Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 11011 |
|---|---|
| ensemblid | ENSG00000146872.19 |
| hgncid | 11842 |
| symbol | TLK2 |
| name | tousled like kinase 2 |
| refseq_nuc | NM_006852.6 |
| refseq_prot | NP_006843.2 |
| ensembl_nuc | ENST00000346027.10 |
| ensembl_prot | ENSP00000275780.7 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 62478825 |
| end | 62615481 |
| strand | + |
| ver | v1.2 |
| region | chr17:62478825-62615481 |
| region5000 | chr17:62473825-62620481 |
| regionname0 | TLK2_chr17_62478825_62615481 |
| regionname5000 | TLK2_chr17_62473825_62620481 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 750 | 292 | 80 | 66 | 100 | 12 | 32 | 78 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 2253 | 151 | 66 | 32 | 36 | 6 | 10 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| c0002 | 0/1 | 2253 | 138 | 12 | 34 | 64 | 6 | 21 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| c0003 | 0/0 | 2253 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| c0004 | 0/0 | 2253 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| c0005 | 0/0 | 2253 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 3388 | 97 | 28 | 20 | 33 | 6 | 9 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| t0002 | 0/1 | 3388 | 76 | 8 | 17 | 32 | 5 | 13 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| t0003 | 0/0 | 3387 | 44 | 11 | 8 | 18 | 0 | 7 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| t0004 | 0/0 | 3388 | 17 | 10 | 4 | 2 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| t0005 | 0/0 | 3389 | 6 | 1 | 3 | 2 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| t0006 | 0/0 | 3388 | 5 | 5 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| t0007 | 0/0 | 3387 | 5 | 1 | 2 | 1 | 1 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| t0008 | 0/0 | 3388 | 4 | 1 | 2 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| t0009 | 0/0 | 3387 | 4 | 4 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| t0010 | 0/0 | 3388 | 4 | 4 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| t0011 | 0/0 | 3388 | 4 | 0 | 0 | 4 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| t0012 | 0/0 | 3388 | 3 | 0 | 3 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| t0013 | 0/0 | 3388 | 3 | 0 | 0 | 3 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| t0014 | 0/0 | 3389 | 2 | 1 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| t0015 | 0/0 | 3389 | 2 | 1 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| t0016 | 0/0 | 3388 | 2 | 0 | 2 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| t0017 | 0/0 | 3389 | 2 | 1 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| t0018 | 0/0 | 3389 | 2 | 1 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| t0019 | 0/0 | 3389 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| t0020 | 0/0 | 3388 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| t0021 | 0/0 | 3388 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| t0022 | 0/0 | 3389 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| t0023 | 0/0 | 3389 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| t0024 | 0/0 | 3389 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| t0025 | 0/0 | 3388 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| t0026 | 0/0 | 3387 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| t0027 | 0/0 | 3387 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| t0028 | 0/0 | 3388 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0114 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0169 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2253 | 151 | 66 | 32 | 36 | 6 | 10 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| a0001c0002 | 0/1 | 2253 | 138 | 12 | 34 | 64 | 6 | 21 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| a0001c0003 | 0/0 | 2253 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| a0001c0004 | 0/0 | 2253 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| a0001c0005 | 0/0 | 2253 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 5640 | 96 | 27 | 20 | 33 | 6 | 9 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| a0001c0001t0003 | 0/0 | 5639 | 14 | 11 | 3 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| a0001c0001t0004 | 0/0 | 5640 | 11 | 9 | 2 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| a0001c0001t0006 | 0/0 | 5640 | 5 | 5 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| a0001c0001t0008 | 0/0 | 5640 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| a0001c0001t0009 | 0/0 | 5639 | 4 | 4 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| a0001c0001t0010 | 0/0 | 5640 | 4 | 4 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| a0001c0001t0012 | 0/0 | 5640 | 3 | 0 | 3 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| a0001c0001t0014 | 0/0 | 5641 | 2 | 1 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| a0001c0001t0016 | 0/0 | 5640 | 2 | 0 | 2 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| a0001c0001t0017 | 0/0 | 5641 | 2 | 1 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| a0001c0001t0018 | 0/0 | 5641 | 2 | 1 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| a0001c0001t0021 | 0/0 | 5640 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| a0001c0001t0024 | 0/0 | 5641 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| a0001c0001t0025 | 0/0 | 5640 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| a0001c0001t0026 | 0/0 | 5639 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| a0001c0001t0027 | 0/0 | 5639 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| a0001c0002t0002 | 0/1 | 5640 | 75 | 7 | 17 | 32 | 5 | 13 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| a0001c0002t0003 | 0/0 | 5639 | 30 | 0 | 5 | 18 | 0 | 7 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| a0001c0002t0004 | 0/0 | 5640 | 6 | 1 | 2 | 2 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| a0001c0002t0005 | 0/0 | 5641 | 6 | 1 | 3 | 2 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| a0001c0002t0007 | 0/0 | 5639 | 5 | 1 | 2 | 1 | 1 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| a0001c0002t0008 | 0/0 | 5640 | 2 | 0 | 2 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| a0001c0002t0011 | 0/0 | 5640 | 4 | 0 | 0 | 4 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| a0001c0002t0013 | 0/0 | 5640 | 3 | 0 | 0 | 3 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| a0001c0002t0015 | 0/0 | 5641 | 2 | 1 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| a0001c0002t0019 | 0/0 | 5641 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| a0001c0002t0020 | 0/0 | 5640 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| a0001c0002t0022 | 0/0 | 5641 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| a0001c0002t0023 | 0/0 | 5641 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| a0001c0002t0028 | 0/0 | 5640 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| a0001c0003t0008 | 0/0 | 5640 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| a0001c0004t0001 | 0/0 | 5640 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| a0001c0005t0002 | 0/0 | 5640 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | copy fasta | chr17 | 62473825 | 62620481 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0169 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0004g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0004g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0004g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0004g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0004g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0006g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0006g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0006g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0006g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0006g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0008g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0009g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0009g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0009g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0009g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0010g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0010g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0010g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0010g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0012g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0012g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0012g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0014g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0014g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0016g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0016g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0017g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0017g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0018g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0018g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0021g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0024g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0025g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0026g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0001t0027g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0114 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0003g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0003g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0003g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0003g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0003g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0003g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0003g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0003g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0004g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0004g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0004g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0004g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0004g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0005g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0005g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0005g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0005g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0005g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0005g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0007g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0007g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0007g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0007g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0007g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0008g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0008g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0011g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0011g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0011g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0011g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0013g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0013g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0013g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0015g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0015g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0019g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0020g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0022g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0023g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0002t0028g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0003t0008g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0004t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| a0001c0005t0002g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0002 | t0002 | g0102 | EUR | GBR | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0246 | EUR | GBR | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG00280 | hp1 | a0001 | c0002 | t0002 | g0040 | EUR | FIN | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0217 | EUR | FIN | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG00323 | hp1 | a0001 | c0002 | t0007 | g0109 | EUR | FIN | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0234 | EUR | FIN | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG00438 | hp1 | a0001 | c0002 | t0003 | g0075 | EAS | CHS | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG00438 | hp2 | a0001 | c0001 | t0025 | g0247 | EAS | CHS | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG00609 | hp1 | a0001 | c0002 | t0002 | g0011 | EAS | CHS | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG00609 | hp2 | a0001 | c0001 | t0024 | g0251 | EAS | CHS | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG00639 | hp1 | a0001 | c0002 | t0007 | g0125 | AMR | PUR | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG00639 | hp2 | a0001 | c0002 | t0007 | g0081 | AMR | PUR | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG00733 | hp2 | a0001 | c0002 | t0002 | g0110 | AMR | PUR | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG00735 | hp2 | a0001 | c0002 | t0002 | g0090 | AMR | PUR | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG00738 | hp1 | a0001 | c0002 | t0002 | g0088 | AMR | PUR | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG00738 | hp2 | a0001 | c0001 | t0012 | g0149 | AMR | PUR | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG00741 | hp1 | a0001 | c0002 | t0004 | g0091 | AMR | PUR | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0165 | AMR | PUR | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG01069 | hp2 | a0001 | c0002 | t0002 | g0089 | AMR | PUR | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG01071 | hp1 | a0001 | c0002 | t0002 | g0093 | AMR | PUR | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0166 | AMR | PUR | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG01074 | hp2 | a0001 | c0001 | t0012 | g0148 | AMR | PUR | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG01081 | hp2 | a0001 | c0002 | t0002 | g0085 | AMR | PUR | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG01099 | hp1 | a0001 | c0002 | t0004 | g0139 | AMR | PUR | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG01099 | hp2 | a0001 | c0002 | t0002 | g0082 | AMR | PUR | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG01109 | hp2 | a0001 | c0001 | t0017 | g0284 | AMR | PUR | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG01167 | hp1 | a0001 | c0002 | t0002 | g0012 | AMR | PUR | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG01168 | hp1 | a0001 | c0002 | t0002 | g0128 | AMR | PUR | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0152 | AMR | PUR | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG01192 | hp1 | a0001 | c0002 | t0008 | g0046 | AMR | PUR | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG01192 | hp2 | a0001 | c0002 | t0019 | g0016 | AMR | PUR | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG01243 | hp1 | a0001 | c0001 | t0016 | g0185 | AMR | PUR | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG01255 | hp1 | a0001 | c0001 | t0016 | g0186 | AMR | CLM | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG01255 | hp2 | a0001 | c0002 | t0002 | g0108 | AMR | CLM | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG01258 | hp1 | a0001 | c0002 | t0002 | g0087 | AMR | CLM | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG01261 | hp1 | a0001 | c0002 | t0003 | g0157 | AMR | CLM | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG01261 | hp2 | a0001 | c0002 | t0002 | g0106 | AMR | CLM | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG01358 | hp2 | a0001 | c0001 | t0012 | g0151 | AMR | CLM | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | CLM | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG01433 | hp2 | a0001 | c0002 | t0003 | g0069 | AMR | CLM | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0291 | AMR | CLM | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG01496 | hp2 | a0001 | c0002 | t0005 | g0084 | AMR | CLM | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG01515 | hp1 | a0001 | c0002 | t0002 | g0103 | EUR | IBS | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0231 | EUR | IBS | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0229 | EUR | IBS | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG01516 | hp2 | a0001 | c0002 | t0002 | g0119 | EUR | IBS | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0050 | AFR | ACB | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | ACB | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ACB | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0172 | AFR | ACB | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PEL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG01928 | hp2 | a0001 | c0002 | t0002 | g0024 | AMR | PEL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PEL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG01934 | hp2 | a0001 | c0002 | t0015 | g0037 | AMR | PEL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG01943 | hp1 | a0001 | c0002 | t0002 | g0010 | AMR | PEL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG01943 | hp2 | a0001 | c0002 | t0003 | g0045 | AMR | PEL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG01952 | hp1 | a0001 | c0002 | t0008 | g0047 | AMR | PEL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG01952 | hp2 | a0001 | c0001 | t0021 | g0153 | AMR | PEL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG01978 | hp1 | a0001 | c0002 | t0005 | g0155 | AMR | PEL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG01978 | hp2 | a0001 | c0002 | t0028 | g0005 | AMR | PEL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PEL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG01993 | hp1 | a0001 | c0002 | t0003 | g0043 | AMR | PEL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG01993 | hp2 | a0001 | c0002 | t0002 | g0015 | AMR | PEL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02004 | hp2 | a0001 | c0002 | t0002 | g0021 | AMR | PEL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02015 | hp1 | a0001 | c0002 | t0002 | g0099 | EAS | KHV | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02015 | hp2 | a0001 | c0002 | t0003 | g0212 | EAS | KHV | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02027 | hp2 | a0001 | c0002 | t0003 | g0057 | EAS | KHV | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02040 | hp1 | a0001 | c0002 | t0003 | g0023 | EAS | KHV | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02040 | hp2 | a0001 | c0002 | t0002 | g0051 | EAS | KHV | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02055 | hp1 | a0001 | c0002 | t0022 | g0138 | AFR | ACB | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | ACB | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02074 | hp1 | a0001 | c0002 | t0002 | g0032 | EAS | KHV | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02074 | hp2 | a0001 | c0002 | t0003 | g0073 | EAS | KHV | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02080 | hp1 | a0001 | c0002 | t0005 | g0038 | EAS | KHV | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02080 | hp2 | a0001 | c0002 | t0002 | g0134 | EAS | KHV | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02083 | hp2 | a0001 | c0002 | t0002 | g0013 | EAS | KHV | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02132 | hp1 | a0001 | c0002 | t0002 | g0034 | EAS | KHV | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02132 | hp2 | a0001 | c0002 | t0003 | g0058 | EAS | KHV | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02155 | hp1 | a0001 | c0002 | t0002 | g0135 | EAS | CDX | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02155 | hp2 | a0001 | c0002 | t0003 | g0068 | EAS | CDX | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02165 | hp1 | a0001 | c0002 | t0002 | g0029 | EAS | CDX | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | CDX | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0164 | AFR | ACB | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02258 | hp2 | a0001 | c0002 | t0005 | g0124 | AFR | ACB | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02273 | hp1 | a0001 | c0002 | t0002 | g0007 | AMR | PEL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0054 | AFR | ACB | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02280 | hp2 | a0001 | c0002 | t0002 | g0094 | AFR | ACB | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02293 | hp1 | a0001 | c0001 | t0004 | g0150 | AMR | PEL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02293 | hp2 | a0001 | c0002 | t0003 | g0044 | AMR | PEL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02300 | hp1 | a0001 | c0002 | t0005 | g0006 | AMR | PEL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0159 | AMR | PEL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02451 | hp1 | a0001 | c0001 | t0010 | g0282 | AFR | ACB | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02451 | hp2 | a0001 | c0001 | t0009 | g0287 | AFR | ACB | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02602 | hp1 | a0001 | c0003 | t0008 | g0071 | SAS | PJL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02602 | hp2 | a0001 | c0001 | t0014 | g0267 | SAS | PJL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | GWD | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02622 | hp2 | a0001 | c0001 | t0006 | g0056 | AFR | GWD | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02630 | hp1 | a0001 | c0001 | t0009 | g0286 | AFR | GWD | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0158 | AFR | GWD | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02647 | hp1 | a0001 | c0001 | t0006 | g0041 | AFR | GWD | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | GWD | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02683 | hp1 | a0001 | c0002 | t0002 | g0116 | SAS | PJL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02683 | hp2 | a0001 | c0002 | t0004 | g0156 | SAS | PJL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02698 | hp2 | a0001 | c0002 | t0002 | g0086 | SAS | PJL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0163 | AFR | GWD | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0049 | AFR | GWD | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02723 | hp2 | a0001 | c0002 | t0002 | g0097 | AFR | GWD | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02735 | hp1 | a0001 | c0002 | t0002 | g0022 | SAS | PJL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02738 | hp1 | a0001 | c0002 | t0002 | g0129 | SAS | PJL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02738 | hp2 | a0001 | c0002 | t0003 | g0078 | SAS | PJL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0161 | AFR | GWD | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0162 | AFR | GWD | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02818 | hp2 | a0001 | c0001 | t0010 | g0281 | AFR | GWD | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02886 | hp1 | a0001 | c0002 | t0004 | g0140 | AFR | GWD | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02897 | hp2 | a0001 | c0001 | t0010 | g0280 | AFR | GWD | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0112 | AFR | ESN | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0160 | AFR | ESN | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0175 | AFR | ESN | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | ESN | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02970 | hp2 | a0001 | c0001 | t0006 | g0074 | AFR | ESN | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02976 | hp1 | a0001 | c0001 | t0009 | g0288 | AFR | ESN | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02976 | hp2 | a0001 | c0004 | t0001 | g0204 | AFR | ESN | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG03017 | hp1 | a0001 | c0002 | t0003 | g0060 | SAS | PJL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG03017 | hp2 | a0001 | c0002 | t0002 | g0096 | SAS | PJL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0144 | AFR | GWD | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | MSL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG03098 | hp2 | a0001 | c0002 | t0002 | g0126 | AFR | MSL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ESN | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | ESN | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG03139 | hp1 | a0001 | c0001 | t0010 | g0283 | AFR | ESN | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG03139 | hp2 | a0001 | c0001 | t0014 | g0221 | AFR | ESN | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0048 | AFR | ESN | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | ESN | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | MSL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG03225 | hp2 | a0001 | c0001 | t0006 | g0042 | AFR | MSL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG03239 | hp2 | a0001 | c0002 | t0002 | g0107 | SAS | PJL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | MSL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG03453 | hp2 | a0001 | c0001 | t0027 | g0277 | AFR | MSL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | MSL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0170 | AFR | MSL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG03490 | hp1 | a0001 | c0002 | t0002 | g0120 | SAS | PJL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG03491 | hp1 | a0001 | c0002 | t0002 | g0092 | SAS | PJL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG03491 | hp2 | a0001 | c0002 | t0003 | g0065 | SAS | PJL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG03492 | hp1 | a0001 | c0002 | t0003 | g0064 | SAS | PJL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0055 | AFR | GWD | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0147 | AFR | GWD | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG03579 | hp1 | a0001 | c0002 | t0002 | g0127 | AFR | MSL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0171 | AFR | MSL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG03654 | hp1 | a0001 | c0002 | t0002 | g0083 | SAS | PJL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG03704 | hp1 | a0001 | c0002 | t0002 | g0115 | SAS | PJL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG03942 | hp1 | a0001 | c0002 | t0002 | g0131 | SAS | BEB | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG03942 | hp2 | a0001 | c0002 | t0003 | g0141 | SAS | BEB | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG04204 | hp1 | a0001 | c0002 | t0003 | g0063 | SAS | STU | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG04204 | hp2 | a0001 | c0002 | t0002 | g0105 | SAS | STU | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0254 | SAS | STU | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG04228 | hp2 | a0001 | c0002 | t0003 | g0079 | SAS | STU | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0167 | AFR | YRI | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | YRI | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0146 | AFR | YRI | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA18906 | hp2 | a0001 | c0001 | t0026 | g0278 | AFR | YRI | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA18940 | hp1 | a0001 | c0002 | t0011 | g0143 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA18941 | hp1 | a0001 | c0002 | t0003 | g0142 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA18941 | hp2 | a0001 | c0002 | t0002 | g0033 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA18942 | hp1 | a0001 | c0002 | t0002 | g0031 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA18943 | hp2 | a0001 | c0002 | t0002 | g0025 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA18947 | hp2 | a0001 | c0002 | t0002 | g0014 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA18948 | hp1 | a0001 | c0002 | t0007 | g0036 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA18952 | hp1 | a0001 | c0002 | t0003 | g0066 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA18952 | hp2 | a0001 | c0002 | t0011 | g0104 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA18954 | hp1 | a0001 | c0002 | t0011 | g0117 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA18959 | hp2 | a0001 | c0002 | t0011 | g0111 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA18960 | hp1 | a0001 | c0002 | t0002 | g0017 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA18963 | hp1 | a0001 | c0002 | t0020 | g0001 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA18966 | hp1 | a0001 | c0002 | t0002 | g0030 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA18973 | hp1 | a0001 | c0002 | t0003 | g0077 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA18977 | hp1 | a0001 | c0002 | t0013 | g0100 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA18977 | hp2 | a0001 | c0002 | t0003 | g0059 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA18983 | hp1 | a0001 | c0002 | t0002 | g0019 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA18983 | hp2 | a0001 | c0002 | t0002 | g0095 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA18986 | hp1 | a0001 | c0002 | t0003 | g0062 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA18988 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA18988 | hp2 | a0001 | c0002 | t0003 | g0067 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA18990 | hp1 | a0001 | c0002 | t0002 | g0035 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA18992 | hp2 | a0001 | c0002 | t0003 | g0052 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA18994 | hp1 | a0001 | c0002 | t0023 | g0098 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA18994 | hp2 | a0001 | c0002 | t0004 | g0177 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA18998 | hp1 | a0001 | c0002 | t0002 | g0039 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA18999 | hp1 | a0001 | c0002 | t0002 | g0027 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA19000 | hp1 | a0001 | c0001 | t0018 | g0243 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA19000 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA19003 | hp1 | a0001 | c0002 | t0002 | g0026 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA19004 | hp1 | a0001 | c0002 | t0002 | g0121 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA19005 | hp2 | a0001 | c0002 | t0013 | g0113 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA19007 | hp2 | a0001 | c0002 | t0002 | g0136 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA19009 | hp1 | a0001 | c0002 | t0002 | g0130 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA19009 | hp2 | a0001 | c0002 | t0003 | g0070 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0168 | AFR | LWK | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA19030 | hp2 | a0001 | c0001 | t0017 | g0279 | AFR | LWK | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA19043 | hp1 | a0001 | c0002 | t0007 | g0123 | AFR | LWK | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | LWK | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA19060 | hp2 | a0001 | c0002 | t0002 | g0122 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA19062 | hp2 | a0001 | c0002 | t0002 | g0018 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA19063 | hp2 | a0001 | c0002 | t0005 | g0137 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA19072 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA19074 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA19079 | hp1 | a0001 | c0002 | t0003 | g0072 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA19080 | hp2 | a0001 | c0002 | t0013 | g0101 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA19085 | hp1 | a0001 | c0002 | t0002 | g0133 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA19085 | hp2 | a0001 | c0002 | t0003 | g0061 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA19086 | hp2 | a0001 | c0002 | t0002 | g0028 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA19090 | hp1 | a0001 | c0002 | t0004 | g0053 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA19091 | hp2 | a0001 | c0002 | t0003 | g0076 | EAS | JPT | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA19240 | hp1 | a0001 | c0002 | t0002 | g0080 | AFR | YRI | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0145 | AFR | YRI | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA20129 | hp1 | a0001 | c0001 | t0009 | g0285 | AFR | ASW | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | ASW | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA20805 | hp1 | a0001 | c0002 | t0002 | g0132 | EUR | TSI | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0238 | EUR | TSI | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | GIH | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA20905 | hp2 | a0001 | c0002 | t0002 | g0118 | SAS | GIH | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02109 | hp1 | a0001 | c0001 | t0008 | g0174 | AFR | ACB | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02486 | hp1 | a0001 | c0002 | t0015 | g0173 | AFR | ACB | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | MSL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | MSL | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG06807 | hp1 | a0001 | c0002 | t0002 | g0154 | AFR | USA | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | USA | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA21309 | hp1 | a0001 | c0001 | t0018 | g0255 | AFR | LWK | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| NA21309 | hp2 | a0001 | c0005 | t0002 | g0002 | AFR | LWK | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0002 | g0114 | REF | REF | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0169 | REF | REF | TLK2_chr17_62473825_62620481 | TLK2 | chr17 | 62473825 | 62620481 |
| 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 |
|---|
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:62573260
|
A | G | 1 | a0001c0005 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.1014A>G | p.Gln338Gln | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 12/22 | 1485/5640 | 1014/2253 | 338/750 | chr17 | 62573260 | ||
| chr17:62600723
|
G | A | 1 | a0001c0003 | 1 | HG02602.hp1 | synonymous_variant | LOW | c.1623G>A | p.Ser541Ser | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 18/22 | 2094/5640 | 1623/2253 | 541/750 | chr17 | 62600723 | ||
| chr17:62606142
|
A | G | 3 | a0001c0002a0001c0003a0001c0005 | 140 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(137): Show |
synonymous_variant | LOW | c.1872A>G | p.Pro624Pro | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 20/22 | 2343/5640 | 1872/2253 | 624/750 | chr17 | 62606142 | ||
| chr17:62608088
|
G | A | 1 | a0001c0004 | 1 | HG02976.hp2 | synonymous_variant | LOW | c.2019G>A | p.Thr673Thr | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 21/22 | 2490/5640 | 2019/2253 | 673/750 | chr17 | 62608088 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:62478894
|
A | AC | 7 | a0001c0001t0008a0001c0001t0014a0001c0002t0005others(4): Show | 14 | HG01192.hp1 HG01192.hp2 HG01496.hp2 others(11): Show |
5_prime_UTR_variant | MODIFIER | c.-395dupC | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 1/22 | 2224 | INFO_REALIGN_3_PRIME | chr17 | 62478894 | ||||
| chr17:62479143
|
C | T | 1 | a0001c0002t0011 | 4 | NA18940.hp1 NA18952.hp2 NA18954.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-153C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 1/22 | 1983 | chr17 | 62479143 | |||||
| chr17:62612784
|
C | T | 1 | a0001c0002t0028 | 1 | HG01978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*219C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 22/22 | 219 | chr17 | 62612784 | |||||
| chr17:62613336
|
T | G | 1 | a0001c0001t0021 | 1 | HG01952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*771T>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 22/22 | 771 | chr17 | 62613336 | |||||
| chr17:62613713
|
G | A | 23 | a0001c0001t0003a0001c0001t0004a0001c0001t0006others(20): Show | 179 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(176): Show |
3_prime_UTR_variant | MODIFIER | c.*1148G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 22/22 | 1148 | chr17 | 62613713 | |||||
| chr17:62613743
|
T | A | 1 | a0001c0001t0024 | 1 | HG00609.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1178T>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 22/22 | 1178 | chr17 | 62613743 | |||||
| chr17:62613863
|
C | T | 10 | a0001c0002t0002a0001c0002t0005a0001c0002t0007others(7): Show | 99 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*1298C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 22/22 | 1298 | chr17 | 62613863 | |||||
| chr17:62613914
|
G | A | 1 | a0001c0001t0016 | 2 | HG01243.hp1 HG01255.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1349G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 22/22 | 1349 | chr17 | 62613914 | |||||
| chr17:62613921
|
C | G | 1 | a0001c0001t0016 | 2 | HG01243.hp1 HG01255.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1356C>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 22/22 | 1356 | chr17 | 62613921 | |||||
| chr17:62614125
|
G | GA | 6 | a0001c0001t0017a0001c0001t0018a0001c0001t0024others(3): Show | 9 | HG00609.hp2 HG01109.hp2 HG01934.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1580dupA | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 22/22 | 1581 | INFO_REALIGN_3_PRIME | chr17 | 62614125 | ||||
| chr17:62614125
|
GA | G | 10 | a0001c0001t0003a0001c0001t0008a0001c0001t0009others(7): Show | 60 | HG00323.hp1 HG00438.hp1 HG00639.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*1580delA | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 22/22 | 1580 | INFO_REALIGN_3_PRIME | chr17 | 62614125 | ||||
| chr17:62614151
|
A | G | 1 | a0001c0001t0025 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1586A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 22/22 | 1586 | chr17 | 62614151 | |||||
| chr17:62614235
|
G | C | 1 | a0001c0001t0009 | 4 | HG02451.hp2 HG02630.hp1 HG02976.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1670G>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 22/22 | 1670 | chr17 | 62614235 | |||||
| chr17:62614329
|
T | G | 1 | a0001c0001t0012 | 3 | HG00738.hp2 HG01074.hp2 HG01358.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1764T>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 22/22 | 1764 | chr17 | 62614329 | |||||
| chr17:62614738
|
C | T | 2 | a0001c0002t0013a0001c0002t0023 | 4 | NA18977.hp1 NA18994.hp1 NA19005.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2173C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 22/22 | 2173 | chr17 | 62614738 | |||||
| chr17:62614879
|
G | A | 4 | a0001c0001t0010a0001c0001t0017a0001c0001t0026others(1): Show | 8 | HG01109.hp2 HG02451.hp1 HG02818.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2314G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 22/22 | 2314 | chr17 | 62614879 | |||||
| chr17:62615085
|
A | G | 1 | a0001c0001t0006 | 5 | HG02622.hp2 HG02647.hp1 HG02970.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2520A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 22/22 | 2520 | chr17 | 62615085 | |||||
| chr17:62615182
|
C | T | 1 | a0001c0001t0027 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2617C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 22/22 | 2617 | chr17 | 62615182 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:62479320
|
A | G | 117 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(114): Show | 117 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.-6+30A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 1/21 | chr17 | 62479320 | ||||||
| chr17:62479323
|
C | G | 2 | a0001c0001t0001g0291a0001c0001t0001g0292 | 2 | HG01175.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.-6+33C>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 1/21 | chr17 | 62479323 | ||||||
| chr17:62479388
|
G | C | 1 | a0001c0002t0020g0001 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-6+98G>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 1/21 | chr17 | 62479388 | ||||||
| chr17:62479438
|
C | T | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-6+148C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 1/21 | chr17 | 62479438 | ||||||
| chr17:62479459
|
C | G | 2 | a0001c0001t0001g0291a0001c0001t0001g0292 | 2 | HG01175.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.-6+169C>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 1/21 | chr17 | 62479459 | ||||||
| chr17:62479873
|
T | C | 270 | a0001c0001t0001g0020a0001c0001t0001g0176a0001c0001t0001g0178others(267): Show | 270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.-6+583T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 1/21 | chr17 | 62479873 | ||||||
| chr17:62480120
|
G | C | 1 | a0001c0005t0002g0002 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-6+830G>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 1/21 | chr17 | 62480120 | ||||||
| chr17:62480574
|
C | T | 2 | a0001c0002t0003g0157a0001c0002t0004g0156 | 2 | HG01261.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.-5-547C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 1/21 | chr17 | 62480574 | ||||||
| chr17:62480628
|
A | T | 278 | a0001c0001t0001g0020a0001c0001t0001g0176a0001c0001t0001g0178others(275): Show | 278 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.-5-493A>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 1/21 | chr17 | 62480628 | ||||||
| chr17:62480732
|
A | G | 2 | a0001c0002t0002g0154a0001c0002t0005g0155 | 2 | HG01978.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-5-389A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 1/21 | chr17 | 62480732 | ||||||
| chr17:62480822
|
A | G | 2 | a0001c0001t0003g0170a0001c0001t0003g0171 | 2 | HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-5-299A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 1/21 | chr17 | 62480822 | ||||||
| chr17:62481256
|
A | G | 10 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0010g0280others(7): Show | 10 | HG01109.hp2 HG02451.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.81+50A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62481256 | ||||||
| chr17:62481283
|
G | T | 10 | a0001c0001t0004g0144a0001c0001t0004g0145a0001c0001t0004g0146others(7): Show | 10 | HG00738.hp2 HG01074.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.81+77G>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62481283 | ||||||
| chr17:62481347
|
TC | T | 8 | a0001c0001t0010g0280a0001c0001t0010g0281a0001c0001t0010g0282others(5): Show | 8 | HG01109.hp2 HG02451.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.81+143delC | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62481347 | |||||
| chr17:62481554
|
A | G | 1 | a0001c0001t0003g0175 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.81+348A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62481554 | ||||||
| chr17:62481723
|
G | A | 37 | a0001c0001t0001g0020a0001c0002t0002g0003a0001c0002t0002g0004others(34): Show | 37 | HG00609.hp1 HG01167.hp1 HG01192.hp2 others(34): Show |
intron_variant | MODIFIER | c.81+517G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62481723 | ||||||
| chr17:62481746
|
G | A | 1 | a0001c0002t0002g0040 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.81+540G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62481746 | ||||||
| chr17:62481902
|
C | T | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | NA18959.hp1 NA18999.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.81+696C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62481902 | ||||||
| chr17:62482180
|
C | T | 1 | a0001c0001t0021g0153 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.81+974C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62482180 | ||||||
| chr17:62482282
|
T | C | 1 | a0001c0001t0006g0041 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.81+1076T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62482282 | ||||||
| chr17:62482371
|
C | T | 1 | a0001c0001t0001g0276 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.81+1165C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62482371 | ||||||
| chr17:62482453
|
G | GT | 99 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(96): Show | 99 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.81+1261dupT | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62482453 | |||||
| chr17:62482523
|
C | T | 2 | a0001c0001t0001g0270a0001c0001t0001g0271 | 2 | NA18942.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.81+1317C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62482523 | ||||||
| chr17:62482581
|
C | T | 3 | a0001c0002t0004g0139a0001c0002t0004g0140a0001c0002t0022g0138 | 3 | HG01099.hp1 HG02055.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.81+1375C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62482581 | ||||||
| chr17:62482695
|
G | C | 1 | a0001c0001t0006g0042 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.81+1489G>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62482695 | ||||||
| chr17:62482946
|
C | T | 1 | a0001c0001t0001g0269 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.81+1740C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62482946 | ||||||
| chr17:62482971
|
G | A | 5 | a0001c0002t0003g0043a0001c0002t0003g0044a0001c0002t0003g0045others(2): Show | 5 | HG01192.hp1 HG01943.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.81+1765G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62482971 | ||||||
| chr17:62483036
|
A | C | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.81+1830A>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62483036 | ||||||
| chr17:62483194
|
C | T | 101 | a0001c0001t0001g0020a0001c0002t0002g0003a0001c0002t0002g0004others(98): Show | 101 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.81+1988C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62483194 | ||||||
| chr17:62483257
|
C | T | 1 | a0001c0002t0003g0157 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.81+2051C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62483257 | ||||||
| chr17:62483392
|
G | A | 2 | a0001c0001t0001g0176a0001c0001t0001g0182 | 2 | HG02486.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.81+2186G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62483392 | ||||||
| chr17:62483418
|
T | C | 1 | a0001c0001t0001g0289 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.81+2212T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62483418 | ||||||
| chr17:62483434
|
T | G | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.81+2228T>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62483434 | ||||||
| chr17:62483496
|
C | T | 99 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(96): Show | 99 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.81+2290C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62483496 | ||||||
| chr17:62483565
|
C | T | 1 | a0001c0001t0008g0174 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.81+2359C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62483565 | ||||||
| chr17:62483824
|
C | A | 1 | a0001c0001t0001g0187 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.81+2618C>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62483824 | ||||||
| chr17:62483897
|
C | T | 1 | a0001c0001t0001g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.81+2691C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62483897 | ||||||
| chr17:62483919
|
G | A | 1 | a0001c0002t0003g0141 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.81+2713G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62483919 | ||||||
| chr17:62483965
|
A | G | 37 | a0001c0001t0001g0020a0001c0002t0002g0003a0001c0002t0002g0004others(34): Show | 37 | HG00609.hp1 HG01167.hp1 HG01192.hp2 others(34): Show |
intron_variant | MODIFIER | c.81+2759A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62483965 | ||||||
| chr17:62484293
|
C | T | 1 | a0001c0001t0001g0268 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.81+3087C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62484293 | ||||||
| chr17:62484444
|
G | A | 2 | a0001c0002t0002g0080a0001c0002t0007g0081 | 2 | HG00639.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.81+3238G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62484444 | ||||||
| chr17:62484546
|
C | T | 3 | a0001c0002t0004g0139a0001c0002t0004g0140a0001c0002t0022g0138 | 3 | HG01099.hp1 HG02055.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.81+3340C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62484546 | ||||||
| chr17:62484589
|
C | T | 3 | a0001c0001t0010g0282a0001c0001t0010g0283a0001c0001t0017g0284 | 3 | HG01109.hp2 HG02451.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.81+3383C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62484589 | ||||||
| chr17:62484715
|
C | T | 1 | a0001c0001t0021g0153 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.81+3509C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62484715 | ||||||
| chr17:62484755
|
T | C | 1 | a0001c0001t0001g0188 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.81+3549T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62484755 | ||||||
| chr17:62484872
|
C | T | 5 | a0001c0002t0002g0133a0001c0002t0002g0134a0001c0002t0002g0135others(2): Show | 5 | HG02080.hp2 HG02155.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.81+3666C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62484872 | ||||||
| chr17:62484937
|
A | G | 113 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(110): Show | 113 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.81+3731A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62484937 | ||||||
| chr17:62485025
|
C | G | 1 | a0001c0002t0002g0132 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.81+3819C>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62485025 | ||||||
| chr17:62485025
|
C | T | 1 | a0001c0002t0002g0039 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.81+3819C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62485025 | ||||||
| chr17:62485026
|
G | A | 1 | a0001c0002t0002g0082 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.81+3820G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62485026 | ||||||
| chr17:62485684
|
A | AGT | 114 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(111): Show | 114 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.81+4479_81+4480dup others(2): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62485684 | |||||
| chr17:62485816
|
G | GT | 69 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0187others(66): Show | 69 | HG00609.hp2 HG00639.hp1 HG01109.hp1 others(66): Show |
intron_variant | MODIFIER | c.81+4632dupT | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62485816 | |||||
| chr17:62485816
|
G | GTT | 13 | a0001c0001t0006g0041a0001c0001t0006g0042a0001c0001t0006g0074others(10): Show | 13 | HG00438.hp1 HG01192.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.81+4631_81+4632dup others(2): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62485816 | |||||
| chr17:62485906
|
C | T | 1 | a0001c0002t0005g0137 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.81+4700C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62485906 | ||||||
| chr17:62486014
|
G | T | 1 | a0001c0001t0001g0250 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.81+4808G>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62486014 | ||||||
| chr17:62486041
|
C | T | 2 | a0001c0001t0001g0248a0001c0001t0001g0249 | 2 | HG01884.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.81+4835C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62486041 | ||||||
| chr17:62486055
|
C | T | 1 | a0001c0001t0025g0247 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.81+4849C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62486055 | ||||||
| chr17:62486201
|
G | A | 1 | a0001c0001t0021g0153 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.81+4995G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62486201 | ||||||
| chr17:62486808
|
T | C | 1 | a0001c0002t0002g0051 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.81+5602T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62486808 | ||||||
| chr17:62486942
|
A | G | 1 | a0001c0002t0003g0079 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.81+5736A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62486942 | ||||||
| chr17:62487075
|
C | T | 10 | a0001c0001t0004g0144a0001c0001t0004g0145a0001c0001t0004g0146others(7): Show | 10 | HG00738.hp2 HG01074.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.81+5869C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62487075 | ||||||
| chr17:62487141
|
A | G | 1 | a0001c0002t0007g0123 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.81+5935A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62487141 | ||||||
| chr17:62487162
|
T | G | 1 | a0001c0001t0021g0153 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.81+5956T>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62487162 | ||||||
| chr17:62487361
|
C | T | 1 | a0001c0002t0005g0038 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.81+6155C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62487361 | ||||||
| chr17:62487480
|
T | C | 291 | a0001c0001t0001g0020a0001c0001t0001g0176a0001c0001t0001g0178others(288): Show | 291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.81+6274T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62487480 | ||||||
| chr17:62487487
|
C | T | 8 | a0001c0002t0002g0121a0001c0002t0002g0122a0001c0002t0002g0133others(5): Show | 8 | HG02080.hp2 HG02155.hp1 NA18963.hp1 others(5): Show |
intron_variant | MODIFIER | c.81+6281C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62487487 | ||||||
| chr17:62487496
|
C | G | 291 | a0001c0001t0001g0020a0001c0001t0001g0176a0001c0001t0001g0178others(288): Show | 291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.81+6290C>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62487496 | ||||||
| chr17:62487507
|
C | A | 291 | a0001c0001t0001g0020a0001c0001t0001g0176a0001c0001t0001g0178others(288): Show | 291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.81+6301C>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62487507 | ||||||
| chr17:62487509
|
C | A | 291 | a0001c0001t0001g0020a0001c0001t0001g0176a0001c0001t0001g0178others(288): Show | 291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.81+6303C>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62487509 | ||||||
| chr17:62487513
|
C | T | 291 | a0001c0001t0001g0020a0001c0001t0001g0176a0001c0001t0001g0178others(288): Show | 291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.81+6307C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62487513 | ||||||
| chr17:62487518
|
C | CA | 9 | a0001c0001t0004g0172a0001c0001t0026g0278a0001c0001t0027g0277others(6): Show | 9 | HG01891.hp2 HG02074.hp2 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.81+6329dupA | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62487518 | |||||
| chr17:62487518
|
CA | C | 11 | a0001c0001t0004g0144a0001c0001t0004g0145a0001c0001t0004g0146others(8): Show | 11 | HG00738.hp2 HG01074.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.81+6329delA | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62487518 | |||||
| chr17:62487557
|
T | C | 8 | a0001c0001t0010g0280a0001c0001t0010g0281a0001c0001t0010g0282others(5): Show | 8 | HG01109.hp2 HG02451.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.81+6351T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62487557 | ||||||
| chr17:62487604
|
A | C | 1 | a0001c0002t0002g0120 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.81+6398A>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62487604 | ||||||
| chr17:62487618
|
A | ATG | 8 | a0001c0002t0003g0072a0001c0002t0003g0073a0001c0002t0003g0077others(5): Show | 8 | HG02074.hp2 HG02602.hp1 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.81+6413_81+6414ins others(2): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62487618 | |||||
| chr17:62487619
|
T | TG | 26 | a0001c0002t0002g0051a0001c0002t0003g0043a0001c0002t0003g0044others(23): Show | 26 | HG00438.hp1 HG01192.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.81+6413_81+6414ins others(1): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62487619 | ||||||
| chr17:62487620
|
C | CT | 190 | a0001c0001t0001g0020a0001c0001t0001g0178a0001c0001t0001g0188others(187): Show | 190 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.81+6434dupT | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62487620 | |||||
| chr17:62487620
|
C | CTT | 27 | a0001c0001t0001g0176a0001c0001t0001g0179a0001c0001t0001g0181others(24): Show | 27 | HG00140.hp2 HG01175.hp1 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.81+6433_81+6434dup others(2): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62487620 | |||||
| chr17:62487620
|
C | T | 34 | a0001c0002t0002g0051a0001c0002t0003g0043a0001c0002t0003g0044others(31): Show | 34 | HG00438.hp1 HG01192.hp1 HG01261.hp1 others(31): Show |
intron_variant | MODIFIER | c.81+6414C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62487620 | ||||||
| chr17:62487701
|
G | A | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.81+6495G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62487701 | ||||||
| chr17:62487751
|
A | G | 111 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(108): Show | 111 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.81+6545A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62487751 | ||||||
| chr17:62487772
|
C | T | 1 | a0001c0002t0002g0003 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.81+6566C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62487772 | ||||||
| chr17:62487810
|
G | A | 270 | a0001c0001t0001g0020a0001c0001t0001g0176a0001c0001t0001g0178others(267): Show | 270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.81+6604G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62487810 | ||||||
| chr17:62487849
|
C | A | 34 | a0001c0002t0002g0051a0001c0002t0003g0043a0001c0002t0003g0044others(31): Show | 34 | HG00438.hp1 HG01192.hp1 HG01261.hp1 others(31): Show |
intron_variant | MODIFIER | c.81+6643C>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62487849 | ||||||
| chr17:62487850
|
C | T | 97 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(94): Show | 97 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.81+6644C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62487850 | ||||||
| chr17:62488512
|
T | C | 111 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(108): Show | 111 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.81+7306T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62488512 | ||||||
| chr17:62488616
|
A | G | 1 | a0001c0002t0002g0034 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.81+7410A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62488616 | ||||||
| chr17:62488820
|
A | AT | 25 | a0001c0001t0001g0276a0001c0001t0004g0150a0001c0001t0004g0152others(22): Show | 25 | HG00738.hp1 HG00738.hp2 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.81+7637dupT | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62488820 | |||||
| chr17:62488820
|
AT | A | 99 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0182others(96): Show | 99 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.81+7637delT | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62488820 | |||||
| chr17:62488974
|
C | T | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.81+7768C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62488974 | ||||||
| chr17:62489171
|
G | T | 1 | a0001c0002t0002g0118 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.81+7965G>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62489171 | ||||||
| chr17:62489174
|
C | CGT | 66 | a0001c0001t0001g0176a0001c0001t0001g0180a0001c0001t0001g0181others(63): Show | 66 | HG00438.hp1 HG00438.hp2 HG00741.hp1 others(63): Show |
intron_variant | MODIFIER | c.81+7993_81+7994dup others(2): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62489174 | |||||
| chr17:62489174
|
C | CGTGT | 152 | a0001c0001t0001g0020a0001c0001t0001g0178a0001c0001t0001g0188others(149): Show | 152 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.81+7991_81+7994dup others(4): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62489174 | |||||
| chr17:62489174
|
C | CGTGTGT | 19 | a0001c0001t0001g0187a0001c0001t0001g0237a0001c0001t0001g0238others(16): Show | 19 | HG01074.hp1 HG01168.hp2 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.81+7989_81+7994dup others(6): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62489174 | |||||
| chr17:62489174
|
CGT | C | 7 | a0001c0001t0001g0252a0001c0001t0004g0048a0001c0001t0004g0049others(4): Show | 7 | HG00735.hp2 HG01069.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.81+7993_81+7994del others(2): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62489174 | |||||
| chr17:62489200
|
T | TGTG | 3 | a0001c0001t0001g0179a0001c0001t0001g0198a0001c0001t0001g0199 | 3 | HG03704.hp2 NA18986.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.81+7994_81+7995ins others(3): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62489200 | ||||||
| chr17:62489201
|
A | T | 3 | a0001c0001t0001g0179a0001c0001t0001g0198a0001c0001t0001g0199 | 3 | HG03704.hp2 NA18986.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.81+7995A>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62489201 | ||||||
| chr17:62489203
|
A | T | 1 | a0001c0001t0006g0042 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.81+7997A>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62489203 | ||||||
| chr17:62489204
|
T | A | 3 | a0001c0001t0001g0179a0001c0001t0001g0198a0001c0001t0001g0199 | 3 | HG03704.hp2 NA18986.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.81+7998T>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62489204 | ||||||
| chr17:62489347
|
C | T | 1 | a0001c0002t0003g0068 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.81+8141C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62489347 | ||||||
| chr17:62489361
|
C | T | 1 | a0001c0002t0002g0034 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.81+8155C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62489361 | ||||||
| chr17:62489483
|
A | G | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.81+8277A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62489483 | ||||||
| chr17:62489534
|
G | A | 1 | a0001c0002t0002g0008 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.81+8328G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62489534 | ||||||
| chr17:62489727
|
C | A | 97 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(94): Show | 97 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.81+8521C>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62489727 | ||||||
| chr17:62489782
|
T | C | 1 | a0001c0001t0001g0271 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.81+8576T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62489782 | ||||||
| chr17:62489952
|
T | A | 9 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(6): Show | 9 | HG01175.hp1 HG01258.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.81+8746T>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62489952 | ||||||
| chr17:62489975
|
C | T | 1 | a0001c0002t0020g0001 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.81+8769C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62489975 | ||||||
| chr17:62490029
|
C | A | 1 | a0001c0002t0002g0092 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.81+8823C>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62490029 | ||||||
| chr17:62490089
|
G | A | 270 | a0001c0001t0001g0020a0001c0001t0001g0176a0001c0001t0001g0178others(267): Show | 270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.81+8883G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62490089 | ||||||
| chr17:62490148
|
G | C | 2 | a0001c0001t0001g0238a0001c0001t0001g0239 | 2 | HG01168.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.81+8942G>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62490148 | ||||||
| chr17:62490181
|
T | C | 1 | a0001c0002t0003g0057 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.81+8975T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62490181 | ||||||
| chr17:62490220
|
C | T | 138 | a0001c0001t0001g0020a0001c0002t0002g0003a0001c0002t0002g0004others(135): Show | 138 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.81+9014C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62490220 | ||||||
| chr17:62490366
|
C | T | 142 | a0001c0001t0001g0020a0001c0001t0004g0048a0001c0001t0004g0049others(139): Show | 142 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.81+9160C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62490366 | ||||||
| chr17:62490540
|
T | G | 1 | a0001c0002t0003g0058 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.81+9334T>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62490540 | ||||||
| chr17:62490590
|
G | A | 97 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(94): Show | 97 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.81+9384G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62490590 | ||||||
| chr17:62490618
|
T | A | 5 | a0001c0002t0002g0083a0001c0002t0002g0087a0001c0002t0002g0088others(2): Show | 5 | HG00738.hp1 HG01258.hp1 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.81+9412T>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62490618 | ||||||
| chr17:62490637
|
G | A | 3 | a0001c0002t0003g0057a0001c0002t0003g0059a0001c0002t0003g0142 | 3 | HG02027.hp2 NA18941.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.81+9431G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62490637 | ||||||
| chr17:62490644
|
C | T | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.81+9438C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62490644 | ||||||
| chr17:62490831
|
C | T | 1 | a0001c0001t0001g0290 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.81+9625C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62490831 | ||||||
| chr17:62490912
|
A | G | 1 | a0001c0001t0004g0152 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.81+9706A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62490912 | ||||||
| chr17:62491004
|
A | G | 271 | a0001c0001t0001g0020a0001c0001t0001g0176a0001c0001t0001g0178others(268): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.81+9798A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62491004 | ||||||
| chr17:62491041
|
G | C | 1 | a0001c0001t0021g0153 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.81+9835G>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62491041 | ||||||
| chr17:62491142
|
TAG | T | 4 | a0001c0001t0004g0048a0001c0001t0004g0049a0001c0001t0004g0050others(1): Show | 4 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+9937_81+9938del others(2): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62491142 | ||||||
| chr17:62491145
|
T | G | 4 | a0001c0001t0004g0048a0001c0001t0004g0049a0001c0001t0004g0050others(1): Show | 4 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+9939T>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62491145 | ||||||
| chr17:62491217
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.81+10011C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62491217 | ||||||
| chr17:62491227
|
A | G | 1 | a0001c0001t0021g0153 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.81+10021A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62491227 | ||||||
| chr17:62491437
|
C | G | 2 | a0001c0001t0001g0235a0001c0001t0001g0236 | 2 | NA18998.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.81+10231C>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62491437 | ||||||
| chr17:62491585
|
A | G | 4 | a0001c0001t0004g0048a0001c0001t0004g0049a0001c0001t0004g0050others(1): Show | 4 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+10379A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62491585 | ||||||
| chr17:62491648
|
G | A | 1 | a0001c0001t0001g0200 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.81+10442G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62491648 | ||||||
| chr17:62491675
|
G | A | 2 | a0001c0001t0018g0255a0001c0004t0001g0204 | 2 | HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.81+10469G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62491675 | ||||||
| chr17:62491681
|
T | C | 111 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(108): Show | 111 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.81+10475T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62491681 | ||||||
| chr17:62491808
|
T | A | 2 | a0001c0002t0002g0089a0001c0002t0002g0090 | 2 | HG00735.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.81+10602T>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62491808 | ||||||
| chr17:62491820
|
A | G | 3 | a0001c0002t0003g0066a0001c0002t0003g0067a0001c0002t0003g0073 | 3 | HG02074.hp2 NA18952.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.81+10614A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62491820 | ||||||
| chr17:62491848
|
C | T | 3 | a0001c0001t0001g0234a0001c0001t0001g0238a0001c0001t0001g0239 | 3 | HG00323.hp2 HG01168.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.81+10642C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62491848 | ||||||
| chr17:62491861
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.81+10655G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62491861 | ||||||
| chr17:62491957
|
A | G | 2 | a0001c0001t0026g0278a0001c0001t0027g0277 | 2 | HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.81+10751A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62491957 | ||||||
| chr17:62492068
|
A | G | 1 | a0001c0001t0001g0242 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.81+10862A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62492068 | ||||||
| chr17:62492079
|
A | G | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.81+10873A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62492079 | ||||||
| chr17:62492088
|
T | C | 1 | a0001c0001t0018g0243 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.81+10882T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62492088 | ||||||
| chr17:62492315
|
G | T | 5 | a0001c0002t0002g0083a0001c0002t0002g0087a0001c0002t0002g0088others(2): Show | 5 | HG00738.hp1 HG01258.hp1 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.81+11109G>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62492315 | ||||||
| chr17:62492369
|
C | T | 139 | a0001c0001t0001g0020a0001c0002t0002g0003a0001c0002t0002g0004others(136): Show | 139 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.81+11163C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62492369 | ||||||
| chr17:62492457
|
G | GT | 8 | a0001c0001t0001g0246a0001c0001t0001g0274a0001c0001t0001g0292others(5): Show | 8 | HG00140.hp2 HG01109.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.81+11262dupT | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62492457 | |||||
| chr17:62492561
|
G | A | 4 | a0001c0001t0004g0048a0001c0001t0004g0049a0001c0001t0004g0050others(1): Show | 4 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+11355G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62492561 | ||||||
| chr17:62492806
|
A | G | 1 | a0001c0002t0002g0112 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.81+11600A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62492806 | ||||||
| chr17:62493009
|
A | G | 1 | a0001c0002t0003g0069 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.81+11803A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62493009 | ||||||
| chr17:62493022
|
G | C | 1 | a0001c0002t0003g0141 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.81+11816G>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62493022 | ||||||
| chr17:62493071
|
T | C | 6 | a0001c0001t0001g0179a0001c0001t0001g0191a0001c0001t0001g0244others(3): Show | 6 | HG00609.hp2 HG01981.hp2 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.81+11865T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62493071 | ||||||
| chr17:62493529
|
A | G | 2 | a0001c0002t0003g0064a0001c0002t0003g0065 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.81+12323A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62493529 | ||||||
| chr17:62493642
|
C | T | 2 | a0001c0002t0003g0064a0001c0002t0003g0065 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.81+12436C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62493642 | ||||||
| chr17:62493734
|
C | T | 1 | a0001c0001t0001g0290 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.81+12528C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62493734 | ||||||
| chr17:62493842
|
C | T | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.81+12636C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62493842 | ||||||
| chr17:62493923
|
A | G | 1 | a0001c0002t0007g0036 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.81+12717A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62493923 | ||||||
| chr17:62494069
|
G | T | 4 | a0001c0001t0004g0048a0001c0001t0004g0049a0001c0001t0004g0050others(1): Show | 4 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+12863G>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62494069 | ||||||
| chr17:62494084
|
C | T | 271 | a0001c0001t0001g0020a0001c0001t0001g0176a0001c0001t0001g0178others(268): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.81+12878C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62494084 | ||||||
| chr17:62494169
|
G | A | 1 | a0001c0002t0003g0141 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.81+12963G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62494169 | ||||||
| chr17:62494205
|
C | T | 2 | a0001c0002t0002g0033a0001c0002t0002g0035 | 2 | NA18941.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.81+12999C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62494205 | ||||||
| chr17:62494633
|
G | A | 1 | a0001c0001t0004g0048 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.81+13427G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62494633 | ||||||
| chr17:62494941
|
G | A | 3 | a0001c0002t0002g0093a0001c0002t0002g0094a0001c0002t0007g0125 | 3 | HG00639.hp1 HG01071.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.81+13735G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62494941 | ||||||
| chr17:62494994
|
C | T | 1 | a0001c0001t0001g0189 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.81+13788C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62494994 | ||||||
| chr17:62495029
|
T | A | 3 | a0001c0001t0010g0280a0001c0001t0010g0281a0001c0001t0017g0279 | 3 | HG02818.hp2 HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.81+13823T>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62495029 | ||||||
| chr17:62495092
|
G | A | 4 | a0001c0001t0004g0048a0001c0001t0004g0049a0001c0001t0004g0050others(1): Show | 4 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+13886G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62495092 | ||||||
| chr17:62495183
|
G | A | 1 | a0001c0002t0003g0069 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.81+13977G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62495183 | ||||||
| chr17:62495259
|
C | T | 3 | a0001c0002t0004g0139a0001c0002t0004g0140a0001c0002t0022g0138 | 3 | HG01099.hp1 HG02055.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.81+14053C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62495259 | ||||||
| chr17:62495397
|
A | G | 1 | a0001c0001t0001g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.81+14191A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62495397 | ||||||
| chr17:62495602
|
A | ATCTTTCT others(23): Show |
1 | a0001c0002t0002g0004 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.81+14400_81+14401i others(32): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62495602 | |||||
| chr17:62495607
|
G | T | 1 | a0001c0002t0002g0004 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.81+14401G>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62495607 | ||||||
| chr17:62495608
|
A | C | 1 | a0001c0002t0002g0004 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.81+14402A>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62495608 | ||||||
| chr17:62495612
|
G | T | 1 | a0001c0002t0002g0004 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.81+14406G>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62495612 | ||||||
| chr17:62495643
|
A | T | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.81+14437A>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62495643 | ||||||
| chr17:62495653
|
T | TTA | 11 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0248others(8): Show | 11 | HG01884.hp2 HG02622.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.81+14467_81+14468d others(4): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62495653 | |||||
| chr17:62495653
|
T | TTATA | 218 | a0001c0001t0001g0020a0001c0001t0001g0176a0001c0001t0001g0179others(215): Show | 218 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.81+14465_81+14468d others(6): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62495653 | |||||
| chr17:62495653
|
T | TTATATA | 19 | a0001c0001t0001g0178a0001c0001t0001g0188a0001c0001t0001g0206others(16): Show | 19 | HG00438.hp1 HG00738.hp1 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.81+14463_81+14468d others(8): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62495653 | |||||
| chr17:62495653
|
T | TTATATAT others(5): Show |
2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.81+14457_81+14468d others(14): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62495653 | |||||
| chr17:62495675
|
T | A | 1 | a0001c0001t0001g0187 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.81+14469T>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62495675 | ||||||
| chr17:62495833
|
T | G | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.81+14627T>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62495833 | ||||||
| chr17:62495834
|
T | G | 2 | a0001c0001t0016g0185a0001c0001t0016g0186 | 2 | HG01243.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.81+14628T>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62495834 | ||||||
| chr17:62495864
|
A | G | 271 | a0001c0001t0001g0020a0001c0001t0001g0176a0001c0001t0001g0178others(268): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.81+14658A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62495864 | ||||||
| chr17:62496030
|
A | G | 6 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0233others(3): Show | 6 | HG01074.hp1 HG01515.hp2 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+14824A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62496030 | ||||||
| chr17:62496095
|
A | T | 2 | a0001c0001t0001g0230a0001c0001t0001g0246 | 2 | HG00140.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.81+14889A>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62496095 | ||||||
| chr17:62496354
|
A | C | 1 | a0001c0001t0021g0153 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.81+15148A>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62496354 | ||||||
| chr17:62496409
|
C | G | 19 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0004g0144others(16): Show | 19 | HG00738.hp2 HG01074.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.81+15203C>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62496409 | ||||||
| chr17:62496478
|
G | T | 3 | a0001c0001t0010g0280a0001c0001t0010g0281a0001c0001t0017g0279 | 3 | HG02818.hp2 HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.81+15272G>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62496478 | ||||||
| chr17:62496486
|
C | T | 3 | a0001c0002t0002g0110a0001c0002t0002g0119a0001c0002t0002g0132 | 3 | HG00733.hp2 HG01516.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.81+15280C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62496486 | ||||||
| chr17:62496520
|
C | A | 1 | a0001c0001t0001g0208 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.81+15314C>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62496520 | ||||||
| chr17:62496838
|
T | C | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.81+15632T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62496838 | ||||||
| chr17:62496956
|
C | CA | 8 | a0001c0001t0001g0240a0001c0001t0006g0042a0001c0001t0025g0247others(5): Show | 8 | HG00438.hp2 HG01074.hp1 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.81+15771dupA | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62496956 | |||||
| chr17:62496956
|
CA | C | 6 | a0001c0001t0001g0229a0001c0002t0002g0004a0001c0002t0004g0139others(3): Show | 6 | HG01099.hp1 HG01516.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+15771delA | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62496956 | |||||
| chr17:62497053
|
T | A | 1 | a0001c0002t0002g0095 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.81+15847T>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62497053 | ||||||
| chr17:62497068
|
G | T | 101 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(98): Show | 101 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.81+15862G>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62497068 | ||||||
| chr17:62497156
|
C | T | 1 | a0001c0001t0001g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.81+15950C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62497156 | ||||||
| chr17:62497208
|
C | T | 2 | a0001c0001t0001g0235a0001c0001t0001g0236 | 2 | NA18998.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.81+16002C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62497208 | ||||||
| chr17:62497467
|
T | C | 1 | a0001c0002t0007g0123 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.81+16261T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62497467 | ||||||
| chr17:62498203
|
C | T | 1 | a0001c0001t0010g0281 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.81+16997C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62498203 | ||||||
| chr17:62498233
|
T | G | 1 | a0001c0001t0001g0268 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.81+17027T>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62498233 | ||||||
| chr17:62498280
|
A | C | 1 | a0001c0002t0015g0173 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.81+17074A>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62498280 | ||||||
| chr17:62498359
|
A | T | 10 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0010g0280others(7): Show | 10 | HG01109.hp2 HG02451.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.81+17153A>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62498359 | ||||||
| chr17:62498370
|
TAGTGTCG others(5): Show |
T | 1 | a0001c0002t0007g0123 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.81+17167_81+17178d others(14): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62498370 | |||||
| chr17:62498390
|
CT | C | 118 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(115): Show | 118 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.81+17201delT | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62498390 | |||||
| chr17:62498391
|
T | C | 2 | a0001c0001t0004g0150a0001c0002t0005g0038 | 2 | HG02080.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.81+17185T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62498391 | ||||||
| chr17:62498392
|
T | C | 105 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(102): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.81+17186T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62498392 | ||||||
| chr17:62498428
|
C | T | 1 | a0001c0002t0002g0094 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.81+17222C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62498428 | ||||||
| chr17:62498565
|
G | A | 271 | a0001c0001t0001g0020a0001c0001t0001g0176a0001c0001t0001g0178others(268): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.81+17359G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62498565 | ||||||
| chr17:62498695
|
C | A | 3 | a0001c0002t0003g0058a0001c0002t0003g0075a0001c0002t0004g0053 | 3 | HG00438.hp1 HG02132.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.81+17489C>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62498695 | ||||||
| chr17:62498698
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.81+17492G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62498698 | ||||||
| chr17:62499158
|
C | T | 8 | a0001c0001t0010g0280a0001c0001t0010g0281a0001c0001t0010g0282others(5): Show | 8 | HG01109.hp2 HG02451.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.81+17952C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62499158 | ||||||
| chr17:62499184
|
C | T | 1 | a0001c0002t0007g0109 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.81+17978C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62499184 | ||||||
| chr17:62499211
|
T | C | 5 | a0001c0001t0004g0150a0001c0001t0004g0152a0001c0001t0012g0148others(2): Show | 5 | HG00738.hp2 HG01074.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.81+18005T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62499211 | ||||||
| chr17:62499299
|
A | C | 3 | a0001c0001t0001g0207a0001c0001t0001g0227a0001c0001t0001g0228 | 3 | HG02055.hp2 HG02965.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.81+18093A>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62499299 | ||||||
| chr17:62499447
|
T | C | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.81+18241T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62499447 | ||||||
| chr17:62499547
|
T | G | 3 | a0001c0001t0001g0192a0001c0001t0001g0248a0001c0001t0001g0249 | 3 | HG01884.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.81+18341T>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62499547 | ||||||
| chr17:62499620
|
T | G | 1 | a0001c0002t0002g0004 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.81+18414T>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62499620 | ||||||
| chr17:62499621
|
G | T | 1 | a0001c0002t0002g0004 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.81+18415G>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62499621 | ||||||
| chr17:62499682
|
T | G | 139 | a0001c0001t0001g0020a0001c0002t0002g0003a0001c0002t0002g0004others(136): Show | 139 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.81+18476T>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62499682 | ||||||
| chr17:62499683
|
C | T | 1 | a0001c0001t0009g0288 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.81+18477C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62499683 | ||||||
| chr17:62499755
|
G | A | 10 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0010g0280others(7): Show | 10 | HG01109.hp2 HG02451.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.81+18549G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62499755 | ||||||
| chr17:62499856
|
A | G | 1 | a0001c0002t0003g0045 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.81+18650A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62499856 | ||||||
| chr17:62499946
|
C | A | 1 | a0001c0001t0021g0153 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.81+18740C>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62499946 | ||||||
| chr17:62499965
|
C | T | 2 | a0001c0002t0003g0064a0001c0002t0003g0065 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.81+18759C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62499965 | ||||||
| chr17:62500027
|
C | G | 8 | a0001c0001t0010g0280a0001c0001t0010g0281a0001c0001t0010g0282others(5): Show | 8 | HG01109.hp2 HG02451.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.81+18821C>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62500027 | ||||||
| chr17:62500072
|
A | G | 1 | a0001c0001t0004g0152 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.81+18866A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62500072 | ||||||
| chr17:62500079
|
T | A | 2 | a0001c0001t0026g0278a0001c0001t0027g0277 | 2 | HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.81+18873T>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62500079 | ||||||
| chr17:62500278
|
A | G | 2 | a0001c0001t0016g0185a0001c0001t0016g0186 | 2 | HG01243.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.81+19072A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62500278 | ||||||
| chr17:62500293
|
ATATAAAA others(21): Show |
A | 1 | a0001c0002t0007g0036 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.81+19101_81+19128d others(30): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62500293 | |||||
| chr17:62500410
|
C | T | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.81+19204C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62500410 | ||||||
| chr17:62500443
|
C | T | 1 | a0001c0001t0016g0186 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.81+19237C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62500443 | ||||||
| chr17:62500458
|
A | G | 1 | a0001c0002t0015g0173 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.81+19252A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62500458 | ||||||
| chr17:62500761
|
A | T | 97 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(94): Show | 97 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.81+19555A>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62500761 | ||||||
| chr17:62501004
|
C | T | 1 | a0001c0001t0001g0208 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.82-19769C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62501004 | ||||||
| chr17:62501005
|
G | A | 1 | a0001c0002t0002g0085 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.82-19768G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62501005 | ||||||
| chr17:62501095
|
G | C | 1 | a0001c0001t0001g0209 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.82-19678G>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62501095 | ||||||
| chr17:62501200
|
T | C | 1 | a0001c0002t0002g0096 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.82-19573T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62501200 | ||||||
| chr17:62501455
|
G | A | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.82-19318G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62501455 | ||||||
| chr17:62501509
|
A | G | 113 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(110): Show | 113 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.82-19264A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62501509 | ||||||
| chr17:62501524
|
G | C | 1 | a0001c0002t0002g0095 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.82-19249G>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62501524 | ||||||
| chr17:62501730
|
C | T | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.82-19043C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62501730 | ||||||
| chr17:62501819
|
TAGTC | T | 3 | a0001c0001t0010g0282a0001c0001t0010g0283a0001c0001t0017g0284 | 3 | HG01109.hp2 HG02451.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.82-18951_82-18948d others(6): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62501819 | |||||
| chr17:62502028
|
A | ATTTTTTT others(2): Show |
7 | a0001c0001t0001g0193a0001c0001t0001g0209a0001c0001t0001g0231others(4): Show | 7 | HG00323.hp2 HG01167.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.82-18745_82-18744i others(11): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62502028 | ||||||
| chr17:62502028
|
A | ATTTTTTT others(3): Show |
69 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0182others(66): Show | 69 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.82-18745_82-18744i others(12): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62502028 | ||||||
| chr17:62502028
|
A | ATTTTTTT others(4): Show |
18 | a0001c0001t0001g0176a0001c0001t0001g0187a0001c0001t0001g0200others(15): Show | 18 | HG00609.hp2 HG00735.hp1 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.82-18745_82-18744i others(13): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62502028 | ||||||
| chr17:62502028
|
A | ATTTTTTT others(5): Show |
1 | a0001c0001t0001g0189 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.82-18745_82-18744i others(14): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62502028 | ||||||
| chr17:62502029
|
A | AT | 23 | a0001c0001t0010g0280a0001c0001t0010g0281a0001c0001t0010g0282others(20): Show | 23 | HG00280.hp1 HG00735.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.82-18727dupT | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62502029 | |||||
| chr17:62502029
|
A | ATTTTTTT others(6): Show |
2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.82-18739_82-18727d others(15): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62502029 | |||||
| chr17:62502029
|
A | T | 96 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(93): Show | 96 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.82-18744A>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62502029 | ||||||
| chr17:62502341
|
A | C | 1 | a0001c0002t0002g0095 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.82-18432A>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62502341 | ||||||
| chr17:62502587
|
A | C | 1 | a0001c0001t0001g0276 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.82-18186A>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62502587 | ||||||
| chr17:62502634
|
T | C | 271 | a0001c0001t0001g0020a0001c0001t0001g0176a0001c0001t0001g0178others(268): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.82-18139T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62502634 | ||||||
| chr17:62502700
|
C | G | 1 | a0001c0002t0002g0029 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.82-18073C>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62502700 | ||||||
| chr17:62502923
|
G | A | 2 | a0001c0001t0026g0278a0001c0001t0027g0277 | 2 | HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.82-17850G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62502923 | ||||||
| chr17:62503052
|
C | CT | 16 | a0001c0001t0001g0226a0001c0001t0001g0242a0001c0001t0001g0254others(13): Show | 16 | HG01175.hp1 HG01934.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.82-17696dupT | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62503052 | |||||
| chr17:62503052
|
CT | C | 130 | a0001c0001t0001g0020a0001c0001t0001g0178a0001c0001t0001g0180others(127): Show | 130 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(127): Show |
intron_variant | MODIFIER | c.82-17696delT | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62503052 | |||||
| chr17:62503052
|
CTT | C | 29 | a0001c0002t0002g0004a0001c0002t0002g0051a0001c0002t0003g0043others(26): Show | 29 | HG00323.hp1 HG00438.hp1 HG01192.hp1 others(26): Show |
intron_variant | MODIFIER | c.82-17697_82-17696d others(4): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62503052 | |||||
| chr17:62503098
|
C | T | 1 | a0001c0001t0001g0233 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.82-17675C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62503098 | ||||||
| chr17:62503099
|
G | A | 9 | a0001c0001t0004g0144a0001c0001t0004g0145a0001c0001t0004g0146others(6): Show | 9 | HG00738.hp2 HG01074.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.82-17674G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62503099 | ||||||
| chr17:62503122
|
C | T | 2 | a0001c0002t0002g0040a0001c0002t0005g0124 | 2 | HG00280.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.82-17651C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62503122 | ||||||
| chr17:62503139
|
A | G | 1 | a0001c0001t0001g0276 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.82-17634A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62503139 | ||||||
| chr17:62503211
|
C | T | 1 | a0001c0001t0001g0276 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.82-17562C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62503211 | ||||||
| chr17:62503213
|
C | T | 1 | a0001c0002t0002g0087 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.82-17560C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62503213 | ||||||
| chr17:62503408
|
G | C | 1 | a0001c0002t0011g0143 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.82-17365G>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62503408 | ||||||
| chr17:62503415
|
C | CT | 6 | a0001c0001t0010g0280a0001c0001t0010g0281a0001c0001t0010g0282others(3): Show | 6 | HG02451.hp1 HG02818.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.82-17338dupT | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62503415 | |||||
| chr17:62503415
|
CT | C | 254 | a0001c0001t0001g0020a0001c0001t0001g0178a0001c0001t0001g0179others(251): Show | 254 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.82-17338delT | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62503415 | |||||
| chr17:62503510
|
C | T | 1 | a0001c0002t0007g0125 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.82-17263C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62503510 | ||||||
| chr17:62503573
|
C | G | 1 | a0001c0002t0002g0136 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.82-17200C>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62503573 | ||||||
| chr17:62503728
|
CT | C | 257 | a0001c0001t0001g0020a0001c0001t0001g0176a0001c0001t0001g0178others(254): Show | 257 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.82-17028delT | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62503728 | |||||
| chr17:62503797
|
C | T | 1 | a0001c0001t0001g0199 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.82-16976C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62503797 | ||||||
| chr17:62503819
|
C | T | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.82-16954C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62503819 | ||||||
| chr17:62503894
|
A | AT | 6 | a0001c0001t0001g0275a0001c0001t0004g0048a0001c0001t0004g0049others(3): Show | 6 | HG01081.hp2 HG01884.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.82-16868dupT | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62503894 | |||||
| chr17:62503919
|
A | T | 1 | a0001c0002t0004g0053 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.82-16854A>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62503919 | ||||||
| chr17:62503922
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.82-16851C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62503922 | ||||||
| chr17:62503954
|
G | A | 1 | a0001c0002t0002g0085 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.82-16819G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62503954 | ||||||
| chr17:62504072
|
G | A | 2 | a0001c0002t0002g0080a0001c0002t0007g0081 | 2 | HG00639.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.82-16701G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62504072 | ||||||
| chr17:62504107
|
A | G | 3 | a0001c0002t0004g0139a0001c0002t0004g0140a0001c0002t0022g0138 | 3 | HG01099.hp1 HG02055.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.82-16666A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62504107 | ||||||
| chr17:62504371
|
G | A | 1 | a0001c0002t0002g0085 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.82-16402G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62504371 | ||||||
| chr17:62504372
|
C | G | 1 | a0001c0002t0002g0085 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.82-16401C>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62504372 | ||||||
| chr17:62504553
|
G | A | 1 | a0001c0001t0006g0042 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.82-16220G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62504553 | ||||||
| chr17:62505407
|
A | AT | 27 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162others(24): Show | 27 | HG00609.hp1 HG00738.hp2 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.82-15340dupT | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62505407 | |||||
| chr17:62505407
|
A | ATT | 132 | a0001c0001t0001g0020a0001c0001t0003g0158a0001c0001t0003g0168others(129): Show | 132 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.82-15341_82-15340d others(4): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62505407 | |||||
| chr17:62505407
|
A | ATTT | 19 | a0001c0001t0001g0181a0001c0001t0001g0275a0001c0001t0006g0041others(16): Show | 19 | HG01081.hp2 HG01261.hp1 HG02074.hp1 others(16): Show |
intron_variant | MODIFIER | c.82-15342_82-15340d others(5): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62505407 | |||||
| chr17:62505407
|
A | ATTTTTTT others(4): Show |
4 | a0001c0001t0001g0190a0001c0001t0001g0193a0001c0001t0001g0228others(1): Show | 4 | HG01109.hp2 HG01167.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-15350_82-15340d others(13): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62505407 | |||||
| chr17:62505407
|
A | ATTTTTTT others(5): Show |
35 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0192others(32): Show | 35 | HG00140.hp2 HG00323.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.82-15351_82-15340d others(14): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62505407 | |||||
| chr17:62505407
|
A | ATTTTTTT others(6): Show |
26 | a0001c0001t0001g0187a0001c0001t0001g0191a0001c0001t0001g0202others(23): Show | 26 | HG00280.hp2 HG00438.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.82-15352_82-15340d others(15): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62505407 | |||||
| chr17:62505407
|
A | ATTTTTTT others(7): Show |
11 | a0001c0001t0001g0200a0001c0001t0001g0203a0001c0001t0001g0220others(8): Show | 11 | HG01243.hp2 HG02273.hp2 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.82-15353_82-15340d others(16): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62505407 | |||||
| chr17:62505407
|
A | ATTTTTTT others(8): Show |
2 | a0001c0001t0010g0282a0001c0001t0010g0283 | 2 | HG02451.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.82-15354_82-15340d others(17): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62505407 | |||||
| chr17:62505407
|
A | ATTTTTTT others(9): Show |
1 | a0001c0001t0001g0231 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.82-15355_82-15340d others(18): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62505407 | |||||
| chr17:62505407
|
A | ATTTTTTT others(10): Show |
2 | a0001c0001t0001g0250a0001c0001t0001g0266 | 2 | HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.82-15356_82-15340d others(19): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62505407 | |||||
| chr17:62505407
|
A | ATTTTTTT others(11): Show |
10 | a0001c0001t0001g0176a0001c0001t0001g0182a0001c0001t0001g0183others(7): Show | 10 | HG00733.hp1 HG00735.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.82-15357_82-15340d others(20): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62505407 | |||||
| chr17:62505407
|
A | ATTTTTTT others(12): Show |
4 | a0001c0001t0001g0188a0001c0001t0001g0223a0001c0001t0001g0226others(1): Show | 4 | NA18940.hp2 NA18948.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-15358_82-15340d others(21): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62505407 | |||||
| chr17:62505407
|
A | ATTTTTTT others(14): Show |
2 | a0001c0001t0001g0241a0001c0001t0001g0289 | 2 | HG02622.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.82-15360_82-15340d others(23): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62505407 | |||||
| chr17:62505407
|
A | ATTTTTTT others(16): Show |
3 | a0001c0001t0001g0189a0001c0001t0016g0185a0001c0001t0026g0278 | 3 | HG01243.hp1 HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.82-15362_82-15340d others(25): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62505407 | |||||
| chr17:62505407
|
A | ATTTTTTT others(17): Show |
1 | a0001c0001t0001g0197 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.82-15363_82-15340d others(26): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62505407 | |||||
| chr17:62505407
|
A | ATTTTTTT others(18): Show |
1 | a0001c0001t0001g0237 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.82-15364_82-15340d others(27): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62505407 | |||||
| chr17:62505407
|
A | ATTTTTTT others(31): Show |
1 | a0001c0001t0010g0281 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.82-15340_82-15339i others(40): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62505407 | |||||
| chr17:62505434
|
G | T | 1 | a0001c0002t0002g0085 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.82-15339G>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62505434 | ||||||
| chr17:62505468
|
G | A | 5 | a0001c0001t0001g0190a0001c0001t0001g0207a0001c0001t0001g0224others(2): Show | 5 | HG02055.hp2 HG02965.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.82-15305G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62505468 | ||||||
| chr17:62505636
|
A | G | 1 | a0001c0001t0001g0270 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.82-15137A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62505636 | ||||||
| chr17:62505786
|
G | T | 1 | a0001c0002t0002g0085 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.82-14987G>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62505786 | ||||||
| chr17:62505788
|
C | T | 1 | a0001c0002t0002g0085 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.82-14985C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62505788 | ||||||
| chr17:62505862
|
T | C | 103 | a0001c0001t0001g0020a0001c0001t0001g0222a0001c0002t0002g0003others(100): Show | 103 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.82-14911T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62505862 | ||||||
| chr17:62505920
|
T | G | 1 | a0001c0002t0002g0085 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.82-14853T>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62505920 | ||||||
| chr17:62505983
|
G | A | 1 | a0001c0001t0016g0186 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.82-14790G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62505983 | ||||||
| chr17:62505989
|
A | G | 1 | a0001c0001t0001g0276 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.82-14784A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62505989 | ||||||
| chr17:62506063
|
C | T | 5 | a0001c0002t0002g0083a0001c0002t0002g0087a0001c0002t0002g0088others(2): Show | 5 | HG00738.hp1 HG01258.hp1 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.82-14710C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62506063 | ||||||
| chr17:62506203
|
G | T | 3 | a0001c0002t0004g0139a0001c0002t0004g0140a0001c0002t0022g0138 | 3 | HG01099.hp1 HG02055.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.82-14570G>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62506203 | ||||||
| chr17:62506274
|
G | A | 2 | a0001c0002t0002g0154a0001c0002t0005g0155 | 2 | HG01978.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.82-14499G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62506274 | ||||||
| chr17:62506405
|
G | A | 5 | a0001c0001t0006g0041a0001c0001t0006g0042a0001c0001t0006g0055others(2): Show | 5 | HG02622.hp2 HG02647.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.82-14368G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62506405 | ||||||
| chr17:62506455
|
C | T | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.82-14318C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62506455 | ||||||
| chr17:62506517
|
T | C | 1 | a0001c0002t0002g0085 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.82-14256T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62506517 | ||||||
| chr17:62506518
|
C | T | 1 | a0001c0002t0002g0085 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.82-14255C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62506518 | ||||||
| chr17:62506881
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.82-13892C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62506881 | ||||||
| chr17:62507188
|
C | T | 99 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(96): Show | 99 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.82-13585C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62507188 | ||||||
| chr17:62507500
|
T | A | 15 | a0001c0001t0001g0176a0001c0001t0001g0182a0001c0001t0001g0183others(12): Show | 15 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.82-13273T>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62507500 | ||||||
| chr17:62507619
|
C | T | 1 | a0001c0001t0003g0175 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.82-13154C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62507619 | ||||||
| chr17:62507871
|
A | G | 97 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(94): Show | 97 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.82-12902A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62507871 | ||||||
| chr17:62508047
|
A | G | 1 | a0001c0001t0001g0276 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.82-12726A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62508047 | ||||||
| chr17:62508163
|
T | G | 5 | a0001c0001t0004g0150a0001c0001t0004g0152a0001c0001t0012g0148others(2): Show | 5 | HG00738.hp2 HG01074.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.82-12610T>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62508163 | ||||||
| chr17:62508168
|
G | GT | 152 | a0001c0001t0001g0020a0001c0001t0001g0187a0001c0001t0001g0200others(149): Show | 152 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.82-12586dupT | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62508168 | |||||
| chr17:62508168
|
G | GTT | 101 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(98): Show | 101 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.82-12587_82-12586d others(4): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62508168 | |||||
| chr17:62508168
|
G | GTTT | 7 | a0001c0001t0001g0188a0001c0001t0001g0206a0001c0001t0001g0261others(4): Show | 7 | HG01109.hp1 HG01243.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.82-12588_82-12586d others(5): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62508168 | |||||
| chr17:62508405
|
T | G | 1 | a0001c0002t0002g0085 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.82-12368T>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62508405 | ||||||
| chr17:62508427
|
G | A | 1 | a0001c0001t0003g0175 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.82-12346G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62508427 | ||||||
| chr17:62508433
|
A | G | 1 | a0001c0002t0002g0093 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.82-12340A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62508433 | ||||||
| chr17:62508558
|
T | C | 1 | a0001c0002t0003g0066 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.82-12215T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62508558 | ||||||
| chr17:62508657
|
C | T | 1 | a0001c0001t0016g0186 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.82-12116C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62508657 | ||||||
| chr17:62508822
|
G | T | 1 | a0001c0002t0002g0092 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.82-11951G>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62508822 | ||||||
| chr17:62508966
|
T | TCAA | 34 | a0001c0002t0002g0051a0001c0002t0003g0043a0001c0002t0003g0044others(31): Show | 34 | HG00438.hp1 HG01192.hp1 HG01261.hp1 others(31): Show |
intron_variant | MODIFIER | c.82-11791_82-11789d others(5): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62508966 | |||||
| chr17:62509106
|
C | T | 1 | a0001c0002t0003g0068 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.82-11667C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62509106 | ||||||
| chr17:62509249
|
C | T | 1 | a0001c0001t0026g0278 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.82-11524C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62509249 | ||||||
| chr17:62509550
|
T | C | 1 | a0001c0001t0001g0292 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.82-11223T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62509550 | ||||||
| chr17:62509663
|
G | A | 1 | a0001c0002t0002g0129 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.82-11110G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62509663 | ||||||
| chr17:62510036
|
T | G | 1 | a0001c0002t0005g0038 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.82-10737T>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62510036 | ||||||
| chr17:62510158
|
A | G | 1 | a0001c0001t0006g0042 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.82-10615A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62510158 | ||||||
| chr17:62510319
|
G | T | 4 | a0001c0001t0009g0285a0001c0001t0009g0286a0001c0001t0009g0287others(1): Show | 4 | HG02451.hp2 HG02630.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.82-10454G>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62510319 | ||||||
| chr17:62510446
|
A | C | 3 | a0001c0001t0006g0055a0001c0001t0006g0056a0001c0001t0006g0074 | 3 | HG02622.hp2 HG02970.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.82-10327A>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62510446 | ||||||
| chr17:62510669
|
T | C | 3 | a0001c0001t0006g0055a0001c0001t0006g0056a0001c0001t0006g0074 | 3 | HG02622.hp2 HG02970.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.82-10104T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62510669 | ||||||
| chr17:62510800
|
C | T | 8 | a0001c0001t0010g0280a0001c0001t0010g0281a0001c0001t0010g0282others(5): Show | 8 | HG01109.hp2 HG02451.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.82-9973C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62510800 | ||||||
| chr17:62510933
|
G | A | 1 | a0001c0002t0002g0092 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.82-9840G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62510933 | ||||||
| chr17:62510967
|
C | T | 2 | a0001c0001t0026g0278a0001c0001t0027g0277 | 2 | HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.82-9806C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62510967 | ||||||
| chr17:62511137
|
A | G | 8 | a0001c0001t0010g0280a0001c0001t0010g0281a0001c0001t0010g0282others(5): Show | 8 | HG01109.hp2 HG02451.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.82-9636A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62511137 | ||||||
| chr17:62511233
|
T | C | 111 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(108): Show | 111 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.82-9540T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62511233 | ||||||
| chr17:62511276
|
T | C | 1 | a0001c0001t0001g0242 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.82-9497T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62511276 | ||||||
| chr17:62511332
|
A | G | 1 | a0001c0001t0010g0283 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.82-9441A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62511332 | ||||||
| chr17:62511485
|
C | T | 1 | a0001c0001t0009g0288 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.82-9288C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62511485 | ||||||
| chr17:62511524
|
C | A | 1 | a0001c0002t0011g0111 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.82-9249C>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62511524 | ||||||
| chr17:62511919
|
A | G | 1 | a0001c0002t0002g0088 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.82-8854A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62511919 | ||||||
| chr17:62511951
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.82-8822A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62511951 | ||||||
| chr17:62512208
|
C | T | 4 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0026g0278others(1): Show | 4 | HG03195.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-8565C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62512208 | ||||||
| chr17:62512213
|
CT | C | 144 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(141): Show | 144 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.82-8535delT | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62512213 | |||||
| chr17:62512213
|
CTT | C | 114 | a0001c0001t0001g0020a0001c0001t0001g0192a0001c0001t0001g0210others(111): Show | 114 | HG00280.hp1 HG00438.hp1 HG00609.hp1 others(111): Show |
intron_variant | MODIFIER | c.82-8536_82-8535del others(2): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62512213 | |||||
| chr17:62512213
|
CTTTTTTT others(8): Show |
C | 1 | a0001c0002t0015g0173 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.82-8549_82-8535del others(15): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62512213 | |||||
| chr17:62512294
|
C | T | 55 | a0001c0002t0002g0040a0001c0002t0002g0082a0001c0002t0002g0083others(52): Show | 55 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.82-8479C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62512294 | ||||||
| chr17:62512317
|
G | A | 1 | a0001c0001t0006g0041 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.82-8456G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62512317 | ||||||
| chr17:62512682
|
T | C | 1 | a0001c0001t0021g0153 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.82-8091T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62512682 | ||||||
| chr17:62512698
|
A | G | 2 | a0001c0002t0002g0133a0001c0002t0002g0134 | 2 | HG02080.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.82-8075A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62512698 | ||||||
| chr17:62512786
|
T | C | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.82-7987T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62512786 | ||||||
| chr17:62512861
|
A | AATT | 90 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0180others(87): Show | 90 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.82-7880_82-7878dup others(3): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62512861 | |||||
| chr17:62512861
|
A | AATTATT | 49 | a0001c0001t0001g0199a0001c0001t0001g0214a0001c0001t0001g0219others(46): Show | 49 | HG00140.hp1 HG00438.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.82-7883_82-7878dup others(6): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62512861 | |||||
| chr17:62512861
|
A | AATTATTA others(2): Show |
57 | a0001c0001t0001g0020a0001c0001t0001g0244a0001c0002t0002g0003others(54): Show | 57 | HG00323.hp1 HG00609.hp1 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.82-7886_82-7878dup others(9): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62512861 | |||||
| chr17:62512861
|
A | AATTATTA others(5): Show |
9 | a0001c0001t0016g0185a0001c0002t0002g0007a0001c0002t0002g0009others(6): Show | 9 | HG00280.hp1 HG01243.hp1 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.82-7889_82-7878dup others(12): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62512861 | |||||
| chr17:62512861
|
A | T | 2 | a0001c0002t0002g0083a0001c0002t0002g0088 | 2 | HG00738.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.82-7912A>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62512861 | ||||||
| chr17:62512861
|
AATT | A | 3 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0009g0288 | 3 | HG02622.hp1 HG02976.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.82-7880_82-7878del others(3): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62512861 | |||||
| chr17:62512896
|
G | T | 2 | a0001c0001t0026g0278a0001c0001t0027g0277 | 2 | HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.82-7877G>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62512896 | ||||||
| chr17:62512897
|
A | T | 2 | a0001c0001t0026g0278a0001c0001t0027g0277 | 2 | HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.82-7876A>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62512897 | ||||||
| chr17:62513129
|
G | A | 1 | a0001c0002t0003g0045 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.82-7644G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62513129 | ||||||
| chr17:62513318
|
C | CT | 145 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(142): Show | 145 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.82-7436dupT | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62513318 | |||||
| chr17:62513318
|
C | CTT | 8 | a0001c0001t0001g0218a0001c0001t0001g0225a0001c0001t0001g0237others(5): Show | 8 | HG01358.hp1 HG02083.hp1 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.82-7437_82-7436dup others(2): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62513318 | |||||
| chr17:62513318
|
CT | C | 17 | a0001c0002t0002g0089a0001c0002t0002g0099a0001c0002t0002g0120others(14): Show | 17 | HG01069.hp2 HG01168.hp1 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.82-7436delT | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62513318 | |||||
| chr17:62513473
|
G | A | 2 | a0001c0001t0018g0255a0001c0004t0001g0204 | 2 | HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.82-7300G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62513473 | ||||||
| chr17:62513665
|
A | G | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.82-7108A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62513665 | ||||||
| chr17:62513709
|
G | A | 1 | a0001c0001t0003g0170 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.82-7064G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62513709 | ||||||
| chr17:62513933
|
C | T | 6 | a0001c0002t0003g0057a0001c0002t0003g0058a0001c0002t0003g0059others(3): Show | 6 | HG00438.hp1 HG02027.hp2 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.82-6840C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62513933 | ||||||
| chr17:62514099
|
C | T | 1 | a0001c0002t0007g0081 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.82-6674C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62514099 | ||||||
| chr17:62514435
|
T | A | 1 | a0001c0001t0004g0172 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.82-6338T>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62514435 | ||||||
| chr17:62514453
|
T | TA | 104 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(101): Show | 104 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.82-6308dupA | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62514453 | |||||
| chr17:62514599
|
A | G | 1 | a0001c0002t0004g0139 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.82-6174A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62514599 | ||||||
| chr17:62514757
|
T | A | 1 | a0001c0001t0001g0197 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.82-6016T>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62514757 | ||||||
| chr17:62514776
|
G | A | 1 | a0001c0002t0003g0075 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.82-5997G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62514776 | ||||||
| chr17:62514870
|
C | T | 11 | a0001c0001t0006g0041a0001c0001t0006g0042a0001c0001t0006g0055others(8): Show | 11 | HG01109.hp2 HG02451.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.82-5903C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62514870 | ||||||
| chr17:62514934
|
A | G | 102 | a0001c0001t0001g0020a0001c0002t0002g0003a0001c0002t0002g0004others(99): Show | 102 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.82-5839A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62514934 | ||||||
| chr17:62515032
|
C | A | 1 | a0001c0002t0002g0131 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.82-5741C>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62515032 | ||||||
| chr17:62515221
|
A | G | 97 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(94): Show | 97 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.82-5552A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62515221 | ||||||
| chr17:62515390
|
A | G | 139 | a0001c0001t0001g0020a0001c0002t0002g0003a0001c0002t0002g0004others(136): Show | 139 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.82-5383A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62515390 | ||||||
| chr17:62515406
|
A | G | 1 | a0001c0001t0001g0276 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.82-5367A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62515406 | ||||||
| chr17:62515544
|
G | A | 1 | a0001c0001t0001g0276 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.82-5229G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62515544 | ||||||
| chr17:62516264
|
CT | C | 98 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(95): Show | 98 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.82-4493delT | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62516264 | |||||
| chr17:62516455
|
G | A | 5 | a0001c0001t0006g0041a0001c0001t0006g0042a0001c0001t0006g0055others(2): Show | 5 | HG02622.hp2 HG02647.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.82-4318G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62516455 | ||||||
| chr17:62516857
|
C | T | 97 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(94): Show | 97 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.82-3916C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62516857 | ||||||
| chr17:62517147
|
C | T | 1 | a0001c0001t0001g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.82-3626C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62517147 | ||||||
| chr17:62517302
|
C | A | 1 | a0001c0002t0015g0173 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.82-3471C>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62517302 | ||||||
| chr17:62517325
|
T | C | 99 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(96): Show | 99 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.82-3448T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62517325 | ||||||
| chr17:62517494
|
A | C | 1 | a0001c0001t0003g0175 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.82-3279A>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62517494 | ||||||
| chr17:62517495
|
C | T | 6 | a0001c0001t0010g0280a0001c0001t0010g0281a0001c0001t0010g0282others(3): Show | 6 | HG01109.hp2 HG02451.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.82-3278C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62517495 | ||||||
| chr17:62517540
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.82-3233G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62517540 | ||||||
| chr17:62517680
|
C | T | 2 | a0001c0001t0026g0278a0001c0001t0027g0277 | 2 | HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.82-3093C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62517680 | ||||||
| chr17:62517769
|
C | T | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.82-3004C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62517769 | ||||||
| chr17:62517783
|
C | T | 1 | a0001c0001t0004g0172 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.82-2990C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62517783 | ||||||
| chr17:62517822
|
C | T | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.82-2951C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62517822 | ||||||
| chr17:62517897
|
C | T | 2 | a0001c0002t0002g0040a0001c0002t0005g0124 | 2 | HG00280.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.82-2876C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62517897 | ||||||
| chr17:62518004
|
A | G | 2 | a0001c0002t0003g0070a0001c0002t0003g0076 | 2 | NA19009.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.82-2769A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62518004 | ||||||
| chr17:62518310
|
G | A | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.82-2463G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62518310 | ||||||
| chr17:62518545
|
A | T | 1 | a0001c0001t0001g0199 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.82-2228A>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62518545 | ||||||
| chr17:62518609
|
G | C | 1 | a0001c0001t0001g0276 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.82-2164G>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62518609 | ||||||
| chr17:62518659
|
T | C | 1 | a0001c0001t0001g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.82-2114T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62518659 | ||||||
| chr17:62518699
|
C | T | 1 | a0001c0002t0002g0086 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.82-2074C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62518699 | ||||||
| chr17:62518933
|
A | C | 94 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(91): Show | 94 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.82-1840A>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62518933 | ||||||
| chr17:62518935
|
T | C | 1 | a0001c0002t0002g0089 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.82-1838T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62518935 | ||||||
| chr17:62519050
|
A | T | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.82-1723A>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62519050 | ||||||
| chr17:62519054
|
T | C | 2 | a0001c0001t0026g0278a0001c0001t0027g0277 | 2 | HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.82-1719T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62519054 | ||||||
| chr17:62519232
|
A | G | 1 | a0001c0001t0014g0221 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.82-1541A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62519232 | ||||||
| chr17:62519341
|
T | A | 1 | a0001c0001t0001g0199 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.82-1432T>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62519341 | ||||||
| chr17:62519378
|
T | G | 1 | a0001c0002t0007g0036 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.82-1395T>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62519378 | ||||||
| chr17:62519449
|
T | C | 1 | a0001c0001t0001g0276 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.82-1324T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62519449 | ||||||
| chr17:62519608
|
G | A | 1 | a0001c0001t0016g0185 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.82-1165G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62519608 | ||||||
| chr17:62519678
|
C | A | 3 | a0001c0001t0001g0207a0001c0001t0001g0227a0001c0001t0001g0228 | 3 | HG02055.hp2 HG02965.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.82-1095C>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62519678 | ||||||
| chr17:62519870
|
A | G | 1 | a0001c0001t0001g0276 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.82-903A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62519870 | ||||||
| chr17:62519917
|
G | T | 9 | a0001c0001t0004g0144a0001c0001t0004g0145a0001c0001t0004g0146others(6): Show | 9 | HG00738.hp2 HG01074.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.82-856G>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62519917 | ||||||
| chr17:62519919
|
G | C | 107 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(104): Show | 107 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.82-854G>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62519919 | ||||||
| chr17:62519936
|
A | G | 99 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(96): Show | 99 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.82-837A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62519936 | ||||||
| chr17:62519989
|
G | A | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.82-784G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62519989 | ||||||
| chr17:62520059
|
T | A | 2 | a0001c0002t0003g0064a0001c0002t0003g0065 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.82-714T>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62520059 | ||||||
| chr17:62520075
|
G | T | 1 | a0001c0001t0001g0276 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.82-698G>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62520075 | ||||||
| chr17:62520086
|
G | A | 1 | a0001c0002t0007g0036 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.82-687G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62520086 | ||||||
| chr17:62520217
|
A | G | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.82-556A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62520217 | ||||||
| chr17:62520625
|
C | T | 81 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0187others(78): Show | 81 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.82-148C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62520625 | ||||||
| chr17:62520676
|
T | TA | 10 | a0001c0001t0001g0226a0001c0001t0001g0236a0001c0001t0001g0292others(7): Show | 10 | HG00438.hp2 HG01175.hp1 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.82-77dupA | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr17 | 62520676 | |||||
| chr17:62520707
|
T | G | 1 | a0001c0001t0001g0259 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.82-66T>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 2/21 | chr17 | 62520707 | ||||||
| chr17:62520964
|
G | C | 4 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0026g0278others(1): Show | 4 | HG03195.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.153+120G>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 3/21 | chr17 | 62520964 | ||||||
| chr17:62521002
|
G | A | 3 | a0001c0002t0002g0097a0001c0002t0002g0112a0001c0002t0002g0127 | 3 | HG02723.hp2 HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.153+158G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 3/21 | chr17 | 62521002 | ||||||
| chr17:62521008
|
A | G | 4 | a0001c0001t0004g0048a0001c0001t0004g0049a0001c0001t0004g0050others(1): Show | 4 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.153+164A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 3/21 | chr17 | 62521008 | ||||||
| chr17:62521141
|
C | T | 1 | a0001c0001t0016g0186 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.153+297C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 3/21 | chr17 | 62521141 | ||||||
| chr17:62521230
|
G | T | 1 | a0001c0001t0001g0276 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.153+386G>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 3/21 | chr17 | 62521230 | ||||||
| chr17:62521233
|
C | T | 105 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(102): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.153+389C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 3/21 | chr17 | 62521233 | ||||||
| chr17:62521423
|
G | A | 1 | a0001c0001t0014g0267 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.153+579G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 3/21 | chr17 | 62521423 | ||||||
| chr17:62521691
|
T | C | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.154-513T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 3/21 | chr17 | 62521691 | ||||||
| chr17:62521789
|
A | G | 9 | a0001c0001t0004g0144a0001c0001t0004g0145a0001c0001t0004g0146others(6): Show | 9 | HG00738.hp2 HG01074.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.154-415A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 3/21 | chr17 | 62521789 | ||||||
| chr17:62521825
|
T | G | 1 | a0001c0001t0016g0186 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.154-379T>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 3/21 | chr17 | 62521825 | ||||||
| chr17:62522413
|
G | T | 1 | a0001c0002t0002g0027 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.223+140G>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 4/21 | chr17 | 62522413 | ||||||
| chr17:62522417
|
A | G | 1 | a0001c0002t0003g0043 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.223+144A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 4/21 | chr17 | 62522417 | ||||||
| chr17:62522436
|
G | A | 278 | a0001c0001t0001g0020a0001c0001t0001g0176a0001c0001t0001g0178others(275): Show | 278 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.223+163G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 4/21 | chr17 | 62522436 | ||||||
| chr17:62522441
|
C | T | 2 | a0001c0001t0001g0199a0001c0001t0001g0209 | 2 | NA18990.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.223+168C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 4/21 | chr17 | 62522441 | ||||||
| chr17:62522680
|
T | C | 1 | a0001c0002t0003g0060 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.223+407T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 4/21 | chr17 | 62522680 | ||||||
| chr17:62522927
|
T | C | 1 | a0001c0001t0017g0284 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.224-207T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 4/21 | chr17 | 62522927 | ||||||
| chr17:62522961
|
A | G | 1 | a0001c0002t0002g0086 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.224-173A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 4/21 | chr17 | 62522961 | ||||||
| chr17:62523346
|
A | G | 1 | a0001c0002t0002g0108 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.267+169A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 5/21 | chr17 | 62523346 | ||||||
| chr17:62523368
|
C | G | 17 | a0001c0002t0002g0083a0001c0002t0002g0087a0001c0002t0002g0088others(14): Show | 17 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.267+191C>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 5/21 | chr17 | 62523368 | ||||||
| chr17:62523478
|
G | A | 1 | a0001c0001t0001g0276 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.267+301G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 5/21 | chr17 | 62523478 | ||||||
| chr17:62523647
|
A | G | 1 | a0001c0002t0008g0047 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.267+470A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 5/21 | chr17 | 62523647 | ||||||
| chr17:62523985
|
T | C | 1 | a0001c0001t0001g0189 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.268-251T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 5/21 | chr17 | 62523985 | ||||||
| chr17:62524354
|
T | C | 1 | a0001c0002t0028g0005 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.363+23T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62524354 | ||||||
| chr17:62524701
|
G | A | 1 | a0001c0003t0008g0071 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.363+370G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62524701 | ||||||
| chr17:62524748
|
T | C | 6 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0233others(3): Show | 6 | HG01074.hp1 HG01515.hp2 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.363+417T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62524748 | ||||||
| chr17:62524870
|
A | G | 1 | a0001c0001t0016g0185 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.363+539A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62524870 | ||||||
| chr17:62524925
|
G | A | 4 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0026g0278others(1): Show | 4 | HG03195.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+594G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62524925 | ||||||
| chr17:62525090
|
T | C | 1 | a0001c0001t0001g0211 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.363+759T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62525090 | ||||||
| chr17:62525374
|
T | C | 2 | a0001c0001t0016g0185a0001c0001t0016g0186 | 2 | HG01243.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.363+1043T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62525374 | ||||||
| chr17:62525403
|
A | G | 1 | a0001c0001t0001g0211 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.363+1072A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62525403 | ||||||
| chr17:62525440
|
A | G | 1 | a0001c0001t0001g0271 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.363+1109A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62525440 | ||||||
| chr17:62525451
|
A | AT | 9 | a0001c0001t0017g0284a0001c0002t0002g0026a0001c0002t0002g0086others(6): Show | 9 | HG01109.hp2 HG01255.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.363+1137dupT | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr17 | 62525451 | |||||
| chr17:62525451
|
AT | A | 105 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(102): Show | 105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.363+1137delT | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr17 | 62525451 | |||||
| chr17:62525605
|
C | T | 16 | a0001c0001t0001g0020a0001c0002t0002g0004a0001c0002t0002g0008others(13): Show | 16 | HG00609.hp1 HG02074.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.363+1274C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62525605 | ||||||
| chr17:62525729
|
C | T | 1 | a0001c0002t0002g0026 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.363+1398C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62525729 | ||||||
| chr17:62525741
|
T | C | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.363+1410T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62525741 | ||||||
| chr17:62526370
|
C | G | 1 | a0001c0001t0001g0190 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.363+2039C>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62526370 | ||||||
| chr17:62526559
|
A | G | 3 | a0001c0001t0001g0209a0001c0001t0001g0253a0001c0001t0001g0262 | 3 | NA18990.hp2 NA19005.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.363+2228A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62526559 | ||||||
| chr17:62526608
|
A | G | 97 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(94): Show | 97 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.363+2277A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62526608 | ||||||
| chr17:62526694
|
G | GTA | 139 | a0001c0001t0001g0020a0001c0002t0002g0003a0001c0002t0002g0004others(136): Show | 139 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.363+2364_363+2365d others(4): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr17 | 62526694 | |||||
| chr17:62526857
|
G | T | 97 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(94): Show | 97 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.363+2526G>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62526857 | ||||||
| chr17:62526911
|
A | G | 13 | a0001c0001t0006g0041a0001c0001t0006g0042a0001c0001t0006g0055others(10): Show | 13 | HG01109.hp2 HG01243.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.363+2580A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62526911 | ||||||
| chr17:62527097
|
A | G | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.363+2766A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62527097 | ||||||
| chr17:62527599
|
C | T | 4 | a0001c0001t0004g0048a0001c0001t0004g0049a0001c0001t0004g0050others(1): Show | 4 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.363+3268C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62527599 | ||||||
| chr17:62527604
|
C | G | 1 | a0001c0001t0001g0276 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.363+3273C>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62527604 | ||||||
| chr17:62527681
|
C | A | 1 | a0001c0001t0001g0224 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.363+3350C>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62527681 | ||||||
| chr17:62527943
|
A | G | 2 | a0001c0001t0016g0185a0001c0001t0016g0186 | 2 | HG01243.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.363+3612A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62527943 | ||||||
| chr17:62527963
|
G | A | 1 | a0001c0002t0002g0136 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.363+3632G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62527963 | ||||||
| chr17:62528037
|
A | G | 1 | a0001c0002t0004g0156 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.363+3706A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62528037 | ||||||
| chr17:62528425
|
G | T | 271 | a0001c0001t0001g0020a0001c0001t0001g0176a0001c0001t0001g0178others(268): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.363+4094G>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62528425 | ||||||
| chr17:62528481
|
A | G | 1 | a0001c0001t0001g0276 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.363+4150A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62528481 | ||||||
| chr17:62528614
|
G | A | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.363+4283G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62528614 | ||||||
| chr17:62528709
|
G | A | 1 | a0001c0002t0002g0008 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.363+4378G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62528709 | ||||||
| chr17:62528721
|
C | T | 4 | a0001c0001t0003g0165a0001c0001t0003g0166a0001c0001t0026g0278others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+4390C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62528721 | ||||||
| chr17:62528988
|
G | A | 1 | a0001c0002t0015g0173 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.363+4657G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62528988 | ||||||
| chr17:62529033
|
C | T | 267 | a0001c0001t0001g0020a0001c0001t0001g0176a0001c0001t0001g0178others(264): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.363+4702C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62529033 | ||||||
| chr17:62529083
|
T | C | 4 | a0001c0001t0004g0048a0001c0001t0004g0049a0001c0001t0004g0050others(1): Show | 4 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.363+4752T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62529083 | ||||||
| chr17:62529188
|
A | G | 1 | a0001c0001t0004g0172 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.363+4857A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62529188 | ||||||
| chr17:62529741
|
A | T | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.363+5410A>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62529741 | ||||||
| chr17:62529921
|
G | A | 1 | a0001c0001t0017g0284 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.363+5590G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62529921 | ||||||
| chr17:62530156
|
C | T | 102 | a0001c0001t0001g0020a0001c0002t0002g0003a0001c0002t0002g0004others(99): Show | 102 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.363+5825C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62530156 | ||||||
| chr17:62530222
|
C | T | 1 | a0001c0001t0003g0175 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.363+5891C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62530222 | ||||||
| chr17:62530273
|
GAAAC | G | 13 | a0001c0001t0001g0190a0001c0001t0001g0224a0001c0001t0006g0041others(10): Show | 13 | HG01109.hp2 HG02451.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.364-5873_364-5870d others(6): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr17 | 62530273 | |||||
| chr17:62530303
|
A | C | 1 | a0001c0002t0003g0078 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.364-5867A>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62530303 | ||||||
| chr17:62530526
|
T | C | 1 | a0001c0002t0008g0046 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.364-5644T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62530526 | ||||||
| chr17:62530794
|
G | C | 1 | a0001c0001t0001g0276 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.364-5376G>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62530794 | ||||||
| chr17:62530932
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.364-5238C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62530932 | ||||||
| chr17:62531115
|
G | A | 2 | a0001c0002t0004g0140a0001c0002t0022g0138 | 2 | HG02055.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.364-5055G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62531115 | ||||||
| chr17:62531270
|
T | TA | 99 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(96): Show | 99 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.364-4900_364-4899i others(3): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62531270 | ||||||
| chr17:62531271
|
T | A | 99 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(96): Show | 99 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.364-4899T>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62531271 | ||||||
| chr17:62531369
|
T | C | 1 | a0001c0001t0001g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.364-4801T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62531369 | ||||||
| chr17:62531541
|
A | G | 1 | a0001c0001t0001g0276 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.364-4629A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62531541 | ||||||
| chr17:62531818
|
T | G | 1 | a0001c0002t0004g0139 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.364-4352T>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62531818 | ||||||
| chr17:62531930
|
T | C | 1 | a0001c0002t0028g0005 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.364-4240T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62531930 | ||||||
| chr17:62532169
|
G | GT | 5 | a0001c0001t0001g0276a0001c0001t0001g0289a0001c0001t0001g0290others(2): Show | 5 | HG01243.hp1 HG01255.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.364-3994dupT | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr17 | 62532169 | |||||
| chr17:62532174
|
T | G | 2 | a0001c0002t0004g0140a0001c0002t0022g0138 | 2 | HG02055.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.364-3996T>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62532174 | ||||||
| chr17:62532177
|
G | T | 1 | a0001c0001t0001g0276 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.364-3993G>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62532177 | ||||||
| chr17:62532203
|
A | G | 1 | a0001c0001t0001g0201 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.364-3967A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62532203 | ||||||
| chr17:62532232
|
C | T | 275 | a0001c0001t0001g0020a0001c0001t0001g0176a0001c0001t0001g0178others(272): Show | 275 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.364-3938C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62532232 | ||||||
| chr17:62532237
|
C | T | 1 | a0001c0002t0002g0121 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.364-3933C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62532237 | ||||||
| chr17:62532248
|
G | C | 1 | a0001c0001t0001g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.364-3922G>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62532248 | ||||||
| chr17:62532274
|
C | G | 1 | a0001c0001t0001g0194 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.364-3896C>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62532274 | ||||||
| chr17:62532373
|
G | A | 107 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(104): Show | 107 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.364-3797G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62532373 | ||||||
| chr17:62532385
|
A | G | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.364-3785A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62532385 | ||||||
| chr17:62532418
|
T | G | 1 | a0001c0001t0001g0180 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.364-3752T>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62532418 | ||||||
| chr17:62532535
|
G | A | 3 | a0001c0001t0001g0208a0001c0001t0001g0222a0001c0001t0014g0267 | 3 | HG00733.hp1 HG00735.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.364-3635G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62532535 | ||||||
| chr17:62532840
|
C | T | 1 | a0001c0002t0003g0077 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.364-3330C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62532840 | ||||||
| chr17:62533117
|
T | C | 6 | a0001c0001t0010g0280a0001c0001t0010g0281a0001c0001t0010g0282others(3): Show | 6 | HG01109.hp2 HG02451.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.364-3053T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62533117 | ||||||
| chr17:62533317
|
T | C | 3 | a0001c0002t0004g0139a0001c0002t0004g0140a0001c0002t0022g0138 | 3 | HG01099.hp1 HG02055.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.364-2853T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62533317 | ||||||
| chr17:62533367
|
G | GGT | 4 | a0001c0001t0001g0211a0001c0001t0026g0278a0001c0001t0027g0277others(1): Show | 4 | HG02165.hp2 HG03239.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-2780_364-2779d others(4): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr17 | 62533367 | |||||
| chr17:62533367
|
G | GGTGT | 17 | a0001c0001t0001g0176a0001c0001t0001g0182a0001c0001t0001g0183others(14): Show | 17 | HG00733.hp1 HG01884.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.364-2782_364-2779d others(6): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr17 | 62533367 | |||||
| chr17:62533367
|
G | GGTGTGT | 76 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0187others(73): Show | 76 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.364-2784_364-2779d others(8): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr17 | 62533367 | |||||
| chr17:62533367
|
G | GGTGTGTG others(1): Show |
3 | a0001c0001t0001g0201a0001c0001t0001g0252a0001c0001t0001g0274 | 3 | HG01258.hp2 NA19086.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.364-2786_364-2779d others(10): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr17 | 62533367 | |||||
| chr17:62533367
|
G | GGTGTGTG others(3): Show |
1 | a0001c0001t0001g0200 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.364-2788_364-2779d others(12): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr17 | 62533367 | |||||
| chr17:62533383
|
TGTGTGTG others(59): Show |
T | 1 | a0001c0001t0001g0248 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.364-2778_364-2713d others(68): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr17 | 62533383 | |||||
| chr17:62533409
|
A | AT | 102 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(99): Show | 102 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.364-2747dupT | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr17 | 62533409 | |||||
| chr17:62533435
|
T | C | 1 | a0001c0002t0002g0021 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.364-2735T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62533435 | ||||||
| chr17:62533462
|
C | G | 1 | a0001c0001t0001g0224 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.364-2708C>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62533462 | ||||||
| chr17:62533479
|
A | AT | 6 | a0001c0001t0001g0241a0001c0001t0001g0263a0001c0002t0002g0129others(3): Show | 6 | HG01192.hp2 HG01928.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.364-2676dupT | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr17 | 62533479 | |||||
| chr17:62533522
|
G | T | 1 | a0001c0002t0002g0027 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.364-2648G>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62533522 | ||||||
| chr17:62533571
|
C | T | 5 | a0001c0002t0002g0099a0001c0002t0013g0100a0001c0002t0013g0101others(2): Show | 5 | HG02015.hp1 NA18977.hp1 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.364-2599C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62533571 | ||||||
| chr17:62533664
|
G | A | 250 | a0001c0001t0001g0020a0001c0001t0001g0176a0001c0001t0001g0178others(247): Show | 250 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.364-2506G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62533664 | ||||||
| chr17:62533726
|
C | T | 9 | a0001c0001t0004g0144a0001c0001t0004g0145a0001c0001t0004g0146others(6): Show | 9 | HG00738.hp2 HG01074.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.364-2444C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62533726 | ||||||
| chr17:62533746
|
G | A | 2 | a0001c0001t0026g0278a0001c0001t0027g0277 | 2 | HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.364-2424G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62533746 | ||||||
| chr17:62533911
|
T | G | 1 | a0001c0001t0001g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.364-2259T>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62533911 | ||||||
| chr17:62533927
|
G | A | 2 | a0001c0002t0004g0140a0001c0002t0022g0138 | 2 | HG02055.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.364-2243G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62533927 | ||||||
| chr17:62534136
|
C | G | 107 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(104): Show | 107 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.364-2034C>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62534136 | ||||||
| chr17:62534248
|
C | T | 1 | a0001c0002t0002g0032 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.364-1922C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62534248 | ||||||
| chr17:62534647
|
T | G | 4 | a0001c0001t0004g0048a0001c0001t0004g0049a0001c0001t0004g0050others(1): Show | 4 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.364-1523T>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62534647 | ||||||
| chr17:62534881
|
C | CT | 27 | a0001c0001t0001g0193a0001c0001t0001g0275a0001c0001t0001g0276others(24): Show | 27 | HG00639.hp2 HG00741.hp1 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.364-1265dupT | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr17 | 62534881 | |||||
| chr17:62534881
|
C | CTT | 82 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(79): Show | 82 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.364-1266_364-1265d others(4): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr17 | 62534881 | |||||
| chr17:62534881
|
C | CTTT | 12 | a0001c0001t0001g0206a0001c0001t0001g0211a0001c0001t0001g0223others(9): Show | 12 | HG01175.hp1 HG02055.hp2 HG02165.hp2 others(9): Show |
intron_variant | MODIFIER | c.364-1267_364-1265d others(5): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr17 | 62534881 | |||||
| chr17:62534984
|
G | A | 2 | a0001c0001t0016g0185a0001c0001t0016g0186 | 2 | HG01243.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.364-1186G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62534984 | ||||||
| chr17:62535222
|
T | C | 271 | a0001c0001t0001g0020a0001c0001t0001g0176a0001c0001t0001g0178others(268): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.364-948T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62535222 | ||||||
| chr17:62535229
|
T | A | 19 | a0001c0002t0003g0057a0001c0002t0003g0058a0001c0002t0003g0059others(16): Show | 19 | HG00438.hp1 HG01261.hp1 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.364-941T>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62535229 | ||||||
| chr17:62535346
|
G | A | 11 | a0001c0001t0006g0041a0001c0001t0006g0042a0001c0001t0006g0055others(8): Show | 11 | HG01109.hp2 HG02451.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.364-824G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62535346 | ||||||
| chr17:62535581
|
A | G | 1 | a0001c0001t0001g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.364-589A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62535581 | ||||||
| chr17:62535799
|
GAAAA | G | 34 | a0001c0002t0002g0051a0001c0002t0003g0043a0001c0002t0003g0044others(31): Show | 34 | HG00438.hp1 HG01192.hp1 HG01261.hp1 others(31): Show |
intron_variant | MODIFIER | c.364-366_364-363del others(4): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr17 | 62535799 | |||||
| chr17:62536069
|
A | G | 1 | a0001c0001t0001g0276 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.364-101A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 6/21 | chr17 | 62536069 | ||||||
| chr17:62536451
|
A | T | 37 | a0001c0001t0001g0020a0001c0002t0002g0003a0001c0002t0002g0004others(34): Show | 37 | HG00609.hp1 HG01167.hp1 HG01192.hp2 others(34): Show |
intron_variant | MODIFIER | c.531+114A>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62536451 | ||||||
| chr17:62536579
|
C | T | 1 | a0001c0001t0021g0153 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.531+242C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62536579 | ||||||
| chr17:62536625
|
G | C | 4 | a0001c0001t0004g0048a0001c0001t0004g0049a0001c0001t0004g0050others(1): Show | 4 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.531+288G>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62536625 | ||||||
| chr17:62536666
|
A | T | 4 | a0001c0001t0004g0048a0001c0001t0004g0049a0001c0001t0004g0050others(1): Show | 4 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.531+329A>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62536666 | ||||||
| chr17:62537053
|
G | C | 81 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0187others(78): Show | 81 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.531+716G>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62537053 | ||||||
| chr17:62537055
|
C | T | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.531+718C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62537055 | ||||||
| chr17:62537092
|
C | G | 250 | a0001c0001t0001g0020a0001c0001t0001g0176a0001c0001t0001g0178others(247): Show | 250 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.531+755C>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62537092 | ||||||
| chr17:62537334
|
G | C | 1 | a0001c0001t0003g0160 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.531+997G>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62537334 | ||||||
| chr17:62537456
|
G | A | 1 | a0001c0001t0016g0185 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.531+1119G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62537456 | ||||||
| chr17:62537456
|
G | C | 1 | a0001c0002t0003g0067 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.531+1119G>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62537456 | ||||||
| chr17:62537536
|
A | T | 2 | a0001c0001t0026g0278a0001c0001t0027g0277 | 2 | HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.531+1199A>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62537536 | ||||||
| chr17:62537640
|
G | A | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.531+1303G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62537640 | ||||||
| chr17:62537855
|
A | T | 1 | a0001c0002t0003g0078 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.531+1518A>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62537855 | ||||||
| chr17:62538033
|
G | GT | 46 | a0001c0001t0001g0020a0001c0001t0001g0276a0001c0001t0001g0290others(43): Show | 46 | HG00438.hp1 HG01192.hp1 HG01261.hp1 others(43): Show |
intron_variant | MODIFIER | c.531+1716dupT | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62538033 | |||||
| chr17:62538033
|
G | GTT | 98 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(95): Show | 98 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.531+1715_531+1716d others(4): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62538033 | |||||
| chr17:62538075
|
G | A | 1 | a0001c0001t0001g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.531+1738G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62538075 | ||||||
| chr17:62538128
|
C | T | 3 | a0001c0001t0004g0144a0001c0001t0004g0147a0001c0002t0022g0138 | 3 | HG02055.hp1 HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.531+1791C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62538128 | ||||||
| chr17:62538248
|
G | A | 97 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(94): Show | 97 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.531+1911G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62538248 | ||||||
| chr17:62538500
|
A | T | 1 | a0001c0002t0002g0133 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.531+2163A>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62538500 | ||||||
| chr17:62538519
|
A | T | 1 | a0001c0001t0006g0041 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.531+2182A>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62538519 | ||||||
| chr17:62538633
|
G | A | 34 | a0001c0002t0002g0051a0001c0002t0003g0043a0001c0002t0003g0044others(31): Show | 34 | HG00438.hp1 HG01192.hp1 HG01261.hp1 others(31): Show |
intron_variant | MODIFIER | c.531+2296G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62538633 | ||||||
| chr17:62538732
|
G | A | 1 | a0001c0002t0005g0038 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.531+2395G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62538732 | ||||||
| chr17:62538970
|
A | T | 1 | a0001c0001t0006g0056 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.531+2633A>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62538970 | ||||||
| chr17:62538972
|
T | G | 1 | a0001c0001t0004g0145 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.531+2635T>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62538972 | ||||||
| chr17:62538995
|
A | C | 2 | a0001c0001t0004g0144a0001c0001t0004g0147 | 2 | HG03041.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.531+2658A>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62538995 | ||||||
| chr17:62539042
|
A | C | 1 | a0001c0001t0001g0270 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.531+2705A>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62539042 | ||||||
| chr17:62539211
|
T | C | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.531+2874T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62539211 | ||||||
| chr17:62539473
|
C | CT | 14 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0004g0144others(11): Show | 14 | HG00738.hp2 HG01074.hp2 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.531+3155dupT | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62539473 | |||||
| chr17:62539473
|
CT | C | 9 | a0001c0001t0001g0194a0001c0001t0001g0197a0001c0001t0003g0167others(6): Show | 9 | HG01952.hp2 HG02109.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.531+3155delT | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62539473 | |||||
| chr17:62539531
|
G | A | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.531+3194G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62539531 | ||||||
| chr17:62539782
|
C | T | 2 | a0001c0001t0001g0248a0001c0001t0001g0249 | 2 | HG01884.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.531+3445C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62539782 | ||||||
| chr17:62539801
|
C | G | 1 | a0001c0002t0002g0132 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.531+3464C>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62539801 | ||||||
| chr17:62539890
|
G | A | 1 | a0001c0001t0004g0172 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.531+3553G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62539890 | ||||||
| chr17:62539948
|
A | G | 1 | a0001c0001t0001g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.531+3611A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62539948 | ||||||
| chr17:62540046
|
T | A | 1 | a0001c0002t0020g0001 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.531+3709T>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62540046 | ||||||
| chr17:62540068
|
CCTTTCTT | C | 34 | a0001c0002t0002g0051a0001c0002t0003g0043a0001c0002t0003g0044others(31): Show | 34 | HG00438.hp1 HG01192.hp1 HG01261.hp1 others(31): Show |
intron_variant | MODIFIER | c.531+3742_531+3748d others(9): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62540068 | |||||
| chr17:62540099
|
C | CT | 9 | a0001c0001t0001g0237a0001c0001t0004g0152a0001c0001t0010g0280others(6): Show | 9 | HG01109.hp2 HG01175.hp2 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.531+3780dupT | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62540099 | |||||
| chr17:62540099
|
CT | C | 22 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0187others(19): Show | 22 | HG00280.hp1 HG01074.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.531+3780delT | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62540099 | |||||
| chr17:62540105
|
T | C | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.531+3768T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62540105 | ||||||
| chr17:62540399
|
A | G | 1 | a0001c0002t0002g0115 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.531+4062A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62540399 | ||||||
| chr17:62540400
|
A | ATTTT | 9 | a0001c0001t0010g0282a0001c0001t0010g0283a0001c0001t0016g0186others(6): Show | 9 | HG01255.hp1 HG01943.hp2 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.531+4083_531+4086d others(6): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62540400 | |||||
| chr17:62540400
|
A | ATTTTTT | 13 | a0001c0001t0001g0187a0001c0001t0001g0199a0001c0001t0001g0209others(10): Show | 13 | HG00438.hp2 HG01109.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.531+4081_531+4086d others(8): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62540400 | |||||
| chr17:62540400
|
A | ATTTTTTT | 58 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0190others(55): Show | 58 | HG00140.hp2 HG00323.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.531+4080_531+4086d others(9): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62540400 | |||||
| chr17:62540400
|
A | ATTTTTTT others(1): Show |
13 | a0001c0001t0001g0188a0001c0001t0001g0216a0001c0001t0001g0217others(10): Show | 13 | HG00280.hp2 HG01168.hp2 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.531+4079_531+4086d others(10): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62540400 | |||||
| chr17:62540400
|
A | ATTTTTTT others(2): Show |
10 | a0001c0001t0001g0195a0001c0001t0001g0201a0001c0001t0001g0208others(7): Show | 10 | HG00735.hp1 HG01099.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.531+4078_531+4086d others(11): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62540400 | |||||
| chr17:62540400
|
A | ATTTTTTT others(3): Show |
3 | a0001c0001t0001g0254a0001c0001t0018g0243a0001c0001t0026g0278 | 3 | HG04228.hp1 NA18906.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.531+4077_531+4086d others(12): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62540400 | |||||
| chr17:62540400
|
A | ATTTTTTT others(4): Show |
3 | a0001c0001t0001g0196a0001c0001t0006g0041a0001c0002t0003g0060 | 3 | HG02647.hp1 HG03017.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.531+4076_531+4086d others(13): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62540400 | |||||
| chr17:62540400
|
A | ATTTTTTT others(5): Show |
1 | a0001c0001t0006g0074 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.531+4075_531+4086d others(14): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62540400 | |||||
| chr17:62540400
|
A | ATTTTTTT others(6): Show |
3 | a0001c0001t0006g0042a0001c0001t0006g0055a0001c0001t0006g0056 | 3 | HG02622.hp2 HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.531+4074_531+4086d others(15): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62540400 | |||||
| chr17:62540400
|
A | ATTTTTTT others(8): Show |
20 | a0001c0001t0004g0147a0001c0001t0021g0153a0001c0002t0002g0083others(17): Show | 20 | HG00140.hp1 HG00323.hp1 HG01258.hp1 others(17): Show |
intron_variant | MODIFIER | c.531+4072_531+4086d others(17): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62540400 | |||||
| chr17:62540400
|
A | ATTTTTTT others(9): Show |
23 | a0001c0001t0004g0144a0001c0001t0004g0152a0001c0002t0002g0004others(20): Show | 23 | HG00280.hp1 HG00639.hp1 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.531+4071_531+4086d others(18): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62540400 | |||||
| chr17:62540400
|
A | ATTTTTTT others(10): Show |
24 | a0001c0001t0001g0020a0001c0001t0012g0149a0001c0002t0002g0010others(21): Show | 24 | HG00438.hp1 HG00609.hp1 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.531+4070_531+4086d others(19): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62540400 | |||||
| chr17:62540400
|
A | ATTTTTTT others(11): Show |
7 | a0001c0002t0002g0008a0001c0002t0002g0021a0001c0002t0002g0027others(4): Show | 7 | HG02004.hp2 HG02055.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.531+4069_531+4086d others(20): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62540400 | |||||
| chr17:62540400
|
A | ATTTTTTT others(12): Show |
3 | a0001c0001t0012g0151a0001c0002t0002g0009a0001c0002t0007g0081 | 3 | HG00639.hp2 HG01358.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.531+4068_531+4086d others(21): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62540400 | |||||
| chr17:62540400
|
A | ATTTTTTT others(13): Show |
5 | a0001c0001t0004g0145a0001c0001t0004g0146a0001c0001t0004g0150others(2): Show | 5 | HG02293.hp1 HG03098.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.531+4067_531+4086d others(22): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62540400 | |||||
| chr17:62540400
|
A | ATTTTTTT others(14): Show |
7 | a0001c0002t0002g0007a0001c0002t0002g0015a0001c0002t0005g0006others(4): Show | 7 | HG01192.hp2 HG01934.hp2 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.531+4066_531+4086d others(23): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62540400 | |||||
| chr17:62540400
|
A | ATTTTTTT others(15): Show |
5 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0002t0003g0065others(2): Show | 5 | HG02683.hp2 HG03041.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.531+4065_531+4086d others(24): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62540400 | |||||
| chr17:62540400
|
A | ATTTTTTT others(16): Show |
8 | a0001c0002t0002g0013a0001c0002t0002g0019a0001c0002t0002g0032others(5): Show | 8 | HG01168.hp1 HG01261.hp1 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.531+4064_531+4086d others(25): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62540400 | |||||
| chr17:62540400
|
A | ATTTTTTT others(17): Show |
6 | a0001c0002t0002g0003a0001c0002t0002g0025a0001c0002t0002g0127others(3): Show | 6 | HG02738.hp2 HG03579.hp1 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.531+4086_531+4087i others(26): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62540400 | |||||
| chr17:62540400
|
A | ATTTTTTT others(18): Show |
5 | a0001c0002t0002g0014a0001c0002t0002g0034a0001c0002t0002g0080others(2): Show | 5 | HG02027.hp2 HG02080.hp2 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.531+4086_531+4087i others(27): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62540400 | |||||
| chr17:62540400
|
A | ATTTTTTT others(20): Show |
2 | a0001c0002t0011g0117a0001c0002t0011g0143 | 2 | NA18940.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.531+4086_531+4087i others(29): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62540400 | |||||
| chr17:62540400
|
A | ATTTTTTT others(21): Show |
1 | a0001c0002t0002g0108 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.531+4086_531+4087i others(30): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62540400 | |||||
| chr17:62540400
|
A | ATTTTTTT others(22): Show |
1 | a0001c0002t0002g0051 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.531+4086_531+4087i others(31): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62540400 | |||||
| chr17:62540400
|
A | ATTTTTTT others(23): Show |
2 | a0001c0002t0002g0107a0001c0002t0003g0073 | 2 | HG02074.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.531+4086_531+4087i others(32): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62540400 | |||||
| chr17:62540400
|
A | ATTTTTTT others(25): Show |
1 | a0001c0002t0002g0026 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.531+4086_531+4087i others(34): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62540400 | |||||
| chr17:62540400
|
A | ATTTTTTT others(26): Show |
1 | a0001c0002t0003g0052 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.531+4086_531+4087i others(35): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62540400 | |||||
| chr17:62540400
|
A | ATTTTTTT others(29): Show |
1 | a0001c0002t0007g0123 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.531+4086_531+4087i others(38): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62540400 | |||||
| chr17:62540400
|
A | ATTTTTTT others(31): Show |
2 | a0001c0002t0002g0039a0001c0002t0003g0062 | 2 | NA18986.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.531+4086_531+4087i others(40): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62540400 | |||||
| chr17:62540400
|
A | ATTTTTTT others(33): Show |
1 | a0001c0002t0003g0072 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.531+4086_531+4087i others(42): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62540400 | |||||
| chr17:62540400
|
A | T | 1 | a0001c0001t0001g0276 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.531+4063A>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62540400 | ||||||
| chr17:62540400
|
ATTTTTTT others(1): Show |
A | 15 | a0001c0001t0001g0176a0001c0001t0001g0182a0001c0001t0001g0183others(12): Show | 15 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.531+4079_531+4086d others(10): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62540400 | |||||
| chr17:62540439
|
G | T | 271 | a0001c0001t0001g0020a0001c0001t0001g0176a0001c0001t0001g0178others(268): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.531+4102G>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62540439 | ||||||
| chr17:62540545
|
C | T | 1 | a0001c0002t0002g0089 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.531+4208C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62540545 | ||||||
| chr17:62540666
|
T | C | 1 | a0001c0001t0001g0276 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.531+4329T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62540666 | ||||||
| chr17:62540689
|
G | T | 1 | a0001c0001t0001g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.531+4352G>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62540689 | ||||||
| chr17:62540748
|
A | G | 97 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(94): Show | 97 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.531+4411A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62540748 | ||||||
| chr17:62540780
|
G | T | 4 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0026g0278others(1): Show | 4 | HG03195.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.531+4443G>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62540780 | ||||||
| chr17:62541036
|
G | C | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | NA18954.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.531+4699G>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62541036 | ||||||
| chr17:62541052
|
C | T | 2 | a0001c0002t0002g0089a0001c0002t0002g0090 | 2 | HG00735.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.531+4715C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62541052 | ||||||
| chr17:62541064
|
A | T | 2 | a0001c0002t0002g0080a0001c0002t0007g0081 | 2 | HG00639.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.531+4727A>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62541064 | ||||||
| chr17:62541242
|
A | G | 3 | a0001c0002t0004g0139a0001c0002t0004g0140a0001c0002t0022g0138 | 3 | HG01099.hp1 HG02055.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.531+4905A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62541242 | ||||||
| chr17:62541768
|
G | GAT | 270 | a0001c0001t0001g0020a0001c0001t0001g0176a0001c0001t0001g0178others(267): Show | 270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.531+5431_531+5432i others(4): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62541768 | ||||||
| chr17:62541768
|
G | GATTGCAC others(22): Show |
1 | a0001c0002t0002g0135 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.531+5431_531+5432i others(31): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62541768 | ||||||
| chr17:62541845
|
GA | G | 36 | a0001c0002t0002g0008a0001c0002t0002g0034a0001c0002t0002g0051others(33): Show | 36 | HG00438.hp1 HG01192.hp1 HG01261.hp1 others(33): Show |
intron_variant | MODIFIER | c.531+5519delA | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62541845 | |||||
| chr17:62541860
|
G | C | 3 | a0001c0001t0006g0055a0001c0001t0006g0056a0001c0001t0006g0074 | 3 | HG02622.hp2 HG02970.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.531+5523G>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62541860 | ||||||
| chr17:62541907
|
T | A | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.531+5570T>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62541907 | ||||||
| chr17:62541912
|
G | A | 11 | a0001c0001t0006g0041a0001c0001t0006g0042a0001c0001t0006g0055others(8): Show | 11 | HG01109.hp2 HG02451.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.531+5575G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62541912 | ||||||
| chr17:62542008
|
A | G | 2 | a0001c0002t0002g0085a0001c0002t0002g0096 | 2 | HG01081.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.531+5671A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62542008 | ||||||
| chr17:62542052
|
A | G | 1 | a0001c0002t0002g0132 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.531+5715A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62542052 | ||||||
| chr17:62542158
|
T | C | 1 | a0001c0002t0015g0173 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.531+5821T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62542158 | ||||||
| chr17:62542175
|
C | T | 1 | a0001c0002t0003g0157 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.531+5838C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62542175 | ||||||
| chr17:62542269
|
A | G | 2 | a0001c0001t0026g0278a0001c0001t0027g0277 | 2 | HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.531+5932A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62542269 | ||||||
| chr17:62542351
|
C | G | 1 | a0001c0001t0001g0259 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.531+6014C>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62542351 | ||||||
| chr17:62542421
|
TTAAG | T | 4 | a0001c0001t0004g0048a0001c0001t0004g0049a0001c0001t0004g0050others(1): Show | 4 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.531+6089_531+6092d others(6): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62542421 | |||||
| chr17:62542432
|
C | G | 2 | a0001c0002t0002g0040a0001c0002t0005g0124 | 2 | HG00280.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.531+6095C>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62542432 | ||||||
| chr17:62542510
|
T | A | 2 | a0001c0001t0016g0185a0001c0001t0016g0186 | 2 | HG01243.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.531+6173T>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62542510 | ||||||
| chr17:62542572
|
C | T | 1 | a0001c0002t0003g0141 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.531+6235C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62542572 | ||||||
| chr17:62543267
|
T | C | 1 | a0001c0001t0001g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.531+6930T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62543267 | ||||||
| chr17:62543465
|
A | T | 1 | a0001c0002t0008g0047 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.531+7128A>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62543465 | ||||||
| chr17:62543717
|
A | G | 1 | a0001c0002t0002g0107 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.531+7380A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62543717 | ||||||
| chr17:62543745
|
T | C | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.531+7408T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62543745 | ||||||
| chr17:62543755
|
G | A | 1 | a0001c0002t0002g0009 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.531+7418G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62543755 | ||||||
| chr17:62543876
|
T | C | 3 | a0001c0001t0006g0055a0001c0001t0006g0056a0001c0001t0006g0074 | 3 | HG02622.hp2 HG02970.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.531+7539T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62543876 | ||||||
| chr17:62543950
|
C | T | 271 | a0001c0001t0001g0020a0001c0001t0001g0176a0001c0001t0001g0178others(268): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.531+7613C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62543950 | ||||||
| chr17:62544116
|
G | A | 254 | a0001c0001t0001g0020a0001c0001t0001g0176a0001c0001t0001g0178others(251): Show | 254 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.531+7779G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62544116 | ||||||
| chr17:62544136
|
TTACA | T | 3 | a0001c0001t0001g0200a0001c0001t0001g0202a0001c0001t0001g0237 | 3 | HG02083.hp1 NA18963.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.531+7800_531+7803d others(6): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62544136 | ||||||
| chr17:62544328
|
T | C | 2 | a0001c0001t0026g0278a0001c0001t0027g0277 | 2 | HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.532-7974T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62544328 | ||||||
| chr17:62544505
|
C | T | 2 | a0001c0002t0002g0107a0001c0002t0002g0108 | 2 | HG01255.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.532-7797C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62544505 | ||||||
| chr17:62544511
|
C | T | 2 | a0001c0001t0018g0255a0001c0004t0001g0204 | 2 | HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.532-7791C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62544511 | ||||||
| chr17:62544799
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.532-7503T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62544799 | ||||||
| chr17:62544854
|
G | A | 1 | a0001c0002t0002g0024 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.532-7448G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62544854 | ||||||
| chr17:62544877
|
A | G | 5 | a0001c0002t0002g0083a0001c0002t0002g0087a0001c0002t0002g0088others(2): Show | 5 | HG00738.hp1 HG01258.hp1 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.532-7425A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62544877 | ||||||
| chr17:62545076
|
T | G | 107 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(104): Show | 107 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.532-7226T>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62545076 | ||||||
| chr17:62545225
|
C | T | 11 | a0001c0001t0006g0041a0001c0001t0006g0042a0001c0001t0006g0055others(8): Show | 11 | HG01109.hp2 HG02451.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.532-7077C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62545225 | ||||||
| chr17:62545367
|
T | A | 1 | a0001c0001t0003g0175 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.532-6935T>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62545367 | ||||||
| chr17:62545476
|
G | A | 1 | a0001c0001t0008g0174 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.532-6826G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62545476 | ||||||
| chr17:62545515
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.532-6787G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62545515 | ||||||
| chr17:62545602
|
A | G | 107 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(104): Show | 107 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.532-6700A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62545602 | ||||||
| chr17:62545668
|
A | G | 10 | a0001c0001t0004g0144a0001c0001t0004g0145a0001c0001t0004g0146others(7): Show | 10 | HG00738.hp2 HG01074.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.532-6634A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62545668 | ||||||
| chr17:62545692
|
C | CTTG | 4 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0002t0002g0004others(1): Show | 4 | HG03041.hp2 HG03130.hp1 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.532-6589_532-6587d others(5): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62545692 | |||||
| chr17:62545804
|
G | A | 2 | a0001c0001t0026g0278a0001c0001t0027g0277 | 2 | HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.532-6498G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62545804 | ||||||
| chr17:62545873
|
T | TTTTG | 97 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(94): Show | 97 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.532-6406_532-6403d others(6): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62545873 | |||||
| chr17:62545929
|
G | A | 1 | a0001c0001t0021g0153 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.532-6373G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62545929 | ||||||
| chr17:62546093
|
G | C | 3 | a0001c0002t0002g0093a0001c0002t0002g0094a0001c0002t0007g0125 | 3 | HG00639.hp1 HG01071.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.532-6209G>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62546093 | ||||||
| chr17:62546213
|
A | G | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.532-6089A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62546213 | ||||||
| chr17:62546292
|
C | T | 1 | a0001c0001t0001g0276 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.532-6010C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62546292 | ||||||
| chr17:62546344
|
G | GTTTGTTT others(13): Show |
1 | a0001c0001t0021g0153 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.532-5955_532-5954i others(22): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62546344 | |||||
| chr17:62546344
|
G | GTTTTTT | 12 | a0001c0001t0006g0041a0001c0001t0006g0042a0001c0001t0006g0055others(9): Show | 12 | HG01109.hp2 HG02451.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.532-5947_532-5942d others(8): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62546344 | |||||
| chr17:62546344
|
G | GTTTTTTT others(3): Show |
1 | a0001c0002t0028g0005 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.532-5951_532-5942d others(12): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62546344 | |||||
| chr17:62546344
|
G | GTTTTTTT others(10): Show |
1 | a0001c0002t0013g0100 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.532-5947_532-5946i others(19): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62546344 | |||||
| chr17:62546344
|
G | GTTTTTTT others(11): Show |
1 | a0001c0002t0023g0098 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.532-5947_532-5946i others(20): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62546344 | |||||
| chr17:62546344
|
G | GTTTTTTT others(5): Show |
3 | a0001c0001t0001g0276a0001c0001t0016g0185a0001c0001t0016g0186 | 3 | HG01243.hp1 HG01255.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.532-5953_532-5942d others(14): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62546344 | |||||
| chr17:62546344
|
G | GTTTTTTT others(6): Show |
19 | a0001c0002t0002g0051a0001c0002t0003g0023a0001c0002t0003g0044others(16): Show | 19 | HG01943.hp2 HG01952.hp1 HG02040.hp1 others(16): Show |
intron_variant | MODIFIER | c.532-5954_532-5942d others(15): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62546344 | |||||
| chr17:62546344
|
G | GTTTTTTT others(7): Show |
82 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(79): Show | 82 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.532-5955_532-5942d others(16): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62546344 | |||||
| chr17:62546344
|
G | GTTTTTTT others(8): Show |
32 | a0001c0001t0001g0184a0001c0001t0001g0187a0001c0001t0001g0189others(29): Show | 32 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.532-5956_532-5942d others(17): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62546344 | |||||
| chr17:62546344
|
G | GTTTTTTT others(9): Show |
23 | a0001c0001t0001g0195a0001c0001t0001g0230a0001c0001t0001g0231others(20): Show | 23 | HG00639.hp1 HG00733.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.532-5957_532-5942d others(18): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62546344 | |||||
| chr17:62546344
|
G | GTTTTTTT others(10): Show |
29 | a0001c0001t0001g0226a0001c0001t0004g0049a0001c0001t0004g0172others(26): Show | 29 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.532-5942_532-5941i others(19): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62546344 | |||||
| chr17:62546344
|
G | GTTTTTTT others(11): Show |
14 | a0001c0002t0002g0026a0001c0002t0002g0034a0001c0002t0002g0040others(11): Show | 14 | HG00280.hp1 HG00639.hp2 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.532-5942_532-5941i others(20): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62546344 | |||||
| chr17:62546344
|
G | GTTTTTTT others(12): Show |
17 | a0001c0002t0002g0007a0001c0002t0002g0009a0001c0002t0002g0021others(14): Show | 17 | HG00323.hp1 HG01099.hp2 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.532-5942_532-5941i others(21): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62546344 | |||||
| chr17:62546344
|
G | GTTTTTTT others(13): Show |
13 | a0001c0001t0001g0180a0001c0002t0002g0011a0001c0002t0002g0013others(10): Show | 13 | HG00609.hp1 HG01993.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.532-5942_532-5941i others(22): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62546344 | |||||
| chr17:62546344
|
G | GTTTTTTT others(14): Show |
14 | a0001c0001t0001g0020a0001c0001t0004g0144a0001c0001t0004g0145others(11): Show | 14 | HG01074.hp2 HG01167.hp1 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.532-5942_532-5941i others(23): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62546344 | |||||
| chr17:62546344
|
G | GTTTTTTT others(15): Show |
4 | a0001c0001t0001g0181a0001c0001t0004g0152a0001c0002t0002g0004others(1): Show | 4 | HG01175.hp2 HG03041.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.532-5942_532-5941i others(24): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62546344 | |||||
| chr17:62546344
|
G | GTTTTTTT others(16): Show |
3 | a0001c0001t0012g0149a0001c0002t0002g0003a0001c0002t0007g0036 | 3 | HG00738.hp2 NA18948.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.532-5942_532-5941i others(25): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62546344 | |||||
| chr17:62546344
|
G | GTTTTTTT others(18): Show |
3 | a0001c0001t0004g0048a0001c0001t0004g0050a0001c0001t0004g0054 | 3 | HG01884.hp1 HG02280.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.532-5942_532-5941i others(27): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62546344 | |||||
| chr17:62546360
|
T | TTTTTTTT others(8): Show |
1 | a0001c0002t0002g0128 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.532-5942_532-5941i others(17): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62546360 | ||||||
| chr17:62546374
|
G | C | 1 | a0001c0001t0001g0276 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.532-5928G>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62546374 | ||||||
| chr17:62547022
|
C | T | 1 | a0001c0002t0002g0130 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.532-5280C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62547022 | ||||||
| chr17:62547028
|
A | C | 271 | a0001c0001t0001g0020a0001c0001t0001g0176a0001c0001t0001g0178others(268): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.532-5274A>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62547028 | ||||||
| chr17:62547040
|
C | T | 2 | a0001c0001t0026g0278a0001c0001t0027g0277 | 2 | HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.532-5262C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62547040 | ||||||
| chr17:62547239
|
T | C | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.532-5063T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62547239 | ||||||
| chr17:62547265
|
T | G | 6 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0233others(3): Show | 6 | HG01074.hp1 HG01515.hp2 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.532-5037T>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62547265 | ||||||
| chr17:62547335
|
G | C | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.532-4967G>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62547335 | ||||||
| chr17:62547348
|
T | C | 3 | a0001c0001t0010g0280a0001c0001t0010g0281a0001c0001t0017g0279 | 3 | HG02818.hp2 HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.532-4954T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62547348 | ||||||
| chr17:62547406
|
C | G | 1 | a0001c0001t0001g0180 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.532-4896C>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62547406 | ||||||
| chr17:62547506
|
A | G | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.532-4796A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62547506 | ||||||
| chr17:62547804
|
C | G | 1 | a0001c0002t0002g0130 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.532-4498C>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62547804 | ||||||
| chr17:62547843
|
C | CA | 9 | a0001c0001t0004g0144a0001c0001t0004g0145a0001c0001t0004g0146others(6): Show | 9 | HG00738.hp2 HG01074.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.532-4458dupA | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62547843 | |||||
| chr17:62548194
|
C | T | 1 | a0001c0002t0002g0120 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.532-4108C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62548194 | ||||||
| chr17:62548236
|
A | ATGTGTGT others(3): Show |
1 | a0001c0002t0002g0105 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.532-4065_532-4064i others(12): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62548236 | |||||
| chr17:62548236
|
A | ATGTGTGT others(5): Show |
1 | a0001c0002t0002g0136 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.532-4065_532-4064i others(14): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62548236 | |||||
| chr17:62548238
|
A | ATG | 4 | a0001c0001t0001g0194a0001c0002t0002g0103a0001c0002t0004g0140others(1): Show | 4 | HG01515.hp1 HG02055.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.532-4063_532-4062i others(4): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62548238 | |||||
| chr17:62548238
|
A | ATGTG | 44 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0187others(41): Show | 44 | HG00323.hp2 HG00741.hp2 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.532-4063_532-4062i others(6): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62548238 | |||||
| chr17:62548238
|
A | ATGTGTG | 40 | a0001c0001t0001g0188a0001c0001t0001g0190a0001c0001t0001g0200others(37): Show | 40 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(37): Show |
intron_variant | MODIFIER | c.532-4063_532-4062i others(8): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62548238 | |||||
| chr17:62548238
|
A | ATGTGTGT others(1): Show |
21 | a0001c0001t0001g0198a0001c0001t0001g0202a0001c0001t0001g0203others(18): Show | 21 | HG00733.hp2 HG00738.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.532-4063_532-4062i others(10): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62548238 | |||||
| chr17:62548238
|
A | ATGTGTGT others(3): Show |
8 | a0001c0001t0001g0218a0001c0001t0001g0268a0001c0001t0001g0274others(5): Show | 8 | HG01071.hp1 HG01243.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.532-4063_532-4062i others(12): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62548238 | |||||
| chr17:62548238
|
A | ATGTGTGT others(5): Show |
8 | a0001c0001t0001g0258a0001c0001t0001g0273a0001c0001t0014g0221others(5): Show | 8 | HG00639.hp1 HG01934.hp1 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.532-4063_532-4062i others(14): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62548238 | |||||
| chr17:62548238
|
A | ATGTGTGT others(9): Show |
1 | a0001c0002t0005g0137 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.532-4063_532-4062i others(18): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62548238 | |||||
| chr17:62548238
|
A | G | 3 | a0001c0001t0001g0259a0001c0002t0002g0105a0001c0002t0002g0136 | 3 | HG04204.hp2 NA18960.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.532-4064A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62548238 | ||||||
| chr17:62548238
|
ATATGTGT others(3): Show |
A | 1 | a0001c0001t0004g0049 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.532-4062_532-4053d others(12): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62548238 | |||||
| chr17:62548238
|
ATATGTGT others(5): Show |
A | 3 | a0001c0001t0004g0048a0001c0001t0004g0050a0001c0001t0004g0054 | 3 | HG01884.hp1 HG02280.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.532-4062_532-4051d others(14): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62548238 | |||||
| chr17:62548240
|
A | ATATATAT others(3): Show |
2 | a0001c0001t0012g0148a0001c0001t0012g0151 | 2 | HG01074.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.532-4061_532-4060i others(12): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62548240 | |||||
| chr17:62548240
|
A | ATATATAT others(5): Show |
1 | a0001c0001t0012g0149 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.532-4061_532-4060i others(14): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62548240 | |||||
| chr17:62548240
|
A | ATATATGT others(3): Show |
1 | a0001c0001t0010g0282 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.532-4061_532-4060i others(12): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62548240 | |||||
| chr17:62548240
|
A | ATATG | 9 | a0001c0001t0006g0041a0001c0002t0002g0080a0001c0002t0002g0097others(6): Show | 9 | HG00639.hp2 HG02647.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.532-4061_532-4060i others(6): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62548240 | |||||
| chr17:62548240
|
A | ATATGTGT others(3): Show |
3 | a0001c0001t0010g0283a0001c0002t0002g0128a0001c0002t0015g0173 | 3 | HG01168.hp1 HG02486.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.532-4061_532-4060i others(12): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62548240 | |||||
| chr17:62548240
|
A | ATATGTGT others(5): Show |
3 | a0001c0002t0002g0013a0001c0002t0002g0028a0001c0002t0002g0032 | 3 | HG02074.hp1 HG02083.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.532-4061_532-4060i others(14): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62548240 | |||||
| chr17:62548240
|
A | ATG | 27 | a0001c0001t0003g0158a0001c0001t0003g0159a0001c0001t0003g0160others(24): Show | 27 | HG01069.hp1 HG01071.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.532-4028_532-4027d others(4): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62548240 | |||||
| chr17:62548240
|
A | ATGTG | 15 | a0001c0001t0001g0176a0001c0001t0001g0182a0001c0001t0001g0183others(12): Show | 15 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.532-4030_532-4027d others(6): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62548240 | |||||
| chr17:62548240
|
A | ATGTGTG | 16 | a0001c0001t0001g0189a0001c0001t0025g0247a0001c0002t0002g0004others(13): Show | 16 | HG00438.hp2 HG01978.hp1 HG02165.hp1 others(13): Show |
intron_variant | MODIFIER | c.532-4032_532-4027d others(8): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62548240 | |||||
| chr17:62548240
|
A | ATGTGTGT others(1): Show |
32 | a0001c0001t0001g0020a0001c0002t0002g0003a0001c0002t0002g0007others(29): Show | 32 | HG00280.hp1 HG00438.hp1 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.532-4034_532-4027d others(10): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62548240 | |||||
| chr17:62548240
|
A | ATGTGTGT others(3): Show |
14 | a0001c0001t0016g0186a0001c0002t0002g0008a0001c0002t0002g0011others(11): Show | 14 | HG00609.hp1 HG01081.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.532-4036_532-4027d others(12): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62548240 | |||||
| chr17:62548240
|
A | ATGTGTGT others(5): Show |
12 | a0001c0001t0016g0185a0001c0002t0002g0022a0001c0002t0002g0051others(9): Show | 12 | HG01243.hp1 HG02040.hp1 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.532-4038_532-4027d others(14): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62548240 | |||||
| chr17:62548240
|
A | ATGTGTGT others(7): Show |
5 | a0001c0002t0002g0012a0001c0002t0003g0044a0001c0002t0003g0045others(2): Show | 5 | HG01167.hp1 HG01192.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.532-4040_532-4027d others(16): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62548240 | |||||
| chr17:62548240
|
A | ATGTGTGT others(9): Show |
1 | a0001c0002t0002g0121 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.532-4042_532-4027d others(18): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62548240 | |||||
| chr17:62548240
|
A | G | 129 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0187others(126): Show | 129 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.532-4062A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62548240 | ||||||
| chr17:62548240
|
ATG | A | 3 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0006g0042 | 3 | HG02622.hp1 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.532-4028_532-4027d others(4): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62548240 | |||||
| chr17:62548244
|
G | A | 1 | a0001c0001t0006g0042 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.532-4058G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62548244 | ||||||
| chr17:62548250
|
G | A | 1 | a0001c0001t0004g0144 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.532-4052G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62548250 | ||||||
| chr17:62548252
|
G | A | 1 | a0001c0001t0004g0144 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.532-4050G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62548252 | ||||||
| chr17:62548254
|
G | A | 1 | a0001c0001t0004g0144 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.532-4048G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62548254 | ||||||
| chr17:62548345
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.532-3957G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62548345 | ||||||
| chr17:62548489
|
G | T | 1 | a0001c0001t0003g0158 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.532-3813G>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62548489 | ||||||
| chr17:62548539
|
C | T | 2 | a0001c0001t0026g0278a0001c0001t0027g0277 | 2 | HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.532-3763C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62548539 | ||||||
| chr17:62548544
|
G | A | 10 | a0001c0001t0001g0176a0001c0001t0001g0182a0001c0001t0001g0183others(7): Show | 10 | HG02486.hp2 HG02647.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.532-3758G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62548544 | ||||||
| chr17:62549113
|
G | T | 9 | a0001c0001t0004g0144a0001c0001t0004g0145a0001c0001t0004g0146others(6): Show | 9 | HG00738.hp2 HG01074.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.532-3189G>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62549113 | ||||||
| chr17:62549253
|
C | G | 291 | a0001c0001t0001g0020a0001c0001t0001g0176a0001c0001t0001g0178others(288): Show | 291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.532-3049C>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62549253 | ||||||
| chr17:62549268
|
G | A | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.532-3034G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62549268 | ||||||
| chr17:62549292
|
G | A | 3 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0003g0159 | 3 | HG02300.hp2 HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.532-3010G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62549292 | ||||||
| chr17:62549398
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0006g0074 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.532-2874_532-2865d others(12): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62549398 | |||||
| chr17:62549398
|
C | CAAAAAAA others(7): Show |
1 | a0001c0001t0006g0055 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.532-2878_532-2865d others(16): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62549398 | |||||
| chr17:62549398
|
CA | C | 10 | a0001c0001t0003g0162a0001c0001t0003g0163a0001c0001t0003g0165others(7): Show | 10 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.532-2865delA | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62549398 | |||||
| chr17:62549398
|
CAA | C | 6 | a0001c0001t0003g0160a0001c0001t0003g0164a0001c0001t0004g0172others(3): Show | 6 | HG01891.hp2 HG02258.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.532-2866_532-2865d others(4): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62549398 | |||||
| chr17:62549398
|
CAAAAAAA others(5): Show |
C | 3 | a0001c0001t0004g0048a0001c0001t0004g0050a0001c0001t0004g0054 | 3 | HG01884.hp1 HG02280.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.532-2876_532-2865d others(14): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62549398 | |||||
| chr17:62549398
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0004g0049 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.532-2877_532-2865d others(15): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62549398 | |||||
| chr17:62549398
|
CAAAAAAA others(8): Show |
C | 1 | a0001c0002t0002g0114 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.532-2879_532-2865d others(17): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62549398 | |||||
| chr17:62549398
|
CAAAAAAA others(12): Show |
C | 1 | a0001c0001t0001g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.532-2883_532-2865d others(21): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62549398 | |||||
| chr17:62549398
|
CAAAAAAA others(13): Show |
C | 6 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0240others(3): Show | 6 | HG01074.hp1 HG01928.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.532-2884_532-2865d others(22): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62549398 | |||||
| chr17:62549398
|
CAAAAAAA others(14): Show |
C | 82 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(79): Show | 82 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.532-2885_532-2865d others(23): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62549398 | |||||
| chr17:62549398
|
CAAAAAAA others(15): Show |
C | 13 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0198others(10): Show | 13 | HG00140.hp2 HG01081.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.532-2886_532-2865d others(24): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62549398 | |||||
| chr17:62549418
|
A | G | 2 | a0001c0001t0010g0282a0001c0002t0002g0108 | 2 | HG01255.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.532-2884A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62549418 | ||||||
| chr17:62549419
|
A | AAAAAAAA others(15): Show |
1 | a0001c0002t0002g0093 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.532-2865_532-2864i others(24): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62549419 | |||||
| chr17:62549419
|
A | AAAAAAAA others(12): Show |
6 | a0001c0002t0002g0086a0001c0002t0002g0094a0001c0002t0003g0069others(3): Show | 6 | HG01433.hp2 HG02074.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.532-2866_532-2865i others(21): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62549419 | |||||
| chr17:62549419
|
A | AAAAAAAA others(11): Show |
18 | a0001c0002t0002g0008a0001c0002t0002g0013a0001c0002t0002g0032others(15): Show | 18 | HG00438.hp1 HG02074.hp1 HG02080.hp1 others(15): Show |
intron_variant | MODIFIER | c.532-2867_532-2866i others(20): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62549419 | |||||
| chr17:62549419
|
A | AAAAAAAA others(10): Show |
47 | a0001c0001t0012g0149a0001c0001t0012g0151a0001c0002t0002g0003others(44): Show | 47 | HG00323.hp1 HG00609.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.532-2868_532-2867i others(19): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62549419 | |||||
| chr17:62549419
|
A | AAAAAAAA others(9): Show |
38 | a0001c0001t0004g0146a0001c0001t0004g0152a0001c0002t0002g0007others(35): Show | 38 | HG00280.hp1 HG00735.hp2 HG01175.hp2 others(35): Show |
intron_variant | MODIFIER | c.532-2869_532-2868i others(18): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62549419 | |||||
| chr17:62549419
|
A | AAAAAAAA others(8): Show |
19 | a0001c0001t0004g0145a0001c0001t0004g0150a0001c0001t0012g0148others(16): Show | 19 | HG00140.hp1 HG00738.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.532-2870_532-2869i others(17): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62549419 | |||||
| chr17:62549419
|
A | AAAAAAAA others(11): Show |
1 | a0001c0002t0002g0130 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.532-2875_532-2874i others(20): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62549419 | |||||
| chr17:62549419
|
A | T | 2 | a0001c0001t0010g0282a0001c0002t0002g0108 | 2 | HG01255.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.532-2883A>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62549419 | ||||||
| chr17:62549420
|
A | AAAAAAAA others(12): Show |
1 | a0001c0002t0003g0079 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.532-2865_532-2864i others(21): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62549420 | |||||
| chr17:62549420
|
A | AAAAAAAA others(10): Show |
2 | a0001c0001t0004g0147a0001c0002t0007g0125 | 2 | HG00639.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.532-2867_532-2866i others(19): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62549420 | |||||
| chr17:62549420
|
A | AAAAAAAA others(9): Show |
1 | a0001c0002t0002g0085 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.532-2868_532-2867i others(18): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62549420 | |||||
| chr17:62549420
|
A | AAAAAAAA others(8): Show |
6 | a0001c0001t0004g0144a0001c0002t0002g0034a0001c0002t0002g0082others(3): Show | 6 | HG01099.hp2 HG02132.hp1 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.532-2869_532-2868i others(17): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62549420 | |||||
| chr17:62549420
|
A | AAAAAAAA others(7): Show |
2 | a0001c0002t0002g0097a0001c0002t0011g0111 | 2 | HG02723.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.532-2870_532-2869i others(16): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62549420 | |||||
| chr17:62549435
|
A | T | 1 | a0001c0002t0003g0043 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.532-2867A>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62549435 | ||||||
| chr17:62549580
|
T | C | 1 | a0001c0001t0003g0167 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.532-2722T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62549580 | ||||||
| chr17:62549611
|
T | C | 1 | a0001c0002t0002g0040 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.532-2691T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62549611 | ||||||
| chr17:62549741
|
C | T | 1 | a0001c0001t0001g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.532-2561C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62549741 | ||||||
| chr17:62549834
|
GT | G | 109 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(106): Show | 109 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.532-2453delT | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62549834 | |||||
| chr17:62550407
|
A | C | 1 | a0001c0001t0001g0276 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.532-1895A>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62550407 | ||||||
| chr17:62550973
|
T | C | 271 | a0001c0001t0001g0020a0001c0001t0001g0176a0001c0001t0001g0178others(268): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.532-1329T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62550973 | ||||||
| chr17:62550984
|
A | G | 1 | a0001c0002t0004g0091 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.532-1318A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62550984 | ||||||
| chr17:62551157
|
G | A | 1 | a0001c0001t0001g0211 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.532-1145G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62551157 | ||||||
| chr17:62551420
|
G | A | 107 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(104): Show | 107 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.532-882G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62551420 | ||||||
| chr17:62551471
|
T | C | 271 | a0001c0001t0001g0020a0001c0001t0001g0176a0001c0001t0001g0178others(268): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.532-831T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62551471 | ||||||
| chr17:62551573
|
C | T | 15 | a0001c0001t0001g0020a0001c0002t0002g0004a0001c0002t0002g0008others(12): Show | 15 | HG00609.hp1 HG02074.hp1 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.532-729C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62551573 | ||||||
| chr17:62551574
|
G | A | 1 | a0001c0001t0001g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.532-728G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62551574 | ||||||
| chr17:62551598
|
G | A | 1 | a0001c0001t0001g0260 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.532-704G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62551598 | ||||||
| chr17:62551709
|
GA | G | 101 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(98): Show | 101 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.532-579delA | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr17 | 62551709 | |||||
| chr17:62551767
|
A | G | 1 | a0001c0002t0002g0095 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.532-535A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62551767 | ||||||
| chr17:62552042
|
A | G | 99 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(96): Show | 99 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.532-260A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62552042 | ||||||
| chr17:62552056
|
C | T | 1 | a0001c0002t0002g0025 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.532-246C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 7/21 | chr17 | 62552056 | ||||||
| chr17:62552582
|
T | C | 1 | a0001c0001t0001g0276 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.627+185T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 8/21 | chr17 | 62552582 | ||||||
| chr17:62552617
|
G | A | 1 | a0001c0001t0006g0042 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.627+220G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 8/21 | chr17 | 62552617 | ||||||
| chr17:62552662
|
C | CT | 13 | a0001c0001t0006g0041a0001c0001t0006g0042a0001c0001t0006g0055others(10): Show | 13 | HG00438.hp2 HG01109.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.627+281dupT | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr17 | 62552662 | |||||
| chr17:62552662
|
CT | C | 39 | a0001c0001t0001g0197a0001c0001t0001g0275a0001c0001t0001g0276others(36): Show | 39 | HG00438.hp1 HG01192.hp1 HG01192.hp2 others(36): Show |
intron_variant | MODIFIER | c.627+281delT | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr17 | 62552662 | |||||
| chr17:62552755
|
T | G | 1 | a0001c0001t0001g0213 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.627+358T>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 8/21 | chr17 | 62552755 | ||||||
| chr17:62552861
|
T | C | 1 | a0001c0001t0001g0276 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.627+464T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 8/21 | chr17 | 62552861 | ||||||
| chr17:62552988
|
T | C | 1 | a0001c0001t0004g0050 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.627+591T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 8/21 | chr17 | 62552988 | ||||||
| chr17:62553170
|
A | G | 1 | a0001c0002t0002g0130 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.628-493A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 8/21 | chr17 | 62553170 | ||||||
| chr17:62553238
|
T | C | 99 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0179others(96): Show | 99 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.628-425T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 8/21 | chr17 | 62553238 | ||||||
| chr17:62553262
|
C | G | 4 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0026g0278others(1): Show | 4 | HG03195.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.628-401C>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 8/21 | chr17 | 62553262 | ||||||
| chr17:62553358
|
G | A | 3 | a0001c0001t0001g0192a0001c0001t0001g0248a0001c0001t0001g0249 | 3 | HG01884.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.628-305G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 8/21 | chr17 | 62553358 | ||||||
| chr17:62553593
|
A | G | 1 | a0001c0002t0002g0097 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.628-70A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 8/21 | chr17 | 62553593 | ||||||
| chr17:62553637
|
A | C | 1 | a0001c0001t0025g0247 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.628-26A>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 8/21 | chr17 | 62553637 | ||||||
| chr17:62553926
|
C | A | 1 | a0001c0001t0009g0286 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.720+171C>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 9/21 | chr17 | 62553926 | ||||||
| chr17:62554220
|
C | T | 2 | a0001c0001t0026g0278a0001c0001t0027g0277 | 2 | HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.720+465C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 9/21 | chr17 | 62554220 | ||||||
| chr17:62554567
|
G | A | 184 | a0001c0001t0001g0020a0001c0001t0003g0158a0001c0001t0003g0159others(181): Show | 184 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.720+812G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 9/21 | chr17 | 62554567 | ||||||
| chr17:62554673
|
G | C | 1 | a0001c0002t0002g0088 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.720+918G>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 9/21 | chr17 | 62554673 | ||||||
| chr17:62554796
|
G | A | 1 | a0001c0001t0021g0153 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.720+1041G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 9/21 | chr17 | 62554796 | ||||||
| chr17:62554834
|
G | A | 20 | a0001c0001t0003g0158a0001c0001t0003g0159a0001c0001t0003g0160others(17): Show | 20 | HG01069.hp1 HG01071.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.720+1079G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 9/21 | chr17 | 62554834 | ||||||
| chr17:62554872
|
G | A | 1 | a0001c0002t0003g0063 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.720+1117G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 9/21 | chr17 | 62554872 | ||||||
| chr17:62554876
|
C | CA | 6 | a0001c0001t0001g0178a0001c0001t0001g0233a0001c0001t0001g0257others(3): Show | 6 | HG01981.hp1 NA18959.hp1 NA18992.hp1 others(3): Show |
intron_variant | MODIFIER | c.720+1136dupA | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr17 | 62554876 | |||||
| chr17:62554876
|
CA | C | 110 | a0001c0001t0001g0020a0001c0001t0001g0190a0001c0001t0001g0199others(107): Show | 110 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.720+1136delA | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr17 | 62554876 | |||||
| chr17:62554896
|
A | G | 2 | a0001c0001t0026g0278a0001c0001t0027g0277 | 2 | HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.720+1141A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 9/21 | chr17 | 62554896 | ||||||
| chr17:62554967
|
A | AT | 22 | a0001c0001t0003g0158a0001c0001t0003g0159a0001c0001t0003g0160others(19): Show | 22 | HG01069.hp1 HG01071.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.720+1222dupT | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr17 | 62554967 | |||||
| chr17:62555023
|
C | T | 194 | a0001c0001t0001g0020a0001c0001t0001g0180a0001c0001t0001g0181others(191): Show | 194 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.720+1268C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 9/21 | chr17 | 62555023 | ||||||
| chr17:62555166
|
G | C | 3 | a0001c0002t0003g0058a0001c0002t0003g0075a0001c0002t0004g0053 | 3 | HG00438.hp1 HG02132.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.720+1411G>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 9/21 | chr17 | 62555166 | ||||||
| chr17:62555410
|
C | T | 1 | a0001c0002t0002g0131 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.720+1655C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 9/21 | chr17 | 62555410 | ||||||
| chr17:62555424
|
C | T | 2 | a0001c0002t0003g0157a0001c0002t0004g0156 | 2 | HG01261.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.720+1669C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 9/21 | chr17 | 62555424 | ||||||
| chr17:62555483
|
AT | A | 8 | a0001c0001t0001g0179a0001c0001t0001g0203a0001c0001t0006g0041others(5): Show | 8 | HG01074.hp2 HG01081.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.720+1745delT | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr17 | 62555483 | |||||
| chr17:62555579
|
G | GTCAAGCA others(11): Show |
2 | a0001c0001t0001g0230a0001c0001t0001g0246 | 2 | HG00140.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.720+1828_720+1845d others(20): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr17 | 62555579 | |||||
| chr17:62555632
|
G | A | 4 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0026g0278others(1): Show | 4 | HG03195.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.720+1877G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 9/21 | chr17 | 62555632 | ||||||
| chr17:62555667
|
C | T | 3 | a0001c0001t0006g0055a0001c0001t0006g0056a0001c0001t0006g0074 | 3 | HG02622.hp2 HG02970.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.720+1912C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 9/21 | chr17 | 62555667 | ||||||
| chr17:62555735
|
C | G | 20 | a0001c0001t0003g0158a0001c0001t0003g0159a0001c0001t0003g0160others(17): Show | 20 | HG01069.hp1 HG01071.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.720+1980C>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 9/21 | chr17 | 62555735 | ||||||
| chr17:62555737
|
A | G | 1 | a0001c0001t0001g0231 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.720+1982A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 9/21 | chr17 | 62555737 | ||||||
| chr17:62555767
|
G | A | 184 | a0001c0001t0001g0020a0001c0001t0003g0158a0001c0001t0003g0159others(181): Show | 184 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.720+2012G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 9/21 | chr17 | 62555767 | ||||||
| chr17:62555773
|
G | A | 1 | a0001c0001t0006g0041 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.720+2018G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 9/21 | chr17 | 62555773 | ||||||
| chr17:62555985
|
G | A | 1 | a0001c0002t0002g0094 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.720+2230G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 9/21 | chr17 | 62555985 | ||||||
| chr17:62556518
|
C | T | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.720+2763C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 9/21 | chr17 | 62556518 | ||||||
| chr17:62556548
|
A | G | 4 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0026g0278others(1): Show | 4 | HG03195.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.720+2793A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 9/21 | chr17 | 62556548 | ||||||
| chr17:62556635
|
A | G | 1 | a0001c0002t0003g0078 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.720+2880A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 9/21 | chr17 | 62556635 | ||||||
| chr17:62556748
|
ATCCCTCT | A | 4 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0026g0278others(1): Show | 4 | HG03195.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.720+2995_720+3001d others(9): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr17 | 62556748 | |||||
| chr17:62556752
|
C | T | 2 | a0001c0001t0001g0218a0001c0001t0001g0268 | 2 | HG01243.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.720+2997C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 9/21 | chr17 | 62556752 | ||||||
| chr17:62556987
|
C | T | 1 | a0001c0001t0001g0276 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.721-3029C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 9/21 | chr17 | 62556987 | ||||||
| chr17:62557034
|
C | T | 1 | a0001c0001t0001g0217 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.721-2982C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 9/21 | chr17 | 62557034 | ||||||
| chr17:62557304
|
G | T | 1 | a0001c0001t0001g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.721-2712G>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 9/21 | chr17 | 62557304 | ||||||
| chr17:62557470
|
A | G | 2 | a0001c0002t0003g0064a0001c0002t0003g0065 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.721-2546A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 9/21 | chr17 | 62557470 | ||||||
| chr17:62557678
|
C | G | 3 | a0001c0001t0001g0207a0001c0001t0001g0227a0001c0001t0001g0228 | 3 | HG02055.hp2 HG02965.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.721-2338C>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 9/21 | chr17 | 62557678 | ||||||
| chr17:62558100
|
G | A | 1 | a0001c0001t0025g0247 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.721-1916G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 9/21 | chr17 | 62558100 | ||||||
| chr17:62558196
|
G | A | 1 | a0001c0001t0001g0258 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.721-1820G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 9/21 | chr17 | 62558196 | ||||||
| chr17:62558307
|
C | T | 1 | a0001c0003t0008g0071 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.721-1709C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 9/21 | chr17 | 62558307 | ||||||
| chr17:62558462
|
T | C | 191 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0275others(188): Show | 191 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.721-1554T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 9/21 | chr17 | 62558462 | ||||||
| chr17:62558481
|
C | T | 183 | a0001c0001t0003g0158a0001c0001t0003g0159a0001c0001t0003g0160others(180): Show | 183 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.721-1535C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 9/21 | chr17 | 62558481 | ||||||
| chr17:62559231
|
T | C | 1 | a0001c0001t0001g0244 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.721-785T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 9/21 | chr17 | 62559231 | ||||||
| chr17:62559299
|
CAT | C | 137 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0007others(134): Show | 137 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.721-715_721-714del others(2): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr17 | 62559299 | |||||
| chr17:62559367
|
A | AT | 9 | a0001c0001t0004g0144a0001c0001t0004g0145a0001c0001t0004g0146others(6): Show | 9 | HG00738.hp2 HG01074.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.721-639dupT | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr17 | 62559367 | |||||
| chr17:62559371
|
T | A | 1 | a0001c0001t0006g0074 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.721-645T>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 9/21 | chr17 | 62559371 | ||||||
| chr17:62559465
|
G | A | 38 | a0001c0002t0002g0083a0001c0002t0002g0086a0001c0002t0002g0087others(35): Show | 38 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.721-551G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 9/21 | chr17 | 62559465 | ||||||
| chr17:62559623
|
C | T | 1 | a0001c0001t0006g0042 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.721-393C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 9/21 | chr17 | 62559623 | ||||||
| chr17:62559856
|
T | C | 2 | a0001c0001t0026g0278a0001c0001t0027g0277 | 2 | HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.721-160T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 9/21 | chr17 | 62559856 | ||||||
| chr17:62559897
|
C | A | 17 | a0001c0002t0002g0040a0001c0002t0002g0082a0001c0002t0002g0085others(14): Show | 17 | HG00280.hp1 HG00735.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.721-119C>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 9/21 | chr17 | 62559897 | ||||||
| chr17:62559970
|
T | G | 2 | a0001c0002t0002g0004a0001c0002t0002g0017 | 2 | NA18960.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.721-46T>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 9/21 | chr17 | 62559970 | ||||||
| chr17:62560239
|
G | GGAACATG others(18): Show |
1 | a0001c0001t0001g0178 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.831+114_831+138dup others(25): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr17 | 62560239 | |||||
| chr17:62560451
|
G | T | 142 | a0001c0001t0004g0048a0001c0001t0004g0049a0001c0001t0004g0050others(139): Show | 142 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.831+325G>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 10/21 | chr17 | 62560451 | ||||||
| chr17:62560486
|
A | G | 6 | a0001c0001t0010g0280a0001c0001t0010g0281a0001c0001t0010g0282others(3): Show | 6 | HG01109.hp2 HG02451.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.831+360A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 10/21 | chr17 | 62560486 | ||||||
| chr17:62560521
|
G | A | 1 | a0001c0002t0002g0130 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.831+395G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 10/21 | chr17 | 62560521 | ||||||
| chr17:62560521
|
G | T | 1 | a0001c0001t0001g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.831+395G>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 10/21 | chr17 | 62560521 | ||||||
| chr17:62560550
|
T | TA | 183 | a0001c0001t0003g0158a0001c0001t0003g0159a0001c0001t0003g0160others(180): Show | 183 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.831+427dupA | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr17 | 62560550 | |||||
| chr17:62560661
|
A | AT | 16 | a0001c0001t0001g0218a0001c0001t0001g0227a0001c0001t0001g0244others(13): Show | 16 | HG00609.hp1 HG01167.hp1 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.831+553dupT | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr17 | 62560661 | |||||
| chr17:62560724
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.831+598G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 10/21 | chr17 | 62560724 | ||||||
| chr17:62560740
|
G | A | 20 | a0001c0001t0003g0158a0001c0001t0003g0159a0001c0001t0003g0160others(17): Show | 20 | HG01069.hp1 HG01071.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.831+614G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 10/21 | chr17 | 62560740 | ||||||
| chr17:62560838
|
T | A | 2 | a0001c0001t0026g0278a0001c0001t0027g0277 | 2 | HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.831+712T>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 10/21 | chr17 | 62560838 | ||||||
| chr17:62561082
|
G | T | 15 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0011others(12): Show | 15 | HG00609.hp1 HG02074.hp1 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.831+956G>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 10/21 | chr17 | 62561082 | ||||||
| chr17:62561185
|
T | G | 1 | a0001c0002t0002g0015 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.831+1059T>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 10/21 | chr17 | 62561185 | ||||||
| chr17:62561492
|
G | A | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.831+1366G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 10/21 | chr17 | 62561492 | ||||||
| chr17:62561759
|
A | T | 6 | a0001c0001t0010g0280a0001c0001t0010g0281a0001c0001t0010g0282others(3): Show | 6 | HG01109.hp2 HG02451.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.831+1633A>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 10/21 | chr17 | 62561759 | ||||||
| chr17:62562047
|
C | A | 1 | a0001c0001t0001g0236 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.831+1921C>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 10/21 | chr17 | 62562047 | ||||||
| chr17:62562436
|
T | A | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.831+2310T>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 10/21 | chr17 | 62562436 | ||||||
| chr17:62562449
|
A | G | 1 | a0001c0002t0003g0073 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.831+2323A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 10/21 | chr17 | 62562449 | ||||||
| chr17:62562541
|
G | A | 1 | a0001c0002t0002g0085 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.831+2415G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 10/21 | chr17 | 62562541 | ||||||
| chr17:62562841
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.832-2160C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 10/21 | chr17 | 62562841 | ||||||
| chr17:62563262
|
A | G | 1 | a0001c0002t0002g0022 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.832-1739A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 10/21 | chr17 | 62563262 | ||||||
| chr17:62563382
|
G | C | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.832-1619G>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 10/21 | chr17 | 62563382 | ||||||
| chr17:62563658
|
C | T | 3 | a0001c0002t0004g0139a0001c0002t0004g0140a0001c0002t0022g0138 | 3 | HG01099.hp1 HG02055.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.832-1343C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 10/21 | chr17 | 62563658 | ||||||
| chr17:62563766
|
C | G | 1 | a0001c0001t0008g0174 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.832-1235C>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 10/21 | chr17 | 62563766 | ||||||
| chr17:62563776
|
C | T | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.832-1225C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 10/21 | chr17 | 62563776 | ||||||
| chr17:62563777
|
G | A | 1 | a0001c0001t0001g0261 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.832-1224G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 10/21 | chr17 | 62563777 | ||||||
| chr17:62564023
|
T | C | 1 | a0001c0001t0009g0285 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.832-978T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 10/21 | chr17 | 62564023 | ||||||
| chr17:62564106
|
A | G | 1 | a0001c0001t0016g0186 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.832-895A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 10/21 | chr17 | 62564106 | ||||||
| chr17:62564259
|
C | T | 9 | a0001c0001t0004g0144a0001c0001t0004g0145a0001c0001t0004g0146others(6): Show | 9 | HG00738.hp2 HG01074.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.832-742C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 10/21 | chr17 | 62564259 | ||||||
| chr17:62564530
|
C | G | 6 | a0001c0001t0010g0280a0001c0001t0010g0281a0001c0001t0010g0282others(3): Show | 6 | HG01109.hp2 HG02451.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.832-471C>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 10/21 | chr17 | 62564530 | ||||||
| chr17:62564535
|
CA | C | 184 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0200others(181): Show | 184 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.832-443delA | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr17 | 62564535 | |||||
| chr17:62564592
|
C | T | 1 | a0001c0001t0004g0172 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.832-409C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 10/21 | chr17 | 62564592 | ||||||
| chr17:62564723
|
CA | C | 9 | a0001c0001t0004g0144a0001c0001t0004g0145a0001c0001t0004g0146others(6): Show | 9 | HG00738.hp2 HG01074.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.832-272delA | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr17 | 62564723 | |||||
| chr17:62564729
|
A | G | 9 | a0001c0001t0004g0144a0001c0001t0004g0145a0001c0001t0004g0146others(6): Show | 9 | HG00738.hp2 HG01074.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.832-272A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 10/21 | chr17 | 62564729 | ||||||
| chr17:62565317
|
C | G | 4 | a0001c0002t0002g0012a0001c0002t0002g0022a0001c0002t0002g0024others(1): Show | 4 | HG01167.hp1 HG01928.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.968+180C>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62565317 | ||||||
| chr17:62565516
|
G | A | 1 | a0001c0001t0001g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.968+379G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62565516 | ||||||
| chr17:62565534
|
T | C | 1 | a0001c0002t0002g0118 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.968+397T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62565534 | ||||||
| chr17:62565630
|
C | T | 2 | a0001c0001t0001g0242a0001c0001t0001g0250 | 2 | HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.968+493C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62565630 | ||||||
| chr17:62565651
|
C | CA | 18 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0207others(15): Show | 18 | HG00280.hp1 HG01243.hp1 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.968+532dupA | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr17 | 62565651 | |||||
| chr17:62565651
|
C | CAA | 169 | a0001c0001t0001g0276a0001c0001t0003g0158a0001c0001t0003g0159others(166): Show | 169 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.968+531_968+532dup others(2): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr17 | 62565651 | |||||
| chr17:62565651
|
C | CAAA | 8 | a0001c0002t0002g0097a0001c0002t0002g0112a0001c0002t0002g0126others(5): Show | 8 | HG00741.hp1 HG02723.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.968+530_968+532dup others(3): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr17 | 62565651 | |||||
| chr17:62565747
|
A | G | 3 | a0001c0001t0001g0219a0001c0001t0001g0225a0001c0002t0005g0137 | 3 | NA18947.hp1 NA19063.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.968+610A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62565747 | ||||||
| chr17:62565781
|
G | T | 142 | a0001c0001t0004g0048a0001c0001t0004g0049a0001c0001t0004g0050others(139): Show | 142 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.968+644G>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62565781 | ||||||
| chr17:62565790
|
G | A | 36 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0007others(33): Show | 36 | HG00609.hp1 HG01167.hp1 HG01192.hp2 others(33): Show |
intron_variant | MODIFIER | c.968+653G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62565790 | ||||||
| chr17:62565817
|
G | T | 1 | a0001c0001t0001g0252 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.968+680G>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62565817 | ||||||
| chr17:62566122
|
G | A | 2 | a0001c0002t0002g0013a0001c0002t0002g0032 | 2 | HG02074.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.968+985G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62566122 | ||||||
| chr17:62566335
|
A | G | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.968+1198A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62566335 | ||||||
| chr17:62566381
|
T | C | 1 | a0001c0001t0001g0226 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.968+1244T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62566381 | ||||||
| chr17:62566382
|
A | T | 1 | a0001c0001t0001g0226 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.968+1245A>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62566382 | ||||||
| chr17:62566384
|
A | T | 1 | a0001c0001t0001g0226 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.968+1247A>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62566384 | ||||||
| chr17:62566387
|
T | A | 1 | a0001c0001t0001g0226 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.968+1250T>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62566387 | ||||||
| chr17:62566388
|
A | T | 1 | a0001c0001t0001g0226 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.968+1251A>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62566388 | ||||||
| chr17:62566390
|
C | G | 1 | a0001c0001t0001g0226 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.968+1253C>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62566390 | ||||||
| chr17:62566391
|
C | T | 1 | a0001c0001t0001g0226 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.968+1254C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62566391 | ||||||
| chr17:62566392
|
T | G | 1 | a0001c0001t0001g0226 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.968+1255T>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62566392 | ||||||
| chr17:62566393
|
C | A | 1 | a0001c0001t0001g0226 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.968+1256C>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62566393 | ||||||
| chr17:62566396
|
A | T | 1 | a0001c0001t0001g0226 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.968+1259A>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62566396 | ||||||
| chr17:62566397
|
G | T | 1 | a0001c0001t0001g0226 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.968+1260G>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62566397 | ||||||
| chr17:62566444
|
A | G | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.968+1307A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62566444 | ||||||
| chr17:62566457
|
G | A | 1 | a0001c0001t0001g0244 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.968+1320G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62566457 | ||||||
| chr17:62566987
|
G | A | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.968+1850G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62566987 | ||||||
| chr17:62567009
|
G | A | 194 | a0001c0001t0001g0020a0001c0001t0001g0180a0001c0001t0001g0181others(191): Show | 194 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.968+1872G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62567009 | ||||||
| chr17:62567086
|
G | A | 1 | a0001c0001t0001g0258 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.968+1949G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62567086 | ||||||
| chr17:62567117
|
A | G | 3 | a0001c0002t0002g0110a0001c0002t0002g0119a0001c0002t0002g0132 | 3 | HG00733.hp2 HG01516.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.968+1980A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62567117 | ||||||
| chr17:62567554
|
A | T | 1 | a0001c0001t0012g0149 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.968+2417A>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62567554 | ||||||
| chr17:62567784
|
C | T | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.968+2647C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62567784 | ||||||
| chr17:62567812
|
T | G | 1 | a0001c0002t0003g0060 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.968+2675T>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62567812 | ||||||
| chr17:62567828
|
T | C | 1 | a0001c0001t0001g0194 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.968+2691T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62567828 | ||||||
| chr17:62567850
|
T | C | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.968+2713T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62567850 | ||||||
| chr17:62568286
|
G | A | 2 | a0001c0001t0016g0185a0001c0001t0016g0186 | 2 | HG01243.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.968+3149G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62568286 | ||||||
| chr17:62568404
|
G | C | 1 | a0001c0001t0001g0276 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.968+3267G>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62568404 | ||||||
| chr17:62568431
|
C | CA | 48 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0192others(45): Show | 48 | HG00438.hp1 HG00639.hp2 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.968+3314dupA | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr17 | 62568431 | |||||
| chr17:62568431
|
CA | C | 6 | a0001c0001t0001g0199a0001c0001t0001g0228a0001c0002t0002g0082others(3): Show | 6 | HG01099.hp1 HG01099.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.968+3314delA | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr17 | 62568431 | |||||
| chr17:62568522
|
G | A | 1 | a0001c0002t0007g0036 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.968+3385G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62568522 | ||||||
| chr17:62568558
|
C | G | 20 | a0001c0001t0003g0158a0001c0001t0003g0159a0001c0001t0003g0160others(17): Show | 20 | HG01069.hp1 HG01071.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.968+3421C>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62568558 | ||||||
| chr17:62568612
|
C | T | 4 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0026g0278others(1): Show | 4 | HG03195.hp2 HG03225.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.968+3475C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62568612 | ||||||
| chr17:62568774
|
G | A | 11 | a0001c0001t0006g0041a0001c0001t0006g0042a0001c0001t0006g0055others(8): Show | 11 | HG01109.hp2 HG02451.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.968+3637G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62568774 | ||||||
| chr17:62568917
|
G | C | 1 | a0001c0001t0001g0234 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.968+3780G>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62568917 | ||||||
| chr17:62568937
|
T | A | 4 | a0001c0001t0004g0048a0001c0001t0004g0049a0001c0001t0004g0050others(1): Show | 4 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.968+3800T>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62568937 | ||||||
| chr17:62568961
|
C | G | 13 | a0001c0002t0003g0023a0001c0002t0003g0043a0001c0002t0003g0044others(10): Show | 13 | HG01192.hp1 HG01943.hp2 HG01952.hp1 others(10): Show |
intron_variant | MODIFIER | c.968+3824C>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62568961 | ||||||
| chr17:62569031
|
GGT | G | 195 | a0001c0001t0001g0020a0001c0001t0001g0180a0001c0001t0001g0181others(192): Show | 195 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.968+3898_968+3899d others(4): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr17 | 62569031 | |||||
| chr17:62569085
|
T | A | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.968+3948T>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62569085 | ||||||
| chr17:62569097
|
G | C | 1 | a0001c0001t0001g0194 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.968+3960G>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62569097 | ||||||
| chr17:62569434
|
C | CT | 12 | a0001c0001t0001g0176a0001c0001t0001g0189a0001c0001t0001g0192others(9): Show | 12 | HG01358.hp1 HG01891.hp1 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.969-3762dupT | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr17 | 62569434 | |||||
| chr17:62569434
|
CT | C | 170 | a0001c0001t0001g0020a0001c0001t0001g0230a0001c0001t0001g0246others(167): Show | 170 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.969-3762delT | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr17 | 62569434 | |||||
| chr17:62569525
|
C | A | 6 | a0001c0002t0002g0102a0001c0002t0002g0114a0001c0002t0002g0115others(3): Show | 6 | HG00140.hp1 HG02683.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.969-3690C>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62569525 | ||||||
| chr17:62570025
|
C | T | 1 | a0001c0001t0008g0174 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.969-3190C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62570025 | ||||||
| chr17:62570090
|
A | G | 5 | a0001c0001t0004g0150a0001c0001t0004g0152a0001c0001t0012g0148others(2): Show | 5 | HG00738.hp2 HG01074.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.969-3125A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62570090 | ||||||
| chr17:62570426
|
C | T | 11 | a0001c0001t0006g0041a0001c0001t0006g0042a0001c0001t0006g0055others(8): Show | 11 | HG01109.hp2 HG02451.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.969-2789C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62570426 | ||||||
| chr17:62570627
|
T | C | 2 | a0001c0002t0003g0058a0001c0002t0004g0053 | 2 | HG02132.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.969-2588T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62570627 | ||||||
| chr17:62570689
|
G | A | 1 | a0001c0001t0001g0270 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.969-2526G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62570689 | ||||||
| chr17:62570781
|
G | T | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.969-2434G>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62570781 | ||||||
| chr17:62570914
|
G | A | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.969-2301G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62570914 | ||||||
| chr17:62570920
|
G | A | 3 | a0001c0001t0001g0198a0001c0001t0001g0218a0001c0001t0001g0268 | 3 | HG01243.hp2 HG01358.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.969-2295G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62570920 | ||||||
| chr17:62570964
|
G | A | 3 | a0001c0001t0001g0208a0001c0001t0001g0222a0001c0001t0014g0267 | 3 | HG00733.hp1 HG00735.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.969-2251G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62570964 | ||||||
| chr17:62571219
|
A | G | 1 | a0001c0002t0011g0117 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.969-1996A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62571219 | ||||||
| chr17:62571395
|
T | A | 1 | a0001c0001t0001g0276 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.969-1820T>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62571395 | ||||||
| chr17:62571544
|
C | T | 1 | a0001c0002t0003g0063 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.969-1671C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62571544 | ||||||
| chr17:62571702
|
T | C | 1 | a0001c0001t0001g0250 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.969-1513T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62571702 | ||||||
| chr17:62571792
|
T | C | 1 | a0001c0002t0002g0131 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.969-1423T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62571792 | ||||||
| chr17:62571919
|
G | T | 1 | a0001c0001t0006g0041 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.969-1296G>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62571919 | ||||||
| chr17:62572023
|
A | G | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.969-1192A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62572023 | ||||||
| chr17:62572176
|
C | CA | 8 | a0001c0001t0001g0273a0001c0001t0003g0162a0001c0001t0004g0152others(5): Show | 8 | HG01175.hp2 HG01258.hp1 HG02300.hp1 others(5): Show |
intron_variant | MODIFIER | c.969-1021dupA | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr17 | 62572176 | |||||
| chr17:62572304
|
G | A | 1 | a0001c0001t0001g0252 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.969-911G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62572304 | ||||||
| chr17:62572417
|
G | GT | 10 | a0001c0001t0001g0194a0001c0001t0001g0289a0001c0001t0001g0290others(7): Show | 10 | HG00738.hp2 HG01884.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.969-786dupT | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr17 | 62572417 | |||||
| chr17:62572417
|
GT | G | 6 | a0001c0001t0001g0193a0001c0001t0001g0205a0001c0001t0001g0215others(3): Show | 6 | HG00323.hp2 HG00741.hp2 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.969-786delT | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr17 | 62572417 | |||||
| chr17:62572575
|
A | G | 1 | a0001c0002t0003g0069 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.969-640A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62572575 | ||||||
| chr17:62572606
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.969-609C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62572606 | ||||||
| chr17:62572657
|
T | G | 1 | a0001c0002t0004g0139 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.969-558T>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62572657 | ||||||
| chr17:62572685
|
G | T | 1 | a0001c0001t0021g0153 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.969-530G>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62572685 | ||||||
| chr17:62572689
|
A | G | 1 | a0001c0002t0003g0079 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.969-526A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62572689 | ||||||
| chr17:62573199
|
T | G | 2 | a0001c0002t0002g0080a0001c0002t0007g0081 | 2 | HG00639.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.969-16T>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 11/21 | chr17 | 62573199 | ||||||
| chr17:62573384
|
C | T | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1121+17C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 12/21 | chr17 | 62573384 | ||||||
| chr17:62573818
|
T | C | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1121+451T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 12/21 | chr17 | 62573818 | ||||||
| chr17:62574020
|
C | T | 190 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0274others(187): Show | 190 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.1121+653C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 12/21 | chr17 | 62574020 | ||||||
| chr17:62574053
|
A | G | 4 | a0001c0002t0002g0012a0001c0002t0002g0022a0001c0002t0002g0024others(1): Show | 4 | HG01167.hp1 HG01928.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1121+686A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 12/21 | chr17 | 62574053 | ||||||
| chr17:62574125
|
A | G | 1 | a0001c0002t0007g0109 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1121+758A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 12/21 | chr17 | 62574125 | ||||||
| chr17:62574201
|
G | A | 1 | a0001c0001t0001g0252 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1121+834G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 12/21 | chr17 | 62574201 | ||||||
| chr17:62574266
|
A | G | 20 | a0001c0001t0003g0158a0001c0001t0003g0159a0001c0001t0003g0160others(17): Show | 20 | HG01069.hp1 HG01071.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1121+899A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 12/21 | chr17 | 62574266 | ||||||
| chr17:62574281
|
T | G | 2 | a0001c0001t0001g0253a0001c0001t0001g0262 | 2 | NA19005.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1121+914T>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 12/21 | chr17 | 62574281 | ||||||
| chr17:62574319
|
T | G | 3 | a0001c0001t0001g0210a0001c0001t0001g0214a0001c0001t0001g0229 | 3 | HG01516.hp1 HG02735.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1121+952T>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 12/21 | chr17 | 62574319 | ||||||
| chr17:62574421
|
C | T | 2 | a0001c0002t0002g0089a0001c0002t0002g0090 | 2 | HG00735.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.1121+1054C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 12/21 | chr17 | 62574421 | ||||||
| chr17:62574435
|
A | G | 1 | a0001c0001t0001g0208 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1121+1068A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 12/21 | chr17 | 62574435 | ||||||
| chr17:62574523
|
GT | G | 193 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0274others(190): Show | 193 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.1121+1168delT | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr17 | 62574523 | |||||
| chr17:62574541
|
G | A | 11 | a0001c0001t0006g0041a0001c0001t0006g0042a0001c0001t0006g0055others(8): Show | 11 | HG01109.hp2 HG02451.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1121+1174G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 12/21 | chr17 | 62574541 | ||||||
| chr17:62574618
|
C | T | 1 | a0001c0001t0001g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1121+1251C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 12/21 | chr17 | 62574618 | ||||||
| chr17:62574756
|
T | A | 6 | a0001c0001t0010g0280a0001c0001t0010g0281a0001c0001t0010g0282others(3): Show | 6 | HG01109.hp2 HG02451.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1121+1389T>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 12/21 | chr17 | 62574756 | ||||||
| chr17:62574950
|
G | A | 2 | a0001c0001t0001g0274a0001c0002t0002g0028 | 2 | NA19086.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.1121+1583G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 12/21 | chr17 | 62574950 | ||||||
| chr17:62575029
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1121+1662G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 12/21 | chr17 | 62575029 | ||||||
| chr17:62575129
|
A | G | 1 | a0001c0001t0004g0144 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1122-1580A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 12/21 | chr17 | 62575129 | ||||||
| chr17:62575321
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1122-1388G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 12/21 | chr17 | 62575321 | ||||||
| chr17:62575442
|
T | A | 2 | a0001c0001t0016g0185a0001c0001t0016g0186 | 2 | HG01243.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.1122-1267T>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 12/21 | chr17 | 62575442 | ||||||
| chr17:62575598
|
C | T | 4 | a0001c0001t0001g0198a0001c0001t0001g0218a0001c0001t0001g0268others(1): Show | 4 | HG01243.hp2 HG01358.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1122-1111C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 12/21 | chr17 | 62575598 | ||||||
| chr17:62575719
|
C | T | 10 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0010g0280others(7): Show | 10 | HG01109.hp2 HG02451.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.1122-990C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 12/21 | chr17 | 62575719 | ||||||
| chr17:62575853
|
T | C | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1122-856T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 12/21 | chr17 | 62575853 | ||||||
| chr17:62575913
|
G | T | 1 | a0001c0001t0001g0210 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1122-796G>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 12/21 | chr17 | 62575913 | ||||||
| chr17:62576085
|
T | G | 1 | a0001c0001t0004g0172 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1122-624T>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 12/21 | chr17 | 62576085 | ||||||
| chr17:62576283
|
A | G | 1 | a0001c0001t0001g0209 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1122-426A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 12/21 | chr17 | 62576283 | ||||||
| chr17:62576423
|
T | C | 8 | a0001c0001t0010g0280a0001c0001t0010g0281a0001c0001t0010g0282others(5): Show | 8 | HG01109.hp2 HG02451.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1122-286T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 12/21 | chr17 | 62576423 | ||||||
| chr17:62576966
|
C | CTTTTTTT others(2): Show |
7 | a0001c0001t0001g0290a0001c0002t0002g0004a0001c0002t0002g0009others(4): Show | 7 | HG01515.hp1 HG03130.hp2 NA18941.hp2 others(4): Show |
intron_variant | MODIFIER | c.1188+197_1188+205d others(11): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr17 | 62576966 | |||||
| chr17:62576966
|
C | CTTTTTTT others(3): Show |
135 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0274others(132): Show | 135 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.1188+196_1188+205d others(12): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr17 | 62576966 | |||||
| chr17:62576966
|
C | CTTTTTTT others(4): Show |
8 | a0001c0001t0001g0289a0001c0002t0002g0134a0001c0002t0003g0068others(5): Show | 8 | HG01099.hp1 HG02055.hp1 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.1188+195_1188+205d others(13): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr17 | 62576966 | |||||
| chr17:62576966
|
C | CTTTTTTT others(5): Show |
7 | a0001c0001t0010g0280a0001c0001t0010g0281a0001c0001t0010g0282others(4): Show | 7 | HG01109.hp2 HG02451.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1188+194_1188+205d others(14): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr17 | 62576966 | |||||
| chr17:62576966
|
C | CTTTTTTT others(6): Show |
1 | a0001c0001t0026g0278 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1188+193_1188+205d others(15): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr17 | 62576966 | |||||
| chr17:62576966
|
CT | C | 38 | a0001c0001t0001g0199a0001c0001t0001g0258a0001c0001t0001g0291others(35): Show | 38 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.1188+205delT | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr17 | 62576966 | |||||
| chr17:62576997
|
G | C | 195 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0274others(192): Show | 195 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.1188+222G>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 13/21 | chr17 | 62576997 | ||||||
| chr17:62577025
|
C | T | 1 | a0001c0001t0001g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1188+250C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 13/21 | chr17 | 62577025 | ||||||
| chr17:62577109
|
C | T | 1 | a0001c0001t0001g0269 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1188+334C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 13/21 | chr17 | 62577109 | ||||||
| chr17:62577121
|
C | A | 1 | a0001c0001t0001g0189 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1188+346C>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 13/21 | chr17 | 62577121 | ||||||
| chr17:62577165
|
T | G | 1 | a0001c0002t0002g0128 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1188+390T>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 13/21 | chr17 | 62577165 | ||||||
| chr17:62577177
|
C | T | 17 | a0001c0002t0002g0083a0001c0002t0002g0087a0001c0002t0002g0088others(14): Show | 17 | HG00140.hp1 HG00738.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.1188+402C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 13/21 | chr17 | 62577177 | ||||||
| chr17:62577178
|
G | A | 1 | a0001c0001t0004g0172 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1188+403G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 13/21 | chr17 | 62577178 | ||||||
| chr17:62577243
|
G | T | 1 | a0001c0001t0001g0276 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1188+468G>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 13/21 | chr17 | 62577243 | ||||||
| chr17:62577605
|
A | G | 2 | a0001c0002t0002g0004a0001c0002t0002g0017 | 2 | NA18960.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.1188+830A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 13/21 | chr17 | 62577605 | ||||||
| chr17:62577759
|
G | A | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1189-718G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 13/21 | chr17 | 62577759 | ||||||
| chr17:62577843
|
C | G | 36 | a0001c0002t0003g0023a0001c0002t0003g0043a0001c0002t0003g0044others(33): Show | 36 | HG00438.hp1 HG01192.hp1 HG01261.hp1 others(33): Show |
intron_variant | MODIFIER | c.1189-634C>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 13/21 | chr17 | 62577843 | ||||||
| chr17:62577875
|
G | A | 2 | a0001c0001t0016g0185a0001c0001t0016g0186 | 2 | HG01243.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.1189-602G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 13/21 | chr17 | 62577875 | ||||||
| chr17:62577876
|
A | T | 2 | a0001c0001t0016g0185a0001c0001t0016g0186 | 2 | HG01243.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.1189-601A>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 13/21 | chr17 | 62577876 | ||||||
| chr17:62577940
|
G | A | 1 | a0001c0002t0013g0101 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1189-537G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 13/21 | chr17 | 62577940 | ||||||
| chr17:62577998
|
G | T | 1 | a0001c0002t0015g0173 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1189-479G>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 13/21 | chr17 | 62577998 | ||||||
| chr17:62578109
|
C | T | 5 | a0001c0001t0006g0041a0001c0001t0006g0042a0001c0001t0006g0055others(2): Show | 5 | HG02622.hp2 HG02647.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1189-368C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 13/21 | chr17 | 62578109 | ||||||
| chr17:62578265
|
T | C | 1 | a0001c0002t0002g0095 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1189-212T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 13/21 | chr17 | 62578265 | ||||||
| chr17:62578289
|
G | T | 1 | a0001c0002t0003g0078 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1189-188G>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 13/21 | chr17 | 62578289 | ||||||
| chr17:62578914
|
A | C | 20 | a0001c0001t0003g0158a0001c0001t0003g0159a0001c0001t0003g0160others(17): Show | 20 | HG01069.hp1 HG01071.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1286+340A>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 14/21 | chr17 | 62578914 | ||||||
| chr17:62579262
|
T | A | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1286+688T>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 14/21 | chr17 | 62579262 | ||||||
| chr17:62579337
|
G | A | 1 | a0001c0002t0002g0154 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1286+763G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 14/21 | chr17 | 62579337 | ||||||
| chr17:62579339
|
T | C | 1 | a0001c0002t0002g0092 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1286+765T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 14/21 | chr17 | 62579339 | ||||||
| chr17:62579973
|
C | T | 93 | a0001c0001t0001g0020a0001c0001t0001g0274a0001c0002t0002g0003others(90): Show | 93 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.1287-138C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 14/21 | chr17 | 62579973 | ||||||
| chr17:62580022
|
T | C | 1 | a0001c0002t0002g0114 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1287-89T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 14/21 | chr17 | 62580022 | ||||||
| chr17:62580411
|
T | G | 1 | a0001c0002t0003g0078 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1368+219T>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 15/21 | chr17 | 62580411 | ||||||
| chr17:62580413
|
G | T | 2 | a0001c0001t0016g0185a0001c0001t0016g0186 | 2 | HG01243.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.1368+221G>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 15/21 | chr17 | 62580413 | ||||||
| chr17:62580453
|
T | TATG | 191 | a0001c0001t0001g0020a0001c0001t0001g0180a0001c0001t0001g0181others(188): Show | 191 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.1368+264_1368+266d others(5): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr17 | 62580453 | |||||
| chr17:62580736
|
A | G | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1368+544A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 15/21 | chr17 | 62580736 | ||||||
| chr17:62580868
|
C | T | 2 | a0001c0001t0004g0145a0001c0001t0004g0146 | 2 | NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1368+676C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 15/21 | chr17 | 62580868 | ||||||
| chr17:62581131
|
A | G | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1368+939A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 15/21 | chr17 | 62581131 | ||||||
| chr17:62581148
|
G | A | 1 | a0001c0002t0002g0031 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1368+956G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 15/21 | chr17 | 62581148 | ||||||
| chr17:62581429
|
T | G | 1 | a0001c0001t0004g0147 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1368+1237T>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 15/21 | chr17 | 62581429 | ||||||
| chr17:62581438
|
CT | C | 198 | a0001c0001t0001g0020a0001c0001t0001g0180a0001c0001t0001g0181others(195): Show | 198 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.1368+1263delT | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr17 | 62581438 | |||||
| chr17:62581489
|
A | G | 2 | a0001c0002t0002g0131a0001c0002t0005g0084 | 2 | HG01496.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1368+1297A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 15/21 | chr17 | 62581489 | ||||||
| chr17:62581508
|
G | A | 1 | a0001c0002t0002g0130 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1368+1316G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 15/21 | chr17 | 62581508 | ||||||
| chr17:62581667
|
T | C | 1 | a0001c0002t0005g0006 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1368+1475T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 15/21 | chr17 | 62581667 | ||||||
| chr17:62581753
|
G | A | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1368+1561G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 15/21 | chr17 | 62581753 | ||||||
| chr17:62581913
|
A | G | 1 | a0001c0001t0001g0271 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1368+1721A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 15/21 | chr17 | 62581913 | ||||||
| chr17:62581996
|
C | G | 5 | a0001c0002t0002g0008a0001c0002t0002g0014a0001c0002t0002g0018others(2): Show | 5 | HG02165.hp1 NA18947.hp2 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.1368+1804C>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 15/21 | chr17 | 62581996 | ||||||
| chr17:62582116
|
T | C | 1 | a0001c0001t0001g0265 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1368+1924T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 15/21 | chr17 | 62582116 | ||||||
| chr17:62582529
|
G | A | 1 | a0001c0002t0002g0118 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1368+2337G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 15/21 | chr17 | 62582529 | ||||||
| chr17:62582689
|
G | A | 1 | a0001c0001t0021g0153 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1368+2497G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 15/21 | chr17 | 62582689 | ||||||
| chr17:62582773
|
C | T | 1 | a0001c0002t0002g0121 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1368+2581C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 15/21 | chr17 | 62582773 | ||||||
| chr17:62583053
|
C | T | 1 | a0001c0002t0011g0117 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1368+2861C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 15/21 | chr17 | 62583053 | ||||||
| chr17:62583061
|
G | A | 2 | a0001c0001t0004g0145a0001c0001t0004g0146 | 2 | NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1368+2869G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 15/21 | chr17 | 62583061 | ||||||
| chr17:62583338
|
G | T | 15 | a0001c0001t0001g0176a0001c0001t0001g0182a0001c0001t0001g0183others(12): Show | 15 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1369-2797G>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 15/21 | chr17 | 62583338 | ||||||
| chr17:62583450
|
A | G | 1 | a0001c0001t0001g0265 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1369-2685A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 15/21 | chr17 | 62583450 | ||||||
| chr17:62583920
|
G | C | 2 | a0001c0002t0003g0064a0001c0002t0003g0065 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1369-2215G>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 15/21 | chr17 | 62583920 | ||||||
| chr17:62583985
|
G | C | 1 | a0001c0002t0002g0008 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1369-2150G>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 15/21 | chr17 | 62583985 | ||||||
| chr17:62584016
|
A | C | 1 | a0001c0002t0013g0100 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1369-2119A>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 15/21 | chr17 | 62584016 | ||||||
| chr17:62584045
|
T | G | 1 | a0001c0002t0015g0173 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1369-2090T>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 15/21 | chr17 | 62584045 | ||||||
| chr17:62584083
|
T | A | 3 | a0001c0002t0002g0012a0001c0002t0002g0022a0001c0002t0002g0024 | 3 | HG01167.hp1 HG01928.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.1369-2052T>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 15/21 | chr17 | 62584083 | ||||||
| chr17:62584107
|
G | GT | 16 | a0001c0001t0001g0187a0001c0001t0001g0189a0001c0001t0001g0192others(13): Show | 16 | HG00438.hp2 HG01358.hp1 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.1369-2003dupT | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr17 | 62584107 | |||||
| chr17:62584107
|
GT | G | 51 | a0001c0001t0001g0237a0001c0001t0001g0239a0001c0001t0001g0272others(48): Show | 51 | HG00438.hp1 HG00639.hp2 HG01168.hp2 others(48): Show |
intron_variant | MODIFIER | c.1369-2003delT | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr17 | 62584107 | |||||
| chr17:62584107
|
GTT | G | 92 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0273others(89): Show | 92 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.1369-2004_1369-200 others(6): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr17 | 62584107 | |||||
| chr17:62584107
|
GTTT | G | 50 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0289others(47): Show | 50 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(47): Show |
intron_variant | MODIFIER | c.1369-2005_1369-200 others(7): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr17 | 62584107 | |||||
| chr17:62584265
|
C | T | 1 | a0001c0002t0003g0059 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1369-1870C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 15/21 | chr17 | 62584265 | ||||||
| chr17:62584514
|
G | C | 1 | a0001c0002t0002g0087 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1369-1621G>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 15/21 | chr17 | 62584514 | ||||||
| chr17:62584633
|
A | T | 2 | a0001c0001t0001g0238a0001c0001t0001g0239 | 2 | HG01168.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1369-1502A>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 15/21 | chr17 | 62584633 | ||||||
| chr17:62584816
|
A | C | 1 | a0001c0001t0001g0200 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1369-1319A>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 15/21 | chr17 | 62584816 | ||||||
| chr17:62584861
|
G | T | 196 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0273others(193): Show | 196 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.1369-1274G>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 15/21 | chr17 | 62584861 | ||||||
| chr17:62585164
|
G | A | 1 | a0001c0001t0004g0147 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1369-971G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 15/21 | chr17 | 62585164 | ||||||
| chr17:62585240
|
T | C | 1 | a0001c0001t0010g0283 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1369-895T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 15/21 | chr17 | 62585240 | ||||||
| chr17:62585341
|
C | T | 4 | a0001c0001t0004g0048a0001c0001t0004g0049a0001c0001t0004g0050others(1): Show | 4 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1369-794C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 15/21 | chr17 | 62585341 | ||||||
| chr17:62585393
|
C | T | 1 | a0001c0001t0012g0148 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1369-742C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 15/21 | chr17 | 62585393 | ||||||
| chr17:62585394
|
C | T | 1 | a0001c0001t0001g0276 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1369-741C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 15/21 | chr17 | 62585394 | ||||||
| chr17:62585408
|
C | T | 1 | a0001c0002t0004g0177 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1369-727C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 15/21 | chr17 | 62585408 | ||||||
| chr17:62585450
|
A | G | 1 | a0001c0001t0003g0161 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1369-685A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 15/21 | chr17 | 62585450 | ||||||
| chr17:62585666
|
T | A | 1 | a0001c0001t0001g0020 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1369-469T>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 15/21 | chr17 | 62585666 | ||||||
| chr17:62585703
|
G | T | 3 | a0001c0001t0001g0192a0001c0001t0001g0248a0001c0001t0001g0249 | 3 | HG01884.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1369-432G>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 15/21 | chr17 | 62585703 | ||||||
| chr17:62585907
|
T | G | 37 | a0001c0001t0001g0273a0001c0002t0002g0003a0001c0002t0002g0004others(34): Show | 37 | HG00609.hp1 HG01167.hp1 HG01192.hp2 others(34): Show |
intron_variant | MODIFIER | c.1369-228T>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 15/21 | chr17 | 62585907 | ||||||
| chr17:62585949
|
C | G | 3 | a0001c0002t0004g0139a0001c0002t0004g0140a0001c0002t0022g0138 | 3 | HG01099.hp1 HG02055.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1369-186C>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 15/21 | chr17 | 62585949 | ||||||
| chr17:62586313
|
G | C | 2 | a0001c0002t0002g0085a0001c0002t0002g0096 | 2 | HG01081.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1460+87G>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62586313 | ||||||
| chr17:62586379
|
C | T | 10 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0010g0280others(7): Show | 10 | HG01109.hp2 HG02451.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.1460+153C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62586379 | ||||||
| chr17:62586414
|
G | C | 1 | a0001c0001t0001g0190 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1460+188G>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62586414 | ||||||
| chr17:62586597
|
A | G | 1 | a0001c0002t0002g0130 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1460+371A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62586597 | ||||||
| chr17:62586607
|
G | A | 8 | a0001c0001t0010g0280a0001c0001t0010g0281a0001c0001t0010g0282others(5): Show | 8 | HG01109.hp2 HG02451.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1460+381G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62586607 | ||||||
| chr17:62586695
|
T | C | 196 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0273others(193): Show | 196 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.1460+469T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62586695 | ||||||
| chr17:62586745
|
C | T | 1 | a0001c0002t0007g0123 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1460+519C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62586745 | ||||||
| chr17:62586826
|
C | CA | 100 | a0001c0001t0001g0273a0001c0002t0002g0004a0001c0002t0002g0007others(97): Show | 100 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.1460+614dupA | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr17 | 62586826 | |||||
| chr17:62586841
|
T | C | 15 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0011others(12): Show | 15 | HG00609.hp1 HG02074.hp1 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.1460+615T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62586841 | ||||||
| chr17:62586917
|
A | G | 212 | a0001c0001t0001g0176a0001c0001t0001g0180a0001c0001t0001g0181others(209): Show | 212 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.1460+691A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62586917 | ||||||
| chr17:62586918
|
G | A | 5 | a0001c0001t0006g0041a0001c0001t0006g0042a0001c0001t0006g0055others(2): Show | 5 | HG02622.hp2 HG02647.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1460+692G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62586918 | ||||||
| chr17:62587000
|
C | T | 9 | a0001c0001t0004g0144a0001c0001t0004g0145a0001c0001t0004g0146others(6): Show | 9 | HG00738.hp2 HG01074.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.1460+774C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62587000 | ||||||
| chr17:62587063
|
A | G | 1 | a0001c0002t0003g0068 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1460+837A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62587063 | ||||||
| chr17:62587193
|
A | C | 1 | a0001c0001t0025g0247 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1460+967A>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62587193 | ||||||
| chr17:62587232
|
A | T | 2 | a0001c0001t0016g0185a0001c0001t0016g0186 | 2 | HG01243.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.1460+1006A>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62587232 | ||||||
| chr17:62587402
|
G | T | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1460+1176G>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62587402 | ||||||
| chr17:62587597
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1460+1371C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62587597 | ||||||
| chr17:62587699
|
G | A | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1460+1473G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62587699 | ||||||
| chr17:62587736
|
T | C | 1 | a0001c0002t0005g0124 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1460+1510T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62587736 | ||||||
| chr17:62587944
|
ATATACAG others(22): Show |
A | 1 | a0001c0002t0002g0028 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1460+1725_1460+175 others(33): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr17 | 62587944 | |||||
| chr17:62587952
|
A | ATGTATAT others(22): Show |
9 | a0001c0001t0001g0193a0001c0001t0001g0199a0001c0001t0001g0200others(6): Show | 9 | HG01167.hp2 HG01433.hp2 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.1460+1902_1460+193 others(33): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr17 | 62587952 | |||||
| chr17:62587952
|
A | ATGTATAT others(51): Show |
5 | a0001c0001t0001g0190a0001c0001t0001g0207a0001c0001t0001g0224others(2): Show | 5 | HG02055.hp2 HG02965.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1460+1873_1460+193 others(62): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr17 | 62587952 | |||||
| chr17:62587952
|
ATGTATAT others(22): Show |
A | 158 | a0001c0001t0001g0176a0001c0001t0001g0180a0001c0001t0001g0181others(155): Show | 158 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.1460+1902_1460+193 others(33): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr17 | 62587952 | |||||
| chr17:62587952
|
ATGTATAT others(51): Show |
A | 6 | a0001c0002t0002g0087a0001c0002t0003g0079a0001c0002t0004g0139others(3): Show | 6 | HG01099.hp1 HG01258.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.1460+1873_1460+193 others(62): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr17 | 62587952 | |||||
| chr17:62587952
|
ATGTATAT others(80): Show |
A | 12 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0010g0280others(9): Show | 12 | HG01109.hp2 HG02451.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.1460+1844_1460+193 others(91): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr17 | 62587952 | |||||
| chr17:62587952
|
ATGTATAT others(109): Show |
A | 4 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0016g0185others(1): Show | 4 | HG01243.hp1 HG01255.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1460+1815_1460+193 others(4): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr17 | 62587952 | |||||
| chr17:62587959
|
T | C | 1 | a0001c0001t0001g0252 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1460+1733T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62587959 | ||||||
| chr17:62588038
|
T | G | 1 | a0001c0002t0015g0173 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1460+1812T>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62588038 | ||||||
| chr17:62588039
|
C | A | 1 | a0001c0002t0015g0173 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1460+1813C>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62588039 | ||||||
| chr17:62588082
|
A | C | 3 | a0001c0002t0003g0057a0001c0002t0003g0059a0001c0002t0003g0142 | 3 | HG02027.hp2 NA18941.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.1460+1856A>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62588082 | ||||||
| chr17:62588244
|
G | C | 1 | a0001c0001t0004g0147 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1460+2018G>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62588244 | ||||||
| chr17:62588256
|
A | C | 1 | a0001c0001t0021g0153 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1460+2030A>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62588256 | ||||||
| chr17:62588612
|
G | T | 2 | a0001c0002t0002g0040a0001c0002t0005g0124 | 2 | HG00280.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1460+2386G>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62588612 | ||||||
| chr17:62588656
|
T | TTTTTG | 15 | a0001c0002t0002g0004a0001c0002t0002g0008a0001c0002t0002g0011others(12): Show | 15 | HG00609.hp1 HG02074.hp1 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.1460+2445_1460+244 others(9): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr17 | 62588656 | |||||
| chr17:62588721
|
C | G | 180 | a0001c0001t0001g0273a0001c0001t0003g0158a0001c0001t0003g0159others(177): Show | 180 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.1460+2495C>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62588721 | ||||||
| chr17:62588972
|
C | T | 3 | a0001c0001t0001g0208a0001c0001t0001g0222a0001c0001t0014g0267 | 3 | HG00733.hp1 HG00735.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.1460+2746C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62588972 | ||||||
| chr17:62588973
|
G | A | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1460+2747G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62588973 | ||||||
| chr17:62589064
|
A | AG | 8 | a0001c0002t0002g0121a0001c0002t0002g0122a0001c0002t0002g0133others(5): Show | 8 | HG02080.hp1 HG02155.hp1 NA18963.hp1 others(5): Show |
intron_variant | MODIFIER | c.1460+2840dupG | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr17 | 62589064 | |||||
| chr17:62589064
|
A | G | 137 | a0001c0001t0001g0273a0001c0001t0004g0048a0001c0001t0004g0049others(134): Show | 137 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.1460+2838A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62589064 | ||||||
| chr17:62589217
|
A | T | 1 | a0001c0002t0002g0031 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1460+2991A>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62589217 | ||||||
| chr17:62589236
|
A | G | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1460+3010A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62589236 | ||||||
| chr17:62589652
|
C | T | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1460+3426C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62589652 | ||||||
| chr17:62589741
|
G | A | 5 | a0001c0001t0006g0041a0001c0001t0006g0042a0001c0001t0006g0055others(2): Show | 5 | HG02622.hp2 HG02647.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1460+3515G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62589741 | ||||||
| chr17:62589819
|
T | C | 3 | a0001c0001t0006g0055a0001c0001t0006g0056a0001c0001t0006g0074 | 3 | HG02622.hp2 HG02970.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1460+3593T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62589819 | ||||||
| chr17:62589931
|
C | T | 20 | a0001c0001t0003g0158a0001c0001t0003g0159a0001c0001t0003g0160others(17): Show | 20 | HG01069.hp1 HG01071.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1460+3705C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62589931 | ||||||
| chr17:62589957
|
C | T | 10 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0010g0280others(7): Show | 10 | HG01109.hp2 HG02451.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.1460+3731C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62589957 | ||||||
| chr17:62590096
|
C | T | 1 | a0001c0001t0001g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1460+3870C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62590096 | ||||||
| chr17:62590116
|
G | C | 1 | a0001c0002t0002g0004 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1460+3890G>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62590116 | ||||||
| chr17:62590462
|
C | G | 1 | a0001c0002t0007g0109 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1460+4236C>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62590462 | ||||||
| chr17:62590601
|
TTAA | T | 3 | a0001c0001t0006g0055a0001c0001t0006g0056a0001c0001t0006g0074 | 3 | HG02622.hp2 HG02970.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1460+4376_1460+437 others(7): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62590601 | ||||||
| chr17:62590604
|
A | C | 192 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0275others(189): Show | 192 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.1460+4378A>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62590604 | ||||||
| chr17:62591286
|
C | T | 1 | a0001c0002t0002g0080 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1460+5060C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62591286 | ||||||
| chr17:62591357
|
T | A | 2 | a0001c0002t0004g0139a0001c0002t0007g0109 | 2 | HG00323.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.1460+5131T>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62591357 | ||||||
| chr17:62591357
|
TA | T | 37 | a0001c0001t0001g0259a0001c0001t0004g0048a0001c0001t0004g0049others(34): Show | 37 | HG00438.hp1 HG01433.hp2 HG01884.hp1 others(34): Show |
intron_variant | MODIFIER | c.1460+5145delA | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr17 | 62591357 | |||||
| chr17:62591424
|
G | A | 3 | a0001c0001t0006g0055a0001c0001t0006g0056a0001c0001t0006g0074 | 3 | HG02622.hp2 HG02970.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1461-5161G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62591424 | ||||||
| chr17:62591473
|
C | T | 1 | a0001c0001t0001g0269 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1461-5112C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62591473 | ||||||
| chr17:62591653
|
G | A | 193 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0275others(190): Show | 193 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.1461-4932G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62591653 | ||||||
| chr17:62591849
|
T | C | 1 | a0001c0002t0007g0109 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1461-4736T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62591849 | ||||||
| chr17:62591925
|
G | A | 1 | a0001c0002t0005g0038 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1461-4660G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62591925 | ||||||
| chr17:62591971
|
C | T | 179 | a0001c0001t0003g0158a0001c0001t0003g0159a0001c0001t0003g0160others(176): Show | 179 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.1461-4614C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62591971 | ||||||
| chr17:62592036
|
C | T | 1 | a0001c0002t0002g0118 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1461-4549C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62592036 | ||||||
| chr17:62592114
|
C | T | 3 | a0001c0001t0010g0282a0001c0001t0010g0283a0001c0001t0017g0284 | 3 | HG01109.hp2 HG02451.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1461-4471C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62592114 | ||||||
| chr17:62592328
|
A | C | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1461-4257A>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62592328 | ||||||
| chr17:62592703
|
A | G | 2 | a0001c0002t0002g0012a0001c0002t0002g0022 | 2 | HG01167.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1461-3882A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62592703 | ||||||
| chr17:62592724
|
A | G | 1 | a0001c0001t0016g0186 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1461-3861A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62592724 | ||||||
| chr17:62592909
|
C | T | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1461-3676C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62592909 | ||||||
| chr17:62593546
|
A | G | 1 | a0001c0002t0002g0090 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1461-3039A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62593546 | ||||||
| chr17:62593558
|
G | A | 1 | a0001c0001t0017g0284 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1461-3027G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62593558 | ||||||
| chr17:62593570
|
A | G | 144 | a0001c0001t0004g0048a0001c0001t0004g0049a0001c0001t0004g0050others(141): Show | 144 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.1461-3015A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62593570 | ||||||
| chr17:62593784
|
A | C | 1 | a0001c0001t0001g0181 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1461-2801A>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62593784 | ||||||
| chr17:62593791
|
A | AT | 22 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0191others(19): Show | 22 | HG00738.hp2 HG01074.hp2 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.1461-2775dupT | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr17 | 62593791 | |||||
| chr17:62593791
|
AT | A | 6 | a0001c0001t0001g0178a0001c0001t0001g0274a0001c0001t0003g0160others(3): Show | 6 | HG01496.hp2 HG02922.hp2 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.1461-2775delT | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr17 | 62593791 | |||||
| chr17:62594268
|
C | T | 8 | a0001c0001t0010g0280a0001c0001t0010g0281a0001c0001t0010g0282others(5): Show | 8 | HG01109.hp2 HG02451.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1461-2317C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62594268 | ||||||
| chr17:62594493
|
G | A | 2 | a0001c0001t0026g0278a0001c0001t0027g0277 | 2 | HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1461-2092G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62594493 | ||||||
| chr17:62594631
|
A | G | 8 | a0001c0001t0010g0280a0001c0001t0010g0281a0001c0001t0010g0282others(5): Show | 8 | HG01109.hp2 HG02451.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1461-1954A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62594631 | ||||||
| chr17:62594789
|
T | TAC | 34 | a0001c0001t0001g0187a0001c0001t0001g0190a0001c0001t0001g0199others(31): Show | 34 | HG00140.hp2 HG00738.hp2 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.1461-1755_1461-175 others(6): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr17 | 62594789 | |||||
| chr17:62594789
|
T | TACAC | 7 | a0001c0001t0001g0020a0001c0001t0001g0180a0001c0001t0001g0271others(4): Show | 7 | HG01175.hp2 HG02293.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1461-1757_1461-175 others(8): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr17 | 62594789 | |||||
| chr17:62594789
|
TAC | T | 19 | a0001c0001t0001g0178a0001c0001t0001g0183a0001c0001t0001g0189others(16): Show | 19 | HG01109.hp2 HG02040.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1461-1755_1461-175 others(6): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr17 | 62594789 | |||||
| chr17:62594789
|
TACAC | T | 17 | a0001c0001t0001g0192a0001c0001t0001g0237a0001c0001t0001g0248others(14): Show | 17 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.1461-1757_1461-175 others(8): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr17 | 62594789 | |||||
| chr17:62594789
|
TACACAC | T | 5 | a0001c0001t0004g0048a0001c0001t0004g0049a0001c0001t0004g0050others(2): Show | 5 | HG00609.hp1 HG01884.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1461-1759_1461-175 others(10): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr17 | 62594789 | |||||
| chr17:62594789
|
TACACACA others(1): Show |
T | 55 | a0001c0001t0003g0158a0001c0001t0003g0160a0001c0001t0003g0161others(52): Show | 55 | HG00639.hp2 HG01069.hp1 HG01071.hp2 others(52): Show |
intron_variant | MODIFIER | c.1461-1761_1461-175 others(12): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr17 | 62594789 | |||||
| chr17:62594789
|
TACACACA others(3): Show |
T | 6 | a0001c0001t0001g0270a0001c0002t0002g0110a0001c0002t0002g0119others(3): Show | 6 | HG00733.hp2 HG01496.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1461-1763_1461-175 others(14): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr17 | 62594789 | |||||
| chr17:62594789
|
TACACACA others(5): Show |
T | 52 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0002t0002g0040others(49): Show | 52 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.1461-1765_1461-175 others(16): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr17 | 62594789 | |||||
| chr17:62594789
|
TACACACA others(9): Show |
T | 1 | a0001c0002t0003g0060 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1461-1769_1461-175 others(20): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr17 | 62594789 | |||||
| chr17:62594789
|
TACACACA others(11): Show |
T | 2 | a0001c0001t0001g0275a0001c0002t0003g0068 | 2 | HG02155.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1461-1771_1461-175 others(22): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr17 | 62594789 | |||||
| chr17:62594822
|
ACACACAC others(3): Show |
A | 1 | a0001c0002t0002g0095 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1461-1761_1461-175 others(14): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr17 | 62594822 | |||||
| chr17:62594968
|
G | T | 1 | a0001c0002t0007g0109 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1461-1617G>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62594968 | ||||||
| chr17:62594977
|
T | A | 1 | a0001c0002t0007g0109 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1461-1608T>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62594977 | ||||||
| chr17:62595081
|
C | T | 3 | a0001c0002t0004g0139a0001c0002t0004g0140a0001c0002t0022g0138 | 3 | HG01099.hp1 HG02055.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1461-1504C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62595081 | ||||||
| chr17:62595283
|
C | CT | 32 | a0001c0001t0001g0259a0001c0001t0003g0158a0001c0001t0003g0159others(29): Show | 32 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.1461-1281dupT | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr17 | 62595283 | |||||
| chr17:62595283
|
CT | C | 21 | a0001c0001t0001g0178a0001c0001t0001g0193a0001c0001t0001g0203others(18): Show | 21 | HG00323.hp2 HG00639.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.1461-1281delT | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr17 | 62595283 | |||||
| chr17:62595465
|
T | C | 10 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0010g0280others(7): Show | 10 | HG01109.hp2 HG02451.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.1461-1120T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62595465 | ||||||
| chr17:62596031
|
A | G | 2 | a0001c0001t0001g0276a0001c0001t0009g0286 | 2 | HG02630.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1461-554A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62596031 | ||||||
| chr17:62596068
|
A | G | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1461-517A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62596068 | ||||||
| chr17:62596158
|
T | A | 195 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0275others(192): Show | 195 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.1461-427T>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62596158 | ||||||
| chr17:62596492
|
A | G | 1 | a0001c0002t0007g0125 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1461-93A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62596492 | ||||||
| chr17:62596518
|
G | A | 10 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0010g0280others(7): Show | 10 | HG01109.hp2 HG02451.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.1461-67G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 16/21 | chr17 | 62596518 | ||||||
| chr17:62596718
|
T | C | 1 | a0001c0002t0002g0025 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1550+44T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 17/21 | chr17 | 62596718 | ||||||
| chr17:62596804
|
T | G | 1 | a0001c0001t0001g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1550+130T>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 17/21 | chr17 | 62596804 | ||||||
| chr17:62596978
|
C | T | 1 | a0001c0001t0021g0153 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1550+304C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 17/21 | chr17 | 62596978 | ||||||
| chr17:62596994
|
GT | G | 9 | a0001c0001t0004g0144a0001c0001t0004g0145a0001c0001t0004g0146others(6): Show | 9 | HG00738.hp2 HG01074.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.1550+329delT | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr17 | 62596994 | |||||
| chr17:62597164
|
A | G | 2 | a0001c0002t0011g0117a0001c0002t0011g0143 | 2 | NA18940.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.1550+490A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 17/21 | chr17 | 62597164 | ||||||
| chr17:62597399
|
C | T | 3 | a0001c0001t0006g0055a0001c0001t0006g0056a0001c0001t0006g0074 | 3 | HG02622.hp2 HG02970.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1550+725C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 17/21 | chr17 | 62597399 | ||||||
| chr17:62597421
|
A | T | 1 | a0001c0001t0001g0273 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1550+747A>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 17/21 | chr17 | 62597421 | ||||||
| chr17:62597509
|
C | A | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | NA18959.hp1 NA18999.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1550+835C>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 17/21 | chr17 | 62597509 | ||||||
| chr17:62597542
|
T | C | 1 | a0001c0002t0003g0157 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1550+868T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 17/21 | chr17 | 62597542 | ||||||
| chr17:62597744
|
T | G | 1 | a0001c0001t0003g0158 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1550+1070T>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 17/21 | chr17 | 62597744 | ||||||
| chr17:62597840
|
T | C | 1 | a0001c0001t0001g0189 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1550+1166T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 17/21 | chr17 | 62597840 | ||||||
| chr17:62598383
|
G | A | 1 | a0001c0001t0001g0210 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1550+1709G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 17/21 | chr17 | 62598383 | ||||||
| chr17:62598537
|
T | G | 1 | a0001c0002t0002g0011 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1550+1863T>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 17/21 | chr17 | 62598537 | ||||||
| chr17:62598579
|
C | T | 170 | a0001c0001t0003g0158a0001c0001t0003g0159a0001c0001t0003g0160others(167): Show | 170 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.1550+1905C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 17/21 | chr17 | 62598579 | ||||||
| chr17:62598873
|
T | C | 36 | a0001c0002t0003g0023a0001c0002t0003g0043a0001c0002t0003g0044others(33): Show | 36 | HG00438.hp1 HG01192.hp1 HG01261.hp1 others(33): Show |
intron_variant | MODIFIER | c.1551-1778T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 17/21 | chr17 | 62598873 | ||||||
| chr17:62598977
|
G | A | 1 | a0001c0001t0001g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1551-1674G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 17/21 | chr17 | 62598977 | ||||||
| chr17:62598992
|
C | T | 1 | a0001c0002t0003g0023 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1551-1659C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 17/21 | chr17 | 62598992 | ||||||
| chr17:62599165
|
T | G | 1 | a0001c0002t0004g0139 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1551-1486T>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 17/21 | chr17 | 62599165 | ||||||
| chr17:62599375
|
A | G | 9 | a0001c0002t0003g0043a0001c0002t0003g0044a0001c0002t0003g0045others(6): Show | 9 | HG01192.hp1 HG01943.hp2 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.1551-1276A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 17/21 | chr17 | 62599375 | ||||||
| chr17:62599455
|
G | A | 3 | a0001c0001t0010g0280a0001c0001t0010g0281a0001c0001t0017g0279 | 3 | HG02818.hp2 HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1551-1196G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 17/21 | chr17 | 62599455 | ||||||
| chr17:62599530
|
G | C | 1 | a0001c0001t0001g0233 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1551-1121G>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 17/21 | chr17 | 62599530 | ||||||
| chr17:62599606
|
C | T | 4 | a0001c0001t0004g0048a0001c0001t0004g0049a0001c0001t0004g0050others(1): Show | 4 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1551-1045C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 17/21 | chr17 | 62599606 | ||||||
| chr17:62599762
|
T | G | 1 | a0001c0001t0001g0180 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1551-889T>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 17/21 | chr17 | 62599762 | ||||||
| chr17:62600243
|
CA | C | 194 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0275others(191): Show | 194 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.1551-397delA | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr17 | 62600243 | |||||
| chr17:62600408
|
A | G | 1 | a0001c0001t0001g0292 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1551-243A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 17/21 | chr17 | 62600408 | ||||||
| chr17:62600437
|
A | G | 1 | a0001c0001t0021g0153 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1551-214A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 17/21 | chr17 | 62600437 | ||||||
| chr17:62600829
|
A | G | 1 | a0001c0001t0021g0153 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1720+9A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 18/21 | chr17 | 62600829 | ||||||
| chr17:62601004
|
G | A | 3 | a0001c0001t0001g0207a0001c0001t0001g0227a0001c0001t0001g0228 | 3 | HG02055.hp2 HG02965.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1720+184G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 18/21 | chr17 | 62601004 | ||||||
| chr17:62601315
|
A | G | 1 | a0001c0002t0002g0099 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1720+495A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 18/21 | chr17 | 62601315 | ||||||
| chr17:62601446
|
T | G | 1 | a0001c0002t0003g0077 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1721-596T>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 18/21 | chr17 | 62601446 | ||||||
| chr17:62601559
|
A | C | 1 | a0001c0001t0001g0195 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1721-483A>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 18/21 | chr17 | 62601559 | ||||||
| chr17:62601768
|
G | A | 193 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0275others(190): Show | 193 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.1721-274G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 18/21 | chr17 | 62601768 | ||||||
| chr17:62601799
|
C | T | 1 | a0001c0002t0007g0036 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1721-243C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 18/21 | chr17 | 62601799 | ||||||
| chr17:62601821
|
T | A | 5 | a0001c0001t0001g0205a0001c0001t0001g0215a0001c0001t0001g0234others(2): Show | 5 | HG00323.hp2 HG00741.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.1721-221T>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 18/21 | chr17 | 62601821 | ||||||
| chr17:62601918
|
G | A | 1 | a0001c0002t0002g0082 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1721-124G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 18/21 | chr17 | 62601918 | ||||||
| chr17:62601961
|
C | G | 2 | a0001c0001t0026g0278a0001c0001t0027g0277 | 2 | HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1721-81C>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 18/21 | chr17 | 62601961 | ||||||
| chr17:62602364
|
T | A | 1 | a0001c0001t0001g0276 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1859+184T>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | chr17 | 62602364 | ||||||
| chr17:62602574
|
C | G | 9 | a0001c0001t0004g0144a0001c0001t0004g0145a0001c0001t0004g0146others(6): Show | 9 | HG00738.hp2 HG01074.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.1859+394C>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | chr17 | 62602574 | ||||||
| chr17:62602797
|
G | C | 1 | a0001c0001t0026g0278 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1859+617G>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | chr17 | 62602797 | ||||||
| chr17:62602820
|
A | G | 1 | a0001c0002t0002g0133 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1859+640A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | chr17 | 62602820 | ||||||
| chr17:62603005
|
G | C | 1 | a0001c0001t0001g0225 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1859+825G>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | chr17 | 62603005 | ||||||
| chr17:62603006
|
C | T | 1 | a0001c0001t0001g0225 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1859+826C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | chr17 | 62603006 | ||||||
| chr17:62603008
|
T | A | 1 | a0001c0001t0001g0225 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1859+828T>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | chr17 | 62603008 | ||||||
| chr17:62603019
|
G | A | 26 | a0001c0001t0003g0158a0001c0001t0003g0159a0001c0001t0003g0160others(23): Show | 26 | HG01069.hp1 HG01071.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.1859+839G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | chr17 | 62603019 | ||||||
| chr17:62603107
|
A | C | 170 | a0001c0001t0003g0158a0001c0001t0003g0159a0001c0001t0003g0160others(167): Show | 170 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.1859+927A>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | chr17 | 62603107 | ||||||
| chr17:62603127
|
T | C | 1 | a0001c0001t0004g0172 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1859+947T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | chr17 | 62603127 | ||||||
| chr17:62603223
|
C | T | 2 | a0001c0001t0016g0185a0001c0001t0016g0186 | 2 | HG01243.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.1859+1043C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | chr17 | 62603223 | ||||||
| chr17:62603262
|
C | T | 1 | a0001c0002t0028g0005 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1859+1082C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | chr17 | 62603262 | ||||||
| chr17:62603348
|
A | T | 1 | a0001c0001t0001g0225 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1859+1168A>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | chr17 | 62603348 | ||||||
| chr17:62603625
|
T | C | 1 | a0001c0001t0027g0277 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1859+1445T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | chr17 | 62603625 | ||||||
| chr17:62603671
|
G | A | 1 | a0001c0001t0004g0172 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1859+1491G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | chr17 | 62603671 | ||||||
| chr17:62603753
|
G | C | 1 | a0001c0002t0011g0143 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1859+1573G>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | chr17 | 62603753 | ||||||
| chr17:62603818
|
C | T | 1 | a0001c0002t0002g0027 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1859+1638C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | chr17 | 62603818 | ||||||
| chr17:62603970
|
C | CTTTA | 3 | a0001c0001t0001g0190a0001c0001t0001g0203a0001c0001t0001g0291 | 3 | HG01496.hp1 HG02698.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1859+1838_1859+184 others(8): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr17 | 62603970 | |||||
| chr17:62603970
|
CTTTA | C | 100 | a0001c0001t0001g0191a0001c0001t0001g0197a0001c0001t0001g0198others(97): Show | 100 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.1859+1838_1859+184 others(8): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr17 | 62603970 | |||||
| chr17:62603970
|
CTTTATTT others(1): Show |
C | 65 | a0001c0001t0001g0176a0001c0001t0001g0182a0001c0001t0001g0183others(62): Show | 65 | HG00140.hp2 HG00280.hp1 HG01069.hp2 others(62): Show |
intron_variant | MODIFIER | c.1859+1834_1859+184 others(12): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr17 | 62603970 | |||||
| chr17:62603970
|
CTTTATTT others(5): Show |
C | 18 | a0001c0001t0001g0290a0001c0001t0003g0165a0001c0001t0003g0166others(15): Show | 18 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.1859+1830_1859+184 others(16): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr17 | 62603970 | |||||
| chr17:62603970
|
CTTTATTT others(9): Show |
C | 33 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0275others(30): Show | 33 | HG00738.hp2 HG01074.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.1859+1826_1859+184 others(20): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr17 | 62603970 | |||||
| chr17:62604007
|
T | C | 9 | a0001c0001t0004g0144a0001c0001t0004g0145a0001c0001t0004g0146others(6): Show | 9 | HG00738.hp2 HG01074.hp2 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.1859+1827T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | chr17 | 62604007 | ||||||
| chr17:62604085
|
G | T | 2 | a0001c0001t0026g0278a0001c0001t0027g0277 | 2 | HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1859+1905G>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | chr17 | 62604085 | ||||||
| chr17:62604153
|
C | T | 1 | a0001c0002t0007g0123 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1859+1973C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | chr17 | 62604153 | ||||||
| chr17:62604254
|
G | A | 1 | a0001c0002t0003g0141 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1860-1876G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | chr17 | 62604254 | ||||||
| chr17:62604255
|
C | T | 3 | a0001c0001t0006g0055a0001c0001t0006g0056a0001c0001t0006g0074 | 3 | HG02622.hp2 HG02970.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1860-1875C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | chr17 | 62604255 | ||||||
| chr17:62604277
|
G | C | 2 | a0001c0001t0026g0278a0001c0001t0027g0277 | 2 | HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1860-1853G>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | chr17 | 62604277 | ||||||
| chr17:62604295
|
C | T | 1 | a0001c0001t0001g0291 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1860-1835C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | chr17 | 62604295 | ||||||
| chr17:62604299
|
G | A | 1 | a0001c0001t0008g0174 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1860-1831G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | chr17 | 62604299 | ||||||
| chr17:62604307
|
G | C | 1 | a0001c0002t0002g0027 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1860-1823G>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | chr17 | 62604307 | ||||||
| chr17:62604372
|
G | T | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1860-1758G>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | chr17 | 62604372 | ||||||
| chr17:62604405
|
CAT | C | 193 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0275others(190): Show | 193 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.1860-1710_1860-170 others(6): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr17 | 62604405 | |||||
| chr17:62604412
|
A | G | 15 | a0001c0001t0001g0176a0001c0001t0001g0182a0001c0001t0001g0183others(12): Show | 15 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1860-1718A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | chr17 | 62604412 | ||||||
| chr17:62604448
|
C | T | 2 | a0001c0002t0004g0140a0001c0002t0022g0138 | 2 | HG02055.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1860-1682C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | chr17 | 62604448 | ||||||
| chr17:62604606
|
T | A | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1860-1524T>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | chr17 | 62604606 | ||||||
| chr17:62604619
|
A | G | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1860-1511A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | chr17 | 62604619 | ||||||
| chr17:62604737
|
C | T | 170 | a0001c0001t0003g0158a0001c0001t0003g0159a0001c0001t0003g0160others(167): Show | 170 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.1860-1393C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | chr17 | 62604737 | ||||||
| chr17:62604781
|
C | T | 2 | a0001c0001t0001g0253a0001c0001t0001g0262 | 2 | NA19005.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1860-1349C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | chr17 | 62604781 | ||||||
| chr17:62604825
|
A | G | 195 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0275others(192): Show | 195 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.1860-1305A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | chr17 | 62604825 | ||||||
| chr17:62605155
|
A | C | 4 | a0001c0001t0004g0048a0001c0001t0004g0049a0001c0001t0004g0050others(1): Show | 4 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1860-975A>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | chr17 | 62605155 | ||||||
| chr17:62605182
|
C | T | 1 | a0001c0002t0002g0039 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1860-948C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | chr17 | 62605182 | ||||||
| chr17:62605231
|
G | A | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1860-899G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | chr17 | 62605231 | ||||||
| chr17:62605294
|
G | A | 1 | a0001c0002t0002g0092 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1860-836G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | chr17 | 62605294 | ||||||
| chr17:62605295
|
G | A | 3 | a0001c0001t0012g0148a0001c0001t0012g0149a0001c0001t0012g0151 | 3 | HG00738.hp2 HG01074.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.1860-835G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | chr17 | 62605295 | ||||||
| chr17:62605347
|
C | T | 3 | a0001c0002t0004g0139a0001c0002t0004g0140a0001c0002t0022g0138 | 3 | HG01099.hp1 HG02055.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1860-783C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | chr17 | 62605347 | ||||||
| chr17:62605457
|
A | G | 2 | a0001c0001t0006g0056a0001c0001t0006g0074 | 2 | HG02622.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1860-673A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | chr17 | 62605457 | ||||||
| chr17:62605494
|
T | C | 1 | a0001c0001t0001g0180 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1860-636T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | chr17 | 62605494 | ||||||
| chr17:62605500
|
G | A | 2 | a0001c0001t0001g0206a0001c0001t0001g0264 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1860-630G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | chr17 | 62605500 | ||||||
| chr17:62605531
|
C | T | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1860-599C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | chr17 | 62605531 | ||||||
| chr17:62605563
|
G | A | 4 | a0001c0001t0004g0048a0001c0001t0004g0049a0001c0001t0004g0050others(1): Show | 4 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1860-567G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | chr17 | 62605563 | ||||||
| chr17:62605899
|
TGGGAGGC others(25): Show |
T | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1860-224_1860-193d others(34): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr17 | 62605899 | |||||
| chr17:62606006
|
C | CA | 12 | a0001c0001t0001g0206a0001c0001t0003g0159a0001c0001t0003g0175others(9): Show | 12 | HG00738.hp2 HG01952.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1860-104dupA | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr17 | 62606006 | |||||
| chr17:62606006
|
C | CAA | 7 | a0001c0001t0006g0056a0001c0001t0010g0280a0001c0001t0010g0283others(4): Show | 7 | HG01109.hp2 HG02622.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1860-105_1860-104d others(4): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr17 | 62606006 | |||||
| chr17:62606006
|
CA | C | 162 | a0001c0001t0001g0020a0001c0001t0001g0176a0001c0001t0001g0178others(159): Show | 162 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.1860-104delA | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr17 | 62606006 | |||||
| chr17:62606006
|
CAA | C | 27 | a0001c0001t0001g0239a0001c0001t0001g0289a0001c0002t0003g0023others(24): Show | 27 | HG00438.hp1 HG01168.hp2 HG01261.hp1 others(24): Show |
intron_variant | MODIFIER | c.1860-105_1860-104d others(4): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr17 | 62606006 | |||||
| chr17:62606024
|
A | C | 2 | a0001c0001t0001g0258a0001c0002t0003g0072 | 2 | HG01934.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1860-106A>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | chr17 | 62606024 | ||||||
| chr17:62606028
|
G | A | 1 | a0001c0001t0001g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1860-102G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | chr17 | 62606028 | ||||||
| chr17:62606037
|
A | G | 5 | a0001c0002t0003g0043a0001c0002t0003g0044a0001c0002t0003g0045others(2): Show | 5 | HG01192.hp1 HG01943.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.1860-93A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 19/21 | chr17 | 62606037 | ||||||
| chr17:62606287
|
GCA | G | 5 | a0001c0001t0006g0041a0001c0001t0006g0042a0001c0001t0006g0055others(2): Show | 5 | HG02622.hp2 HG02647.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1971+59_1971+60del others(2): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr17 | 62606287 | |||||
| chr17:62606303
|
T | G | 1 | a0001c0001t0001g0276 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1971+62T>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 20/21 | chr17 | 62606303 | ||||||
| chr17:62606807
|
T | G | 1 | a0001c0002t0002g0096 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1971+566T>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 20/21 | chr17 | 62606807 | ||||||
| chr17:62606877
|
A | G | 2 | a0001c0002t0002g0154a0001c0002t0005g0155 | 2 | HG01978.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1971+636A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 20/21 | chr17 | 62606877 | ||||||
| chr17:62606893
|
C | T | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | NA18959.hp1 NA18999.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1971+652C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 20/21 | chr17 | 62606893 | ||||||
| chr17:62607012
|
C | CAT | 3 | a0001c0001t0006g0055a0001c0001t0006g0056a0001c0001t0006g0074 | 3 | HG02622.hp2 HG02970.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1971+771_1971+772i others(4): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 20/21 | chr17 | 62607012 | ||||||
| chr17:62607012
|
C | CT | 114 | a0001c0001t0001g0020a0001c0001t0001g0176a0001c0001t0001g0178others(111): Show | 114 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.1971+789dupT | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr17 | 62607012 | |||||
| chr17:62607012
|
C | CTT | 153 | a0001c0001t0003g0175a0001c0001t0004g0048a0001c0001t0004g0049others(150): Show | 153 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.1971+788_1971+789d others(4): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr17 | 62607012 | |||||
| chr17:62607012
|
C | CTTT | 9 | a0001c0001t0001g0275a0001c0002t0002g0009a0001c0002t0002g0097others(6): Show | 9 | HG00323.hp1 HG01168.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1971+787_1971+789d others(5): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr17 | 62607012 | |||||
| chr17:62607100
|
A | T | 1 | a0001c0002t0002g0034 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1971+859A>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 20/21 | chr17 | 62607100 | ||||||
| chr17:62607413
|
C | T | 1 | a0001c0002t0003g0062 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1972-628C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 20/21 | chr17 | 62607413 | ||||||
| chr17:62607520
|
C | T | 1 | a0001c0001t0001g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1972-521C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 20/21 | chr17 | 62607520 | ||||||
| chr17:62607615
|
C | G | 1 | a0001c0001t0001g0196 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1972-426C>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 20/21 | chr17 | 62607615 | ||||||
| chr17:62607622
|
T | C | 1 | a0001c0001t0001g0020 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1972-419T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 20/21 | chr17 | 62607622 | ||||||
| chr17:62607723
|
G | T | 1 | a0001c0002t0002g0106 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1972-318G>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 20/21 | chr17 | 62607723 | ||||||
| chr17:62608288
|
C | T | 6 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0233others(3): Show | 6 | HG01074.hp1 HG01515.hp2 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.2079+140C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 21/21 | chr17 | 62608288 | ||||||
| chr17:62608446
|
G | A | 3 | a0001c0001t0001g0192a0001c0001t0001g0248a0001c0001t0001g0249 | 3 | HG01884.hp2 HG01891.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2079+298G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 21/21 | chr17 | 62608446 | ||||||
| chr17:62608637
|
C | T | 2 | a0001c0002t0002g0136a0001c0002t0005g0137 | 2 | NA19007.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.2079+489C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 21/21 | chr17 | 62608637 | ||||||
| chr17:62608659
|
G | A | 1 | a0001c0002t0003g0078 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2079+511G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 21/21 | chr17 | 62608659 | ||||||
| chr17:62608702
|
A | G | 1 | a0001c0002t0003g0068 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2079+554A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 21/21 | chr17 | 62608702 | ||||||
| chr17:62608705
|
A | T | 291 | a0001c0001t0001g0020a0001c0001t0001g0176a0001c0001t0001g0178others(288): Show | 291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.2079+557A>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 21/21 | chr17 | 62608705 | ||||||
| chr17:62608744
|
G | A | 1 | a0001c0001t0001g0219 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2079+596G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 21/21 | chr17 | 62608744 | ||||||
| chr17:62608854
|
C | CA | 195 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0275others(192): Show | 195 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.2079+706_2079+707i others(3): Show |
TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 21/21 | chr17 | 62608854 | ||||||
| chr17:62609259
|
T | C | 2 | a0001c0001t0001g0199a0001c0001t0001g0209 | 2 | NA18990.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.2079+1111T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 21/21 | chr17 | 62609259 | ||||||
| chr17:62609283
|
C | T | 179 | a0001c0001t0003g0158a0001c0001t0003g0159a0001c0001t0003g0160others(176): Show | 179 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.2079+1135C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 21/21 | chr17 | 62609283 | ||||||
| chr17:62609344
|
A | G | 1 | a0001c0002t0003g0141 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2079+1196A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 21/21 | chr17 | 62609344 | ||||||
| chr17:62609563
|
T | C | 2 | a0001c0002t0011g0117a0001c0002t0011g0143 | 2 | NA18940.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.2079+1415T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 21/21 | chr17 | 62609563 | ||||||
| chr17:62609819
|
A | T | 1 | a0001c0002t0003g0060 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2079+1671A>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 21/21 | chr17 | 62609819 | ||||||
| chr17:62609829
|
G | A | 1 | a0001c0001t0001g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2079+1681G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 21/21 | chr17 | 62609829 | ||||||
| chr17:62610279
|
C | T | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2080-2113C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 21/21 | chr17 | 62610279 | ||||||
| chr17:62610573
|
G | A | 1 | a0001c0001t0001g0291 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2080-1819G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 21/21 | chr17 | 62610573 | ||||||
| chr17:62610602
|
A | C | 1 | a0001c0001t0001g0020 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2080-1790A>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 21/21 | chr17 | 62610602 | ||||||
| chr17:62610633
|
G | A | 5 | a0001c0001t0006g0041a0001c0001t0006g0042a0001c0001t0006g0055others(2): Show | 5 | HG02622.hp2 HG02647.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2080-1759G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 21/21 | chr17 | 62610633 | ||||||
| chr17:62610787
|
A | C | 36 | a0001c0002t0002g0003a0001c0002t0002g0004a0001c0002t0002g0007others(33): Show | 36 | HG00609.hp1 HG01167.hp1 HG01192.hp2 others(33): Show |
intron_variant | MODIFIER | c.2080-1605A>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 21/21 | chr17 | 62610787 | ||||||
| chr17:62610823
|
T | C | 1 | a0001c0001t0001g0276 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2080-1569T>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 21/21 | chr17 | 62610823 | ||||||
| chr17:62611098
|
C | T | 1 | a0001c0001t0008g0174 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2080-1294C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 21/21 | chr17 | 62611098 | ||||||
| chr17:62611101
|
G | T | 2 | a0001c0001t0016g0185a0001c0001t0016g0186 | 2 | HG01243.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.2080-1291G>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 21/21 | chr17 | 62611101 | ||||||
| chr17:62611333
|
G | A | 1 | a0001c0001t0001g0270 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2080-1059G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 21/21 | chr17 | 62611333 | ||||||
| chr17:62611558
|
A | G | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2080-834A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 21/21 | chr17 | 62611558 | ||||||
| chr17:62611691
|
A | C | 2 | a0001c0002t0003g0066a0001c0002t0003g0067 | 2 | NA18952.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.2080-701A>C | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 21/21 | chr17 | 62611691 | ||||||
| chr17:62611741
|
A | T | 1 | a0001c0001t0003g0175 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2080-651A>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 21/21 | chr17 | 62611741 | ||||||
| chr17:62611746
|
G | A | 1 | a0001c0001t0001g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2080-646G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 21/21 | chr17 | 62611746 | ||||||
| chr17:62611819
|
G | A | 5 | a0001c0002t0002g0099a0001c0002t0013g0100a0001c0002t0013g0101others(2): Show | 5 | HG02015.hp1 NA18977.hp1 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.2080-573G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 21/21 | chr17 | 62611819 | ||||||
| chr17:62611836
|
A | G | 1 | a0001c0001t0009g0285 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2080-556A>G | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 21/21 | chr17 | 62611836 | ||||||
| chr17:62611920
|
G | A | 1 | a0001c0001t0001g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2080-472G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 21/21 | chr17 | 62611920 | ||||||
| chr17:62611940
|
G | A | 1 | a0001c0002t0003g0045 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2080-452G>A | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 21/21 | chr17 | 62611940 | ||||||
| chr17:62612059
|
C | T | 1 | a0001c0001t0001g0202 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2080-333C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 21/21 | chr17 | 62612059 | ||||||
| chr17:62612222
|
C | T | 2 | a0001c0001t0001g0199a0001c0001t0001g0209 | 2 | NA18990.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.2080-170C>T | TLK2 | ENSG00000146872.19 | transcript | ENST00000346027.10 | protein_coding | 21/21 | chr17 | 62612222 |