
|
T | TGC | 3 | a0001c0001t0001g0364a0001c0002t0001g0180a0002c0023t0001g0207 | 3 | HG01175.hp1 HG03041.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.163+648_163+649dup others(2): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/15 | chr3 | 195887776 | ||||||
| chr3:195887782
|
C | CGT | 122 | a0001c0001t0001g0001a0001c0001t0001g0076a0001c0001t0001g0103others(119): Show | 126 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(123): Show |
intron_variant | MODIFIER | c.163+642_163+643dup others(2): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/15 | chr3 | 195887782 | ||||||
| chr3:195887792
|
C | T | 1 | a0001c0002t0001g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.163+634G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/15 | chr3 | 195887792 | ||||||
| chr3:195887804
|
C | G | 26 | a0001c0002t0001g0130a0001c0002t0001g0174a0001c0002t0001g0175others(23): Show | 26 | HG01109.hp1 HG01175.hp1 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.163+622G>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/15 | chr3 | 195887804 | ||||||
| chr3:195887804
|
C | T | 1 | a0001c0001t0002g0062 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.163+622G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/15 | chr3 | 195887804 | ||||||
| chr3:195887830
|
A | G | 2 | a0001c0003t0001g0150a0001c0003t0001g0195 | 2 | HG00609.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.163+596T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/15 | chr3 | 195887830 | ||||||
| chr3:195887835
|
CGT | C | 101 | a0001c0001t0001g0076a0001c0001t0001g0103a0001c0001t0001g0104others(98): Show | 104 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.163+589_163+590del others(2): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/15 | chr3 | 195887835 | ||||||
| chr3:195887835
|
CGTGT | C | 7 | a0001c0002t0001g0018a0001c0017t0006g0012a0001c0017t0006g0013others(4): Show | 7 | HG02486.hp2 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.163+587_163+590del others(4): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/15 | chr3 | 195887835 | ||||||
| chr3:195887845
|
TGTGTGC | T | 43 | a0001c0002t0001g0029a0001c0002t0001g0031a0001c0002t0001g0036others(40): Show | 43 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.163+575_163+580del others(6): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/15 | chr3 | 195887845 | ||||||
| chr3:195887849
|
T | C | 3 | a0001c0001t0001g0311a0001c0003t0001g0122a0001c0014t0004g0093 | 3 | HG02280.hp1 HG02523.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.163+577A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/15 | chr3 | 195887849 | ||||||
| chr3:195887853
|
T | C | 44 | a0001c0002t0001g0029a0001c0002t0001g0031a0001c0002t0001g0036others(41): Show | 44 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.163+573A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/15 | chr3 | 195887853 | ||||||
| chr3:195887887
|
C | CGCACGTG others(11): Show |
2 | a0001c0002t0001g0205a0002c0023t0001g0207 | 2 | HG01175.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.163+538_163+539ins others(18): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/15 | chr3 | 195887887 | ||||||
| chr3:195887887
|
C | CGCACGTG others(11): Show |
23 | a0001c0002t0001g0130a0001c0002t0001g0174a0001c0002t0001g0175others(20): Show | 23 | HG01109.hp1 HG01192.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.163+521_163+538dup others(18): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/15 | chr3 | 195887887 | ||||||
| chr3:195887887
|
C | CGCACGTG others(29): Show |
1 | a0001c0003t0001g0122 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.163+538_163+539ins others(36): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/15 | chr3 | 195887887 | ||||||
| chr3:195887887
|
CGCACGTG others(11): Show |
C | 28 | a0001c0001t0002g0264a0001c0001t0002g0340a0001c0002t0001g0003others(25): Show | 31 | HG01192.hp1 HG01884.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.163+521_163+538del others(18): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/15 | chr3 | 195887887 | ||||||
| chr3:195887898
|
GCGTGTGT others(21): Show |
G | 2 | a0014c0063t0002g0247a0015c0064t0001g0347 | 2 | HG04199.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.163+500_163+527del others(28): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/15 | chr3 | 195887898 | ||||||
| chr3:195887903
|
T | TGTGCACG others(11): Show |
1 | a0001c0001t0007g0232 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.163+505_163+522dup others(18): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/15 | chr3 | 195887903 | ||||||
| chr3:195887908
|
A | ACGTGCAT others(21): Show |
4 | a0001c0001t0001g0274a0001c0001t0002g0273a0001c0001t0008g0269others(1): Show | 4 | NA18948.hp1 NA18990.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.163+517_163+518ins others(28): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/15 | chr3 | 195887908 | ||||||
| chr3:195887914
|
A | G | 4 | a0001c0014t0004g0002a0001c0014t0004g0109a0001c0037t0004g0110others(1): Show | 5 | HG01884.hp1 HG01891.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.163+512T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/15 | chr3 | 195887914 | ||||||
| chr3:195887919
|
T | G | 1 | a0001c0014t0004g0093 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.163+507A>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/15 | chr3 | 195887919 | ||||||
| chr3:195887928
|
GTGTGTGC others(3): Show |
G | 1 | a0001c0003t0001g0122 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.163+488_163+497del others(10): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/15 | chr3 | 195887928 | ||||||
| chr3:195887931
|
T | C | 4 | a0001c0014t0004g0002a0001c0014t0004g0109a0001c0037t0004g0110others(1): Show | 5 | HG01884.hp1 HG01891.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.163+495A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/15 | chr3 | 195887931 | ||||||
| chr3:195887938
|
ATGTGCGT others(35): Show |
A | 2 | a0001c0001t0002g0094a0001c0001t0002g0361 | 2 | NA18983.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.163+446_163+487del others(42): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/15 | chr3 | 195887938 | ||||||
| chr3:195887939
|
T | C | 1 | a0001c0014t0004g0002 | 2 | HG01884.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.163+487A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/15 | chr3 | 195887939 | ||||||
| chr3:195887955
|
C | CGT | 4 | a0001c0001t0001g0285a0001c0001t0002g0173a0001c0020t0002g0252others(1): Show | 4 | HG00280.hp2 HG01361.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.163+469_163+470dup others(2): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/15 | chr3 | 195887955 | ||||||
| chr3:195887955
|
CGT | C | 179 | a0001c0001t0001g0001a0001c0001t0001g0076a0001c0001t0001g0103others(176): Show | 183 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.163+469_163+470del others(2): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/15 | chr3 | 195887955 | ||||||
| chr3:195887955
|
CGTGT | C | 50 | a0001c0001t0001g0095a0001c0001t0001g0209a0001c0001t0001g0210others(47): Show | 50 | HG01069.hp2 HG01071.hp1 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.163+467_163+470del others(4): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/15 | chr3 | 195887955 | ||||||
| chr3:195887955
|
CGTGTGT | C | 18 | a0001c0001t0001g0116a0001c0001t0002g0333a0001c0001t0002g0334others(15): Show | 18 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(15): Show |
intron_variant | MODIFIER | c.163+465_163+470del others(6): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/15 | chr3 | 195887955 | ||||||
| chr3:195887960
|
G | A | 24 | a0001c0002t0001g0130a0001c0002t0001g0174a0001c0002t0001g0175others(21): Show | 24 | HG01175.hp1 HG01192.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.163+466C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/15 | chr3 | 195887960 | ||||||
| chr3:195887962
|
G | A | 1 | a0001c0002t0001g0181 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.163+464C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/15 | chr3 | 195887962 | ||||||
| chr3:195887974
|
G | A | 1 | a0001c0002t0001g0235 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.163+452C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/15 | chr3 | 195887974 | ||||||
| chr3:195887986
|
G | A | 1 | a0001c0003t0003g0142 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.163+440C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/15 | chr3 | 195887986 | ||||||
| chr3:195888017
|
A | C | 7 | a0001c0001t0001g0323a0001c0001t0002g0321a0001c0001t0002g0322others(4): Show | 7 | HG00408.hp2 NA18939.hp1 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.163+409T>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/15 | chr3 | 195888017 | ||||||
| chr3:195888082
|
G | C | 41 | a0001c0002t0001g0029a0001c0002t0001g0031a0001c0002t0001g0036others(38): Show | 41 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(38): Show |
intron_variant | MODIFIER | c.163+344C>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/15 | chr3 | 195888082 | ||||||
| chr3:195888089
|
G | C | 1 | a0001c0001t0001g0336 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.163+337C>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/15 | chr3 | 195888089 | ||||||
| chr3:195888096
|
C | CG | 4 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(1): Show | 4 | HG01975.hp2 HG02976.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.163+329dupC | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/15 | chr3 | 195888096 | ||||||
| chr3:195888227
|
G | A | 55 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(52): Show | 55 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.163+199C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/15 | chr3 | 195888227 | ||||||
| chr3:195888289
|
G | A | 1 | a0001c0042t0001g0234 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.163+137C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/15 | chr3 | 195888289 | ||||||
| chr3:195888360
|
G | A | 1 | a0001c0012t0001g0071 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.163+66C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 2/15 | chr3 | 195888360 | ||||||
| chr3:195888612
|
G | A | 6 | a0001c0002t0001g0018a0001c0017t0006g0012a0001c0017t0006g0013others(3): Show | 6 | HG02486.hp2 HG02630.hp2 HG02896.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.-18-6C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195888612 | ||||||
| chr3:195888613
|
G | A | 2 | a0001c0002t0001g0205a0002c0023t0001g0207 | 2 | HG01175.hp1 HG06807.hp1 |
splice_region_variant&intron_variant | LOW | c.-18-7C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195888613 | ||||||
| chr3:195888748
|
C | T | 1 | a0001c0002t0001g0130 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-18-142G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195888748 | ||||||
| chr3:195888768
|
G | A | 2 | a0001c0001t0001g0308a0002c0004t0001g0350 | 2 | HG02055.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-18-162C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195888768 | ||||||
| chr3:195888901
|
C | T | 112 | a0001c0002t0001g0003a0001c0002t0001g0011a0001c0002t0001g0018others(109): Show | 115 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.-18-295G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195888901 | ||||||
| chr3:195889016
|
T | C | 1 | a0017c0035t0004g0233 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-18-410A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195889016 | ||||||
| chr3:195889113
|
C | T | 1 | a0001c0001t0002g0050 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-18-507G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195889113 | ||||||
| chr3:195889200
|
G | C | 4 | a0001c0014t0004g0002a0001c0014t0004g0109a0001c0037t0004g0110others(1): Show | 5 | HG01884.hp1 HG01891.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18-594C>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195889200 | ||||||
| chr3:195889337
|
C | T | 111 | a0001c0002t0001g0003a0001c0002t0001g0011a0001c0002t0001g0018others(108): Show | 114 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.-18-731G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195889337 | ||||||
| chr3:195889409
|
G | A | 1 | a0001c0020t0002g0335 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-18-803C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195889409 | ||||||
| chr3:195889490
|
C | T | 1 | a0001c0020t0002g0251 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-18-884G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195889490 | ||||||
| chr3:195889505
|
C | G | 57 | a0001c0001t0001g0001a0001c0001t0001g0076a0001c0001t0001g0095others(54): Show | 58 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.-18-899G>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195889505 | ||||||
| chr3:195889668
|
G | A | 1 | a0001c0002t0001g0185 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-18-1062C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195889668 | ||||||
| chr3:195889718
|
G | A | 1 | a0001c0001t0002g0062 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-18-1112C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195889718 | ||||||
| chr3:195889773
|
C | T | 5 | a0001c0058t0004g0237a0001c0061t0001g0238a0001c0062t0001g0239others(2): Show | 5 | HG02922.hp2 HG03130.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18-1167G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195889773 | ||||||
| chr3:195889802
|
G | A | 225 | a0001c0001t0001g0001a0001c0001t0001g0076a0001c0001t0001g0095others(222): Show | 229 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.-18-1196C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195889802 | ||||||
| chr3:195889824
|
C | T | 1 | a0003c0043t0001g0025 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-18-1218G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195889824 | ||||||
| chr3:195889836
|
G | A | 1 | a0003c0030t0001g0072 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-18-1230C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195889836 | ||||||
| chr3:195889868
|
C | T | 1 | a0001c0001t0001g0284 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-18-1262G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195889868 | ||||||
| chr3:195889906
|
C | A | 7 | a0001c0002t0001g0036a0002c0010t0001g0035a0002c0010t0001g0043others(4): Show | 7 | HG01074.hp2 HG01099.hp2 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-18-1300G>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195889906 | ||||||
| chr3:195889910
|
C | A | 1 | a0001c0002t0001g0045 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-18-1304G>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195889910 | ||||||
| chr3:195889981
|
A | G | 1 | a0001c0042t0001g0234 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-18-1375T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195889981 | ||||||
| chr3:195890036
|
C | T | 1 | a0003c0015t0001g0020 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-18-1430G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195890036 | ||||||
| chr3:195890139
|
G | A | 1 | a0001c0001t0001g0336 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-18-1533C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195890139 | ||||||
| chr3:195890377
|
A | C | 2 | a0001c0019t0003g0132a0001c0019t0003g0133 | 2 | NA18964.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.-18-1771T>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195890377 | ||||||
| chr3:195890454
|
G | GT | 18 | a0001c0001t0001g0281a0001c0001t0001g0348a0001c0001t0002g0188others(15): Show | 19 | HG00423.hp1 HG01884.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-18-1849dupA | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195890454 | ||||||
| chr3:195890454
|
G | GTT | 6 | a0001c0002t0001g0011a0001c0002t0001g0018a0002c0008t0001g0010others(3): Show | 6 | HG02647.hp1 HG02723.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18-1850_-18-1849d others(4): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195890454 | ||||||
| chr3:195890454
|
GT | G | 107 | a0001c0001t0001g0001a0001c0001t0001g0076a0001c0001t0001g0095others(104): Show | 108 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.-18-1849delA | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195890454 | ||||||
| chr3:195890454
|
GTT | G | 24 | a0001c0002t0001g0130a0001c0002t0001g0174a0001c0002t0001g0175others(21): Show | 24 | HG01175.hp1 HG01192.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.-18-1850_-18-1849d others(4): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195890454 | ||||||
| chr3:195890507
|
A | G | 2 | a0001c0001t0001g0116a0007c0021t0001g0113 | 2 | HG00323.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.-18-1901T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195890507 | ||||||
| chr3:195890543
|
C | T | 1 | a0001c0006t0001g0066 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-18-1937G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195890543 | ||||||
| chr3:195890596
|
G | A | 2 | a0001c0058t0004g0237a0002c0057t0004g0236 | 2 | HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-18-1990C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195890596 | ||||||
| chr3:195890630
|
G | C | 2 | a0001c0024t0001g0189a0001c0024t0001g0190 | 2 | HG01099.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-18-2024C>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195890630 | ||||||
| chr3:195890798
|
T | C | 1 | a0001c0001t0001g0351 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-18-2192A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195890798 | ||||||
| chr3:195890936
|
A | G | 226 | a0001c0001t0001g0001a0001c0001t0001g0076a0001c0001t0001g0095others(223): Show | 230 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.-18-2330T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195890936 | ||||||
| chr3:195891088
|
T | C | 1 | a0001c0002t0001g0214 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-18-2482A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195891088 | ||||||
| chr3:195891168
|
C | T | 42 | a0001c0001t0001g0001a0001c0001t0001g0076a0001c0001t0002g0062others(39): Show | 43 | HG00140.hp1 HG00639.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.-18-2562G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195891168 | ||||||
| chr3:195891292
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-18-2686C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195891292 | ||||||
| chr3:195891544
|
C | T | 1 | a0001c0002t0001g0235 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-18-2938G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195891544 | ||||||
| chr3:195891558
|
G | A | 9 | a0001c0001t0001g0076a0001c0006t0001g0077a0001c0006t0001g0092others(6): Show | 9 | HG01884.hp2 HG02451.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.-18-2952C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195891558 | ||||||
| chr3:195891624
|
G | A | 57 | a0001c0001t0001g0001a0001c0001t0001g0076a0001c0001t0001g0095others(54): Show | 58 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.-18-3018C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195891624 | ||||||
| chr3:195891656
|
A | AC | 38 | a0001c0001t0001g0254a0001c0001t0001g0315a0001c0001t0002g0161others(35): Show | 40 | HG00408.hp2 HG00597.hp2 HG01261.hp1 others(37): Show |
intron_variant | MODIFIER | c.-18-3051dupG | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195891656 | ||||||
| chr3:195891663
|
C | G | 3 | a0001c0040t0001g0019a0002c0010t0001g0053a0003c0005t0001g0054 | 3 | HG00673.hp2 HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-18-3057G>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195891663 | ||||||
| chr3:195891663
|
C | T | 2 | a0001c0001t0001g0363a0001c0001t0001g0364 | 2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-18-3057G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195891663 | ||||||
| chr3:195891664
|
C | G | 60 | a0001c0001t0001g0001a0001c0001t0001g0076a0001c0001t0001g0095others(57): Show | 61 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.-18-3058G>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195891664 | ||||||
| chr3:195891705
|
G | A | 2 | a0001c0002t0001g0202a0001c0002t0001g0203 | 2 | NA18948.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.-18-3099C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195891705 | ||||||
| chr3:195891797
|
C | G | 1 | a0001c0001t0001g0076 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-18-3191G>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195891797 | ||||||
| chr3:195892126
|
T | C | 1 | a0001c0002t0001g0031 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-18-3520A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195892126 | ||||||
| chr3:195892150
|
T | TCTGCATG others(8): Show |
3 | a0002c0008t0001g0010a0012c0045t0001g0009a0025c0047t0001g0008 | 3 | HG02647.hp1 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-18-3559_-18-3545d others(17): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195892150 | ||||||
| chr3:195892249
|
T | C | 8 | a0001c0002t0001g0036a0002c0010t0001g0035a0002c0010t0001g0043others(5): Show | 8 | HG01074.hp1 HG01074.hp2 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.-18-3643A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195892249 | ||||||
| chr3:195892256
|
G | A | 1 | a0003c0005t0001g0039 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-18-3650C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195892256 | ||||||
| chr3:195892383
|
A | G | 58 | a0001c0001t0001g0001a0001c0001t0001g0076a0001c0001t0001g0095others(55): Show | 59 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.-18-3777T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195892383 | ||||||
| chr3:195892400
|
C | T | 4 | a0001c0014t0004g0002a0001c0014t0004g0109a0001c0037t0004g0110others(1): Show | 5 | HG01884.hp1 HG01891.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18-3794G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195892400 | ||||||
| chr3:195892404
|
C | A | 1 | a0001c0002t0001g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-18-3798G>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195892404 | ||||||
| chr3:195892473
|
G | A | 1 | a0001c0013t0001g0121 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-18-3867C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195892473 | ||||||
| chr3:195892500
|
G | A | 2 | a0001c0053t0003g0129a0016c0051t0001g0208 | 2 | NA18949.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.-18-3894C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195892500 | ||||||
| chr3:195892510
|
C | T | 2 | a0001c0002t0001g0029a0001c0002t0001g0031 | 2 | HG00323.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.-18-3904G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195892510 | ||||||
| chr3:195892511
|
G | A | 3 | a0001c0002t0001g0211a0001c0002t0001g0214a0001c0050t0001g0213 | 3 | HG02895.hp2 HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-18-3905C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195892511 | ||||||
| chr3:195892678
|
A | AGAG | 230 | a0001c0001t0001g0001a0001c0001t0001g0076a0001c0001t0001g0095others(227): Show | 234 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.-18-4075_-18-4073d others(5): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195892678 | ||||||
| chr3:195892705
|
G | A | 42 | a0001c0001t0001g0001a0001c0001t0001g0076a0001c0001t0002g0062others(39): Show | 43 | HG00140.hp1 HG00639.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.-18-4099C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195892705 | ||||||
| chr3:195892741
|
C | A | 1 | a0001c0003t0001g0122 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-18-4135G>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195892741 | ||||||
| chr3:195892768
|
C | T | 1 | a0001c0001t0001g0315 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-18-4162G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195892768 | ||||||
| chr3:195892795
|
G | C | 362 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0056others(359): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.-18-4189C>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195892795 | ||||||
| chr3:195892798
|
G | T | 1 | a0001c0009t0002g0263 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-18-4192C>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195892798 | ||||||
| chr3:195892818
|
C | T | 5 | a0001c0058t0004g0237a0001c0061t0001g0238a0001c0062t0001g0239others(2): Show | 5 | HG02922.hp2 HG03130.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18-4212G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195892818 | ||||||
| chr3:195893037
|
C | T | 1 | a0001c0002t0001g0235 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-18-4431G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195893037 | ||||||
| chr3:195893166
|
C | T | 41 | a0001c0002t0001g0029a0001c0002t0001g0031a0001c0002t0001g0036others(38): Show | 41 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(38): Show |
intron_variant | MODIFIER | c.-18-4560G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195893166 | ||||||
| chr3:195893167
|
G | A | 73 | a0001c0001t0001g0006a0001c0001t0001g0056a0001c0001t0001g0244others(70): Show | 74 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.-18-4561C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195893167 | ||||||
| chr3:195893297
|
G | C | 1 | a0002c0008t0001g0010 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-18-4691C>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195893297 | ||||||
| chr3:195893368
|
C | T | 1 | a0010c0059t0001g0021 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-18-4762G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195893368 | ||||||
| chr3:195893564
|
C | T | 1 | a0002c0008t0001g0219 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-18-4958G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195893564 | ||||||
| chr3:195893624
|
C | A | 1 | a0002c0008t0002g0267 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-18-5018G>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195893624 | ||||||
| chr3:195893638
|
AC | A | 55 | a0001c0001t0001g0001a0001c0001t0001g0103a0001c0001t0001g0104others(52): Show | 56 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.-18-5033delG | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195893638 | ||||||
| chr3:195893652
|
G | A | 1 | a0001c0001t0001g0343 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-18-5046C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195893652 | ||||||
| chr3:195893747
|
T | G | 2 | a0001c0002t0001g0011a0001c0002t0001g0186 | 2 | HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-18-5141A>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195893747 | ||||||
| chr3:195893937
|
G | C | 1 | a0001c0001t0002g0050 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-18-5331C>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195893937 | ||||||
| chr3:195893946
|
A | G | 1 | a0003c0054t0001g0134 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-18-5340T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195893946 | ||||||
| chr3:195893989
|
C | A | 1 | a0001c0006t0001g0092 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-18-5383G>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195893989 | ||||||
| chr3:195894178
|
ACCGGGGG | A | 36 | a0001c0001t0002g0050a0001c0002t0001g0029a0001c0002t0001g0031others(33): Show | 36 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.-18-5579_-18-5573d others(9): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195894178 | ||||||
| chr3:195894269
|
G | A | 1 | a0004c0007t0001g0312 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-18-5663C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195894269 | ||||||
| chr3:195894335
|
C | T | 3 | a0001c0061t0001g0238a0001c0062t0001g0239a0002c0060t0001g0240 | 3 | HG02922.hp2 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-18-5729G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195894335 | ||||||
| chr3:195894415
|
A | T | 23 | a0001c0002t0001g0003a0001c0002t0001g0211a0001c0002t0001g0214others(20): Show | 26 | HG01192.hp1 HG01884.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.-18-5809T>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195894415 | ||||||
| chr3:195894426
|
C | CT | 115 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(112): Show | 115 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.-18-5821dupA | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195894426 | ||||||
| chr3:195894427
|
T | C | 2 | a0001c0042t0001g0234a0006c0025t0001g0096 | 2 | HG02109.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-18-5821A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195894427 | ||||||
| chr3:195894517
|
G | A | 1 | a0001c0003t0001g0168 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-18-5911C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195894517 | ||||||
| chr3:195894557
|
A | AT | 17 | a0001c0001t0001g0270a0001c0002t0001g0228a0001c0011t0001g0060others(14): Show | 17 | HG00621.hp1 HG01109.hp1 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.-18-5952dupA | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195894557 | ||||||
| chr3:195894557
|
A | ATT | 6 | a0001c0001t0001g0095a0001c0002t0001g0101a0001c0006t0001g0098others(3): Show | 6 | HG02622.hp2 HG02630.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18-5953_-18-5952d others(4): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195894557 | ||||||
| chr3:195894557
|
AT | A | 6 | a0001c0002t0001g0235a0001c0058t0004g0237a0001c0061t0001g0238others(3): Show | 6 | HG02257.hp1 HG02922.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18-5952delA | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195894557 | ||||||
| chr3:195894633
|
C | T | 103 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0116others(100): Show | 103 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.-18-6027G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195894633 | ||||||
| chr3:195894649
|
A | G | 2 | a0001c0002t0001g0220a0001c0002t0001g0221 | 2 | HG02280.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-18-6043T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195894649 | ||||||
| chr3:195894836
|
C | T | 76 | a0001c0001t0001g0144a0001c0001t0001g0164a0001c0001t0001g0165others(73): Show | 76 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.-18-6230G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195894836 | ||||||
| chr3:195894905
|
A | G | 1 | a0001c0042t0001g0234 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-18-6299T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195894905 | ||||||
| chr3:195894907
|
G | A | 1 | a0001c0001t0001g0313 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-18-6301C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195894907 | ||||||
| chr3:195894992
|
C | T | 1 | a0001c0002t0001g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-18-6386G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195894992 | ||||||
| chr3:195895015
|
A | G | 1 | a0001c0001t0001g0317 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-18-6409T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195895015 | ||||||
| chr3:195895111
|
C | T | 103 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0116others(100): Show | 103 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.-18-6505G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195895111 | ||||||
| chr3:195895170
|
G | A | 18 | a0001c0002t0001g0003a0001c0002t0001g0211a0001c0002t0001g0212others(15): Show | 20 | HG01934.hp1 HG02145.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-18-6564C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195895170 | ||||||
| chr3:195895174
|
T | C | 1 | a0001c0001t0001g0314 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-18-6568A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195895174 | ||||||
| chr3:195895411
|
G | A | 1 | a0001c0014t0004g0093 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-18-6805C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195895411 | ||||||
| chr3:195895427
|
T | C | 15 | a0001c0002t0001g0011a0001c0002t0001g0018a0001c0014t0004g0093others(12): Show | 15 | HG00673.hp2 HG01069.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.-18-6821A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195895427 | ||||||
| chr3:195895436
|
G | A | 2 | a0001c0001t0001g0315a0001c0001t0001g0316 | 2 | HG00741.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-18-6830C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195895436 | ||||||
| chr3:195895463
|
C | T | 1 | a0001c0002t0001g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-18-6857G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195895463 | ||||||
| chr3:195895595
|
G | A | 1 | a0001c0014t0004g0093 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-18-6989C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195895595 | ||||||
| chr3:195895624
|
G | A | 41 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0116others(38): Show | 41 | HG00323.hp2 HG01099.hp1 HG01175.hp1 others(38): Show |
intron_variant | MODIFIER | c.-18-7018C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195895624 | ||||||
| chr3:195895682
|
C | T | 42 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0116others(39): Show | 42 | HG00323.hp2 HG01099.hp1 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.-18-7076G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195895682 | ||||||
| chr3:195895720
|
G | A | 1 | a0008c0016t0001g0224 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-18-7114C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195895720 | ||||||
| chr3:195895745
|
G | A | 40 | a0001c0001t0002g0050a0001c0002t0001g0029a0001c0002t0001g0031others(37): Show | 40 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.-18-7139C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195895745 | ||||||
| chr3:195895817
|
G | C | 2 | a0001c0002t0001g0174a0001c0002t0001g0187 | 2 | NA18959.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.-18-7211C>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195895817 | ||||||
| chr3:195895835
|
C | G | 1 | a0006c0025t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-18-7229G>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195895835 | ||||||
| chr3:195895896
|
T | A | 1 | a0001c0006t0001g0100 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-18-7290A>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195895896 | ||||||
| chr3:195895909
|
G | T | 75 | a0001c0001t0001g0006a0001c0001t0001g0056a0001c0001t0001g0244others(72): Show | 76 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.-18-7303C>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195895909 | ||||||
| chr3:195895914
|
T | A | 1 | a0001c0002t0001g0228 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-18-7308A>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195895914 | ||||||
| chr3:195896123
|
C | T | 1 | a0002c0023t0001g0017 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-18-7517G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195896123 | ||||||
| chr3:195896201
|
C | T | 1 | a0001c0042t0001g0234 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-18-7595G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195896201 | ||||||
| chr3:195896205
|
G | T | 1 | a0001c0001t0001g0268 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-18-7599C>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195896205 | ||||||
| chr3:195896252
|
G | A | 2 | a0003c0005t0001g0058a0003c0005t0001g0059 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-18-7646C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195896252 | ||||||
| chr3:195896314
|
G | C | 1 | a0028c0079t0001g0044 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-18-7708C>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195896314 | ||||||
| chr3:195896318
|
G | T | 1 | a0001c0001t0007g0232 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-18-7712C>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195896318 | ||||||
| chr3:195896332
|
C | A | 11 | a0001c0002t0001g0011a0001c0002t0001g0018a0001c0017t0006g0012others(8): Show | 11 | HG02486.hp2 HG02630.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.-18-7726G>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195896332 | ||||||
| chr3:195896359
|
T | G | 1 | a0002c0074t0001g0073 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-18-7753A>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195896359 | ||||||
| chr3:195896378
|
T | G | 4 | a0001c0014t0004g0093a0001c0040t0001g0019a0002c0010t0001g0053others(1): Show | 4 | HG00673.hp2 HG01069.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-7772A>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195896378 | ||||||
| chr3:195896569
|
G | A | 1 | a0006c0025t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-18-7963C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195896569 | ||||||
| chr3:195896569
|
G | C | 43 | a0001c0001t0002g0050a0001c0002t0001g0029a0001c0002t0001g0031others(40): Show | 43 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.-18-7963C>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195896569 | ||||||
| chr3:195896617
|
T | A | 11 | a0001c0002t0001g0011a0001c0002t0001g0018a0001c0017t0006g0012others(8): Show | 11 | HG02486.hp2 HG02630.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.-18-8011A>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195896617 | ||||||
| chr3:195896777
|
C | G | 2 | a0001c0002t0001g0215a0002c0008t0001g0219 | 2 | HG01192.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.-18-8171G>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195896777 | ||||||
| chr3:195896802
|
T | C | 1 | a0002c0010t0001g0028 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-18-8196A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195896802 | ||||||
| chr3:195896851
|
C | G | 1 | a0001c0037t0004g0110 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-18-8245G>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195896851 | ||||||
| chr3:195896909
|
T | A | 1 | a0002c0010t0001g0043 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-18-8303A>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195896909 | ||||||
| chr3:195896910
|
C | A | 1 | a0002c0010t0001g0043 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-18-8304G>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195896910 | ||||||
| chr3:195896974
|
C | T | 1 | a0001c0002t0001g0218 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-18-8368G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195896974 | ||||||
| chr3:195897034
|
A | C | 2 | a0001c0014t0004g0093a0001c0040t0001g0019 | 2 | HG00673.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.-18-8428T>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195897034 | ||||||
| chr3:195897304
|
A | C | 1 | a0010c0059t0001g0021 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-18-8698T>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195897304 | ||||||
| chr3:195897439
|
C | T | 1 | a0001c0009t0002g0255 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-18-8833G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195897439 | ||||||
| chr3:195897474
|
T | C | 1 | a0001c0014t0004g0093 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-18-8868A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195897474 | ||||||
| chr3:195897489
|
T | C | 1 | a0002c0010t0001g0028 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-18-8883A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195897489 | ||||||
| chr3:195897522
|
G | A | 1 | a0001c0040t0001g0019 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-18-8916C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195897522 | ||||||
| chr3:195897613
|
T | C | 36 | a0001c0001t0002g0050a0001c0002t0001g0029a0001c0002t0001g0031others(33): Show | 36 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.-18-9007A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195897613 | ||||||
| chr3:195897650
|
C | T | 1 | a0001c0002t0001g0235 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-18-9044G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195897650 | ||||||
| chr3:195897798
|
GCCCACCC others(20): Show |
G | 2 | a0001c0019t0003g0132a0001c0019t0003g0133 | 2 | NA18964.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.-18-9219_-18-9193d others(29): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195897798 | ||||||
| chr3:195897810
|
ACCCCCCC others(4): Show |
A | 11 | a0001c0002t0001g0011a0001c0002t0001g0018a0001c0017t0006g0012others(8): Show | 11 | HG02486.hp2 HG02630.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.-18-9215_-18-9205d others(13): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195897810 | ||||||
| chr3:195897817
|
CA | C | 11 | a0001c0001t0001g0104a0001c0001t0002g0173a0001c0001t0002g0265others(8): Show | 11 | HG00735.hp1 HG01109.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.-18-9212delT | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195897817 | ||||||
| chr3:195897818
|
A | AC | 20 | a0001c0001t0002g0005a0001c0001t0002g0062a0001c0006t0001g0066others(17): Show | 21 | HG00642.hp1 HG00733.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.-18-9213dupG | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195897818 | ||||||
| chr3:195897818
|
A | C | 7 | a0001c0001t0001g0254a0001c0003t0005g0197a0001c0013t0001g0145others(4): Show | 7 | HG01099.hp1 HG01261.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.-18-9212T>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195897818 | ||||||
| chr3:195897818
|
AC | A | 77 | a0001c0001t0001g0103a0001c0001t0001g0164a0001c0001t0001g0165others(74): Show | 77 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.-18-9213delG | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195897818 | ||||||
| chr3:195897818
|
ACC | A | 193 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0056others(190): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.-18-9214_-18-9213d others(4): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195897818 | ||||||
| chr3:195897819
|
C | A | 5 | a0001c0001t0001g0254a0001c0003t0005g0197a0001c0013t0001g0145others(2): Show | 5 | HG01099.hp1 HG01261.hp1 HG02080.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18-9213G>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195897819 | ||||||
| chr3:195897820
|
C | A | 11 | a0001c0001t0001g0104a0001c0001t0002g0173a0001c0001t0002g0265others(8): Show | 11 | HG00735.hp1 HG01109.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.-18-9214G>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195897820 | ||||||
| chr3:195897827
|
C | A | 2 | a0005c0029t0010g0345a0009c0028t0001g0344 | 2 | HG02698.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.-18-9221G>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195897827 | ||||||
| chr3:195897828
|
C | A | 1 | a0002c0004t0001g0131 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-18-9222G>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195897828 | ||||||
| chr3:195897829
|
A | C | 2 | a0002c0004t0001g0131a0005c0029t0010g0345 | 2 | HG04199.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.-18-9223T>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195897829 | ||||||
| chr3:195897830
|
C | A | 1 | a0001c0002t0001g0225 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-18-9224G>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195897830 | ||||||
| chr3:195897835
|
C | G | 1 | a0005c0029t0010g0345 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-18-9229G>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195897835 | ||||||
| chr3:195897836
|
G | A | 1 | a0001c0002t0001g0228 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-18-9230C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195897836 | ||||||
| chr3:195897836
|
G | C | 1 | a0005c0029t0010g0345 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-18-9230C>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195897836 | ||||||
| chr3:195898150
|
G | A | 1 | a0001c0003t0003g0170 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-18-9544C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195898150 | ||||||
| chr3:195898226
|
G | A | 1 | a0001c0034t0006g0016 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-18-9620C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195898226 | ||||||
| chr3:195898272
|
T | A | 1 | a0006c0025t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-18-9666A>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195898272 | ||||||
| chr3:195898455
|
A | G | 227 | a0001c0001t0001g0001a0001c0001t0001g0076a0001c0001t0001g0095others(224): Show | 231 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.-18-9849T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195898455 | ||||||
| chr3:195898472
|
T | A | 3 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0049 | 3 | HG00280.hp1 HG01433.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.-18-9866A>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195898472 | ||||||
| chr3:195898499
|
C | T | 4 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0209others(1): Show | 4 | HG01361.hp2 HG02559.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-9893G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195898499 | ||||||
| chr3:195898660
|
CT | C | 40 | a0001c0001t0002g0050a0001c0002t0001g0029a0001c0002t0001g0031others(37): Show | 40 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.-19+9824delA | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195898660 | ||||||
| chr3:195898665
|
G | A | 59 | a0001c0001t0001g0144a0001c0001t0001g0164a0001c0001t0001g0165others(56): Show | 59 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.-19+9820C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195898665 | ||||||
| chr3:195898670
|
G | A | 11 | a0001c0002t0001g0011a0001c0002t0001g0018a0001c0017t0006g0012others(8): Show | 11 | HG02486.hp2 HG02630.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.-19+9815C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195898670 | ||||||
| chr3:195898684
|
G | C | 1 | a0020c0071t0002g0346 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-19+9801C>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195898684 | ||||||
| chr3:195898824
|
G | C | 3 | a0001c0014t0004g0002a0001c0014t0004g0109a0001c0037t0004g0110 | 4 | HG01884.hp1 HG01891.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+9661C>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195898824 | ||||||
| chr3:195898928
|
C | T | 1 | a0001c0012t0001g0088 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-19+9557G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195898928 | ||||||
| chr3:195898999
|
G | A | 1 | a0001c0012t0001g0088 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-19+9486C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195898999 | ||||||
| chr3:195899018
|
C | T | 1 | a0001c0014t0004g0093 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-19+9467G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195899018 | ||||||
| chr3:195899050
|
C | T | 2 | a0001c0042t0001g0234a0017c0035t0004g0233 | 2 | HG02615.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-19+9435G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195899050 | ||||||
| chr3:195899333
|
AT | A | 10 | a0001c0001t0001g0210a0001c0001t0001g0348a0001c0002t0001g0130others(7): Show | 10 | HG01993.hp1 HG02055.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.-19+9151delA | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195899333 | ||||||
| chr3:195899488
|
A | G | 1 | a0001c0001t0001g0249 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-19+8997T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195899488 | ||||||
| chr3:195899552
|
G | A | 20 | a0001c0002t0001g0003a0001c0002t0001g0211a0001c0002t0001g0212others(17): Show | 22 | HG01192.hp1 HG01934.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.-19+8933C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195899552 | ||||||
| chr3:195899667
|
T | C | 1 | a0001c0012t0001g0088 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-19+8818A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195899667 | ||||||
| chr3:195899863
|
G | T | 1 | a0001c0002t0001g0202 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-19+8622C>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195899863 | ||||||
| chr3:195899868
|
A | ACGGTGGC others(12): Show |
3 | a0001c0014t0004g0002a0001c0014t0004g0109a0001c0037t0004g0110 | 4 | HG01884.hp1 HG01891.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+8598_-19+8616d others(21): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195899868 | ||||||
| chr3:195899869
|
C | T | 1 | a0001c0001t0001g0363 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-19+8616G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195899869 | ||||||
| chr3:195899953
|
C | T | 1 | a0001c0001t0002g0248 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-19+8532G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195899953 | ||||||
| chr3:195899992
|
C | T | 1 | a0001c0001t0002g0062 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-19+8493G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195899992 | ||||||
| chr3:195900170
|
G | A | 1 | a0006c0025t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-19+8315C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195900170 | ||||||
| chr3:195900188
|
G | A | 2 | a0001c0058t0004g0237a0002c0057t0004g0236 | 2 | HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-19+8297C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195900188 | ||||||
| chr3:195900308
|
G | A | 2 | a0001c0031t0001g0089a0001c0031t0001g0090 | 2 | NA18940.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.-19+8177C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195900308 | ||||||
| chr3:195900338
|
G | A | 1 | a0001c0014t0004g0093 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-19+8147C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195900338 | ||||||
| chr3:195900423
|
C | A | 1 | a0001c0003t0001g0200 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-19+8062G>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195900423 | ||||||
| chr3:195900446
|
T | G | 1 | a0001c0003t0001g0171 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-19+8039A>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195900446 | ||||||
| chr3:195900699
|
C | T | 3 | a0001c0001t0002g0050a0001c0002t0001g0052a0003c0005t0001g0051 | 3 | HG01081.hp1 HG01255.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-19+7786G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195900699 | ||||||
| chr3:195900769
|
C | T | 1 | a0014c0063t0002g0247 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-19+7716G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195900769 | ||||||
| chr3:195900845
|
C | T | 1 | a0006c0025t0001g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-19+7640G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195900845 | ||||||
| chr3:195900868
|
C | G | 2 | a0002c0010t0001g0024a0003c0043t0001g0025 | 2 | HG02071.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.-19+7617G>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195900868 | ||||||
| chr3:195900870
|
G | T | 1 | a0001c0014t0004g0109 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-19+7615C>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195900870 | ||||||
| chr3:195900969
|
A | G | 1 | a0001c0001t0002g0050 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-19+7516T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195900969 | ||||||
| chr3:195901011
|
A | G | 105 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(102): Show | 105 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.-19+7474T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195901011 | ||||||
| chr3:195901019
|
A | G | 4 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(1): Show | 4 | HG01975.hp2 HG02976.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+7466T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195901019 | ||||||
| chr3:195901130
|
G | T | 60 | a0001c0001t0002g0050a0001c0002t0001g0003a0001c0002t0001g0029others(57): Show | 62 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.-19+7355C>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195901130 | ||||||
| chr3:195901133
|
C | T | 60 | a0001c0001t0002g0050a0001c0002t0001g0003a0001c0002t0001g0029others(57): Show | 62 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.-19+7352G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195901133 | ||||||
| chr3:195901199
|
G | A | 1 | a0001c0001t0001g0349 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-19+7286C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195901199 | ||||||
| chr3:195901200
|
G | A | 3 | a0001c0014t0004g0002a0001c0014t0004g0109a0001c0037t0004g0110 | 4 | HG01884.hp1 HG01891.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+7285C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195901200 | ||||||
| chr3:195901268
|
C | T | 11 | a0001c0002t0001g0011a0001c0002t0001g0018a0001c0017t0006g0012others(8): Show | 11 | HG02486.hp2 HG02630.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.-19+7217G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195901268 | ||||||
| chr3:195901379
|
C | T | 2 | a0001c0001t0001g0355a0001c0001t0001g0356 | 2 | HG03491.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.-19+7106G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195901379 | ||||||
| chr3:195901401
|
G | A | 238 | a0001c0001t0001g0001a0001c0001t0001g0076a0001c0001t0001g0095others(235): Show | 242 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.-19+7084C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195901401 | ||||||
| chr3:195901510
|
G | C | 3 | a0001c0014t0004g0002a0001c0014t0004g0109a0001c0037t0004g0110 | 4 | HG01884.hp1 HG01891.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+6975C>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195901510 | ||||||
| chr3:195901521
|
T | TGAGGTAC others(12): Show |
4 | a0001c0002t0001g0011a0002c0008t0001g0010a0012c0045t0001g0009others(1): Show | 4 | HG02647.hp1 HG02723.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+6963_-19+6964i others(21): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195901521 | ||||||
| chr3:195901676
|
C | T | 1 | a0001c0036t0001g0023 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-19+6809G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195901676 | ||||||
| chr3:195901688
|
TGA | T | 3 | a0001c0040t0001g0019a0002c0010t0001g0053a0003c0005t0001g0054 | 3 | HG00673.hp2 HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-19+6795_-19+6796d others(4): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195901688 | ||||||
| chr3:195901739
|
T | C | 1 | a0010c0059t0001g0021 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-19+6746A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195901739 | ||||||
| chr3:195901747
|
C | T | 1 | a0001c0003t0001g0122 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-19+6738G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195901747 | ||||||
| chr3:195901765
|
C | A | 153 | a0001c0001t0001g0001a0001c0001t0001g0076a0001c0001t0001g0095others(150): Show | 155 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.-19+6720G>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195901765 | ||||||
| chr3:195901853
|
G | C | 1 | a0001c0042t0001g0234 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-19+6632C>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195901853 | ||||||
| chr3:195901864
|
A | G | 3 | a0001c0040t0001g0019a0002c0010t0001g0053a0003c0005t0001g0054 | 3 | HG00673.hp2 HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-19+6621T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195901864 | ||||||
| chr3:195901904
|
C | T | 1 | a0001c0006t0001g0061 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-19+6581G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195901904 | ||||||
| chr3:195901944
|
T | C | 52 | a0001c0001t0002g0050a0001c0002t0001g0011a0001c0002t0001g0018others(49): Show | 52 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.-19+6541A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195901944 | ||||||
| chr3:195902212
|
C | T | 2 | a0001c0061t0001g0238a0001c0062t0001g0239 | 2 | HG02922.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-19+6273G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195902212 | ||||||
| chr3:195902213
|
G | A | 105 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0116others(102): Show | 106 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.-19+6272C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195902213 | ||||||
| chr3:195902369
|
G | A | 3 | a0001c0002t0001g0226a0001c0002t0001g0227a0001c0002t0001g0228 | 3 | HG02486.hp1 HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-19+6116C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195902369 | ||||||
| chr3:195902415
|
C | T | 1 | a0001c0001t0002g0128 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-19+6070G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195902415 | ||||||
| chr3:195902526
|
G | A | 1 | a0010c0059t0001g0021 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-19+5959C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195902526 | ||||||
| chr3:195902612
|
C | T | 1 | a0001c0002t0001g0130 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-19+5873G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195902612 | ||||||
| chr3:195902617
|
C | CA | 7 | a0001c0001t0001g0351a0001c0014t0004g0093a0001c0040t0001g0019others(4): Show | 7 | HG00597.hp1 HG00673.hp2 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19+5867dupT | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195902617 | ||||||
| chr3:195902617
|
CA | C | 14 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(11): Show | 15 | HG01884.hp1 HG01891.hp2 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.-19+5867delT | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195902617 | ||||||
| chr3:195902629
|
A | C | 96 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0116others(93): Show | 96 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.-19+5856T>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195902629 | ||||||
| chr3:195902630
|
C | A | 98 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0116others(95): Show | 98 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.-19+5855G>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195902630 | ||||||
| chr3:195902631
|
A | C | 1 | a0001c0011t0001g0060 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-19+5854T>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195902631 | ||||||
| chr3:195902646
|
T | G | 2 | a0001c0002t0001g0018a0002c0023t0001g0017 | 2 | HG02809.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.-19+5839A>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195902646 | ||||||
| chr3:195902646
|
T | TA | 24 | a0001c0001t0001g0353a0001c0002t0001g0003a0001c0002t0001g0045others(21): Show | 26 | HG00621.hp2 HG01192.hp1 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.-19+5838dupT | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195902646 | ||||||
| chr3:195902646
|
TA | T | 55 | a0001c0001t0001g0001a0001c0001t0001g0076a0001c0001t0001g0246others(52): Show | 56 | HG00140.hp1 HG00639.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.-19+5838delT | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195902646 | ||||||
| chr3:195902646
|
TAA | T | 110 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(107): Show | 111 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.-19+5837_-19+5838d others(4): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195902646 | ||||||
| chr3:195902685
|
A | C | 3 | a0001c0040t0001g0019a0002c0010t0001g0053a0003c0005t0001g0054 | 3 | HG00673.hp2 HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-19+5800T>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195902685 | ||||||
| chr3:195902770
|
G | A | 1 | a0001c0003t0005g0201 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-19+5715C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195902770 | ||||||
| chr3:195902819
|
G | A | 28 | a0001c0001t0002g0050a0001c0002t0001g0029a0001c0002t0001g0031others(25): Show | 28 | HG00323.hp1 HG00597.hp1 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.-19+5666C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195902819 | ||||||
| chr3:195902908
|
C | T | 1 | a0001c0003t0002g0127 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-19+5577G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195902908 | ||||||
| chr3:195902911
|
G | A | 113 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(110): Show | 114 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.-19+5574C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195902911 | ||||||
| chr3:195902943
|
T | G | 1 | a0003c0005t0001g0046 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-19+5542A>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195902943 | ||||||
| chr3:195902956
|
C | A | 8 | a0001c0003t0001g0195a0001c0003t0001g0200a0001c0003t0005g0196others(5): Show | 8 | HG00558.hp2 HG02132.hp1 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.-19+5529G>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195902956 | ||||||
| chr3:195903009
|
C | CA | 116 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(113): Show | 117 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.-19+5475dupT | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195903009 | ||||||
| chr3:195903029
|
C | T | 1 | a0001c0001t0001g0001 | 2 | HG03017.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.-19+5456G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195903029 | ||||||
| chr3:195903046
|
G | A | 5 | a0001c0058t0004g0237a0001c0061t0001g0238a0001c0062t0001g0239others(2): Show | 5 | HG02922.hp2 HG03130.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19+5439C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195903046 | ||||||
| chr3:195903109
|
C | T | 42 | a0001c0001t0001g0001a0001c0001t0001g0076a0001c0001t0002g0062others(39): Show | 43 | HG00140.hp1 HG00639.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.-19+5376G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195903109 | ||||||
| chr3:195903265
|
C | T | 20 | a0001c0002t0001g0003a0001c0002t0001g0211a0001c0002t0001g0212others(17): Show | 22 | HG01192.hp1 HG01934.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.-19+5220G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195903265 | ||||||
| chr3:195903315
|
C | T | 102 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0116others(99): Show | 102 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.-19+5170G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195903315 | ||||||
| chr3:195903347
|
A | C | 1 | a0003c0005t0001g0245 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-19+5138T>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195903347 | ||||||
| chr3:195903364
|
G | C | 3 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0049 | 3 | HG00280.hp1 HG01433.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.-19+5121C>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195903364 | ||||||
| chr3:195903389
|
T | C | 3 | a0001c0002t0001g0202a0001c0002t0001g0203a0002c0008t0001g0204 | 3 | NA18940.hp2 NA18948.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.-19+5096A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195903389 | ||||||
| chr3:195903469
|
G | A | 1 | a0001c0006t0001g0092 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-19+5016C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195903469 | ||||||
| chr3:195903494
|
G | C | 1 | a0001c0002t0001g0049 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-19+4991C>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195903494 | ||||||
| chr3:195903497
|
A | G | 1 | a0001c0002t0001g0101 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-19+4988T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195903497 | ||||||
| chr3:195903503
|
G | A | 1 | a0007c0021t0001g0118 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-19+4982C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195903503 | ||||||
| chr3:195903662
|
T | A | 116 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(113): Show | 117 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.-19+4823A>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195903662 | ||||||
| chr3:195903941
|
C | T | 42 | a0001c0001t0001g0001a0001c0001t0001g0076a0001c0001t0002g0062others(39): Show | 43 | HG00140.hp1 HG00639.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.-19+4544G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195903941 | ||||||
| chr3:195904009
|
G | A | 3 | a0001c0001t0002g0050a0001c0002t0001g0052a0003c0005t0001g0051 | 3 | HG01081.hp1 HG01255.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-19+4476C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195904009 | ||||||
| chr3:195904014
|
C | A | 1 | a0002c0060t0001g0240 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-19+4471G>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195904014 | ||||||
| chr3:195904099
|
C | CA | 116 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(113): Show | 117 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.-19+4385dupT | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195904099 | ||||||
| chr3:195904120
|
T | C | 5 | a0001c0058t0004g0237a0001c0061t0001g0238a0001c0062t0001g0239others(2): Show | 5 | HG02922.hp2 HG03130.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19+4365A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195904120 | ||||||
| chr3:195904184
|
G | T | 102 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0116others(99): Show | 102 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.-19+4301C>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195904184 | ||||||
| chr3:195904228
|
G | T | 22 | a0001c0001t0007g0232a0001c0002t0001g0003a0001c0002t0001g0211others(19): Show | 24 | HG01192.hp1 HG01934.hp1 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.-19+4257C>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195904228 | ||||||
| chr3:195904262
|
T | TA | 28 | a0001c0002t0001g0003a0001c0002t0001g0101a0001c0002t0001g0215others(25): Show | 30 | HG00673.hp2 HG01069.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.-19+4222dupT | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195904262 | ||||||
| chr3:195904361
|
GA | G | 11 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(8): Show | 11 | HG01975.hp2 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.-19+4123delT | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195904361 | ||||||
| chr3:195904401
|
T | A | 2 | a0001c0001t0001g0355a0001c0001t0001g0356 | 2 | HG03491.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.-19+4084A>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195904401 | ||||||
| chr3:195904591
|
A | T | 116 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(113): Show | 117 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.-19+3894T>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195904591 | ||||||
| chr3:195904747
|
T | A | 3 | a0001c0002t0001g0226a0001c0002t0001g0227a0001c0002t0001g0228 | 3 | HG02486.hp1 HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-19+3738A>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195904747 | ||||||
| chr3:195904918
|
A | G | 1 | a0001c0001t0001g0244 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-19+3567T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195904918 | ||||||
| chr3:195904984
|
C | T | 3 | a0001c0003t0003g0124a0001c0003t0003g0125a0001c0003t0003g0126 | 3 | HG01496.hp2 HG02148.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.-19+3501G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195904984 | ||||||
| chr3:195905157
|
G | A | 2 | a0001c0001t0001g0358a0002c0004t0001g0357 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-19+3328C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195905157 | ||||||
| chr3:195905174
|
G | C | 11 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(8): Show | 11 | HG01975.hp2 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.-19+3311C>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195905174 | ||||||
| chr3:195905259
|
G | A | 102 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0116others(99): Show | 102 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.-19+3226C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195905259 | ||||||
| chr3:195905303
|
G | A | 2 | a0003c0005t0001g0058a0003c0005t0001g0059 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-19+3182C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195905303 | ||||||
| chr3:195905362
|
G | A | 1 | a0001c0012t0011g0102 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-19+3123C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195905362 | ||||||
| chr3:195905629
|
G | A | 1 | a0001c0002t0001g0235 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-19+2856C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195905629 | ||||||
| chr3:195905808
|
C | A | 106 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0116others(103): Show | 107 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.-19+2677G>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195905808 | ||||||
| chr3:195905949
|
A | C | 113 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(110): Show | 114 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.-19+2536T>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195905949 | ||||||
| chr3:195905950
|
G | A | 113 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(110): Show | 114 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.-19+2535C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195905950 | ||||||
| chr3:195905991
|
T | C | 363 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0056others(360): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.-19+2494A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195905991 | ||||||
| chr3:195906061
|
CAT | C | 4 | a0001c0002t0001g0205a0001c0011t0001g0107a0001c0011t0001g0108others(1): Show | 4 | HG01175.hp1 HG01884.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+2422_-19+2423d others(4): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195906061 | ||||||
| chr3:195906075
|
C | T | 100 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0116others(97): Show | 100 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.-19+2410G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195906075 | ||||||
| chr3:195906255
|
A | C | 2 | a0001c0003t0001g0122a0026c0048t0001g0123 | 2 | HG02523.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.-19+2230T>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195906255 | ||||||
| chr3:195906257
|
A | G | 2 | a0001c0003t0001g0122a0026c0048t0001g0123 | 2 | HG02523.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.-19+2228T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195906257 | ||||||
| chr3:195906298
|
T | C | 1 | a0016c0051t0001g0208 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-19+2187A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195906298 | ||||||
| chr3:195906306
|
C | G | 42 | a0001c0001t0002g0050a0001c0002t0001g0029a0001c0002t0001g0031others(39): Show | 42 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.-19+2179G>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195906306 | ||||||
| chr3:195906316
|
C | A | 4 | a0001c0002t0001g0011a0002c0008t0001g0010a0012c0045t0001g0009others(1): Show | 4 | HG02647.hp1 HG02723.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+2169G>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195906316 | ||||||
| chr3:195906356
|
A | C | 2 | a0001c0058t0004g0237a0002c0057t0004g0236 | 2 | HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-19+2129T>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195906356 | ||||||
| chr3:195906490
|
C | T | 13 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0116others(10): Show | 13 | HG00323.hp2 HG01361.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.-19+1995G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195906490 | ||||||
| chr3:195906564
|
C | T | 35 | a0001c0001t0002g0050a0001c0002t0001g0029a0001c0002t0001g0031others(32): Show | 35 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.-19+1921G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195906564 | ||||||
| chr3:195906567
|
G | A | 105 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0116others(102): Show | 106 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.-19+1918C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195906567 | ||||||
| chr3:195906677
|
G | A | 105 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0116others(102): Show | 106 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.-19+1808C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195906677 | ||||||
| chr3:195906746
|
T | C | 242 | a0001c0001t0001g0001a0001c0001t0001g0076a0001c0001t0001g0095others(239): Show | 246 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.-19+1739A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195906746 | ||||||
| chr3:195906825
|
G | A | 105 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0116others(102): Show | 106 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.-19+1660C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195906825 | ||||||
| chr3:195906925
|
T | C | 11 | a0001c0002t0001g0011a0001c0002t0001g0018a0001c0017t0006g0012others(8): Show | 11 | HG02486.hp2 HG02630.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.-19+1560A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195906925 | ||||||
| chr3:195906929
|
G | A | 2 | a0001c0001t0001g0209a0001c0001t0001g0210 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-19+1556C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195906929 | ||||||
| chr3:195907110
|
C | T | 1 | a0002c0066t0002g0242 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-19+1375G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195907110 | ||||||
| chr3:195907156
|
A | G | 1 | a0002c0004t0002g0241 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-19+1329T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195907156 | ||||||
| chr3:195907373
|
T | C | 103 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0116others(100): Show | 103 | HG00323.hp2 HG00423.hp2 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.-19+1112A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195907373 | ||||||
| chr3:195907433
|
C | G | 40 | a0001c0001t0002g0050a0001c0002t0001g0029a0001c0002t0001g0031others(37): Show | 40 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.-19+1052G>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195907433 | ||||||
| chr3:195907444
|
C | T | 1 | a0010c0059t0001g0021 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-19+1041G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195907444 | ||||||
| chr3:195907720
|
G | A | 11 | a0001c0002t0001g0011a0001c0002t0001g0018a0001c0017t0006g0012others(8): Show | 11 | HG02486.hp2 HG02630.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.-19+765C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195907720 | ||||||
| chr3:195907754
|
C | G | 1 | a0017c0035t0004g0233 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-19+731G>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195907754 | ||||||
| chr3:195908051
|
A | G | 4 | a0001c0002t0001g0011a0002c0008t0001g0010a0012c0045t0001g0009others(1): Show | 4 | HG02647.hp1 HG02723.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+434T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195908051 | ||||||
| chr3:195908106
|
A | ACTTGTGT others(46): Show |
1 | a0003c0015t0001g0020 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-19+326_-19+378dup others(53): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195908106 | ||||||
| chr3:195908122
|
C | T | 1 | a0001c0040t0001g0019 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-19+363G>A | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195908122 | ||||||
| chr3:195908134
|
C | CAT | 11 | a0001c0002t0001g0011a0001c0002t0001g0018a0001c0017t0006g0012others(8): Show | 11 | HG02486.hp2 HG02630.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.-19+349_-19+350dup others(2): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195908134 | ||||||
| chr3:195908138
|
T | C | 23 | a0001c0002t0001g0003a0001c0002t0001g0211a0001c0002t0001g0212others(20): Show | 25 | HG01192.hp1 HG01934.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.-19+347A>G | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195908138 | ||||||
| chr3:195908177
|
G | A | 1 | a0001c0001t0007g0232 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-19+308C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195908177 | ||||||
| chr3:195908241
|
C | A | 2 | a0001c0042t0001g0234a0017c0035t0004g0233 | 2 | HG02615.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-19+244G>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195908241 | ||||||
| chr3:195908373
|
G | A | 6 | a0001c0002t0001g0235a0001c0058t0004g0237a0001c0061t0001g0238others(3): Show | 6 | HG02257.hp1 HG02922.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19+112C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195908373 | ||||||
| chr3:195908386
|
A | G | 240 | a0001c0001t0001g0001a0001c0001t0001g0056a0001c0001t0001g0076others(237): Show | 244 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.-19+99T>C | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195908386 | ||||||
| chr3:195908423
|
G | A | 2 | a0001c0001t0001g0363a0001c0001t0001g0364 | 2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-19+62C>T | TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 1/15 | chr3 | 195908423 |